Modulation of virulence within a pathogenicity island in vancomycin-resistant Enterococcus faecalis (original) (raw)
References
Richards, M. J., Edwards, J. R., Culver, D. H. & Gaynes, R. P. Nosocomial infections in combined medical-surgical intensive care units in the United States. Infect. Control Hosp. Epidemiol.21, 510–515 (2000) ArticleCAS Google Scholar
Huycke, M. M., Spiegel, C. A. & Gilmore, M. S. Bacteremia caused by hemolytic, high-level gentamicin-resistant Enterococcus faecalis. Antimicrob. Agents Chemother.35, 1626–1634 (1991) ArticleCAS Google Scholar
Sahm, D. F. et al. In vitro susceptibility studies of vancomycin-resistant Enterococcus faecalis. Antimicrob. Agents Chemother.33, 1588–1591 (1989) ArticleCAS Google Scholar
Arthur, M. & Courvalin, P. Genetics and mechanisms of glycopeptide resistance in enterococci. Antimicrob. Agents Chemother.37, 1563–1571 (1993) ArticleCAS Google Scholar
Jett, B. D., Huycke, M. M. & Gilmore, M. S. Virulence of enterococci. Clin. Microbiol. Rev.7, 462–478 (1994) ArticleCAS Google Scholar
Haas, W., Shepard, B. D. & Gilmore, M. S. Two-component regulator of Enterococcus faecalis cytolysin responds to quorum-sensing autoinduction. Nature415, 84–87 (2002) ArticleADSCAS Google Scholar
Ike, Y., Hashimoto, H. & Clewell, D. B. Hemolysin of Streptococcus faecalis subspecies zymogenes contributes to virulence in mice. Infect. Immun.45, 528–530 (1984) CASPubMedPubMed Central Google Scholar
Shankar, V., Baghdayan, A. S., Huycke, M. M., Lindahl, G. & Gilmore, M. S. Infection-derived Enterococcus faecalis strains are enriched in esp, a gene encoding a novel surface protein. Infect. Immun.67, 193–200 (1999) CASPubMedPubMed Central Google Scholar
Shankar, N. et al. Role of Enterococcus faecalis surface protein Esp in the pathogenesis of ascending urinary tract infection. Infect. Immun.69, 4366–4372 (2001) ArticleCAS Google Scholar
Toledo-Arana, A. et al. The enterococcal surface protein, Esp, is involved in Enterococcus faecalis biofilm formation. Appl. Environ. Microbiol.67, 4538–4545 (2001) ArticleCAS Google Scholar
Willems, R. J. L. et al. Variant esp gene as a marker of a distinct genetic lineage of vancomycin-resistant Enterococcus faecium spreading in hospitals. Lancet357, 853–855 (2001) ArticleCAS Google Scholar
Woodford, N., Soltani, M. & Hardy, K. J. Frequency of esp in Enterococcus faecium isolates. Lancet358, 584 (2001) ArticleCAS Google Scholar
Baldassarri, L., Bertuccini, L., Ammendolia, M. G., Gherardi, G. & Creti, R. Variant esp gene in vancomycin-sensitive Enterococcus faecium. Lancet357, 1802 (2001) ArticleCAS Google Scholar
Rouch, D. A., Byrne, M. E., Kong, Y. C. & Skurray, R. A. The _aac_A-aph_D gentamicin and kanamycin resistance determinant of Tn_4001 from Staphylococcus aureus: expression and nucleotide sequence analysis. J. Gen. Microbiol.133, 3039–3052 (1987) CASPubMed Google Scholar
Dodd, H. M., Horn, N. & Gasson, M. J. Characterization of IS_905_, a new multicopy insertion sequence identified in lactococci. J. Bacteriol.176, 3393–3396 (1994) ArticleCAS Google Scholar
Fierer, J. & Guiney, D. G. Diverse virulence traits underlying different clinical outcomes of Salmonella infection. J. Clin. Invest.107, 775–780 (2001) ArticleCAS Google Scholar
Gold, O. G., Jordan, H. V. & van Houte, J. The prevalence of enterococci in the human mouth and their pathogenicity in animal models. Arch. Oral Biol.20, 473–477 (1975) ArticleCAS Google Scholar
Ferat, J. L. & Michel, F. Group II self-splicing introns in bacteria. Nature364, 358–361 (1993) ArticleADSCAS Google Scholar
Huang, C. C., Narita, M., Yamagata, T. & Endo, G. Identification of three _mer_B genes and characterization of a broad-spectrum mercury resistance module encoded by a class II transposon of Bacillus megaterium strain MB1. Gene239, 361–366 (1999) ArticleCAS Google Scholar
Francia, M. V. et al. Completion of the nucleotide sequence of the Enterococcus faecalis conjugative virulence plasmid pAD1 and identification of a second transfer origin. Plasmid46, 117–127 (2001) ArticleCAS Google Scholar
Hacker, J. & Kaper, J. B. Pathogenicity islands and the evolution of microbes. Annu. Rev. Microbiol.54, 641–679 (2000) ArticleCAS Google Scholar
Galli, D. & Wirth, R. Comparative analysis of Enterococcus faecalis sex pheromone plasmids identifies a single homologous DNA region which codes for aggregation substance. J. Bacteriol.173, 3029–3033 (1991) ArticleCAS Google Scholar
Rakita, R. M. et al. Enterococcus faecalis bearing aggregation substance is resistant to killing by human neutrophils despite phagocytosis and neutrophil activation. Infect. Immun.67, 6067–6075 (1999) CASPubMedPubMed Central Google Scholar
Rozdzinski, E., Marre, R., Susa, M., Wirth, R. & Muscholl-Silberhorn, A. Aggregation substance-mediated adherence of Enterococcus faecalis to immobilized extracellular matrix proteins. Microb. Pathog.30, 211–220 (2001) ArticleCAS Google Scholar
Giard, J. C., Rince, A., Capiaux, H., Auffray, Y. & Hartke, A. Inactivation of the stress-and starvation-inducible gls24 operon has a pleiotrophic effect on cell morphology, stress sensitivity, and gene expression in Enterococcus faecalis. J. Bacteriol.182, 4512–4520 (2000) ArticleCAS Google Scholar
Novick, R. P., Schlievert, P. & Ruzin, A. Pathogenicity and resistance islands of staphylococci. Microbes Infect.3, 585–594 (2001) ArticleCAS Google Scholar
Brown, J. S., Gilliland, S. M. & Holden, D. W. A Streptococcus pneumoniae pathogenicity island encoding an ABC transporter involved in iron uptake and virulence. Mol. Microbiol.40, 572–585 (2001) ArticleCAS Google Scholar
Sambrook, J., Fritsch, E. F. & Maniatis, T. Molecular Cloning. A Laboratory Manual (Cold Spring Harbor Laboratory Press, New York, 1990) Google Scholar
Rutherford, K. et al. Artemis: sequence visualization and annotation. Bioinformatics16, 944–945 (2000) ArticleCAS Google Scholar