Emergence of high-level colistin resistance mediated by multiple determinants, including mcr-1.1, mcr-8.2 and crrB mutations, combined with tigecycline resistance in an ST656 Klebsiella pneumoniae

被引:6
|
作者
Wang, Yanfei [1 ,2 ,3 ]
Zhou, Junxin [1 ,2 ,3 ]
Liu, Haiyang [1 ,2 ,3 ]
Wang, Qian [2 ,3 ,4 ]
Zhang, Ping [1 ,2 ,3 ]
Zhu, Jingyi [1 ,2 ,3 ]
Zhao, Dongdong [1 ,2 ,3 ]
Wu, Xueqing [1 ,2 ,3 ]
Yu, Yunsong [1 ,2 ,3 ]
Jiang, Yan [1 ,2 ,3 ]
机构
[1] Zhejiang Univ Sch Med, Sir Run Run Shaw Hosp, Dept Infect Dis, Hangzhou, Peoples R China
[2] Key Lab Microbial Technol & Bioinformat Zhejiang P, Hangzhou, Peoples R China
[3] Zhejiang Univ Sch Med, Sir Run Run Shaw Hosp, Reg Med Ctr Natl Inst Resp Dis, Hangzhou, Peoples R China
[4] Zhejiang Univ Sch Med, Sir Run Run Shaw Hosp, Dept Gen Practice, Hangzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
colistin; mcr; tigecycline; tmexCD1-toprJ1; co-integration; GENE; IDENTIFICATION; PLASMIDS;
D O I
10.3389/fcimb.2023.1122532
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Colistin and tigecycline are usually regarded as the last resort for multidrug-resistant Klebsiella pneumoniae infection treatment. Emergence of colistin and tigecycline resistance poses a global healthcare challenge and is associated with high mortality due to limited therapeutic options. Here, we report the ST656 extensively drug-resistant K. pneumoniae strain KP15-652, which was isolated from a patient's urine in China. Antimicrobial susceptibility testing showed it to be resistant to tigecycline, amikacin, levofloxacin, ciprofloxacin, and high-level colistin resistance (> 2048 mg/L). Whole-genome sequencing revealed that it harbors one chromosome and seven plasmids, including four plasmids carrying multiple acquired resistance genes. Transformation/conjugation tests and plasmid curing assays confirmed that mcr-1.1, mcr-8.2 and crrB mutations are responsible for the high-level colistin resistance and that a series of efflux pump genes, such as tmexCD1-toprJ1, tet(A) and tet(M), contribute to tigecycline resistance. mcr-1.1 and tet(M) are located on an IncX1 plasmid, which has conjugation transfer potential. mcr-8.2 and tet(A) are located on a multireplicon IncR/IncN plasmid but unable to be transferred via conjugation. Moreover, another conjugable and fusion plasmid carries the tmexCD1-toprJ1 gene cluster, which may have arisen due to IS26-mediated replicative transposition based on 8-bp target-site duplications. Importantly, a complex class 1 integron carrying various resistance genes was detected on this fusion plasmid. In conclusion, it is possible that the high-level of colistin resistance is caused by the accumulated effect of several factors on the chromosome and mcr-carrying plasmids, combined with many other resistances, including tigecycline. Effective surveillance should be performed to prevent further dissemination.
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页数:10
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