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Level of biofilm production by Staphylococcus aureus isolates is critical for resistance against most but not all antimicrobial drugs

BACKGROUND AND OBJECTIVE: Staphylococcal biofilms cause a wide range of acute and chronic infections, both in hospital and community settings across the world. This study explores biofilm forming propensity among Staphylococcus aureus clinical isolates from Faisalabad, Pakistan and their association...

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Autores principales: Salah-ud-din, Awan, Asad Bashir, Arshad, Muhammad Mohsin, Haque, Abdul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Professional Medical Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9676570/
https://www.ncbi.nlm.nih.gov/pubmed/36415244
http://dx.doi.org/10.12669/pjms.38.8.6276
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author Salah-ud-din,
Awan, Asad Bashir
Arshad, Muhammad Mohsin
Haque, Abdul
author_facet Salah-ud-din,
Awan, Asad Bashir
Arshad, Muhammad Mohsin
Haque, Abdul
author_sort Salah-ud-din,
collection PubMed
description BACKGROUND AND OBJECTIVE: Staphylococcal biofilms cause a wide range of acute and chronic infections, both in hospital and community settings across the world. This study explores biofilm forming propensity among Staphylococcus aureus clinical isolates from Faisalabad, Pakistan and their association with antimicrobial drug resistance. METHODS: The study was conducted during July to December 2020. The biofilm forming ability of S. aureus isolates was assessed by crystal violet staining in 96 well plates. Antimicrobial susceptibility was determined by disk diffusion method against ten antimicrobials representing whole spectrum of antimicrobial drugs. RESULTS: All the isolates (n=22) produced biofilm; 14 (63.6%) were strong, and 8 (36.4%) moderate biofilm producers. Comparative data were obtained for moderate and strong biofilm producers. Increased biofilm production did not affect azithromycin, clindamycin and mupirocin. However, stronger biofilm production significantly increased resistant isolates in case of augmentin (23.2%), cefoxitin (17.9%), levofloxacin (26.8%), tetracycline (23.2%), vancomycin (14.3%) and trimethoprim (21.4%). CONCLUSIONS: Our findings indicate that the ability to produce large amount of biofilm is an important factor, and S. aureus isolates with this ability, do not require acquisition of drug resistance genes from other bacteria. Our study also provides a guideline for selection of antimicrobials which are not adversely affected by level of biofilm production by various strains of S. aureus.
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spelling pubmed-96765702022-11-21 Level of biofilm production by Staphylococcus aureus isolates is critical for resistance against most but not all antimicrobial drugs Salah-ud-din, Awan, Asad Bashir Arshad, Muhammad Mohsin Haque, Abdul Pak J Med Sci Original Article BACKGROUND AND OBJECTIVE: Staphylococcal biofilms cause a wide range of acute and chronic infections, both in hospital and community settings across the world. This study explores biofilm forming propensity among Staphylococcus aureus clinical isolates from Faisalabad, Pakistan and their association with antimicrobial drug resistance. METHODS: The study was conducted during July to December 2020. The biofilm forming ability of S. aureus isolates was assessed by crystal violet staining in 96 well plates. Antimicrobial susceptibility was determined by disk diffusion method against ten antimicrobials representing whole spectrum of antimicrobial drugs. RESULTS: All the isolates (n=22) produced biofilm; 14 (63.6%) were strong, and 8 (36.4%) moderate biofilm producers. Comparative data were obtained for moderate and strong biofilm producers. Increased biofilm production did not affect azithromycin, clindamycin and mupirocin. However, stronger biofilm production significantly increased resistant isolates in case of augmentin (23.2%), cefoxitin (17.9%), levofloxacin (26.8%), tetracycline (23.2%), vancomycin (14.3%) and trimethoprim (21.4%). CONCLUSIONS: Our findings indicate that the ability to produce large amount of biofilm is an important factor, and S. aureus isolates with this ability, do not require acquisition of drug resistance genes from other bacteria. Our study also provides a guideline for selection of antimicrobials which are not adversely affected by level of biofilm production by various strains of S. aureus. Professional Medical Publications 2022 /pmc/articles/PMC9676570/ /pubmed/36415244 http://dx.doi.org/10.12669/pjms.38.8.6276 Text en Copyright: © Pakistan Journal of Medical Sciences https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0 (https://creativecommons.org/licenses/by/3.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Salah-ud-din,
Awan, Asad Bashir
Arshad, Muhammad Mohsin
Haque, Abdul
Level of biofilm production by Staphylococcus aureus isolates is critical for resistance against most but not all antimicrobial drugs
title Level of biofilm production by Staphylococcus aureus isolates is critical for resistance against most but not all antimicrobial drugs
title_full Level of biofilm production by Staphylococcus aureus isolates is critical for resistance against most but not all antimicrobial drugs
title_fullStr Level of biofilm production by Staphylococcus aureus isolates is critical for resistance against most but not all antimicrobial drugs
title_full_unstemmed Level of biofilm production by Staphylococcus aureus isolates is critical for resistance against most but not all antimicrobial drugs
title_short Level of biofilm production by Staphylococcus aureus isolates is critical for resistance against most but not all antimicrobial drugs
title_sort level of biofilm production by staphylococcus aureus isolates is critical for resistance against most but not all antimicrobial drugs
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9676570/
https://www.ncbi.nlm.nih.gov/pubmed/36415244
http://dx.doi.org/10.12669/pjms.38.8.6276
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