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10 pages, 827 KB  
Article
Moraxella osloensis Isolated from the Intraoperative Field After Reverse Total Shoulder Arthroplasty
by Enrico Bellato, Fabio Longo, Francesca Menotti, Claudia Pagano, Antonio Curtoni, Alessandro Bondi, Filippo Castoldi, Giuliana Banche and Valeria Allizond
Microorganisms 2025, 13(12), 2699; https://doi.org/10.3390/microorganisms13122699 (registering DOI) - 26 Nov 2025
Abstract
Moraxella osloensis is an infrequently reported component of the human skin microbiota, but it has recently been recognized as a potential source of intraoperative contamination. Its pathogenic role remains poorly defined, particularly in shoulder arthroplasty. This study describes the recovery and characterization of [...] Read more.
Moraxella osloensis is an infrequently reported component of the human skin microbiota, but it has recently been recognized as a potential source of intraoperative contamination. Its pathogenic role remains poorly defined, particularly in shoulder arthroplasty. This study describes the recovery and characterization of M. osloensis from intraoperative periprosthetic tissue samples collected immediately after reverse total shoulder arthroplasty in five patients. All isolates exhibited low colony counts (10–50 CFU/mL), were uniformly susceptible to the antimicrobial agents tested, and did not produce β-lactamases. Biofilm formation—an important virulence determinant in periprosthetic joint infections—was detected in two of the five isolates. Clinically, no patient developed postoperative infection within 12 months, and only one experienced a transient superficial wound-healing delay, which resolved with a short administration of oral antibiotics. These findings indicate that M. osloensis may be present in the operative field despite stringent skin preparation and aseptic protocols, likely reflecting endogenous colonization rather than environmental contamination. Although its clinical impact appears limited in this context, the bacteria’s biofilm-forming potential and underrecognized presence in the operating room underscore the importance of continued surveillance and careful interpretation when isolated from surgical specimens. Full article
(This article belongs to the Special Issue Emerging Pathogen Infections and Host Immune)
20 pages, 3351 KB  
Article
Preliminary Study of Microbial Corrosion of Stainless Steel AISI 304 Under Conditions Simulating Deep Radioactive Waste Disposal
by Elena Abramova, Oleg Tripachev, Natalia Shapagina and Alexey Safonov
Materials 2025, 18(23), 5329; https://doi.org/10.3390/ma18235329 - 26 Nov 2025
Abstract
This work involved the laboratory modeling of biogenic and biogenically mediated corrosion of AISI 304 stainless steel under geochemical conditions representative of the geological disposal of radioactive waste at the Yeniseisky site (Russia). Experiments with a single glucose stimulation of a microbial community [...] Read more.
This work involved the laboratory modeling of biogenic and biogenically mediated corrosion of AISI 304 stainless steel under geochemical conditions representative of the geological disposal of radioactive waste at the Yeniseisky site (Russia). Experiments with a single glucose stimulation of a microbial community sampled from a depth of 450 m established that the initial dominance of organotrophic microflora (primarily genera such as Xanthobacterium, Novosphingobium, Hydrogenophaga, and Pseudomonas) during the first stage (up to 30 days) led to the formation of a microbial biofilm. This biofilm resulted in uniform surface corrosion at a rate of up to 16 µm/year, which is more than 30 times higher than the corrosion rate in the abiotic control. This acceleration is attributed to the accumulation of microbial metabolites, including acetate, ethanol, formate, succinate, n-butyrate, and lactate. The subsequent development of chemotrophic iron- and sulfur-cycling microflora (dominated by genera such as Sideroxydans, Pseudomonas, Geobacter, Desulfuromonas, Desulfovibrio, and Desulfomicrobium) during the second stage of microbial succession (days 60–120) led to the formation of a pit density 10 times greater than that in the abiotic control. It is important to note that the maximum corrosion rates and pit densities were observed upon the addition of a mixture of glucose and sulfate. An assessment of the role of various microbial metabolites and medium components using the potentiodynamic method demonstrated that the combined presence of hydrocarbonate, sulfide, and microbial metabolites in the solution caused a more than fivefold increase in the corrosion current. Thus, the results demonstrate the complex nature of corrosion processes under conditions modeling the geological disposal of radioactive waste, where biological and abiotic factors interact, creating a synergistic effect that significantly enhances corrosion. Full article
(This article belongs to the Section Corrosion)
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19 pages, 3908 KB  
Article
C14-HSL Quorum Sensing Signal Molecules: Promoting Role in Chalcopyrite Bioleaching Efficiency
by Shiqi Chen, Wang Luo, Zexing Yao, Yiran Li, Xinhong Wu, Nazidi Ibrahim, Shadab Begum and Yili Liang
Minerals 2025, 15(12), 1248; https://doi.org/10.3390/min15121248 - 26 Nov 2025
Abstract
N-tetradecanoyl-L-homoserine lactone (C14-HSL) is a long-chain signaling molecule belonging to acyl-homoserine lactones (AHLs), which is widely present in the quorum sensing (QS) system of Gram-negative bacteria. In this study, the effects of C14-HSL on chalcopyrite bioleaching [...] Read more.
