Genomic analysis of Mycobacterium abscessus isolates from non-cystic fibrosis patients in Thailand: phylogeny, subspecies distribution, and antimicrobial resistance profiles.

IF 3.7 2区 医学 Q2 IMMUNOLOGY
Ajala Prommi, Vorthon Sawaswong, Suthidee Petsong, Kanphai Wongjarit, Ubonwan Somsukpiroh, Sunchai Payungporn, Suwatchareeporn Rotcheewaphan
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引用次数: 0

Abstract

Background: Mycobacterium abscessus (MABS) is a clinically significant nontuberculous mycobacterium, and its drug resistance poses substantial therapeutic challenges. Comprehensive genomic and phenotypic analyses are essential for elucidating the mechanisms underlying this resistance and enhancing understanding of its epidemiology.

Methods: Whole-genome sequencing (WGS) using the Illumina platform was conducted on 61 clinical MABS isolates obtained from patients in Thailand. MABS subspecies classification was performed using FastANI, TYGS, and NTM-Profiler. Phenotypic drug susceptibility testing (pDST) was determined using a broth microdilution method. Resistance mutations were identified through NTM-Profiler and Snippy pipelines.

Results: The analysis classified MABS isolates into three subspecies: subsp. abscessus (40/61, 65.57 %), subsp. massiliense (15/61, 24.59 %), and subsp. bolletii (6/61, 9.83 %). Phylogenetic analysis revealed genetic diversity among the majority of the MABS clinical isolates. These isolates clustered into distinct clades, separate from globally recognized clinical strains and dominant circulating clones. Inducible clarithromycin resistance was detected in 60.66 % of MABS isolates, associated with the T28 variant in erm(41). The Ile80Val mutation in erm(41) was significantly associated with inducible clarithromycin resistance (χ2 = 12.61, p < 0.001). Acquired clarithromycin resistance associated with rrl mutations (A2270C, A2270G, A2271C) and amikacin resistance linked to the rrs mutation A1375G were detected in 11.48 % and 4.92 % of isolates, respectively. The categorical agreement between WGS-based DST and pDST was 95.08 %, 88.33 %, and 96.43 % for inducible clarithromycin, clarithromycin, and amikacin, respectively.

Conclusion: This study provides valuable insights into the genomic diversity and antimicrobial resistance of MABS isolates in Thailand, emphasizing regional variations in dominant clones and resistance mechanisms.

泰国非囊性纤维化患者脓肿分枝杆菌分离株的基因组分析:系统发育、亚种分布和抗菌素耐药性谱
背景:脓肿分枝杆菌(MABS)是临床上重要的非结核分枝杆菌,其耐药性给治疗带来了重大挑战。全面的基因组和表型分析对于阐明这种抗性的机制和加强对其流行病学的理解是必不可少的。方法:采用Illumina平台对61株泰国患者临床分离的单克隆抗体进行全基因组测序(WGS)。使用FastANI、TYGS和NTM-Profiler进行单克隆抗体亚种分类。采用微量肉汤稀释法测定表型药敏试验(pDST)。通过NTM-Profiler和Snippy管道鉴定抗性突变。结果:分析将MABS分离株分为3个亚种:亚种;脓肿(40/61,65.57%),亚科;马尾虫(15/61,24.59%);Bolletii(6/61, 9.83%)。系统发育分析显示,大多数MABS临床分离株具有遗传多样性。这些分离株聚集成不同的分支,与全球公认的临床菌株和主要的循环克隆分开。60.66%的MABS分离株检测到可诱导的克拉霉素耐药,与erm中的T28变异相关(41)。结论:本研究为了解泰国单克隆抗体(MABS)分离株的基因组多样性和耐药性提供了有价值的见解,强调了优势克隆的区域差异和耐药机制。
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来源期刊
Journal of Microbiology Immunology and Infection
Journal of Microbiology Immunology and Infection IMMUNOLOGY-INFECTIOUS DISEASES
CiteScore
15.90
自引率
5.40%
发文量
159
审稿时长
67 days
期刊介绍: Journal of Microbiology Immunology and Infection is an open access journal, committed to disseminating information on the latest trends and advances in microbiology, immunology, infectious diseases and parasitology. Article types considered include perspectives, review articles, original articles, brief reports and correspondence. With the aim of promoting effective and accurate scientific information, an expert panel of referees constitutes the backbone of the peer-review process in evaluating the quality and content of manuscripts submitted for publication.
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