{"title":"Antibacterial, anti-biofilm and anti-virulence activity of biosynthesized silver nanoparticles against drug-resistant Staphylococcus aureus.","authors":"Jaideep Singh, Ravi Kant Agrawal, Kajal Bankoti, Richa Sarkar, Mrinalini Saini, Keshav Kashyap, Deepak Kumar, Gaurav Kumar Sharma, Prabhat Nath Jha, Sonali Jain, Bhoj Raj Singh","doi":"10.1007/s11259-025-10900-y","DOIUrl":null,"url":null,"abstract":"<p><p>Antibiotic resistance in bacteria has become a major concern for the effective treatment of infections; therefore, alternatives to antibiotics are being extensively researched to combat drug-resistant microbes. In this study, silver nanoparticles (AgNPs) were biosynthesized using aqueous extracts of papaya leaves (Carica papaya), cannabis leaves (Cannabis sativa), and cardamom (Elettaria cardamomum) and characterized by field-emission scanning electron microscopy (FE-SEM) and UV-visible spectrophotometry. Biosynthesized AgNPs were evaluated for their antibacterial, anti-biofilm, and anti-virulence potential by phenotypic and genotypic methods. AgNPs biosynthesized by all three extracts had spherical morphology and sizes in the nanoscale, average diameter ranging from 46.05 to 94.12 nm. Antibacterial susceptibility testing of S. aureus field isolates under study revealed 48% (24/50) and 38% (19/50) to be resistant to methicillin and amoxycillin-clavulanic acid, respectively. Antibacterial activity of biosynthesized AgNPs against S. aureus strains was determined by the well diffusion method. AgNPs were found to be effective on 90.90% (50/55) S. aureus strains with a zone of inhibition varying from 10 to 21 mm. The AgNPs were also found to be effective on other important bacterial pathogens (viz. Bacillus cereus ATCC 10876, Pseudomonas aeruginosa ATCC 27853, Salmonella Enteritidis ATCC 13070, Escherichia coli ATCC 43888, and Listeria monocytogenes MTCC 657) screened in the study with a ZOI of 15-18 mm. The minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) of AgNPs against S. aureus ranged between 0.015625-0.125 mg/mL and 0.015625-0.25 mg/mL, respectively. In the time kill assay, AgNPs were able to kill S. aureus rapidly within 0.5-1.0 h. In the haemolytic assay, 4-9% haemolysis was observed at concentrations ranging from 0.015625 to 0.25 mg/mL of AgNPs. Biofilm-forming ability of all strains of S. aureus (n = 55) determined by crystal violet assay revealed that 87.27% (48/55) were biofilm formers, while 12.73% (7/55) were non-biofilm formers. Out of 48 biofilm-forming strains, 81.25% (39/48) were strong biofilm producers, 10.41% (5/48) were moderate biofilm producers, and 8.33% (4/48) were weak biofilm producers. Anti-biofilm effect of AgNPs was found at sub-MIC (0.03125 mg/mL), phenotypically. Exopolysaccharide production was found to be reduced by 53.38% indicating the anti-virulence potential of AgNPs at sub-MIC. Relative expression analysis revealed that AgNPs downregulated the expression of biofilm-related genes, namely icaC, icaD, and spa, by 14.2, 10.6, and 8.7-fold, respectively, compared to the control at 3 h of incubation. Other biofilm-related and virulence genes, including icaA, icaB, icaR, agr, ebps, fnb-B, sar-A, and katA, were also found to be downregulated by 7.4, 7.5, 6.2, 5, 4.2, 7.3, 4, and 3.6-fold, respectively, at 3 h. All the target genes were also found to be downregulated at 24 h post-treatment with AgNPs, except icaD, icaR, and agr, which were slightly upregulated. In the present study, AgNPs were successfully biosynthesized and found to possess broad-spectrum antibacterial activity, reduce biofilm formation, and EPS production. Biosynthesized AgNPs has potential to be utilized as antibacterial, anti-biofilm, and anti-virulence agents against S. aureus, as alternative to conventional antibacterial agents.