scholarly journals Sex pheromones and plasmid transfer in Enterococcus faecalis

Plasmid ◽  
1989 ◽  
Vol 21 (3) ◽  
pp. 175-184 ◽  
Author(s):  
Don B. Clewell ◽  
Keith E. Weaver
2006 ◽  
Vol 52 (4) ◽  
pp. 358-367 ◽  
Author(s):  
Takumi Kajiura ◽  
Hideki Wada ◽  
Kenji Ito ◽  
Yojiro Anzai ◽  
Fumio Kato

2002 ◽  
Vol 70 (2) ◽  
pp. 716-723 ◽  
Author(s):  
Helmut Hirt ◽  
Patrick M. Schlievert ◽  
Gary M. Dunny

ABSTRACT Enterococcus faecalis has become one of the most notable nosocomial pathogens in the last decade. Aggregation substance (AS) on the sex pheromone plasmids of E. faecalis has been implicated as a virulence factor in several model systems. We investigated the AS-encoding plasmid pCF10 for its ability to increase virulence in a rabbit endocarditis model. Cells containing pCF10 increased the virulence in the model significantly, as assessed by an increase in aortic valve vegetation size. The results confirmed in vivo induction of the normally tightly controlled AS. In addition to the expression of AS when E. faecalis cells were in contact with plasma, plasmid transfer of the tetracycline resistance-carrying plasmid was also activated in vitro and in vivo. In vivo, plasmid transfer reached remarkable frequencies of 8 × 10−2 to 9 × 10−2. These values are comparable to the highest frequencies ever observed in vitro. Cells harboring pCF10 had a significant survival advantage over plasmid-free cells indicated by pCF10 present in two-thirds of the recipient population. Plasma induction was dependent on the presence of the plasmid-encoded PrgZ protein, indicating the requirement of the pheromone-sensing system in the induction process. The data suggested that the mechanism of in vivo induction may involve interference of plasma with the normal function of the pheromone peptide and its inhibitor.


1990 ◽  
Vol 87 (1) ◽  
pp. 66-70 ◽  
Author(s):  
P. Sannomiya ◽  
R. A. Craig ◽  
D. B. Clewell ◽  
A. Suzuki ◽  
M. Fujino ◽  
...  

Plasmid ◽  
1979 ◽  
Vol 2 (3) ◽  
pp. 454-465 ◽  
Author(s):  
Gary M. Dunny ◽  
Ronald A. Craig ◽  
Richard L. Carron ◽  
Don B. Clewell

mBio ◽  
2018 ◽  
Vol 9 (1) ◽  
Author(s):  
Helmut Hirt ◽  
Kerryl E. Greenwood-Quaintance ◽  
Melissa J. Karau ◽  
Lisa M. Till ◽  
Purna C. Kashyap ◽  
...  

ABSTRACT Cell-cell communication mediated by peptide pheromones (cCF10 [CF]) is essential for high-frequency plasmid transfer in vitro in Enterococcus faecalis. To examine the role of pheromone signaling in vivo, we established either a CF-producing (CF+) recipient or a recipient producing a biologically inactive variant of CF (CF− recipient) in a germfree mouse model 3 days before donor inoculation and determined transfer frequencies of the pheromone-inducible plasmid pCF10. Plasmid transfer was detected in the upper and middle sections of the intestinal tract 5 h after donor inoculation and was highly efficient in the absence of antibiotic selection. The transconjugant/donor ratio reached a maximum level approaching 1 on day 4 in the upper intestinal tract. Plasmid transfer was significantly lower with the CF− recipient. While rescue of the CF− mating defect by coculture with CF+ recipients is easily accomplished in vitro, no extracellular complementation occurred in vivo. This suggests that most pheromone signaling in the gut occurs between recipient and donor cells in very close proximity. Plasmid-bearing cells (donors plus transconjugants) steadily increased in the population from 0.1% after donor inoculation to about 10% at the conclusion of the experiments. This suggests a selective advantage of pCF10 carriage distinct from antibiotic resistance or bacteriocin production. Our results demonstrate that pheromone signaling is required for efficient pCF10 transfer in vivo. In the absence of CF+ recipients, a low level of transfer to CF− recipients occurred in the gut. This may result from low-level host-mediated induction of the donors in the gastrointestinal (GI) tract, similar to that previously observed in serum. IMPORTANCE Horizontal gene transfer is a major factor in the biology of Enterococcus faecalis, an important nosocomial pathogen. Previous studies showing efficient conjugative plasmid transfer in the gastrointestinal (GI) tracts of experimental animals did not examine how the enterococcal sex pheromone response impacts the efficiency of transfer. Our study demonstrates for the first time pheromone-enhanced, high-frequency plasmid transfer of E. faecalis plasmid pCF10 in a mouse model in the absence of antibiotic or bacteriocin selection. Pheromone production by recipients dramatically increased plasmid transfer in germfree mice colonized initially with recipients, followed by donors. The presence of a coresident community of common gut microbes did not significantly reduce in vivo plasmid transfer between enterococcal donors and recipients. In mice colonized with enterococcal recipients, we detected plasmid transfer in the intestinal tract within 5 h of addition of donors, before transconjugants could be cultured from feces. Surprisingly, pCF10 carriage provided a competitive fitness advantage unrelated to antibiotic resistance or bacteriocin production.


mBio ◽  
2014 ◽  
Vol 5 (5) ◽  
Author(s):  
Sriram Varahan ◽  
Nathan Harms ◽  
Michael S. Gilmore ◽  
John M. Tomich ◽  
Lynn E. Hancock

ABSTRACTEnterococci are leading causes of hospital-acquired infection in the United States and continue to develop resistances to new antibiotics. ManyEnterococcus faecalisisolates harbor pheromone-responsive plasmids that mediate horizontal transfer of even large blocks of chromosomal genes, resulting in hospital-adapted strains over a quarter of whose genomes consist of mobile elements. Pheromones to which the donor cells respond derive from lipoprotein signal peptides. Using a novel bacterial killing assay dependent on the presence of sex pheromones, we screened a transposon mutant library for functions that relate to the production and/or activity of the effector pheromone. Here we describe a previously uncharacterized, but well-conserved, ABC transporter that contributes to pheromone production. Using three distinct pheromone-dependent mating systems, we show that mutants defective in expressing this transporter display a 5- to 6-order-of-magnitude reduction in conjugation efficiency. In addition, we demonstrate that the ABC transporter mutant displays an altered biofilm architecture, with a significant reduction in biofilm biomass compared to that of its isogenic parent, suggesting that pheromone activity also influences biofilm development. The conservation of this peptide transporter across theFirmicutessuggests that it may also play an important role in cell-cell communication in other species within this important phylum.IMPORTANCEEnterococcus faecalisranks as one of the leading causes of hospital-associated infections. Strains possessing resistance to multiple antibiotics are becoming all too common in clinical settings. Pheromone-responsive plasmids play an important role in harboring and disseminating these antibiotic resistance genes. Here we have identified a novel ABC transporter that is responsible for the secretion of peptide pheromones, which enables communication between cells to mediate plasmid transfer. We have also shown that this transporter is important for biofilm formation, providing a strong rationale for its use as a viable therapeutic target which could be targeted to curb infection, as well as the spread of existing drug resistance.


1989 ◽  
Vol 151 (6) ◽  
pp. 486-490 ◽  
Author(s):  
Dominique Galli ◽  
Reinhard Wirth ◽  
Gerhard Wanner

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