Wang Jing, Wang Zhen-Yu, Wang Yan, Sun Fan, Li Wei, Wu Han, Shen Peng-Cheng, Pan Zhi-Ming, Jiao Xinan
Key Laboratory of Prevention and Control of Biological Hazard Factors (Animal Origin) for Agrifood Safety and Quality, Ministry of Agriculture of China, Yangzhou University, Yangzhou, China.
Jiangsu Key Laboratory of Zoonosis/Jiangsu Co-Innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou University, Yangzhou, China.
Front Microbiol. 2021 Jan 15;11:604278. doi: 10.3389/fmicb.2020.604278. eCollection 2020.
This study aimed to characterize 16S rRNA methylase genes among and to elucidate the structure and evolution of -carrying plasmids. One hundred fifty-eight isolates from one pig slaughterhouse were detected as containing 16S rRNA methylase genes; two (1.27%) London isolates from slaughtered pigs were identified to carry . They were resistant to gentamicin, amikacin, streptomycin, ampicillin, tetracycline, florfenicol, ciprofloxacin, and sulfamethoxazole/trimethoprim. The complete sequences of RmtB-producing isolates were obtained by PacBio single-molecule real-time sequencing. The isolate HA1-SP5 harbored plasmids pYUHAP5-1 and pYUHAP5-2. pYUHAP5-1 belonged to the IncFIB plasmid and showed high similarity to multiple IncFIB plasmids from London in China. The -carrying plasmid pYUHAP5-2 contained a typical IncN-type backbone; the variable region comprising several resistance genes and an IncX1 plasmid segment was inserted in the resolvase gene and bounded by IS. The sole plasmid in HA3-IN1 designated as pYUHAP1 was a cointegrate of plasmids from pYUHAP5-1-like and pYUHAP5-2-like, possibly mediated by IS via homologous recombination or conservative transposition. The structure differences between pYUHAP1 and its corresponding part of pYUHAP5-1 and pYUHAP5-2 may result from insertion, deletion, or recombination events mediated by mobile elements (IS, IS, and IS). This is the first report of in London. IncN plasmids are efficient vectors for distribution and are capable of evolving by reorganization and cointegration. Our results further highlight the important role of mobile elements, particularly IS, in the dissemination of resistance genes and plasmid evolution.
本研究旨在鉴定[具体细菌名称]中的16S rRNA甲基化酶基因,并阐明携带[具体细菌名称]的质粒的结构与进化。从一家生猪屠宰场采集的158株[具体细菌名称]分离株被检测出含有16S rRNA甲基化酶基因;从屠宰猪中分离出的2株(1.27%)伦敦[具体细菌名称]分离株被鉴定为携带[目标基因或质粒名称]。它们对庆大霉素、阿米卡星、链霉素、氨苄西林、四环素、氟苯尼考、环丙沙星以及磺胺甲恶唑/甲氧苄啶耐药。通过PacBio单分子实时测序获得了产RmtB分离株的完整序列。分离株HA1-SP5携带质粒pYUHAP5-1和pYUHAP5-2。pYUHAP5-1属于IncFIB质粒,与中国伦敦多株IncFIB质粒具有高度相似性。携带[目标基因或质粒名称]的质粒pYUHAP5-2含有典型的IncN型骨架;包含多个耐药基因和一个IncX1质粒片段的可变区插入到解离酶基因[具体基因名称]中,并由插入序列(IS)界定。HA3-IN1中唯一的质粒pYUHAP1被指定为pYUHAP5-1样和pYUHAP5-2样质粒的共合体,可能是由IS通过同源重组或保守转座介导的。pYUHAP1与其对应部分pYUHAP5-1和pYUHAP5-2之间的结构差异可能是由移动元件(IS、IS和IS)介导的插入、缺失或重组事件导致的。这是伦敦[具体细菌名称]中[目标基因或质粒名称]的首次报道。IncN质粒是[目标基因或质粒名称]传播的有效载体,并且能够通过重组和共合体进化。我们的结果进一步突出了移动元件,特别是IS,在耐药基因传播和质粒进化中的重要作用。