Use of a MAMA-PCR Method to detect gyrA Mutations in Nalidixic Acid-Resistant Clinical Isolates of Escherichia coli

Background: enterobacteriaceae are a large group of bacteria widely distributed in nature. escherichia coli is the mostcommon cause of urinary tract infection. two amino acid substitutions, in gyra, are commonly responsible for quinoloneresistance in e. coli. the aim of this study was molecular survey of nalidixic acid resistance e.coli isolated from patients inthe codones of 83 and 87 gyra genes.methods: during 5 months (january to june 2005) of molecular survey of nalidixic acid resistance, one hundred andtwenty-one e. coli isolates from urine samples of patients referred to clinical laboratory of baqiyatallah hospital were cultured.differential tests were done for diagnosis of e.coli. an economical and time-efficient mismatch amplification mutationassay (mama) pcr was developed to detect mutations in the chromosomal gyra gene causing these substitutions.results: in nalidixic acid antibiogram test, 55 cases (45.5%) were sensitive, 63 cases (52%) were resistant and 3 cases(2.5%) were intermediate. results of pcr and mic were similar to antibiogram. there was not any mutation in the sensitivesamples but there were performed five mutations on the 85, 81, 107, 97 and 87 codones of resistance samples. thecodone number 87s mutation is one of the main mutations of nalidixic acid resistance.conclusion: depending on results of this study and comparison with other studies, trend of resistance of e.coli is increasing.therefore, we recommend control of antibiotic misusage and application of mic and pcr tests (if possible) prior totreatment for suitable selection of antibiotic and prevention of microbial resistance.