Infect. Immun.

Anaplasma marginale is a tick-borne pathogen, one of several closely related ehrlichial organisms that cause disease in animals and humans. These Ehrlichia species have complex life cycles that require, in addition to replication and development within the tick vector, evasion of the immune system in order to persist in the mammalian reservoir host. This complexity requires efficient use of the small ehrlichial genome. A. marginale and related ehrlichiae express immunoprotective, variable outer membrane proteins that have similar structures and are encoded by polymorphic multigene families. We show here that the major outer membrane protein of A. marginale, MSP2, is encoded on a polycistronic mRNA. The genomic expression site for this mRNA is polymorphic and encodes numerous amino acid sequence variants in bloodstream populations of A. marginale. A potential mechanism for persistence is segmental gene conversion of the expression site to link hypervariable msp2 sequences to the promoter and polycistron.

Source:http://purl.uniprot.org/citations/11035716

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http://purl.uniprot.org/cit...rdfs:commentAnaplasma marginale is a tick-borne pathogen, one of several closely related ehrlichial organisms that cause disease in animals and humans. These Ehrlichia species have complex life cycles that require, in addition to replication and development within the tick vector, evasion of the immune system in order to persist in the mammalian reservoir host. This complexity requires efficient use of the small ehrlichial genome. A. marginale and related ehrlichiae express immunoprotective, variable outer membrane proteins that have similar structures and are encoded by polymorphic multigene families. We show here that the major outer membrane protein of A. marginale, MSP2, is encoded on a polycistronic mRNA. The genomic expression site for this mRNA is polymorphic and encodes numerous amino acid sequence variants in bloodstream populations of A. marginale. A potential mechanism for persistence is segmental gene conversion of the expression site to link hypervariable msp2 sequences to the promoter and polycistron.lld:uniprot
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http://purl.uniprot.org/cit...uniprot:nameInfect. Immun.lld:uniprot
http://purl.uniprot.org/cit...uniprot:authorPalmer G.H.lld:uniprot
http://purl.uniprot.org/cit...uniprot:authorBarbet A.F.lld:uniprot
http://purl.uniprot.org/cit...uniprot:authorRurangirwa F.R.lld:uniprot
http://purl.uniprot.org/cit...uniprot:authorYi J.lld:uniprot
http://purl.uniprot.org/cit...uniprot:authorLundgren A.lld:uniprot
http://purl.uniprot.org/cit...uniprot:date2000lld:uniprot
http://purl.uniprot.org/cit...uniprot:pages6133-6138lld:uniprot
http://purl.uniprot.org/cit...uniprot:titleAntigenic variation of Anaplasma marginale by expression of MSP2 mosaics.lld:uniprot
http://purl.uniprot.org/cit...uniprot:volume68lld:uniprot
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