基于全基因组序列对一家大型家禽屠宰场三年来从肉鸡屠体中分离出的弯曲杆菌进行特征分析,发现空肠弯曲杆菌具有高度的遗传多样性和重复出现的基因组系。

IF 2.6 4区 医学 Q3 INFECTIOUS DISEASES
Marc J.A. Stevens , Roger Stephan , Jule Anna Horlbog , Nicole Cernela , Magdalena Nüesch-Inderbinen
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引用次数: 0

摘要

弯曲杆菌是欧洲最常见的细菌性肠胃炎病原体之一,主要与食用受污染的食物有关。本研究的目的是评估基因组多样性,并鉴定三年内从瑞士一家大型家禽屠宰场的肉鸡屠体(颈部皮肤样本)中分离出的 155 个弯曲杆菌的抗菌药耐药性和毒力基因。样本来自三种不同类型养殖系统(特别是动物友好饲养系统(PAFS)、散养农场和有机农场)的肉鸡。采用全基因组测序(WGS)方法(MiniSeq;Illumina)对空肠弯曲菌(n = 127)和大肠弯曲菌(n = 28)进行了分析。根据 WGS 数据确定序列类型 (ST),并使用 cgMLST SeqSphere+ 方案将分离物归入复合类型 (CT)。使用抗性基因鉴定器(RGI)鉴定了抗菌性基因,使用毒力因子数据库(VFDB)鉴定了毒力基因。观察到了高度的遗传多样性。许多序列类型(空肠大肠杆菌 ST19、ST21、ST48、ST50、ST122、ST262 和大肠杆菌 ST827)出现了不止一次,并且分布在整个研究期间,与分离年份和肉鸡养殖类型无关。抗菌药耐药性决定因素包括 blaOXA 和 tet(O)基因,以及 GyrA 中的 T86I 取代。已知在人类弯曲菌感染中发挥作用的毒力基因已被确定,如 wlaN、cstIII、neuA1、neuB1 和 neuC1。对弯曲杆菌分离物进行亚型分析后发现,空肠弯曲杆菌 ST21 存在一个高度克隆的种群,该种群在三年的研究期间一直从不同地理位置和不同养殖系统的农场的屠体中分离出来。在肉鸡屠体分离物中观察到的高度遗传多样性与之前的研究结果一致。空肠大肠杆菌 ST21 亚型的高克隆性持续存在,这表明屠宰场可能是空肠大肠杆菌 ST21 的生存环境,但可能维持该克隆的生态库仍是未知数。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Whole genome sequence-based characterization of Campylobacter isolated from broiler carcasses over a three-year period in a big poultry slaughterhouse reveals high genetic diversity and a recurring genomic lineage of Campylobacter jejuni

Campylobacter is among the most frequent agents of bacterial gastroenteritis in Europe and is primarily linked to the consumption of contaminated food. The aim of this study was to assess genomic diversity and to identify antimicrobial resistance and virulence genes of 155 Campylobacter isolated from broiler carcasses (neck skin samples) in a large-scale Swiss poultry abattoir over a three-year period. Samples originated from broilers from three different types of farming systems (particularly animal-friendly stabling (PAFS), free-range farms, and organic farms).

Campylobacter jejuni (n = 127) and Campylobacter coli (n = 28) were analysed using a whole genome sequencing (WGS) approach (MiniSeq; Illumina). Sequence types (STs) were determined in silico from the WGS data and isolates were assigned into complex types (CTs) using the cgMLST SeqSphere+ scheme. Antimicrobial resistance genes were identified using the Resistance Gene Identifier (RGI), and virulence genes were identified using the virulence factor database (VFDB).

A high degree of genetic diversity was observed. Many sequence types (C. jejuni ST19, ST21, ST48, ST50, ST122, ST262 and C. coli ST827) occurred more than once and were distributed throughout the study period, irrespective of the year of isolation and of the broiler farming type. Antimicrobial resistance determinants included blaOXA and tet(O) genes, as well as the T86I substitution within GyrA. Virulence genes known to play a role in human Campylobacter infection were identified such as the wlaN, cstIII, neuA1, neuB1, and neuC1. Subtyping of the Campylobacter isolates identified the occurrence of a highly clonal population of C. jejuni ST21 that was isolated throughout the three-year study period from carcasses from farms with geographically different locations and different farming systems.

The high rate of genetic diversity observed among broiler carcass isolates is consistent with previous studies. The identification of a persisting highly clonal C. jejuni ST21 subtype suggests that the slaughterhouse may represent an environment in which C. jejuni ST21 may survive, however, the ecological reservoir potentially maintaining this clone remains unknown.

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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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