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Characterization of the biofilm forming ability of Staphylococcus pseudintermedius from dogs
BACKGROUND: Staphylococcus pseudintermedius is an opportunistic pathogen of dogs and has emerged as a leading cause of skin, wound and surgical site infections worldwide. Methicillin resistance is common and clinical infections as a result of methicillin-resistant S. pseudintermedius (MRSP) pose a c...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3681638/ https://www.ncbi.nlm.nih.gov/pubmed/23641755 http://dx.doi.org/10.1186/1746-6148-9-93 |
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author | Singh, Ameet Walker, Meagan Rousseau, Joyce Weese, Jeffrey Scott |
author_facet | Singh, Ameet Walker, Meagan Rousseau, Joyce Weese, Jeffrey Scott |
author_sort | Singh, Ameet |
collection | PubMed |
description | BACKGROUND: Staphylococcus pseudintermedius is an opportunistic pathogen of dogs and has emerged as a leading cause of skin, wound and surgical site infections worldwide. Methicillin resistance is common and clinical infections as a result of methicillin-resistant S. pseudintermedius (MRSP) pose a clinical challenge. In other staphylococci, biofilm formation has been shown to be a virulence factor for infection, however, it has received little attention in S. pseudintermedius. The objectives of this study were to evaluate the biofilm forming ability of clinical isolates of S. pseudintermedius obtained from dogs using phenotypic and genotypic techniques. RESULTS: 96% (136/140) of S. pseudintermedius isolates were classified as strong or moderate biofilm producers, with the majority of isolates being able to produce biofilm. There was no difference in biofilm formation between MRSP and MSSP (p=0.8), amongst isolates from clinical infections compared with isolates obtained from colonized dogs (p=0.08), and between isolates from sequence type (ST) 71 and ST 68 (P=0.09). icaA was detected in 77.9% (109/140) of isolates and icaD was detected in 75.7% (106/140) of isolates. Scanning electron microscopic evaluation of S. pseudintermedius biofilm production revealed aggregates of cocci and irregularly produced extracellular polymeric matrix. CONCLUSION: The majority of S. pseudintermedius isolates evaluated in this study were able to produce biofilm and this may be an important virulence factor in the rapid emergence of this bacterium in veterinary hospitals worldwide. Further study into the mechanisms of biofilm formation by S. pseudintermedius is warranted. |
format | Online Article Text |
id | pubmed-3681638 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-36816382013-06-14 Characterization of the biofilm forming ability of Staphylococcus pseudintermedius from dogs Singh, Ameet Walker, Meagan Rousseau, Joyce Weese, Jeffrey Scott BMC Vet Res Research Article BACKGROUND: Staphylococcus pseudintermedius is an opportunistic pathogen of dogs and has emerged as a leading cause of skin, wound and surgical site infections worldwide. Methicillin resistance is common and clinical infections as a result of methicillin-resistant S. pseudintermedius (MRSP) pose a clinical challenge. In other staphylococci, biofilm formation has been shown to be a virulence factor for infection, however, it has received little attention in S. pseudintermedius. The objectives of this study were to evaluate the biofilm forming ability of clinical isolates of S. pseudintermedius obtained from dogs using phenotypic and genotypic techniques. RESULTS: 96% (136/140) of S. pseudintermedius isolates were classified as strong or moderate biofilm producers, with the majority of isolates being able to produce biofilm. There was no difference in biofilm formation between MRSP and MSSP (p=0.8), amongst isolates from clinical infections compared with isolates obtained from colonized dogs (p=0.08), and between isolates from sequence type (ST) 71 and ST 68 (P=0.09). icaA was detected in 77.9% (109/140) of isolates and icaD was detected in 75.7% (106/140) of isolates. Scanning electron microscopic evaluation of S. pseudintermedius biofilm production revealed aggregates of cocci and irregularly produced extracellular polymeric matrix. CONCLUSION: The majority of S. pseudintermedius isolates evaluated in this study were able to produce biofilm and this may be an important virulence factor in the rapid emergence of this bacterium in veterinary hospitals worldwide. Further study into the mechanisms of biofilm formation by S. pseudintermedius is warranted. BioMed Central 2013-05-03 /pmc/articles/PMC3681638/ /pubmed/23641755 http://dx.doi.org/10.1186/1746-6148-9-93 Text en Copyright © 2013 Singh et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Singh, Ameet Walker, Meagan Rousseau, Joyce Weese, Jeffrey Scott Characterization of the biofilm forming ability of Staphylococcus pseudintermedius from dogs |
title | Characterization of the biofilm forming ability of Staphylococcus pseudintermedius from dogs |
title_full | Characterization of the biofilm forming ability of Staphylococcus pseudintermedius from dogs |
title_fullStr | Characterization of the biofilm forming ability of Staphylococcus pseudintermedius from dogs |
title_full_unstemmed | Characterization of the biofilm forming ability of Staphylococcus pseudintermedius from dogs |
title_short | Characterization of the biofilm forming ability of Staphylococcus pseudintermedius from dogs |
title_sort | characterization of the biofilm forming ability of staphylococcus pseudintermedius from dogs |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3681638/ https://www.ncbi.nlm.nih.gov/pubmed/23641755 http://dx.doi.org/10.1186/1746-6148-9-93 |
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