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Borrelia burgdorferi elongation factor EF-Tu is an immunogenic protein during Lyme borreliosis
Borrelia burgdorferi, the etiological agent of Lyme disease, does not produce lipopolysaccharide but expresses a large number of lipoproteins on its cell surface. These outer membrane lipoproteins are highly immunogenic and have been used for serodiagnosis of Lyme disease. Recent studies have shown...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5176084/ https://www.ncbi.nlm.nih.gov/pubmed/26954993 http://dx.doi.org/10.1038/emi.2015.54 |
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author | Carrasco, Sebastian E Yang, Youyun Troxell, Bryan Yang, Xiuli Pal, Utpal Yang, X Frank |
author_facet | Carrasco, Sebastian E Yang, Youyun Troxell, Bryan Yang, Xiuli Pal, Utpal Yang, X Frank |
author_sort | Carrasco, Sebastian E |
collection | PubMed |
description | Borrelia burgdorferi, the etiological agent of Lyme disease, does not produce lipopolysaccharide but expresses a large number of lipoproteins on its cell surface. These outer membrane lipoproteins are highly immunogenic and have been used for serodiagnosis of Lyme disease. Recent studies have shown that highly conserved cytosolic proteins such as enolase and elongation factor Tu (EF-Tu) unexpectedly localized on the surface of bacteria including B. burgdorferi, and surface-localized enolase has shown to contribute to the enzootic cycle of B. burgdorferi. In this study, we studied the immunogenicity, surface localization, and function of B. burgdorferi EF-Tu. We found that EF-Tu is highly immunogenic in mice, and EF-Tu antibodies were readily detected in Lyme disease patients. On the other hand, active immunization studies showed that EF-Tu antibodies did not protect mice from infection when challenged with B. burgdorferi via either needle inoculation or tick bites. Borrelial mouse-tick cycle studies showed that EF-Tu antibodies also did not block B. burgdorferi migration and survival in ticks. Consistent with these findings, we found that EF-Tu primarily localizes in the protoplasmic cylinder of spirochetes and is not on the surface of B. burgdorferi. Taken together, our studies suggest that B. burgdorferi EF-Tu is not surfaced exposed, but it is highly immunogenic and is a potential serodiagnostic marker for Lyme borreliosis. |
format | Online Article Text |
id | pubmed-5176084 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-51760842017-01-09 Borrelia burgdorferi elongation factor EF-Tu is an immunogenic protein during Lyme borreliosis Carrasco, Sebastian E Yang, Youyun Troxell, Bryan Yang, Xiuli Pal, Utpal Yang, X Frank Emerg Microbes Infect Original Article Borrelia burgdorferi, the etiological agent of Lyme disease, does not produce lipopolysaccharide but expresses a large number of lipoproteins on its cell surface. These outer membrane lipoproteins are highly immunogenic and have been used for serodiagnosis of Lyme disease. Recent studies have shown that highly conserved cytosolic proteins such as enolase and elongation factor Tu (EF-Tu) unexpectedly localized on the surface of bacteria including B. burgdorferi, and surface-localized enolase has shown to contribute to the enzootic cycle of B. burgdorferi. In this study, we studied the immunogenicity, surface localization, and function of B. burgdorferi EF-Tu. We found that EF-Tu is highly immunogenic in mice, and EF-Tu antibodies were readily detected in Lyme disease patients. On the other hand, active immunization studies showed that EF-Tu antibodies did not protect mice from infection when challenged with B. burgdorferi via either needle inoculation or tick bites. Borrelial mouse-tick cycle studies showed that EF-Tu antibodies also did not block B. burgdorferi migration and survival in ticks. Consistent with these findings, we found that EF-Tu primarily localizes in the protoplasmic cylinder of spirochetes and is not on the surface of B. burgdorferi. Taken together, our studies suggest that B. burgdorferi EF-Tu is not surfaced exposed, but it is highly immunogenic and is a potential serodiagnostic marker for Lyme borreliosis. Nature Publishing Group 2015-09 2015-09-02 /pmc/articles/PMC5176084/ /pubmed/26954993 http://dx.doi.org/10.1038/emi.2015.54 Text en Copyright © 2015 Shanghai Shangyixun Cultural Communication Co., Ltd http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 Unported License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Original Article Carrasco, Sebastian E Yang, Youyun Troxell, Bryan Yang, Xiuli Pal, Utpal Yang, X Frank Borrelia burgdorferi elongation factor EF-Tu is an immunogenic protein during Lyme borreliosis |
title | Borrelia burgdorferi elongation factor EF-Tu is an immunogenic protein during Lyme borreliosis |
title_full | Borrelia burgdorferi elongation factor EF-Tu is an immunogenic protein during Lyme borreliosis |
title_fullStr | Borrelia burgdorferi elongation factor EF-Tu is an immunogenic protein during Lyme borreliosis |
title_full_unstemmed | Borrelia burgdorferi elongation factor EF-Tu is an immunogenic protein during Lyme borreliosis |
title_short | Borrelia burgdorferi elongation factor EF-Tu is an immunogenic protein during Lyme borreliosis |
title_sort | borrelia burgdorferi elongation factor ef-tu is an immunogenic protein during lyme borreliosis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5176084/ https://www.ncbi.nlm.nih.gov/pubmed/26954993 http://dx.doi.org/10.1038/emi.2015.54 |
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