Transfer of the Pheromone-Inducible Plasmid pCF10 among Enterococcus faecalis Microorganisms Colonizing the Intestine of Mini-Pigs

ABSTRACT A new animal model, the streptomycin-treated mini-pig, was developed in order to allow colonization of defined strains of Enterococcus faecalis in numbers sufficient to study plasmid transfer. Transfer of the pheromone-inducible pCF10 plasmid between streptomycin-resistant strains of E. faecalis OG1 was investigated in the model. The plasmid encodes resistance to tetracycline. Numbers of recipient, donor, and transconjugant bacteria were monitored by selective plating of fecal samples, and transconjugants were subsequently verified by PCR. After being ingested by the mini-pigs, the recipient strain persisted in the intestine at levels between 106 and 107 CFU per g of feces throughout the experiment. The donor strain, which carried different resistance markers but was otherwise chromosomally isogenic to the recipient strain, was given to the pigs 3 weeks after the recipient strain. The donor cells were initially present in high numbers (106 CFU per g) in feces, but they did not persist in the intestine at detectable levels. Immediately after introduction of the donor bacteria, transconjugant cells appeared and persisted in fecal samples at levels between 103 and 104 CFU per g until the end of the experiment. These observations showed that even in the absence of selective tetracycline pressure, plasmid pCF10 was transferred from ingested E. faecalis cells to other E. faecalis organisms already present in the intestinal environment and that the plasmid subsequently persisted in the intestine.

[1]  T. R. Licht,et al.  Effect of pheromone induction on transfer of the Enterococcus faecalis plasmid pCF10 in intestinal mucus ex vivo. , 2001, FEMS microbiology letters.

[2]  F. Aarestrup,et al.  Antimicrobial susceptibility and presence of resistance genes in staphylococci from poultry. , 2000, Veterinary microbiology.

[3]  R. Andrews,et al.  Isolation of Tn916-like conjugal elements from swine lot effluent. , 2000, Canadian journal of microbiology.

[4]  F. Aarestrup,et al.  Comparison of antimicrobial resistance phenotypes and resistance genes in Enterococcus faecalis and Enterococcus faecium from humans in the community, broilers, and pigs in Denmark. , 2000, Diagnostic microbiology and infectious disease.

[5]  F. Aarestrup,et al.  Characterization of vancomycin-resistant and vancomycin-susceptible Enterococcus faecium isolates from humans, chickens and pigs by RiboPrinting and pulsed-field gel electrophoresis. , 2000, The Journal of antimicrobial chemotherapy.

[6]  G. Beran,et al.  Effects of heat stress on the antimicrobial drug resistance of Escherichia coli of the intestinal flora of swine , 2000, Journal of applied microbiology.

[7]  Albert Balows,et al.  Manual of Clinical Microbiology, 7th ed. , 2000 .

[8]  T. R. Licht,et al.  Klebsiella pneumoniae Capsule Expression Is Necessary for Colonization of Large Intestines of Streptomycin-Treated Mice , 1999, Infection and Immunity.

[9]  T. R. Licht,et al.  Plasmid transfer in the animal intestine and other dynamic bacterial populations: the role of community structure and environment. , 1999, Microbiology.

[10]  L Andrup,et al.  A comparison of the kinetics of plasmid transfer in the conjugation systems encoded by the F plasmid from Escherichia coli and plasmid pCF10 from Enterococcus faecalis. , 1999, Microbiology.

[11]  L. Jensen,et al.  Horizontal Transfer of the satA Gene Encoding Streptogramin A Resistance Between Isogenic Enterococcus faecium Strains in the Gastrointestinal Tract of Gnotobiotic Rats , 1999 .

[12]  K. Wu,et al.  Enterococcus faecalis pheromone-responding plasmid pAD1 gives rise to an aggregation (clumping) response when cells are exposed to subinhibitory concentrations of chloramphenicol, erythromycin, or tetracycline. , 1999, Plasmid.

[13]  W. Witte,et al.  Medical Consequences of Antibiotic Use in Agriculture , 1998, Science.

[14]  R. Wirth,et al.  Enterococcus faecalis Gene Transfer under Natural Conditions in Municipal Sewage Water Treatment Plants , 1998, Applied and Environmental Microbiology.

[15]  T. R. Licht,et al.  Role of lipopolysaccharide in colonization of the mouse intestine by Salmonella typhimurium studied by in situ hybridization , 1996, Infection and immunity.

