Species-specific recruitment of transcription factors dictates toxin expression

Author:

Trouillon Julian1ORCID,Sentausa Erwin1,Ragno Michel1,Robert-Genthon Mylène1,Lory Stephen2,Attrée Ina1ORCID,Elsen Sylvie1ORCID

Affiliation:

1. Université Grenoble Alpes, CNRS ERL5261, CEA-IRIG-BCI, INSERM UMR1036, Grenoble 38000, France

2. Department of Microbiology, Harvard Medical School, Boston, Massachusetts 02115, USA

Abstract

Abstract Tight and coordinate regulation of virulence determinants is essential for bacterial biology and involves dynamic shaping of transcriptional regulatory networks during evolution. The horizontally transferred two-partner secretion system ExlB–ExlA is instrumental in the virulence of different Pseudomonas species, ranging from soil- and plant-dwelling biocontrol agents to the major human pathogen Pseudomonas aeruginosa. Here, we identify a Cro/CI-like repressor, named ErfA, which together with Vfr, a CRP-like activator, controls exlBA expression in P. aeruginosa. The characterization of ErfA regulon across P. aeruginosa subfamilies revealed a second conserved target, the ergAB operon, with functions unrelated to virulence. To gain insights into this functional dichotomy, we defined the pan-regulon of ErfA in several Pseudomonas species and found ergAB as the sole conserved target of ErfA. The analysis of 446 exlBA promoter sequences from all exlBA+ genomes revealed a wide variety of regulatory sequences, as ErfA- and Vfr-binding sites were found to have evolved specifically in P. aeruginosa and nearly each species carries different regulatory sequences for this operon. We propose that the emergence of different regulatory cis-elements in the promoters of horizontally transferred genes is an example of plasticity of regulatory networks evolving to provide an adapted response in each individual niche.

Funder

Agence Nationale de la Recherche

Laboratory of Excellence GRAL

CBH-EUR-GS

Fondation pour la Recherche Médicale

French Ministry of Education and Research

CNRS

Inserm

CEA

Publisher

Oxford University Press (OUP)

Subject

Genetics

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