Genome-scale analysis of Mycobacterium avium complex isolates from Portugal reveals extensive genetic diversity

IF 2.6 4区 医学 Q3 INFECTIOUS DISEASES Infection Genetics and Evolution Pub Date : 2024-10-20 DOI:10.1016/j.meegid.2024.105682
Sofia Carneiro , Miguel Pinto , Joana Rodrigues , João Paulo Gomes , Rita Macedo
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Abstract

Opportunist infections caused by nontuberculous mycobacteria (NTM) have emerged as a significant public health problem. Among these, species of the Mycobacterium avium complex (MAC) are the main responsible for the increase in the number of human disease cases. In order to address the current needs in the detection and surveillance of MAC disease cases, we evaluated different species classification methodologies (BLASTn-based marker-gene approach, Kraken v2, rMLST and MLST databases) and their congruence with a core-SNP phylogenetic approach, based on whole genome sequencing (WGS) data. For this purpose, we used a collection of 142 MAC isolates from Portuguese patients diagnosed between 2014 and 2022. The marker-gene approach (based on the rpoB, hsp65 and groEL genes), showed the best results, allowing the identification of the 142 MAC isolates to the species/subspecies level (M. avium subsp. hominissuis, M. intracellulare, M. intracellulare subsp. chimaera, M. intracellulare subsp. yongonense, M. marseillence and M. colombiense). Additionally, we performed drug susceptibility testing that confirmed clarithromycin efficacy as a first-line treatment for MAC disease, as 93 % of the Portuguese isolates were susceptible. Using a core-SNP approach we also performed an in-depth phylogenetic analysis within each identified species group, and despite the high genetic diversity within the MAC species, we were able to clearly distinguish all the species/subspecies and identify genetic clusters with epidemiological potential.
We highlight not only the need for the standardization of an appropriate genotyping approach for species identification and management of MAC disease, but also a more robust large-scale WGS data analysis, in a One Health perspective, in order to identify potential routes of transmission.
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对葡萄牙的复合分枝杆菌分离物进行基因组规模的分析,发现了广泛的遗传多样性。
由非结核分枝杆菌(NTM)引起的机会性感染已成为一个重要的公共卫生问题。其中,非结核分枝杆菌复合体(MAC)是导致人类疾病病例增加的主要原因。为了满足当前检测和监控 MAC 疾病病例的需要,我们评估了不同的物种分类方法(基于 BLASTn 的标记基因方法、Kraken v2、rMLST 和 MLST 数据库)及其与基于全基因组测序(WGS)数据的核心-SNP 系统发生学方法的一致性。为此,我们从 2014 年至 2022 年期间确诊的葡萄牙患者中收集了 142 个 MAC 分离物。标记基因方法(基于 rpoB、hsp65 和 groEL 基因)显示出最佳结果,可将 142 个 MAC 分离物鉴定为种/亚种水平(M. avium subsp. hominissuis、M. intracellulare、M. intracellulare subsp.)此外,我们还进行了药物敏感性测试,证实克拉霉素可作为治疗 MAC 疾病的一线药物,因为 93% 的葡萄牙分离株对克拉霉素敏感。尽管 MAC 物种的遗传多样性很高,但我们仍能清楚地区分所有物种/亚种,并识别出具有流行病学潜力的基因群。我们强调,不仅需要标准化适当的基因分型方法来识别和管理 MAC 疾病,还需要从 "一体健康 "的角度进行更强大的大规模 WGS 数据分析,以确定潜在的传播途径。
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
Infection Genetics and Evolution
Infection Genetics and Evolution 医学-传染病学
CiteScore
8.40
自引率
0.00%
发文量
215
审稿时长
82 days
期刊介绍: (aka Journal of Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases -- MEEGID) Infectious diseases constitute one of the main challenges to medical science in the coming century. The impressive development of molecular megatechnologies and of bioinformatics have greatly increased our knowledge of the evolution, transmission and pathogenicity of infectious diseases. Research has shown that host susceptibility to many infectious diseases has a genetic basis. Furthermore, much is now known on the molecular epidemiology, evolution and virulence of pathogenic agents, as well as their resistance to drugs, vaccines, and antibiotics. Equally, research on the genetics of disease vectors has greatly improved our understanding of their systematics, has increased our capacity to identify target populations for control or intervention, and has provided detailed information on the mechanisms of insecticide resistance. However, the genetics and evolutionary biology of hosts, pathogens and vectors have tended to develop as three separate fields of research. This artificial compartmentalisation is of concern due to our growing appreciation of the strong co-evolutionary interactions among hosts, pathogens and vectors. Infection, Genetics and Evolution and its companion congress [MEEGID](http://www.meegidconference.com/) (for Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases) are the main forum acting for the cross-fertilization between evolutionary science and biomedical research on infectious diseases. Infection, Genetics and Evolution is the only journal that welcomes articles dealing with the genetics and evolutionary biology of hosts, pathogens and vectors, and coevolution processes among them in relation to infection and disease manifestation. All infectious models enter the scope of the journal, including pathogens of humans, animals and plants, either parasites, fungi, bacteria, viruses or prions. The journal welcomes articles dealing with genetics, population genetics, genomics, postgenomics, gene expression, evolutionary biology, population dynamics, mathematical modeling and bioinformatics. We also provide many author benefits, such as free PDFs, a liberal copyright policy, special discounts on Elsevier publications and much more. Please click here for more information on our author services .
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