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PMID: 18046333 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Distinct physiological states of Plasmodium falciparum in malaria-infected patients.

Nature ·Vol. 450 ·No. 7172 ·2007-12-13 ·Pages 1091-5

Daily JP, Scanfeld D, Pochet N, Le Roch K, Plouffe D, Kamal M, Sarr O, Mboup S, Ndir O, Wypij D, Levasseur K, Thomas E, Tamayo P, Dong C, Zhou Y, Lander ES, Ndiaye D, Wirth D, Winzeler EA, Mesirov JP, Regev A

Abstract

Infection with the malaria parasite Plasmodium falciparum leads to widely different clinical conditions in children, ranging from mild flu-like symptoms to coma and death. Despite the immense medical implications, the genetic and molecular basis of this diversity remains largely unknown. Studies of in vitro gene expression have found few transcriptional differences between different parasite strains. Here we present a large study of in vivo expression profiles of parasites derived directly from blood samples from infected patients. The in vivo expression profiles define three distinct transcriptional states. The biological basis of these states can be interpreted by comparison with an extensive compendium of expression data in the yeast Saccharomyces cerevisiae. The three states in vivo closely resemble, first, active growth based on glycolytic metabolism, second, a starvation response accompanied by metabolism of alternative carbon sources, and third, an environmental stress response. The glycolytic state is highly similar to the known profile of the ring stage in vitro, but the other states have not been observed in vitro. The results reveal a previously unknown physiological diversity in the in vivo biology of the malaria parasite, in particular evidence for a functional mitochondrion in the asexual-stage parasite, and indicate in vivo and in vitro studies to determine how this variation may affect disease manifestations and treatment.

MeSH Terms
Animals Cluster Analysis Fatty Acids/metabolism Gene Expression Profiling Gene Expression Regulation Glycolysis/genetics Humans Malaria, Falciparum/blood,parasitology Oligonucleotide Array Sequence Analysis Plasmodium falciparum/genetics,growth & development,metabolism,pathogenicity Transcription, Genetic Tricarboxylic Acids/metabolism
Chemicals
Fatty Acids Tricarboxylic Acids
Authors & Affiliations
21 authors, click to expand affiliations / ORCID
Daily J P
Department of Immunology and Infectious Disease, [Harvard School of Public Health, 665 Huntington Avenue, Boston, Massachusetts 02115, USA.
Scanfeld D
Pochet N
Le Roch K
Plouffe D
Kamal M
Sarr O
Mboup S
Ndir O
Wypij D
Levasseur K
Thomas E
Tamayo P
Dong C
Zhou Y
Lander E S
Ndiaye D
Wirth D
Winzeler E A
Mesirov J P
Regev A
Article Info
Journal
Nature
Abbr.
Nature
ISSN
1476-4687
Published
2007-12-13
Epub
2007-00-28
Pages
1091-5
Language
English
Region
England
NLM ID
0410462
Subset
IM
Grants
NIAID NIH HHS · K23 AI054518 · United States
Databases
GEO
Corrections
CommentIn
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