bims-fagtap Biomed News
on Phage therapies and applications
Issue of 2026–07–26
47 papers selected by
Luca Bolliger, lxBio



  1. Front Cell Infect Microbiol. 2026 ;16 1879718
      The advancement of synthetic biology and the rise of antimicrobial resistance have led to the development of bacteriophage therapy for more than antibacterial applications. This review focuses on applications to multidrug-resistant infections, biofilm diseases, cancer research, veterinary medicine and animal production. Recent research suggests phages can be used in combination with antibiotics to enhance treatment of large multidrug resistant pathogens such as Pseudomonas aeruginosa, Acinetobacter baumannii and Klebsiella pneumoniae. This could also help to restore antibiotic sensitivity by making bacteria change resistance related structures or mechanisms. Despite this, there are several challenges for the use of phage therapy prior to its widespread clinical application, including phage resistance, difference in patient response, unknown pharmacokinetic parameters, immune issues, and unclear regulatory guidelines. Additionally, in some cases, phages could also play a role in horizontal gene transfer, raising further safety concerns. Beyond antimicrobial therapy, phage display platforms derived from M13, T7 and λ phages have enabled the identification of tumor-targeting peptides, the development of immunomodulatory constructs, and targeted delivery of therapeutic molecules. Over 100 clinical cases and 44 registered trials support the generally favorable safety profile of personalized phage therapy, and highlight the need for better treatment standardization, controlled clinical evaluation, and better regulatory processes. Additionally, engineered phages expressing biofilm degrading enzymes represent promising tools for disrupting matrix-embedded bacterial communities associated with chronic infections and medical devices. In summary, CRISPR-based engineering and genome refactoring highlight the potential of phage-based therapeutics as complements to conventional antimicrobial therapy, although their broader use depends on overcoming biological, clinical, and regulatory challenges.
    Keywords:  antimicrobial resistance; bacteriophage therapy; biofilm eradication; personalized medicine; phage antibiotic synergy
    DOI:  https://doi.org/10.3389/fcimb.2026.1879718
  2. Int J Pharm. 2026 Jul 22. pii: S0378-5173(26)00672-1. [Epub ahead of print]702 127224
      The global rise of antimicrobial resistance poses a persistent challenge in chronic wound care, where limited perfusion and biofilm-embedded bacterial communities severely restrict the efficacy of conventional antibiotics. Despite renewed interest and promising approaches, bacteriophage-based therapy remains constrained by intrinsic phage susceptibility to complex wound environments and the emergence of phage resistance. While synergistic pairings of phages and antibiotics offer a compelling strategy to counteract these limitations, the lack of systems capable of protecting and delivering respective pairs continues to impair clinical translation. To address these challenges, we developed an electrospun nanofiber-based co-delivery platform that spatially separates the lytic bacteriophage JG004 and the β-lactam antibiotic aztreonam within a protective core-shell matrix. The nanofibers exhibit high mechanical robustness, maintain phage viability for at least 28 days, and enable rapid release of both antimicrobials, while reducing exposure to environmental and oxidative stresses. In vitro assays revealed pronounced phage-antibiotic synergy, achieving up to 99% bacterial reduction of Pseudomonas aeruginosa, outperforming the corresponding monotherapies in treatment of both planktonic and biofilm-associated bacteria. Additionally, the modular architecture of our delivery system enables flexible integration of alternative phage-antibiotic pairings, enabling rapid adaptation to patient-specific pathogens and resistance profiles. By combining sustained antimicrobial performance with a clinically adaptable delivery system, this nanofiber platform offers a promising route towards personalized infection management and supports the clinical integration of phage-based strategies into modern wound care.
    Keywords:  Biofilm infection; Core–shell nanofibers; Electrospinning; Localized anti-infective therapy; Phage-antibiotic-synergy; Pseudomonas aeruginosa
    DOI:  https://doi.org/10.1016/j.ijpharm.2026.127224
  3. Front Microbiol. 2026 ;17 1876186
      Burkholderia gladioli is an opportunistic pathogen with intrinsic antimicrobial resistance and is therefore a compelling target for phage therapy (PT), yet bacteriophages infecting this species remain largely uncharacterized. Here, we show that the functionally lytic (FL), lipopolysaccharide (LPS)-binding myovirus KS12, originally isolated against Burkholderia cenocepacia, suppresses B. gladioli growth in vitro and infection-associated mortality in Galleria mellonella. KS12 selects for resistant subpopulations carrying mutations in the O-antigen biosynthesis and export pathways that compromise outer membrane (OM) integrity, resulting in attenuated virulence in vivo and hypersensitivity to human serum, antimicrobial peptides, and polymyxins. Consistent with this trade-off, KS12 and colistin interact synergistically to substantially reduce bacterial densities, suggesting that predation by KS12 may impose an evolutionary trap on B. gladioli. Furthermore, comparative analyses indicate that outer membrane permeability correlates strongly with colistin susceptibility across Gram-negative pathogens, implying that antivirulence steering with LPS-binding phages could provide a strategy to sensitize intrinsically resistant pathogens to antibiotics of last resort. Although KS12 particles were inactivated by innate humoral immunity, they did not appear to be degraded by or stimulate pro-inflammatory responses in phagocytes, indicating that the antibacterial activity of this phage is not driven by direct immunostimulation. Together, these results identify KS12 as a promising phage targeting B. gladioli and highlight the potential of LPS-binding phages to steer bacterial populations toward attenuated virulence and hypersensitivity, thereby yielding more clinically tractable phenotypes.
    Keywords:  Burkholderia gladioli; bacteriophage; lipopolysaccharide; membrane permeability; phage immunogenicity; phage steering; phage therapy; phage-antibiotic synergy
    DOI:  https://doi.org/10.3389/fmicb.2026.1876186
  4. J Fish Dis. 2026 Jul 24. e70246
      The aquaculture sector faces increasing challenges from bacterial diseases and growing restrictions on antibiotic use due to concerns regarding antimicrobial resistance (AMR). Phage therapy, the therapeutic application of bacteriophages to selectively infect and lyse pathogenic bacteria, offers a targeted strategy to combat AMR pathogens while minimizing ecological disruption. This review synthesizes current evidence on major bacterial pathogens in aquaculture, with particular emphasis on infections caused by Aeromonas, Vibrio, Edwardsiella, Flavobacterium and Streptococcus species. Available in vivo studies indicate that phage-based interventions, particularly phage cocktails, can significantly improve survival rates in aquaculture species, including catfish, salmonids, and shrimp. However, the current evidence base is dominated by laboratory challenge studies, and substantial heterogeneity in experimental designs, outcome measures, dosing strategies, and host-pathogen systems limits direct cross-study comparisons and broader translational interpretation. Additional challenges include large-scale field implementation, the emergence of phage-resistant bacterial variants, formulation and delivery constraints, and the absence of standardized regulatory frameworks. This review critically evaluates the translational readiness of phage therapy in aquaculture, examines advances in phage isolation, formulation and delivery strategies, and discusses key practical, regulatory and scientific barriers to commercial adoption. Finally, it identifies priority research areas and strategic investments required to facilitate the transition of phage therapy from experimental proof-of-concept to routine practice.
    Keywords:  antimicrobial resistance (AMR); aquaculture disease management; aquatic animal health; bacteriophages; fish bacterial diseases; phage therapy; regulatory challenges; therapeutic efficacy
    DOI:  https://doi.org/10.1111/jfd.70246
  5. J Dent. 2026 Jul 24. pii: S0300-5712(26)00597-X. [Epub ahead of print] 106927
       OBJECTIVE: This systematic review investigated differences in the oral microbiome among dentate older adults, edentate older adults, and older adults wearing complete dentures (CDs).
    DATA AND SOURCES: Online databases (PubMed, Embase, and the Cochrane Library) were systematically searched. The last search update was on 16th April 2026.
    STUDY SELECTION AND METHODS: Studies were eligible if they reported on oral microbiome outcomes in older adults (≥65 years) who were dentate or edentate (with and without CDs). Meta-analyses were performed for studies comparing edentate versus dentate individuals and for studies evaluating pre- and post-CD insertion.
    RESULTS: Fifteen studies (descriptive analysis: n = 10; meta-analysis: n = 5) were included from 444 identified records. Two studies reported lower microbial diversity and distinct microbial patterns in edentate individuals, with or without CDs, compared with dentate individuals. Two studies reported that individuals with denture stomatitis exhibited different microbial patterns from healthy CD wearers, suggesting microbial dysbiosis. The meta-analysis revealed that Porphyromonas gingivalis (p < 0.001), Tannerella forsythia (p < 0.001), Treponema denticola (p < 0.001), and Prevotella intermedia (p < 0.001) were less prevalent in edentate than dentate individuals. While Porphyromonas gingivalis (p = 0.002) and Tannerella forsythia (p = 0.006) increased during short-term follow-up after CD insertion. Risk of bias ranged from low to moderate.
    CONCLUSIONS: The review concluded that edentate older adults had a distinct oral microbiome when compared with dentate older adults. Denture stomatitis in CD wearers was associated with microbial dysbiosis. The review further found that P. Gingivalis and T. Forsythia may reappear transiently in edentate older adults rehabilitated with CDs.
    CLINICAL SIGNIFICANCE: In older adults, CD therapy requires consistent follow-up with an emphasis on maintaining optimal mucosal health and denture hygiene. Although longitudinal evidence on changes in species associated with periodontitis remains limited, the prevention and management of denture stomatitis-associated dysbiosis should be prioritized because it may contribute to inflammaging.
