Ricardo E. Ahumada-Cota , Ulises Hernández-Chiñas , Brenda Recillas-Farfán , Armando Navarro-Ocaña , José Molina-López , María G. Balbuena-Alonso , María E. Chávez-Berrocal , Carlos A. Eslava-Campos
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引用次数: 0
Abstract
The identification of key genes responsible for the colonization and infection of E. coli strains associated with diarrhea (DEC) has made significant progress. Unfortunately, for uropathogenic E. coli (UPEC) strains, there are currently no defined genes that contribute to the identification of strains associated with urinary tract infections. This paper presents data regarding genes associated with the virulence and adaptability of UPEC strains isolated from urinary tract infections (UTI), aiming to evaluate the possibility of identifying a molecular marker for this pathotype. We analyzed 166 E. coli strains (90 recovered from urine and 76 isolated from feces) characterized by serotyping, phylogenetic analysis, and PCR detection of fimH, iutA, fyuA, feoB, ompT, kguS and kguR, genes associated with the virulence and metabolism of UPEC. Herein, results showed a higher prevalence of kguS/kguR combination in strains isolated from persistent UTI (peUTI), which correlated with strains of classic UPEC serogroups, a higher virulence gene load, and inclusion in pathogenic phylogroups (B2 and D). The presence of the genes in strains isolated from feces showed that the kguS/kguR presence was minimal (14%), while the presence of kguR was almost inexistent (1%), contrary to kguS (39%). The results obtained suggest that the presence of the kguS/kguR pair encoding the homonymous two-component system (TCS) plays an important role in the adaptation and colonization of the urinary tract by E. coli strains that cause UTI. In conclusion, the combination of kguS/kguR could be used as a molecular marker to identify pathogenic strains with a high capacity for adaptation to the urinary environment.
期刊介绍:
The Journal of Microbiological Methods publishes scholarly and original articles, notes and review articles. These articles must include novel and/or state-of-the-art methods, or significant improvements to existing methods. Novel and innovative applications of current methods that are validated and useful will also be published. JMM strives for scholarship, innovation and excellence. This demands scientific rigour, the best available methods and technologies, correctly replicated experiments/tests, the inclusion of proper controls, calibrations, and the correct statistical analysis. The presentation of the data must support the interpretation of the method/approach.
All aspects of microbiology are covered, except virology. These include agricultural microbiology, applied and environmental microbiology, bioassays, bioinformatics, biotechnology, biochemical microbiology, clinical microbiology, diagnostics, food monitoring and quality control microbiology, microbial genetics and genomics, geomicrobiology, microbiome methods regardless of habitat, high through-put sequencing methods and analysis, microbial pathogenesis and host responses, metabolomics, metagenomics, metaproteomics, microbial ecology and diversity, microbial physiology, microbial ultra-structure, microscopic and imaging methods, molecular microbiology, mycology, novel mathematical microbiology and modelling, parasitology, plant-microbe interactions, protein markers/profiles, proteomics, pyrosequencing, public health microbiology, radioisotopes applied to microbiology, robotics applied to microbiological methods,rumen microbiology, microbiological methods for space missions and extreme environments, sampling methods and samplers, soil and sediment microbiology, transcriptomics, veterinary microbiology, sero-diagnostics and typing/identification.