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J Clin Microbiol. 2020 Sep 22;58(10). doi: 10.1128/JCM.01269-20.
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Molecular and Biological Characterization of a Cervidpoxvirus Isolated From Moose with Necrotizing Dermatitis.从患有坏死性皮炎的驼鹿中分离的鹿痘病毒的分子和生物学特性。
Vet Pathol. 2020 Mar;57(2):296-310. doi: 10.1177/0300985819891240. Epub 2020 Feb 25.
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Large Fecal Reservoir of Escherichia coli Sequence Type 131-H30 Subclone Strains That Are Shared Within Households and Resemble Clinical ST131-H30 Isolates.大肠杆菌序列型 131-H30 亚克隆株在家庭内共享的大型粪便储库,类似于临床 ST131-H30 分离株。
J Infect Dis. 2020 Apr 27;221(10):1659-1668. doi: 10.1093/infdis/jiz669.
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The EnteroBase user's guide, with case studies on transmissions, phylogeny, and core genomic diversity.《EnteroBase 用户指南》,内含传播、系统发育和核心基因组多样性方面的案例研究。
Genome Res. 2020 Jan;30(1):138-152. doi: 10.1101/gr.251678.119. Epub 2019 Dec 6.
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Pneumonia-Specific Escherichia coli with Distinct Phylogenetic and Virulence Profiles, France, 2012-2014.2012-2014 年法国具有不同进化和毒力特征的肺炎克雷伯菌
Emerg Infect Dis. 2019 Apr;25(4):710-718. doi: 10.3201/eid2504.180944.
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Pathophysiology of Escherichia coli pneumonia: Respective contribution of pathogenicity islands to virulence.产肠杆菌肺炎的病理生理学:致病岛对毒力的各自贡献。
Int J Med Microbiol. 2018 Mar;308(2):290-296. doi: 10.1016/j.ijmm.2018.01.003. Epub 2018 Jan 5.
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J Clin Microbiol. 2017 Aug;55(8):2538-2543. doi: 10.1128/JCM.00737-17. Epub 2017 Jun 7.
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Household Clustering of Sequence Type 131 Clinical and Fecal Isolates According to Whole Genome Sequence Analysis.基于全基因组序列分析的131型序列临床和粪便分离株的家庭聚集性
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10
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引起动物出血性肺炎的大肠杆菌菌株的分子特征、生态和人畜共患病潜力。

Molecular Characteristics, Ecology, and Zoonotic Potential of Escherichia coli Strains That Cause Hemorrhagic Pneumonia in Animals.

机构信息

Department of Veterinary Clinical Sciences, University of Minnesotagrid.17635.36grid.411111.5, Saint Paul, Minnesota, USA.

Preclinical Research, Ethicon-Endo Surgery Inc., Cincinnati, Ohio, USA.

出版信息

Appl Environ Microbiol. 2021 Nov 10;87(23):e0147121. doi: 10.1128/AEM.01471-21. Epub 2021 Sep 22.

DOI:10.1128/AEM.01471-21
PMID:34550758
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8580006/
Abstract

Hemorrhagic pneumonia (HP) is a rare but highly lethal disease, mainly of dogs and cats, caused by hemolytic Escherichia coli strains that contain (encoding cytotoxic necrotizing factor 1). After encountering fatal HP in two dogs, we used contemporary molecular methods, including multilocus sequence typing and whole-genome sequencing, to compare the corresponding case isolates with published HP clinical isolates and newly obtained fecal E. coli isolates from 20 humans and animals in the index HP case household. We also compared the aggregated HP clinical isolates, which represented 13 discrete strains, by pulsotype with a large, private pulsotype library of diverse-source E. coli. The HP clinical isolates represented a narrow range of phylogenetic group B2 lineages (mainly sequence types 12 and 127), O types (mainly O4 and O6), and H types (mainly H5 and H31), but diverse alleles (type-1 fimbriae adhesin). Their extensive, highly conserved virulence genotypes, which qualified as extraintestinal pathogenic E. coli (ExPEC), encoded diverse adhesins, toxins, iron uptake systems, and protectins. Household surveillance identified multiple HP-like fecal strains, plus abundant between-host strain sharing, including of the household's index HP strain. The pulsotype library search identified, for five HP clinical strains, same-pulsotype human and animal fecal and clinical (predominantly urine) isolates, from diverse locales and time periods. Thus, E. coli strains that cause HP derive from a narrow range of ExPEC lineages within phylogroup B2, contain multiple virulence genes other than , are shared extensively between hosts, and likely function in nature mainly as intestinal colonizers and uropathogens. This study clarifies the clonal background and extensive virulence genotypes of the E. coli strains that cause hemorrhagic pneumonia in domestic animals (mainly dogs and cats), shows that such strains circulate among animals and humans, identifies a substantial intestinal colonization component to their lifestyle, and extends their known clinical manifestations to include bacteremia and urinary tract infection. The findings place these strains better into context vis-à-vis current understandings of E. coli phylogeny, ecology, and pathogenesis; identify questions for future research; and may prove relevant for surveillance and prevention efforts.

摘要

出血性肺炎(HP)是一种罕见但高度致命的疾病,主要发生在犬和猫中,由含有 (编码细胞毒性坏死因子 1)的溶血大肠杆菌菌株引起。在两只狗中遇到致命的 HP 后,我们使用了当代分子方法,包括多位点序列分型和全基因组测序,将相应的病例分离株与已发表的 HP 临床分离株以及从指数 HP 病例家庭的 20 只人和动物中新获得的粪便大肠杆菌分离株进行了比较。我们还通过脉冲型与大量多样化来源的大肠杆菌的私有脉冲型库比较了聚集的 HP 临床分离株,这些分离株代表了 13 个离散的菌株。HP 临床分离株代表了一个狭窄的 B2 群进化枝(主要是序列类型 12 和 127)、O 型(主要是 O4 和 O6)和 H 型(主要是 H5 和 H31)的范围,但多样化的 等位基因(1 型菌毛粘附素)。它们广泛而高度保守的毒力基因型被认为是肠外致病性大肠杆菌(ExPEC),编码多种粘附素、毒素、铁摄取系统和保护素。家庭监测发现了多种类似 HP 的粪便菌株,以及宿主之间大量的菌株共享,包括家庭的指数 HP 菌株。脉冲型文库搜索确定了五个 HP 临床菌株的同脉冲型人、动物粪便和临床(主要是尿液)分离株,来自不同地点和时间段。因此,引起 HP 的大肠杆菌菌株源自 B2 群内的一小部分 ExPEC 谱系,除了 外还含有多个毒力基因,在宿主之间广泛共享,并且可能在自然界中主要作为肠道定植菌和尿路病原体发挥作用。本研究阐明了引起家养动物(主要是犬和猫)出血性肺炎的大肠杆菌菌株的克隆背景和广泛的毒力基因型,表明这些菌株在动物和人类之间传播,确定了其生活方式中存在大量肠道定植成分,并将其已知的临床表现扩展到包括菌血症和尿路感染。这些发现使这些菌株在当前对大肠杆菌系统发育、生态学和发病机制的理解方面更加清晰;确定了未来研究的问题;并且可能与监测和预防工作有关。