    Keywords:  Complete Denture; Edentulism; Geriatric dentistry; Gerodontology; Meta-analysis; Older Adult; Oral Microbiome; Systematic Review
    DOI:  https://doi.org/10.1016/j.jdent.2026.106927
  6. Microbiol Spectr. 2026 Jul 20. e0397925
      Colibacillosis, caused by avian pathogenic Escherichia coli (APEC), results in substantial economic losses in global poultry production. The emergence of multidrug-resistant (MDR) APEC poses zoonotic risks through horizontal transfer of antimicrobial resistance (AMR) genes. Bacteriophage therapy emerges as a safe alternative to antibiotherapy; however, comprehensive characterization of phages targeting MDR-APEC from diverse geographical regions remains limited. We isolated five lytic bacteriophages from poultry fecal samples collected from five Indian states and characterized them through morphological analysis, physiological stability testing, whole-genome sequencing, and in vivo efficacy assessment. Host range was determined against APEC isolates, and therapeutic potential was validated in the Galleria mellonella infection model. All phages showed Myovirus-like morphology and stability across physiologically relevant temperatures (up to 55°C-70°C) and pH conditions (3-11). Phages were classified as Escherichia phage vB_EcoM_fRPOT1, vB_EcoM_fDMYT1, vB_EcoM_fBSZT1, vB_EcoM_fUAMT1, and vB_EcoM_fPKPT2. Their genome size ranges from 170 to 356 kb, belonging to three distinct genera: Dhakavirus, Gaprivervirus, and Asteriusvirus. Genomic analysis confirmed the absence of antimicrobial resistance, virulence, toxin, or lysogeny genes. Fifty-one APEC strains were isolated, of which 23 (45.1%) were MDR. Individual phages lysed 37%-51% of tested APEC and 17%-39% of MDR strains. Three phages (fBSZT1, fUAMT1, and fPKPT2) significantly improved larval survival to 60%-80% at an MOI of 10 in G. mellonella infection models compared to the untreated control. This study establishes a well-characterized phage bank targeting MDR-APEC strains, providing a foundation for developing phage-based interventions to reduce antibiotic dependency and mitigate AMR transmission risks under the One Health framework.
    IMPORTANCE: The overuse of antibiotics in poultry farming has created a crisis. The multidrug-resistant (MDR) bacteria threaten both animal health and human safety through the food chain. When antibiotics fail, farmers face devastating losses, and resistant bacteria can transfer to humans through consumption or environmental contamination. Bacteriophages offer a practical solution as they kill target bacteria without harming beneficial microbes or leaving chemical residues. Our comprehensive characterization confirms that these five phages are safe and effective as they lack any resistance or toxin genes and rescue 60%-80% of infected larvae. This represents a characterized phage bank targeting the specific resistant strains in Indian poultry. By providing a validated alternative to antibiotics, this work supports sustainable food production while reducing the spread of antimicrobial resistance from farms to humans.
    Keywords:  Galleria mellonella; One Health; avian pathogenic Escherichia coli (APEC); bacteriophage therapy; genomics; multidrug resistance (MDR)
    DOI:  https://doi.org/10.1128/spectrum.03979-25
  7. Cureus. 2026 Jun;18(6): e110999
       BACKGROUND: Neutrophil gelatinase-associated lipocalin (NGAL) is an inflammatory biomarker implicated in periodontal tissue destruction and tumor progression. Tobacco use, both smoked and smokeless, is a key risk factor for periodontitis and oral squamous cell carcinoma (OSCC) and may influence NGAL expression. However, comparative evaluation of salivary NGAL levels across periodontal disease, tobacco users, and OSCC remains limited.
    AIM: To compare salivary NGAL levels among patients with OSCC, periodontitis, smoked tobacco users, smokeless tobacco (SLT) users, and healthy controls, and to assess the correlation of NGAL levels with periodontal clinical parameters.
    MATERIALS AND METHODS: This cross-sectional study included 125 participants divided into five groups (n = 25 each): OSCC, periodontitis, smokers, SLT users, and healthy controls. Periodontal parameters such as Oral Hygiene Index (OHI), Russell's Periodontal Index, probing pocket depth (PPD), and clinical attachment level (CAL) were recorded. Unstimulated whole saliva samples were collected and analyzed for NGAL levels using enzyme-linked immunosorbent assay (ELISA). Statistical analysis was performed using analysis of variance (ANOVA) with Tukey's post-hoc test and Pearson's correlation analysis (p < 0.05).
    RESULTS: Salivary NGAL levels showed a statistically significant difference among all groups (p < 0.001), with the highest levels observed in SLT users, followed by patients with OSCC, patients with periodontitis, smoked tobacco users, and healthy controls. Periodontal parameters were significantly worse in patients with periodontitis and SLT users, with no significant difference between these two groups. Salivary NGAL exhibited strong positive correlations with OHI, Russell's Index, PPD, and CAL (p < 0.001).
    CONCLUSION: Elevated salivary NGAL levels are significantly associated with periodontal disease severity, both smoked and SLT use, and OSCC. NGAL shows promise as a potential non-invasive biomarker for assessing inflammatory burden and disease risk in periodontal and tobacco-related oral conditions.
    Keywords:  neutrophil gelatinase-associated lipocalin; oral squamous cell carcinoma; periodontitis; saliva; smoked tobacco; smokeless tobacco
    DOI:  https://doi.org/10.7759/cureus.110999
  8. Front Pharmacol. 2026 ;17 1907819
      
    Keywords:  antimicrobial resistance; drug repurposing; infectious disease pharmacology; neglected tropical diseases; phage therapy; pharmacokinetics/pharmacodynamics; precision medicine; therapeutic drug monitoring
    DOI:  https://doi.org/10.3389/fphar.2026.1907819
  9. Cancer Cell Int. 2026 Jul 22. pii: 269. [Epub ahead of print]26(1):
      Originating in the mucosal lining of the mouth, oral squamous cell carcinoma is the most common malignancy of the head and neck regions. Its pathogenesis is multifactorial, involving environmental exposures, genetic susceptibility, and lifestyle-related risk factors. Increasing evidence indicates that oral microbial dysbiosis contributes to the initiation and progression of OSCC. Under healthy conditions, the oral cavity harbors a diverse and functionally balanced microbial ecosystem that maintains mucosal integrity, supports immune homeostasis, and prevents colonization by pathogenic species. Disruption of this equilibrium, known as oral dysbiosis, is increasingly recognized as a key event in oral carcinogenesis. In OSCC, a shift toward pathogenic and pro-inflammatory microbial communities has been consistently observed, particularly involving periodontal bacteria such as Porphyromonas gingivalis, Treponema denticola, and Fusobacterium nucleatum. These organisms contribute to tumor progression by activating inflammatory and oncogenic signaling pathways, including NF-κB, STAT3, and PI3K/Akt; suppressing apoptosis; inducing epithelial-mesenchymal transition; and immune evasion, thereby creating a tumor-promoting microenvironment. In addition to bacterial dysbiosis, viral and fungal components of the oral microbiome may act as important cofactors in OSCC. High-risk Epstein-Barr virus (EBV) and human papillomavirus (HPV) have been implicated in disrupting tumor suppressor pathways, causing genomic instability, and modulating the immune response. Fungal species, particularly Candida albicans, may further contribute by producing carcinogenic metabolites and inducing chronic inflammation. This review provides an integrated overview of the oral microbiome in OSCC, focusing on the composition and protective roles of the core microbiota, factors influencing microbial stability, and mechanisms by which dysbiosis contributes to carcinogenesis. It also highlights the oral microbiome as a potential source of non-invasive biomarkers and discusses microbiome-targeted strategies, including prebiotics, probiotics, and postbiotics, as promising adjunctive approaches to restore microbial balance and reduce tumor-promoting inflammation.
    Keywords:   Fusobacterium nucleatum ; Porphyromonas gingivalis ; Treponema denticola ; Dysbiosis; Oncogenic viruses; Oral microbiome; Oral squamous cell carcinoma
    DOI:  https://doi.org/10.1186/s12935-026-04414-z
  10. JAAD Case Rep. 2026 Aug;74 192-194
      
    Keywords:  Darier disease; bacteriophage therapy; cutaneous dysbiosis; genodermatosis; keratosis follicularis; multidrug-resistant infection
    DOI:  https://doi.org/10.1016/j.jdcr.2026.06.010
  11. Iran J Vet Res. 2025 ;26(3): 213-228
      Today, many poultry production systems require no antibiotics ever. Due to the unavailability of novel antibiotics for veterinary use, presence of multidrug resistant bacteria, and official banning of many antibiotic classes for use in veterinary medicine for production animals, the need for alternative therapeutics such as competitive exclusion compounds, vaccines, nano-medicine, etc. has become an urgent need. In this context, bacteriophages are regarded as an antibiotic alternative. Bacteriophages are viruses that target to infect, replicate, and lyse numerus types of bacteria in humans, animals, water, plants, and food. They are classified into several orders and 15 families. Different preparations of bacteriophages have been approved by the United States of Food and Drug Administration for managing some bacterial infections. They have been globally used in the poultry production and processing. Therefore, the present review intends to expose every aspect of bacteriophages in poultry health and production which include the mechanisms of phages as therapeutics, their usage in the industry, and the limitations/threats associated with the usage of bacteriophages.
    Keywords:  Bacteriophages; Chickens; Immunity; Limitations; Performance
    DOI:  https://doi.org/10.22099/ijvr.2025.51640.7678
  12. mSystems. 2026 Jul 20. e0050526
      When bacteriophages infect starved host bacteria, the restrictive host physiology may lead to prolonged latent periods and/or reduced burst sizes, compared to infection of a fast-growing bacterium. Using a mathematical model, we explore a system of two types of virulent phages that have distinct host physiology dependencies and are infecting a shared bacterial host population. We consider different environmental regimes to test whether they can compete and coexist under fluctuating conditions, putting emphasis on phases with limited resources for bacterial growth. We find that the fitness of a phage that can modulate lysis timing in response to changes in the host physiology is elevated in fluctuating feast-famine environments compared to more stable environments, which favor rapid lysis with a reduced burst size. This effect is closely coupled to the increased mortality of free phages due to abortive adsorption to already infected host bacteria during starvation phases. We identify specific system dynamics that either support or suppress the propagation of the delayed lysis phage. This theoretical analysis highlights the competitive benefits and limitations of lysis delay as a phage propagation strategy. Our results underscore the importance of considering the bacterial physiology dependence of bacteriophage replication in order to correctly predict phage fitness and population dynamics in complex environments.IMPORTANCEBacteriophage replication depends strongly on the physiological state of the host, yet most ecological and theoretical studies treat phage life histories as fixed traits. This overlooks how nutrient limitation, starvation, and fluctuating growth conditions reshape infection outcomes. By examining competition between phages with different responses to host physiology, our work shows how environmentally driven changes in the latent period can alter which phages persist, spread, or are lost. These insights clarify when delayed lysis is a beneficial strategy and when it becomes a liability. More broadly, our results highlight the need to integrate host physiology into models of phage-host dynamics to better understand microbial ecosystems and to guide applications such as rational phage therapy design.
