Distinct physiological states of Plasmodium falciparum in malaria-infected patients
Triple identity for malaria A major puzzle in understanding malaria is the wide range of clinical conditions seen in infected children — from mild flu-like symptoms to coma and death. A large-scale transcriptional analysis of malaria parasites isolated from human patients has uncovered a possible cl...
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Veröffentlicht in: | Nature 2007-12, Vol.450 (7172), p.1091-1095 |
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description | Triple identity for malaria
A major puzzle in understanding malaria is the wide range of clinical conditions seen in infected children — from mild flu-like symptoms to coma and death. A large-scale transcriptional analysis of malaria parasites isolated from human patients has uncovered a possible clue to this variation:
Plasmodium falciparum
exists in its human host in three different physiological states. These can be described as active growth, a response to starvation, and an environmental stress response. This finding has important implications both for treatment with current drugs and for future drug and vaccine development.
This study presents the first large scale transcriptional analysis of malaria parasites isolated from human patients, and defines three distinct transcriptional patterns that can be described as active growth, response to starvation and environmental stress response.
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
1
. Despite the immense medical implications, the genetic and molecular basis of this diversity remains largely unknown
2
. Studies of
in vitro
gene expression have found few transcriptional differences between different parasite strains
3
. 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. |
doi_str_mv | 10.1038/nature06311 |
format | Article |
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A major puzzle in understanding malaria is the wide range of clinical conditions seen in infected children — from mild flu-like symptoms to coma and death. A large-scale transcriptional analysis of malaria parasites isolated from human patients has uncovered a possible clue to this variation:
Plasmodium falciparum
exists in its human host in three different physiological states. These can be described as active growth, a response to starvation, and an environmental stress response. This finding has important implications both for treatment with current drugs and for future drug and vaccine development.
This study presents the first large scale transcriptional analysis of malaria parasites isolated from human patients, and defines three distinct transcriptional patterns that can be described as active growth, response to starvation and environmental stress response.
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
1
. Despite the immense medical implications, the genetic and molecular basis of this diversity remains largely unknown
2
. Studies of
in vitro
gene expression have found few transcriptional differences between different parasite strains
3
. 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.</description><identifier>ISSN: 0028-0836</identifier><identifier>EISSN: 1476-4687</identifier><identifier>EISSN: 1476-4679</identifier><identifier>DOI: 10.1038/nature06311</identifier><identifier>PMID: 18046333</identifier><identifier>CODEN: NATUAS</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Animals ; Biological and medical sciences ; Biomedical research ; Blood ; Blood tests ; Carbon sources ; Cluster Analysis ; Diagnosis ; Environmental stress ; Fatty Acids - metabolism ; Gene expression ; Gene Expression Profiling ; Gene Expression Regulation ; Genetic aspects ; Genetic transcription ; Glycolysis - genetics ; Health aspects ; Human protozoal diseases ; Humanities and Social Sciences ; Humans ; Infectious diseases ; letter ; Malaria ; Malaria, Falciparum - blood ; Malaria, Falciparum - parasitology ; Medical sciences ; Metabolism ; multidisciplinary ; Oligonucleotide Array Sequence Analysis ; Parasites ; Parasitic diseases ; Parasitology ; Physiology ; Plasmodium falciparum ; Plasmodium falciparum - genetics ; Plasmodium falciparum - growth & development ; Plasmodium falciparum - metabolism ; Plasmodium falciparum - pathogenicity ; Protozoal diseases ; Saccharomyces cerevisiae ; Science ; Science (multidisciplinary) ; Transcription, Genetic ; Tricarboxylic Acids - metabolism ; Vector-borne diseases ; Yeasts</subject><ispartof>Nature, 2007-12, Vol.450 (7172), p.1091-1095</ispartof><rights>Springer Nature Limited 2007</rights><rights>2008 INIST-CNRS</rights><rights>COPYRIGHT 2007 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Dec 13, 2007</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1125t-e336b440878e2e84212cba25694c3ed717fd7d979817423fdf39b010f0f611fa3</citedby><cites>FETCH-LOGICAL-c1125t-e336b440878e2e84212cba25694c3ed717fd7d979817423fdf39b010f0f611fa3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/nature06311$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/nature06311$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19893825$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18046333$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Daily, J. P.