Babesia microti-Group Parasites Compared Phylogenetically by Complete Sequencing of the CCT eta Gene in 36 Isolates

Babesia microti, the erythroparasitie Cause or human babesiosis. has long been taken to be a single species because classification by parasite morphology and host spectrum blurred distinctions between the parasites. Phylogenetic analyses of the 18S ribosomal RNA gene (18S rDNA) and, more recently, the beta-tubulin gene have Suggested inter-group heterogeneity. Intra-group relationships, however, remain unknown. This Study Was Conducted to clarify the intra- and inter-group phylogenetic features of the B. microti-group parasites with the eta subunit of the chaperonin-containing t-complex polypeptide I (CCT eta) gene as a candidate genetic marker for defining the B. microti group. We prepared complete sequences or the CCT eta gene from 36 piroplasms and compared the phylogenetic trees. The B. microti-group parasites clustered in a monophyletic assemblage separate from the Babesia sensu stricto and Theileria genera and subdivided predominantly into 4 clades (U.S., Kobe, Hobetsu, Munich) With highly significant evolutionary distances between the clades, B. rodhaini branched at the base of the B. microti-group parasites. Ill addition, a unique intron presence/absence matrix not observable in I SS rDNA or beta-tubulin set the B. microti group entirely apart from either Babesia sensu stricto or Theileria. These results have strong implications for public health, suggesting that the B. microti-group parasites are a full-fledged genus comprising, for now, four core species, i.e., U.S., Kobe, Hobetsu, and Munich species nova. Furthermore, the CCT eta gene is all instructive and definitive genetic marker for analyzing B. microti and related parasites.