<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7</volume><submitter>Tabassum N</submitter><pubmed_abstract>The increasing incidence of antimicrobial resistance exhibited by biofilm-forming microbial pathogens has been recognized as one of the major issues in the healthcare sector. In the present study, nanomaterial-based controlling the biofilm and virulence properties has been considered an alternative approach. Pyoverdine (PVD) isolated from the &lt;i>Pseudomonas aeruginosa&lt;/i> was utilized as a biological corona to synthesize silver nanoparticles (AgNPs), which will be helpful in a targeted action to microbial pathogens due to the recognition of the corona of the nanoparticles by the pathogenic membrane. Synthesized PVD-AgNPs were spherical to irregular, with an average size value of 251.87 ± 21.8 nm and zeta potential with a value of -36.51 ± 0.69 mV. The MIC value of PVD-AgNPs towards &lt;i>P. aeruginosa&lt;/i>, &lt;i>Listeria monocytogenes&lt;/i>, &lt;i>Staphylococcus aureus&lt;/i>, &lt;i>Streptococcus mutans&lt;/i>, &lt;i>Escherichia coli&lt;/i>, and &lt;i>Candida albicans&lt;/i> in the standard and host-mimicking media were observed in decreasing order in a multi-fold, such as standard growth media > sputum > synthetic human urine > saliva. Both the initial stage and the well-established biofilms of these microbial pathogens have been effectively inhibited and eradicated by PVD-AgNPs. PVD-AgNPs increase the susceptibility of tetracycline, PVD, and amphotericin B towards established mature mono- and mixed-species biofilms of &lt;i>S. aureus&lt;/i> and &lt;i>C. albicans&lt;/i>. Additionally, PVD-AgNPs attenuate several virulence properties, such as inhibition of protease activity, motility, and PVD and pyocyanin production in &lt;i>P. aeruginosa&lt;/i>. The inhibition of gene expression of biofilm and virulence-associated genes in &lt;i>P. aeruginosa&lt;/i> validates its phenotypic effects.</pubmed_abstract><journal>Biofilm</journal><pagination>100192</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10966193</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Silver nanoparticles synthesized from &lt;i>Pseudomonas aeruginosa&lt;/i> pyoverdine: Antibiofilm and antivirulence agents.</pubmed_title><pmcid>PMC10966193</pmcid><pubmed_authors>Kim YM</pubmed_authors><pubmed_authors>Jo DM</pubmed_authors><pubmed_authors>Khan F</pubmed_authors><pubmed_authors>Jeong GJ</pubmed_authors><pubmed_authors>Tabassum N</pubmed_authors></additional><is_claimable>false</is_claimable><name>Silver nanoparticles synthesized from &lt;i>Pseudomonas aeruginosa&lt;/i> pyoverdine: Antibiofilm and antivirulence agents.</name><description>The increasing incidence of antimicrobial resistance exhibited by biofilm-forming microbial pathogens has been recognized as one of the major issues in the healthcare sector. In the present study, nanomaterial-based controlling the biofilm and virulence properties has been considered an alternative approach. Pyoverdine (PVD) isolated from the &lt;i>Pseudomonas aeruginosa&lt;/i> was utilized as a biological corona to synthesize silver nanoparticles (AgNPs), which will be helpful in a targeted action to microbial pathogens due to the recognition of the corona of the nanoparticles by the pathogenic membrane. Synthesized PVD-AgNPs were spherical to irregular, with an average size value of 251.87 ± 21.8 nm and zeta potential with a value of -36.51 ± 0.69 mV. The MIC value of PVD-AgNPs towards &lt;i>P. aeruginosa&lt;/i>, &lt;i>Listeria monocytogenes&lt;/i>, &lt;i>Staphylococcus aureus&lt;/i>, &lt;i>Streptococcus mutans&lt;/i>, &lt;i>Escherichia coli&lt;/i>, and &lt;i>Candida albicans&lt;/i> in the standard and host-mimicking media were observed in decreasing order in a multi-fold, such as standard growth media > sputum > synthetic human urine > saliva. Both the initial stage and the well-established biofilms of these microbial pathogens have been effectively inhibited and eradicated by PVD-AgNPs. PVD-AgNPs increase the susceptibility of tetracycline, PVD, and amphotericin B towards established mature mono- and mixed-species biofilms of &lt;i>S. aureus&lt;/i> and &lt;i>C. albicans&lt;/i>. Additionally, PVD-AgNPs attenuate several virulence properties, such as inhibition of protease activity, motility, and PVD and pyocyanin production in &lt;i>P. aeruginosa&lt;/i>. The inhibition of gene expression of biofilm and virulence-associated genes in &lt;i>P. aeruginosa&lt;/i> validates its phenotypic effects.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jun</publication><modification>2025-04-04T23:52:56.738Z</modification><creation>2025-04-04T23:52:56.738Z</creation></dates><accession>S-EPMC10966193</accession><cross_references><pubmed>38544742</pubmed><doi>10.1016/j.bioflm.2024.100192</doi></cross_references></HashMap>