2019-2020 年美国新发感染计划站点非结核分枝杆菌肺外菌株基因组流行病学。

IF 5 2区 医学 Q2 IMMUNOLOGY
Thao L Masters, Nadege Charles Toney, Thomas O Ewing, Gillian A McAllister, Marsenia H Mathis, Cheri Grigg, Shelley S Magill, Kelly A Jackson, Rebecca Byram, Isaac See, Max Salfinger, Devra Barter, Helen Johnston, Ruth Lynfield, Paula Snippes Vagnone, Laura Tourdot, Bridget J Anderson, Ghinwa Dumyati, Rebecca Pierce, Joseph D Lutgring, Amy Gargis, Susannah L McKay
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引用次数: 0

摘要

背景:非结核分枝杆菌(NTM)可引起肺部和肺外感染。尽管从临床标本中分离出的非结核分枝杆菌在全国范围内有所增加,但很少有研究对肺外非结核分枝杆菌的分子特征进行描述:方法:2019 年 10 月至 2020 年 3 月期间,四个新发感染项目点收集了肺外分离物,并对其进行了实验室特征描述,包括基质辅助激光解吸电离飞行时间质谱、桑格 DNA 测序和全基因组测序。生物信息学分析用于确定物种、序列类型(ST)、抗菌药耐药性(AR)和毒力基因;通过系统发育分析进一步确定分离物的特征:结果:在 45 个分离株中,最主要的菌种是鸟分枝杆菌(20 个,占 44%)、螯合分枝杆菌(7 个,占 16%)和富特分枝杆菌(6 个,占 13%)。收集到的 10 种分枝杆菌中有 31 种 ST;最常见的 ST 是 ST11(M. avium,n=7)。福氏分枝杆菌和脓肿分枝杆菌分离株含有多种基因,可产生对氨基糖苷类、β-内酰胺类和大环内酯类药物的耐药性。在 rpoB、16S 或 23S rRNA 中未检测到已知的 AR 突变。生长缓慢的 NTM 物种含有多种毒力基因,包括 VII 型分泌成分、粘附因子和磷脂酶 C:继续积极开展基于实验室和人群的监测将进一步了解 NTM 物种和 ST 的流行情况,监测新出现的克隆,并对 AR 进行定性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genomic Epidemiology of Extrapulmonary Nontuberculous Mycobacteria Isolates at Emerging Infections Program Sites-United States, 2019-2020.

Background: Nontuberculous mycobacteria (NTM) cause pulmonary and extrapulmonary infections. Although isolation of NTM from clinical specimens has increased nationally, few studies delineated the molecular characteristics of extrapulmonary NTM.

Methods: Extrapulmonary isolates were collected by 4 Emerging Infections Program sites from October 2019 to March 2020 and underwent laboratory characterization, including matrix-assisted laser desorption ionization-time of flight mass spectrometry, Sanger DNA sequencing, and whole genome sequencing. Bioinformatics analyses were employed to identify species, sequence types (STs), antimicrobial resistance (AR), and virulence genes; isolates were further characterized by phylogenetic analyses.

Results: Among 45 isolates, the predominant species were Mycobacterium avium (n = 20, 44%), Mycobacterium chelonae (n = 7, 16%), and Mycobacterium fortuitum (n = 6, 13%). The collection represented 31 STs across 10 species; the most common ST was ST11 (M. avium, n = 7). M. fortuitum and Mycobacterium abscessus isolates harbored multiple genes conferring resistance to aminoglycosides, β-lactams, and macrolides. No known AR mutations were detected in rpoB, 16S, or 23S rRNAs. Slow-growing NTM species harbored multiple virulence genes, including type VII secretion components, adhesion factors, and phospholipase C.

Conclusions: Continued active laboratory- and population-based surveillance will further inform the prevalence of NTM species and STs, monitor emerging clones, and allow AR characterization.

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来源期刊
Journal of Infectious Diseases
Journal of Infectious Diseases 医学-传染病学
CiteScore
13.50
自引率
3.10%
发文量
449
审稿时长
2-4 weeks
期刊介绍: Published continuously since 1904, The Journal of Infectious Diseases (JID) is the premier global journal for original research on infectious diseases. The editors welcome Major Articles and Brief Reports describing research results on microbiology, immunology, epidemiology, and related disciplines, on the pathogenesis, diagnosis, and treatment of infectious diseases; on the microbes that cause them; and on disorders of host immune responses. JID is an official publication of the Infectious Diseases Society of America.
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