Sukmawinata Eddy, Uemura Ryoko, Sato Wataru, Mitoma Shuya, Kanda Takuya, 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.
Antibiotics (Basel). 2020 Feb 7;9(2):70. doi: 10.3390/antibiotics9020070.
In our previous study, extended spectrum β-lactamase (ESBL)-producing (ESBLEC) were isolated from healthy Thoroughbred racehorse feces samples in Japan. Some ESBL genes were predicted to be located on the conjugative plasmid. PCR-based replicon typing (PBRT) is a useful method to monitor and detect the association of replicons with specific plasmid-borne resistant genes. This study aimed to evaluate the plasmid replicon associated with ESBLEC isolated from healthy Thoroughbred racehorses at Japan Racing Association Training Centers in Japan. A total of 24 ESBLECs isolated from 23 (10.8%) individual Thoroughbred racehorse feces samples were used in this study. ESBL gene transfer was performed using a conjugation assay. Then, replicon types of ESBLEC isolates and their transconjugants were determined using PBRT. Pulsed-field gel electrophoresis (PFGE) was performed to look at the clonality of the ESBLECs isolates. ESBLECs were detected from 10.8% of healthy Thoroughbred racehorses. The was identified as the dominant type of ESBL gene, followed by and . In this study, only the and the IncI1 plasmid were transferred to transconjugants. The PFGE results showed that ESBL genes were distributed in diversity of ESBLECs. This finding suggested that the IncI1 plasmid was associated with the dissemination of in Thoroughbred racehorses in Japan.
在我们之前的研究中,从日本健康纯种赛马的粪便样本中分离出了产超广谱β-内酰胺酶(ESBL)的大肠杆菌(ESBLEC)。一些ESBL基因预计位于接合质粒上。基于PCR的复制子分型(PBRT)是监测和检测复制子与特定质粒携带的抗性基因之间关联的有用方法。本研究旨在评估与从日本赛马协会训练中心的健康纯种赛马中分离出的ESBLEC相关的质粒复制子。本研究共使用了从23匹(10.8%)个体纯种赛马粪便样本中分离出的24株ESBLEC。使用接合试验进行ESBL基因转移。然后,使用PBRT确定ESBLEC分离株及其接合子的复制子类型。进行脉冲场凝胶电泳(PFGE)以观察ESBLEC分离株的克隆性。从10.8%的健康纯种赛马中检测到了ESBLEC。 被鉴定为ESBL基因的主要类型,其次是 和 。在本研究中,只有 和IncI1质粒被转移到了接合子中。PFGE结果表明ESBL基因在ESBLEC中呈多样化分布。这一发现表明IncI1质粒与日本纯种赛马中 的传播有关。