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dc.creatorGraca, Telmo
dc.creatorParadiso, Lydia
dc.creatorBroschat, Shira L.
dc.creatorNoh, Susan M.
dc.creatorPalmer, Guy H.
dc.date.accessioned2016-03-22T00:17:25Z
dc.date.available2016-03-22T00:17:25Z
dc.date.issued2015-11
dc.identifier.urihttp://hdl.handle.net/2376/6004
dc.description.abstractAntigenic variation allows microbial pathogens to evade immune clearance and establish persistent infection. Anaplasma marginale utilizes gene conversion of a repertoire of silent msp2 alleles into a single active expression site to encode unique Msp2 variants. As the genomic complement of msp2 alleles alone is insufficient to generate the number of variants required for persistence, A. marginale uses segmental gene conversion, in which oligonucleotide segments from multiple alleles are recombined into the expression site to generate a novel msp2 mosaic, not represented elsewhere in the genome. Whether these segmental changes are sufficient to evade a broad antibody response is unknown. We addressed this question by identifying Msp2 variants that differed in primary structure within the immunogenic hypervariable region microdomains and tested whether these represented true antigenic variants. The minimal primary structural difference between variants was a single amino acid resulting from a codon insertion and overall the amino acid identity among paired microdomains ranged from 18-92%. Collectively, 89% of the expressed structural variants were also antigenic variants across all biological replicates, independent of a specific host major histocompatibility complex haplotype. Biologic relevance is supported by the following: i) all structural variants were expressed during infection of a natural host; ii) the structural variation observed in the microdomains corresponded to the mean length of variants generated by segmental gene conversion; and iii) antigenic variants were identified using a broad antibody response that developed during infection of a natural host. The findings demonstrate that segmental gene conversion efficiently generates Msp2 antigenic variants.en_US
dc.language.isoEnglish
dc.publisherInfection and Immunityen_US
dc.rightsIn copyright
dc.rightsopenAccess
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/
dc.rights.urihttp://purl.org/eprint/accessRights/OpenAccess
dc.subjectAntigenic variationen_US
dc.subjectImmunologyen_US
dc.subjectMicrobial pathogensen_US
dc.titlePrimary structural variation in Anaplasma marginale Msp2 efficiently generates immune escape variants
dc.typeText
dc.description.citationGraca, T., L. Paradiso, S.L. Broschat, S. Noh, and G. Palmer, ���Primary structural variation in Anaplasma marginale Msp2 efficiently generates immune escape variants,�� Infection and Immunity, Vol. 83, No. 11, pp. 4178-4184, Nov. 2015. doi:10.1128/IAI.00851-15.


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  • Broschat, Shira
    This collection features research and educational materials by Shira Broschat, Professor and Curriculum Coordinator for the School of Electrical Engineering and Computer Science at Washington State University.

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