This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Eaton, T. J.
Right arrow Articles by Gasson, M. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Eaton, T. J.
Right arrow Articles by Gasson, M. J.
Agricola
Right arrow Articles by Eaton, T. J.
Right arrow Articles by Gasson, M. J.

 Previous Article  |  Next Article 

Applied and Environmental Microbiology, April 2001, p. 1628-1635, Vol. 67, No. 4
0099-2240/01/$04.00+0   DOI: 10.1128/AEM.67.4.1628-1635.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.

Molecular Screening of Enterococcus Virulence Determinants and Potential for Genetic Exchange between Food and Medical Isolates

Tracy J. Eaton* and Michael J. Gasson

Division of Food Safety Sciences, Institute of Food Research, Norwich, United Kingdom

Received 29 September 2000/Accepted 1 February 2001

Enterococci are used as starter and probiotic cultures in foods, and they occur as natural food contaminants. The genus Enterococcus is of increased significance as a cause of nosocomial infections, and this trend is exacerbated by the development of antibiotic resistance. In this study, we investigated the incidence of known virulence determinants in starter, food, and medical strains of Enterococcus faecalis, E. faecium, and E. durans. PCR and gene probe strategies were used to screen enterococcal isolates from both food and medical sources. Different and distinct patterns of incidence of virulence determinants were found for the E. faecalis and E. faecium strains. Medical E. faecalis strains had more virulence determinants than did food strains, which, in turn, had more than did starter strains. All of the E. faecalis strains tested possessed multiple determinants (between 6 and 11). E. faecium strains were generally free of virulence determinants, with notable exceptions. Significantly, esp and gelE determinants were identified in E. faecium medical strains. These virulence determinants have not previously been identified in E. faecium strains and may result from regional differences or the evolution of pathogenic E. faecium. Phenotypic testing revealed the existence of apparently silent gelE and cyl genes. In E. faecalis, the trend in these silent genes mirrors that of the expressed determinants. The potential for starter strains to acquire virulence determinants by natural conjugation mechanisms was investigated. Transconjugation in which starter strains acquired additional virulence determinants from medical strains was demonstrated. In addition, multiple pheromone-encoding genes were identified in both food and starter strains, indicating their potential to acquire other sex pheromone plasmids. These results suggest that the use of Enterococcus spp. in foods requires careful safety evaluation.


* Corresponding author. Mailing address: Division of Food Safety Sciences, Institute of Food Research, Norwich Research Park, Colney, Norwich NR4 7UA, United Kingdom. Phone: (1603) 255000. Fax: (1603) 507723. E-mail: Tracy.Eaton{at}bbsrc.ac.uk.


