The two-component system WalKR provides an essential link between cell wall homeostasis and DNA replication in Staphylococcus aureus

Author:

Sharkey Liam K. R.1ORCID,Guerillot Romain1ORCID,Walsh Calum J.1,Turner Adrianna M.1,Lee Jean Y. H.1ORCID,Neville Stephanie L.1ORCID,Klatt Stephan2ORCID,Baines Sarah L.1ORCID,Pidot Sacha J.1ORCID,Rossello Fernando J.34ORCID,Seemann Torsten15ORCID,McWilliam Hamish E. G.1ORCID,Cho Ellie6,Carter Glen P.1ORCID,Howden Benjamin P.15ORCID,McDevitt Christopher A.1ORCID,Hachani Abderrahman1ORCID,Stinear Timothy P.15ORCID,Monk Ian R.1ORCID

Affiliation:

1. Department of Microbiology and Immunology, Doherty Institute for Infection and Immunity, University of Melbourne, Melbourne, Victoria, Australia

2. The Florey Institute of Neuroscience and Mental Health, Melbourne Dementia Research Centre, The University of Melbourne, Parkville, Victoria, Australia

3. University of Melbourne Centre for Cancer Research, The University of Melbourne, Melbourne, Victoria, Australia

4. Australian Regenerative Medicine Institute, Monash University, Melbourne, Victoria, Australia

5. Department of Microbiology and Immunology, Centre for Pathogen Genomics, Doherty Institute for Infection and Immunity, University of Melbourne, Melbourne, Victoria, Australia

6. Biological Optical Microscopy Platform, University of Melbourne, Melbourne, Victoria, Australia

Abstract

ABSTRACT Among the 16 two-component systems in the opportunistic human pathogen Staphylococcus aureus , only WalKR is essential. Like the orthologous systems in other Bacillota, S. aureus WalKR controls autolysins involved in peptidoglycan remodeling and is therefore intimately involved in cell division. However, despite the importance of WalKR in S. aureus , the basis for its essentiality is not understood and the regulon is poorly defined. Here, we defined a consensus WalR DNA-binding motif and the direct WalKR regulon by using functional genomics, including chromatin immunoprecipitation sequencing, with a panel of isogenic walKR mutants that had a spectrum of altered activities. Consistent with prior findings, the direct regulon includes multiple autolysin genes. However, this work also revealed that WalR directly regulates at least five essential genes involved in lipoteichoic acid synthesis ( ltaS ): translation ( rplK ), DNA compaction ( hup ), initiation of DNA replication ( dnaA , hup ) and purine nucleotide metabolism ( prs ). Thus, WalKR in S. aureus serves as a polyfunctional regulator that contributes to fundamental control over critical cell processes by coordinately linking cell wall homeostasis with purine biosynthesis, protein biosynthesis, and DNA replication. Our findings further address the essentiality of this locus and highlight the importance of WalKR as a bona fide target for novel anti-staphylococcal therapeutics. IMPORTANCE The opportunistic human pathogen Staphylococcus aureus uses an array of protein sensing systems called two-component systems (TCS) to sense environmental signals and adapt its physiology in response by regulating different genes. This sensory network is key to S. aureus versatility and success as a pathogen. Here, we reveal for the first time the full extent of the regulatory network of WalKR, the only staphylococcal TCS that is indispensable for survival under laboratory conditions. We found that WalKR is a master regulator of cell growth, coordinating the expression of genes from multiple, fundamental S. aureus cellular processes, including those involved in maintaining cell wall metabolism, protein biosynthesis, nucleotide metabolism, and the initiation of DNA replication.

Funder

DHAC | National Health and Medical Research Council

Australian Government Research Training Program Scholarship

Publisher

American Society for Microbiology

Subject

Virology,Microbiology

Reference93 articles.

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