The effect of Silver nanoparticles on biofilm production of vancomycin resistant Staphylococcus aureus
Background & Aims: The increasing rate of vancomycin resistant Staphylococcus aureus (VRSA) with biofilm formation may become a new threat to humans. In such cases, finding an effective treatment strategy such as using Nanotechnology (Nano- drugs) to deal with these types of infections may be p...
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Format: | Article |
Language: | English |
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Urmia University of Medical Sciences
2020-04-01
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Series: | Journal of Research in Applied and Basic Medical Sciences |
Subjects: | |
Online Access: | http://ijrabms.umsu.ac.ir/article-1-102-en.pdf |
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author | Maryam Ghahremani Ali Haghi Ghahremanloi Olia Yaeghob Sharifi |
author_facet | Maryam Ghahremani Ali Haghi Ghahremanloi Olia Yaeghob Sharifi |
author_sort | Maryam Ghahremani |
collection | DOAJ |
description | Background & Aims: The increasing rate of vancomycin resistant Staphylococcus aureus (VRSA) with biofilm formation may become a new threat to humans. In such cases, finding an effective treatment strategy such as using Nanotechnology (Nano- drugs) to deal with these types of infections may be promising. This study aimed to investigate the inhibitory effects of silver nanoparticles (SNPs) on biofilm formation of VRSAs.
Materials and Methods: Clinical S. aureus isolates were identified to the species level by conventional methods, and their identities were later confirmed by PCR. Following the determination of susceptibility patterns of the isolates; all the screened S.aureus isolates have been assessed regarding their susceptibility to vancomycin. Detection of vanA gene and determination of minimum inhibitory concentrations (MICs) of VRSAs were carried out using PCR and Etest methods, respectively. The biofilm production was assessed on all VRSA isolates in the presence/absence of SNPs using micro-titer plate method.
Results: In total, 11 (6.21%) VRSAs were identified among 177 S. aureus clinical isolates. These isolates were included in the biofilm production assay. All of the VRSAs were multidrug resistance and biofilm producers. The inhibitory effect of SNPs in concentration of 250 µg/ml on biofilm formation of VRSA isolates was significant (Pv = 0.01).
Conclusion: Based on our findings, SNPs can prevent biofilm formation of VRSAs and applying of these nanoparticles may prohibit from the persistence and colonization of such resistant isolates. |
first_indexed | 2024-03-12T14:54:26Z |
format | Article |
id | doaj.art-29fc1d1a1bd94cb4a9acf5e9a9be872b |
institution | Directory Open Access Journal |
issn | 2717-0098 |
language | English |
last_indexed | 2024-03-12T14:54:26Z |
publishDate | 2020-04-01 |
publisher | Urmia University of Medical Sciences |
record_format | Article |
series | Journal of Research in Applied and Basic Medical Sciences |
spelling | doaj.art-29fc1d1a1bd94cb4a9acf5e9a9be872b2023-08-15T04:45:40ZengUrmia University of Medical SciencesJournal of Research in Applied and Basic Medical Sciences2717-00982020-04-01627278The effect of Silver nanoparticles on biofilm production of vancomycin resistant Staphylococcus aureusMaryam Ghahremani0Ali Haghi Ghahremanloi Olia1Yaeghob Sharifi2 Urmia university of medical sciences Urmia university of medical sciences Urmia university of medical sciences Background & Aims: The increasing rate of vancomycin resistant Staphylococcus aureus (VRSA) with biofilm formation may become a new threat to humans. In such cases, finding an effective treatment strategy such as using Nanotechnology (Nano- drugs) to deal with these types of infections may be promising. This study aimed to investigate the inhibitory effects of silver nanoparticles (SNPs) on biofilm formation of VRSAs. Materials and Methods: Clinical S. aureus isolates were identified to the species level by conventional methods, and their identities were later confirmed by PCR. Following the determination of susceptibility patterns of the isolates; all the screened S.aureus isolates have been assessed regarding their susceptibility to vancomycin. Detection of vanA gene and determination of minimum inhibitory concentrations (MICs) of VRSAs were carried out using PCR and Etest methods, respectively. The biofilm production was assessed on all VRSA isolates in the presence/absence of SNPs using micro-titer plate method. Results: In total, 11 (6.21%) VRSAs were identified among 177 S. aureus clinical isolates. These isolates were included in the biofilm production assay. All of the VRSAs were multidrug resistance and biofilm producers. The inhibitory effect of SNPs in concentration of 250 µg/ml on biofilm formation of VRSA isolates was significant (Pv = 0.01). Conclusion: Based on our findings, SNPs can prevent biofilm formation of VRSAs and applying of these nanoparticles may prohibit from the persistence and colonization of such resistant isolates.http://ijrabms.umsu.ac.ir/article-1-102-en.pdfvancomycin resistantstaphylococcus aureusbiofilminhibitory effects |
spellingShingle | Maryam Ghahremani Ali Haghi Ghahremanloi Olia Yaeghob Sharifi The effect of Silver nanoparticles on biofilm production of vancomycin resistant Staphylococcus aureus Journal of Research in Applied and Basic Medical Sciences vancomycin resistant staphylococcus aureus biofilm inhibitory effects |
title | The effect of Silver nanoparticles on biofilm production of vancomycin resistant Staphylococcus aureus |
title_full | The effect of Silver nanoparticles on biofilm production of vancomycin resistant Staphylococcus aureus |
title_fullStr | The effect of Silver nanoparticles on biofilm production of vancomycin resistant Staphylococcus aureus |
title_full_unstemmed | The effect of Silver nanoparticles on biofilm production of vancomycin resistant Staphylococcus aureus |
title_short | The effect of Silver nanoparticles on biofilm production of vancomycin resistant Staphylococcus aureus |
title_sort | effect of silver nanoparticles on biofilm production of vancomycin resistant staphylococcus aureus |
topic | vancomycin resistant staphylococcus aureus biofilm inhibitory effects |
url | http://ijrabms.umsu.ac.ir/article-1-102-en.pdf |
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