In vitro screening of multidrug resistance uropathogenic Escherichia coli from the urban area of Namakkal district

The aim of the study is to screen the multiple drug resistance (MDR) Uropathogenic Escherichia coli (UPEC) fromthe urban area of Namakkal district. To detect UPEC resistant by using different antibiotics and to analyze the virulentcharacteristics of UPEC and amplification of extended-spectrum beta-lactamases genes by multiplex polymerasechain reaction. Total 450 samples individually collected from the urinary tract infection (UTI) patients’ and directstreaked on to the eosin methylene blue agar plates. Significant growth indicates E. coli. HiCrome UTI agar was usedfor rapid identification of uropathogenic E. coli. Out of 450 samples, only 62 isolates of E. coli were subjected tovirulence characteristics, such as slime production (34%), hemolytic activity (56%), and beta-lactamase production(43%). Antibiotic sensitivity test was performed with 13 different antibiotics. Among them, 62 isolates were E. coli,only five were resistant to 10 antibiotics, possess virulence characteristics. Four strains (E-12, E23, E-58, and E-97)have Temoneira, sulfhydryl variable, and cefotaxime hydrolyzing capabilities (CTX-M) antibiotic resistance genes,and E-07 have only CTX-M gene. As E. coli is the main infectious agent in patients with UTI and a potent pathogen,it was difficult to treat with routine antibiotics because day-by-day microbes are resisting to common drugs. Hence,they need alternative therapy

Detection of Uropathogens by Using Chromogenic Media (Hicrome UTI agar), CLED agar and other Conventional Media.

This study was undertaken to find media better than routinely used media in isolation of uropathogens.Three hundred urine samples having pus cells >_ 5/ HPF were enrolled for the study. Comparison of isolation and identification of uropathogens among HiCrome UTI Agar media, 5% Sheep Blood agar & MacConkey agar and CLED agar media were done. Among them 95(31.67%) samples showed single growth, 6 (2%) showed mixed growth and 199 (66.67%) showed no growth. Rate of presumptive identification of organisms in primary culture plate were high in HiCrome UTI agar media. For Escherichia coli, it was 94.20% whereas in CLED agar it was 79.71% and by Blood agar and MacConkey agar media in combination it was 82.61%. All the Enterococcus spp. were identified in HiCrome UTI agar media, 33.33% in CLED agar media but none in Blood agar and MacConkey agar media. Among the mixed growth, 100% organisms were identified on HiCrome UTI Agar media due to distinct colour produced by the different organisms, whereas in one (16.67%) sample (mixed Esch.coli and Pseudomonas spp.) organisms were identified on other three media.