Abstract
Blastocystis is a unicellular stramenopile of controversial pathogenicity in humans [1, 2]. Although it is a strict anaerobe, Blastocystis has mitochondrion-like organelles with cristae, a transmembrane potential and DNA [2-4]. An apparent lack of several typical mitochondrial pathways has led some to suggest that these organelles might be hydrogenosomes, anaerobic organelles related to mitochondria [5, 6]. We generated 12,767 expressed sequence tags (ESTs) from Blastocystis and identified 115 clusters that encode putative mitochondrial and hydrogenosomal proteins. Among these is the canonical hydrogenosomal protein iron-only [FeFe] hydrogenase that we show localizes to the organelles. The organelles also have mitochondrial characteristics, including pathways for amino acid metabolism, iron-sulfur cluster biogenesis, and an incomplete tricarboxylic acid cycle as well as a mitochondrial genome. Although complexes I and II of the electron transport chain (ETC) are present, we found no evidence for complexes III and IV or F1Fo ATPases. The Blastocystis organelles have metabolic properties of aerobic and anaerobic mitochondria and of hydrogenosomes [7, 8]. They are convergently similar to organelles recently described in the unrelated ciliate Nyctotherus ovalis [9]. These findings blur the boundaries between mitochondria, hydrogenosomes, and mitosomes, as currently defined, underscoring the disparate selective forces that shape these organelles in eukaryotes.
Original language | English |
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Pages (from-to) | 580-585 |
Number of pages | 6 |
Journal | Current Biology |
Volume | 18 |
Issue number | 8 |
DOIs | |
Publication status | Published - Apr 22 2008 |
Bibliographical note
Funding Information:A.S. is supported by a postdoctoral fellowship from the Canadian Institutes of Health Research. K.H. is supported by a Queen Mary University of London PhD Studentship. A.J.R. is supported by a New Investigator fellowship from the Canadian Institutes of Health Research (CIHR), the Canadian Institute for Advanced Research, and a Natural Sciences and Engineering Research Council of Canada E.W.R. Steacie Memorial fellowship. EST data from Blastocystis were generated as part of the Genome Canada sponsored Protist EST Program. This work was supported by CIHR grant MOP-62809 awarded to A.J.R. The cell biology and mitochondrial genome sequencing were supported by grant 078566/A/05/Z from the Wellcome Trust awarded to M.v.d.G. and C.G.C. A.S. and A.J.R. would like to thank Dr. Maria José Barberà and Dr. Sara Diaz-Triviño for discussions, Jessica Leigh for supplying NADH alignments and help with phylogenetic analyses, Thomas Perley and Jacqueline de Mestral for technical help, Dr. Michael Gray and Dr. Gabino Sanchez-Perez for critically reading the manuscript, and Dr. William Martin and Dr. Louis Tielens for constructive criticism. C.G.C. would like to thank Alex Karcanias for her preliminary work on the mitochondrial genome. C.G.C. and A.J.R. would like to thank Dr. Tetsuo Hashimoto for providing DNA from Blastocystis strain NandII. K.H. and M.v.d.G. would like to thank Dr. Matthew Rogers for discussion. Some of this work formed part of a Master of Science thesis submitted by G.S.R.
ASJC Scopus Subject Areas
- General Neuroscience
- General Biochemistry,Genetics and Molecular Biology
- General Agricultural and Biological Sciences
PubMed: MeSH publication types
- Journal Article
- Research Support, Non-U.S. Gov't