Evidence map›Paper›PMID 15747257›Full record

ArticleThe Journal of infectious diseases2005

In vivo transcriptome of Plasmodium falciparum reveals overexpression of transcripts that encode surface proteins.

Johanna P Daily, Karine G Le Roch, Ousmane Sarr, Daouda Ndiaye, Amanda Lukens, Yingyao Zhou, Omar Ndir, Soulyemane Mboup, Ali Sultan, Elizabeth A Winzeler and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
11.8field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

49 citing papers in PubMed, 107 citations in OpenAlex.

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  8. Merozoite Proteins Discovered by qRT-PCR-Based Transcriptome Screening ofFrontiers in cellular and infection microbiology · 2021
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  20. A subset of group A-like var genes encodes the malaria parasite ligands for binding to human brain endothelial cells.Proceedings of the National Academy of Sciences of the United States of America · 2012
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 5 institutions in 2 countries.

Johanna P DailyDepartment of Immunology and Infectious Disease, Harvard School of Public Health, Boston, Massachusetts 02115, USA. jdaily@partners.org
Karine G Le Roch
Ousmane Sarr
Daouda Ndiaye
Amanda Lukens
Yingyao Zhou
Omar Ndir
Soulyemane Mboup
Ali Sultan
Elizabeth A Winzeler
Dyann F Wirth
Cheikh Anta Diop University · SNHarvard University · USScripps Research Institute · USBrigham and Women's Hospital · USGenomics Institute of the Novartis Research Foundation · US

Funding

TRAINING IN MALARIA PATHOGENESIS AND DIVERSITY IN AFRICAD43TW001503 · FIC · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI WIRTH, DYANN F · 2000 to 2009
$1.6M
Drug resistance in Plasmodium falciparumK23AI054518 · NIAID · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI DAILY, JOHANNA PATRICIA · 2003 to 2007
$623k
FIC NIH HHS 5D43TW001503FIC NIH HHS D43 TW001503NIAID NIH HHS 5K23AI054518NIAID NIH HHS K23 AI054518
6 · The paper itself

Abstract

Infections with the human parasite Plasmodium falciparum continue to present a great challenge to global health. Fundamental questions regarding the molecular basis of virulence and immune evasion in P. falciparum have been only partially answered. Because of the parasite's intracellular location and complex life cycle, standard genetic approaches to the study of the pathogenesis of malaria have been limited. The present study presents a novel approach to the identification of the biological processes involved in host-pathogen interactions, one that is based on the analysis of in vivo P. falciparum transcripts. We demonstrate that a sufficient quantity of P. falciparum RNA transcripts can be derived from a small blood sample from infected patients for whole-genome microarray analysis. Overall, excellent correlation was observed between the transcriptomes derived from in vivo samples and in vitro samples with ring-stage P. falciparum 3D7 reference strain. However, gene families that encode surface proteins are overexpressed in vivo. Moreover, this analysis has identified a new family of hypothetical genes that may encode surface variant antigens. Comparative studies of the transcriptomes derived from in vivo samples and in vitro 3D7 samples may identify important strategies used by the pathogen for survival in the human host and highlight, for vaccine development, new candidate antigens that were not previously identified through the use of in vitro cultures.

Indexed as

Gene Expression ProfilingGene Expression RegulationAdaptation, PhysiologicalAdultAmino Acid SequenceAnimalsChildFemaleGenes, ProtozoanHost-Parasite InteractionsHumansMalaria, FalciparumMaleMembrane ProteinsMolecular Sequence DataOligonucleotide Array Sequence AnalysisMembrane ProteinsProtozoan ProteinsRNA, MessengerRNA, Protozoan

Identifiers

PMID15747257
PMCPMC2582152
OpenAlexW2110952939

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.