Hyperexpression of a-hemolysin explains enhanced virulence of sequence type 93 community-associated methicillin-resistant Staphylococcus aureus

Background: The community-associated methicillin-resistant S. aureus (CA-MRSA) ST93 clone is becoming dominant in Australia and is clinically highly virulent. In addition, sepsis and skin infection models demonstrate that ST93 CA-MRSA is the most virulent global clone of S. aureus tested to date. Wh...

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Main Authors: Chua, K., Monk, I., Lin, Y., Seemann, T., Tuck, K., Porter, J., Stepnell, J., Coombs, Geoffrey, Davies, J., Stinear, T., Howden, B.
Format: Journal Article
Published: BioMed Central Ltd. 2014
Subjects:
Online Access:http://hdl.handle.net/20.500.11937/38640
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author Chua, K.
Monk, I.
Lin, Y.
Seemann, T.
Tuck, K.
Porter, J.
Stepnell, J.
Coombs, Geoffrey
Davies, J.
Stinear, T.
Howden, B.
author_facet Chua, K.
Monk, I.
Lin, Y.
Seemann, T.
Tuck, K.
Porter, J.
Stepnell, J.
Coombs, Geoffrey
Davies, J.
Stinear, T.
Howden, B.
author_sort Chua, K.
building Curtin Institutional Repository
collection Online Access
description Background: The community-associated methicillin-resistant S. aureus (CA-MRSA) ST93 clone is becoming dominant in Australia and is clinically highly virulent. In addition, sepsis and skin infection models demonstrate that ST93 CA-MRSA is the most virulent global clone of S. aureus tested to date. While the determinants of virulence have been studied in other clones of CA-MRSA, the basis for hypervirulence in ST93 CA-MRSA has not been defined. Results: Here, using a geographically and temporally dispersed collection of ST93 isolates we demonstrate that the ST93 population hyperexpresses key CA-MRSA exotoxins, in particular a-hemolysin, in comparison to other global clones. Gene deletion and complementation studies, and virulence comparisons in a murine skin infection model, showed unequivocally that increased expression of a-hemolysin is the key staphylococcal virulence determinant for this clone. Genome sequencing and comparative genomics of strains with divergent exotoxin profiles demonstrated that, like other S. aureus clones, the quorum sensing agr system is the master regulator of toxin expression and virulence in ST93 CA-MRSA. However, we also identified a previously uncharacterized AraC/XylS family regulator (AryK) that potentiates toxin expression and virulence in S. aureus. Conclusions: These data demonstrate that hyperexpression of a-hemolysin mediates enhanced virulence in ST93 CA-MRSA, and additional control of exotoxin production, in particular a-hemolysin, mediated by regulatory systems other than agr have the potential to fine-tune virulence in CA-MRSA.
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spelling curtin-20.500.11937-386402017-11-15T08:03:33Z Hyperexpression of a-hemolysin explains enhanced virulence of sequence type 93 community-associated methicillin-resistant Staphylococcus aureus Chua, K. Monk, I. Lin, Y. Seemann, T. Tuck, K. Porter, J. Stepnell, J. Coombs, Geoffrey Davies, J. Stinear, T. Howden, B. Alpha-hemolysin CA-MRSA Pathogenesis Staphylococcus aureus Background: The community-associated methicillin-resistant S. aureus (CA-MRSA) ST93 clone is becoming dominant in Australia and is clinically highly virulent. In addition, sepsis and skin infection models demonstrate that ST93 CA-MRSA is the most virulent global clone of S. aureus tested to date. While the determinants of virulence have been studied in other clones of CA-MRSA, the basis for hypervirulence in ST93 CA-MRSA has not been defined. Results: Here, using a geographically and temporally dispersed collection of ST93 isolates we demonstrate that the ST93 population hyperexpresses key CA-MRSA exotoxins, in particular a-hemolysin, in comparison to other global clones. Gene deletion and complementation studies, and virulence comparisons in a murine skin infection model, showed unequivocally that increased expression of a-hemolysin is the key staphylococcal virulence determinant for this clone. Genome sequencing and comparative genomics of strains with divergent exotoxin profiles demonstrated that, like other S. aureus clones, the quorum sensing agr system is the master regulator of toxin expression and virulence in ST93 CA-MRSA. However, we also identified a previously uncharacterized AraC/XylS family regulator (AryK) that potentiates toxin expression and virulence in S. aureus. Conclusions: These data demonstrate that hyperexpression of a-hemolysin mediates enhanced virulence in ST93 CA-MRSA, and additional control of exotoxin production, in particular a-hemolysin, mediated by regulatory systems other than agr have the potential to fine-tune virulence in CA-MRSA. 2014 Journal Article http://hdl.handle.net/20.500.11937/38640 10.1186/1471-2180-14-31 http://creativecommons.org/licenses/by/2.0/ BioMed Central Ltd. fulltext
spellingShingle Alpha-hemolysin
CA-MRSA
Pathogenesis
Staphylococcus aureus
Chua, K.
Monk, I.
Lin, Y.
Seemann, T.
Tuck, K.
Porter, J.
Stepnell, J.
Coombs, Geoffrey
Davies, J.
Stinear, T.
Howden, B.
Hyperexpression of a-hemolysin explains enhanced virulence of sequence type 93 community-associated methicillin-resistant Staphylococcus aureus
title Hyperexpression of a-hemolysin explains enhanced virulence of sequence type 93 community-associated methicillin-resistant Staphylococcus aureus
title_full Hyperexpression of a-hemolysin explains enhanced virulence of sequence type 93 community-associated methicillin-resistant Staphylococcus aureus
title_fullStr Hyperexpression of a-hemolysin explains enhanced virulence of sequence type 93 community-associated methicillin-resistant Staphylococcus aureus
title_full_unstemmed Hyperexpression of a-hemolysin explains enhanced virulence of sequence type 93 community-associated methicillin-resistant Staphylococcus aureus
title_short Hyperexpression of a-hemolysin explains enhanced virulence of sequence type 93 community-associated methicillin-resistant Staphylococcus aureus
title_sort hyperexpression of a-hemolysin explains enhanced virulence of sequence type 93 community-associated methicillin-resistant staphylococcus aureus
topic Alpha-hemolysin
CA-MRSA
Pathogenesis
Staphylococcus aureus
url http://hdl.handle.net/20.500.11937/38640