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
-
dosS
[Δ
dosR-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
Cited by
132 articles.
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