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食品中单增李斯特菌携带 tetM 基因的质粒可在加工干酪表面与粪肠球菌发生水平基因转移。

Food isolate Listeria monocytogenes harboring tetM gene plasmid-mediated exchangeable to Enterococcus faecalis on the surface of processed cheese.

机构信息

Núcleo de Biotecnologia, Centro de Desenvolvimento Tecnológico (CDTec), Universidade Federal de Pelotas (UFPel), Pelotas, RS, Brazil; Departamento de Ciência e Tecnologia Agroindustrial (DCTA), Faculdade de Agronomia Eliseu Maciel (FAEM), Universidade Federal de Pelotas (UFPel), Pelotas, RS, Brazil.

Núcleo de Biotecnologia, Centro de Desenvolvimento Tecnológico (CDTec), Universidade Federal de Pelotas (UFPel), Pelotas, RS, Brazil.

出版信息

Food Res Int. 2018 May;107:503-508. doi: 10.1016/j.foodres.2018.02.062. Epub 2018 Mar 1.

Abstract

The genetic basis of tetracycline resistance in a food isolate Listeria monocytogenes (Lm16) was evaluated. Resistance to tetracycline was associated with the presence of the tetM gene in plasmid DNA. The sequence of tetM showed 100% of similarity with the Enterococcus faecalis sequences found in the EMBL database, suggesting that Lm16 received this gene from E. faecalis. Various size bands were detected in the DNA plasmid analysis, the largest being approximately 54.38 kb. Transferability of the tetM gene was achieved in vitro by agar matings between Lm16 and E. faecalis JH2-2, proving the potential for the spread of tetM by horizontal gene transfer. Furthermore, the conjugation experiments were performed on the surface of processed cheese, confirming the transferability in a food matrix. PCR assays were used to confirm the identity of E. faecalis and to detect the tetM gene in transconjugant bacteria. Additionally, the minimal inhibitory concentration for tetracycline and rifampicin and plasmid profiling were performed. This is the first report of a food isolate L. monocytogenes carrying the tetM gene in plasmid DNA, and it highlights the potential risk of spreading antimicrobial resistance genes between different bacteria.

摘要

评估了食品分离李斯特菌 (Lm16) 中四环素耐药性的遗传基础。对四环素的抗性与质粒 DNA 中 tetM 基因的存在有关。tetM 序列与 EMBL 数据库中发现的粪肠球菌序列完全相同,表明 Lm16 从粪肠球菌获得了该基因。在 DNA 质粒分析中检测到各种大小的带,最大的约为 54.38 kb。通过 Lm16 和粪肠球菌 JH2-2 之间的琼脂交配在体外实现了 tetM 基因的可转移性,证明了通过水平基因转移传播 tetM 的潜力。此外,在加工奶酪表面进行了接合实验,证实了在食品基质中的可转移性。PCR 检测用于确认粪肠球菌的身份,并检测转导细菌中的 tetM 基因。此外,还进行了最低抑菌浓度和质粒图谱分析。这是第一个报告食品分离李斯特菌在质粒 DNA 中携带 tetM 基因的报告,它突出了不同细菌之间传播抗生素耐药基因的潜在风险。

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