Document Detail


A composite bacteriophage alters colonization by an intestinal commensal bacterium.
MedLine Citation:
PMID:  23045666     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The mammalian intestine is home to a dense community of bacteria and its associated bacteriophage (phage). Virtually nothing is known about how phages impact the establishment and maintenance of resident bacterial communities in the intestine. Here, we examine the phages harbored by Enterococcus faecalis, a commensal of the human intestine. We show that E. faecalis strain V583 produces a composite phage (ΦV1/7) derived from two distinct chromosomally encoded prophage elements. One prophage, prophage 1 (ΦV1), encodes the structural genes necessary for phage particle production. Another prophage, prophage 7 (ΦV7), is required for phage infection of susceptible host bacteria. Production of ΦV1/7 is controlled, in part, by nutrient availability, because ΦV1/7 particle numbers are elevated by free amino acids in culture and during growth in the mouse intestine. ΦV1/7 confers an advantage to E. faecalis V583 during competition with other E. faecalis strains in vitro and in vivo. Thus, we propose that E. faecalis V583 uses phage particles to establish and maintain dominance of its intestinal niche in the presence of closely related competing strains. Our findings indicate that bacteriophages can impact the dynamics of bacterial colonization in the mammalian intestinal ecosystem.
Authors:
Breck A Duerkop; Charmaine V Clements; Darcy Rollins; Jorge L M Rodrigues; Lora V Hooper
Related Documents :
7615766 - Evaluation of a new agar in uricult-trio for rapid detection of escherichia coli in urine.
14197906 - Cultivation of leptospirae. ii. growth and lysis in synthetic medium.
23770966 - Staphylococcus aureus nasal carriers among medical students in a medical school.
2338726 - A medium for the selective isolation of edwardsiella ictaluri.
24167266 - Chronic exposure to arsenic in drinking water can lead to resistance to antimonial drug...
10830896 - Larval susceptibility of the diamondback moth, plutella xylostella (lepidoptera: plutel...
Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't     Date:  2012-10-08
Journal Detail:
Title:  Proceedings of the National Academy of Sciences of the United States of America     Volume:  109     ISSN:  1091-6490     ISO Abbreviation:  Proc. Natl. Acad. Sci. U.S.A.     Publication Date:  2012 Oct 
Date Detail:
Created Date:  2012-10-24     Completed Date:  2013-01-07     Revised Date:  2013-07-11    
Medline Journal Info:
Nlm Unique ID:  7505876     Medline TA:  Proc Natl Acad Sci U S A     Country:  United States    
Other Details:
Languages:  eng     Pagination:  17621-6     Citation Subset:  IM    
Affiliation:
Department of Immunology and The Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Amino Acids / metabolism
Animals
Bacteriophages / physiology*
Germ-Free Life
Humans
Intestines / microbiology*
Mice
Mice, Inbred C57BL
Polymerase Chain Reaction
Grant Support
ID/Acronym/Agency:
F32 DK089718/DK/NIDDK NIH HHS; F32 DK089718/DK/NIDDK NIH HHS; R01DK070855/DK/NIDDK NIH HHS; //Howard Hughes Medical Institute
Chemical
Reg. No./Substance:
0/Amino Acids
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Prenatal exposure to antidepressants and depressed maternal mood alter trajectory of infant speech p...
Next Document:  Impact of experience-dependent and -independent factors on gene expression in songbird brain.