Regulatory interactions between daptomycin‐ and bacitracin‐responsive pathways coordinate the cell envelope antibiotic resistance response of Enterococcus faecalis

Author:

Morris Sali M.1,Wiens Laura2,Rose Olivia1,Fritz Georg3ORCID,Rogers Tim4,Gebhard Susanne12ORCID

Affiliation:

1. Life Sciences Department, Milner Centre for Evolution University of Bath Bath UK

2. Institute of Molecular Physiology Johannes‐Gutenberg‐University Mainz Mainz Germany

3. School of Molecular Sciences The University of Western Australia Crawley WA Australia

4. Department of Mathematical Sciences University of Bath Bath UK

Abstract

AbstractEnterococcal infections frequently show high levels of antibiotic resistance, including to cell envelope‐acting antibiotics like daptomycin (DAP). While we have a good understanding of the resistance mechanisms, less is known about the control of such resistance genes in enterococci. Previous work unveiled a bacitracin resistance network, comprised of the sensory ABC transporter SapAB, the two‐component system (TCS) SapRS and the resistance ABC transporter RapAB. Interestingly, components of this system have recently been implicated in DAP resistance, a role usually regulated by the TCS LiaFSR. To better understand the regulation of DAP resistance and how this relates to mutations observed in DAP‐resistant clinical isolates of enterococci, we here explored the interplay between these two regulatory pathways. Our results show that SapR regulates an additional resistance operon, dltXABCD, a known DAP resistance determinant, and show that LiaFSR regulates the expression of sapRS. This regulatory structure places SapRS‐target genes under dual control, where expression is directly controlled by SapRS, which itself is up‐regulated through LiaFSR. The network structure described here shows how Enterococcus faecalis coordinates its response to cell envelope attack and can explain why clinical DAP resistance often emerges via mutations in regulatory components.

Funder

Medical Research Council

Publisher

Wiley

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