Evidence map›Paper›PMID 20974003›Full record

ArticleBMC genomics2010

A novel multifunctional oligonucleotide microarray for Toxoplasma gondii.

Amit Bahl, Paul H Davis, Michael Behnke, Florence Dzierszinski, Manjunatha Jagalur, Feng Chen, Dhanasekaran Shanmugam, Michael W White, David Kulp, David S Roos

Abstract read
In one paragraph

Article in BMC genomics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
–field-weighted citation impact
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

33 citing papers in PubMed.

  1. Article
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  4. R Script Approach to InferBioinformatics and biology insights · 2017
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  18. ApiAP2 transcription factor restricts development of the Toxoplasma tissue cyst.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  19. Article
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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

10 authors.

Amit BahlGenomics and Computational Biology, University of Pennsylvania, Philadelphia, PA 19104, USA.
Paul H Davis
Michael Behnke
Florence Dzierszinski
Manjunatha Jagalur
Feng Chen
Dhanasekaran Shanmugam
Michael W White
David Kulp
David S Roos

Funding

ZINC FINGER-INSPIRED FLUORESCENT CHEMOSENSORSP20RR016469 · NCRR · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI TURPEN, JAMES B · 2001 to 2011
$36.2M
GENETIC DISSECTION OF TOXOPLASMA GONDIIR37AI028724 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI ROOS, DAVID S. · 1999 to 2008
$4.3M
Improved design and analysis of diploid resequencing microarraysR01HG003880 · NHGRI · UNIVERSITY OF MASSACHUSETTS AMHERST · PI KULP, DAVID · 2006 to 2008
$711k
Transcriptional mechanisms in Toxoplasma gondiiR21AI072739 · NIAID · MONTANA STATE UNIVERSITY - BOZEMAN · PI WHITE, MICHAEL W · 2007 to 2008
$386k
Molecular Dissection of Early Toxoplasma gondii Bradyzoite DifferentiationF32AI077268 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI DAVIS, PAUL H · 2008 to 2010
$112k
FOLATE METABOLISM AND DRUG RESISTANCE IN TOXOPLASMAR01AI028724 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI ROOS, DAVID S. · 1989 to 1997
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NCRR NIH HHS RR016469NHGRI NIH HHS HG003880NIAID NIH HHS AI028724NIAID NIH HHS AI072739NIAID NIH HHS AI077268
6 · The paper itself

Abstract

backgroundMicroarrays are invaluable tools for genome interrogation, SNP detection, and expression analysis, among other applications. Such broad capabilities would be of value to many pathogen research communities, although the development and use of genome-scale microarrays is often a costly undertaking. Therefore, effective methods for reducing unnecessary probes while maintaining or expanding functionality would be relevant to many investigators.

resultsTaking advantage of available genome sequences and annotation for Toxoplasma gondii (a pathogenic parasite responsible for illness in immunocompromised individuals) and Plasmodium falciparum (a related parasite responsible for severe human malaria), we designed a single oligonucleotide microarray capable of supporting a wide range of applications at relatively low cost, including genome-wide expression profiling for Toxoplasma, and single-nucleotide polymorphism (SNP)-based genotyping of both T. gondii and P. falciparum. Expression profiling of the three clonotypic lineages dominating T. gondii populations in North America and Europe provides a first comprehensive view of the parasite transcriptome, revealing that ~49% of all annotated genes are expressed in parasite tachyzoites (the acutely lytic stage responsible for pathogenesis) and 26% of genes are differentially expressed among strains. A novel design utilizing few probes provided high confidence genotyping, used here to resolve recombination points in the clonal progeny of sexual crosses. Recent sequencing of additional T. gondii isolates identifies >620 K new SNPs, including ~11 K that intersect with expression profiling probes, yielding additional markers for genotyping studies, and further validating the utility of a combined expression profiling/genotyping array design. Additional applications facilitating SNP and transcript discovery, alternative statistical methods for quantifying gene expression, etc. are also pursued at pilot scale to inform future array designs.

conclusionsIn addition to providing an initial global view of the T. gondii transcriptome across major lineages and permitting detailed resolution of recombination points in a historical sexual cross, the multifunctional nature of this array also allowed opportunities to exploit probes for purposes beyond their intended use, enhancing analyses. This array is in widespread use by the T. gondii research community, and several aspects of the design strategy are likely to be useful for other pathogens.

Indexed as

AnimalsExonsGene Expression ProfilingGene Expression RegulationGenotypeHost-Parasite InteractionsHumansMiceModels, GeneticOligonucleotide Array Sequence AnalysisParasitesPhylogenyPolymorphism, Single NucleotideReproducibility of ResultsRNA, MessengerSpecies SpecificityRNA, Messenger

Identifiers

PMID20974003
PMCPMC3017859

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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.