Hamidian Mohammad, Kenyon Johanna J, Holt Kathryn E, Pickard Derek, Hall Ruth M
School of Molecular Bioscience, The University of Sydney, NSW 2006, Australia.
Department of Biochemistry and Molecular Biology and Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Melbourne, Victoria, Australia.
J Antimicrob Chemother. 2014 Oct;69(10):2625-8. doi: 10.1093/jac/dku188. Epub 2014 Jun 6.
To locate the acquired bla(OXA-23) carbapenem resistance gene in an Australian A. baumannii global clone 1 (GC1) isolate.
The genome of the extensively antibiotic-resistant GC1 isolate A85 harbouring bla(OXA-23) in Tn2006 was sequenced using Illumina HiSeq, and the reads were used to generate a de novo assembly. PCR was used to assemble relevant contigs. Sequences were compared with ones in GenBank. Conjugation experiments were conducted.
The sporadic GC1 isolate A85, recovered in 2003, was extensively resistant, exhibiting resistance to imipenem, meropenem and ticarcillin/clavulanate, to cephalosporins and fluoroquinolones and to the older antibiotics gentamicin, kanamycin and neomycin, sulfamethoxazole, trimethoprim and tetracycline. Genes for resistance to older antibiotics are in the chromosome, in an AbaR3 resistance island. A second copy of the ampC gene in Tn6168 confers cephalosporin resistance and the gyrA and parC genes have mutations leading to fluoroquinolone resistance. An 86 335 bp repAci6 plasmid, pA85-3, carrying bla(OXA-23) in Tn2006 in AbaR4, was shown to transfer imipenem, meropenem and ticarcillin/clavulanate resistance into a susceptible recipient. A85 also contains two small cryptic plasmids of 2.7 and 8.7 kb. A85 is sequence type ST126 (Oxford scheme) and carries a novel KL15 capsule locus and the OCL3 outer core locus.
A85 represents a new GC1 lineage identified by the novel capsule locus but retains AbaR3 carrying genes for resistance to older antibiotics. Resistance to imipenem, meropenem and ticarcillin/clavulanate has been introduced into A85 by pA85-3, a repAci6 conjugative plasmid carrying Tn2006 in AbaR4.
在一株澳大利亚鲍曼不动杆菌全球克隆1(GC1)分离株中定位获得性bla(OXA - 23)碳青霉烯耐药基因。
使用Illumina HiSeq对携带位于Tn2006中的bla(OXA - 23)的广泛耐药GC1分离株A85的基因组进行测序,并将测序读数用于从头组装。采用PCR组装相关重叠群。将序列与GenBank中的序列进行比较。进行了接合实验。
2003年分离出的散发GC1分离株A85具有广泛耐药性,对亚胺培南、美罗培南和替卡西林/克拉维酸、头孢菌素和氟喹诺酮类以及较老的抗生素庆大霉素、卡那霉素和新霉素、磺胺甲恶唑、甲氧苄啶和四环素均耐药。对较老抗生素的耐药基因位于染色体上的一个AbaR3耐药岛中。Tn6168中的ampC基因的第二个拷贝赋予头孢菌素耐药性,gyrA和parC基因发生突变导致氟喹诺酮耐药性。一个86 335 bp的repAci6质粒pA85 - 3,在AbaR4中携带位于Tn2006中的bla(OXA - 23),被证明可将亚胺培南、美罗培南和替卡西林/克拉维酸耐药性转移至敏感受体。A85还包含两个大小分别为2.7 kb和8.7 kb的小隐蔽质粒。A85是序列型ST126(牛津分型法),携带一个新的KL15荚膜位点和OCL3外核心位点。
A85代表了一个由新的荚膜位点鉴定出的新GC1谱系,但保留了携带对较老抗生素耐药基因的AbaR3。pA85 - 3(一个在AbaR4中携带Tn2006的repAci6接合质粒)已将对亚胺培南、美罗培南和替卡西林/克拉维酸的耐药性引入A85。