M Protein and Hyaluronic Acid Capsule Are Essential for <italic toggle="yes">In Vivo</italic> Selection of <italic toggle="yes">covRS</italic> Mutations Characteristic of Invasive Serotype M1T1 Group A <italic toggle="yes">Streptococcus</italic>

ABSTRACT The initiation of hyperinvasive disease in group A Streptococcus (GAS) serotype M1T1 occurs by mutation within the covRS two-component regulon (named covRS for control of virulence regulatory sensor kinase), which promotes resistance to neutrophil-mediated killing through the upregulation o...

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Autores principales: Jason N. Cole, Morgan A. Pence, Maren von Köckritz-Blickwede, Andrew Hollands, Richard L. Gallo, Mark J. Walker, Victor Nizet
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Publicado: American Society for Microbiology 2010
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spelling oai:doaj.org-article:29d2718b948441769760790a552143282021-11-15T15:38:15ZM Protein and Hyaluronic Acid Capsule Are Essential for <italic toggle="yes">In Vivo</italic> Selection of <italic toggle="yes">covRS</italic> Mutations Characteristic of Invasive Serotype M1T1 Group A <italic toggle="yes">Streptococcus</italic>10.1128/mBio.00191-102150-7511https://doaj.org/article/29d2718b948441769760790a552143282010-10-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mBio.00191-10https://doaj.org/toc/2150-7511ABSTRACT The initiation of hyperinvasive disease in group A Streptococcus (GAS) serotype M1T1 occurs by mutation within the covRS two-component regulon (named covRS for control of virulence regulatory sensor kinase), which promotes resistance to neutrophil-mediated killing through the upregulation of bacteriophage-encoded Sda1 DNase. To determine whether other virulence factors contribute to this phase-switching phenomenon, we studied a panel of 10 isogenic GAS serotype M1T1 virulence gene knockout mutants. While loss of several individual virulence factors did not prevent GAS covRS switching in vivo, we found that M1 protein and hyaluronic acid capsule are indispensable for the switching phenotype, a phenomenon previously attributed uniquely to the Sda1 DNase. We demonstrate that like M1 protein and Sda1, capsule expression enhances survival of GAS serotype M1T1 within neutrophil extracellular traps. Furthermore, capsule shares with M1 protein a role in GAS resistance to human cathelicidin antimicrobial peptide LL-37. We conclude that a quorum of GAS serotype M1T1 virulence genes with cooperative roles in resistance to neutrophil extracellular killing is essential for the switch to a hyperinvasive phenotype in vivo. IMPORTANCE The pathogen group A Streptococcus (GAS) causes a wide range of human infections ranging from the superficial “strep throat” to potentially life-threatening conditions, such as necrotizing fasciitis, also known as “flesh-eating disease.” A marked increase in the number of cases of severe invasive GAS infection during the last 30 years has been traced to the emergence and spread of a single clone of the M1T1 serotype. Recent studies have shown that GAS serotype M1T1 bacteria undergo a genetic “switch” in vivo to a hypervirulent state that allows dissemination into the bloodstream. The present study was undertaken to identify specific GAS serotype M1T1 virulence factors required for this switch to hypervirulence. The surface-anchored GAS M1 protein and hyaluronic acid capsule are found to be essential for the switching phenotype, and a novel role for capsule in GAS resistance to host defense peptides and neutrophil extracellular killing is revealed.Jason N. ColeMorgan A. PenceMaren von Köckritz-BlickwedeAndrew HollandsRichard L. GalloMark J. WalkerVictor NizetAmerican Society for MicrobiologyarticleMicrobiologyQR1-502ENmBio, Vol 1, Iss 4 (2010)
institution DOAJ
collection DOAJ
language EN
topic Microbiology
QR1-502
spellingShingle Microbiology
QR1-502
Jason N. Cole
Morgan A. Pence
Maren von Köckritz-Blickwede
Andrew Hollands
Richard L. Gallo
Mark J. Walker
Victor Nizet
M Protein and Hyaluronic Acid Capsule Are Essential for <italic toggle="yes">In Vivo</italic> Selection of <italic toggle="yes">covRS</italic> Mutations Characteristic of Invasive Serotype M1T1 Group A <italic toggle="yes">Streptococcus</italic>
