Elhadidy Mohamed, Elkhatib Walid F, Elfadl Eman A Abo, Verstraete Karen, Denayer Sarah, Barbau-Piednoir Elodie, De Zutter Lieven, Verhaegen Bavo, De Rauw Klara, Piérard Denis, De Reu Koen, Heyndrickx Marc
Department of Bacteriology, Mycology and Immunology, Faculty of Veterinary Medicine, Mansoura University, Mansoura 35516, Egypt.
Department of Pharmacy Practice, School of Pharmacy, Hampton University, Kittrell Hall Hampton, VA 23668, USA.
Microbiology (Reading). 2015 Jan;161(Pt 1):112-119. doi: 10.1099/mic.0.083063-0. Epub 2014 Nov 19.
The aim of this study was to identify an epidemiological association between Shiga toxin-producing Escherichia coli O157 : H7 strains associated with human infection and with food sources. Frequency distributions of different genetic markers of E. coli O157 : H7 strains recovered from human and food sources were compared using molecular assays to identify E. coli O157 : H7 genotypes associated with variation in pathogenic potential and host specificity. Genotypic characterization included: lineage-specific polymorphism assay (LSPA-6), clade typing, tir (A255T) polymorphism, Shiga toxin-encoding bacteriophage insertion site analysis and variant analysis of Shiga toxin 2 gene (stx2a and stx2c) and antiterminator Q genes (Q933 and Q21). The intermediate lineage (LI/II) dominated among both food and human strains. Compared to other clades, clades 7 and 8 were more frequent among food and human strains, respectively. The tir (255T) polymorphism occurred more frequently among human strains than food strains. Q21 and Q933 + Q21 were found at significantly higher frequencies among food and human strains, respectively. Moreover, stx2a and stx2a+c were detected at significantly higher frequencies among human strains compared to food strains. Bivariate analysis revealed significant concordance (P<0.05) between the LSPA-6 assay and the other typing methods. Multivariable regression analysis suggested that tir (255T) was the most distinctive genotype that can be used to detect bacterial clones with potential risk for human illness from food sources. This study supported previous reports of the existence of diversity in genetic markers among different isolation sources by including E. coli O157 : H7 strains from both food and human sources. This might enable tracking genotypes with potential risk for human illness from food sources.
本研究的目的是确定产志贺毒素大肠杆菌O157 : H7菌株与人类感染及食物来源之间的流行病学关联。使用分子检测方法比较从人类和食物来源分离出的大肠杆菌O157 : H7菌株不同遗传标记的频率分布,以鉴定与致病潜力和宿主特异性变异相关的大肠杆菌O157 : H7基因型。基因型特征分析包括:谱系特异性多态性检测(LSPA-6)、进化枝分型、tir(A255T)多态性、志贺毒素编码噬菌体插入位点分析以及志贺毒素2基因(stx2a和stx2c)和抗终止子Q基因(Q933和Q21)的变异分析。中间谱系(LI/II)在食物和人类菌株中均占主导地位。与其他进化枝相比,进化枝7和8分别在食物和人类菌株中更为常见。tir(255T)多态性在人类菌株中比在食物菌株中更频繁出现。Q21以及Q933 + Q21分别在食物和人类菌株中以显著更高的频率被发现。此外,与食物菌株相比,stx2a和stx2a + c在人类菌株中的检测频率显著更高。双变量分析显示LSPA-6检测与其他分型方法之间存在显著一致性(P<0.05)。多变量回归分析表明,tir(255T)是最具特征性的基因型,可用于从食物来源中检测具有人类疾病潜在风险的细菌克隆。本研究通过纳入来自食物和人类来源的大肠杆菌O157 : H7菌株,支持了先前关于不同分离来源之间遗传标记存在多样性的报道。这可能有助于追踪来自食物来源的具有人类疾病潜在风险的基因型。