[R01] Impact of polymicrobial interactions and within-host adaptation on CAUTI pathogenesis
Ente: National Institute of Diabetes and Digestive and Kidney Diseases
Scadenza: 2030-06-30
Importo max: 782.322 EUR
Paese: US
Descrizione
Project Summary/Abstract
Urinary tract infection (UTI) is one of the most common infections worldwide and a leading cause of morbidity
and healthcare expenditures across all ages. Older adults and individuals with catheters have a particularly high
risk of UTI sequelae, including kidney infection, permanent renal damage, and urosepsis. The average mortality
rate for urosepsis is 20-40%, but ranges as high as 66% for patients with catheter-associated UTI (CAUTI).
Catheterization also promotes persistent polymicrobial colonization and infection by a wide range of
understudied microbes, including multidrug-resistant organisms that threaten the utility of last-resort antibiotics.
There is a substantial gap in knowledge regarding the impact of microbe-microbe interactions and within-host
adaptation on progression from initial colonization to urosepsis and development of antimicrobial resistance. Our
preliminary data demonstrates that the three most common and persistent colonizers of the catheterized urinary
tract are Enterococcus faecalis, Proteus mirabilis, and Escherichia coli, with some patients being co-colonized
by all three species for up to 6 months. We further demonstrate that dual-species interactions involving these
species enhance formation of recalcitrant catheter biofilms and increase infection severity in a mouse model of
CAUTI. However, it is not yet known how all three species interact under physiologically-relevant conditions, nor
the impact of their interactions on biofilm formation and CAUTI pathogenesis. We have further determined that
P. mirabilis accumulates phenotypic and genotypic changes during persistent colonization of the urinary tract,
many of which are likely to alter pathogenic potential as well as fitness within a polymicrobial community. We
hypothesize that the interactions between P. mirabilis, E. coli, and E. faecalis will alter i) biofilm architecture,
composition, and antimicrobial resistance, ii) stimulation of the innate immune response, and iii) incidence of
disseminated infection and urosepsis. We further hypothesize that within-host adaptation during persistent
colonization will promote biofilm formation and bladder colonization but decrease incidence of severe disease,
and will also select for greater codependence among co-colonizing isolates, thereby modifying polymicrobial
interactions. In Aim 1, we will determine the impact of polymicrobial interactions and inoculation order on
bacterial viability, transcription profiles, and biofilm composition in an “artificial bladder model” and on
colonization, immune stimulation, and infection progression in a mouse CAUTI model. In Aim 2, we will identify
genotypic and phenotypic changes that occur in all three species during persistent colonization and examine
contribution to biofilm formation, CAUTI severity, and polymicrobial interactions. The long-term objective of the
proposed studies is to identify new targets for preventing or disrupting the formation of recal
Istituzione: STATE UNIVERSITY OF NEW YORK AT BUFFALO
PI: Chelsie Elizabeth Armbruster
Progetto: 5R01DK140371-02
Settori: National Institute of Diabetes and Digestive and Kidney Diseases
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