Tokajian Sima, Eisen Jonathan A, Jospin Guillaume, Farra Anna, Coil David A
Department of Natural Sciences, School of Arts and Sciences, Lebanese American University Byblos, Lebanon.
University of California Davis Genome Center Davis, CA, USA.
Front Cell Infect Microbiol. 2015 Apr 8;5:32. doi: 10.3389/fcimb.2015.00032. eCollection 2015.
The emergence of extended-spectrum β-lactamase (ESBL)-producing bacteria is now a critical concern. The ESBL-producing Klebsiella pneumoniae constitutes one of the most common multidrug-resistant (MDR) groups of gram-negative bacteria involved in nosocomial infections worldwide. In this study we report on the molecular characterization through whole genome sequencing of an ESBL-producing K. pneumoniae strain, LAU-KP1, isolated from a stool sample from a patient admitted for a gastrointestinal procedure/surgery at the Lebanese Amrican University Medical Center-Rizk Hospital (LAUMCRH) in Lebanon.
Illumina paired-end libraries were prepared and sequenced, which resulted in 4,220,969 high-quality reads. All sequence processing and assembly were performed using the A5 assembly pipeline.
The initial assembly produced 86 contigs, for which no scaffolding was obtained. The final collection of contigs was submitted to GenBank. The final draft genome sequence consists of a combined 5,632,663 bases with 57% G+C content. Automated annotation was performed using the RAST annotation server. Sequencing analysis revealed that the isolate harbored different β-lactamase genes, including bla oxa-1, bla CTX-M-15, bla SHV-11, and bla TEM-1b. The isolate was also characterized by the concomitant presence of other resistance determinants most notably acc(6')-lb-cr and qnrb1. The entire plasmid content was also investigated and revealed homology with four major plasmids pKPN-IT, pBS512_2, pRSF1010_SL1344, and pKPN3.
The potential role of K. pneumonia as a reservoir for ESBL genes and other resistance determinants is along with the presence of key factors that favor the spread of antimicrobial resistance a clear cause of concern and the problem that Carbapenem-non-susceptible ESBL isolates are posing in hospitals should be reconsidered through systematic exploration and molecular characterization.
产超广谱β-内酰胺酶(ESBL)细菌的出现目前是一个关键问题。产ESBL的肺炎克雷伯菌是全球医院感染中最常见的多重耐药(MDR)革兰氏阴性菌群体之一。在本研究中,我们报告了通过全基因组测序对一株从黎巴嫩美国大学医学中心 - 里兹克医院(LAUMCRH)因胃肠道手术入院患者的粪便样本中分离出的产ESBL肺炎克雷伯菌菌株LAU-KP1进行的分子特征分析。
制备并测序Illumina双末端文库,产生了4,220,969条高质量读段。所有序列处理和组装均使用A5组装流程进行。
初始组装产生了86个重叠群,未获得支架。最终的重叠群集合提交给了GenBank。最终的基因组草图序列由5,632,663个碱基组成,G + C含量为57%。使用RAST注释服务器进行自动注释。测序分析表明,该分离株携带不同的β-内酰胺酶基因,包括bla oxa-1、bla CTX-M-15、bla SHV-11和bla TEM-1b。该分离株的特征还在于同时存在其他耐药决定因素,最显著的是acc(6')-lb-cr和qnrb1。还对整个质粒含量进行了研究,发现与四个主要质粒pKPN-IT、pBS512_2、pRSF1010_SL1344和pKPN3具有同源性。
肺炎克雷伯菌作为ESBL基因和其他耐药决定因素储存库的潜在作用,以及有利于抗菌药物耐药性传播的关键因素的存在,显然令人担忧,并且应通过系统探索和分子特征分析重新审视碳青霉烯不敏感ESBL分离株在医院中造成的问题。