</creatorcontrib><creatorcontrib>Scanfeld, D.</creatorcontrib><creatorcontrib>Pochet, N.</creatorcontrib><creatorcontrib>Le Roch, K.</creatorcontrib><creatorcontrib>Plouffe, D.</creatorcontrib><creatorcontrib>Kamal, M.</creatorcontrib><creatorcontrib>Sarr, O.</creatorcontrib><creatorcontrib>Mboup, S.</creatorcontrib><creatorcontrib>Ndir, O.</creatorcontrib><creatorcontrib>Wypij, D.</creatorcontrib><creatorcontrib>Levasseur, K.</creatorcontrib><creatorcontrib>Thomas, E.</creatorcontrib><creatorcontrib>Tamayo, P.</creatorcontrib><creatorcontrib>Dong, C.</creatorcontrib><creatorcontrib>Zhou, Y.</creatorcontrib><creatorcontrib>Lander, E. S.</creatorcontrib><creatorcontrib>Ndiaye, D.</creatorcontrib><creatorcontrib>Wirth, D.</creatorcontrib><creatorcontrib>Winzeler, E. A.</creatorcontrib><creatorcontrib>Mesirov, J. P.</creatorcontrib><creatorcontrib>Regev, A.</creatorcontrib><title>Distinct physiological states of Plasmodium falciparum in malaria-infected patients</title><title>Nature</title><addtitle>Nature</addtitle><addtitle>Nature</addtitle><description>Triple identity for malaria
A major puzzle in understanding malaria is the wide range of clinical conditions seen in infected children — from mild flu-like symptoms to coma and death. A large-scale transcriptional analysis of malaria parasites isolated from human patients has uncovered a possible clue to this variation:
Plasmodium falciparum
exists in its human host in three different physiological states. These can be described as active growth, a response to starvation, and an environmental stress response. This finding has important implications both for treatment with current drugs and for future drug and vaccine development.
This study presents the first large scale transcriptional analysis of malaria parasites isolated from human patients, and defines three distinct transcriptional patterns that can be described as active growth, response to starvation and environmental stress response.
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
1
. Despite the immense medical implications, the genetic and molecular basis of this diversity remains largely unknown
2
. Studies of
in vitro
gene expression have found few transcriptional differences between different parasite strains
3
. 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.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Biomedical research</subject><subject>Blood</subject><subject>Blood tests</subject><subject>Carbon sources</subject><subject>Cluster Analysis</subject><subject>Diagnosis</subject><subject>Environmental stress</subject><subject>Fatty Acids - metabolism</subject><subject>Gene expression</subject><subject>Gene Expression Profiling</subject><subject>Gene Expression Regulation</subject><subject>Genetic aspects</subject><subject>Genetic transcription</subject><subject>Glycolysis - genetics</subject><subject>Health aspects</subject><subject>Human protozoal diseases</subject><subject>Humanities and Social Sciences</subject><subject>Humans</subject><subject>Infectious diseases</subject><subject>letter</subject><subject>Malaria</subject><subject>Malaria, Falciparum - blood</subject><subject>Malaria, Falciparum - parasitology</subject><subject>Medical sciences</subject><subject>Metabolism</subject><subject>multidisciplinary</subject><subject>Oligonucleotide Array Sequence Analysis</subject><subject>Parasites</subject><subject>Parasitic diseases</subject><subject>Parasitology</subject><subject>Physiology</subject><subject>Plasmodium falciparum</subject><subject>Plasmodium falciparum - genetics</subject><subject>Plasmodium falciparum - growth & development</subject><subject>Plasmodium falciparum - metabolism</subject><subject>Plasmodium falciparum - pathogenicity</subject><subject>Protozoal diseases</subject><subject>Saccharomyces cerevisiae</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Transcription, Genetic</subject><subject>Tricarboxylic Acids - metabolism</subject><subject>Vector-borne diseases</subject><subject>Yeasts</subject><issn>0028-0836</issn><issn>1476-4687</issn><issn>1476-4679</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqV1Ftv0zAUAOAIgdgYPPGOIiZuggzfEtuPVblNmgCxCR4j17GLp9xmOxL795zRSk2hXYvykMj5fC5WcpLkMUYnGFHxtlVx8AYVFOM7ySFmvMhYIfjd5BAhIjIkaHGQPAjhEiGUY87uJwdYIFZQSg-T83cuRNfqmPY_r4Pr6m7utKrTEFU0Ie1s-rVWoekqNzSpVbV2vfLw6Nq0UbXyTmWutUZHU6W9is60MTxM7oEM5tHyfpR8__D-YvopO_vy8XQ6Ocs0xiSPmaG0mDGGBBeGGMEIJnqmSF5IpqmpOOa24pXkUkDVhNrKUjlDGFlkC4ytokfJi0Xg3ndXgwmxbFzQpq5Va7ohlJxRLCCJBPn8VklznBOKdkOCqGR5TgG-vBVCPEQ5R5wAffoXvewG38LRQDiWF4QyBuh4geaqNiWcaRe90jcxywkIWQhoA1S2Qc1Na7yqu9ZYB8v_7bGkjHPyp_29vJCcSUzxqrU1r3t3VY6L2IrGmbejUbqTDQiuyjROb-x_rw3jMvbbMCrp1doGMNH8inM1hFCenn9br2aXHRey045qeL3dTi5-TD-vR95D_xtb-y4Eb2zZe9cof11iVN7Mn3I0f0A_WX7qw6wx1couBw6AZ0ugAswZ61WrXVg5KSQVJAf3ZuECvGrnxq_-mU15fwNiP4-N</recordid><startdate>20071213</startdate><enddate>20071213</enddate><creator>Daily, J. 