Global Disease Detection and Response Program, U,S, Naval Medical Research Unit No, 3 (NAMRU-3), Abbassia, Cairo, Egypt.
Ann Clin Microbiol Antimicrob. 2013 Jul 18;12:16. doi: 10.1186/1476-0711-12-16.
Klebsiella pneumoniae outbreaks possessing extended-spectrum β-lactamase- (ESBL) mediated resistance to third-generation cephalosporins have increased significantly in hospital and community settings worldwide. The study objective was to characterize prevalent genetic determinants of TEM, SHV and CTX-M types ESBL activity in K. pneumoniae isolates from Egypt.
Sixty five ESBL-producing K. pneumoniae strains, isolated from nosocomial and community-acquired infections from 10 Egyptian University hospitals (2000-2003), were confirmed with double disc-synergy method and E-test. blaTEM, blaSHV and blaCTX-m genes were identified by PCR and DNA sequencing. Pulsed-field gel electrophoresis (PFGE) was conducted for genotyping.
All isolates displayed ceftazidime and cefotaxime resistance. blaTEM and blaSHV genes were detected in 98% of the isolates' genomes, while 11% carried blaCTX-m. DNA sequencing revealed plasmid-borne SHV-12,-5,-2a (17%), CTX-m-15 (11%), and TEM-1 (10%) prevalence. Among SHV-12 (n=8), one isolate displayed 100% blaSHV-12 amino acid identity, while others had various point mutations: T17G (Leu to Arg, position 6 of the enzyme: n=2); A8T and A10G (Tyr and Ile to Phe and Val, positions 3 and 4, respectively: n=4), and; A703G (Lys to Glu 235: n=1). SHV-5 and SHV-2a variants were identified in three isolates: T17G (n=1); A703G and G705A (Ser and Lys to Gly and Glu: n=1); multiple mutations at A8T, A10G, T17G, A703G and G705A (n=1). Remarkably, 57% of community-acquired isolates carried CTX-m-15. PFGE demonstrated four distinct genetic clusters, grouping strains of different genetic backgrounds.
This is the first study demonstrating the occurrence of SHV-12, SHV-5 and SHV-2a variants in Egypt, indicating the spread of class A ESBL in K. pneumoniae through different mechanisms.
具有第三代头孢菌素中介导的扩展谱β-内酰胺酶(ESBL)耐药性的肺炎克雷伯菌爆发在全球医院和社区环境中显著增加。本研究的目的是描述从埃及分离的肺炎克雷伯菌中 TEM、SHV 和 CTX-M 型 ESBL 活性的流行遗传决定因素。
65 株产 ESBL 的肺炎克雷伯菌分离自埃及 10 所大学医院的医院获得性和社区获得性感染(2000-2003 年),通过双碟协同试验和 E 试验确认。通过 PCR 和 DNA 测序鉴定 blaTEM、blaSHV 和 blaCTX-m 基因。进行脉冲场凝胶电泳(PFGE)进行基因分型。
所有分离株均表现出对头孢他啶和头孢噻肟的耐药性。98%的分离株基因组中检测到 blaTEM 和 blaSHV 基因,而 11%的分离株携带 blaCTX-m。DNA 测序显示质粒携带 SHV-12、-5、-2a(17%)、CTX-m-15(11%)和 TEM-1(10%)。在 SHV-12(n=8)中,有 1 株分离株 blaSHV-12 氨基酸同一性为 100%,而其他株则存在不同的点突变:T17G(Leu 到 Arg,酶的位置 6:n=2);A8T 和 A10G(Tyr 和 Ile 到 Phe 和 Val,分别为位置 3 和 4:n=4)和;A703G(Lys 到 Glu 235:n=1)。在 3 株分离株中鉴定出 SHV-5 和 SHV-2a 变体:T17G(n=1);A703G 和 G705A(Ser 和 Lys 到 Gly 和 Glu:n=1);A8T、A10G、T17G、A703G 和 G705A 多处突变(n=1)。值得注意的是,57%的社区获得性分离株携带 CTX-m-15。PFGE 显示出四个不同的遗传簇,将不同遗传背景的菌株分组。
这是首次在埃及发现 SHV-12、SHV-5 和 SHV-2a 变体的研究,表明通过不同机制,A 类 ESBL 在肺炎克雷伯菌中的传播。