Genetic diversity of Mycobacterium leprae: Need to move towards genome-wide approaches.

IF 2.7 4区 医学 Q3 IMMUNOLOGY Indian Journal of Medical Research Pub Date : 2024-02-01 Epub Date: 2024-04-04 DOI:10.4103/ijmr.ijmr_2383_22
Purna Dwivedi, Mukul Sharma, Afzal Ansari, Pushpendra Singh
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Abstract

Abstract: Leprosy, an ancient disease, continues to be a public health concern as it remains endemic in several countries. After reaching the elimination target (1/10,000) as a public health problem in 2005 in India, around 1.2 lakh cases have been detected every year over the last decade indicating active transmission of leprosy bacillus (Mycobacterium leprae). Single-nucleotide polymorphisms (SNPs), genomic insertions/deletions and variable-number tandem repeats (VNTRs) have been identified as genetic markers for tracking M. leprae transmission. As the leprosy bacilli cannot be cultured in vitro, molecular testing of M. leprae genotypes is done by polymerase chain reaction-based sequencing which provides a practical alternative for the identification of strains as well as drug resistance-associated mutations. Whole-genome sequencing (WGS) of M. leprae directly from clinical samples has also proven to be an effective tool for identifying genetic variations which can further help refine the molecular epidemiological schemes based on SNPs and VNTRs. However, the WGS data of M. leprae strains from India are scarce, being responsible for a gross under-representation of the genetic diversity of M. leprae strains present in India and need to be addressed suitably. Molecular studies of leprosy can provide better insight into phylogeographic markers to monitor the transmission dynamics and emergence of antimicrobial resistance. An improved understanding of M. leprae transmission is essential to guide efficient leprosy control strategies. Therefore, this review compiles and discusses the current status of molecular epidemiology, genotyping and the potential of genome-wide analysis of M. leprae strains in the Indian context.

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麻风分枝杆菌的遗传多样性:需要转向全基因组方法。
摘要:麻风病是一种古老的疾病,在一些国家仍然流行,因此仍然是一个公共卫生问题。印度于 2005 年实现了消除麻风病这一公共卫生问题的目标(1/10,000),但在过去十年中,每年发现的麻风病例约为 120 万例,表明麻风杆菌(麻风分枝杆菌)的传播十分活跃。单核苷酸多态性(SNPs)、基因组插入/缺失和变数串联重复序列(VNTRs)已被确定为追踪麻风杆菌传播的遗传标记。由于麻风杆菌无法在体外培养,麻风杆菌基因型的分子检测是通过聚合酶链反应测序完成的,这为鉴定菌株和耐药性相关突变提供了一种实用的替代方法。直接从临床样本中对麻风杆菌进行全基因组测序(WGS)也被证明是鉴定基因变异的有效工具,有助于进一步完善基于 SNP 和 VNTR 的分子流行病学方案。然而,印度麻风杆菌菌株的 WGS 数据很少,导致印度麻风杆菌菌株的遗传多样性代表性严重不足,需要适当解决。麻风病的分子研究可以更好地了解系统地理标记,从而监测传播动态和抗菌药耐药性的出现。加深对麻风杆菌传播的了解对于指导有效的麻风病控制策略至关重要。因此,本综述汇编并讨论了印度麻风杆菌菌株的分子流行病学、基因分型和全基因组分析潜力的现状。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.80
自引率
2.40%
发文量
191
审稿时长
3-8 weeks
期刊介绍: The Indian Journal of Medical Research (IJMR) [ISSN 0971-5916] is one of the oldest medical Journals not only in India, but probably in Asia, as it started in the year 1913. The Journal was started as a quarterly (4 issues/year) in 1913 and made bimonthly (6 issues/year) in 1958. It became monthly (12 issues/year) in the year 1964.
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