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Differential Expression of miR-146 and miR-155 in Active and Latent Tuberculosis Infection

BACKGROUND: Tuberculosis (TB) is one of the leading causes of death worldwide. Besides, one-third of the world population is infected with Mycobacterium tuberculosis (MTB) while staying clinically asymptomatic; the situation is called latent TB infection (LTBI). MiR-21, miR-31, miR-146a, and miR-155...

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Autores principales: Alijani, Ebrahim, Rad, Farhad Riazi, Katebi, Asal, Ajdary, Soheila
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10512130/
https://www.ncbi.nlm.nih.gov/pubmed/37744552
http://dx.doi.org/10.18502/ijph.v52i8.13414
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author Alijani, Ebrahim
Rad, Farhad Riazi
Katebi, Asal
Ajdary, Soheila
author_facet Alijani, Ebrahim
Rad, Farhad Riazi
Katebi, Asal
Ajdary, Soheila
author_sort Alijani, Ebrahim
collection PubMed
description BACKGROUND: Tuberculosis (TB) is one of the leading causes of death worldwide. Besides, one-third of the world population is infected with Mycobacterium tuberculosis (MTB) while staying clinically asymptomatic; the situation is called latent TB infection (LTBI). MiR-21, miR-31, miR-146a, and miR-155 play an important role in many immune and inflammatory pathways. In the present study the expression levels of MiR-21, miR-31, miR-146a, and miR-155 in peripheral blood mononuclear cells (PBMCs) from patients with active TB, latently infected individuals (LTBI), and healthy controls (HC) were investigated. Participants were recruited at the Bouali Hospital, Zahedan University of Medical Sciences, Zahedan, Iran from 2010 to 2011. METHODS: PBMCs were stimulated with PPD before RNA extraction. TaqMan RT-qPCR assay was used to analyze the expression levels of miRNAs. RESULTS: The results indicated no significant differences in the expression of miR-21 and miR-31 between different groups; however, in patients with active TB, the expression of miR-21 (P=0.03) and miR-31 (P=0.04) were significantly increased after stimulation with PPD compared to the unstimulated condition. The expression of miR-146 in response to PPD in both LTBI (P=0.02) and TB (P=0.03) groups compared to the HC group was increased. No significant differences were found in the expression level of miR-155 in response to PPD between LTBI and HC groups. However, the fold change was significantly higher in the TB group in comparison with the HC (P=0.03) and LTBI (P=0.05) groups. CONCLUSION: The results confirm the main role of miR-146 and miR-155 in TB infection and suggest a role for miR-146 and miR-155 as infection and activation markers in tuberculosis infection, respectively.
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spelling pubmed-105121302023-09-22 Differential Expression of miR-146 and miR-155 in Active and Latent Tuberculosis Infection Alijani, Ebrahim Rad, Farhad Riazi Katebi, Asal Ajdary, Soheila Iran J Public Health Original Article BACKGROUND: Tuberculosis (TB) is one of the leading causes of death worldwide. Besides, one-third of the world population is infected with Mycobacterium tuberculosis (MTB) while staying clinically asymptomatic; the situation is called latent TB infection (LTBI). MiR-21, miR-31, miR-146a, and miR-155 play an important role in many immune and inflammatory pathways. In the present study the expression levels of MiR-21, miR-31, miR-146a, and miR-155 in peripheral blood mononuclear cells (PBMCs) from patients with active TB, latently infected individuals (LTBI), and healthy controls (HC) were investigated. Participants were recruited at the Bouali Hospital, Zahedan University of Medical Sciences, Zahedan, Iran from 2010 to 2011. METHODS: PBMCs were stimulated with PPD before RNA extraction. TaqMan RT-qPCR assay was used to analyze the expression levels of miRNAs. RESULTS: The results indicated no significant differences in the expression of miR-21 and miR-31 between different groups; however, in patients with active TB, the expression of miR-21 (P=0.03) and miR-31 (P=0.04) were significantly increased after stimulation with PPD compared to the unstimulated condition. The expression of miR-146 in response to PPD in both LTBI (P=0.02) and TB (P=0.03) groups compared to the HC group was increased. No significant differences were found in the expression level of miR-155 in response to PPD between LTBI and HC groups. However, the fold change was significantly higher in the TB group in comparison with the HC (P=0.03) and LTBI (P=0.05) groups. CONCLUSION: The results confirm the main role of miR-146 and miR-155 in TB infection and suggest a role for miR-146 and miR-155 as infection and activation markers in tuberculosis infection, respectively. Tehran University of Medical Sciences 2023-08 /pmc/articles/PMC10512130/ /pubmed/37744552 http://dx.doi.org/10.18502/ijph.v52i8.13414 Text en Copyright © 2023 Alijani et al. Published by Tehran University of Medical Sciences https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International license. (https://creativecommons.org/licenses/by-nc/4.0/). Non-commercial uses of the work are permitted, provided the original work is properly cited
spellingShingle Original Article
Alijani, Ebrahim
Rad, Farhad Riazi
Katebi, Asal
Ajdary, Soheila
Differential Expression of miR-146 and miR-155 in Active and Latent Tuberculosis Infection
title Differential Expression of miR-146 and miR-155 in Active and Latent Tuberculosis Infection
title_full Differential Expression of miR-146 and miR-155 in Active and Latent Tuberculosis Infection
title_fullStr Differential Expression of miR-146 and miR-155 in Active and Latent Tuberculosis Infection
title_full_unstemmed Differential Expression of miR-146 and miR-155 in Active and Latent Tuberculosis Infection
title_short Differential Expression of miR-146 and miR-155 in Active and Latent Tuberculosis Infection
title_sort differential expression of mir-146 and mir-155 in active and latent tuberculosis infection
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10512130/
https://www.ncbi.nlm.nih.gov/pubmed/37744552
http://dx.doi.org/10.18502/ijph.v52i8.13414
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