N-tetradecanoyl-L-homoserine lactone (C14-HSL) is a long-chain signaling molecule belonging to acyl-homoserine lactones (AHLs), which is widely present in the quorum sensing (QS) system of Gram-negative bacteria. In this study, the effects of C14-HSL on chalcopyrite bioleaching mediated by Acidithiobacillus ferrooxidans (A. ferrooxidans) were investigated. After cultivating A. ferrooxidans with different energy substrates and exploring the potential mechanisms of signal molecule production, chalcopyrite was selected as the energy substrate for further study. Molecular docking analysis revealed that the high binding affinity between AHL and the receptor protein AfeR in A. ferrooxidans was beneficial for the activation of transcription by the AfeR-AHL complex, promoting their biological impact. The variations in the physicochemical parameters of pH, redox potential, and copper ions revealed that after adding C14-HSL, the leaching rate of chalcopyrite increased (1.15 times during the initial 12 days). Further analysis of the mechanism of extracellular polymers formation indicated that the presence of C14-HSL could promote the formation of biofilms and the adhesion of bacteria, facilitating mineral leaching rate of A. ferrooxidans. This research provides a theoretical basis for regulating the biological leaching process of chalcopyrite and metal recovery using signaling molecules, which could also be used to control environmental damage caused by acid mine/rock drainage. Full article
(This article belongs to the Special Issue Hydrometallurgical Treatments of Copper Ores, By-Products and Waste)
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2 pages, 125 KB  
Abstract
Assessing the Immune-Modulatory Effects of Indigenous Plants on Lymphocytes and Neutrophils
by Kgothatso Ashley Rakgate and Mxolisi Justice Ndlovu
Proceedings 2025, 130(1), 30; https://doi.org/10.3390/proceedings2025130030 - 26 Nov 2025
Abstract
Background: Infectious diseases continue to pose a worldwide health issue, intensified by the capacity of bacteria such as Staphylococcus aureus and Pseudomonas aeruginosa to elude host immune responses through mechanisms involving biofilm formation, intracellular survival, and the release of cytolytic toxins [...] Full article
18 pages, 12557 KB  
Article
Differential Proteomic Analysis of Extracellular Vesicles Produced by Granulicatella adiacens in Biofilm vs. Planktonic Lifestyle
by Maribasappa Karched and Sarah Alkandari
Dent. J. 2025, 13(12), 557; https://doi.org/10.3390/dj13120557 - 26 Nov 2025
Abstract
Background: Gram-positive bacteria, once considered incapable of producing extracellular vesicles (EVs) due to their thick peptidoglycan layer, are now known to secrete EVs that transport virulence factors and modulate host immunity. These EVs contribute to bacterial pathogenicity by facilitating biofilm formation, immune evasion, [...] Read more.
