Proteomics analysis of three different strains of Mycobacterium tuberculosis under in vitro hypoxia and evaluation of hypoxia associated antigen's specific memory T cells in healthy household contacts.

Santhi, D.; A kilandeswari, G.; Das, S.D .; Raja, A .

Frontiers in Microbiology; 2016; 7; 1275.

Abstract: In vitro mimicking conditions are thought to reflect the environment experienced by Mycobacterium tuberculosis inside the host granuloma. The majority of in vitro dormancy experimental models use laboratory-adapted strains H37Rv or Erdman instead of prevalent clinical strains involved during disease outbreaks. Thus, we included the most prevalent clinical strains (S7 and S10) of M. tuberculosis from south India in addition to H37Rv for our in vitro oxygen depletion (hypoxia) experimental model. Cytosolic proteins were prepared from hypoxic cultures, resolved by two-dimensional electrophoresis and protein spots were characterized by mass spectrometry. In total, 49 spots were characterized as over-expressed or newly emergent between the three strains. Two antigens (ESAT-6, Lpd) out of the 49 characterized spots were readily available in recombinant form in our lab. Hence, these two genes were overexpressed, purified and used for in vitro stimulation of whole blood collected from healthy household contacts (HHC) and active pulmonary tuberculosis patients (PTB). Multicolor flow cytometry analysis showed high levels of antigen specific CD4 + central memory T cells in the circulation of HHC compared to PTB ( p < 0.005 for ESAT-6 and p < 0.0005 for Lpd). This shows proteins that are predicted to be up regulated during in vitro hypoxia in most prevalent clinical strains would indicate possible potential immunogens. In vitro hypoxia experiments with most prevalent clinical strains would also elucidate the probable true representative antigens involved in adaptive mechanisms.

Keywords: M. tuberculosis , hypoxia, prevalent clinical strains, two-dimensional electrophoresis, mass spectrometry, multicolor flow cytometry

Back to List of publications / Home