Borrelia burgdorferi complement regulator-acquiring surface protein 2 does not contribute to complement resistance or host infectivity.
Borrelia burgdorferi, the pathogen of Lyme disease, cycles in nature through Ixodes ticks and mammalian hosts. At least five Complement Regulator-Acquiring Surface Proteins (BbCRASPs) are produced by B. burgdorferi, which are thought to assist spirochetes in host immune evasion. Recent studies estab...
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Format: | Article |
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Public Library of Science (PLoS)
2008-08-01
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Series: | PLoS ONE |
Online Access: | http://europepmc.org/articles/PMC2526170?pdf=render |
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author | Adam S Coleman Xiuli Yang Manish Kumar Xinyue Zhang Kamoltip Promnares Deborah Shroder Melisha R Kenedy John F Anderson Darrin R Akins Utpal Pal |
author_facet | Adam S Coleman Xiuli Yang Manish Kumar Xinyue Zhang Kamoltip Promnares Deborah Shroder Melisha R Kenedy John F Anderson Darrin R Akins Utpal Pal |
author_sort | Adam S Coleman |
collection | DOAJ |
description | Borrelia burgdorferi, the pathogen of Lyme disease, cycles in nature through Ixodes ticks and mammalian hosts. At least five Complement Regulator-Acquiring Surface Proteins (BbCRASPs) are produced by B. burgdorferi, which are thought to assist spirochetes in host immune evasion. Recent studies established that BbCRASP-2 is preferentially expressed in mammals, and elicits robust antibody response in infected hosts, including humans. We show that BbCRASP-2 is ubiquitously expressed in diverse murine tissues, but not in ticks, reinforcing a role of BbCRASP-2 in conferring B. burgdorferi defense against persistent host immune threats, such as complement. BbCRASP-2 immunization, however, fails to protect mice from B. burgdorferi infection and does not modify disease, as reflected by the development of arthritis. An infectious BbCRASP-2 mutant was generated, therefore, to examine the precise role of the gene product in spirochete infectivity. Similar to wild type B. burgdorferi, BbCRASP-2 mutants remain insensitive to complement-mediated killing in vitro, retain full murine infectivity and induce arthritis. Quantitative RT-PCR assessment indicates that survivability of BbCRASP-2-deficient B. burgdorferi is not due to altered expression of other BbCRASPs. Together, these results suggest that the function of a selectively expressed B. burgdorferi gene, BbCRASP-2, is not essential for complement resistance or infectivity in the murine host. |
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id | doaj.art-5fdd03cbe3a9452db35e1d0db7c50a67 |
institution | Directory Open Access Journal |
issn | 1932-6203 |
language | English |
last_indexed | 2024-12-10T03:47:50Z |
publishDate | 2008-08-01 |
publisher | Public Library of Science (PLoS) |
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series | PLoS ONE |
spelling | doaj.art-5fdd03cbe3a9452db35e1d0db7c50a672022-12-22T02:03:22ZengPublic Library of Science (PLoS)PLoS ONE1932-62032008-08-01383010e10.1371/journal.pone.0003010Borrelia burgdorferi complement regulator-acquiring surface protein 2 does not contribute to complement resistance or host infectivity.Adam S ColemanXiuli YangManish KumarXinyue ZhangKamoltip PromnaresDeborah ShroderMelisha R KenedyJohn F AndersonDarrin R AkinsUtpal PalBorrelia burgdorferi, the pathogen of Lyme disease, cycles in nature through Ixodes ticks and mammalian hosts. At least five Complement Regulator-Acquiring Surface Proteins (BbCRASPs) are produced by B. burgdorferi, which are thought to assist spirochetes in host immune evasion. Recent studies established that BbCRASP-2 is preferentially expressed in mammals, and elicits robust antibody response in infected hosts, including humans. We show that BbCRASP-2 is ubiquitously expressed in diverse murine tissues, but not in ticks, reinforcing a role of BbCRASP-2 in conferring B. burgdorferi defense against persistent host immune threats, such as complement. BbCRASP-2 immunization, however, fails to protect mice from B. burgdorferi infection and does not modify disease, as reflected by the development of arthritis. An infectious BbCRASP-2 mutant was generated, therefore, to examine the precise role of the gene product in spirochete infectivity. Similar to wild type B. burgdorferi, BbCRASP-2 mutants remain insensitive to complement-mediated killing in vitro, retain full murine infectivity and induce arthritis. Quantitative RT-PCR assessment indicates that survivability of BbCRASP-2-deficient B. burgdorferi is not due to altered expression of other BbCRASPs. Together, these results suggest that the function of a selectively expressed B. burgdorferi gene, BbCRASP-2, is not essential for complement resistance or infectivity in the murine host.http://europepmc.org/articles/PMC2526170?pdf=render |
spellingShingle | Adam S Coleman Xiuli Yang Manish Kumar Xinyue Zhang Kamoltip Promnares Deborah Shroder Melisha R Kenedy John F Anderson Darrin R Akins Utpal Pal Borrelia burgdorferi complement regulator-acquiring surface protein 2 does not contribute to complement resistance or host infectivity. PLoS ONE |
title | Borrelia burgdorferi complement regulator-acquiring surface protein 2 does not contribute to complement resistance or host infectivity. |
title_full | Borrelia burgdorferi complement regulator-acquiring surface protein 2 does not contribute to complement resistance or host infectivity. |
title_fullStr | Borrelia burgdorferi complement regulator-acquiring surface protein 2 does not contribute to complement resistance or host infectivity. |
title_full_unstemmed | Borrelia burgdorferi complement regulator-acquiring surface protein 2 does not contribute to complement resistance or host infectivity. |
title_short | Borrelia burgdorferi complement regulator-acquiring surface protein 2 does not contribute to complement resistance or host infectivity. |
title_sort | borrelia burgdorferi complement regulator acquiring surface protein 2 does not contribute to complement resistance or host infectivity |
url | http://europepmc.org/articles/PMC2526170?pdf=render |
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