    Keywords:  bacteriophages; feast-famine cycle; fluctuating environment; latent period; lysis inhibition; physiology dependence; starvation; superinfection exclusion
    DOI:  https://doi.org/10.1128/msystems.00505-26
  13. Oral Dis. 2026 Jul 22.
       BACKGROUND: This study examines the relationship between the microbial load of selected periodontitis-associated bacteria (PAB) and proinflammatory biomarkers in gingival crevicular fluid (GCF) from patients with periodontitis.
    METHODS: GCF and subgingival biofilm samples were collected from the deepest periodontal pocket of each quadrant of 515 patients diagnosed with periodontitis using sterile GCF collection strips for GCF and sterile paper points for subgingival biofilm. Selected PAB (i.e., Porphyromonas gingivalis, Aggregatibacter actinomycetemcomitans, Prevotella intermedia, Fusobacterium nucleatum, Treponema denticola, and Tannerella forsythia) were analyzed and associated with the concentrations of interleukin-8 (IL-8) and active-matrix metalloproteinase-8 (aMMP-8).
    RESULTS: Increased aMMP-8 (β:187.75, CI:[132.45;243.05], p < 0.001) and IL-8 levels (β:144.27, CI:[84.04;204.50], p < 0.001) were associated with deeper mean probing pocket depths. Smoking was significantly associated with decreased aMMP-8 (β:-121.81, CI:[-202.51;-41.11], p = 0.003) and IL-8 (β:-95.44, CI:[-182.03;-8.86], p = 0.031) expression. Multivariate analysis adjusted for confounding factors revealed a significant association between IL-8 and P. gingivalis (β: 26.68, CI:[2.00;51.37], p = 0.034).
    CONCLUSION: Higher levels of proinflammatory biomarkers were observed in patients with advanced periodontal disease. Notably, the findings suggest that IL-8 levels, but not aMMP-8, might be associated with P. gingivalis levels. The results further confirm that smoking is an important confounder when examining biomarkers.
    Keywords:  biomarker; interleukin‐8; pathogens; periodontitis
    DOI:  https://doi.org/10.1111/odi.70433
  14. Biologicals. 2026 Jul 23. pii: S1045-1056(26)00030-8. [Epub ahead of print]95 101902
       INTRODUCTION: Bacteriophages are increasingly recognized as vital modulators of the human microbiome and promising candidates for alternative antimicrobial therapies. Critics raise concerns about immune neutralization with prolonged use. This study examines the presence of bacteriophages in human body fluids and assesses their interaction with autologous and heterologous serum to evaluate immune neutralization of human phage isolates.
    METHODS: Inactivation and neutralization experiments were conducted by exposing samples to neat serum and complement-inactivated serum for 1 h to assess their ability to inactivate human-origin phages.
    RESULTS: This finding suggests that autologous bacteriophages from human subjects are recognized as self. These phages were not inactivated by either the complement system or neutralized by either homologous or heterologous antibodies.
    CONCLUSION: This finding indicates that endogenous phages may reduce worries that antibody or complement activation could inactivate them. It provides evidence that these phages might bypass antibody- or complement-induced neutralization, thereby strengthening their case for therapeutic use.
    Keywords:  Antibodies; Antigen; Bacteriophages; Complement; Heterologous; Neutralization
    DOI:  https://doi.org/10.1016/j.biologicals.2026.101902
  15. Diabetes Obes Metab. 2026 Jul 21.
       INTRODUCTION: Diabetic foot ulcers and heart failure are severe complications of diabetes mellitus, both associated with high morbidity and mortality. Whether diabetic foot ulcers worsen prognosis in people with heart failure remains unclear. This study evaluated the association between diabetic foot ulcers, mortality and heart failure hospitalisations in people with diabetes and heart failure.
    METHODS: We performed a retrospective cohort study including adults with diabetes and heart failure treated at a large, single centre in the Netherlands (2002-2021). People were stratified by diabetic foot ulcer status. Primary outcomes were all-cause mortality and hospitalisation for decompensated heart failure during 3 years of follow-up, with additional 5-year mortality analyses. Multivariable Cox regression was adjusted for age, renal disease, neuropathy, hypertension and other significant comorbidities. To address immortal time bias, an additional time-varying Cox model was performed.
    RESULTS: Among 4937 people with diabetes and heart failure, 908 had a current or previous diabetic foot ulcer. These people had more comorbidities, including renal disease and neuropathy. Mortality differences were modest during the first 3 years after heart failure diagnosis but became significant at 5 years (32.0% vs. 25.1%, p < 0.001). When follow-up started at ulcer diagnosis, mortality was substantially higher in the diabetic foot ulcer group (1-year: 32.9% vs. 6.0%, p < 0.001). Multivariable analysis showed no independent association, whereas the time-varying Cox model demonstrated an independent association between diabetic foot ulcer occurrence and mortality (HR 2.88, 95% CI 2.26-3.66; p < 0.001). Hospitalization rates showed similar patterns.
    CONCLUSIONS: In people with diabetes and heart failure, diabetic foot ulcer occurrence was independently associated with increased mortality in the time-varying analysis. Diabetic foot ulceration may therefore represent an important clinical marker of disease burden and identify people with advanced cardiometabolic disease who may benefit from intensified multidisciplinary management.
    Keywords:  cohort study; diabetes complications; heart failure; real‐world evidence
    DOI:  https://doi.org/10.1111/dom.71121
  16. Front Cell Infect Microbiol. 2026 ;16 1851410
      Extensively drug-resistant (XDR) Acinetobacter baumannii pneumonia carries severe pneumonia, respiratory failure and high mortality, showing limited therapeutic options in critically ill patients. Although bacteriophage (phage) therapy represents a promising alternative against drug-resistant infections, its clinical use remains largely empirical. Here, we reported a systematically planned phage-antibiotic combination strategy in a critically ill patient with refractory XDR A. baumannii pneumonia. A virulent phage targeting the patient-derived strain was isolated from hospital wastewater and classified within the class Caudoviricetes, with no virulence, toxin, or antibiotic resistance genes. In vitro time-kill assays showed that phage monotherapy failed to persistently suppress bacteria proliferation, whereas phage-antibiotic therapy achieved synergistic inhibition of A. baumannii growth for over 48 h. The patient received nebulized phage therapy (5 × 109 PFU/mL twice daily) combined with intravenous fosfomycin (8 g, every 8 hours), amikacin (0.2 g, every 12 hours), and polymyxin B (500, 000 U, every 12 hours). Clinically, treatment was associated with rapid normalization of arterial carbon dioxide tension (PaCO2), clearance of A. baumannii sputum cultures by day 4, declining inflammatory markers, and no treatment-related toxicity.Longitudinal metagenomic sequencing further revealed approximately 52-fold reduction in pathogen abundance and significant decrease of A. baumannii-associated antimicrobial resistance genes (ARGs) in the lung, highlighting the potential of precision phage-antibiotic therapy for recalcitrant XDR bacterial infections.
    Keywords:  Acinetobacter baumannii; antibiotics; antimicrobial resistance genes; bacteriophage; extensive drug resistance
    DOI:  https://doi.org/10.3389/fcimb.2026.1851410
  17. Int J Low Extrem Wounds. 2026 Jul 24. 15347346261469630
      Diabetic foot ulcers (DFU), a prevalent chronic wound, pose severe threats to patients' quality of life. Recently hydrogel dressings have emerged as a promising therapeutic option for DFU. This study aimed to gain the current status, hotspots and research orientation of the field via analyzing the characteristics of both literature and patents on hydrogel dressings for DFU therapy. The literature and patents were retrieved and screened from the Web of Science Core Collection database and the IncoPat global patent database, respectively. The bibliometric analysis was conducted by CiteSpace 6.1.R6. We found that both articles and patents related to the field surged since 2019 in parallel. Research on this topic has involved 43 countries worldwide; two large-scale collaborative clusters were respectively led by China and Spain; Wenzhou Medical University and D.G. Armstrong are the core institution and researcher. Through analyzing literature, angiogenesis, drug delivery and inflammation are the core focus, while conductive hydrogels and therapy strategy have become emerging research hotspots. Given the patents, the focus of hydrogels for DFU are concentrated on clinical application scenarios, hydrogel preparation and drug loading. In conclusion, both literature publication and patent application have garnered increasing academic attention and recognition. Effective and productive hydrogel represent a promising therapeutic option for DFU patients.
    Keywords:  Hydrogel; bibliometric analysis; citespace; diabetic foot ulcers; patent
    DOI:  https://doi.org/10.1177/15347346261469630
  18. Adv Pediatr. 2026 Aug;pii: S0065-3101(25)00029-5. [Epub ahead of print]73(1): 179-190
      This review synthesizes emerging evidence on gastrointestinal (GI) disorders, specifically luminal and pancreatic function in the era of triple cystic fibrosis transmembrane conductance regulator (CFTR) modulator therapy. Elexacaftor-tezacaftor-ivacaftor has been associated with mild improvements in GI symptoms and disease burden in patients' reported outcomes and has shown a significant increase in growth and body mass index reflecting improved nutritional status, even among individuals who remain pancreatic insufficient. Long-term data on triple CFTR modulators remain limited, highlighting the need to understand their long-term impact on GI manifestations, as survival improves and chronic intestinal inflammation persists.