Background: Gram-positive bacteria, once considered incapable of producing extracellular vesicles (EVs) due to their thick peptidoglycan layer, are now known to secrete EVs that transport virulence factors and modulate host immunity. These EVs contribute to bacterial pathogenicity by facilitating biofilm formation, immune evasion, and inflammation. Granulicatella adiacens, an oral commensal associated with infective endocarditis, represents a clinically relevant model to study EV-mediated virulence. Objectives: This study’s aim was to investigate whether the proteomic composition and immunomodulatory activity of G. adiacens EVs differ between biofilm and planktonic lifestyles, thereby contributing to distinct pathogenic behaviours. Methods: EVs isolated from G. adiacens CCUG 27809 cultures were characterized using nano LC-ESI-MS/MS, followed by comprehensive bioinformatic and cytokine assays. Results: Quantitative proteomic profiling identified 1017 proteins, revealing distinct signatures between biofilm- and planktonic-derived EVs. Principal component analysis showed clear segregation between the two states, with biofilm EVs enriched in proteins linked to stress adaptation, adhesion, and structural integrity, while planktonic EVs exhibited growth- and metabolism-related proteins. A total of 114 virulence-associated proteins were identified, including several novel candidates. Functionally, EVs from both conditions significantly induced pro-inflammatory cytokines IL-8 and IL-1β in a dose-dependent manner (p < 0.05), whereas IL-17 remained unchanged. Conclusions: G. adiacens EVs exhibit lifestyle-dependent proteomic and immunomodulatory differences, underscoring their role in host–pathogen interactions and endocardial infection. These findings provide a foundation for future mechanistic and in vivo studies exploring EV-mediated virulence and potential therapeutic modulation. Full article
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17 pages, 3210 KB  
Article
HtrA Contributes to Biofilm Formation in Mycobacterium smegmatis by Downregulating the Cell Wall Amidase Ami3
by Jiachen Zheng, Yueqi Li, Yizhang Wei, Kang Li, Jie Lu, Xiaolin Liu and Weihui Li
Microorganisms 2025, 13(12), 2688; https://doi.org/10.3390/microorganisms13122688 - 25 Nov 2025
Abstract
Mycobacterium tuberculosis, the causative agent of tuberculosis, utilizes biofilm formation as a key mechanism to withstand host-derived stresses. To identify novel factors involved in this process, we performed a CRISPRi screen in the model organism Mycobacterium smegmatis. This screen identified trypsin [...] Read more.
Mycobacterium tuberculosis, the causative agent of tuberculosis, utilizes biofilm formation as a key mechanism to withstand host-derived stresses. To identify novel factors involved in this process, we performed a CRISPRi screen in the model organism Mycobacterium smegmatis. This screen identified trypsin HtrA as a critical factor for growth and biofilm formation. Deletion of htrA led to a profound upregulation of the cell wall amidase Ami3. We demonstrated that Ami3 is a crucial negative regulator of biofilm formation, as overexpression of ami3 recapitulated the biofilm and growth defects of the ΔhtrA strain. Furthermore, we found that the essential role of periplasmic protease HtrA for normal growth could be suppressed by novel mutations in pmt, a gene encoding a phosphomyoinositol mannosyltransferase, at residues F53 and N55, distinct from the previously reported D68 site. Our findings establish a novel regulatory pathway in which HtrA modulates mycobacterial biofilm formation by controlling the levels of Ami3 and reveal new genetic interactions within this network. Full article
(This article belongs to the Section Biofilm)
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2 pages, 132 KB  
Abstract
Computational and Experimental Validation of Aloe Vera Against Pseudomonas Aeruginosa PsrA in Interventive Antibacterial Therapeutics
by Karabo Ramatapa, Mduduzi Mokoena, Ivy Rukasha and Sabiu Saheed
Proceedings 2025, 130(1), 24; https://doi.org/10.3390/proceedings2025130024 - 24 Nov 2025
Abstract
Background: Pseudomonas aeruginosa, a multidrug-resistant pathogen, employs biofilm formation as a key virulence strategy, complicating treatment [...] Full article
47 pages, 3252 KB  
Review
Wounds and the Microbiota: The Healing Interplay Between Host and Microbial Communities
by Raghad Al-Taweel, Ayat S Hammad, Ali Tajammul, Sergio Crovella and Maha Al-Asmakh
Int. J. Mol. Sci. 2025, 26(23), 11365; https://doi.org/10.3390/ijms262311365 - 24 Nov 2025
Abstract
Chronic, non-healing wounds represent a major global health challenge, often aggravated by microbial dysbiosis and impaired host responses. Wound healing progresses through four overlapping phases—hemostasis, inflammation, proliferation, and remodeling—yet recent findings reveal that the skin microbiota actively participates in each step through immune, [...] Read more.
