4.6 Article

The Bacterial Amyloid Curli Is Associated with Urinary Source Bloodstream Infection

Journal

PLOS ONE
Volume 9, Issue 1, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0086009

Keywords

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Funding

  1. NIH CTSA [UL1RR024992]
  2. CDC Prevention Epicenters Program grant [U54 CK000162]
  3. KL2 Career Development Award [KL2RR024994]
  4. Washington University Building Interdisciplinary Research Careers in Women's Health (BIRCWH) program [5K12HD001459-13]
  5. Barnes-Jewish Hospital Patient Safety & Quality Fellowship Program
  6. Barnes-Jewish Hospital Foundation & Washington University's Institute of Clinical and Translational Sciences
  7. Burroughs-Wellcome Career Award for Medical Scientists
  8. NIH [HD001459-09, DK064540-09]

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Urinary tract infections are the most common cause of E. coli bloodstream infections (BSI) but the mechanism of bloodstream invasion is poorly understood. Some clinical isolates have been observed to shield themselves with extracellular amyloid fibers called curli at physiologic temperature. We hypothesize that curli fiber assembly at 37 degrees C promotes bacteremic progression by urinary E. coli strains. Curli expression by cultured E. coli isolates from bacteriuric patients in the presence and absence of bacteremia were compared using Western blotting following amyloid fiber disruption with hexafluoroisopropanol. At 37 degrees C, urinary isolates from bacteremic patients were more likely to express curli than those from non-bacteremic patients [16/22 (73%) vs. 7/21 (33%); p = 0.01]. No significant difference in curli expression was observed at 30 degrees C [86% (19/22) vs. 76% (16/21); p = 0.5]. Isolates were clonally diverse between patients, indicating that this phenotype is distributed across multiple lineages. Most same-patient urine and blood isolates were highly related, consistent with direct invasion of urinary bacteria into the bloodstream. 37 degrees C curli expression was associated with bacteremic progression of urinary E. coli isolates in this population. These findings suggest new future diagnostic and virulence-targeting therapeutic approaches.

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