    Keywords:  CFTR modulators; Cystic fibrosis; Cystic fibrosis transmembrane conductance regulator; Digestive diseases; Motility disorders; Pancreatic insufficiency
    DOI:  https://doi.org/10.1016/j.yapd.2025.11.001
  19. J Med Microbiol. 2026 Jul;75(7):
      Introduction. High rates of recurrent Clostridioides difficile infection (CDI) and environmental contamination are attributed to its ability to form spores. Periodontal diseases are characterized by gingival inflammation, caused by dental plaque accumulation.Hypothesis. Periodontal plaque could harbour C. difficile spores, acting as a reservoir for reinfection.Aim. Compare the prevalence and abundance of C. difficile in metagenomic sequences of saliva and dental plaque from healthy and periodontal disease patients.Methodology. Publicly available metagenomic reads from oral samples of healthy (n=80) and periodontitis (n=204) patients were analysed for C. difficile presence through an in-house bioinformatic pipeline. Briefly, reads underwent quality control (cutadapt/fastQC) prior to subsampling of 3 million reads (seqtk). Reads and MEGAHIT-assembled contigs were aligned to a C. difficile reference genome (ASM1888508v1) or a full non-redundant protein DIAMOND database. Outputs were filtered, annotated (Entrez Direct) and top hits identified via National Center for Biotechnology Information blast. Abundance and prevalence were compared between cohorts.Results. Low levels of C. difficile sequences were observed, with significantly higher prevalence in periodontitis (7.4%, n=15/204) vs. healthy cohorts (5.0%, n=4/80) (P=0.0087) with reference genome alignment. Using the full non-redundant database, prevalence was also higher in periodontitis (14.2% vs. 3.8%; P=0.012), along with significantly greater average C. difficile sequence counts (0.608 vs. 0.075; P=0.018) and relative abundance (0.00029% vs. 0.0000003%; P=0.009).Conclusion. Sequences pertaining to C. difficile were detected in oral samples, with significantly more observed in periodontal disease compared to healthy cohorts. This highlights the possibility for dental plaque to act as a reservoir, potentially contributing to reinfection in CDI patients.
    Keywords:  Clostridioides difficile; bioinformatics; dental plaque; metagenomics; periodontal disease; saliva
    DOI:  https://doi.org/10.1099/jmm.0.002188
  20. Adv Immunol. 2026 ;pii: S0065-2776(26)00012-X. [Epub ahead of print]170 35-74
      This chapter explores the significant role of oral microbiome dysbiosis in oral squamous cell carcinoma (OSCC) pathogenesis, highlighting mechanisms such as chronic inflammation via NF-κB activation by Porphyromonas gingivalis and Fusobacterium nucleatum, production of oncogenic metabolites (for example, acetaldehyde, N-nitrosamines), immune evasion through PD-L1 upregulation and T-cell suppression, and direct carcinogenic effects including epithelial-mesenchymal transition and apoptosis inhibition. In this comprehensive overview, microbes with key role in OSCC pathogenesis, including F. nucleatum (invasion promotion, hypoxia mimicry), P. gingivalis (EMT induction), Capnocytophaga gingivalis (diagnostic potential), and Candida albicans (acetaldehyde synthesis), are examined, alongside interactions with established risk factors. Diagnostic advancements could potentially include salivary biomarkers (IL-6, miRNAs, bacterial panels) and AI-driven models achieving AUC >0.9, with microbial diversity shifts aiding early detection and prognosis. Recent research investigate findings in mycobiome and HPV influences, therapy modulation (e.g., radiotherapy-induced dysbiosis), epigenetic effects, and hypoxia pathways. Challenges include establishing causality, study inconsistencies, and the need for multiomics approaches, with future directions emphasizing longitudinal research, standardized protocols, and microbiome-targeted therapies to enhance OSCC prevention, diagnosis, and management.
    Keywords:  Biomarkers; Dysbiosis; Microbiota; Mouth neoplasms; Squamous cell carcinoma of head and neck; Tumor
    DOI:  https://doi.org/10.1016/bs.ai.2026.03.011
  21. Adv Immunol. 2026 ;pii: S0065-2776(26)00008-8. [Epub ahead of print]170 75-90
      OSCC affects over 377,000 patients annually with poor prognosis. While conventional prognostic indicators like TNM staging provide structural information, they inadequately explain clinical outcome variability. The oral microbiome has emerged as a dynamic prognostic factor offering functional insights through non-invasive sampling and longitudinal monitoring. Specific microbial signatures strongly associate with clinical outcomes. Pathogens including Fusobacterium nucleatum, Porphyromonas gingivalis, Eubacterium, and Lactobacillus correlate with increased recurrence and reduced survival, while commensals like Veillonella, Streptococcus, and Staphylococcus predict favorable outcomes. Microbiome-based models outperform traditional parameters in recurrence stratification, with beta diversity distinguishing recurrent from non-recurrent cases. Functional pathways involving PI3K/AKT/mTOR signaling and immunomodulation demonstrate prognostic relevance. High-risk patterns promote immune evasion through CD8+ T-cell depletion, while favorable patterns maintain anti-tumor immunity. The microbiome influences treatment response, with dysbiosis reducing therapy effectiveness and increasing mucositis. Probiotic interventions show promise in restoring diversity and improving outcomes. Despite standardization challenges, the oral microbiome represents a promising non-invasive prognostic indicator for refining risk stratification and personalizing OSCC management.
    Keywords:  Dysbiosis; Fusobacterium nucleatum; Immune evasion; Immunomodulation; Microbial biomarkers; Oral microbiome; Oral mucositis; Oral squamous cell carcinoma; PI3K/AKT/mTOR pathway; Personalized medicine; Porphyromonas gingivalis; Prognosis; Recurrence prediction; Treatment response; Tumor microenvironment
    DOI:  https://doi.org/10.1016/bs.ai.2026.03.007
  22. J Appl Microbiol. 2026 Jul 24. pii: lxag188. [Epub ahead of print]
       AIMS: Zoonotic infections with Salmonella spp. transmitted from reptiles to humans are an increasing concern due to the growing number of documented cases and the close contact between humans and reptiles. Reptiles, such as bearded dragons (Pogona vitticeps), frequently carry Salmonella enterica asymptomatically as part of their intestinal microbiota.Given the rise of antibiotic-resistant Salmonella strains in reptiles, bacteriophages (phages) may provide a targeted and sustainable alternative for preventing reptile-to-human transmission.
    METHODS AND RESULTS: Seventeen phages were isolated from ten of eighteen faecal samples collected from bearded dragons. Seven of these phages were selected for further analyses. Host range assays on 41 S. enterica and nine non-Salmonella isolates revealed a narrow spectrum: phages infected up to 63.4% of Salmonella isolates and lysed one non-Salmonella strain. Planktonic killing assays at 25 °C and 37 °C showed pronounced bacterial growth reduction, with 8 of 12 significant inhibitions observed at 37 °C. Phage cocktails generally showed stronger inhibition than individual phages. Electron microscopy and whole-genome sequencing identified six Myovirus-like and one Siphovirus-like phage, all temperate with integrase or transposase genes despite lytic activity.
    CONCLUSIONS: This study expands knowledge of S. enterica-specific phages from reptiles, detailing host specificity, morphology and genomic features. While in vitro results are promising, in vivo efficacy may be influenced by host physiology, immunity and microbiome interactions. The predominance of temperate phages may limit direct therapeutic use, though low lysogeny rates in related phages and genetic engineering advances may enable future applications.
    Keywords:  Antibiotica Resistance; Bacteriophage; Public Health; Salmonella; Veterinary Medicine; Zoonoses
    DOI:  https://doi.org/10.1093/jambio/lxag188
  23. Lancet Microbe. 2026 Jul 22. pii: S2666-5247(26)00122-9. [Epub ahead of print] 101467
    European Society of Clinical Microbiology and Infectious Diseases (ESCMID) Study Group for Host and Microbiota Interactions (ESGHAMI)
      Antimicrobial resistance (AMR) has made multidrug-resistant organisms (MDROs), particularly ESKAPE-E pathogens (including Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, Enterobacter spp, and Escherichia coli), a major threat to modern medicine. Although novel antibiotics, antimicrobial stewardship, and infection prevention remain essential, such interventions are unlikely to offset projected AMR trends on their own. Vaccines can help to mitigate AMR by preventing infections and reducing antibiotic exposure. WHO estimates that vaccines targeting 23 pathogens (excluding Neisseria gonorrhoea) could reduce global antibiotic need by 22%, equivalent to 2·5 billion defined daily doses annually. In the mRNA era, modular vaccine platforms enable rapid design of protein antigens and multivalent constructs, with emerging preclinical proof of concept against selected bacterial pathogens. In this Personal View, we argue that mRNA vaccines should be considered enabling platforms for selected protein-based MDRO targets rather than universal solutions for antibacterial vaccine development. We propose a microbiome-informed framework that distinguishes systemic protection from mucosal decolonisation and aligns antigen selection, delivery route, and trial endpoints with colonisation dynamics, microbiome resilience, and AMR reduction goals.
