中国大熊猫保护研究中心都江堰基地圈养大熊猫大肠杆菌的全基因组分析。

IF 1.9 2区 农林科学 Q2 VETERINARY SCIENCES
Hongyan Yu, Mengru Zhao, Maolin Lu, Hongjia Li, Shu Fang, Ruisi Zhang, Tianlu Liu, Zhiyou Lü, Mengchao Zhou, Yaxian Lu, Tongzuo Zhang, Zhijun Hou
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引用次数: 0

摘要

大熊猫(Ailuropoda melanoleuca)是一种罕见的脆弱物种,面临着细菌感染的威胁。在疾病预防中广泛使用抗生素引起了人们对抗生素耐药性的关注,这降低了治疗效果,并对环境和公共卫生构成风险。本研究旨在分析圈养大熊猫的大肠杆菌耐药谱,为其肠道菌群中的抗生素耐药基因提供见解。从22只圈养大熊猫粪便中分离得到22株大肠杆菌,并进行全基因组测序。通过多位点序列分型(Multi-Locus Sequence Typing, MLST)和核心基因组多位点序列分型(core genome Multi-Locus Sequence Typing, cgMLST)确定序列类型和进化关系,鉴定毒力和抗性基因。核心基因组SNP分析建立遗传关系,AST分析评估抗生素耐药谱。全基因组测序显示15种不同的序列类型(STs),其中ST48(22.7%, 5株)和ST212(18.2%, 4株)为优势谱系。利用cgMLST进一步分析发现,ST48包含分布在不同进化分支上的多个cgST,而所有ST212分离株都属于一个cgST。这些结果证明了cgMLST在解决遗传多样性和分离优势系关系方面的实用性。基于核心基因组snp的系统发育分析将具有相似血清型和STs的分离株分组,包括与熊猫来源的大肠杆菌分离株(AMSHJX04)密切相关的致病簇。共有88个毒力基因(平均每个分离物52个)广泛存在,包括与铁获取系统(yagZ/Y)、菌毛相关基因(fimA/H)和II型分泌系统(gspM/K)有关的基因。药敏试验(AST)对环丙沙星、诺氟沙星和四环素的耐药率分别为59.1%、18.2%和13.6%,对庆大霉素和阿米卡星均保持敏感。耐药性分析鉴定出78个耐药基因,主要是外排泵(acrB/D, emrA/B)和四环素相关突变(emrK/Y)。圈养大熊猫的肠道菌群中含有多种抗生素耐药基因,表明存在耐药基因传播的风险。不同的序列类型、毒力基因和系统发育关系揭示了该物种大肠杆菌的遗传复杂性。一些分离株显示出与致病性大肠杆菌的遗传相似性,强调需要持续进行细菌监测。这威胁到抗生素的有效性,增加了感染风险,并使健康管理复杂化,强调了解决熊猫保护中的耐药性问题的紧迫性。
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 analysis of escherichia coli isolated from captive giant pandas (ailuropoda melanoleuca) at the Dujiangyan base of the China conservation and research center for the giant panda, Sichuan, China.

The giant panda (Ailuropoda melanoleuca) is a rare and vulnerable species facing threats from bacterial infections. The extensive use of antibiotics in disease prevention has raised concerns about antibiotic resistance, which reduces treatment efficacy and poses environmental and public health risks. This study aims to analyze the resistance profiles of Escherichia coli (E. coli) in captive pandas, providing insights into the antibiotic resistance genes within their gut microbiota. Twenty-two E. coli isolates were obtained from the feces of 22 captive giant pandas, and whole-genome sequencing was conducted. Sequence types and evolutionary relationships were determined through Multi-Locus Sequence Typing (MLST) and core genome Multi-Locus Sequence Typing (cgMLST), while virulence and resistance genes were identified. Core genome SNP analysis was performed to establish genetic relationships, and AST was conducted to evaluate antibiotic resistance profiles. Whole-genome sequencing revealed 15 distinct sequence types (STs), with ST48 (22.7%, 5 isolates) and ST212 (18.2%, 4 isolates) identified as the dominant lineages. Further resolution using cgMLST revealed that ST48 encompassed multiple cgSTs distributed across different evolutionary branches, while all ST212 isolates belonged to a single cgST. These results demonstrate the utility of cgMLST in resolving genetic diversity and isolate relationships within dominant lineages. Core genome SNP-based phylogenetic analysis grouped isolates with similar serotypes and STs, including a pathogenic cluster closely related to a panda-derived E. coli isolate (AMSHJX04). A total of 88 virulence genes (average 52 per isolate) were widespread, including those involved in iron acquisition systems (yagZ/Y), fimbriae-associated genes (fimA/H), and type II secretion systems (gspM/K). Antimicrobial susceptibility testing (AST) showed 59.1% resistance to ciprofloxacin, 18.2% to norfloxacin, and 13.6% to tetracycline, while all isolates remained sensitive to gentamicin and amikacin. Resistance profiling identified 78 resistance genes, primarily efflux pumps (acrB/D, emrA/B) and tetracycline-related mutations (emrK/Y). The gut microbiota of captive giant pandas harbors multiple antibiotic resistance genes, indicating a risk of resistance gene spread. Diverse sequence types, virulence genes, and phylogenetic relationships reveal the genetic complexity of E. coli in this species. Some isolates showed genetic similarities to pathogenic E. coli, emphasizing the need for continuous bacterial monitoring. This threatens antibiotic efficacy, increases infection risks, and complicates health management, underscoring the urgency of addressing resistance in panda conservation.

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来源期刊
Acta Veterinaria Scandinavica
Acta Veterinaria Scandinavica 农林科学-兽医学
CiteScore
3.60
自引率
0.00%
发文量
28
审稿时长
18-36 weeks
期刊介绍: Acta Veterinaria Scandinavica is an open access journal encompassing all aspects of veterinary research and medicine of domestic and wild animals.
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