Role of the dosR - dosS Two-Component Regulatory System in Mycobacterium tuberculosis Virulence in Three Animal Models

Author:

Converse Paul J.1,Karakousis Petros C.1,Klinkenberg Lee G.1,Kesavan Anup K.1,Ly Lan H.2,Allen Shannon Sedberry2,Grosset Jacques H.1,Jain Sanjay K.1,Lamichhane Gyanu1,Manabe Yukari C.1,McMurray David N.2,Nuermberger Eric L.1,Bishai William R.1

Affiliation:

1. Center for Tuberculosis Research, Johns Hopkins University School of Medicine, Baltimore, Maryland

2. Department of Microbial and Molecular Pathogenesis, Texas A&M University System Health Science Center, College Station, Texas 77843

Abstract

ABSTRACT The Mycobacterium tuberculosis dosR gene (Rv3133c) is part of an operon, Rv3134c-Rv3132c, and encodes a response regulator that has been shown to be upregulated by hypoxia and other in vitro stress conditions and may be important for bacterial survival within granulomatous lesions found in tuberculosis. DosR is activated in response to hypoxia and nitric oxide by DosS (Rv3132c) or DosT (Rv2027c). We compared the virulence levels of an M. tuberculosis dosR - dosS deletion mutant (Δ dosR - dosSdosR-S ]), a dosR -complemented strain, and wild-type H37Rv in rabbits, guinea pigs, and mice infected by the aerosol route and in a mouse hollow-fiber model that may mimic in vivo granulomatous conditions. In the mouse and the guinea pig models, the Δ dosR - S mutant exhibited a growth defect. In the rabbit, the Δ dosR - S mutant did not replicate more than the wild type. In the hollow-fiber model, the mutant phenotype was not different from that of the wild-type strain. Our analyses reveal that the dosR and dosS genes are required for full virulence and that there may be differences in the patterns of attenuation of this mutant between the animal models studied.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

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