Background: Urinary tract infections are a significant health problem, with Escherichia coli as a primary pathogen in approximately 80% of cases. The pathogenesis of E. coli in urinary tract infections is attributed to the production of virulence factors and phylogenetic background groups. Objectives: The aim of this study was to determine differences in prevalence of virulence factors of E. coli isolates from phylogenetic groups B2 and D, collected from patients with urinary tract infections. Materials and Methods: A total of 100 E. coli isolates were identified by conventional biochemical tests from patients with urinary tracts infections (UTIs) in teaching hospitals of Zabol, Iran. DNA was extracted using the boiling method. Analysis of phylogenetic groups, along with detection of virulence factor genes was performed by the multiplex-PCR method. Associations were assessed between type 1 fimberiaencoding gene, siderophore receptor encoding genes and hemolysin encoding gene among 55 B2 group E. coli isolates and 22 D group E. coli isolates. Statistical analysis was performed using the Fisher exact test. Results: Phylogenetic analysis showed that 55 and 22 of 100 isolates belonged to the B2 and D phylogenetic groups, respectively. The hlyA, iroN, iucD and fimH genes were present in 29 (52.72%), 22 (40%), 46 (83.63%) and 55 (100%) isolates belonging to the phylogenetic group B2, whereas in 2 (9.09%), 2 (9.09%), 10 (45.45%) and 22 (100%) isolates belonging to the phylogenetic group D, respectively. The comparison showed that there was a significant difference between the presence of hlyA and iroN genes in isolates belonging to the phylogenetic group B2 and D (P ≤ 0.05). Conclusions: This study determined that strains belonging to group B2 are the most important and abundant E. coli strains causing urinary tract infections.
Background: The importance of microbiome in the progression and development of colorectal cancer (CRC) has been discussed in the last decade. Like colon bacteria, other intestinal microorganisms, including archaea, could also be involved in the CRC progression, so it's important to work out the archaeal microbiome (archaeome) composition among CRC patients. Objectives: The aim of this study was to determine the archaeome composition of CRC and healthy controls based on age and gender. Methods: Total bacterial DNA was extracted from 30 biopsy samples (17 CRC and 13 healthy controls). Archaeome communities were profiled by 16S rRNA high throughput sequencing, then compared to clinicopathological features, including CRC patients’ gender and age. Results: In the CRC patients, archaeal methanogens including Methanobrevibacter (86%) and Methanomassiliicoccus (8%) were overrepresented at the genus level. In contrast in the healthy controls, only two genera of haloarchaea including Natronococcus (58%) and Haloterrigena (42%) were presented. The results showed that the number of archaeal genera in men is higher than women in both the CRC and healthy controls. moreover, our results showed that the most genera of archaea are present in the CRC-32-50 group, six archaeal genera. The differential abundance taxa analysis results showed significant differences between healthy controls and CRC patients (P ≤ 0.05). Conclusions: The high abundance of methanogens in the colon archaeome of CRC patients compared to healthy controls suggests that methanogens may be involved in CRC development.
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