    DOI:  https://doi.org/10.1016/j.lanmic.2026.101467
  24. Virulence. 2026 Jul 21. 2707728
      Phage therapy represents a promising alternative for combating bacterial infections. This study employed an A. baumannii isolate harboring the I-F CRISPR-Cas system as a host to isolate phage and evaluate its biological characteristics. Phage-resistant mutants were screened using a double-layer agar plate assay, and the underlying molecular mechanisms were identified through whole-genome sequencing, followed by validation via gene knockout. Transcriptome sequencing was subsequently applied to alterations in the global regulatory networks of these mutants. Our results demonstrate the successful isolation of a novel myovirus, stable at 40-50 ℃, which was successfully isolated and found to utilize the capsule as its adsorption receptor. Whole-genomic analysis confirmed its taxonomic distinction from currently published phages. Investigation into the primary resistance mechanism revealed that the capsule loss, due to an insertional mutation in the UDP-glucose 4-epimerase encoding gene galE. This conclusion was further validated through targeted gene knockout of galE. This defect concurrently attenuated bacterial virulence, as demonstrated by significantly reduced lethality in the Galleria mellonella infection model and enhanced susceptibility to serum killing, while concurrently enhancing the capacity for biofilm formation. Transcriptomic profiling indicated that the ΔgalE significantly upregulated multiple biofilm-associated genes and remodeled the transcriptomic-wide regulatory. Furthermore, the combination of carbenicillin or ceftazidime with the phage exhibited a synergistic effect in vitro, effectively inhibiting biofilm formation and suppressing the emergence of phage resistance. Overall, this work characterizes a novel phage and delineates the host's biological network changes triggered by phage resistance, offering valuable insights for developing phage-based antimicrobial strategies.
    Keywords:  Acinetobacter baumannii; biofilm; capsule; phage resistance; virulence
    DOI:  https://doi.org/10.1080/21505594.2026.2707728
  25. Expert Opin Pharmacother. 2026 Jul 22. 1-4
      
    Keywords:  GLP-1 receptor agonist; Wound healing; chronic wounds; diabetic foot ulcers; epidermolysis bullosa; gene therapy; hypertrophic scar; wound pharmacotherapy
    DOI:  https://doi.org/10.1080/14656566.2026.2706077
  26. Adv Pediatr. 2026 Aug;pii: S0065-3101(26)00003-4. [Epub ahead of print]73(1): 161-178
      There have been advances in the care of children with cystic fibrosis (CF) that allow for early disease identification and intervention in early childhood. Universal and the rise of modulator therapy have revolutionized CF care, so the life expectancy in children with CF has improved. With the changing landscape in advances in CF care, there is uncertainty in interpretation of tests and clinical phenotypes that are indeterminate for CF diagnosis.
    Keywords:  Cystic fibrosis (CF); Cystic fibrosis screen positive; Cystic fibrosis transmembrane conductance regulator (CFTR)-Related metabolic syndrome (CRMS); Health equity; Highly effective modulator therapy (HEMT); Inconclusive diagnosis (CFSPID); Modulators; Newborn screening (NBS)
    DOI:  https://doi.org/10.1016/j.yapd.2026.02.002
  27. Front Med (Lausanne). 2026 ;13 1861751
       Background: Treponema denticola, Porphyromonas gingivalis and Tannerella forsythia are common oral pathogens collectively referred to as the "red complex bacteria", serve as crucial periodontopathic agents. Owing to the challenges associated with anaerobic culture, their contribution to lower respiratory tract infections, especially lung abscess, is often undervalued. Metagenomic next-generation sequencing (mNGS) has evolved as a potent instrument for the identification of fastidious organisms.
    Case presentation: A 63-year-old male with chronic cough and hemoptysis was admitted to our hospital. Chest computed tomography showed an indeterminate space-occupying lesion in the right upper lobe, and repeated sputum cultures were negative. Lung cancer was the primary consideration, so a CT-guided percutaneous core needle biopsy of the lung lesion was performed. Nevertheless, the pathology favored inflammation over lung cancer, leading us to continue investigating the causative pathogen. Following mNGS analysis of the puncture biopsy tissue, Treponema denticola and Porphyromonas gingivalis were detected. Both organisms belong to the red complex bacteria, closely associated with periodontitis that the patient had. Intravenous piperacillin-tazobactam followed by oral amoxicillin-clavulanate was prescribed. The patient recovered and subsequent chest computed tomography confirmed the improvement.
    Conclusions: This case highlights the role of oral red complex bacteria in culture-negative chronic lung abscesses. mNGS is a crucial diagnostic tool for identifying these fastidious anaerobes, enabling targeted therapy and improving clinical outcomes.
    Keywords:  Porphyromonas gingivalis; Tannerella forsythia; Treponema denticola; lung abscess; metagenomic next-generation sequencing (mNGS)
    DOI:  https://doi.org/10.3389/fmed.2026.1861751
  28. J Oral Microbiol. 2026 ;18(1): 2701564
       Background: Porphyromonas gingivalis (P. gingivalis) is a Gram-negative anaerobic bacterium and a keystone pathogen in chronic periodontitis. Beyond oral disease, it has been implicated in systemic conditions, including cardiovascular disease, type 2 diabetes, rheumatoid arthritis, and neurodegeneration. Marked strain-to-strain differences in tissue invasion, immune evasion, and pathogenicity suggest that virulence is shaped by complex genetic and regulatory interactions rather than a single determinant.
    Objective: To summarize current knowledge of the genetic diversity of P. gingivalis virulence determinants and their contribution to strain-specific pathogenicity.
    Design: This narrative review synthesizes current evidence on the diversity of major virulence determinants, including fimbriae (FimA and Mfa1), gingipains (RgpA/RgpB/Kgp), Hag-family hemagglutinins, capsular polysaccharide loci, lipopolysaccharide variants, the RagAB nutrient acquisition system, and the type IX secretion system. It also examines the roles of allelic variation, domain rearrangements, phase variation, and horizontal gene transfer in shaping strain-specific virulence repertoires.
    Conclusions: The reviewed evidence indicates that genetic variation across multiple virulence-associated loci contributes to substantial phenotypic diversity among P. gingivalis strains, influencing host interaction, tissue tropism, immune modulation, and pathogenic potential. Integrating comparative genomics with functional phenotyping provides a framework for predicting strain-specific virulence and may facilitate the development of improved diagnostic tools and targeted therapeutic strategies.
    Keywords:  Porphyromonas gingivalis; capsular polysaccharide; comparative genomics; fimbriae; gingipain; lipopolysaccharide (LPS); strain diversity; virulence factors
    DOI:  https://doi.org/10.1080/20002297.2026.2701564
  29. J Oral Microbiol. 2026 ;18(1): 2705699
       Background: Periodontal diseases may influence systemic health through the oral-gut axis, with three mechanistic pathways proposed. Periodontitis-associated gut dysbiosis has been repeatedly observed and may plausibly extend to effects on drug metabolism, yet the literature on periodontitis-associated dysbiosis and that on its potential effects on medicine pharmacokinetics have not previsouly been bridged.
    Objective: To synthesise the available human evidence for each of the three pathways with a distinct focus on the interventional evidence, and to position the evidence to its clinical context alongside downstream outcomes and the implications for patients and clinicians. Our secondary aim was to connect the dysbiosis and pharmacokinetic literatures in a hypothesis-generating section.
    Design: This systematic review was registered on PROSPERO. PubMed and Scopus were searched and eligibility restricted to human studies.
    Results: A total of 76 studies were included following full-text assessment by two independent reviewers. Across the three pathways, the human evidence was placed in clinical context with its downstream outcomes. Direct evidence that periodontitis modeifies drug response in humans was not identified, however, we were able to provide a hypothesis-generating section that identifies four drug classes for which a periodontitis-mediated modification of drug response would be most clinically relevant.
    Conclusions: The oral-gut axis is a biologically plausible but, currently, under-evidenced route from periodontal disease to systemic and pharmacological outcomes. Future reserach should prioritise prospective comparative pharmacokinetic studies in periodontitis-affected popualtions and field-wide standardisation of methodology across oral-gut microbiome research.
    Keywords:  Periodontitis; drug metabolism; gut microbiome; intestinal permeability; oral–gut axis; systemic inflammation
    DOI:  https://doi.org/10.1080/20002297.2026.2705699
  30. Acta Vet Hung. 2026 Jul 20. pii: 004.2026.01273. [Epub ahead of print]
      Canine pyoderma is a common bacterial skin infection predominantly caused by Staphylococcus species. This study, conducted from June to December 2024, analysed 71 PCR-confirmed cases of staphylococcal pyoderma to investigate epidemiological and host-associated risk factors and antimicrobial resistance (AMR) patterns. Bacterial isolates from PCR-positive samples were identified using MALDI-TOF MS and tested for antimicrobial susceptibility. Of the cases analysed, 63.38% involved monomicrobial infections, whereas 36.62% were accounted for polymicrobial infections. Staphylococcus pseudintermedius and Staphylococcus aureus were the predominant pathogens in both infection types, occurring alone or in combination with Escherichia coli, Pseudomonas aeruginosa or Klebsiella pneumoniae. Polymicrobial infections were significantly associated with recurrent disease, longer disease duration, tissue invasion and allergic skin manifestations. Both major Staphylococcus species exhibited high resistance to β-lactams and third-generation cephalosporins, with notable interspecies differences in resistance to ceftizoxime, trimethoprim-sulfonamide, amikacin, enrofloxacin and clindamycin. Although overall AMR did not differ significantly between major staphylococci species associated to monomicrobial and polymicrobial infections, however isolates from polymicrobial cases showed a consistent trend toward higher resistance across multiple antimicrobial classes. The findings emphasise the complexity of canine pyoderma characterised by bacterial communities dominated by Staphylococcus pseudintermedius and the increasingly relevant Staphylococcus aureus with potential zoonotic implications. Routine species-level identification, culture-guided therapy and continuous AMR surveillance are crucial for effective treatment and antimicrobial stewardship within a One Health framework.
    Keywords:  MALDI-TOF MS; Staphylococcus aureus; Staphylococcus pseudintermedius; antimicrobial resistance; canine pyoderma; polymicrobial infection
    DOI:  https://doi.org/10.1556/004.2026.01273
  31. JMIR Form Res. 2026 Jul 23. 10 e94016
       Background: Diabetic foot ulcers (DFUs) are a leading cause of hospitalizations, amputations, and health care costs among individuals with diabetes, often due to delayed detection and treatment. Early identification of skin changes is critical for preventing ulcer progression, yet daily visual foot self-inspections are often limited by impaired mobility, visual deficits, and poor compliance. Although some foot-focused remote patient monitoring technologies are in use, most of these approaches do not provide standardized, full-color visual documentation, which can affect clinicians' ability to interpret findings using familiar visual cues.
