Modulation of host ubiquitin system genes in human endometrial cell line infected with Mycobacterium tuberculosis
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  • 作者:S. Meenu ; S. Thiagarajan ; Sudha Ramalingam…
  • 关键词:Mycobacterium tuberculosis ; Endometrial cells ; Ubiquitin ; Subtractive cDNA library ; Ishikawa cell lines
  • 刊名:Medical Microbiology and Immunology
  • 出版年:2016
  • 出版时间:April 2016
  • 年:2016
  • 卷:205
  • 期:2
  • 页码:163-171
  • 全文大小:673 KB
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  • 作者单位:S. Meenu (1) (2)
    S. Thiagarajan (1)
    Sudha Ramalingam (1)
    A. Michael (2)
    Sankaran Ramalingam (1)

    1. PSG Center for Molecular Medicine and Therapeutics, PSG Institute of Medical Sciences and Research, Coimbatore, Tamil Nadu, 641 004, India
    2. PSG College of Arts and Science, Coimbatore, Tamil Nadu, 641 004, India
  • 刊物类别:Biomedical and Life Sciences
  • 刊物主题:Biomedicine
    Medical Microbiology
    Immunology
  • 出版者:Springer Berlin / Heidelberg
  • ISSN:1432-1831
文摘
Endometrium is one of the most commonly affected sites in genital tuberculosis. The understanding of its interaction with the tubercle bacilli is of paramount importance for studying the pathogenesis of this disease. The main objective of this work was to study the interplay between Mycobacterium tuberculosis and host endometrial epithelial cell lines (Ishikawa cell lines), and to identify the differentially expressed genes upon tuberculosis infection. To study this, suppression subtractive hybridization library was constructed using M. tuberculosis H37Rv-infected Ishikawa cell line harvested 24 h post-infection. The subtracted cDNA library was screened, and 105 differentially expressed genes were identified and grouped based on their functions. Since ubiquitination process has gained importance in targeting M. tuberculosis to xenophagy, ubiquitin system genes obtained in the library were selected, and time course analysis of their gene expression was performed. We observed an upregulation of mkrn1 and cops5 and downregulation of zfp91, ndfip2, ube2f, rnft1, psmb6, and psmd13 at 24 h post-infection. From the results obtained, we surmise that ubiquitination pathway genes may have roles in combating tuberculosis which are yet uncharted.

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