Université de Carthage, Faculté des Sciences de Bizerte, Jarzouna 7021, Tunisia; Service des Laboratoires, Centre National de Greffe de la Moelle Osseuse, Tunis 1006, Tunisia; Université de Tunis El Manar, Faculté de Médecine de Tunis, UR 12ES02, Tunis 1007, Tunisia.
Service des Laboratoires, Centre National de Greffe de la Moelle Osseuse, Tunis 1006, Tunisia; Université de Tunis El Manar, Faculté de Médecine de Tunis, UR 12ES02, Tunis 1007, Tunisia.
J Glob Antimicrob Resist. 2018 Jun;13:154-160. doi: 10.1016/j.jgar.2017.12.014. Epub 2018 Jan 5.
This study investigated the prevalence of extended-spectrum β-lactamase-producing Klebsiella pneumoniae (ESBL-KP) strains in the National Bone Marrow Transplant Center of Tunis between 2002 and 2011 as well as their associated antimicrobial resistance patterns and molecular features.
Antimicrobial susceptibility was determined by the disk diffusion method according to CA-SFM guidelines. All of the strains were screened for β-lactamase genes, plasmid-encoded AmpC genes and integrons. Carbapenemase genes were analysed by PCR and sequencing for strains showing reduced susceptibility to ertapenem. Genetic relatedness was determined by pulsed-field gel electrophoresis (PFGE) and multilocus sequencing typing (MLST).
A total of 128 non-repetitive ESBL-KP strains (23.4%) responsible for infection or colonisation were recovered among 548 K. pneumoniae strains. The isolates were also multidrug-resistant. Molecular analysis revealed the prevalence of bla (92.2%), followed by bla (81.3%) and bla group (73.4%). Four ertapenem-resistant ESBL-KP strains (3.1%) carried the bla gene associated with the bla gene. Class 1 integrons were the most prevalent among the isolates (85.2%). High diversity was demonstrated by PFGE with limited clonal dissemination of 1 major (n=13 strains) and 11 minor clusters (each comprising 2-3 strains). MLST of representative strains also showed high diversity with two main epidemic clones: ST15, associated with the major cluster; and ST101, associated with five minor clusters (n=11 strains).
This study provides relevant information on the epidemiology of ESBL-KP strains in oncohaematology patients, of which 18.8% belonged to the specific CTX-M-15 K. pneumoniae clones ST15 and ST101.
本研究旨在调查 2002 年至 2011 年期间突尼斯国家骨髓移植中心产超广谱β-内酰胺酶肺炎克雷伯菌(ESBL-KP)的流行情况及其相关的抗菌药物耐药模式和分子特征。
采用 CA-SFM 指南中的纸片扩散法测定抗菌药物敏感性。所有菌株均进行β-内酰胺酶基因、质粒编码 AmpC 基因和整合子筛查。对表现出对厄他培南敏感性降低的菌株进行碳青霉烯酶基因分析,采用 PCR 和测序。通过脉冲场凝胶电泳(PFGE)和多位点序列分型(MLST)确定遗传相关性。
在 548 株肺炎克雷伯菌中,共分离出 128 株非重复的产 ESBL-KP 菌株(23.4%),这些菌株可引起感染或定植。这些分离株还表现出多重耐药性。分子分析显示,bla(92.2%)、bla(81.3%)和 bla(73.4%)基因最为常见。4 株耐厄他培南的产 ESBL-KP 菌株(3.1%)携带与 bla基因相关的 bla基因。在分离株中,I 类整合子最为常见(85.2%)。PFGE 显示高度多样性,仅传播 1 个主要克隆(n=13 株)和 11 个次要克隆(每个克隆由 2-3 株组成)。代表性菌株的 MLST 也显示出高度多样性,有两个主要流行克隆:与主要克隆相关的 ST15 型和与 5 个次要克隆相关的 ST101 型(n=11 株)。
本研究提供了有关血液肿瘤患者产 ESBL-KP 菌株的流行病学信息,其中 18.8%属于特定的 CTX-M-15 型肺炎克雷伯菌 ST15 和 ST101 克隆。