Previous Article | Next Article 
Infection and Immunity, April 2002, p. 2010-2015, Vol. 70, No. 4
0019-9567/02/$04.00+0 DOI: 10.1128/IAI.70.4.2010-2015.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
Evidence that the Enterococcal Polysaccharide Antigen Gene (epa) Cluster Is Widespread in Enterococcus faecalis and Influences Resistance to Phagocytic Killing of E. faecalis
Fang Teng,1,2 Karen D. Jacques-Palaz,2,3 George M. Weinstock,1,2 and Barbara E. Murray1,2,3*
Department of Microbiology and Molecular Genetics, Division of Infectious Diseases,1
Department of Medicine,3
Center for the Study of Emerging and Re-emerging Pathogens, University of Texas Medical School, Houston, Texas 770302
Received 28 September 2001/
Returned for modification 1 November 2001/
Accepted 18 January 2002
In previous studies, we cloned a cluster of genes involved in polysaccharide biosynthesis (epa) from Enterococcus faecalis strain OG1RF and showed that this gene cluster mediated synthesis of a polysaccharide in Escherichia coli. Disruption of two open reading frames in the epa gene cluster of OG1RF generated two mutants, TX5179 and TX5180, which were attenuated in a mouse peritonitis model. In the current study, Western blotting was performed with serum from a patient with E. faecalis endocarditis and polysaccharide extracts from OG1RF and the mutants TX5179 and TX5180. OG1RF showed a smear in the high-molecular-weight region and discrete bands in the low-molecular-weight region, which were missing from the mutants; periodate treatment and carbohydrate staining confirmed the polysaccharide nature of this material. In a neutrophil killing assay using OG1RF-absorbed normal human serum, the mutants TX5179 and TX5180, respectively, were 50 and 2.4 times more susceptible to killing than wild-type OG1RF (P
0.01). With a fluorescence phagocytosis assay, 2.5 to 3 times more of the mutants were taken up by neutrophils than OG1RF (P
0.001). Finally, with restriction digestion and hybridization under high-stringency conditions, the epa gene cluster of OG1RF (which is also present in the sequenced E. faecalis strain V583) was detected in 12 of 12 other clonally distinct E. faecalis strains tested: a similar polysaccharide pattern was detected for the 12 strains on Western blots using an E. faecalis endocarditis patient serum, and sera from four other patients with E. faecalis endocarditis all reacted with polysaccharide extracts of OG1RF. These results indicate that the epa gene cluster is widespread among E. faecalis and confers some protection against human host defenses.
* Corresponding author. Mailing address: Center for the Study of Emerging and Re-emerging Pathogens, Division of Infectious Diseases, 1728 JFB, University of Texas Medical School, 6431 Fannin St., Houston, TX 77030. Phone: (713) 500-6745. Fax: (713) 500-5495. E-mail:
Barbara.E.Murray{at}uth.tmc.edu.
Editor: E. I. Tuomanen
Infection and Immunity, April 2002, p. 2010-2015, Vol. 70, No. 4
0019-9567/02/$04.00+0 DOI: 10.1128/IAI.70.4.2010-2015.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
This article has been cited by other articles:
-
Thurlow, L. R., Thomas, V. C., Hancock, L. E.
(2009). Capsular Polysaccharide Production in Enterococcus faecalis and Contribution of CpsF to Capsule Serospecificity. J. Bacteriol.
191: 6203-6210
[Abstract]
[Full Text]
-
Teng, F., Singh, K. V., Bourgogne, A., Zeng, J., Murray, B. E.
(2009). Further Characterization of the epa Gene Cluster and Epa Polysaccharides of Enterococcus faecalis. Infect. Immun.
77: 3759-3767
[Abstract]
[Full Text]
-
Brinster, S., Posteraro, B., Bierne, H., Alberti, A., Makhzami, S., Sanguinetti, M., Serror, P.
(2007). Enterococcal Leucine-Rich Repeat-Containing Protein Involved in Virulence and Host Inflammatory Response. Infect. Immun.
75: 4463-4471
[Abstract]
[Full Text]
-
Brinster, S., Furlan, S., Serror, P.
(2007). C-Terminal WxL Domain Mediates Cell Wall Binding in Enterococcus faecalis and Other Gram-Positive Bacteria. J. Bacteriol.
189: 1244-1253
[Abstract]
[Full Text]
-
Verneuil, N., Sanguinetti, M., Le Breton, Y., Posteraro, B., Fadda, G., Auffray, Y., Hartke, A., Giard, J.-C.
(2004). Effects of the Enterococcus faecalis hypR Gene Encoding a New Transcriptional Regulator on Oxidative Stress Response and Intracellular Survival within Macrophages. Infect. Immun.
72: 4424-4431
[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]
-
Johnson, J. R., Clabots, C., Hirt, H., Waters, C., Dunny, G.
(2004). Enterococcal Aggregation Substance and Binding Substance Are Not Major Contributors to Urinary Tract Colonization by Enterococcus faecalis in a Mouse Model of Ascending Unobstructed Urinary Tract Infection. Infect. Immun.
72: 2445-2448
[Abstract]
[Full Text]
-
Zeng, J., Teng, F., Weinstock, G. M., Murray, B. E.
(2004). Translocation of Enterococcus faecalis Strains across a Monolayer of Polarized Human Enterocyte-Like T84 Cells. J. Clin. Microbiol.
42: 1149-1154
[Abstract]
[Full Text]
-
Teng, F., Kawalec, M., Weinstock, G. M., Hryniewicz, W., Murray, B. E.
(2003). An Enterococcus faecium Secreted Antigen, SagA, Exhibits Broad-Spectrum Binding to Extracellular Matrix Proteins and Appears Essential for E. faecium Growth. Infect. Immun.
71: 5033-5041
[Abstract]
[Full Text]
-
Hancock, L. E., Shepard, B. D., Gilmore, M. S.
(2003). Molecular Analysis of the Enterococcus faecalis Serotype 2 Polysaccharide Determinant. J. Bacteriol.
185: 4393-4401
[Abstract]
[Full Text]