Phylogenetic Groups/B2 Subgroup Distributions, Serogrouping and Identification of Virulence Factors in Extended-Spectrum Cephalosporin-Resistant Escherichia coli Strains Isolated from the Stool of Healthy Children Under 10 Years Old

IF 0.5 Q4 PEDIATRICS Archives of Pediatric Infectious Diseases Pub Date : 2022-04-19 DOI:10.5812/pedinfect-118889
M. Mansuri, M. Karbalaei, Zahra Abdolvand, A. Mohabati Mobarez
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Abstract

Background: Segregation of Escherichia coli (E. coli) into the phylogenetic groups was observed in the experiments so that group B2 contained the enteropathogenic E. coli (EPEC) strains and extraintestinal pathogenic E. coli (ExPEC). Objectives: This study aimed to identify B2 phylogenetic groups in the extended-spectrum Cephalosporins resistant E. coli isolated from the stool of healthy children under 10 years old. Methods: One hundred E. coli resistant to broad-spectrum Cephalosporins were collected from the feces of healthy children under 10. Subsequently, we grouped phylogenetic via PCR based on the genes yjaA, chuA, arpA, as well, as TspE4.C2. Then, according to Clermont et al.’s study, we used two individual multiplex PCRs for identifying B2 sub-groups (I-X subgroups). Serogroup typing with the 12 O-antigen was analyzed via PCR, and finally, 10 virulence genes (cnf1, papG, ibeA, malX, usp, cdt, eae, bfp, and afa-Dr) were identified with PCR. Results: The age range of the healthy children was between 1 and 10 years. The B2 and unknown phylogroups were the most common strains in this study. The most common B2 subgroups were I (STc131) (2%), IX (1%), V (8%), IV, V, VII (1%), IX, V (3%), IX, V, III, I (1%), IX, V, III, VII, I (%1), V, I (6%), V, III, I (3%), and V, III, VII (1%), with each subgroup carrying distinctive sets of ExPEC virulence markers. The results also showed that 29% of E. coli in the healthy children had malX and 23% had papGII. It was also found that 32% of the strains isolated from the healthy children had antigens O2 and 36% were unknown. Conclusions: In this study, 27% of the strains belonged to B2 phylogroup and 6% to B1 phylogroup. Moreover, serogroups O2, O16, and O25 were predominant and belonged to B2 phylogroup. Moreover, malX, papGII, usp, papGIII, aggR, and eae virulence genes also had the highest to lowest supply among the tested strains, respectively. Moreover, B2 isolates were shown to have further virulence-related genes in comparison to the non B2 isolates.
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10岁以下健康儿童粪便中广谱耐头孢菌素大肠杆菌的系统发育群/B2亚群分布、血清分型及毒力因子鉴定
背景:实验中观察到大肠杆菌(E. coli)分离为系统发育组,B2组包含肠致病性大肠杆菌(EPEC)菌株和肠外致病性大肠杆菌(ExPEC)菌株。目的:本研究旨在鉴定10岁以下健康儿童粪便中广谱耐头孢菌素大肠杆菌的B2系统发育群。方法:从10岁以下健康儿童粪便中收集100株对广谱头孢菌素耐药的大肠杆菌。随后,我们根据基因yjaA、chuA、arpA以及TspE4.C2进行了系统发育分组。然后,根据Clermont等人的研究,我们使用了两个单独的多重pcr来鉴定B2亚群(I-X亚群)。用12 o抗原进行PCR分型,最终鉴定出cnf1、papG、ibeA、malX、usp、cdt、eae、bfp、afa-Dr等10个毒力基因。结果:健康儿童年龄在1 ~ 10岁之间。B2和未知系群是本研究中最常见的菌株。最常见的B2亚群是I (STc131) (2%), IX (1%), V (8%), IV, V, VII (1%), IX, V, III, I (3%), IX, V, III, I (1%), IX, V, III, VII, I (%1), V, I (6%), V, III, I (3%), V, III, I (1%), V, III, I(3%)和V, III, VII(1%),每个亚群携带独特的expc毒力标记组。结果还显示,29%的健康儿童大肠杆菌携带malX, 23%携带papGII。还发现,从健康儿童中分离的菌株中有32%具有抗原O2, 36%未知。结论:本研究中,27%的菌株属于B2系统群,6%属于B1系统群。O2、O16和O25为主要血清群,属于B2系统群。此外,malX、papGII、usp、papGIII、aggR和eae毒力基因的供应量也分别最高至最低。此外,与非B2分离株相比,B2分离株具有更多的毒力相关基因。
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来源期刊
CiteScore
1.80
自引率
14.30%
发文量
22
期刊介绍: Archives Of Pediatric Infectious Disease is a clinical journal which is informative to all practitioners like pediatric infectious disease specialists and internists. This authoritative clinical journal was founded by Professor Abdollah Karimi in 2012. The Journal context is devoted to the particular compilation of the latest worldwide and interdisciplinary approach and findings including original manuscripts, meta-analyses and reviews, health economic papers, debates and consensus statements of clinical relevance to pediatric disease field, especially infectious diseases. In addition, consensus evidential reports not only highlight the new observations, original research and results accompanied by innovative treatments and all the other relevant topics but also include highlighting disease mechanisms or important clinical observations and letters on articles published in the journal.
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