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SLC11A1 genetic variation and low expression may cause immune response impairment in TB patients.
Shahzad, Faheem; Bashir, Noman; Ali, Atia; Nadeem, Ayesha; Ammar, Ali; Kashif, Mohammad; Javaid, Khursheed; Jahan, Shah; Tahir, Romeeza; Rizwan, Muhammad; Mushtaq, Abid; Afzal, Nadeem.
Affiliation
  • Shahzad F; Department of Immunology, University of Health Sciences, Lahore, Pakistan. Faheem599@gmail.com.
  • Bashir N; Department of Livestock Management, Agriculture University Faisalabad, Faisalabad, Pakistan.
  • Ali A; Department of Immunology, University of Health Sciences, Lahore, Pakistan.
  • Nadeem A; Continental Medical College, Lahore, Pakistan.
  • Ammar A; Department of Immunology, University of Health Sciences, Lahore, Pakistan.
  • Kashif M; Department of Immunology, University of Health Sciences, Lahore, Pakistan.
  • Javaid K; Department of Immunology, University of Health Sciences, Lahore, Pakistan.
  • Jahan S; Department of Immunology, University of Health Sciences, Lahore, Pakistan.
  • Tahir R; Department of Immunology, University of Health Sciences, Lahore, Pakistan.
  • Rizwan M; Ameer-Ud-Din Medical College, Lahore, Pakistan.
  • Mushtaq A; Services Institute of Medical Sciences, Lahore, Pakistan.
  • Afzal N; Department of Immunology, University of Health Sciences, Lahore, Pakistan.
Genes Immun ; 23(2): 85-92, 2022 04.
Article in En | MEDLINE | ID: mdl-35140349
Tuberculosis (TB) is caused by Mycobacterium tuberculosis. Host genetic factors are important for the detection of TB susceptibility. SLC11A1 is located in monocyte phagolysosomes that help to limit M. tuberculosis growth by transferring divalent cations across the membrane. Genetic variation in SLC11A1 may alter its expression and increase the susceptibility of individuals to TB. The current study aimed to provide insight into host genetic variations and gene expression in TB patients. A total of 164 TB patients and 85 healthy controls were enrolled in this study. SLC11A1 polymorphisms were detected by PCR-RFLP. Real-time qPCR was used for SLC11A1 gene expression, and ELISA was used for protein estimation. GTEx Portal was used for quantitative trait loci analysis, while the STRING (v.11) web platform was used for gene interactive network construction. Data were analyzed using SPSS, GraphPad Prism, Haploview, and SNPstats. SLC11A1 polymorphisms and combinatorial genotypes were strongly associated with TB susceptibility, which may explain the greater prevalence of tuberculosis in the local population. Polymorphisms in SLC11A1 have also been linked to gene expression variation. Furthermore, the expression of SLC11A1 was downregulated in TB patients, which may influence the function of other associated genes and may impair the immunological response to tuberculosis.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tuberculosis / Cation Transport Proteins / Mycobacterium tuberculosis Type of study: Risk_factors_studies Limits: Humans Language: En Journal: Genes Immun Journal subject: ALERGIA E IMUNOLOGIA / BIOLOGIA MOLECULAR Year: 2022 Document type: Article Affiliation country: Pakistan Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tuberculosis / Cation Transport Proteins / Mycobacterium tuberculosis Type of study: Risk_factors_studies Limits: Humans Language: En Journal: Genes Immun Journal subject: ALERGIA E IMUNOLOGIA / BIOLOGIA MOLECULAR Year: 2022 Document type: Article Affiliation country: Pakistan Country of publication: United kingdom