Publication:
A Borrelia burgdorferi Surface-Exposed Transmembrane Protein Lacking Detectable Immune Responses Supports Pathogen Persistence and Constitutes a Vaccine Target

dc.authorscopusid55534268700
dc.authorscopusid57213734423
dc.authorscopusid24401885500
dc.authorscopusid35084558100
dc.authorscopusid26032490200
dc.authorscopusid57199714621
dc.authorscopusid6504499889
dc.contributor.authorKung, F.
dc.contributor.authorKaur, S.
dc.contributor.authorSmith, A.A.
dc.contributor.authorYang, X.
dc.contributor.authorWilder, C.N.
dc.contributor.authorSharma, K.
dc.contributor.authorBüyüktanir Yaş, O.
dc.date.accessioned2020-06-21T13:33:08Z
dc.date.available2020-06-21T13:33:08Z
dc.date.issued2016
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Kung] Faith, Department of Veterinary Medicine, University of Maryland, College Park, College Park, MD, United States; [Kaur] Simarjot, Department of Veterinary Medicine, University of Maryland, College Park, College Park, MD, United States; [Smith] Alexis A., Department of Veterinary Medicine, University of Maryland, College Park, College Park, MD, United States; [Yang] Xiuli, Department of Veterinary Medicine, University of Maryland, College Park, College Park, MD, United States; [Wilder] Cara N., Department of Veterinary Medicine, University of Maryland, College Park, College Park, MD, United States; [Sharma] Kavita, Department of Veterinary Medicine, University of Maryland, College Park, College Park, MD, United States; [Büyüktanir Yaş] Özlem, Department of Microbiology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Pal] Utpal, Department of Veterinary Medicine, University of Maryland, College Park, College Park, MD, United Statesen_US
dc.description.abstractBorrelia burgdorferi harbors a limited set of transmembrane surface proteins, most of which constitute key targets of humoral immune responses. Here we show that BB0405, a conserved membrane-spanning protein of unknown function, fails to evoke detectable antibody responses despite its extracellular exposure. bb0405 is a member of an operon and ubiquitously expressed throughout the rodent-tick infection cycle. The gene product serves an essential function in vivo, as bb0405-deletion mutants are unable to transmit from ticks and establish infection in mammalian hosts. Despite the lack of BB0405-specific immunoglobulin M or immunoglobulin G antibodies during natural infection, mice immunized with a recombinant version of the protein elicited high-titer and remarkably long-lasting antibody responses, conferring significant host protection against tick-borne infection. Taken together, these studies highlight the essential role of an apparently immune-invisible borrelial transmembrane protein in facilitating infection and its usefulness as a target of protective host immunity blocking the transmission of B. burgdorferi. © The Author 2016. Published by Oxford University Press for the Infectious Diseases Society of America.en_US
dc.identifier.doi10.1093/infdis/jiw013
dc.identifier.endpage1795en_US
dc.identifier.issn0022-1899
dc.identifier.issn1537-6613
dc.identifier.issue11en_US
dc.identifier.pmid26747708
dc.identifier.scopus2-s2.0-84978698507
dc.identifier.scopusqualityQ1
dc.identifier.startpage1786en_US
dc.identifier.urihttps://doi.org/10.1093/infdis/jiw013
dc.identifier.volume213en_US
dc.identifier.wosWOS:000377443400016
dc.identifier.wosqualityQ1
dc.language.isoenen_US
dc.publisherOxford University Press jnl.info@oup.co.uken_US
dc.relation.ispartofJournal of Infectious Diseasesen_US
dc.relation.journalJournal of Infectious Diseasesen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectBB0405en_US
dc.subjectBorrelia Burgdorferien_US
dc.subjectPathogen Persistenceen_US
dc.subjectTransmission-Blockingen_US
dc.subjectVaccineen_US
dc.titleA Borrelia burgdorferi Surface-Exposed Transmembrane Protein Lacking Detectable Immune Responses Supports Pathogen Persistence and Constitutes a Vaccine Targeten_US
dc.typeArticleen_US
dspace.entity.typePublication

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