Chronic, non-healing wounds represent a major global health challenge, often aggravated by microbial dysbiosis and impaired host responses. Wound healing progresses through four overlapping phases—hemostasis, inflammation, proliferation, and remodeling—yet recent findings reveal that the skin microbiota actively participates in each step through immune, metabolic, and signaling mechanisms. Beneficial microorganisms such as Staphylococcus epidermidis and Lactobacillus plantarum promote tissue repair by inducing antimicrobial peptides and modulating cytokine production, whereas opportunistic pathogens (Staphylococcus aureus, Pseudomonas aeruginosa, Enterococcus faecalis) delay closure via biofilm formation and proteolytic activity. This review integrates current molecular insights and bibliometric trends to highlight advances and remaining challenges in understanding the wound–microbiome axis. A deeper grasp of these interactions can inform next-generation, microbiome-targeted therapies for chronic wounds. Full article
(This article belongs to the Special Issue Wound Repair: From Basic Biology to Tissue Engineering)
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2 pages, 3958 KB  
Correction
Correction: Zeng et al. Myricetin Potentiates Antibiotics Against Resistant Pseudomonas aeruginosa by Disrupting Biofilm Formation and Inhibiting Motility Through FimX-Mediated c-di-GMP Signaling Interference. Biology 2025, 14, 859
by Derong Zeng, Fangfang Jiao, Yuqi Yang, Shuai Dou, Jiahua Yu, Xiang Yu, Yongqiang Zhou, Juan Xue, Xue Li, Hongliang Duan, Yan Zhang, Jingjing Guo and Wude Yang
Biology 2025, 14(12), 1660; https://doi.org/10.3390/biology14121660 - 24 Nov 2025
Abstract
Error in Figure [...] Full article
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21 pages, 3206 KB  
Article
Lacticaseibacillus casei Combats Biofilm Formation and Exhibits Antibacterial Activity Against Clinical Isolates of Staphylococcus aureus, Salmonella enterica, and Escherichia coli
by Despoina Eugenia Kiousi, Sotiris Kyriakou, Christos Efstathiou, Stylianos Didaskalou, Maria Koffa, Aglaia Pappa, Maria Panopoulou, Mihalis I. Panayiotidis and Alex Galanis
Microorganisms 2025, 13(12), 2667; https://doi.org/10.3390/microorganisms13122667 - 24 Nov 2025
Abstract
Biofilm-forming pathogens are a major cause of persistent infections, showing limited response to antibiotic treatment. The search for alternative strategies has therefore driven extensive research into the antimicrobial potential of beneficial microorganisms. In the present study, the antibacterial and antibiofilm activity of the [...] Read more.
