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Australian Group on Antimicrobial Resistance (AGAR) Australian Enterococcal Sepsis Outcome Programme (AESOP) Annual Report 2018.澳大利亚抗菌药物耐药性小组(AGAR)澳大利亚肠球菌败血症结局项目(AESOP)2018年年度报告。
Commun Dis Intell (2018). 2020 Mar 16;44. doi: 10.33321/cdi.2020.44.19.
2
A three-year whole genome sequencing perspective of Enterococcus faecium sepsis in Australia.澳大利亚肠球菌败血病的三年全基因组测序观察。
PLoS One. 2020 Feb 14;15(2):e0228781. doi: 10.1371/journal.pone.0228781. eCollection 2020.
3
Surveillance of vancomycin-resistant enterococci reveals shift in dominating clones and national spread of a vancomycin-variable ST1421-CT1134 clone, Denmark, 2015 to March 2019.万古霉素耐药肠球菌的监测显示,优势克隆发生变化,丹麦 2015 年至 2019 年 3 月期间,具有万古霉素可变表型的 ST1421-CT1134 克隆出现全国性传播。
Euro Surveill. 2019 Aug;24(34). doi: 10.2807/1560-7917.ES.2019.24.34.1900503.
4
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Nucleic Acids Res. 2019 Jul 2;47(W1):W256-W259. doi: 10.1093/nar/gkz239.
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VFDB 2019: a comparative pathogenomic platform with an interactive web interface.VFDB 2019:一个具有交互式网络界面的比较病原体基因组学平台。
Nucleic Acids Res. 2019 Jan 8;47(D1):D687-D692. doi: 10.1093/nar/gky1080.
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Antimicrobial-resistant CC17 Enterococcus faecium: The past, the present and the future.耐抗生素的 CC17 粪肠球菌:过去、现在和未来。
J Glob Antimicrob Resist. 2019 Mar;16:36-47. doi: 10.1016/j.jgar.2018.08.016. Epub 2018 Aug 24.
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Dissemination and persistence of extended-spectrum cephalosporin-resistance encoding IncI1-bla plasmid among Escherichia coli in pigs.肠杆菌科细菌中携带 IncI1-bla 质粒的超广谱头孢菌素耐药基因的传播和持续存在。
ISME J. 2018 Oct;12(10):2352-2362. doi: 10.1038/s41396-018-0200-3. Epub 2018 Jun 13.
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Characteristic of Enterococcus faecium clinical isolates with quinupristin/dalfopristin resistance in China.中国粪肠球菌临床分离株对奎奴普丁/达福普汀耐药的特征
BMC Microbiol. 2016 Oct 21;16(1):246. doi: 10.1186/s12866-016-0863-8.
10
Multilevel population genetic analysis of vanA and vanB Enterococcus faecium causing nosocomial outbreaks in 27 countries (1986-2012).对在27个国家(1986 - 2012年)引起医院感染暴发的vanA和vanB型粪肠球菌进行的多级群体遗传学分析。
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澳大利亚猪肠球菌的抗药性及其对人类健康的影响。

Antimicrobial Resistance in Porcine Enterococci in Australia and the Ramifications for Human Health.

机构信息

Antimicrobial Resistance and Infectious Diseases Laboratory, Murdoch University, Murdoch, WA, Australia

New South Wales Department of Primary Industries, Wollongbar, NSW, Australia.

出版信息

Appl Environ Microbiol. 2021 Apr 27;87(10). doi: 10.1128/AEM.03037-20.

DOI:10.1128/AEM.03037-20
PMID:33712430
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8117772/
Abstract

