Paralogs vs. genotypes? Variability of Babesia canis assessed by 18S rDNA and two mitochondrial markers
Language English Country Netherlands Media print-electronic
Document type Journal Article
PubMed
30736942
DOI
10.1016/j.vetpar.2018.12.017
PII: S0304-4017(19)30017-2
Knihovny.cz E-resources
- Keywords
- 18S rDNA paralog, Babesia canis, COI, Cytb, Genotype,
- MeSH
- Babesia genetics MeSH
- Babesiosis blood diagnosis parasitology MeSH
- Phylogeny MeSH
- Genetic Variation * MeSH
- Genetic Markers MeSH
- Genome, Protozoan MeSH
- Genotype * MeSH
- Haplotypes MeSH
- Cohort Studies MeSH
- Mitochondria genetics MeSH
- Dog Diseases diagnosis parasitology MeSH
- DNA, Protozoan genetics MeSH
- Dogs MeSH
- RNA, Ribosomal, 18S genetics MeSH
- Sequence Analysis, DNA MeSH
- Animals MeSH
- Check Tag
- Dogs MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Geographicals
- Europe MeSH
- Names of Substances
- Genetic Markers MeSH
- DNA, Protozoan MeSH
- RNA, Ribosomal, 18S MeSH
Canine babesiosis caused by Babesia canis sensu stricto became an emerging disease of dogs across Europe calling for attention also in countries where it was an only rare imported disease. An easy accessibility of molecular methods and the growing amount of sequencing data led to the description of intraspecific variability in 18S rDNA sequences designated as "genotypes". Using material from a homogenous cohort of dogs with microscopically confirmed canine babesiosis caused by B. canis, we evaluated Babesia intraspecific variability and amplification sensitivity of three different genes (18S rDNA, COI, Cytb) to assess their potential as diagnostic or phylogenetic markers. In raw sequencing data obtained, we observed at least 3 ambiguous positions in up to 86% of chromatograms within the ∼560 bp fragment of 18S rDNA suggesting the existence of several, not identical copies of this gene. Our COI haplotype analysis resulted in a star-like pattern indicating a recent origin of most haplotypes, but not supporting the existence of two dominant haplotypes. Similarly, the Cytb sequences obtained from samples with all variants of 18S rDNA were identical. We corroborate previous observations from three other European countries and bring the evidence of the existence of 18S rDNA paralogs in B. canis genome replacing currently used "genotype" theory.
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