Biofilm-forming pathogens are a major cause of persistent infections, showing limited response to antibiotic treatment. The search for alternative strategies has therefore driven extensive research into the antimicrobial potential of beneficial microorganisms. In the present study, the antibacterial and antibiofilm activity of the commercial probiotic strain Lacticaseibacillus casei ATCC 393 (Lc393) was examined against clinical isolates of Staphylococcus aureus, Salmonella enterica subsp. enterica serovar Enteritidis and Escherichia coli. Lc393 reduced pathogen viability and attachment to the colon adenocarcinoma cell line HT-29, with maximal effects recorded against S. aureus. Confocal microscopy visualization of the lactobacilli-pathogens-host interface revealed that Lc393 binds loosely to both host cells and pathogens. The Lc393 cell-free culture supernatant (CFCS) significantly reduced planktonic growth, biofilm mass, and viability of cells in biofilm (>2 logCFU reduction, p < 0.05) and downregulated genes involved in the early stages of biofilm formation in S. aureus (i.e., icaA, fnbpA, eno). In silico analysis of the Lc393 genome identified two bacteriocin clusters, along with genes related to ethanol and organic acid production. Based on in silico predictions and a bacteriocin zymogram, the strain cannot produce functional antimicrobial peptides. Untargeted metabolomics based on UPLC/MS further revealed the presence of putative antimicrobial metabolites. Collectively, our findings highlight the antimicrobial potential of Lc. casei ATCC 393 and support its further investigation for combating clinically relevant human pathogens. Full article
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24 pages, 6251 KB  
Article
Gut-Protective and Multifunctional Exopolysaccharide from Enterococcus faecium HDRsEf1: Structural Characterization and Protective Effects Against Enteropathogenic E. coli-Induced Intestinal Inflammation
by Zeyuan Dong, Xinyang Li, Yaxin Wu, Zhaoyang Wang, Weitao Cui, Sishun Hu, Deshi Shi, Qi Huang, Yuncai Xiao, Hongbo Zhou, Zili Li and Zutao Zhou
Nutrients 2025, 17(23), 3667; https://doi.org/10.3390/nu17233667 - 24 Nov 2025
Abstract
Background: Enteropathogenic Escherichia coli (EPEC) disrupts intestinal barrier integrity by adhering to epithelial cells, leading to diarrhea, impaired nutrient absorption, oxidative stress, and intestinal inflammation in young animals. This study aimed to isolate and characterize a neutral exopolysaccharide (EPS-T1) from Enterococcus faecium HDRsEf1, [...] Read more.
Background: Enteropathogenic Escherichia coli (EPEC) disrupts intestinal barrier integrity by adhering to epithelial cells, leading to diarrhea, impaired nutrient absorption, oxidative stress, and intestinal inflammation in young animals. This study aimed to isolate and characterize a neutral exopolysaccharide (EPS-T1) from Enterococcus faecium HDRsEf1, evaluate its functional activities in vitro, and assess its protective effects against EPEC-induced enteritis in vivo. Results: EPS-T1, with a molecular weight of 81.21 ± 1.28 kDa, was mainly composed of glucose, galactose, rhamnose, and mannose, and exhibited a porous, sheet structure with relatively high thermal stability. In vitro, EPS-T1 (200 μg/mL) significantly inhibited EPEC growth and biofilm formation, reduced bacterial adhesion to intestinal epithelial cells, and exhibited broad-spectrum free radical scavenging activity. In vivo, EPS-T1 treatment alleviated EPEC-induced weight loss and intestinal tissue damage, reduced the intestinal EPEC load, downregulated pro-inflammatory cytokines (TNF-α, IL-1β, and IL-6), upregulated the anti-inflammatory cytokine IL-10, and improved serum antioxidant indices (T-AOC, SOD, and GSH-PX) while decreasing MDA levels. Conclusions: These results demonstrate that EPS-T1 derived from Enterococcus effectively mitigates EPEC-induced intestinal inflammation and oxidative stress, highlighting its potential as an immunobiotic functional candidate. Full article
(This article belongs to the Section Prebiotics and Probiotics)
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19 pages, 981 KB  
Article
Assessment of the Antimicrobial Activity of Cistus salviifolius L. and Helichrysum stoechas (L.) DC Extracts and Their Synergistic Potential with Conventional Antibiotics Against Staphylococcus aureus
by Alexandra Coimbra, Ângelo Luís, Pedro Dinis Gaspar, Susana Ferreira and Ana Paula Duarte
Int. J. Mol. Sci. 2025, 26(23), 11331; https://doi.org/10.3390/ijms262311331 - 24 Nov 2025
Abstract
This study aimed to evaluate the antibacterial activity of Cistus salviifolius L. and Helichrysum stoechas (L.) DC extracts against S. aureus, including methicillin-resistant S. aureus (MRSA) strains. To this end, assays were conducted to assess killing kinetics, antibiotic combination effects, modulatory effects [...] Read more.
