DOI: 10.1126/sciadv.aee0675 ISSN: 2375-2548
Metabolic cross-talk promotes persistence of
Enterococcus
in a model of polymicrobial catheter-associated urinary tract infection
Zongsen Zou, Jerome S. Pinkner, Chloe L. P. Obernuefemann, Kent R. Kleinschmidt, Denise A. Sanick, Suzanne M. Hickerson, Karen W. Dodson, Jeffrey P. Henderson, Scott J. Hultgren, Michael G. Caparon
Catheter-associated urinary tract infections (CAUTIs) account for approximately 80% of urinary tract infections (UTI) and can lead to adverse outcomes. Most CAUTIs are polymicrobial with resilient communities maintaining a consistent composition of species over time. However, the mechanisms promoting persistence are poorly understood. Here, we examine how a chemical interaction between
Enterococcus faecalis
and
Klebsiella pneumoniae
can explain their high rate of co-occurrence on long-term indwelling catheters. Sequence analyses of longitudinal isolates from several patients coinfected with
E. faecalis
and
K. pneumoniae
revealed that despite frequent replacement, catheters became recolonized with the same or a nearly identical consortium of strains throughout the collection period. Using artificial urine medium (AUM), monoculture revealed that the
K. pneumoniae
isolates grew robustly and formed biofilm, while the
E. faecalis
isolates grew poorly and did not form biofilm. However, coculture of paired isolates resulted in enhanced
E. faecalis
growth and biofilm, which could be reproduced by supplementing
E. faecalis
with
K. pneumoniae
conditioned AUM supernatant (KpAUMSup). Analyses using comparative transcriptomics, mutant strains, and chemical inhibitors with cell culture and murine CAUTI models revealed that (i) KpAUMSup, but not AUM, stimulated expression of the
E. faecalis
Fsr quorum sensing system; (ii) Fsr was required for
E. faecalis
to respond to KpAUMSup; (iii)
E. faecalis
cultured in KpAUMSup was more efficient in initiating CAUTI; and (iv) disruption of Fsr inhibited initiation of CAUTI. This interspecies signaling may help explain the high rate of co-colonization of these CAUTI pathogens and highlights therapeutic strategies to treat polymicrobial CAUTI.