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Significant variability exists in the cytotoxicity of global methicillin-resistant Staphylococcus aureus lineages

Staphylococcus aureus is a major human pathogen where the emergence of antibiotic resistant lineages, such as methicillin-resistant S. aureus (MRSA), is a major health concern. While some MRSA lineages are restricted to the healthcare setting, the epidemiology of MRSA is changing globally, with the...

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Autores principales: Laabei, Maisem, Peacock, Sharon J., Blane, Beth, Baines, Sarah L., Howden, Benjamin P., Stinear, Timothy P., Massey, Ruth C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Microbiology Society 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8744995/
https://www.ncbi.nlm.nih.gov/pubmed/34928202
http://dx.doi.org/10.1099/mic.0.001119
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author Laabei, Maisem
Peacock, Sharon J.
Blane, Beth
Baines, Sarah L.
Howden, Benjamin P.
Stinear, Timothy P.
Massey, Ruth C.
author_facet Laabei, Maisem
Peacock, Sharon J.
Blane, Beth
Baines, Sarah L.
Howden, Benjamin P.
Stinear, Timothy P.
Massey, Ruth C.
author_sort Laabei, Maisem
collection PubMed
description Staphylococcus aureus is a major human pathogen where the emergence of antibiotic resistant lineages, such as methicillin-resistant S. aureus (MRSA), is a major health concern. While some MRSA lineages are restricted to the healthcare setting, the epidemiology of MRSA is changing globally, with the rise of specific lineages causing disease in healthy people in the community. In the past two decades, community-associated MRSA (CA-MRSA) has emerged as a clinically important and virulent pathogen associated with serious skin and soft-tissue infections (SSTI). These infections are primarily cytotoxin driven, leading to the suggestion that hypervirulent lineages/multi-locus sequence types (STs) exist. To examine this, we compared the cytotoxicity of 475 MRSA isolates representing five major MRSA STs (ST22, ST93, ST8, ST239 and ST36) by employing a monocyte-macrophage THP-1 cell line as a surrogate for measuring gross cytotoxicity. We demonstrate that while certain MRSA STs contain highly toxic isolates, there is such variability within lineages to suggest that this aspect of virulence should not be inferred from the genotype of any given isolate. Furthermore, by interrogating the accessory gene regulator (Agr) sequences in this collection we identified several Agr mutations that were associated with reduced cytotoxicity. Interestingly, the majority of isolates that were attenuated in cytotoxin production contained no mutations in the agr locus, indicating a role of other undefined genes in S. aureus toxin regulation.
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spelling pubmed-87449952022-01-12 Significant variability exists in the cytotoxicity of global methicillin-resistant Staphylococcus aureus lineages Laabei, Maisem Peacock, Sharon J. Blane, Beth Baines, Sarah L. Howden, Benjamin P. Stinear, Timothy P. Massey, Ruth C. Microbiology (Reading) Microbial Virulence and Pathogenesis Staphylococcus aureus is a major human pathogen where the emergence of antibiotic resistant lineages, such as methicillin-resistant S. aureus (MRSA), is a major health concern. While some MRSA lineages are restricted to the healthcare setting, the epidemiology of MRSA is changing globally, with the rise of specific lineages causing disease in healthy people in the community. In the past two decades, community-associated MRSA (CA-MRSA) has emerged as a clinically important and virulent pathogen associated with serious skin and soft-tissue infections (SSTI). These infections are primarily cytotoxin driven, leading to the suggestion that hypervirulent lineages/multi-locus sequence types (STs) exist. To examine this, we compared the cytotoxicity of 475 MRSA isolates representing five major MRSA STs (ST22, ST93, ST8, ST239 and ST36) by employing a monocyte-macrophage THP-1 cell line as a surrogate for measuring gross cytotoxicity. We demonstrate that while certain MRSA STs contain highly toxic isolates, there is such variability within lineages to suggest that this aspect of virulence should not be inferred from the genotype of any given isolate. Furthermore, by interrogating the accessory gene regulator (Agr) sequences in this collection we identified several Agr mutations that were associated with reduced cytotoxicity. Interestingly, the majority of isolates that were attenuated in cytotoxin production contained no mutations in the agr locus, indicating a role of other undefined genes in S. aureus toxin regulation. Microbiology Society 2021-12-20 /pmc/articles/PMC8744995/ /pubmed/34928202 http://dx.doi.org/10.1099/mic.0.001119 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License. This article was made open access via a Publish and Read agreement between the Microbiology Society and the corresponding author’s institution.
spellingShingle Microbial Virulence and Pathogenesis
Laabei, Maisem
Peacock, Sharon J.
Blane, Beth
Baines, Sarah L.
Howden, Benjamin P.
Stinear, Timothy P.
Massey, Ruth C.
Significant variability exists in the cytotoxicity of global methicillin-resistant Staphylococcus aureus lineages
title Significant variability exists in the cytotoxicity of global methicillin-resistant Staphylococcus aureus lineages
title_full Significant variability exists in the cytotoxicity of global methicillin-resistant Staphylococcus aureus lineages
title_fullStr Significant variability exists in the cytotoxicity of global methicillin-resistant Staphylococcus aureus lineages
title_full_unstemmed Significant variability exists in the cytotoxicity of global methicillin-resistant Staphylococcus aureus lineages
title_short Significant variability exists in the cytotoxicity of global methicillin-resistant Staphylococcus aureus lineages
title_sort significant variability exists in the cytotoxicity of global methicillin-resistant staphylococcus aureus lineages
topic Microbial Virulence and Pathogenesis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8744995/
https://www.ncbi.nlm.nih.gov/pubmed/34928202
http://dx.doi.org/10.1099/mic.0.001119
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