</p>","PeriodicalId":23690,"journal":{"name":"Veterinary Research Communications","volume":"49 6","pages":"345"},"PeriodicalIF":2.0000,"publicationDate":"2025-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Veterinary Research Communications","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1007/s11259-025-10900-y","RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"VETERINARY SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Antibiotic resistance in bacteria has become a major concern for the effective treatment of infections; therefore, alternatives to antibiotics are being extensively researched to combat drug-resistant microbes. In this study, silver nanoparticles (AgNPs) were biosynthesized using aqueous extracts of papaya leaves (Carica papaya), cannabis leaves (Cannabis sativa), and cardamom (Elettaria cardamomum) and characterized by field-emission scanning electron microscopy (FE-SEM) and UV-visible spectrophotometry. Biosynthesized AgNPs were evaluated for their antibacterial, anti-biofilm, and anti-virulence potential by phenotypic and genotypic methods. AgNPs biosynthesized by all three extracts had spherical morphology and sizes in the nanoscale, average diameter ranging from 46.05 to 94.12 nm. Antibacterial susceptibility testing of S. aureus field isolates under study revealed 48% (24/50) and 38% (19/50) to be resistant to methicillin and amoxycillin-clavulanic acid, respectively. Antibacterial activity of biosynthesized AgNPs against S. aureus strains was determined by the well diffusion method. AgNPs were found to be effective on 90.90% (50/55) S. aureus strains with a zone of inhibition varying from 10 to 21 mm. The AgNPs were also found to be effective on other important bacterial pathogens (viz. Bacillus cereus ATCC 10876, Pseudomonas aeruginosa ATCC 27853, Salmonella Enteritidis ATCC 13070, Escherichia coli ATCC 43888, and Listeria monocytogenes MTCC 657) screened in the study with a ZOI of 15-18 mm. The minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) of AgNPs against S. aureus ranged between 0.015625-0.125 mg/mL and 0.015625-0.25 mg/mL, respectively. In the time kill assay, AgNPs were able to kill S. aureus rapidly within 0.5-1.0 h. In the haemolytic assay, 4-9% haemolysis was observed at concentrations ranging from 0.015625 to 0.25 mg/mL of AgNPs. Biofilm-forming ability of all strains of S. aureus (n = 55) determined by crystal violet assay revealed that 87.27% (48/55) were biofilm formers, while 12.73% (7/55) were non-biofilm formers. Out of 48 biofilm-forming strains, 81.25% (39/48) were strong biofilm producers, 10.41% (5/48) were moderate biofilm producers, and 8.33% (4/48) were weak biofilm producers. Anti-biofilm effect of AgNPs was found at sub-MIC (0.03125 mg/mL), phenotypically. Exopolysaccharide production was found to be reduced by 53.38% indicating the anti-virulence potential of AgNPs at sub-MIC. Relative expression analysis revealed that AgNPs downregulated the expression of biofilm-related genes, namely icaC, icaD, and spa, by 14.2, 10.6, and 8.7-fold, respectively, compared to the control at 3 h of incubation. Other biofilm-related and virulence genes, including icaA, icaB, icaR, agr, ebps, fnb-B, sar-A, and katA, were also found to be downregulated by 7.4, 7.5, 6.2, 5, 4.2, 7.3, 4, and 3.6-fold, respectively, at 3 h. All the target genes were also found to be downregulated at 24 h post-treatment with AgNPs, except icaD, icaR, and agr, which were slightly upregulated. In the present study, AgNPs were successfully biosynthesized and found to possess broad-spectrum antibacterial activity, reduce biofilm formation, and EPS production. Biosynthesized AgNPs has potential to be utilized as antibacterial, anti-biofilm, and anti-virulence agents against S. aureus, as alternative to conventional antibacterial agents.
期刊介绍:
Veterinary Research Communications publishes fully refereed research articles and topical reviews on all aspects of the veterinary sciences. Interdisciplinary articles are particularly encouraged, as are well argued reviews, even if they are somewhat controversial.
The journal is an appropriate medium in which to publish new methods, newly described diseases and new pathological findings, as these are applied to animals. The material should be of international rather than local interest. As it deliberately seeks a wide coverage, Veterinary Research Communications provides its readers with a means of keeping abreast of current developments in the entire field of veterinary science.