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来自猪的氟苯尼考耐药性大肠杆菌分离株的分子分析

Molecular analysis of florfenicol-resistant Escherichia coli isolates from pigs.

作者信息

Blickwede Maren, Schwarz Stefan

机构信息

Institut für Tierzucht, Bundesforschungsanstalt für Landwirtschaft (FAL), Höltystrasse 10, 31535 Neustadt-Mariensee, Germany.

出版信息

J Antimicrob Chemother. 2004 Jan;53(1):58-64. doi: 10.1093/jac/dkh007. Epub 2003 Nov 25.

DOI:10.1093/jac/dkh007
PMID:14645321
Abstract

OBJECTIVES

The aim of this study was to analyse florfenicol-resistant Escherichia coli isolates from pigs for the genetic basis of florfenicol resistance, and to compare these data with those previously determined for E. coli isolates from cattle and poultry.

METHODS

Fourteen porcine E. coli isolates were included in this study and subjected to serotyping, plasmid profiling and macrorestriction analysis. MICs of florfenicol were determined by broth microdilution. The presence of the gene floR was confirmed by hybridization and PCR analysis. Transformation experiments were conducted to isolate florfenicol resistance plasmids. The floR region of a florfenicol resistance plasmid was cloned and sequenced.

RESULTS

All florfenicol-resistant E. coli isolates exhibited MICs of florfenicol >128 mg/L and carried the floR gene. A single isolate had a floR-carrying plasmid of approximately 35 kb, designated pMBSF1. Sequence analysis identified the floR gene flanked by truncated transposase genes. Moreover, a truncated copy of Tn5393 with complete streptomycin resistance genes strA and strB was found upstream of the floR gene of pMBSF1. Chromosomally resistant E. coli isolates, which shared the same BlnI macrorestriction pattern, differed in their floR hybridization patterns.

CONCLUSION

The plasmid pMBSF1 is the smallest floR-carrying plasmid reported to date. Its floR region differed from those previously found in E. coli isolates from cattle. Variations in the RFLPs of chromosomal EcoRI fragments carrying floR in isolates that had the same macrorestriction pattern might suggest variable chromosomal integration sites.

摘要

目的

本研究旨在分析猪源氟苯尼考耐药性大肠杆菌分离株的氟苯尼考耐药遗传基础,并将这些数据与先前针对牛和家禽源大肠杆菌分离株所确定的数据进行比较。

方法

本研究纳入了14株猪源大肠杆菌分离株,进行血清型鉴定、质粒图谱分析和宏观限制性分析。通过肉汤微量稀释法测定氟苯尼考的最低抑菌浓度(MIC)。通过杂交和PCR分析确认floR基因的存在。进行转化实验以分离氟苯尼考耐药质粒。对一个氟苯尼考耐药质粒的floR区域进行克隆和测序。

结果

所有氟苯尼考耐药性大肠杆菌分离株的氟苯尼考MIC均>128 mg/L,并携带floR基因。单个分离株有一个约35 kb携带floR的质粒,命名为pMBSF1。序列分析确定floR基因两侧为截短的转座酶基因。此外,在pMBSF1的floR基因上游发现了一个带有完整链霉素抗性基因strA和strB的截短的Tn5393拷贝。具有相同BlnI宏观限制性图谱的染色体耐药性大肠杆菌分离株,其floR杂交图谱有所不同。

结论

质粒pMBSF1是迄今为止报道的最小的携带floR的质粒。其floR区域与先前在牛源大肠杆菌分离株中发现的不同。具有相同宏观限制性图谱的分离株中,携带floR的染色体EcoRI片段的限制性片段长度多态性(RFLP)的变化可能表明染色体整合位点不同。

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