TY - JOUR
T1 - Dynamics of plasmid-mediated niche invasion, immunity to invasion, and pheromone-inducible conjugation in the murine gastrointestinal tract
AU - Hirt, Helmut
AU - Greenwood-Quaintance, Kerryl E.
AU - Barnes, Aaron M.T.
AU - Karau, Melissa J.
AU - Till, Lisa M.
AU - Palzer, Elise
AU - Guan, Weihua
AU - VanNieuwenhze, Michael S.
AU - Kashyap, Purna C.
AU - Patel, Robin
AU - Dunny, Gary M.
N1 - Funding Information:
We would like to thank Michael Travisano and William Harcombe for their input and critical review of the manuscript, as well as Tim Leonard for assistance with graphics. This work was supported by PHS grants 1R35GM118079 to G.M.D. and R35 GM 136365 to M.S.VN., with additional support for A.M.T.B via NIH training grant AI055433.
Funding Information:
We would like to thank Michael Travisano and William Harcombe for their input and critical review of the manuscript, as well as Tim Leonard for assistance with graphics. This work was supported by PHS grants 1R35GM118079 to G.M.D. and R35 GM 136365 to M.S.VN., with additional support for A.M.T.B via NIH training grant AI055433.
Publisher Copyright:
© 2022, The Author(s).
PY - 2022/12
Y1 - 2022/12
N2 - Microbial communities provide protection to their hosts by resisting pathogenic invasion. Microbial residents of a host often exclude subsequent colonizers, but this protection is not well understood. The Enterococcus faecalis plasmid pCF10, whose conjugative transfer functions are induced by a peptide pheromone, efficiently transfers in the intestinal tract of mice. Here we show that an invading donor strain established in the gastrointestinal tract of mice harboring resident recipients, resulting in a stable, mixed population comprised of approximately 10% donors and 90% recipients. We also show that the plasmid-encoded surface protein PrgB (Aggregation Substance), enhanced donor invasion of resident recipients, and resistance of resident donors to invasion by recipients. Imaging of the gastrointestinal mucosa of mice infected with differentially labeled recipients and donors revealed pheromone induction within microcolonies harboring both strains in close proximity, suggesting that adherent microcolonies on the mucosal surface of the intestine comprise an important niche for cell-cell signaling and plasmid transfer.
AB - Microbial communities provide protection to their hosts by resisting pathogenic invasion. Microbial residents of a host often exclude subsequent colonizers, but this protection is not well understood. The Enterococcus faecalis plasmid pCF10, whose conjugative transfer functions are induced by a peptide pheromone, efficiently transfers in the intestinal tract of mice. Here we show that an invading donor strain established in the gastrointestinal tract of mice harboring resident recipients, resulting in a stable, mixed population comprised of approximately 10% donors and 90% recipients. We also show that the plasmid-encoded surface protein PrgB (Aggregation Substance), enhanced donor invasion of resident recipients, and resistance of resident donors to invasion by recipients. Imaging of the gastrointestinal mucosa of mice infected with differentially labeled recipients and donors revealed pheromone induction within microcolonies harboring both strains in close proximity, suggesting that adherent microcolonies on the mucosal surface of the intestine comprise an important niche for cell-cell signaling and plasmid transfer.
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U2 - 10.1038/s41467-022-29028-7
DO - 10.1038/s41467-022-29028-7
M3 - Article
C2 - 35296679
AN - SCOPUS:85126695178
SN - 2041-1723
VL - 13
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 1377
ER -