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Mycobacterium tuberculosis WhiB4 regulates oxidative stress response to modulate survival and dissemination in vivo
Author(s) -
Chawla Manbeena,
Parikh Pankti,
Saxena Alka,
Munshi MohamedHusen,
Mehta Mansi,
Mai Deborah,
Srivastava Anup K.,
Narasimhulu K. V.,
Redding Kevin E.,
Vashi Nimi,
Kumar Dhiraj,
Steyn Adrie J. C.,
Singh Amit
Publication year - 2012
Publication title -
molecular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.857
H-Index - 247
eISSN - 1365-2958
pISSN - 0950-382X
DOI - 10.1111/j.1365-2958.2012.08165.x
Subject(s) - oxidative stress , biology , mycobacterium tuberculosis , oxidative phosphorylation , nitric oxide , dna damage , virulence , microbiology and biotechnology , biochemistry , dna , tuberculosis , gene , medicine , pathology , endocrinology
Summary Host‐generated oxidative stress is considered one of the main mechanisms constraining Mycobacterium tuberculosis ( Mtb ) growth. The redox‐sensing mechanisms in Mtb are not completely understood. Here we show that WhiB4 responds to oxygen (O 2 ) and nitric oxide (NO) via its 4Fe‐4S cluster and controls the oxidative stress response in Mtb . The WhiB4 mutant ( Mtb Δ whiB4 ) displayed an altered redox balance and a reduced membrane potential. Microarray analysis demonstrated that Mtb Δ whiB4 overexpresses the antioxidant systems including alkyl hydroperoxidase ( ahpC‐ahpD ) and rubredoxins ( rubA‐rubB ). DNA binding assays showed that WhiB4 [4Fe‐4S] cluster is dispensable for DNA binding. However, oxidation of the apo‐WhiB4 Cys thiols induced disulphide‐linked oligomerization, DNA binding and transcriptional repression, whereas reduction reversed the effect. Furthermore, WhiB4 binds DNA with a preference for GC‐rich sequences. Expression analysis showed that oxidative stress repressed whiB4 and induced antioxidants in Mtb , while their hyper‐induction was observed in Mtb Δ whiB4 . Mtb Δ whiB4 showed increased resistance to oxidative stress in vitro and enhanced survival inside the macrophages. Lastly, Mtb Δ whiB4 displayed hypervirulence in the lungs of guinea pigs, but showed a defect in dissemination to their spleen. These findings suggest that WhiB4 systematically calibrates the activation of oxidative stress response in Mtb to maintain redox balance, and to modulate virulence.