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对捷克奶牛犊及其饲养员中产超广谱β-内酰胺酶菌株的基因组分析。

Genomic analysis of extended-spectrum beta-lactamase-producing from Czech diary calves and their caretakers.

作者信息

Masarikova Martina, Papouskova Aneta, Sukkar Iva, Lausova Jarmila, Cejkova Darina, Cizek Alois

机构信息

Department of Infectious Diseases and Microbiology, Faculty of Veterinary Medicine, University of Veterinary Sciences Brno, Brno, Czechia.

CEITEC VETUNI Brno, University of Veterinary Sciences Brno, Brno, Czechia.

出版信息

Front Vet Sci. 2025 Mar 12;12:1552297. doi: 10.3389/fvets.2025.1552297. eCollection 2025.

Abstract

INTRODUCTION

The increasing prevalence of antimicrobial resistance in livestock, particularly the dissemination of extended-spectrum beta-lactamase-producing , poses a significant zoonotic and public health risk. This study investigates the genomic characteristics of cefotaxime-resistant isolates from dairy calves across 23 Czech farms and their caretakers.

MATERIALS AND METHODS

Bacteriological cultivation on McConkey agar with cefotaxime was used for their isolation, susceptibility to selected antibiotics was determined by disc diffusion method, production of extended-spectrum beta-lactamases (ESBL) was demonstrated by double disc synergy test. The PCR was applied to confirm the presence of selected genes encoding resistance to some beta-lactams and genes encoding resistance to quinolones carried on plasmids. Using whole-genome sequencing, we evaluated resistance genotypes, sequence types, serotypes, plasmid replicons, and virulence genes.

RESULTS AND DISCUSSION

Among 266 rectal samples obtained from the calves, 128 (48%) harbored cefotaxime-resistant . Whole-genome analysis revealed genes in 91% (116/128) of isolates, with (44%) and (34%) being the dominant variants. Other beta-lactamase gene was found in 40% (51/128) of isolates. Notably, no cephamycin resistance genes have been identified. The plasmid-mediated quinolone resistance (PMQR) gene was present at 21% (27/128) of isolates. The colistin resistance gene was found in a single ST2325 isolate. Sequence typing revealed significant clonal diversity, with 21 different STs detected among 68 sequenced isolates. ST10 was the most prevalent (27%), followed by ST69 (12%), ST29 (7%) and others. The phylogenetic distribution showed a predominance of commensal groups A (54%) and B1 (21%). The most common serotypes included O101:H9 (21%), O15:H18 (12%), H12, and O70:H11 (7%). Analysis of plasmid content revealed a complex distribution of 18 distinct plasmid replicon types, especially IncF, followed by Col-type and IncI1-type plasmids. Cross-species transmission was indicated by the detection of clonal strains shared between calves and caretakers, notably ST10-O101:H9 and ST34-O68:H30. The prevalence of high-risk clones and the presence of mobile resistance elements underscore the urgent need for stringent monitoring, antimicrobial stewardship, and improved biosecurity measures in livestock environments like increased caution and personal hygiene of animal handlers to mitigate the spread of resistant between animals and humans.

摘要

引言

家畜中抗菌药物耐药性的日益普遍,尤其是产超广谱β-内酰胺酶细菌的传播,构成了重大的人畜共患病和公共卫生风险。本研究调查了来自捷克23个农场的奶牛犊及其饲养员中对头孢噻肟耐药的分离株的基因组特征。

材料与方法

采用含头孢噻肟的麦康凯琼脂进行细菌培养以分离菌株,通过纸片扩散法测定其对选定抗生素的敏感性,通过双纸片协同试验证明超广谱β-内酰胺酶(ESBL)的产生。应用聚合酶链反应(PCR)确认某些编码对β-内酰胺耐药的选定基因以及质粒上携带的编码对喹诺酮耐药的基因的存在。使用全基因组测序,我们评估了耐药基因型、序列类型、血清型、质粒复制子和毒力基因。

结果与讨论

在从犊牛获得的266份直肠样本中,128份(48%)含有对头孢噻肟耐药的[细菌名称未给出]。全基因组分析显示,91%(116/128)的分离株含有[相关基因未给出]基因,其中[基因变体1未给出](44%)和[基因变体2未给出](34%)是主要变体。在40%(51/128)的分离株中发现了其他β-内酰胺酶基因[基因名称未给出]。值得注意的是,未鉴定出头孢霉素耐药基因。质粒介导的喹诺酮耐药(PMQR)基因[基因名称未给出]在21%(27/128)的分离株中存在。在一个ST2325分离株中发现了黏菌素耐药基因[基因名称未给出]。序列分型显示出显著的克隆多样性,在68个测序分离株中检测到21种不同的序列类型。ST10最为常见(27%),其次是ST69(12%)、ST29(7%)等。系统发育分布显示共生菌群A(54%)和B1(21%)占主导。最常见的血清型包括O101:H9(21%)、O15:H18(12%)、H12和O70:H11(7%)。质粒含量分析显示18种不同质粒复制子类型的复杂分布,尤其是IncF,其次是Col型和IncI1型质粒。犊牛和饲养员之间共享的克隆菌株的检测表明存在跨物种传播,特别是ST10-O101:H9和ST34-O68:H30。高风险克隆的流行以及移动耐药元件的存在强调了在牲畜环境中进行严格监测、抗菌药物管理以及改善生物安全措施的迫切需求,如提高动物处理人员的警惕性和个人卫生,以减轻耐药[细菌名称未给出]在动物和人类之间的传播。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b8b/11938843/09ccec6d9840/fvets-12-1552297-g001.jpg

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