Gene expression, levels and polymorphism (Ala16Val) of mitochondrial superoxide dismutase in tuberculosis patients of Rajasthan.


Journal

Microbes and infection
ISSN: 1769-714X
Titre abrégé: Microbes Infect
Pays: France
ID NLM: 100883508

Informations de publication

Date de publication:
05 2023
Historique:
received: 14 04 2022
revised: 31 10 2022
accepted: 03 11 2022
medline: 18 4 2023
pubmed: 11 11 2022
entrez: 10 11 2022
Statut: ppublish

Résumé

Infectious diseases cause redox imbalance and oxidative stress (OS) in host. Superoxide Dismutases(SOD) decrease this OS. SOD2 gene polymorphism can influence the expression and levels of enzyme. To investigate the association of genetic polymorphism of MnSOD with enzyme levels and mRNA expression in TB patients. A total of 87 TB patients and 85 healthy individuals participated in the study. The serum SOD2 levels were measured by ELISA. Gene polymorphism was analysed using PCR-RFLP with BsaW1 as the restriction enzyme. Expression was studied by Real-TimePCR. Statistical significance was determined using the Mann-Whitney, Chi-square and Kruskal-Wallis tests and p value < 0.05 was considered statistically significant. The median(IQR) serum SOD2 levels of TB patients were lower than those of healthy subjects (4.64(6.48) vs 11.35(20.36)ng/mL respectively,p < 0.001). SOD2 expression was significantly down-regulated in TB patients with a fold change value of 0.312. The Val/Val genotype was higher in the patient group than healthy subjects (36.8% vs 23.5%). However, the difference observed between serum SOD2 levels and mRNA expression in the different genotypes were statistically non-significant. Significant difference was found between levels and expression of SOD2 in TB patients and healthy controls, but not for SOD2 gene polymorphism.

Sections du résumé

BACKGROUND
Infectious diseases cause redox imbalance and oxidative stress (OS) in host. Superoxide Dismutases(SOD) decrease this OS. SOD2 gene polymorphism can influence the expression and levels of enzyme.
AIM
To investigate the association of genetic polymorphism of MnSOD with enzyme levels and mRNA expression in TB patients.
METHODS
A total of 87 TB patients and 85 healthy individuals participated in the study. The serum SOD2 levels were measured by ELISA. Gene polymorphism was analysed using PCR-RFLP with BsaW1 as the restriction enzyme. Expression was studied by Real-TimePCR. Statistical significance was determined using the Mann-Whitney, Chi-square and Kruskal-Wallis tests and p value < 0.05 was considered statistically significant.
RESULTS
The median(IQR) serum SOD2 levels of TB patients were lower than those of healthy subjects (4.64(6.48) vs 11.35(20.36)ng/mL respectively,p < 0.001). SOD2 expression was significantly down-regulated in TB patients with a fold change value of 0.312. The Val/Val genotype was higher in the patient group than healthy subjects (36.8% vs 23.5%). However, the difference observed between serum SOD2 levels and mRNA expression in the different genotypes were statistically non-significant.
CONCLUSION
Significant difference was found between levels and expression of SOD2 in TB patients and healthy controls, but not for SOD2 gene polymorphism.

Identifiants

pubmed: 36356830
pii: S1286-4579(22)00145-9
doi: 10.1016/j.micinf.2022.105075
pii:
doi:

Substances chimiques

Superoxide Dismutase EC 1.15.1.1
RNA, Messenger 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

105075

Informations de copyright

Copyright © 2022 Institut Pasteur. Published by Elsevier Masson SAS. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors have declared that no competing interests exist.

Auteurs

Kavya Gauba (K)

Department of Biochemistry, All India Institute of Medical Sciences Jodhpur, 342005, India.

Shruti Gupta (S)

Department of Biochemistry, All India Institute of Medical Sciences Jodhpur, 342005, India.

Jyoti Shekhawat (J)

Department of Biochemistry, All India Institute of Medical Sciences Jodhpur, 342005, India.

Naveen Dutt (N)

Department of Pulmonary Medicine, All India Institute of Medical Sciences Jodhpur, 342005, India.

Dharmveer Yadav (D)

Department of Biochemistry, All India Institute of Medical Sciences Jodhpur, 342005, India.

Vijaya Lakshmi Nag (VL)

Department of Microbiology, All India Institute of Medical Sciences Jodhpur, 342005, India.

Mahadev Rao (M)

Department of Pharmacy Practice, Manipal College of Pharmaceutical Sciences Manipal, 576104, India.

Praveen Sharma (P)

Department of Biochemistry, All India Institute of Medical Sciences Jodhpur, 342005, India.

Mithu Banerjee (M)

Department of Biochemistry, All India Institute of Medical Sciences Jodhpur, 342005, India. Electronic address: mithu.banerjee.3@gmail.com.

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