Rhoptry-associated protein (rap-1) genes in the sheep pathogen Babesia sp. Xinjiang: Multiple transcribed copies differing by 3′ end repeated sequences
•We demonstrated the presence of tandemly arranged copies of rap-1a in Babesia sp. Xinjiang.•These copies varied in the 3′ region, due to the presence of a variable number of 36bp repeats.•These copies were probably generated by gene duplication and gene conversion.•At least 6 of the 7 copies are tr...
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Veröffentlicht in: | Veterinary parasitology 2015-07, Vol.211 (3-4), p.158-169 |
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Zusammenfassung: | •We demonstrated the presence of tandemly arranged copies of rap-1a in Babesia sp. Xinjiang.•These copies varied in the 3′ region, due to the presence of a variable number of 36bp repeats.•These copies were probably generated by gene duplication and gene conversion.•At least 6 of the 7 copies are transcribed in vitro cultivated parasite.•The 5′ UTR region contains the 3 boxes conserved in all rap-1 intergenic regions analyzed.
Sheep babesiosis occurs mainly in tropical and subtropical areas. The sheep parasite Babesia sp. Xinjiang is widespread in China, and our goal is to characterize rap-1 (rhoptry-associated protein 1) gene diversity and expression as a first step of a long term goal aiming at developing a recombinant subunit vaccine. Seven different rap-1a genes were amplified in Babesia sp. Xinjiang, using degenerate primers designed from conserved motifs. Rap-1b and rap-1c gene types could not be identified. In all seven rap-1a genes, the 5′ regions exhibited identical sequences over 936nt, and the 3′ regions differed at 28 positions over 147nt, defining two types of genes designated α and β. The remaining 3′ part varied from 72 to 360nt in length, depending on the gene. This region consists of a succession of two to ten 36nt repeats, which explains the size differences. Even if the nucleotide sequences varied, 6 repeats encoded the same stretch of amino acids. Transcription of at least four α and two β genes was demonstrated by standard RT-PCR. |
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ISSN: | 0304-4017 1873-2550 |
DOI: | 10.1016/j.vetpar.2015.04.030 |