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Restriction of major surface protein 2 (MSP2) variants during tick transmission of the ehrlichia Anaplasma marginale.

TitleRestriction of major surface protein 2 (MSP2) variants during tick transmission of the ehrlichia Anaplasma marginale.
Publication TypeJournal Article
Year of Publication1999
AuthorsRurangirwa, FR, Stiller, D, French, DM, Palmer, GH
JournalProc Natl Acad Sci U S A
Volume96
Issue6
Pagination3171-6
Date Published1999 Mar 16
ISSN0027-8424
KeywordsAmino Acid Sequence, Anaplasma, Animals, Antigens, Bacterial, Arthropod Vectors, Bacterial Outer Membrane Proteins, Cattle, Molecular Sequence Data, Sequence Alignment, Sequence Analysis, Tick-Borne Diseases, Ticks, Transcription, Genetic
Abstract

Anaplasma marginale is an ehrlichial pathogen of cattle that establishes lifelong persistent infection. Persistence is characterized by rickettsemic cycles in which new A. marginale variant types, defined by the sequence of the expressed msp2 transcripts, emerge. The polymorphic msp2 transcripts encode structurally distinct MSP2 proteins and result in an antigenically diverse and continually changing A. marginale population within the blood. In this manuscript, we used sequence analysis of msp2 transcripts to show that a restricted repertoire of variant types, designated SGV1 and SGV2, is expressed within the tick salivary gland. The same SGV1 and SGV2 variant types were expressed in ticks regardless of the variant types expressed in the blood of infected cattle at the time of acquisition feeding by the ticks. Importantly, subsequent tick transmission to susceptible cattle resulted in acute rickettsemia composed of organisms expressing only the same SGV1 and SGV2 variant types. This indicates that the msp2 expressed by organisms within the tick salivary gland predicts the variant type responsible for acute rickettsemia and disease. This restriction of transmitted A. marginale variant types, in contrast to the marked diversity within persistently infected cattle, supports development of MSP2 vaccines to prevent acute rickettsemia in tick-transmitted infections.

Alternate JournalProc. Natl. Acad. Sci. U.S.A.
PubMed ID10077656
PubMed Central IDPMC15914
Grant ListK08 AI01371 / AI / NIAID NIH HHS / United States
R01 AI44005 / AI / NIAID NIH HHS / United States