description ABSTRACT The initiation of hyperinvasive disease in group A Streptococcus (GAS) serotype M1T1 occurs by mutation within the covRS two-component regulon (named covRS for control of virulence regulatory sensor kinase), which promotes resistance to neutrophil-mediated killing through the upregulation of bacteriophage-encoded Sda1 DNase. To determine whether other virulence factors contribute to this phase-switching phenomenon, we studied a panel of 10 isogenic GAS serotype M1T1 virulence gene knockout mutants. While loss of several individual virulence factors did not prevent GAS covRS switching in vivo, we found that M1 protein and hyaluronic acid capsule are indispensable for the switching phenotype, a phenomenon previously attributed uniquely to the Sda1 DNase. We demonstrate that like M1 protein and Sda1, capsule expression enhances survival of GAS serotype M1T1 within neutrophil extracellular traps. Furthermore, capsule shares with M1 protein a role in GAS resistance to human cathelicidin antimicrobial peptide LL-37. We conclude that a quorum of GAS serotype M1T1 virulence genes with cooperative roles in resistance to neutrophil extracellular killing is essential for the switch to a hyperinvasive phenotype in vivo. IMPORTANCE The pathogen group A Streptococcus (GAS) causes a wide range of human infections ranging from the superficial “strep throat” to potentially life-threatening conditions, such as necrotizing fasciitis, also known as “flesh-eating disease.” A marked increase in the number of cases of severe invasive GAS infection during the last 30 years has been traced to the emergence and spread of a single clone of the M1T1 serotype. Recent studies have shown that GAS serotype M1T1 bacteria undergo a genetic “switch” in vivo to a hypervirulent state that allows dissemination into the bloodstream. The present study was undertaken to identify specific GAS serotype M1T1 virulence factors required for this switch to hypervirulence. The surface-anchored GAS M1 protein and hyaluronic acid capsule are found to be essential for the switching phenotype, and a novel role for capsule in GAS resistance to host defense peptides and neutrophil extracellular killing is revealed.
format article
author Jason N. Cole
Morgan A. Pence
Maren von Köckritz-Blickwede
Andrew Hollands
Richard L. Gallo
Mark J. Walker
Victor Nizet
author_facet Jason N. Cole
Morgan A. Pence
Maren von Köckritz-Blickwede
Andrew Hollands
Richard L. Gallo
Mark J. Walker
Victor Nizet
author_sort Jason N. Cole
title M Protein and Hyaluronic Acid Capsule Are Essential for <italic toggle="yes">In Vivo</italic> Selection of <italic toggle="yes">covRS</italic> Mutations Characteristic of Invasive Serotype M1T1 Group A <italic toggle="yes">Streptococcus</italic>
title_short M Protein and Hyaluronic Acid Capsule Are Essential for <italic toggle="yes">In Vivo</italic> Selection of <italic toggle="yes">covRS</italic> Mutations Characteristic of Invasive Serotype M1T1 Group A <italic toggle="yes">Streptococcus</italic>
title_full M Protein and Hyaluronic Acid Capsule Are Essential for <italic toggle="yes">In Vivo</italic> Selection of <italic toggle="yes">covRS</italic> Mutations Characteristic of Invasive Serotype M1T1 Group A <italic toggle="yes">Streptococcus</italic>
title_fullStr M Protein and Hyaluronic Acid Capsule Are Essential for <italic toggle="yes">In Vivo</italic> Selection of <italic toggle="yes">covRS</italic> Mutations Characteristic of Invasive Serotype M1T1 Group A <italic toggle="yes">Streptococcus</italic>
title_full_unstemmed M Protein and Hyaluronic Acid Capsule Are Essential for <italic toggle="yes">In Vivo</italic> Selection of <italic toggle="yes">covRS</italic> Mutations Characteristic of Invasive Serotype M1T1 Group A <italic toggle="yes">Streptococcus</italic>
title_sort m protein and hyaluronic acid capsule are essential for <italic toggle="yes">in vivo</italic> selection of <italic toggle="yes">covrs</italic> mutations characteristic of invasive serotype m1t1 group a <italic toggle="yes">streptococcus</italic>
publisher American Society for Microbiology
publishDate 2010
url https://doaj.org/article/29d2718b948441769760790a55214328
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