IJSEM Applied and Environmental Microbiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Moreira, D.
Right arrow Articles by Vickerman, K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Moreira, D.
Right arrow Articles by Vickerman, K.
Agricola
Right arrow Articles by Moreira, D.
Right arrow Articles by Vickerman, K.
Int J Syst Evol Microbiol 54 (2004), 1861-1875; DOI  10.1099/ijs.0.63081-0
© 2004 International Union of Microbiological Societies

An updated view of kinetoplastid phylogeny using environmental sequences and a closer outgroup: proposal for a new classification of the class Kinetoplastea

David Moreira1, Purificación López-García1 and Keith Vickerman2

1 UMR CNRS 8079, Ecologie, Systématique et Evolution, Université Paris-Sud, bâtiment 360, 91405 Orsay Cedex, France
2 Division of Environmental & Evolutionary Biology, University of Glasgow, Glasgow G12 8QQ, UK

Correspondence
David Moreira
david.moreira{at}ese.u-psud.fr

Given their ecological and medical importance, the classification of the kinetoplastid protists (class Kinetoplastea) has attracted much scientific attention for a long time. Morphology-based taxonomic schemes distinguished two major kinetoplastid groups: the strictly parasitic, uniflagellate trypanosomatids and the biflagellate bodonids. Molecular phylogenetic analyses based on 18S rRNA sequence comparison suggested that the trypanosomatids emerged from within the bodonids. However, these analyses revealed a huge evolutionary distance between the kinetoplastids and their closest relatives (euglenids and diplonemids) that makes very difficult the correct inference of the phylogenetic relationships between the different kinetoplastid groups. Using direct PCR amplification of 18S rRNA genes from hydrothermal vent samples, several new kinetoplastid-like sequences have been reported recently. Three of them emerge robustly at the base of the kinetoplastids, breaking the long branch leading to the euglenids and diplonemids. One of these sequences belongs to a close relative of Ichthyobodo necator (a fish parasite) and of the ‘Perkinsiella amoebae’-like endosymbiont of Neoparamoeba spp. amoebae. The authors have studied the reliability of their basal position and used all these slow-evolving basal-emerging sequences as a close outgroup to analyse the phylogeny of the apical kinetoplastids. They thus find a much more stable and resolved kinetoplastid phylogeny, which supports the monophyly of groups that very often emerged as polyphyletic in the trees rooted using the traditional, distant outgroup sequences. A new classification of the class Kinetoplastea is proposed based on the results of the phylogenetic analysis presented. This class is now subdivided into two new subclasses, Prokinetoplastina (accommodating the basal species I. necator and ‘Perkinsiella amoebae’) and Metakinetoplastina (containing the Trypanosomatida together with three additional new orders: Eubodonida, Parabodonida and Neobodonida). The classification of the species formerly included in the genus Bodo is also revised, with the amendment of this genus and the genus Parabodo and the creation of a new genus, Neobodo.


Abbreviations: GTR, general time reversible; kDNA, kinetoplast DNA; LBA, long branch attraction; ML, maximum-likelihood; MP, maximum-parsimony; NJ, neighbour-joining; PP, posterior probability

Published online ahead of print on 12 March 2004 as DOI 10.1099/ijs.0.63081-0.

The GenBank/EMBL/DDBJ accession numbers for the 18S rRNA gene sequences obtained from uncultured kinetoplastid-like species discussed in this study are AF530516 to AF530522.




This article has been cited by other articles:


Home page
Appl. Environ. Microbiol.Home page
A. Behnke, J. Bunge, K. Barger, H.-W. Breiner, V. Alla, and T. Stoeck
Microeukaryote Community Patterns along an O2/H2S Gradient in a Supersulfidic Anoxic Fjord (Framvaren, Norway).
Appl. Envir. Microbiol., May 1, 2006; 72(5): 3626 - 3636.
[Abstract] [Full Text] [PDF]


Home page
Int. J. Syst. Evol. Microbiol.Home page
S. von der Heyden and T. Cavalier-Smith
Culturing and environmental DNA sequencing uncover hidden kinetoplastid biodiversity and a major marine clade within ancestrally freshwater Neobodo designis
Int J Syst Evol Microbiol, November 1, 2005; 55(6): 2605 - 2621.
[Abstract] [Full Text] [PDF]


Home page
Int. J. Syst. Evol. Microbiol.Home page
T. Stoeck, M. V. J. Schwarz, J. Boenigk, M. Schweikert, S. von der Heyden, and A. Behnke
Cellular identity of an 18S rRNA gene sequence clade within the class Kinetoplastea: the novel genus Actuariola gen. nov. (Neobodonida) with description of the type species Actuariola framvarensis sp. nov.
Int J Syst Evol Microbiol, November 1, 2005; 55(6): 2623 - 2635.
[Abstract] [Full Text] [PDF]


Home page
Eukaryot CellHome page
W. Marande, J. Lukes, and G. Burger
Unique Mitochondrial Genome Structure in Diplonemids, the Sister Group of Kinetoplastids
Eukaryot. Cell, June 1, 2005; 4(6): 1137 - 1146.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 2004 by the International Union of Microbiological Societies.