Enterococci are ubiquitous opportunistic pathogens that have become a major public health issue globally. The increasing prevalence of antimicrobial resistance in hospital-adapted enterococci had been thought to originate from livestock. However, this association between livestock and hospital-adapted enterococci is currently unclear. This study investigates the antimicrobial susceptibilities of enterococci isolated from pig cecal samples and compares the genomic characteristics of from pigs to those of isolates from meat chickens and from human sepsis cases. From 200 cecal samples, antimicrobial susceptibility testing was performed for ( = 84), ( = 36), and ( = 17). Whole-genome sequencing was performed for all isolates, and the sequences were compared to those of previously studied isolates from meat chickens and human sepsis cases through bioinformatics analysis. Resistance (non-wild type) to erythromycin, gentamicin, tetracycline, ampicillin, daptomycin, virginiamycin, and quinupristin-dalfopristin was identified. More importantly, except for a single isolate harboring the operon, no resistance was observed in the three species to vancomycin, teicoplanin, and linezolid, which are critically important antimicrobials used to treat enterococcal infections in humans. The isolates from chickens were genetically distinct from human and pig isolates, which were more closely related. Human strains that were closely related to pig strains were not typical "hospital-adapted strains" as previously identified. The results of this study show that enterococci from Australian finisher pigs are not a source of resistance to critically important antimicrobials and that from pigs is not part of the current human hospital-adapted population. Resistance to the critically important antimicrobials vancomycin, teicoplanin, and linezolid is not found in enterococci collected from Australian finisher pigs. However, some antimicrobial resistance was observed. In particular, resistance to quinupristin-dalfopristin, a combination of two streptogramin class antimicrobials, was identified despite the absence of streptogramin use Australia-wide since 2005. Other observed resistance among enterococci from pigs include chloramphenicol, erythromycin, and tetracycline resistance. Genomic comparison of from Australian pigs to isolates collected from previous studies on chickens and humans indicate that from pigs are genetically more similar to those of humans than those from chickens. Despite the increased genetic similarities, strains from pigs are phylogenetically distinct and did not belong to the dominant sequence types found in hospital-adapted strains causing sepsis in humans. Therefore, the results indicate that Australian finisher pigs are not a source of hospital-adapted in Australia.

摘要

肠球菌是一种普遍存在的机会致病菌,已成为全球主要的公共卫生问题。医院适应肠球菌对抗菌药物的耐药性日益增加,人们曾认为这种耐药性源自家畜。然而,目前尚不清楚家畜与医院适应肠球菌之间的这种关联。本研究调查了从猪盲肠样本中分离出的肠球菌的抗菌药物敏感性,并比较了来自猪、鸡肉鸡和人类败血症病例的 的基因组特征。从 200 个盲肠样本中,对 ( = 84)、 ( = 36)和 ( = 17)进行了抗菌药物敏感性测试。对所有 分离株进行了全基因组测序,并通过生物信息学分析将序列与先前从鸡肉鸡和人类败血症病例中研究过的分离株进行比较。鉴定出对红霉素、庆大霉素、四环素、氨苄西林、达托霉素、维吉尼亚霉素和奎奴普丁/达福普汀的耐药性(非野生型)。更重要的是,除了单个分离株携带 操纵子外,三种物种对万古霉素、替考拉宁和利奈唑胺均未表现出耐药性,这些药物是治疗人类肠球菌感染的关键抗菌药物。来自鸡的 分离株在基因上与人类和猪分离株不同,与猪分离株的关系更密切。与猪分离株密切相关的人类菌株并非以前确定的典型“医院适应株”。本研究结果表明,来自澳大利亚育肥猪的肠球菌不是对关键抗菌药物耐药的来源,而且来自猪的肠球菌也不是当前人类医院适应人群的一部分。在从澳大利亚育肥猪中收集的肠球菌中未发现对关键抗菌药物万古霉素、替考拉宁和利奈唑胺的耐药性。然而,观察到了一些抗菌药物耐药性。特别是,尽管自 2005 年以来,澳大利亚已全面停止使用两种糖肽类抗菌药物组合的奎奴普丁/达福普汀,但仍观察到对其的耐药性。猪源肠球菌中其他观察到的耐药性包括氯霉素、红霉素和四环素耐药性。对来自澳大利亚猪的 与之前在鸡和人类上的研究中收集的分离株进行基因组比较表明,来自猪的 在基因上与人类的更相似,而不是与鸡的相似。尽管遗传相似性增加,但猪源 菌株在系统发育上是不同的,不属于引起人类败血症的医院适应株的主要序列类型。因此,结果表明,澳大利亚育肥猪不是澳大利亚医院适应 的来源。