    Objective: This formative evaluation aimed to assess the usability, compliance, and feasibility of an in-home full-color imaging scale for the remote monitoring of patients with DFUs to inform the design of larger prospective studies.
    Methods: We conducted a retrospective formative feasibility evaluation analyzing 7 months of preexisting data from adults with a history of DFUs who had enrolled in an outpatient remote monitoring program. During this program, participants were provided with an internet-connected in-home scale that captured high-resolution, full-color scans of the plantar surface of the feet during daily use. Scans were securely transmitted to a HIPAA (Health Insurance Portability and Accountability Act)-compliant web portal for podiatrist review. Usability was assessed through compliance with daily scanning, patient and physician surveys, and descriptive review of clinical workflows.
    Results: A total of 21 participants aged 43 to 86 years (median 65, IQR 59-74; mean 65.3, SD 10.6 years) were retrospectively analyzed. Participants demonstrated high compliance and feasibility of home use, with device use on 82.5% (3638/4410) of possible days, a median use of 27 days (IQR 21-30) per 30-day period, and a mean use of 23 (SD 6.4) days per 30-day period. Participants reported high satisfaction and minimal burden associated with daily use, with most rating the device as physically easy to use (median 7.0, IQR 7-7; mean 6.9, SD 0.45), expressing willingness to use it daily (median 7.0, IQR 7-7; mean 6.9, SD 0.31), and indicating trust in the system (median 7.0, IQR 7-7; mean 6.9, SD 0.32) on a 7-point Likert scale (1=worst; 7=best). Clinician usability was supported by podiatrist review of 3295 scans, of which 3220 (97.7%) were rated as usable for clinical assessment. Three representative cases illustrated real-world device use and longitudinal image review, demonstrating the ability to visualize skin changes such as foreign body presence, new ulceration, and early skin breakdown.
    Conclusions: This retrospective formative evaluation demonstrates the preliminary usability and feasibility of an in-home, full-color imaging scale for daily remote visual monitoring of diabetic feet in a real-world outpatient setting. High compliance and usability in clinical workflows suggest that this approach may support early identification of foot-related concerns. Future prospective studies are warranted to evaluate the impact of this technology on clinical outcomes, including ulcer progression and health care use.
    Keywords:  chronic care management; diabetes; diabetic foot ulcer; digital health; early detection of neuropathic wounds; neuropathy; remote patient monitoring
    DOI:  https://doi.org/10.2196/94016
  32. J Mater Chem B. 2026 Jul 20.
      Chronic and complex wounds remain a major clinical challenge due to persistent inflammation, infection, impaired angiogenesis, and dysregulated immune responses. In response, microneedle (MN) technology has emerged as a minimally invasive, highly versatile platform for wound healing by enabling direct delivery of therapeutics into viable tissue while also supporting wound monitoring and microenvironment modulation. Moreover, advances in MN fabrication techniques, such as micromolding, 3D printing, and centrifugal drawing, enable precise control over needle geometry, mechanical strength, and drug-loading strategies. Diverse MN designs, including dissolvable, swellable, porous, hollow, separable, and multifunctional types, have consequently expanded therapeutic functionality beyond passive drug delivery to encompass immunomodulation, antimicrobial action, angiogenesis, neurovascular regeneration, antioxidative protection, and scar remodeling. Further, intelligent MN systems combine biosensing with stimuli-responsive drug release, enabling real-time monitoring and on-demand therapy tailored to the changing wound environment. This review summarizes recent advances in MN fabrication methods, structural designs, and integration with other scaffolds. It also discusses diagnostic and sensing capabilities, as well as therapeutic mechanisms across diverse wound types, highlighting the translational potential of multifunctional MN systems for next-generation wound care.
    DOI:  https://doi.org/10.1039/d6tb00716c
  33. Eur J Clin Microbiol Infect Dis. 2026 Jul 20.
       PURPOSE: Methicillin-resistant Staphylococcus aureus (MRSA) continues to compromise the efficacy of conventional antibiotics, highlighting the urgent need for alternative antimicrobial strategies. This study aimed to isolate, characterize, and evaluate the therapeutic potential of two strictly lytic bacteriophages, Staphylococcus phages EAS1 and EAS2, against MRSA, including their safety and efficacy in an in vivo myositis model.
    METHODS: EAS1 and EAS2 were isolated from wastewater and characterized using transmission electron microscopy, whole-genome sequencing, and in vitro functional assays. Genomic and comparative analyses were performed to assess genome organization and safety-related features. Therapeutic efficacy and toxicity were evaluated in a rat model of MRSA-induced myositis, with assessment of inflammatory mediators and histopathological tissue damage.
    RESULTS: Both phages exhibited broad and potent lytic activity against S. aureus, including MRSA strains, and demonstrated high physicochemical stability and biocompatibility. Both phages possessed large linear dsDNA genomes (∼138-140 kb) encoding over 240 CDSs without lysogeny, virulence, or antibiotic resistance genes and were classified within the Kayvirus genus based on comparative genomics. In vivo, phage treatment caused no detectable hepatic or renal toxicity. EAS2 treatment led to significant modulation of inflammatory mediators, including TNF-α, IL-10, NF-κB, and COX-2, and resulted in reduced histopathological tissue damage compared with untreated control and vancomycin-treated groups.
    CONCLUSION: These findings demonstrate the stability, safety, and therapeutic efficacy of bacteriophages EAS1 and EAS2, particularly EAS2, supporting phage therapy as a promising alternative approach for the treatment of MRSA infections.
    Keywords:   Kayvirus phages; Methicillin-resistant S. aureus ; Myositis model; Phage therapy
    DOI:  https://doi.org/10.1007/s10096-026-05604-3
  34. Ann Plast Surg. 2026 Jul 23.
      The Little Book of Bad Wounds by Yvette Godwin is a concise field manual intended to guide civilian surgeons managing complex traumatic and wartime wounds in resource-limited environments. Written from the perspective of frontline surgical experience rather than tertiary academic practice, the text emphasizes practical wound stabilization strategies over definitive reconstruction and introduces the concept of the "delayed acute wound" (DAW), a wound that may present days after injury yet still requires acute management principles. This editorial evaluates the book's practicality, readability, and consistency with current wound care literature. Godwin work succeeds in presenting a highly accessible framework for the management of blast and ballistic injuries, particularly its "blueprint recipe" structure, which allows for rapid bedside reference. The text appropriately emphasizes repeated debridement, antimicrobial stewardship, preservation of reconstructive options, and the clinical significance of biofilm in delayed traumatic wounds. Additional strengths include pragmatic discussion of austere-resource solutions, realistic commentary on limb salvage versus amputation, and a writing style that remains engaging without sacrificing clinical utility. Several recommendations, however, differ from current guideline-supported practice and warrant contextualization. These include the use of high-concentration povidone-iodine solutions, broad rejection of pulse lavage, omission of negative pressure wound therapy, and selective recommendations regarding topical antimicrobials and antibiotic timing. While many of these viewpoints are grounded in extensive field experience, they should be interpreted as practice-based recommendations rather than universal standards of care. Despite these limitations, The Little Book of Bad Wounds provides a valuable and timely contribution to modern reconstructive and wartime wound literature. As civilian health care systems increasingly encounter injuries associated with armed conflict and mass trauma, this work offers surgeons a practical framework for stabilizing complex wounds in compromised circumstances. When used with appropriate clinical discernment, the book serves as an effective field guide for surgeons managing devastating injuries under austere conditions.
    Keywords:  complex wound management; reconstructive surgery; traumatic fracture; wartime wounds; wound stabilization
    DOI:  https://doi.org/10.1097/SAP.0000000000004812
  35. Front Immunol. 2026 ;17 1841874
       Background: Alterations of the gut microbiome are well documented in connective tissue diseases, whereas the oral microbiome has largely been studied in isolation. Emerging evidence suggests coordinated dysbiosis across mucosal sites with oral-gut relocation of pathobionts occurring in animal models; however, it remains unclear whether consistent oral and gut microbiome alterations occur in systemic lupus erythematosus (SLE) and primary Sjögren's syndrome (pSS). This review systematically synthesizes evidence on oral and gut microbiome alterations in SLE and pSS with a focus on recurrent opposing abundance patterns across anatomical sites compatible with oral-gut microbial relocation.
    Methods: Observational studies comparing adult patients with SLE or pSS to healthy controls and reporting oral and/or gut microbiome data were included. Interventional studies, case reports, reviews, and non-human studies were excluded. PubMed was searched from inception to November 2024. Study quality was assessed using the Newcastle-Ottawa Scale. Microbial alterations were harmonized using current NCBI taxonomy and synthesized descriptively without meta-analysis.
    Results: Thirty-three studies comprising 1,385 patients and 2,131 healthy controls were included. Intestinal Shannon and Simpson α-diversity were frequently reduced, whereas oral diversity was preserved or increased. Recurrent opposing abundance patterns were observed for specific taxa, most consistently involving Streptococcus and Actinomycetota in SLE and Pseudomonadota in pSS, characterized by decreased oral and increased intestinal relative abundance. Several taxa, including Veillonella and Veillonellaceae, showed parallel enrichment across both sites.
    Discussion: SLE and pSS are characterized by coordinated dysregulation of the oral and gut microbiomes. Opposing abundance patterns across anatomical sites support the concept of disease-associated microbial redistribution although causal inference is limited given the data was derived primarily from cross-sectional studies with relative abundances. Overall, this study highlights the oral-gut axis as an underexplored dimension of mucosal immune dysregulation in connective tissue diseases.
