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Genetic structure of community acquired methicillin-resistant Staphylococcus aureus USA300

BACKGROUND: Community-associated methicillin-resistant Staphylococcus aureus (CA-MRSA) is a significant bacterial pathogen that poses considerable clinical and public health challenges. The majority of the CA-MRSA disease burden consists of skin and soft tissue infections (SSTI) not associated with...

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Autores principales: Tewhey, Ryan, Cannavino, Christopher R, Leake, John AD, Bansal, Vikas, Topol, Eric J, Torkamani, Ali, Bradley, John S, Schork, Nicholas J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3598774/
https://www.ncbi.nlm.nih.gov/pubmed/23009684
http://dx.doi.org/10.1186/1471-2164-13-508
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author Tewhey, Ryan
Cannavino, Christopher R
Leake, John AD
Bansal, Vikas
Topol, Eric J
Torkamani, Ali
Bradley, John S
Schork, Nicholas J
author_facet Tewhey, Ryan
Cannavino, Christopher R
Leake, John AD
Bansal, Vikas
Topol, Eric J
Torkamani, Ali
Bradley, John S
Schork, Nicholas J
author_sort Tewhey, Ryan
collection PubMed
description BACKGROUND: Community-associated methicillin-resistant Staphylococcus aureus (CA-MRSA) is a significant bacterial pathogen that poses considerable clinical and public health challenges. The majority of the CA-MRSA disease burden consists of skin and soft tissue infections (SSTI) not associated with significant morbidity; however, CA-MRSA also causes severe, invasive infections resulting in significant morbidity and mortality. The broad range of disease severity may be influenced by bacterial genetic variation. RESULTS: We sequenced the complete genomes of 36 CA-MRSA clinical isolates from the predominant North American community acquired clonal type USA300 (18 SSTI and 18 severe infection-associated isolates). While all 36 isolates shared remarkable genetic similarity, we found greater overall time-dependent sequence diversity among SSTI isolates. In addition, pathway analysis of non-synonymous variations revealed increased sequence diversity in the putative virulence genes of SSTI isolates. CONCLUSIONS: Here we report the first whole genome survey of diverse clinical isolates of the USA300 lineage and describe the evolution of the pathogen over time within a defined geographic area. The results demonstrate the close relatedness of clinically independent CA-MRSA isolates, which carry implications for understanding CA-MRSA epidemiology and combating its spread.
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spelling pubmed-35987742013-03-16 Genetic structure of community acquired methicillin-resistant Staphylococcus aureus USA300 Tewhey, Ryan Cannavino, Christopher R Leake, John AD Bansal, Vikas Topol, Eric J Torkamani, Ali Bradley, John S Schork, Nicholas J BMC Genomics Research Article BACKGROUND: Community-associated methicillin-resistant Staphylococcus aureus (CA-MRSA) is a significant bacterial pathogen that poses considerable clinical and public health challenges. The majority of the CA-MRSA disease burden consists of skin and soft tissue infections (SSTI) not associated with significant morbidity; however, CA-MRSA also causes severe, invasive infections resulting in significant morbidity and mortality. The broad range of disease severity may be influenced by bacterial genetic variation. RESULTS: We sequenced the complete genomes of 36 CA-MRSA clinical isolates from the predominant North American community acquired clonal type USA300 (18 SSTI and 18 severe infection-associated isolates). While all 36 isolates shared remarkable genetic similarity, we found greater overall time-dependent sequence diversity among SSTI isolates. In addition, pathway analysis of non-synonymous variations revealed increased sequence diversity in the putative virulence genes of SSTI isolates. CONCLUSIONS: Here we report the first whole genome survey of diverse clinical isolates of the USA300 lineage and describe the evolution of the pathogen over time within a defined geographic area. The results demonstrate the close relatedness of clinically independent CA-MRSA isolates, which carry implications for understanding CA-MRSA epidemiology and combating its spread. BioMed Central 2012-09-25 /pmc/articles/PMC3598774/ /pubmed/23009684 http://dx.doi.org/10.1186/1471-2164-13-508 Text en Copyright ©2012 Tewhey 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
Tewhey, Ryan
Cannavino, Christopher R
Leake, John AD
Bansal, Vikas
Topol, Eric J
Torkamani, Ali
Bradley, John S
Schork, Nicholas J
Genetic structure of community acquired methicillin-resistant Staphylococcus aureus USA300
title Genetic structure of community acquired methicillin-resistant Staphylococcus aureus USA300
title_full Genetic structure of community acquired methicillin-resistant Staphylococcus aureus USA300
title_fullStr Genetic structure of community acquired methicillin-resistant Staphylococcus aureus USA300
title_full_unstemmed Genetic structure of community acquired methicillin-resistant Staphylococcus aureus USA300
title_short Genetic structure of community acquired methicillin-resistant Staphylococcus aureus USA300
title_sort genetic structure of community acquired methicillin-resistant staphylococcus aureus usa300
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3598774/
https://www.ncbi.nlm.nih.gov/pubmed/23009684
http://dx.doi.org/10.1186/1471-2164-13-508
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