Enterococcal infection is a leading health concern. They rank among most common causes of hospital acquired infection, and the enterococci that cause these infections are often resistant to multiple antibiotics - and with increasing frequency, to all antibiotics. After examining available data, we recently proposed that most nosocomial enterococcal infections are the result of a 2 step process: 1) virulent hospital strains of antibiotic resistant enterococci colonize the gastrointestinal tract of the patient, where their numbers are greatly amplified; followed by 2) infection of extra intestinal sites, such as the bloodstream, urinary tract, or surgical wound. Studies of GI tract colonization and the transition to infection are intractable because of their complexity. There are an estimated 500 taxa represented among bacterial species in the colon. Moreover, species representation in this consortium varies by age and diet, and is further confounded by the health status of the host and antimicrobial therapy. We recently found that Drosophila are naturally colonized by enterococci, that these bacteria occur in the posterior intestine, and that they are represented in proportions similar to that found in the human colon. Development of a simple, tractable model to study the complex interactions between enterococci, other organisms of the GI tract consortium, and the host, would represent a substantial advance in the effort to develop rational approaches for limiting the occurrence and spread of multiple antibiotic resistant strains of enterococci among hospitalized patients.
The aims of this R-21 Exploratory Proposal, which was submitted in response to a call for proposals from the National Center for Research Resources, are to verify preliminary observations on the natural colonization of Drosophila by enterococci, to determine whether replacement of indigenous enterococci with clinical isolates that vary in virulence potential (as would be needed to use this model to study enterococcal virulence and pathogenesis) impacts the physiology of the fly or colonization pattern, and to determine the extent to which antimicrobial peptides produced by Drosophila regulate colonization pattern of the GI tract.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21RR020596-02
Application #
7140416
Study Section
Special Emphasis Panel (ZRG1-DDR (01))
Program Officer
Chang, Michael
Project Start
2005-07-01
Project End
2008-06-30
Budget Start
2006-07-01
Budget End
2008-06-30
Support Year
2
Fiscal Year
2006
Total Cost
$287,091
Indirect Cost
Name
Schepens Eye Research Institute
Department
Type
DUNS #
073826000
City
Boston
State
MA
Country
United States
Zip Code
02114
Cox, Christopher R; Gilmore, Michael S (2007) Native microbial colonization of Drosophila melanogaster and its use as a model of Enterococcus faecalis pathogenesis. Infect Immun 75:1565-76
Spoering, Amy L; Gilmore, Michael S (2006) Quorum sensing and DNA release in bacterial biofilms. Curr Opin Microbiol 9:133-7