Transcription and translation products of the cytolysin gene psm-mec on the mobile genetic element SCCmec regulate Staphylococcus aureus virulence.

The F region downstream of the mecI gene in the SCCmec element in hospital-associated methicillin-resistant Staphylococcus aureus (HA-MRSA) contains two bidirectionally overlapping open reading frames (ORFs), the fudoh ORF and the psm-mec ORF. The psm-mec ORF encodes a cytolysin, phenol-soluble modu...

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Autores principales: Chikara Kaito, Yuki Saito, Gentaro Nagano, Mariko Ikuo, Yosuke Omae, Yuichi Hanada, Xiao Han, Kyoko Kuwahara-Arai, Tomomi Hishinuma, Tadashi Baba, Teruyo Ito, Keiichi Hiramatsu, Kazuhisa Sekimizu
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Publicado: Public Library of Science (PLoS) 2011
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Acceso en línea:https://doaj.org/article/01181988587c4409935821e4ed22c88e
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spelling oai:doaj.org-article:01181988587c4409935821e4ed22c88e2021-11-18T06:03:38ZTranscription and translation products of the cytolysin gene psm-mec on the mobile genetic element SCCmec regulate Staphylococcus aureus virulence.1553-73661553-737410.1371/journal.ppat.1001267https://doaj.org/article/01181988587c4409935821e4ed22c88e2011-02-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21304931/pdf/?tool=EBIhttps://doaj.org/toc/1553-7366https://doaj.org/toc/1553-7374The F region downstream of the mecI gene in the SCCmec element in hospital-associated methicillin-resistant Staphylococcus aureus (HA-MRSA) contains two bidirectionally overlapping open reading frames (ORFs), the fudoh ORF and the psm-mec ORF. The psm-mec ORF encodes a cytolysin, phenol-soluble modulin (PSM)-mec. Transformation of the F region into the Newman strain, which is a methicillin-sensitive S. aureus (MSSA) strain, or into the MW2 (USA400) and FRP3757 (USA300) strains, which are community-acquired MRSA (CA-MRSA) strains that lack the F region, attenuated their virulence in a mouse systemic infection model. Introducing the F region to these strains suppressed colony-spreading activity and PSMα production, and promoted biofilm formation. By producing mutations into the psm-mec ORF, we revealed that (i) both the transcription and translation products of the psm-mec ORF suppressed colony-spreading activity and promoted biofilm formation; and (ii) the transcription product of the psm-mec ORF, but not its translation product, decreased PSMα production. These findings suggest that both the psm-mec transcript, acting as a regulatory RNA, and the PSM-mec protein encoded by the gene on the mobile genetic element SCCmec regulate the virulence of Staphylococcus aureus.Chikara KaitoYuki SaitoGentaro NaganoMariko IkuoYosuke OmaeYuichi HanadaXiao HanKyoko Kuwahara-AraiTomomi HishinumaTadashi BabaTeruyo ItoKeiichi HiramatsuKazuhisa SekimizuPublic Library of Science (PLoS)articleImmunologic diseases. AllergyRC581-607Biology (General)QH301-705.5ENPLoS Pathogens, Vol 7, Iss 2, p e1001267 (2011)
institution DOAJ
collection DOAJ
language EN
topic Immunologic diseases. Allergy
RC581-607
Biology (General)
QH301-705.5
spellingShingle Immunologic diseases. Allergy
RC581-607
Biology (General)
QH301-705.5
Chikara Kaito
Yuki Saito
Gentaro Nagano
Mariko Ikuo
Yosuke Omae
Yuichi Hanada
Xiao Han
Kyoko Kuwahara-Arai
Tomomi Hishinuma
Tadashi Baba
Teruyo Ito
Keiichi Hiramatsu
Kazuhisa Sekimizu
Transcription and translation products of the cytolysin gene psm-mec on the mobile genetic element SCCmec regulate Staphylococcus aureus virulence.
description The F region downstream of the mecI gene in the SCCmec element in hospital-associated methicillin-resistant Staphylococcus aureus (HA-MRSA) contains two bidirectionally overlapping open reading frames (ORFs), the fudoh ORF and the psm-mec ORF. The psm-mec ORF encodes a cytolysin, phenol-soluble modulin (PSM)-mec. Transformation of the F region into the Newman strain, which is a methicillin-sensitive S. aureus (MSSA) strain, or into the MW2 (USA400) and FRP3757 (USA300) strains, which are community-acquired MRSA (CA-MRSA) strains that lack the F region, attenuated their virulence in a mouse systemic infection model. Introducing the F region to these strains suppressed colony-spreading activity and PSMα production, and promoted biofilm formation. By producing mutations into the psm-mec ORF, we revealed that (i) both the transcription and translation products of the psm-mec ORF suppressed colony-spreading activity and promoted biofilm formation; and (ii) the transcription product of the psm-mec ORF, but not its translation product, decreased PSMα production. These findings suggest that both the psm-mec transcript, acting as a regulatory RNA, and the PSM-mec protein encoded by the gene on the mobile genetic element SCCmec regulate the virulence of Staphylococcus aureus.
format article
author Chikara Kaito
Yuki Saito
Gentaro Nagano
Mariko Ikuo
Yosuke Omae
Yuichi Hanada
Xiao Han
Kyoko Kuwahara-Arai
Tomomi Hishinuma
Tadashi Baba
Teruyo Ito
Keiichi Hiramatsu
Kazuhisa Sekimizu
author_facet Chikara Kaito
Yuki Saito
Gentaro Nagano
Mariko Ikuo
Yosuke Omae
Yuichi Hanada
Xiao Han
Kyoko Kuwahara-Arai
Tomomi Hishinuma
Tadashi Baba
Teruyo Ito
Keiichi Hiramatsu
Kazuhisa Sekimizu
author_sort Chikara Kaito
title Transcription and translation products of the cytolysin gene psm-mec on the mobile genetic element SCCmec regulate Staphylococcus aureus virulence.
title_short Transcription and translation products of the cytolysin gene psm-mec on the mobile genetic element SCCmec regulate Staphylococcus aureus virulence.
title_full Transcription and translation products of the cytolysin gene psm-mec on the mobile genetic element SCCmec regulate Staphylococcus aureus virulence.
title_fullStr Transcription and translation products of the cytolysin gene psm-mec on the mobile genetic element SCCmec regulate Staphylococcus aureus virulence.
title_full_unstemmed Transcription and translation products of the cytolysin gene psm-mec on the mobile genetic element SCCmec regulate Staphylococcus aureus virulence.
title_sort transcription and translation products of the cytolysin gene psm-mec on the mobile genetic element sccmec regulate staphylococcus aureus virulence.
publisher Public Library of Science (PLoS)
publishDate 2011
url https://doaj.org/article/01181988587c4409935821e4ed22c88e
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