Applied and Environmental Microbiology, April 2001, p. 1628-1635, Vol. 67, No. 4
0099-2240/01/$04.00+0   DOI: 10.1128/AEM.67.4.1628-1635.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Semedo-Lemsaddek, T., Barreto-Crespo, M. T., Tenreiro, R. (2009). Occurrence of Putative Pathogenicity Islands in Enterococci from Distinct Species and of Differing Origins. Appl. Environ. Microbiol. 75: 7271-7274 [Abstract] [Full Text]  
  • Gaspar, F., Teixeira, N., Rigottier-Gois, L., Marujo, P., Nielsen-LeRoux, C., Crespo, M. T. B., Lopes, M. d. F. S., Serror, P. (2009). Virulence of Enterococcus faecalis dairy strains in an insect model: the role of fsrB and gelE. Microbiology 155: 3564-3571 [Abstract] [Full Text]  
  • Toomey, N., Monaghan, A., Fanning, S., Bolton, D. (2009). Transfer of Antibiotic Resistance Marker Genes between Lactic Acid Bacteria in Model Rumen and Plant Environments. Appl. Environ. Microbiol. 75: 3146-3152 [Abstract] [Full Text]  
  • Zheng, B., Tomita, H., Inoue, T., Ike, Y. (2009). Isolation of VanB-Type Enterococcus faecalis Strains from Nosocomial Infections: First Report of the Isolation and Identification of the Pheromone-Responsive Plasmids pMG2200, Encoding VanB-Type Vancomycin Resistance and a Bac41-Type Bacteriocin, and pMG2201, Encoding Erythromycin Resistance and Cytolysin (Hly/Bac). Antimicrob. Agents Chemother. 53: 735-747 [Abstract] [Full Text]  
  • Vankerckhoven, V., Huys, G., Vancanneyt, M., Snauwaert, C., Swings, J., Klare, I., Witte, W., Van Autgaerden, T., Chapelle, S., Lammens, C., Goossens, H. (2008). Genotypic Diversity, Antimicrobial Resistance, and Virulence Factors of Human Isolates and Probiotic Cultures Constituting Two Intraspecific Groups of Enterococcus faecium Isolates. Appl. Environ. Microbiol. 74: 4247-4255 [Abstract] [Full Text]  
  • Riboulet-Bisson, E., Sanguinetti, M., Budin-Verneuil, A., Auffray, Y., Hartke, A., Giard, J.-C. (2008). Characterization of the Ers Regulon of Enterococcus faecalis. Infect. Immun. 76: 3064-3074 [Abstract] [Full Text]  
  • Izquierdo, E., Bednarczyk, A., Schaeffer, C., Cai, Y., Marchioni, E., Van Dorsselaer, A., Ennahar, S. (2008). Production of Enterocins L50A, L50B, and IT, a New Enterocin, by Enterococcus faecium IT62, a Strain Isolated from Italian Ryegrass in Japan. Antimicrob. Agents Chemother. 52: 1917-1923 [Abstract] [Full Text]  
  • Biavasco, F., Foglia, G., Paoletti, C., Zandri, G., Magi, G., Guaglianone, E., Sundsfjord, A., Pruzzo, C., Donelli, G., Facinelli, B. (2007). VanA-Type Enterococci from Humans, Animals, and Food: Species Distribution, Population Structure, Tn1546 Typing and Location, and Virulence Determinants. Appl. Environ. Microbiol. 73: 3307-3319 [Abstract] [Full Text]  
  • Paoletti, C., Foglia, G., Princivalli, M. S., Magi, G., Guaglianone, E., Donelli, G., Pruzzo, C., Biavasco, F., Facinelli, B. (2007). Co-transfer of vanA and aggregation substance genes from Enterococcus faecalis isolates in intra- and interspecies matings. J Antimicrob Chemother 59: 1005-1009 [Abstract] [Full Text]  
  • Lepage, E., Brinster, S., Caron, C., Ducroix-Crepy, C., Rigottier-Gois, L., Dunny, G., Hennequet-Antier, C., Serror, P. (2006). Comparative Genomic Hybridization Analysis of Enterococcus faecalis: Identification of Genes Absent from Food Strains.. J. Bacteriol. 188: 6858-6868 [Abstract] [Full Text]  
  • Macovei, L., Zurek, L. (2006). Ecology of antibiotic resistance genes: characterization of enterococci from houseflies collected in food settings.. Appl. Environ. Microbiol. 72: 4028-4035 [Abstract] [Full Text]  
  • Gutierrez, J., Criado, R., Martin, M., Herranz, C., Cintas, L. M., Hernandez, P. E. (2005). Production of Enterocin P, an Antilisterial Pediocin-Like Bacteriocin from Enterococcus faecium P13, in Pichia pastoris. Antimicrob. Agents Chemother. 49: 3004-3008 [Abstract] [Full Text]  
  • Novais, C., Coque, T. M., Ferreira, H., Sousa, J. C., Peixe, L. (2005). Environmental Contamination with Vancomycin-Resistant Enterococci from Hospital Sewage in Portugal. Appl. Environ. Microbiol. 71: 3364-3368 [Abstract] [Full Text]  
  • Reviriego, C., Eaton, T., Martin, R., Jimenez, E., Fernandez, L., Gasson, M. J., Rodriguez, J. M. (2005). Screening of Virulence Determinants in Enterococcus faecium Strains Isolated From Breast Milk. J Hum Lact 21: 131-137 [Abstract]  
  • Middleton, J. H., Ambrose, A. (2005). ENUMERATION AND ANTIBIOTIC RESISTANCE PATTERNS OF FECAL INDICATOR ORGANISMS ISOLATED FROM MIGRATORY CANADA GEESE (BRANTA CANADENSIS). J Wildl Dis 41: 334-341 [Abstract] [Full Text]  
  • Bittencourt de Marques, E., Suzart, S. (2004). Occurrence of virulence-associated genes in clinical Enterococcus faecalis strains isolated in Londrina, Brazil. J Med Microbiol 53: 1069-1073 [Abstract] [Full Text]  
  • Vankerckhoven, V., Van Autgaerden, T., Vael, C., Lammens, C., Chapelle, S., Rossi, R., Jabes, D., Goossens, H. (2004). Development of a Multiplex PCR for the Detection of asa1, gelE, cylA, esp, and hyl Genes in Enterococci and Survey for Virulence Determinants among European Hospital Isolates of Enterococcus faecium. J. Clin. Microbiol. 42: 4473-4479 [Abstract] [Full Text]  
