
pmid: 18977349
The first and second internal transcribed spacers (ITS1, ITS2) as well as the intervening 5.8S coding region of the rRNA gene for six Babesia spp. isolated from different geographic origins were characterized. Varying degrees of ITS1 and ITS2 intra- and inter-species sequence polymorphism were found among these isolates. Phylogenetic analysis of the ITS1-5.8S gene-ITS2 region clearly separated the isolates into two clusters. One held an unidentified Babesia sp. transmitted by Hyalomma anatolicum anatolicum. The second held five other isolates, which were considered to be Babesia motasi. Each Babesia species cluster possessed ITS1 and ITS2 of unique size(s) and species specific nucleotide sequences. The results showed that ITS1, ITS2 and the complete ITS1-5.8S-ITS2 region could be used to discriminate these ovine Babesia spp. effectively.
Genetic Markers, China, Polymorphism, Genetic, Sheep, Base Sequence, Ixodidae, Molecular Sequence Data, Babesia, RNA, Ribosomal, 5.8S, DNA, Ribosomal Spacer, Animals, Sequence Alignment, Phylogeny
Genetic Markers, China, Polymorphism, Genetic, Sheep, Base Sequence, Ixodidae, Molecular Sequence Data, Babesia, RNA, Ribosomal, 5.8S, DNA, Ribosomal Spacer, Animals, Sequence Alignment, Phylogeny
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