Molecular Biology and Evolution, Vol 8, 345-355, Copyright © 1991 by Society for Molecular Biology and Evolution
JR Barta, MC Jenkins and HD Danforth
Direct, reverse transcriptase-mediated, partial sequencing of the small-
subunit (16S-like) ribosomal RNA (srRNA) of Eimeria tenella and E.
acervulina was performed. Sequences were aligned by eye with six previously
published, partial or complete srRNA sequences of apicomplexan protists
(Plasmodium berghei, Theileria annulata, Cryptosporidium sp., Toxoplasma
gondii, Sarcocystis muris, and S. gigantea). Six eukaryotic protists (a
slime mold, a yeast, two dinoflagellates, and two ciliates) acted as an
outgroup for a parsimony- based phylogenetic analysis (PAUP Ver. 3.0). The
188 phylogenetically informative sites (i.e., those positions that neither
were unvaried nor had only autapomorphic substitutions) supported a single
tree topology 481 steps in length with a consistency index of 0.65 in which
the monophyly of the Apicomplexa was supported. The two Eimeria species and
S. muris, S. gigantea, and T. gondii formed a pair of monophyletic groups
that were sister groups. The two Sarcocystis species were not hypothesized
to be sister taxa. The genera Plasmodium and Cryptosporidium were
hypothesized to form the sister group to these five coccidia and T.
annulata. A priori data-editing techniques that deleted "variable"
positions prior to analysis failed to recognize the monophyly of the
Apicomplexa when the same parsimony-based tree- building algorithm was
used. Inability of the outgroup taxa to root the well-supported ingroup
tree (Apicomplexa) at a unique site when these taxa were used individually
for this purpose reinforces the need for an appropriate, multiple-taxon
outgroup in such analyses.
ORIGINAL ARTICLE
Evolutionary relationships of avian Eimeria species among other Apicomplexan protozoa: monophyly of the apicomplexa is supported
Department of Pathology, University of Guelph, Ontario, Canada.
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