| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 3416393 | Microbial Pathogenesis | 2016 | 6 Pages |
•All genetic clusters were not equally involved in pathogenesis of urinary tract infections.•Isolates from urinary infections which belonged to common pulsotypes showed common hsp60 genetics clusters.•PFGE genotyping showed more discriminatory power than hsp60 genotyping for differentiation of Enterobacter cloacae complex.•The expression of curli biogenesis genes and its positive regulator did not vary significantly between members of different hsp60 clusters, which rules out its role in un-equivalent contribution of clusters in human pathogenesis.
The objective of this study was to determine the correlation between Enterobacter cloacae complex subspecies and clusters involved in UTI infections and specific pulsotypes, and to assess the contribution of major curli biogenesis genes (csgD, csgA) expression level to pathogenesis of clusters and genotypes.Based on the PFGE analysis, 37 different profiles were observed among which 8 profiles were common types. Real time PCR of csgD and csgA genes of 50 E. cloacae complex in relation to PFGE and hsp60 genotypes showed that all the genetic clusters are not equally involved in pathogenesis of urinary tract infections. It was elucidated in this study that isolates with common PFGE genotypes belonged to identical hsp60 clusters, and the foremost clusters (VI, III, and V) mainly comprised within PFGE common types. In our study, no significant correlation was detected between the specific hsp60 clusters or PFGE genotypes and the expression level of csgD and csgA genes (P-value > 0.05).This is the first study describing that unequivalent contribution of E. cloacae genotypes and clusters in pathogenesis of UTI, is not owing to varied curli biogenesis expression potential. The PFGE genotyping showed more discriminatory power than hsp60 genotyping for epidemiological studies and source tracking purpose.