    Keywords:  Sjögren´s disease; connective tissue diseases; dysbiosis; gastrointestinal microbiome; microbiota; mouth; mucosal immunity; systemic lupus erythematosus
    DOI:  https://doi.org/10.3389/fimmu.2026.1841874
  36. Diabetes Res Clin Pract. 2026 Jul 18. pii: S0168-8227(26)00361-X. [Epub ahead of print]239 113441
       AIMS: Diabetic foot disease (DFD) is a leading cause of amputation and preventable morbidity among persons with diabetes. This study explored healthcare professionals' (HCPs) perceptions of DFD management in Oman, examining access to diabetic foot care (DFC), quality of care, service challenges, and improvement recommendations.
    METHODS: Four focus group discussions were conducted in February 2025 with 35 HCPs: podiatrists (10), followed by nurses (9), physicians (including endocrinologist) (10), and surgeons (6). Sessions were audio-recorded, transcribed, and analysed using hybrid thematic analysis within an Interpretative Phenomenological Analysis framework. Themes were mapped onto the COM-B (Capability, Opportunity, Motivation-Behaviour) framework.
    RESULTS: Participants (mean age 39 years [SD 5]; 82.9% female; mean experience 12.4 years [SD 6]) identified five principal barriers: regional access disparities, poor DFC integration into primary care, absent quality indicators, fragmented specialist services, and cultural misconceptions favouring traditional remedies. Recommendations included expanded screening, personalised care plans, multidisciplinary collaboration, telemedicine, and advanced wound care. Application of the COM-B framework to the emergent themes provides a multilayered strategy to advance DFC through targeted policy, educational, and structural interventions.
    CONCLUSIONS: A national coordinating governance structure for DFD is urgently recommended.
    Keywords:  COM-B framework; Diabetic foot disease; Focus group discussions; Healthcare professionals; Oman; Qualitative research
    DOI:  https://doi.org/10.1016/j.diabres.2026.113441
  37. Front Cell Infect Microbiol. 2026 ;16 1833939
      Wound odor is a common symptom in patients with chronic wounds. Malodorous wounds can result in embarrassment, anxiety, and, therefore, in social isolation of the patient. Current treatment options are limited and focused on masking the odor. Current approaches to wound odor management have notable limitations and fail to adequately address existing therapeutic needs. Wound odor is multifactorial, with a major contribution from volatile organic compounds (VOCs) emitted by microorganisms and necrotic tissue. Several VOCs have been identified as key drivers of malodor, such as short-chain fatty acids, dimethyl-trisulfide, specific alcohols, ketones, and aldehydes. These compounds are detected by the human olfactory system, including olfactory receptors (ORs) expressed on olfactory sensory neurons (OSNs). The human olfactory system comprises more than 400 ORs, which enable the detection of a vast array of odorants, however only a small fraction of these receptors has been deorphanized. This systematic review will evaluate therapeutic clinical strategies addressing malodor and compile current knowledge on VOCs that cause wound odor and the ORs associated with their detection. It summarizes the existing evidence on deorphanized ORs that detect these VOCs in malodorous wounds and outlines experimental mechanisms of deorphanization. Identifying wound-odor-associated VOCs and their corresponding ORs provides a framework for novel therapeutic strategies, such as antagonizing the OR to suppress odor perception. This may directly improve the quality of life of patients with chronic malodorous wounds, particularly in malignant wounds and palliative care.
    Keywords:  chronic wounds; olfactory receptors; volatile organic compounds; wound malodor; wound microbiome
    DOI:  https://doi.org/10.3389/fcimb.2026.1833939
  38. Pharmacol Ther. 2026 Jul 23. pii: S0163-7258(26)00119-1. [Epub ahead of print] 109092
      Multidrug-resistant (MDR) Staphylococcus aureus remains a leading cause of life-threatening infections worldwide and is designated a high-priority pathogen by the WHO. The accumulation of resistance mechanisms, such as β-lactam insensitivity, reduced vancomycin susceptibility, and multidrug efflux, has limited effective therapies and sustained high morbidity and mortality. Conventional antibiotic discovery is too slow, costly, and inefficient to keep pace with resistance. Artificial intelligence-driven drug design (AIDD) has emerged to address these limitations through high-precision virtual screening, generative de novo design, and multi-parameter property optimization. This review synthesizes the clinical burden and resistance mechanisms of MDR S. aureus, evaluates AIDD technologies spanning data resource curation, resistance prediction, generative design, and structure-based optimization, and examines the structure-activity relationships (SAR) that guide rational anti-staphylococcal design. By integrating AI methodology with mechanistic antibacterial pharmacology, it illustrates how AI-driven approaches can accelerate the discovery of novel antibiotics against MDR S. aureus and other priority pathogens.
    Keywords:  AIDD; Drug design; Multidrug resistance; Staphylococcus aureus; Structure-activity relationships
    DOI:  https://doi.org/10.1016/j.pharmthera.2026.109092
  39. Brief Bioinform. 2026 Jul 03. pii: bbag389. [Epub ahead of print]27(4):
      Fecal microbiota transplantation (FMT) has emerged as a highly effective treatment for recurrent Clostridioides difficile infection and is being actively investigated for numerous other conditions. While multi-omics studies have revealed dynamic changes in microbial communities and host metabolism following FMT, existing approaches are primarily descriptive and lack the ability to model individual patient trajectories or identify early biomarkers of treatment response. Small-sample, multi-omics, longitudinal prediction presents unique computational challenges: high dimensionality ($p \gg n$), multi-omics integration, temporal dynamics, and interpretability. Here, we present Hierarchical Multi-Omics Trajectory Prediction (HMOTP), a purpose-built machine learning framework that addresses these challenges through hierarchical feature construction, multilevel attention mechanisms, and patient-specific trajectory prediction. We evaluated HMOTP on 15 patients with recurrent Clostridioides difficile infection who underwent FMT, with lipidomics and metagenomics profiling at four timepoints spanning 6 months. Notably, naively concatenating multi-omics features degraded Random Forest performance ($93.33\%$ to $87.18\%$ accuracy), whereas HMOTP's hierarchical integration benefited from the additional omics layer, demonstrating that its advantage stems from structure, not from access to more data. Through hierarchical interpretability, HMOTP identified key biomarkers and revealed cross-omics associations between host lipid metabolism and microbial energy pathways, demonstrating utility for longitudinal modeling and biological discovery in FMT response. HMOTP provides a generalizable, principled framework for personalized medicine applications across small-sample multi-omics problems. Source code and a demo dataset are publicly available.
    Keywords:  fecal microbiota transplantation; hierarchical attention; longitudinal machine learning; multi-omics integration; small-sample learning; trajectory prediction
    DOI:  https://doi.org/10.1093/bib/bbag389
  40. BMJ Health Care Inform. 2026 Jul 23. pii: e102115. [Epub ahead of print]33(1):
       OBJECTIVES: Shigella remains a major cause of diarrhoea and mortality in children under five in low- and middle-income countries, where laboratory confirmation is often inaccessible and dysentery-based management lacks sensitivity. This study aimed to develop and internally evaluate machine learning models to predict microbiologically confirmed Shigella infection and secondarily to demonstrate the feasibility of translating the best-performing model into a prototype web-based decision-support application.
    METHODS: We analysed data from 3356 children with diarrhoea enrolled in the Global Enteric Multicentre Study, excluding co-infections and non-diarrhoeal controls. Multiple machine learning algorithms were trained using 32 predictors and evaluated with 10-fold cross-validation. Performance was assessed using area under the receiver operating characteristic curve (AUC), recall and Brier score, with recall prioritised to minimise false negatives. The selected model was simplified using the 10 most informative predictors and integrated into a prototype web-based application. All analyses were restricted to internal validation.
    RESULTS: Support vector machine (SVM) demonstrated the highest recall (0.64) with modest but potentially useful discrimination (AUC 0.74). The parsimonious SVM model achieved recall 0.67, AUC 0.77 and Brier score 0.16. A web-based prototype was developed to illustrate real-time model outputs for research purposes.
    DISCUSSION: The model achieved moderate internal performance while prioritising recall, supporting its potential role as a research-stage risk stratification tool in settings with limited diagnostic capacity.
    CONCLUSION: This internally validated model shows potential for supporting risk stratification for shigellosis. External validation and impact evaluation are required before clinical or operational use.
    Keywords:  Artificial intelligence; Data Science; Decision Making, Computer-Assisted; Machine Learning; Public health informatics
    DOI:  https://doi.org/10.1136/bmjhci-2026-102115
  41. Diabetes Ther. 2026 Jul 24.
      Diabetic foot (DF) is a severe and common complication of diabetes mellitus, involving peripheral neuropathy, vascular disease, immune-inflammatory disorders, and impaired tissue repair, with high amputation rates and a heavy medical burden. The Notch1 signaling pathway is highly conserved and participates in regulating cell proliferation, differentiation, apoptosis, angiogenesis, and inflammatory responses. Emerging evidence indicates that dysregulated Notch1 signaling is closely associated with the pathological progression of diabetic foot ulcers (DFU). This review systematically summarizes the role of Notch1 signaling in angiogenesis, inflammation, peripheral neuropathy, and cell fate regulation during DF pathogenesis, and discusses the potential therapeutic strategies targeting Notch1 pathway for DFU. We aim to provide new insights into the molecular mechanism and targeted therapy of DF.Infographic available for this article.
    Keywords:  Angiogenesis; Apoptosis; Diabetic foot; Inflammatory response; Notch1 signaling pathway; Therapeutic strategy
    DOI:  https://doi.org/10.1007/s13300-026-01893-1
  42. Front Cell Infect Microbiol. 2026 ;16 1846125
       Background/Objective: Periodontitis pathogenesis is driven by oral microbiome dysbiosis and dysregulated host immune responses. This cross-sectional study characterized salivary microbiome and inflammatory mediator profiles to identify candidate biomarkers distinguishing periodontal health from periodontitis (PD) using hyperplex PCR, multiplex assay and exploratory machine learning.
