Department of Infectious Diseases and Public Health, Jockey Club College of Veterinary Medicine and Life Sciences, City University of Hong Kong, Kowloon, Hong Kong.
State Key Lab of Chemical Biology and Drug Discovery, Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong.
Adv Biosyst. 2020 Apr;4(4):e1900239. doi: 10.1002/adbi.201900239. Epub 2020 Feb 13.
The rapid dissemination of non-conjugative virulence plasmids among non-K1/K2 types of Klebsiella pneumoniae poses an unprecedented threat to human health, yet the underlying mechanisms governing dissemination of such plasmids is unclear. In this study, a novel 68 581 bp IncFIA plasmid is discovered that can be fused to a hypervirulence-encoding plasmid to form a hybrid conjugative virulence plasmid in conjugation experiments; such fusion events involve homologous recombination between a 241 bp homologous region located in each of the two plasmids. The fusion hypervirulence-encoding plasmid can be conjugated to both classic and bla -bearing carbapenem-resistant K. pneumoniae strains through conjugation, enabling such strains to acquire the ability to express the hypervirulence phenotype. Dissemination of this fusion virulence plasmid will impose an enormous burden on current efforts to control and treat infections caused by multidrug resistant and hypervirulent K. pneumoniae.
非 K1/K2 型肺炎克雷伯菌中非共轭毒力质粒的快速传播对人类健康构成了前所未有的威胁,但控制此类质粒传播的潜在机制尚不清楚。在这项研究中,发现了一种新型的 68581bp IncFIA 质粒,它可以与一种高毒力编码质粒融合,在接合实验中形成一种杂交可接合毒力质粒;这种融合事件涉及位于两个质粒中的 241bp 同源区域之间的同源重组。融合的高毒力编码质粒可以通过接合将经典和 bla 携带的碳青霉烯类耐药肺炎克雷伯菌菌株进行转导,使这些菌株获得表达高毒力表型的能力。这种融合毒力质粒的传播将对当前控制和治疗多药耐药和高毒力肺炎克雷伯菌引起的感染的努力造成巨大负担。