Prevalence of blaCTX-M, blaSHV and blaTEM β-Lactamase Genes Among Escherichia coli Isolates in Foodborne Outbreak in Iran
Author(s) -
Mohammad Mehdi Soltan Dallal,
Fereshteh Fani,
Zahra Rajabi,
Mohsen Karami-Talab,
Hedroosha Molla Agha Mirzaei
Publication year - 2018
Publication title -
international journal of enteric pathogens
Language(s) - English
Resource type - Journals
eISSN - 2345-3362
pISSN - 2322-5866
DOI - 10.15171/ijep.2018.13
Subject(s) - ampicillin , polymerase chain reaction , microbiology and biotechnology , antimicrobial , escherichia coli , diarrhea , agar diffusion test , cephalosporin , beta lactamase , antibiotic resistance , outbreak , biology , multiplex polymerase chain reaction , drug resistance , gene , antibiotics , virology , medicine , genetics
Aim: In this study we focused on evaluating the prevalence of ESBL enzymes genes that are including CTX-M, SHV, TEM β-lactamase among E. coli isolates in foodborne outbreak. Background: Extended Spectrum Beta-Lactamase (ESBL) has known as enzymes that are responsible for creating of high level of antimicrobial resistance in gram negative microorganism especially in E.coli. -Therefore, survey and identify of generating genes of these enzymes can be effective in controlling of resistance and helpful in using of appropriate βlactam drug against them. Material and Methods: Five hundredstool samples are including diarrhea with nausea, vomiting, abdominal cramps, fever and headache were selected by IMVIC biochemical test for E.coli . By making antimicrobial susceptibility test base on CLSI and using disk diffusion method and confirmatory test (combined disk) ,ESBLs samples were determined. Subsequently polymerase chain reaction (PCR) were performed for the following relative genes. Result: The highest - resistance in E. coli isolates was related to ampicillin (56%) -ESBLs positive were showed in (36%) samples , after PCR prosseccing the prevalence of SHV, TEM and CTX-M1 genes was (0%) , (18%) and (38%) respectively. Conclusions: Due to the prevalence of β-lactamase genes , accurate and rapid identification methods as PCR assay is essential. So, this can be considered as routine methods -
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