    Materials and methods: Stimulated saliva samples from 57 participants (28 periodontally healthy, 29 with PD stage III/IV) were collected and analyzed using Hyperplex PCR (simultaneously amplifying multiple targets in a single assay) for oral bacteria and a multiplex immunoassay including 37 inflammatory mediators. Random forest modeling explored the discriminatory performance of individual and combined biomarkers.
    Results: Individuals with PD stage III/IV showed elevated relative abundance of Filifactor alocis, Fretibacterium spp., Parvimonas micra (P < 0.05) compared to periodontally healthy individuals. Among determined inflammatory mediators, the levels of Chitinase 3-like 1, sIL-6Rβ, sIL-6Rα, IL-19, pentraxin-3, sTNF-R1 and TWEAK were elevated in PD stage III/IV. Exploratory modeling identified Fretibacterium spp. as the strongest individual discriminator (AUC = 0.82), a performance that was not improved by two- or three-marker combinations incorporating additional bacteria or inflammatory mediators.
    Conclusion: In exploratory unadjusted analyses, salivary Fretibacterium spp. showed the highest discriminatory performance (AUC = 0.82), although this association was not statistically significant after adjustment for age, smoking, and cardiovascular disease. These exploratory findings require further validation in larger, diverse cohorts to assess their potential clinical utility.
    Keywords:  Inflammatory mediator; biomarker; host response; microbiome; periodontitis; saliva
    DOI:  https://doi.org/10.3389/fcimb.2026.1846125
  43. Biochem Genet. 2026 Jul 20.
      Periodontitis (PD) is a complex inflammatory condition driven by the interplay of microbial, genetic, epigenetic, and environmental factors. While bacterial biofilms are regarded as the primary cause, growing evidence underscores the significant role of genetic predisposition in determining susceptibility to the disease, its progression, and treatment outcomes. This review explores the genetic polymorphisms of PD, focusing on genes related to inflammatory mediators, immune responses, antimicrobial peptides, matrix metalloproteinases, and vitamin D receptor pathways. Key epigenetic mechanisms including DNA methylation, histone modifications, non-coding RNAs, and emerging RNA methylation pathways are explored in their roles in modulating inflammation, tissue destruction, bone metabolism, and interactions between the host and microbes. Advances in transcriptomic technologies, particularly RNA sequencing, have enhanced our ability to identify molecular biomarkers and cell-specific gene expression profiles associated with disease severity and responses to treatment. The potential for leveraging genetic and epigenetic profiling presents an exciting avenue for personalized periodontal care, including the use of epigenetic therapies targeting pathways involved in inflammation and tissue regeneration. Nonetheless, the current body of evidence has limitations. These include significant variability across studies, inconsistent disease classification systems, small sample sizes, and a predominance of preclinical or exploratory research. Many biomarkers and therapeutic targets proposed to date require further validation before they can be routinely applied in clinical practice. While integrating genetic, epigenetic, transcriptomic, and clinical data holds promise for advancing precision periodontology, rigorous large-scale, and multicenter studies are essential to confirm clinical applicability, validate biomarkers, and facilitate their incorporation into evidence-based treatment protocols.
    Keywords:  Epigenetic; Genetic variation; MicroRNA; Periodontitis; Treatment outcome
    DOI:  https://doi.org/10.1007/s10528-026-11435-w
  44. Exploration (Beijing). 2026 May 28. 20250129
      Diabetic foot ulcers (DFUs) present a persistent clinical challenge, posing a significant and ongoing threat to patient health. Current treatment strategies are failing to concurrently address the excessive oxidative stress and impaired angiogenesis during whole-course management of diabetic wounds. To overcome these limitations, this study developed an innovative microneedle (MN)-based drug delivery system incorporating cerium-based metal‒organic frameworks (MOFs) loaded with dihydrocapsaicin (DHC). Fabricated from a Gelatin Methacryloyl (GelMA) hydrogel, the resulting MN-MOF@DHC system exhibited a sustained release profile of DHC that nearly covered the whole-course management of diabetic wounds. Our results revealed that the MN-MOF@DHC system effectively reduced the levels of reactive oxygen species (ROS), promoted the transformation of macrophage phenotypes from the pro-inflammatory M1 subtype to the anti-inflammatory M2 subtype, and significantly enhanced endothelial cell angiogenesis. These combined actions markedly accelerated wound closure. Collectively, the advanced MN platform offers a highly promising strategy for the treatment of DFUs.
    Keywords:  angiogenesis; diabetic foot ulcers; diabetic wound; dihydrocapsaicin; metal‐organic frameworks; microneedle; reactive oxygen species
    DOI:  https://doi.org/10.1002/EXP.20250129
  45. Chirurgia (Bucur). 2026 Jun;pii: 12. [Epub ahead of print]121(3): 348-357
      Diabetic foot disease in end-stage kidney disease (ESKD) represents the convergence of diabetic peripheral neuropathy, accelerated atherosclerosis, medial arterial calcification, uremic immune dysfunction and impaired wound healing. The combination yields amputation rates three- to five-fold higher than in non-uremic diabetics and one-year postamputation mortality approaching 40â?"50%. In this paper we synthesised the current anatomical, diabetological, nephrological and surgical evidence into a practical framework for the surgeon caring for the dialysis-dependent or kidney-transplant recipient with a diabetic foot. We conducted a narrative review of guidelines and consensus statements from the American Diabetes Association (ADA) Standards of Care 2025, KDIGO 2022/2024, the 2023 intersocietal International Working Group on the Diabetic Foot (IWGDF), European Society for Vascular Surgery (ESVS) and Society for Vascular Surgery (SVS) PAD guideline, the 2024 ACC/AHA Lower-Extremity PAD Guideline, the 2019 Global Vascular Guidelines on chronic limb-threatening ischemia (CLTI), and the KDOQI 2019/2020 vascular access update, supplemented by high-quality reviews published through 2026. Anatomical understanding of the tibioperoneal trifurcation, pedal-plantar loop and the angiosomal territories is now central to revascularization planning; belowthe- knee disease in ESKD is diffuse, calcified and pedal-dominant, mandating individualized choice between bypass, endovascular and transcatheter arterialization of the deep veins; perioperative care must integrate dialysis timing, hyperkalaemia control, anaemia and mineral-bone disease management, and ipsilateral vascular-access preservation; the threshold to definitive, well-planned amputation should be lower than in non-uremic diabetics, but only after a structured limb-salvage attempt within a multidisciplinary "toe-and-flow" team.
    Keywords:  IWGDF; KDIGO; amputation; angiosome; chroniclimb-threateningischemia; diabeticfoot; end-stagekidneydisease; medialarterialcalcification; revascularization; transcatheterarterializationofdeepveins
    DOI:  https://doi.org/10.21614/chirurgia.3307
  46. Probiotics Antimicrob Proteins. 2026 Jul 23.
      Antimicrobial Peptides (AMPs) are widely distributed and serve as innate immune responses in various organisms to combat a broad range of pathogens. Bacteriocins are narrow-spectrum antibacterial agents that are found to exhibit bactericidal effects against closely related bacteria of the strain that produces them. The expression of AMPs in plants is considered to be induced by the invasion of pathogenic microorganisms. Thus, the AMPs in plants are part of the immunological response to counter the infection caused by a variety of microorganisms. Biofilms pose a significant challenge in treatment due to their ability to adapt and develop resistance to antibiotics, which is more pronounced than their planktonic counterparts. In this review, AMPs are being explored as potential alternative agents to conventional antibiotics in the quest to combat chronic infections caused by biofilms. AMPs can be potentially effective strategy for fighting infections caused by biofilms. This is because many AMPs specifically target the microbial membrane, making them potentially effective even against cells that are not actively metabolizing. We have also explored the possible mechanisms involved in the eradication of biofilm, which include interference with cell wall and cell membrane-related processes, inhibiting the attachment of microorganisms to the surface, and disrupting cell-to-cell communication within the biofilm.
    Keywords:  AMPs; Antibiotic resistance; Bacteriocins; Biofilm inhibition; Plant defensins; Quorum sensing
    DOI:  https://doi.org/10.1007/s12602-026-11151-2
  47. Biomed Mater. 2026 Jul 21.
      Bone tissue has an inherent capacity for regeneration; however, this process is significantly impaired when the bone defects is large and infected by bacteria, particularly with multidrug-resistant strains. In this study, an injectable β-lactoglobulin fibrils/oxidized dextran/collagen (BLGFs/ODEX/COL) hydrogel biomaterial embedded with Acinetobacter baumannii bacteriophages was developed and evaluated for treating infected partial-thickness cortical tibia bone defects in rat models. The bacteriophage was successfully isolated from hospital sewage, amplified, purified, and morphologically confirmed using TEM. The SEM results showed that the hydrogel exhibited a highly porous and interconnected structure with pore sizes exceeding 50 µm, conducive for cell infiltration and tissue regeneration. ATR-FTIR analysis verified the chemical interactions amongst BLGFs, ODEX, and COL, confirming successful hydrogel formation. In vivo results demonstrated that bone defects treated with the phage-loaded hydrogel showed significantly accelerated bone regeneration by day 21 compared to antibiotic-treated and phage-only groups. Micro-CT analysis revealed superior outcomes in the hydrogel group, including higher tissue volume (above 4000 mm³), increased percent bone volume (above 2.4%), and greater bone surface density (above 0.1/mm), indicating enhanced osteogenesis and bone remodeling despite infection. The incorporation of bacteriophages into the BLGFs/ODEX/COL hydrogel provides a synergistic therapeutic strategy by combining localized antimicrobial activity with structural and biological support, thereby promoting improved healing of infected bone defects.
    Keywords:  Acinetobacter baumannii; bone defects; bone tissue regeneration; injectable hydrogel; phage therapy
    DOI:  https://doi.org/10.1088/1748-605X/ae8e14