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Phylogenomic analysis of gastroenteritis-associated Clostridium perfringens in England and Wales over a 7-year period indicates distribution of clonal toxigenic strains in multiple outbreaks and extensive involvement of enterotoxin-encoding (CPE) plasmids

机译:对英格兰和威尔士胃肠炎相关的产气荚膜梭状芽胞杆菌的7年时间进行的系统生物学分析表明无毒毒素菌株在多次暴发中分布并且肠毒素编码(CPE)质粒广泛参与

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摘要

is a major enteric pathogen known to cause gastroenteritis in human adults. Although major outbreak cases are frequently reported, only limited whole-genome sequencing (WGS) based studies have been performed to understand the genomic epidemiology and virulence gene content of outbreak-associated strains. We performed phylogenomic analysis on 109 . isolates (human and food) obtained from disease cases in England and Wales between 2011 and 2017. Initial findings highlighted the enhanced discriminatory power of WGS in profiling outbreak strains, when compared to the current Public Health England referencing laboratory technique of fluorescent amplified fragment length polymorphism analysis. Further analysis identified that isogenic strains were associated with nine distinct care-home-associated outbreaks over the course of a 5-year interval, indicating a potential common source linked to these outbreaks or transmission over time and space. As expected, the enterotoxin gene was encoded in all but 4 isolates (96.3 %; 105/109), with virulence plasmids encoding (particularly pCPF5603 and pCPF4969 plasmids) extensively distributed (82.6 %; 90/109). Genes encoding accessory virulence factors, such as beta-2 toxin, were commonly detected (46.7 %; 51/109), and genes encoding phage proteins were also frequently identified. Overall, this large-scale genomic study of gastroenteritis-associated suggested that three major -encoding (toxinotype F) genotypes underlie these outbreaks: strains carrying (1) pCPF5603 plasmid, (2) pCPF4969 plasmid and (3) chromosomal- strains. Our findings substantially expanded our knowledge on type F involved in human-associated gastroenteritis, with further studies required to fully probe the dissemination and regional reservoirs of this enteric pathogen, which may help devise effective prevention strategies to reduce the food-poisoning disease burden in vulnerable patients, such as the elderly.
机译:是已知的导致成年人肠胃炎的主要肠道病原体。尽管经常报告主要暴发病例,但仅进行了基于有限的全基因组测序(WGS)的研究来了解暴发相关菌株的基因组流行病学和毒力基因含量。我们对109进行了植物学分析。从2011年至2017年间从英格兰和威尔士的疾病病例中分离出的分离物(人和食物)。与当前英国公共卫生所引用的荧光扩增片段长度多态性实验室技术相比,最​​初的发现突出了WGS在特征性暴发菌株中的歧视能力增强分析。进一步的分析表明,在5年的时间间隔内,同基因菌株与9个与疗养院相关的暴发相关,表明与这些暴发或时间和空间传播相关的潜在共同来源。正如预期的那样,除4个分离株(96.3%; 105/109)外,肠毒素基因均被编码,编码的毒性质粒(尤其是pCPF5603和pCPF4969质粒)广泛分布(82.6%; 90/109)。通常检测到编码辅助毒力因子(例如β-2毒素)的基因(46.7%; 51/109),并且还经常鉴定出编码噬菌体蛋白的基因。总的来说,这项与胃肠炎相关的大规模基因组研究表明,三种主要的编码(毒素型F)基因型是这些暴发的基础:携带(1)pCPF5603质粒,(2)pCPF4969质粒和(3)染色体菌株的菌株。我们的发现大大扩展了我们对与人类相关的肠胃炎有关的F型的知识,需要进行进一步的研究以充分探查这种肠道病原体的传播和区域性储库,这可能有助于制定有效的预防策略,以减轻易感人群的食物中毒疾病负担患者,例如老人。

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