Cargando…

An Immune Evasion Mechanism for Spirochetal Persistence in Lyme Borreliosis

Borrelia burgdorferi, the Lyme disease spirochete, persistently infects mammalian hosts despite the development of strong humoral responses directed against the pathogen. Here we describe a novel mechanism of immune evasion by B. burgdorferi. In immunocompetent mice, spirochetes that did not express...

Descripción completa

Detalles Bibliográficos
Autores principales: Liang, Fang Ting, Jacobs, Mary B., Bowers, Lisa C., Philipp, Mario T.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2193615/
https://www.ncbi.nlm.nih.gov/pubmed/11854355
http://dx.doi.org/10.1084/jem.20011870
_version_ 1782147512710201344
author Liang, Fang Ting
Jacobs, Mary B.
Bowers, Lisa C.
Philipp, Mario T.
author_facet Liang, Fang Ting
Jacobs, Mary B.
Bowers, Lisa C.
Philipp, Mario T.
author_sort Liang, Fang Ting
collection PubMed
description Borrelia burgdorferi, the Lyme disease spirochete, persistently infects mammalian hosts despite the development of strong humoral responses directed against the pathogen. Here we describe a novel mechanism of immune evasion by B. burgdorferi. In immunocompetent mice, spirochetes that did not express ospC (the outer-surface protein C gene) were selected within 17 d after inoculation, concomitantly with the emergence of anti-OspC antibody. Spirochetes with no detectable OspC transcript that were isolated from immunocompetent mice reexpressed ospC after they were either cultured in vitro or transplanted to naive immunocompetent mice, but not in OspC-immunized mice. B. burgdorferi persistently expressed ospC in severe combined immune-deficient (SCID) mice. Passive immunization of B. burgdorferi–infected SCID mice with an anti-OspC monoclonal antibody selectively eliminated ospC-expressing spirochetes but did not clear the infection. OspC-expressing spirochetes reappeared in SCID mice after the anti-OspC antibody was eliminated. We submit that selection of surface-antigen nonexpressers is an immune evasion mechanism that contributes to spirochetal persistence.
format Text
id pubmed-2193615
institution National Center for Biotechnology Information
language English
publishDate 2002
publisher The Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-21936152008-04-14 An Immune Evasion Mechanism for Spirochetal Persistence in Lyme Borreliosis Liang, Fang Ting Jacobs, Mary B. Bowers, Lisa C. Philipp, Mario T. J Exp Med Original Article Borrelia burgdorferi, the Lyme disease spirochete, persistently infects mammalian hosts despite the development of strong humoral responses directed against the pathogen. Here we describe a novel mechanism of immune evasion by B. burgdorferi. In immunocompetent mice, spirochetes that did not express ospC (the outer-surface protein C gene) were selected within 17 d after inoculation, concomitantly with the emergence of anti-OspC antibody. Spirochetes with no detectable OspC transcript that were isolated from immunocompetent mice reexpressed ospC after they were either cultured in vitro or transplanted to naive immunocompetent mice, but not in OspC-immunized mice. B. burgdorferi persistently expressed ospC in severe combined immune-deficient (SCID) mice. Passive immunization of B. burgdorferi–infected SCID mice with an anti-OspC monoclonal antibody selectively eliminated ospC-expressing spirochetes but did not clear the infection. OspC-expressing spirochetes reappeared in SCID mice after the anti-OspC antibody was eliminated. We submit that selection of surface-antigen nonexpressers is an immune evasion mechanism that contributes to spirochetal persistence. The Rockefeller University Press 2002-02-18 /pmc/articles/PMC2193615/ /pubmed/11854355 http://dx.doi.org/10.1084/jem.20011870 Text en Copyright © 2002, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Original Article
Liang, Fang Ting
Jacobs, Mary B.
Bowers, Lisa C.
Philipp, Mario T.
An Immune Evasion Mechanism for Spirochetal Persistence in Lyme Borreliosis
title An Immune Evasion Mechanism for Spirochetal Persistence in Lyme Borreliosis
title_full An Immune Evasion Mechanism for Spirochetal Persistence in Lyme Borreliosis
title_fullStr An Immune Evasion Mechanism for Spirochetal Persistence in Lyme Borreliosis
title_full_unstemmed An Immune Evasion Mechanism for Spirochetal Persistence in Lyme Borreliosis
title_short An Immune Evasion Mechanism for Spirochetal Persistence in Lyme Borreliosis
title_sort immune evasion mechanism for spirochetal persistence in lyme borreliosis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2193615/
https://www.ncbi.nlm.nih.gov/pubmed/11854355
http://dx.doi.org/10.1084/jem.20011870
work_keys_str_mv AT liangfangting animmuneevasionmechanismforspirochetalpersistenceinlymeborreliosis
AT jacobsmaryb animmuneevasionmechanismforspirochetalpersistenceinlymeborreliosis
AT bowerslisac animmuneevasionmechanismforspirochetalpersistenceinlymeborreliosis
AT philippmariot animmuneevasionmechanismforspirochetalpersistenceinlymeborreliosis
AT liangfangting immuneevasionmechanismforspirochetalpersistenceinlymeborreliosis
AT jacobsmaryb immuneevasionmechanismforspirochetalpersistenceinlymeborreliosis
AT bowerslisac immuneevasionmechanismforspirochetalpersistenceinlymeborreliosis
AT philippmariot immuneevasionmechanismforspirochetalpersistenceinlymeborreliosis