This study aimed to evaluate the antibacterial activity of Cistus salviifolius L. and Helichrysum stoechas (L.) DC extracts against S. aureus, including methicillin-resistant S. aureus (MRSA) strains. To this end, assays were conducted to assess killing kinetics, antibiotic combination effects, modulatory effects on ethidium bromide, inhibition of quorum sensing, and biofilm formation. H. stoechas extract demonstrated the strongest activity, with MIC values ranging from 7.8 to 62.5 µg/mL. When combined with antibiotics such as ampicillin, ciprofloxacin, or vancomycin, the extracts of C. salviifolius and H. stoechas predominantly exhibited synergistic (FICI value ≤ 0.5) or additive effects (0.5 < FICI ≤ 1), with some combinations resensitizing resistant strains. The aerial parts of C. salviifolius displayed modulatory effects on ethidium bromide MIC, reducing the concentration from 32 to 8 µg/mL, suggesting efflux pump inhibitory activity. In addition, this extract displayed slight quorum-sensing inhibition at a concentration of 125 µg/mL. Moreover, C. salviifolius and H. stoechas extracts inhibit the formation of biofilm by S. aureus strains, even at subinhibitory concentrations (0.5× and 0.25× MIC). The presence of compounds such as myricetin 3 O-galactoside, catechin derivatives, gallic acid, kaempferol, and chlorogenic acid in the extracts may contribute to their anti-Staphylococcus activity. These results demonstrated the dual antimicrobial and antivirulence potential of C. salviifolius and H. stoechas extracts, highlighting their promise as therapeutic agents or adjuvants against S. aureus. These extracts can be promising candidates for further studies on the development of novel strategies targeting multiple pathogenic pathways. Full article
(This article belongs to the Section Bioactives and Nutraceuticals)
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16 pages, 3801 KB  
Article
Integration of a Fluoride- and Mint-Based Spray in Nighttime Aligner Therapy: Effects on Salivary Concentration and Biofilm
by Francesca Cremonini, Anna Bernardi, Alberto Bernardi and Luca Lombardo
Appl. Sci. 2025, 15(23), 12435; https://doi.org/10.3390/app152312435 - 24 Nov 2025
Viewed by 26
Abstract
Continuous use of clear aligners modifies the oral environment and may favor bacterial colonization. Integration of topical fluoride-based agents could strengthen enamel and reduce biofilm formation. This study evaluated the effects of a galenic fluoride-mint spray (225–250 ppm fluoride and 1–2% peppermint essential [...] Read more.
Continuous use of clear aligners modifies the oral environment and may favor bacterial colonization. Integration of topical fluoride-based agents could strengthen enamel and reduce biofilm formation. This study evaluated the effects of a galenic fluoride-mint spray (225–250 ppm fluoride and 1–2% peppermint essential oil) on salivary fluoride concentration and bacterial biofilm during orthodontic treatment. Ten patients using 3D-printed nighttime aligners were enrolled. Saliva samples were analyzed with an ion-selective electrode (ISE) at baseline, immediately after inserting the sprayed aligners and after 15, 30, 45 min post application. Biofilm morphology was qualitatively assessed by scanning electron microscope (SEM) in three aligners: unused, worn 14 nights without spray, worn 14 nights with spray. Salivary fluoride increased from 0.7–0.8 mg/L at baseline to 5.96 mg/L when the spray was applied on a new aligner and 8.42 mg/L on a used aligner, then progressively decreased, returning close to baseline at 45 min with the new aligner and remaining higher with the used aligner. SEM images showed mature and heterogeneous biofilm on used aligners without the spray, while aligners with nightly spray application exhibited qualitatively reduced and less organized surface deposits. The fluoride- and mint-based spray rapidly increases salivary fluoride and reduces biofilm formation on nighttime clear aligners, improving preventive oral health during orthodontic treatment. Full article
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23 pages, 2661 KB  
Article
Biosynthesized Silver Selenide Nanoparticles from Meyerozyma guilliermondii as a Novel Adjuvant to Revolutionize Gentamicin Therapy
by Min Xu, Lei Yang, Ya-Wei Zhang, Chao Wu, Yuan-Yuan Cheng and Hao Xue
Microorganisms 2025, 13(12), 2657; https://doi.org/10.3390/microorganisms13122657 - 22 Nov 2025
Viewed by 111
Abstract
The increasing prevalence of antibiotic resistance necessitates the development of novel antimicrobial agents and therapeutic strategies. This study reports the extracellular biosynthesis of silver selenide nanoparticles (Ag2Se NPs) using Meyerozyma guilliermondii PG-1 and evaluates their antimicrobial and antibiofilm efficacy, both alone [...] Read more.
