Comparative phylogenomics of extended-spectrum beta-lactamase-producing Escherichia coli revealed a wide diversity of clones and plasmids in Spanish chicken meat

IF 5 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY
Sandra Martínez-Álvarez , Pierre Châtre , Pauline François , Myriam Zarazaga , Jean-Yves Madec , Marisa Haenni , Carmen Torres
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引用次数: 0

Abstract

Animal food products are important sources of zoonotic agents, increasing the risk of exposure to antibiotic-resistant bacteria from farm to fork. Therefore, we aimed to detect and fully characterise Extended-Spectrum Beta-Lactamase (ESBL)-producing E. coli from the poultry sector in a One Health approach. From December 2021 to March 2022, 48 chicken meat samples were collected from 16 establishments in La Rioja (Northern Spain). Antibiotic susceptibility testing was assessed by the disk-diffusion method. Forty E. coli isolates were recovered from 33 of the 48 chicken meat samples tested (68.8%) when plated on MacConkey-agar. In addition, six ESBL-E. coli (6/48, 12.5%) were obtained on cefotaxime-supplemented MacConkey-agar, which were Whole-Genome Sequenced. A large diversity of clones and ESBL genes was observed, namely ST1140-E/blaCTX-M-32 (n = 1), ST752-A/blaTEM-52 (n = 1), ST117-B2/blaCTX-M-1/blaSHV-12 (n = 2), ST10-A/blaSHV-12 (n = 1) and ST223-B1/blaSHV-12 (n = 1). Three IncI1-plasmids (pST3-CC3) were found carrying the blaSHV-12/blaCTX-M-1/blaCTX-M-32 genes in two genetic environments: i) IS26-smc-glpR-blaSHV-12-IS26; and ii) wbuC-blaCTX-M-32/blaCTX-M-1-ISEcp1. The blaTEM-52 gene was carried on a P1-like phage-plasmid flanked by an IS4-mediated composite transposon. An IncHI2 plasmid harboured a blaSHV-12 gene flanked by an IS26-mediated composite transposon but also additional genes conferring resistance to aminoglycosides, chloramphenicol, and sulphonamides. To analyse the cross-sectoral relatedness of our ESBL-E. coli isolates, our six genomes were mapped with publicly available genomes (n = 2588) related to the STs detected, revealing that one of our genomes (X3078-ST117) displayed strong similarities (34–40 allelic differences) with few genomes belonging to ST117 from the poultry sector from Germany and USA. This study demonstrated that the proportion of ESBL-E. coli is still high in chicken meat in Spain. In addition, the ST117 clone and the IncI1-blaCTX-M-1-32/blaSHV-12 plasmids might represent successful clones and plasmids adapted to the chicken host.

西班牙鸡肉中产广谱β-内酰胺酶大肠埃希菌的比较系统发生组学揭示了克隆和质粒的广泛多样性
动物食品是人畜共患病病原体的重要来源,增加了从农场到餐桌接触耐抗生素细菌的风险。因此,我们的目标是采用 "统一健康 "方法检测家禽业中产广谱β-内酰胺酶(ESBL)的大肠杆菌,并对其进行全面鉴定。从 2021 年 12 月到 2022 年 3 月,我们从拉里奥哈(西班牙北部)的 16 家企业采集了 48 份鸡肉样本。抗生素敏感性检测采用盘扩散法进行评估。在检测的 48 个鸡肉样本中,有 33 个样本(68.8%)在 MacConkey-agar 平板上分离出 40 个大肠杆菌。此外,在添加了头孢他啶的 MacConkey-agar 上还获得了 6 个 ESBL-E. coli(6/48,12.5%),并对其进行了全基因组测序。观察到克隆和 ESBL 基因具有很大的多样性,即 ST1140-E/blaCTX-M-32(n = 1)、ST752-A/blaTEM-52(n = 1)、ST117-B2/blaCTX-M-1/blaSHV-12(n = 2)、ST10-A/blaSHV-12(n = 1)和 ST223-B1/blaSHV-12(n = 1)。在两种遗传环境中发现了三个携带 blaSHV-12/blaCTX-M-1/blaCTX-M-32 基因的 IncI1 质粒(pST3-CC3):i) IS26-smc-glpR-blaSHV-12-IS26;ii) wbuC-blaCTX-M-32/blaCTX-M-1-ISEcp1。blaTEM-52 基因携带在一个 P1 类噬菌体质粒上,质粒两侧有一个 IS4 介导的复合转座子。一个 IncHI2 质粒携带有 blaSHV-12 基因,其两侧是一个由 IS26 介导的复合转座子,同时还携带有对氨基糖苷类、氯霉素和磺胺类药物产生抗性的其他基因。为了分析我们分离出的 ESBL-E.大肠杆菌的跨部门亲缘关系,我们将六个基因组与与检测到的 ST 相关的公开基因组(n = 2588)进行了映射,结果显示,我们的一个基因组(X3078-ST117)与德国和美国家禽业中属于 ST117 的少数基因组显示出很强的相似性(34-40 个等位基因差异)。这项研究表明,ESBL-E. 大肠杆菌在西班牙鸡肉中的比例仍然很高。此外,ST117 克隆和 IncI1-blaCTX-M-1-32/blaSHV-12 质粒可能代表了适应鸡宿主的成功克隆和质粒。
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来源期刊
International journal of food microbiology
International journal of food microbiology 工程技术-食品科技
CiteScore
10.40
自引率
5.60%
发文量
322
审稿时长
65 days
期刊介绍: The International Journal of Food Microbiology publishes papers dealing with all aspects of food microbiology. Articles must present information that is novel, has high impact and interest, and is of high scientific quality. They should provide scientific or technological advancement in the specific field of interest of the journal and enhance its strong international reputation. Preliminary or confirmatory results as well as contributions not strictly related to food microbiology will not be considered for publication.
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