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Immunochemical characterization of polysaccharide antigens from six clinical strains of Enterococci

BACKGROUND: Enterococci have become major nosocomial pathogens due to their intrinsic and acquired resistance to a broad spectrum of antibiotics. Their increasing drug resistance prompts us to search for prominent antigens to develop vaccines against enterococci. Given the success of polysaccharide-...

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Autores principales: Hsu, Carolyn T, Ganong, Amanda L, Reinap, Barbara, Mourelatos, Zafiria, Huebner, Johannes, Wang, Julia Y
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1538600/
https://www.ncbi.nlm.nih.gov/pubmed/16836754
http://dx.doi.org/10.1186/1471-2180-6-62
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author Hsu, Carolyn T
Ganong, Amanda L
Reinap, Barbara
Mourelatos, Zafiria
Huebner, Johannes
Wang, Julia Y
author_facet Hsu, Carolyn T
Ganong, Amanda L
Reinap, Barbara
Mourelatos, Zafiria
Huebner, Johannes
Wang, Julia Y
author_sort Hsu, Carolyn T
collection PubMed
description BACKGROUND: Enterococci have become major nosocomial pathogens due to their intrinsic and acquired resistance to a broad spectrum of antibiotics. Their increasing drug resistance prompts us to search for prominent antigens to develop vaccines against enterococci. Given the success of polysaccharide-based vaccines against various bacterial pathogens, we isolated and characterized the immunochemical properties of polysaccharide antigens from five strains of Enterococcus faecalis and one strain of vancomycin-resistant E. faecium. RESULTS: We cultured large batches of each strain, isolated sufficient quantities of polysaccharides, analyzed their chemical structures, and compared their antigenic specificity. Three classes of polysaccharides were isolated from each strain, including a polyglucan, a teichoic acid, and a heteroglycan composed of rhamnose, glucose, galactose, mannosamine, and glucosamine. The polyglucans from all six strains are identical and appear to be dextran. Yields of the teichoic acids were generally low. The most abundant polysaccharides are the heteroglycans. The six heteroglycans are structurally different as evidenced by NMR spectroscopy. They also differ in their antigenic specificities as revealed by competitive ELISA. The heteroglycans are not immunogenic by themselves but conjugation to protein carriers significantly enhanced their ability to induce antibodies. CONCLUSION: The six clinical strains of enterococci express abundant, strain-specific cell-surface heteroglycans. These polysaccharides may provide a molecular basis for serological typing of enterococcal strains and antigens for the development of vaccines against multi-drug resistant enterococci.
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spelling pubmed-15386002006-08-10 Immunochemical characterization of polysaccharide antigens from six clinical strains of Enterococci Hsu, Carolyn T Ganong, Amanda L Reinap, Barbara Mourelatos, Zafiria Huebner, Johannes Wang, Julia Y BMC Microbiol Research Article BACKGROUND: Enterococci have become major nosocomial pathogens due to their intrinsic and acquired resistance to a broad spectrum of antibiotics. Their increasing drug resistance prompts us to search for prominent antigens to develop vaccines against enterococci. Given the success of polysaccharide-based vaccines against various bacterial pathogens, we isolated and characterized the immunochemical properties of polysaccharide antigens from five strains of Enterococcus faecalis and one strain of vancomycin-resistant E. faecium. RESULTS: We cultured large batches of each strain, isolated sufficient quantities of polysaccharides, analyzed their chemical structures, and compared their antigenic specificity. Three classes of polysaccharides were isolated from each strain, including a polyglucan, a teichoic acid, and a heteroglycan composed of rhamnose, glucose, galactose, mannosamine, and glucosamine. The polyglucans from all six strains are identical and appear to be dextran. Yields of the teichoic acids were generally low. The most abundant polysaccharides are the heteroglycans. The six heteroglycans are structurally different as evidenced by NMR spectroscopy. They also differ in their antigenic specificities as revealed by competitive ELISA. The heteroglycans are not immunogenic by themselves but conjugation to protein carriers significantly enhanced their ability to induce antibodies. CONCLUSION: The six clinical strains of enterococci express abundant, strain-specific cell-surface heteroglycans. These polysaccharides may provide a molecular basis for serological typing of enterococcal strains and antigens for the development of vaccines against multi-drug resistant enterococci. BioMed Central 2006-07-12 /pmc/articles/PMC1538600/ /pubmed/16836754 http://dx.doi.org/10.1186/1471-2180-6-62 Text en Copyright © 2006 Hsu et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Hsu, Carolyn T
Ganong, Amanda L
Reinap, Barbara
Mourelatos, Zafiria
Huebner, Johannes
Wang, Julia Y
Immunochemical characterization of polysaccharide antigens from six clinical strains of Enterococci
title Immunochemical characterization of polysaccharide antigens from six clinical strains of Enterococci
title_full Immunochemical characterization of polysaccharide antigens from six clinical strains of Enterococci
title_fullStr Immunochemical characterization of polysaccharide antigens from six clinical strains of Enterococci
title_full_unstemmed Immunochemical characterization of polysaccharide antigens from six clinical strains of Enterococci
title_short Immunochemical characterization of polysaccharide antigens from six clinical strains of Enterococci
title_sort immunochemical characterization of polysaccharide antigens from six clinical strains of enterococci
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1538600/
https://www.ncbi.nlm.nih.gov/pubmed/16836754
http://dx.doi.org/10.1186/1471-2180-6-62
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