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P.</creator><creator>Regev, A.</creator><general>Nature Publishing Group UK</general><general>Nature Publishing</general><general>Nature Publishing Group</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ATWCN</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7T5</scope><scope>7TG</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88G</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>BKSAR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M2O</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PCBAR</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PSYQQ</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>Q9U</scope><scope>R05</scope><scope>RC3</scope><scope>S0X</scope><scope>SOI</scope><scope>F1W</scope><scope>H95</scope><scope>H97</scope><scope>L.G</scope><scope>7SC</scope><scope>7SP</scope><scope>7SR</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>F28</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope></search><sort><creationdate>20071213</creationdate><title>Distinct physiological states of Plasmodium falciparum in malaria-infected patients</title><author>Daily, J. P. ; 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. 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P.</au><au>Scanfeld, D.</au><au>Pochet, N.</au><au>Le Roch, K.</au><au>Plouffe, D.</au><au>Kamal, M.</au><au>Sarr, O.</au><au>Mboup, S.</au><au>Ndir, O.</au><au>Wypij, D.</au><au>Levasseur, K.</au><au>Thomas, E.</au><au>Tamayo, P.</au><au>Dong, C.</au><au>Zhou, Y.</au><au>Lander, E. S.</au><au>Ndiaye, D.</au><au>Wirth, D.</au><au>Winzeler, E. A.</au><au>Mesirov, J. P.</au><au>Regev, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Distinct physiological states of Plasmodium falciparum in malaria-infected patients</atitle><jtitle>Nature</jtitle><stitle>Nature</stitle><addtitle>Nature</addtitle><date>2007-12-13</date><risdate>2007</risdate><volume>450</volume><issue>7172</issue><spage>1091</spage><epage>1095</epage><pages>1091-1095</pages><issn>0028-0836</issn><eissn>1476-4687</eissn><eissn>1476-4679</eissn><coden>NATUAS</coden><abstract>Triple identity for malaria
A major puzzle in understanding malaria is the wide range of clinical conditions seen in infected children — from mild flu-like symptoms to coma and death. A large-scale transcriptional analysis of malaria parasites isolated from human patients has uncovered a possible clue to this variation:
Plasmodium falciparum
exists in its human host in three different physiological states. These can be described as active growth, a response to starvation, and an environmental stress response. This finding has important implications both for treatment with current drugs and for future drug and vaccine development.
This study presents the first large scale transcriptional analysis of malaria parasites isolated from human patients, and defines three distinct transcriptional patterns that can be described as active growth, response to starvation and environmental stress response.
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
1
. Despite the immense medical implications, the genetic and molecular basis of this diversity remains largely unknown
2
. Studies of
in vitro
gene expression have found few transcriptional differences between different parasite strains
3
. 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.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>18046333</pmid><doi>10.1038/nature06311</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0028-0836 |
ispartof | Nature, 2007-12, Vol.450 (7172), p.1091-1095 |
issn | 0028-0836 1476-4687 1476-4679 |
language | eng |
recordid | cdi_proquest_miscellaneous_743183369 |
source | MEDLINE; SpringerLink Journals; Nature |
subjects | Animals Biological and medical sciences Biomedical research Blood Blood tests Carbon sources Cluster Analysis Diagnosis Environmental stress Fatty Acids - metabolism Gene expression Gene Expression Profiling Gene Expression Regulation Genetic aspects Genetic transcription Glycolysis - genetics Health aspects Human protozoal diseases Humanities and Social Sciences Humans Infectious diseases letter Malaria Malaria, Falciparum - blood Malaria, Falciparum - parasitology Medical sciences Metabolism multidisciplinary Oligonucleotide Array Sequence Analysis Parasites Parasitic diseases Parasitology Physiology Plasmodium falciparum Plasmodium falciparum - genetics Plasmodium falciparum - growth & development Plasmodium falciparum - metabolism Plasmodium falciparum - pathogenicity Protozoal diseases Saccharomyces cerevisiae Science Science (multidisciplinary) Transcription, Genetic Tricarboxylic Acids - metabolism Vector-borne diseases Yeasts |
title | Distinct physiological states of Plasmodium falciparum in malaria-infected patients |
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