Heterogeneity in <scp><i>ess</i></scp> transcriptional organization and variable contribution of the <scp>Ess</scp>/Type <scp>VII</scp> protein secretion system to virulence across closely related <scp><i>S</i></scp><i>taphylocccus aureus</i> strains

Holger Kneuper(University of Dundee), Zhen Cao(University of Dundee), Kate B. Twomey(University College Cork), Martin Zoltner(University of Dundee), Franziska Jäger(University of Dundee), James S. Cargill(University of Dundee), James D. Chalmers(University of Dundee), Magdalena M. van der Kooi‐Pol(University Medical Center Groningen), Jan Maarten van Dijl(University Medical Center Groningen), Robert P. Ryan(University of Dundee), William N. Hunter(University of Dundee), Tracy Palmer(University of Dundee)
Molecular Microbiology
July 9, 2014
Cited by 97Open Access
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Abstract

The Type VII protein secretion system, found in Gram-positive bacteria, secretes small proteins, containing a conserved W-x-G amino acid sequence motif, to the growth medium. Staphylococcus aureus has a conserved Type VII secretion system, termed Ess, which is dispensable for laboratory growth but required for virulence. In this study we show that there are unexpected differences in the organization of the ess gene cluster between closely related strains of S. aureus. We further show that in laboratory growth medium different strains of S. aureus secrete the EsxA and EsxC substrate proteins at different growth points, and that the Ess system in strain Newman is inactive under these conditions. Systematic deletion analysis in S. aureus RN6390 is consistent with the EsaA, EsaB, EssA, EssB, EssC and EsxA proteins comprising core components of the secretion machinery in this strain. Finally we demonstrate that the Ess secretion machinery of two S. aureus strains, RN6390 and COL, is important for nasal colonization and virulence in the murine lung pneumonia model. Surprisingly, however, the secretion system plays no role in the virulence of strain SA113 under the same conditions.


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