AI Article Synopsis

  • * A study sequenced the genomes of 66 bladder bacteria isolates from women with varying urinary symptoms to understand their characteristics and potential links to UTIs.
  • * Findings indicated that the genetic content of the bacteria didn't align with the women’s symptoms, suggesting that UTI symptoms might be influenced more by the overall composition of the urobiome rather than just the presence of specific bacteria.

Article Abstract

Urinary tract infections (UTIs) are one of the most common human bacterial infections. While UTIs are commonly associated with colonization by , members of this species also have been found within the bladder of individuals with no lower urinary tract symptoms (no LUTS), also known as asymptomatic bacteriuria. Prior studies have found that both uropathogenic (UPEC) strains and isolates that are not associated with UTIs encode for virulence factors. Thus, the reason(s) why sometimes causes UTI-like symptoms remain(s) elusive. In this study, the genomes of 66 isolates from adult female bladders were sequenced. These isolates were collected from four cohorts, including women: (1) without lower urinary tract symptoms, (2) overactive bladder symptoms, (3) urgency urinary incontinence, and (4) a clinical diagnosis of UTI. Comparative genomic analyses were conducted, including core and accessory genome analyses, virulence and motility gene analyses, and antibiotic resistance prediction and testing. We found that the genomic content of these 66 isolates does not correspond with the participant's symptom status. We thus looked beyond coli genomes to the composition of the entire urobiome and found that the presence of alone was not sufficient to distinguish between the urobiomes of individuals with UTI and those with no LUTS. Because presence, abundance, and genomic content appear to be weak predictors of UTI status, we hypothesize that UTI symptoms associated with detection of are more likely the result of urobiome composition.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7500147PMC
http://dx.doi.org/10.3389/fmicb.2020.02094DOI Listing

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