Sukmawinata Eddy, Uemura Ryoko, Sato Wataru, Thu Htun Myo, Sueyoshi Masuo
Graduate School of Medicine and Veterinary Medicine, University of Miyazaki, Miyazaki 889-1692, Japan.
Department of Veterinary Sciences, Faculty of Agriculture, University of Miyazaki, Miyazaki 889-2192, Japan.
Animals (Basel). 2020 Feb 25;10(3):369. doi: 10.3390/ani10030369.
Extended-spectrum β-lactamase (ESBL)- and AmpC β-lactamase (AmpC)-producing spp. have become a major health problem, leading to treatment failure in humans and animals. This study aimed to evaluate the presence of ESBL/AmpC-producing spp. isolated from racehorses in Japan. Feces samples from 212 healthy Thoroughbred racehorses were collected from the Japan Racing Association Training Centers between March 2017 and August 2018. ESBL/AmpC-producing spp. were isolated using selective medium containing 1 µg/mL cefotaxime. All isolates were subjected to bacterial species identification (MALDI-TOF MS), antimicrobial susceptibility test (disk diffusion test), characterization of resistance genes (PCR), conjugation assay, and genetic relatedness (multilocus sequence typing/MLST). Twelve ESBL/AmpC-producing (ESBL/AmpC-KP) were isolated from 3.3% of horse samples. Antimicrobial resistance profiling for 17 antimicrobials showed all ESBL/AmpC-KP were multidrug-resistant (MDR). Only 1 isolate was confirmed as an ESBL producer (positive), whereas the other 11 isolates were plasmid-mediated AmpC (pAmpC) producers ( positive). On the basis of MLST analysis, the ESBL-KP isolate was identified as sequence type (ST)-133 and four different STs among AmpC-KP isolates, ST-145, ST-4830, ST-4831, and ST-4832, were found to share six of the seven loci constituting a single-locus variant. This is the first study to show carrying MDR pAmpC isolated from a racehorse.
产超广谱β-内酰胺酶(ESBL)和AmpCβ-内酰胺酶(AmpC)的[具体菌名未给出]已成为一个主要的健康问题,导致人类和动物的治疗失败。本研究旨在评估从日本赛马中分离出的产ESBL/AmpC的[具体菌名未给出]的存在情况。2017年3月至2018年8月期间,从日本赛马协会训练中心收集了212匹健康纯种赛马的粪便样本。使用含有1μg/mL头孢噻肟的选择性培养基分离出产ESBL/AmpC的[具体菌名未给出]。所有分离株均进行细菌种类鉴定(基质辅助激光解吸电离飞行时间质谱法)、抗菌药物敏感性试验(纸片扩散法)、耐药基因特征分析(聚合酶链反应)、接合试验和遗传相关性分析(多位点序列分型/MLST)。从3.3%的马样本中分离出12株产ESBL/AmpC的[具体菌名未给出](ESBL/AmpC-KP)。对17种抗菌药物的耐药性分析表明,所有ESBL/AmpC-KP均为多重耐药(MDR)。仅1株分离株被确认为ESBL生产者(阳性),而其他11株分离株为质粒介导的AmpC(pAmpC)生产者(阳性)。基于MLST分析,ESBL-KP分离株被鉴定为序列型(ST)-133,在AmpC-KP分离株中发现了四种不同的ST,即ST-145、ST-4830、ST-4831和ST-4832,它们在构成单一位点变体的七个位点中的六个位点上相同。这是首次显示从赛马中分离出携带MDR pAmpC的[具体菌名未给出]的研究。