Role of a Putative Alkylhydroperoxidase Rv2159c in the Oxidative Stress Response and Virulence of Mycobacterium tuberculosis

• Published in: Pathogens (Basel) Vol. 11; no. 6; p. 684
• Main Authors: Bhargavi, Gunapati, Singh, Amit Kumar, Deenadayalan, Anbarasu, Ponnuraja, Chinnaiyan, Patil, Shripad A., Palaniyandi, Kannan
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 14.06.2022; MDPI
• Subjects: alkylhydroperoxidases; Alveoli; Antiinfectives and antibacterials; Bacteria; Binding sites; Cellular stress response; Drug resistance; Enzymes; Guinea pigs; Homeostasis; IL-1β; Immune response; Infections; Inflammation; Inhalation; IP-10 protein; Kinases; Macrophages; Metals; Monocytes; Mycobacterium tuberculosis; oxidative and transition metal stress response; Oxidative stress; Peroxidase; Phagocytes; Proteins; Reactive oxygen species; Reductases; Respiration; Rv2159c; Strains (organisms); Transition metals; Tuberculosis; Virulence
• ISSN: 2076-0817; 2076-0817
• DOI: 10.3390/pathogens11060684

Mycobacterium tuberculosis, which causes tuberculosis, is one of the leading infectious agents worldwide with a high rate of mortality. Following aerosol inhalation, M. tuberculosis primarily infects the alveolar macrophages, which results in a host immune response that gradually activates various antimicrobial mechanisms, including the production of reactive oxygen species (ROS), within the phagocytes to neutralize the bacteria. OxyR is the master regulator of oxidative stress response in several bacterial species. However, due to the absence of a functional oxyR locus in M. tuberculosis, the peroxidase stress is controlled by alkylhydroperoxidases. M. tuberculosis expresses alkylhydroperoxide reductase to counteract the toxic effects of ROS. In the current study, we report the functional characterization of an orthologue of alkylhydroperoxidase family member, Rv2159c, a conserved protein with putative peroxidase activity, during stress response and virulence of M. tuberculosis. We generated a gene knockout mutant of M. tuberculosis Rv2159c (MtbΔ2159) by specialized transduction. The MtbΔ2159 was sensitive to oxidative stress and exposure to toxic transition metals. In a human monocyte (THP-1) cell infection model, MtbΔ2159 showed reduced uptake and intracellular survival and increased expression of pro-inflammatory molecules, including IL-1β, IP-10, and MIP-1α, compared to the wild type M. tuberculosis and Rv2159c-complemented MtbΔ2159 strains. Similarly, in a guinea pig model of pulmonary infection, MtbΔ2159 displayed growth attenuation in the lungs, compared to the wild type M. tuberculosis and Rv2159c-complemented MtbΔ2159 strains. Our study suggests that Rv2159c has a significant role in maintaining the cellular homeostasis during stress and virulence of M. tuberculosis.