Lee Ji-Young, Lim Suk-Kyung, Choi Yujin, Moon Dong-Chan, Shin Juyoun, Ko Kwan Soo
1 Department of Molecular Cell Biology, and Samsung Medical Center, Sungkyunkwan University School of Medicine , Suwon, South Korea .
2 Bacterial Disease Division, Animal and Plant Quarantine Agency , Gimcheon, South Korea .
Microb Drug Resist. 2018 May;24(4):489-492. doi: 10.1089/mdr.2017.0369. Epub 2018 Feb 27.
Of 11 mcr-1-harboring plasmids previously identified from livestock in Korea, we performed whole plasmid sequencing on 3 plasmids and determined the genetic structure surrounding mcr-1 for all 11 plasmids. Transconjugation frequencies were measured for all mcr-1-harboring plasmids and competitive growth experiments were performed to investigate the fitness cost of each plasmid. Although they belong to different clones, the mcr-1-harboring plasmids, pEC006 and pEC019, were highly similar to the first identified mcr-1-carrying Incl2-type plasmid, pHNSHP45. Another IncX4-type plasmid, pEC111, had completely different structure from these plasmids, but was similar to pMCR1-IncX4. A nearly identical 11.3 kb mcr-1 region (nikB-ISApl1-mcr-1-pap2-topB) was shared by all mcr-1-harboring plasmids except pEC111. The transfer rate of mcr-1-harboring plasmids was highly variable (10 to 10) and was not related to plasmid structure. Competitive growth experiments revealed that the fitness of all three transconjugants with mcr-1-harboring plasmids increased compared with that of the recipient strain, Escherichia coli J53. The mcr-1-harboring plasmids may have been repeatedly introduced into bacterial isolates since the initial introduction of the mcr-1-positive strain from other countries into South Korea. Transferability and reduced burden to the host of mcr-1-harboring plasmid may lead to the proliferation of colistin-resistant isolates in the future. Therefore, continuous monitoring is necessary.
在先前从韩国家畜中鉴定出的11种携带mcr-1的质粒中,我们对3种质粒进行了全质粒测序,并确定了所有11种质粒中mcr-1周围的遗传结构。测量了所有携带mcr-1的质粒的接合转移频率,并进行了竞争性生长实验以研究每种质粒的适应性代价。尽管携带mcr-1的质粒pEC006和pEC019属于不同的克隆,但它们与首次鉴定出的携带mcr-1的IncI2型质粒pHNSHP45高度相似。另一种IncX4型质粒pEC111与这些质粒的结构完全不同,但与pMCR1-IncX4相似。除pEC111外,所有携带mcr-1的质粒都共享一个几乎相同的11.3 kb的mcr-1区域(nikB-ISApl1-mcr-1-pap2-topB)。携带mcr-1的质粒的转移率变化很大(10-10),且与质粒结构无关。竞争性生长实验表明,与受体菌株大肠杆菌J53相比,所有三种携带mcr-1的质粒的转接合子的适应性均有所提高。自从携带mcr-1的阳性菌株从其他国家首次引入韩国以来,携带mcr-1的质粒可能已被反复引入细菌分离株中。携带mcr-1的质粒的可转移性和对宿主负担的减轻可能会导致未来耐黏菌素分离株的增殖。因此,有必要进行持续监测。