Pérez-Vázquez María, Oteo Jesús, García-Cobos Silvia, Aracil Belén, Harris Simon R, Ortega Adriana, Fontanals Dionisia, Hernández Juan Manuel, Solís Sonia, Campos José, Dougan Gordon, Kingsley Robert A
Centro Nacional de Microbiología, Instituto de Salud Carlos III, Majadahonda, Madrid, Spain
Centro Nacional de Microbiología, Instituto de Salud Carlos III, Majadahonda, Madrid, Spain.
J Antimicrob Chemother. 2016 Apr;71(4):887-96. doi: 10.1093/jac/dkv458. Epub 2016 Jan 13.
The global emergence of OXA-48-producing Klebsiella pneumoniae clones is a significant threat to public health. We used WGS and phylogenetic analysis of Spanish isolates to investigate the population structure of blaOXA-48-like-expressing K. pneumoniae ST11 and ST405 and to determine the distribution of resistance genes and plasmids encoding blaOXA-48-like carbapenemases.
SNPs identified in whole-genome sequences were used to reconstruct phylogenetic trees, identify resistance determinants and de novo assemble the genomes of 105 blaOXA-48-like-expressing K. pneumoniae isolates.
Genome variation was generally lower in outbreak-associated isolates compared with those associated with sporadic infections. The relatively limited variation observed within the outbreak-associated isolates was on average 7-10 SNPs per outbreak. Of 24 isolates from suspected sporadic infections, 7 were very closely related to isolates causing hospital outbreaks and 17 were more diverse and therefore probably true sporadic cases. On average, 14 resistance genes were identified per isolate. The 17 ST405 isolates from sporadic cases of infection had four distinct resistance gene profiles, while the resistance gene profile differed in all ST11 isolates from sporadic cases. Sequence analysis of 94 IncL/M plasmids carrying blaOXA-48-like genes revealed an average of two SNP differences, indicating a conserved plasmid clade.
Whole-genome sequence analysis enabled the discrimination of outbreak and sporadic isolates. Significant inter-regional spread within Spain of highly related isolates was evident for both ST11 and ST405 K. pneumoniae. IncL/M plasmids carrying blaOXA-48-like carbapenemase genes were highly conserved geographically and across the outbreaks, sporadic cases and clones.
产OXA - 48型肺炎克雷伯菌克隆在全球范围内的出现对公共卫生构成重大威胁。我们利用全基因组测序(WGS)和对西班牙分离株的系统发育分析,来研究表达blaOXA - 48样基因的肺炎克雷伯菌ST11和ST405的种群结构,并确定编码blaOXA - 48样碳青霉烯酶的耐药基因和质粒的分布。
利用全基因组序列中鉴定出的单核苷酸多态性(SNP)来重建系统发育树、鉴定耐药决定因素,并对105株表达blaOXA - 48样基因的肺炎克雷伯菌分离株的基因组进行从头组装。
与散发感染相关的分离株相比,与暴发相关的分离株的基因组变异通常更低。在与暴发相关的分离株中观察到的相对有限的变异平均每起暴发为7 - 10个SNP。在24株疑似散发感染的分离株中,7株与导致医院暴发的分离株密切相关,17株差异更大,因此可能是真正的散发病例。平均每株分离株鉴定出14个耐药基因。来自散发感染病例的17株ST405分离株有四种不同的耐药基因谱,而来自散发病例的所有ST11分离株的耐药基因谱均不同。对94个携带blaOXA - 48样基因的IncL/M质粒进行序列分析,平均发现两个SNP差异,表明存在一个保守的质粒分支。
全基因组序列分析能够区分暴发株和散发株。ST11和ST405肺炎克雷伯菌在西班牙境内均有明显的高度相关分离株的跨区域传播。携带blaOXA - 48样碳青霉烯酶基因的IncL/M质粒在地理上以及在暴发、散发病例和克隆中都高度保守。