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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1991-8-21
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pubmed:databankReference |
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M59473,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M59474,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M61203,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M61204,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M61205,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M61206,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M61207,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M61208,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S43018,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S78950
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pubmed:abstractText |
A clone expressing a surface exposed, conserved epitope of a 60-kDa merozoite polypeptide was identified in a cDNA library constructed from a cloned Mexico strain of Babesia bovis. Sequencing of the 1.9-kb insert (pBv60) revealed an open reading frame encoding a 65-kDa polypeptide with a signal peptide and a tandemly repeated region. Monoclonal antibody 23/56.156, which binds a surface exposed epitope on the native polypeptide, specifically immunoprecipitated [35S]methionine-labeled polypeptides ranging from 60-30 kDa from pBv60 directed transcription and translation. Antibodies raised in rabbits against recombinant polypeptide reacted with the live merozoite surface in a polar immunofluorescence pattern, immunoprecipitated the native 60-kDa polypeptide, and were used to deplete the polypeptide by adsorption from a preparation of native [35S]methionine-labeled merozoite antigen. Restriction enzyme analysis indicated a single gene copy and the absence of introns. Hybridization demonstrated the presence of the gene in Mexico, Australia 'L', and Texas strains of B. bovis, but not in Babesia bigemina. A slightly different hybridization pattern was present in uncloned Australia 'L' B. bovis, indicating sequence diversity in the Bv60 gene among isolates. Cloning and structural analysis of pBv60 provides a source of defined antigen for determining the role of conserved merozoite surface epitopes in protective immunity against babesiosis.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0166-6851
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
46
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
45-52
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:1712911-Amino Acid Sequence,
pubmed-meshheading:1712911-Animals,
pubmed-meshheading:1712911-Antigens, Protozoan,
pubmed-meshheading:1712911-Antigens, Surface,
pubmed-meshheading:1712911-Babesia,
pubmed-meshheading:1712911-Base Sequence,
pubmed-meshheading:1712911-Blotting, Southern,
pubmed-meshheading:1712911-Cloning, Molecular,
pubmed-meshheading:1712911-DNA, Protozoan,
pubmed-meshheading:1712911-Epitopes,
pubmed-meshheading:1712911-Molecular Sequence Data,
pubmed-meshheading:1712911-Open Reading Frames,
pubmed-meshheading:1712911-Precipitin Tests,
pubmed-meshheading:1712911-Sequence Alignment
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pubmed:year |
1991
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pubmed:articleTitle |
Characterization of the gene encoding a 60-kilodalton Babesia bovis merozoite protein with conserved and surface exposed epitopes.
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pubmed:affiliation |
Department of Veterinary Microbiology and Pathology, Washington State University, Pullman.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't
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