奶牛犊牛中产 ESBL/AmpC 型大肠埃希菌的场内动态:纵向研究。

Within-farm dynamics of ESBL/AmpC-producing Escherichia coli in veal calves: a longitudinal approach.

机构信息

Department of Infectious Diseases and Immunology, Faculty of Veterinary Medicine, Utrecht University, PO Box 80.165, 3508 TD Utrecht, The Netherlands.

出版信息

J Antimicrob Chemother. 2013 Nov;68(11):2468-76. doi: 10.1093/jac/dkt219. Epub 2013 Jun 11.

Abstract

OBJECTIVES

To assess the within-farm dynamics of extended-spectrum β-lactamase (ESBL)/AmpC-producing Escherichia coli in veal calves.

METHODS

Three veal-calf fattening farms were screened. Faecal samples from all calves within a compartment (109-150 per farm) were taken upon arrival on the farm (T0) and after 3, 6, 8 and 10 weeks (T3-T10). ESBL/AmpC genes were characterized by PCR and sequencing. Plasmids were characterized by transformation, PCR-based replicon typing and plasmid multilocus sequence typing (MLST). E. coli genotypes were analysed by MLST.

RESULTS

At T0 the prevalence of ESBL/AmpC-producing E. coli ranged from 18% to 26%. These were predominantly isolates carrying blaCTX-M-1 and blaCTX-M-15 genes, located on various plasmids and E. coli sequence types (STs). Farm 1 was negative for ESBL/AmpC-producing E. coli after T0. Farm 2 showed an increase up to 37% at T3, which subsequently decreased gradually to 0% at T10. The presence from T3 to T10 on farm 2 was mainly caused by the clonal spread of a multiresistant E. coli ST57 harbouring blaCTX-M-14 on an IncF F2:A-:B- plasmid. Farm 3 showed a gradual decrease in prevalence to 1.4% at T10, with a relative increase of the identical clonal variant as shown for farm 2. A second clonal variant found in farm 3 was a multiresistant E. coli ST10 harbouring blaCTX-M-14 on an IncK plasmid.

CONCLUSIONS

The prevalence of ESBL/AmpC-producing E. coli decreased over time. A clonal spread was observed on farm 2 and farm 3, illustrative of the complex dynamics probably associated with the use of antimicrobials.

摘要

目的

评估产extended-spectrum β-lactamase (ESBL)/AmpC 的大肠杆菌在小牛肉犊牛中的农场内动态。

方法

对 3 个小牛肉育肥农场进行筛查。每个畜栏(每个农场 109-150 头)的所有小牛在抵达农场时(T0)以及 3、6、8 和 10 周后(T3-T10)采集粪便样本。通过 PCR 和测序来鉴定 ESBL/AmpC 基因。通过转化、基于 PCR 的复制子分型和质粒多位点序列分型(MLST)来鉴定质粒。通过 MLST 分析大肠杆菌基因型。

结果

在 T0,产 ESBL/AmpC 大肠杆菌的流行率为 18%至 26%。这些主要是携带 blaCTX-M-1 和 blaCTX-M-15 基因的分离株,位于各种质粒和大肠杆菌序列型(ST)上。T0 后,1 号农场无产 ESBL/AmpC 大肠杆菌。2 号农场在 T3 时增加到 37%,随后逐渐降至 T10 时的 0%。从 T3 到 T10,2 号农场的存在主要是由携带 blaCTX-M-14 的多药耐药大肠杆菌 ST57 的克隆传播引起的,该 ST57 位于 IncF F2:A-:B-质粒上。3 号农场的流行率逐渐降至 T10 时的 1.4%,与 2 号农场一样,相同的克隆变异相对增加。在 3 号农场发现的第二种克隆变异是携带 blaCTX-M-14 的多药耐药大肠杆菌 ST10,该 ST10 位于 IncK 质粒上。

结论

产 ESBL/AmpC 大肠杆菌的流行率随时间逐渐降低。在 2 号和 3 号农场观察到了克隆传播,这表明与使用抗生素相关的复杂动态。

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