| Literature DB >> 28893918 |
Brenda Yin Qi Tien1,2, Hwee Mian Sharon Goh1, Kelvin Kian Long Chong1,2, Soumili Bhaduri-Tagore1,2, Sarah Holec1, Regine Dress3, Florent Ginhoux3, Molly A Ingersoll4,5, Rohan B H Williams6, Kimberly A Kline7.
Abstract
Enterococcus faecalis, a member of the human gastrointestinal microbiota, is an opportunistic pathogen associated with hospital-acquired wound, bloodstream, and urinary tract infections. E. faecalis can subvert or evade immune-mediated clearance, although the mechanisms are poorly understood. In this study, we examined E. faecalis-mediated subversion of macrophage activation. We observed that E. faecalis actively prevents NF-κB signaling in mouse RAW264.7 macrophages in the presence of Toll-like receptor agonists and during polymicrobial infection with Escherichia coliE. faecalis and E. coli coinfection in a mouse model of catheter-associated urinary tract infection (CAUTI) resulted in a suppressed macrophage transcriptional response in the bladder compared to that with E. coli infection alone. Finally, we demonstrated that coinoculation of E. faecalis with a commensal strain of E. coli into catheterized bladders significantly augmented E. coli CAUTI. Taken together, these results support the hypothesis that E. faecalis suppression of NF-κB-driven responses in macrophages promotes polymicrobial CAUTI pathogenesis, especially during coinfection with less virulent or commensal E. coli strains.Entities:
Keywords: Enterococcus faecalis; Escherichia coli; catheter-associated UTI; coinfection; immune suppression; macrophage; polymicrobial; urinary tract infection
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Year: 2017 PMID: 28893918 PMCID: PMC5695114 DOI: 10.1128/IAI.00378-17
Source DB: PubMed Journal: Infect Immun ISSN: 0019-9567 Impact factor: 3.441