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Expression of polymorphic msp1beta genes during acute anaplasma Marginale rickettsemia.

TitleExpression of polymorphic msp1beta genes during acute anaplasma Marginale rickettsemia.
Publication TypeJournal Article
Year of Publication2000
AuthorsCamacho-Nuez, M, M Muñoz, deLourdes, Suarez, CE, McGuire, TC, Brown, WC, Palmer, GH
JournalInfect Immun
Volume68
Issue4
Pagination1946-52
Date Published2000 Apr
ISSN0019-9567
KeywordsAmino Acid Sequence, Amino Acids, Anaplasma, Animals, Antibodies, B-Lymphocytes, Bacteremia, Cattle, Cloning, Molecular, Conserved Sequence, Epitopes, Gene Expression, Merozoite Surface Protein 1, Models, Genetic, Molecular Sequence Data, Polymorphism, Genetic, Reverse Transcriptase Polymerase Chain Reaction, Sequence Homology, Amino Acid, Transcription, Genetic
Abstract

Immunization of cattle with native MSP1 induces protection against Anaplasma marginale. The native immunogen is composed of a single MSP1a protein and multiple, undefined MSP1b polypeptides. In addition to the originally sequenced gene, designated msp1beta(F1), we identified three complete msp1beta genes in the Florida strain: msp1beta(F2), msp1beta(F3), and msp1beta(F4). Each of these polymorphic genes encodes a structurally unique MSP1b protein, and unique transcripts can be identified during acute A. marginale rickettsemia. The structural polymorphism is clustered in discrete variable regions, and each MSP1b protein results from a unique mosaic of five variable regions. Although each of the MSP1b proteins in the Florida strain contains epitopes recognized by serum antibody induced by protective immunization with the native MSP1 complex, the variable regions also include epitopes expressed by some but not all of the MSP1b proteins. These data support testing recombinant vaccines composed of the multiple antigenically and structurally unique MSP1b proteins combined with MSP1a in order to mimic the efficacy of native MSP1 immunization.

Alternate JournalInfect. Immun.
PubMed ID10722587
PubMed Central IDPMC97371
Grant ListR01 AI44005 / AI / NIAID NIH HHS / United States