Expression of mammalian cell entry genes in clinical isolates of M. tuberculosis and the cell entry potential and immunological reactivity of the Rv0590A protein.
Chanchal KumarKamal ShrivastavaAnupriya SinghVarsha ChauhanAstha GiriShraddha GuptaNaresh Kumar SharmaMridula BoseSadhna SharmaMandira Varma-BasilPublished in: Medical microbiology and immunology (2023)
Mammalian cell entry (mce) operons play a vital role in cell invasion and survival of M. tuberculosis. Of the mce genes, the function of Rv0590A is still unknown. The present study was performed to investigate the function and immunogenic properties of the protein Rv0590A. Human leukemia monocytic cell line (THP-1) derived macrophages were infected with M. tuberculosis H37Rv at 3, 6, and 24 h of infection. The maximum colony forming units (CFU) were observed at 6 h (p < 0.005), followed by 3 h after infection. M. tuberculosis H37Rv and clinical isolates representative of Delhi/CAS, EAI, Beijing, Haarlem and Euro-American-superlineage were included in the study for expression analysis of mce1A, mce2A, mce3A, mce4A, and Rv0590A genes. Maximum upregulation of all mce genes was observed at 3 h of infection. All the five clinical isolates and H37Rv upregulated Rv0590A at various time points. Macrophage infection with M. tuberculosis H37Rv-overexpressing Rv0590A gene showed higher intracellular CFU as compared to that of wild-type H37Rv. Further, purified Rv0590A protein stimulated the production of TNFα, IFNγ, and IL-10 in macrophages. Thus, Rv0590A was found to be involved in cell invasion and showed good immunological response.
Keyphrases
- mycobacterium tuberculosis
- pulmonary tuberculosis
- genome wide
- cell therapy
- emergency department
- endothelial cells
- gene expression
- genome wide identification
- crispr cas
- adipose tissue
- cell proliferation
- transcription factor
- dendritic cells
- bone marrow
- protein protein
- wild type
- hepatitis c virus
- risk assessment
- drug induced
- hiv infected
- bioinformatics analysis