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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.
Afiliación
  • 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 en 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.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Tuberculosis / Proteínas de Transporte de Catión / Mycobacterium tuberculosis Tipo de estudio: Risk_factors_studies Límite: Humans Idioma: En Revista: Genes Immun Asunto de la revista: ALERGIA E IMUNOLOGIA / BIOLOGIA MOLECULAR Año: 2022 Tipo del documento: Article País de afiliación: Pakistán

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Tuberculosis / Proteínas de Transporte de Catión / Mycobacterium tuberculosis Tipo de estudio: Risk_factors_studies Límite: Humans Idioma: En Revista: Genes Immun Asunto de la revista: ALERGIA E IMUNOLOGIA / BIOLOGIA MOLECULAR Año: 2022 Tipo del documento: Article País de afiliación: Pakistán