[16]  T. R. Licht,et al.  Physiological state of Escherichia coli BJ4 growing in the large intestines of streptomycin-treated mice , 1995, Journal of bacteriology.

[17]  J. Morris,et al.  Enterococci Resistant to Multiple Antimicrobial Agents, Including Vancomycin: Establishment of Endemicity in a University Medical Center , 1995, Annals of Internal Medicine.

[18]  D. Clewell,et al.  Unconstrained bacterial promiscuity: the Tn916-Tn1545 family of conjugative transposons. , 1995, Trends in microbiology.

[19]  G. Dunny,et al.  Pheromone-inducible conjugation in Enterococcus faecalis: interbacterial and host-parasite chemical communication , 1995, Journal of bacteriology.

[20]  R. Wirth,et al.  The sex pheromone system of Enterococcus faecalis. More than just a plasmid-collection mechanism? , 1994, European journal of biochemistry.

[21]  G. Wormser,et al.  Outbreak of vancomycin-, ampicillin-, and aminoglycoside-resistant Enterococcus faecium bacteremia in an adult oncology unit , 1994, Antimicrobial Agents and Chemotherapy.

[22]  J. Boyce,et al.  Outbreak of multidrug-resistant Enterococcus faecium with transferable vanB class vancomycin resistance , 1994, Journal of clinical microbiology.

[23]  J. Schlundt,et al.  Conjugal Transfer of Plasmid DNA between Lactococcus lactis Strains and Distribution of Transconjugants in the Digestive Tract of Gnotobiotic Rats , 1994 .

[24]  B. Farber,et al.  Multidrug-resistant Enterococcus faecium. An untreatable nosocomial pathogen. , 1994, Drugs.

[25]  K. Singh,et al.  Nosocomial outbreak due to Enterococcus faecium highly resistant to vancomycin, penicillin, and gentamicin. , 1993, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

[26]  M. Gilmore,et al.  Transfer of pheromone-inducible plasmids between Enterococcus faecalis in the Syrian hamster gastrointestinal tract. , 1992, The Journal of infectious diseases.

[27]  R. Moellering Emergence of Enterococcus as a significant pathogen. , 1992, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

[28]  R. Gaynes,et al.  Major trends in the microbial etiology of nosocomial infection. , 1991, The American journal of medicine.

[29]  B. Murray New aspects of antimicrobial resistance and the resulting therapeutic dilemmas. , 1991, The Journal of infectious diseases.

[30]  F. M. Stewart,et al.  Estimating the rate of plasmid transfer: an end-point method. , 1990, Journal of general microbiology.

[31]  B. Murray The life and times of the Enterococcus , 1990, Clinical Microbiology Reviews.

[32]  K. Weaver,et al.  Sex pheromones and plasmid transfer in Enterococcus faecalis. , 1989, Plasmid.

[33]  G. Dunny,et al.  Two conjugation systems associated with Streptococcus faecalis plasmid pCF10: identification of a conjugative transposon that transfers between S. faecalis and Bacillus subtilis , 1987, Journal of bacteriology.

[34]  J. Que,et al.  Factors responsible for increased susceptibility of mice to intestinal colonization after treatment with streptomycin , 1986, Infection and immunity.

[35]  G. Dunny,et al.  Identification of regions of the Streptococcus faecalis plasmid pCF-10 that encode antibiotic resistance and pheromone response functions. , 1986, Plasmid.

[36]  J. Que,et al.  Effect of streptomycin administration on colonization resistance to Salmonella typhimurium in mice , 1985, Infection and immunity.

[37]  E. Ehrenfeld,et al.  Genetic and physiological analysis of conjugation in Streptococcus faecalis , 1982, Journal of bacteriology.

[38]  D. Clewell,et al.  Evidence for a chromosome-borne resistance transposon (Tn916) in Streptococcus faecalis that is capable of "conjugal" transfer in the absence of a conjugative plasmid , 1981, Journal of bacteriology.

[39]  G. Dunny,et al.  Transmissible toxin (hemolysin) plasmid in Streptococcus faecalis and its mobilization of a noninfectious drug resistance plasmid , 1975, Journal of bacteriology.

[40]  D. van der Waaij,et al.  Colonization resistance of the digestive tract in conventional and antibiotic-treated mice. , 1971 .

[41]  D. van der Waaij,et al.  Colonization resistance of the digestive tract in conventional and antibiotic-treated mice , 1971, Journal of Hygiene.