Literature DB >> 18180199

Implications of the new eukaryotic systematics for parasitologists.

Joel B Dacks1, Giselle Walker, Mark C Field.   

Abstract

An accurate understanding of evolutionary relationships is central in biology. For parasitologists, understanding the relationships among eukaryotic organisms allows the prediction of virulence mechanisms, reconstruction of metabolic pathways, identification of potential drug targets, elucidation of parasite-specific cellular processes and understanding of interactions with the host or vector. Here we consider the impact of major recent revisions of eukaryotic systematics and taxonomy on parasitology. The previous, ladder-like model placed some protists as early diverging, with the remaining eukaryotes "progressing" towards a "crown radiation" of animals, plants, Fungi and some additional protistan lineages. This model has been robustly disproven. The new model is based on vastly increased amounts of molecular sequence data, integration with morphological information and the rigorous application of phylogenetic methods to those data. It now divides eukaryotes into six major supergroups; the relationships between those groups and the order of branching remain unknown. This new eukaryotic phylogeny emphasizes that organisms including Giardia, Trypanosoma and Trichomonas are not primitive, but instead highly evolved and specialised for their specific environments. The wealth of newly available comparative genomic data has also allowed the reconstruction of ancient suites of characteristics and mapping of character evolution in diverse parasites. For example, the last common eukaryotic ancestor was apparently complex, suggesting that lineage-specific adaptations and secondary losses have been important in the evolution of protistan parasites. Referring to the best evidence-based models for eukaryotic evolution will allow parasitologists to make more accurate and reliable inferences about pathogens that cause significant morbidity and mortality.

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Year:  2007        PMID: 18180199     DOI: 10.1016/j.parint.2007.11.004

Source DB:  PubMed          Journal:  Parasitol Int        ISSN: 1383-5769            Impact factor:   2.230


  24 in total

Review 1.  Evolution of macromolecular import pathways in mitochondria, hydrogenosomes and mitosomes.

Authors:  Trevor Lithgow; André Schneider
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2010-03-12       Impact factor: 6.237

2.  Functional analysis of sequence motifs involved in the polyadenylation of Trichomonas vaginalis mRNAs.

Authors:  Vanessa Fuentes; Guadalupe Barrera; Joaquín Sánchez; Roberto Hernández; Imelda López-Villaseñor
Journal:  Eukaryot Cell       Date:  2012-03-30

3.  Comparative analyses among the Trichomonas vaginalis, Trichomonas tenax, and Tritrichomonas foetus 5S ribosomal RNA genes.

Authors:  Ana Lilia Torres-Machorro; Roberto Hernández; John F Alderete; Imelda López-Villaseñor
Journal:  Curr Genet       Date:  2009-03-17       Impact factor: 3.886

4.  Mitochondrial outer membrane proteome of Trypanosoma brucei reveals novel factors required to maintain mitochondrial morphology.

Authors:  Moritz Niemann; Sebastian Wiese; Jan Mani; Astrid Chanfon; Christopher Jackson; Chris Meisinger; Bettina Warscheid; André Schneider
Journal:  Mol Cell Proteomics       Date:  2012-12-06       Impact factor: 5.911

Review 5.  New eukaryotic systematics: a phylogenetic perspective of developmental gene expression in the Apicomplexa.

Authors:  Mathieu Gissot; Kami Kim; Dick Schaap; James W Ajioka
Journal:  Int J Parasitol       Date:  2008-10-21       Impact factor: 3.981

6.  The canonical pathway for selenocysteine insertion is dispensable in Trypanosomes.

Authors:  Eric Aeby; Sotiria Palioura; Mascha Pusnik; Janine Marazzi; Allyson Lieberman; Elisabetta Ullu; Dieter Söll; André Schneider
Journal:  Proc Natl Acad Sci U S A       Date:  2009-03-11       Impact factor: 11.205

7.  The mitochondrial genome and a 60-kb nuclear DNA segment from Naegleria fowleri, the causative agent of primary amoebic meningoencephalitis.

Authors:  Emily K Herman; Alexander L Greninger; Govinda S Visvesvara; Francine Marciano-Cabral; Joel B Dacks; Charles Y Chiu
Journal:  J Eukaryot Microbiol       Date:  2013-01-29       Impact factor: 3.346

8.  Trypanosoma brucei harbours a divergent XPB helicase paralogue that is specialized in nucleotide excision repair and conserved among kinetoplastid organisms.

Authors:  Nitika Badjatia; Tu N Nguyen; Ju Huck Lee; Arthur Günzl
Journal:  Mol Microbiol       Date:  2013-11-08       Impact factor: 3.501

9.  Evidence for a shared nuclear pore complex architecture that is conserved from the last common eukaryotic ancestor.

Authors:  Jeffrey A DeGrasse; Kelly N DuBois; Damien Devos; T Nicolai Siegel; Andrej Sali; Mark C Field; Michael P Rout; Brian T Chait
Journal:  Mol Cell Proteomics       Date:  2009-06-13       Impact factor: 5.911

10.  Hydroxyurea-induced synchronisation of bloodstream stage Trypanosoma brucei.

Authors:  Glynn R Forsythe; Richard McCulloch; Tansy C Hammarton
Journal:  Mol Biochem Parasitol       Date:  2008-12-27       Impact factor: 1.759

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