The increasing prevalence of antibiotic resistance necessitates the development of novel antimicrobial agents and therapeutic strategies. This study reports the extracellular biosynthesis of silver selenide nanoparticles (Ag2Se NPs) using Meyerozyma guilliermondii PG-1 and evaluates their antimicrobial and antibiofilm efficacy, both alone and in combination with gentamicin. The NPs were thoroughly characterized, confirming their nanoscale size, crystallinity, and biomolecule-mediated stability. Ag2Se NPs exhibited broad-spectrum antibacterial activity against Gram-positive (Staphylococcus aureus) and Gram-negative (Pseudomonas aeruginosa, Escherichia coli) pathogens and showed strong synergy with gentamicin, particularly against P. aeruginosa and E. coli, as demonstrated through checkerboard and time–kill assays. The NPs also significantly inhibited biofilm formation and disrupted pre-formed biofilms. Mechanistic studies revealed that the antibacterial effects involved membrane disruption, ATP leakage, and elevated oxidative stress, while gene expression analysis in S. aureus indicated triggered stress responses related to biofilm formation. These findings suggest that biosynthesized Ag2Se NPs represent a promising synergistic agent for enhancing antibiotic efficacy and combating biofilm-related infections. Full article
(This article belongs to the Topic Antimicrobial Agents and Nanomaterials—2nd Edition)
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13 pages, 987 KB  
Article
Transfer and Fitness of ISAba52-Mediated tet(X3) Transposon in Acinetobacter spp.
by Chong Chen, Jing Liu, Jie Gao, Yubing Hua, Taotao Wu and Jinlin Huang
Microorganisms 2025, 13(12), 2656; https://doi.org/10.3390/microorganisms13122656 - 22 Nov 2025
Viewed by 210
Abstract
The global spread of tigecycline resistance conferred by tet(X3) poses a serious threat to clinical treatment of multidrug-resistant (MDR) Acinetobacter infections. Despite tet(X3) being detected in diverse Acinetobacter species, its transposition mechanism and fitness in these pathogens remain poorly characterized. Here, [...] Read more.
The global spread of tigecycline resistance conferred by tet(X3) poses a serious threat to clinical treatment of multidrug-resistant (MDR) Acinetobacter infections. Despite tet(X3) being detected in diverse Acinetobacter species, its transposition mechanism and fitness in these pathogens remain poorly characterized. Here, we reported the first plasmid-borne ISAba52-mediated transposable element harboring tet(X3) in Acinetobacter amyesii YH16040. Conjugation experiments demonstrated the transferability of tet(X3) into the chromosome of Acinetobacter baylyi ADP1 at an efficiency of (7.1 ± 2.5) × 10−8. High-throughput sequencing revealed six tandem copies of ISAba52-flanked tet(X3), floR, and sul2 forming a 231.6 Kb complex transposon in the obtained transconjugant A. baylyi YH16040C. Phenotypic assays showed that YH16040C exhibited elevated resistance to tigecycline, chlortetracycline, florfenicol, and trimethoprim-sulfamethoxazole by 64- to 256-fold. Notably, YH16040C exhibited a growth advantage, reduced competition ability, and non-significant difference in biofilm formation compared to ADP1 in antibiotic-free backgrounds. Under moderate antibiotic treatment of tigecycline, chlortetracycline, florfenicol, and trimethoprim-sulfamethoxazole, the competition ability of YH16040C against ADP1 was significantly higher than that without antibiotics. All of these highlight the importance of ISAba52-mediated transposition in disseminating tet(X3) between Acinetobacter species and elucidate the fitness changes employed by MDR strains under antibiotic selection pressures. Our study advocates the urgent need for surveillance of ISAba52-associated resistance elements in human, animal, and environmental settings. Full article
(This article belongs to the Section Antimicrobial Agents and Resistance)
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