Nazir Amina, Zhao Yachao, Li Manli, Manzoor Rakia, Tahir Rana Adnan, Zhang Xianglilan, Qing Hong, Tong Yigang
Key Laboratory of Molecular Medicine and Biotherapy in the Ministry of Industry and Information Technology, Department of Biology, School of Life Sciences, Beijing Institute of Technology, Beijing, People's Republic of China.
State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Beijing 100071, People's Republic of China.
Infect Drug Resist. 2020 Jun 22;13:1889-1903. doi: 10.2147/IDR.S228704. eCollection 2020.
Multidrug-resistant plasmids carrying replication genes have been widely present in various strains of and were found in plasmids belong to the IncFIB, but their detailed structural and genomic characterization was not reported yet. This is the first study that delivers structural and functional insights of and -carrying IncFIB plasmids.
strains A1705, 911021, and 1642 were isolated from the human urine samples and bronchoalveolar fluids collected from different hospitals of China. Antibacterial susceptibility and plasmid transfer ability were tested to characterize the resistant phenotypes mediated by the pA1705-, p911021-, and p1642-. The complete nucleotide sequences of these plasmids were determined through high-throughput sequencing technology and comparative genomic analyses of plasmids belong to the same incompatibility group were executed to extract the genomic variations and features.
The pA1705-, p911021-, and p1642- are defined as non-conjugative plasmids, having two replication genes, and associated with IncFIB family, and unknown incompatible group, respectively. Comparative genomic analysis revealed that relatively small backbones of IncFIB plasmids integrated massive accessory module at one "hotspot" that was located between and . These IncFIB plasmids exhibited the distinct profiles of accessory modules including one or two multidrug-resistant regions, many complete and remnant mobile elements comprising integrons, transposons and insertion sequences. The clusters of resistant genes were recognized in this study against different classes of antibiotics including β-lactam, phenicol, aminoglycoside, tetracycline, quinolone, trimethoprim, sulfonamide, tunicamycin, and macrolide. It has been observed that all resistant genes were located in multidrug resistance regions.
It is concluded that multidrug-resistant and -carrying IncFIB plasmids are a key source to mediate the resistance through mobile elements among . Current findings provide a deep understanding of horizontal gene transfer among plasmids of the IncFIB family via mobile elements that will be utilized in further in vitro studies.
携带复制基因的多重耐药质粒广泛存在于各种菌株中,在属于IncFIB的质粒中被发现,但其详细的结构和基因组特征尚未见报道。这是第一项对携带IncFIB质粒的[具体物质1]和[具体物质2]进行结构和功能研究的报道。
从中国不同医院收集的人类尿液样本和支气管肺泡灌洗液中分离出菌株A1705、911021和1642。测试了抗菌药敏性和质粒转移能力,以表征由pA1705 -、p911021 -和p1642 -介导的耐药表型。通过高通量测序技术测定这些质粒的完整核苷酸序列,并对属于同一不相容群的质粒进行比较基因组分析,以提取基因组变异和特征。
pA1705 -、p911021 -和p1642 -被定义为非接合性质粒,分别具有两个与IncFIB家族相关的复制基因[具体基因1]和[具体基因2],以及未知的不相容群。比较基因组分析表明,IncFIB质粒相对较小的主干在位于[具体基因1]和[具体基因2]之间的一个“热点”整合了大量辅助模块。这些IncFIB质粒表现出不同的辅助模块特征,包括一个或两个多重耐药区域,许多完整和残余的移动元件,包括整合子、转座子和插入序列。在本研究中识别出了针对不同类抗生素(包括β-内酰胺类、氯霉素类、氨基糖苷类、四环素类、喹诺酮类、甲氧苄啶、磺胺类、衣霉素和大环内酯类)的耐药基因簇。据观察,所有耐药基因都位于多重耐药区域。
得出结论,携带多重耐药[具体物质1]和[具体物质2]的IncFIB质粒是通过移动元件在[相关物种]中介导耐药性的关键来源。目前的研究结果为深入了解IncFIB家族质粒之间通过移动元件进行的水平基因转移提供了依据,这将在进一步的体外研究中得到应用。