  • Kayaoglu, G., Orstavik, D. (2004). VIRULENCE FACTORS OF ENTEROCOCCUS FAECALIS: RELATIONSHIP TO ENDODONTIC DISEASE. CROBM 15: 308-320 [Abstract] [Full Text]  
  • Donelli, G., Paoletti, C., Baldassarri, L., Guaglianone, E., Di Rosa, R., Magi, G., Spinaci, C., Facinelli, B. (2004). Sex Pheromone Response, Clumping, and Slime Production in Enterococcal Strains Isolated from Occluded Biliary Stents. J. Clin. Microbiol. 42: 3419-3427 [Abstract] [Full Text]  
  • Mohamed, J. A., Huang, W., Nallapareddy, S. R., Teng, F., Murray, B. E. (2004). Influence of Origin of Isolates, Especially Endocarditis Isolates, and Various Genes on Biofilm Formation by Enterococcus faecalis. Infect. Immun. 72: 3658-3663 [Abstract] [Full Text]  
  • Leavis, H., Top, J., Shankar, N., Borgen, K., Bonten, M., van Embden, J., Willems, R. J. L. (2004). A Novel Putative Enterococcal Pathogenicity Island Linked to the esp Virulence Gene of Enterococcus faecium and Associated with Epidemicity. J. Bacteriol. 186: 672-682 [Abstract] [Full Text]  
  • Creti, R., Imperi, M., Bertuccini, L., Fabretti, F., Orefici, G., Di Rosa, R., Baldassarri, L. (2004). Survey for virulence determinants among Enterococcus faecalis isolated from different sources. J Med Microbiol 53: 13-20 [Abstract] [Full Text]  
  • Lund, B., Edlund, C. (2003). Bloodstream Isolates of Enterococcus faecium Enriched with the Enterococcal Surface Protein Gene, esp, Show Increased Adhesion to Eukaryotic Cells. J. Clin. Microbiol. 41: 5183-5185 [Abstract] [Full Text]  
  • Woodford, N., Reynolds, R., Turton, J., Scott, F., Sinclair, A., Williams, A., Livermore, D. (2003). Two widely disseminated strains of Enterococcus faecalis highly resistant to gentamicin and ciprofloxacin from bacteraemias in the UK and Ireland. J Antimicrob Chemother 52: 711-714 [Abstract] [Full Text]  
  • Semedo, T., Almeida Santos, M., Martins, P., Silva Lopes, M. F., Figueiredo Marques, J. J., Tenreiro, R., Barreto Crespo, M. T. (2003). Comparative Study Using Type Strains and Clinical and Food Isolates To Examine Hemolytic Activity and Occurrence of the cyl Operon in Enterococci. J. Clin. Microbiol. 41: 2569-2576 [Abstract] [Full Text]  
  • Dupre, I., Zanetti, S., Schito, A. M., Fadda, G., Sechi, L. A. (2003). Incidence of virulence determinants in clinical Enterococcus faecium and Enterococcus faecalis isolates collected in Sardinia (Italy). J Med Microbiol 52: 491-498 [Abstract] [Full Text]  
  • Magi, G., Capretti, R., Paoletti, C., Pietrella, M., Ferrante, L., Biavasco, F., Varaldo, P. E., Facinelli, B. (2003). Presence of a vanA-Carrying Pheromone Response Plasmid (pBRG1) in a Clinical Isolate of Enterococcus faecium. Antimicrob. Agents Chemother. 47: 1571-1576 [Abstract] [Full Text]  
  • Hickey, R. M., Twomey, D. P., Ross, R. P., Hill, C. (2003). Production of enterolysin A by a raw milk enterococcal isolate exhibiting multiple virulence factors. Microbiology 149: 655-664 [Abstract] [Full Text]  
  • Hancock, L., Perego, M. (2002). Two-Component Signal Transduction in Enterococcus faecalis. J. Bacteriol. 184: 5819-5825 [Full Text]  
  • Nakayama, J., Kariyama, R., Kumon, H. (2002). Description of a 23.9-Kilobase Chromosomal Deletion Containing a Region Encoding fsr Genes Which Mainly Determines the Gelatinase-Negative Phenotype of Clinical Isolates of Enterococcus faecalis in Urine. Appl. Environ. Microbiol. 68: 3152-3155 [Abstract] [Full Text]  
  • Lund, B., Agvald-Ohman, C., Hultberg, A., Edlund, C. (2002). Frequent Transmission of Enterococcal Strains between Mechanically Ventilated Patients Treated at an Intensive Care Unit. J. Clin. Microbiol. 40: 2084-2088 [Abstract] [Full Text]  
  • Balish, E., Warner, T. (2002). Enterococcus faecalis Induces Inflammatory Bowel Disease in Interleukin-10 Knockout Mice. Am. J. Pathol. 160: 2253-2257 [Abstract] [Full Text]  
  • Vancanneyt, M., Lombardi, A., Andrighetto, C., Knijff, E., Torriani, S., Bjorkroth, K. J., Franz, C. M. A. P., Foulquie Moreno, M. R., Revets, H., De Vuyst, L., Swings, J., Kersters, K., Dellaglio, F., Holzapfel, W. H. (2002). Intraspecies Genomic Groups in Enterococcus faecium and Their Correlation with Origin and Pathogenicity. Appl. Environ. Microbiol. 68: 1381-1391 [Abstract] [Full Text]  
  • Toledo-Arana, A., Valle, J., Solano, C., Arrizubieta, M. J., Cucarella, C., Lamata, M., Amorena, B., Leiva, J., Penades, J. R., Lasa, I. (2001). The Enterococcal Surface Protein, Esp, Is Involved in Enterococcus faecalis Biofilm Formation. Appl. Environ. Microbiol. 67: 4538-4545 [Abstract] [Full Text]  
  • Franz, C. M. A. P., Muscholl-Silberhorn, A. B., Yousif, N. M. K., Vancanneyt, M., Swings, J., Holzapfel, W. H. (2001). Incidence of Virulence Factors and Antibiotic Resistance among Enterococci Isolated from Food. Appl. Environ. Microbiol. 67: 4385-4389 [Abstract] [Full Text]