Zowawi Hosam M, Forde Brian M, Alfaresi Mubarak, Alzarouni Abdulqadir, Farahat Yasser, Chong Teik-Min, Yin Wai-Fong, Chan Kok-Gan, Li Jian, Schembri Mark A, Beatson Scott A, Paterson David L
The University of Queensland, Centre for Clinical Research (UQCCR), Herston QLD 4029, Australia.
Australian Infectious Diseases Research Centre, The University of Queensland, Brisbane, Australia.
Sci Rep. 2015 Oct 19;5:15082. doi: 10.1038/srep15082.
Carbapenem resistant Enterobacteriaceae (CRE) pose an urgent risk to global human health. CRE that are non-susceptible to all commercially available antibiotics threaten to return us to the pre-antibiotic era. Using Single Molecule Real Time (SMRT) sequencing we determined the complete genome of a pandrug-resistant Klebsiella pneumoniae isolate, representing the first complete genome sequence of CRE resistant to all commercially available antibiotics. The precise location of acquired antibiotic resistance elements, including mobile elements carrying genes for the OXA-181 carbapenemase, were defined. Intriguingly, we identified three chromosomal copies of an ISEcp1-bla(OXA-181) mobile element, one of which has disrupted the mgrB regulatory gene, accounting for resistance to colistin. Our findings provide the first description of pandrug-resistant CRE at the genomic level, and reveal the critical role of mobile resistance elements in accelerating the emergence of resistance to other last resort antibiotics.
耐碳青霉烯类肠杆菌科细菌(CRE)对全球人类健康构成了紧迫风险。对所有市售抗生素均不敏感的CRE有可能使我们重回抗生素出现之前的时代。我们利用单分子实时(SMRT)测序技术测定了一株全耐药肺炎克雷伯菌分离株的完整基因组,这是对所有市售抗生素均耐药的CRE的首个完整基因组序列。确定了获得性抗生素耐药元件的精确位置,包括携带OXA - 181碳青霉烯酶基因的移动元件。有趣的是,我们鉴定出ISEcp1 - bla(OXA - 181)移动元件的三个染色体拷贝,其中一个破坏了mgrB调控基因,导致对黏菌素耐药。我们的研究结果首次在基因组水平描述了全耐药CRE,并揭示了移动耐药元件在加速对其他最后手段抗生素耐药性出现方面的关键作用。