Evidence map›Paper›PMID 34823519›Full record

ArticleMalaria journal2021

Analysis of pir gene expression across the Plasmodium life cycle.

Timothy S Little, Deirdre A Cunningham, Audrey Vandomme, Carlos Talavera Lopez, Sarah Amis, Christopher Alder, John W G Addy, Sarah McLaughlin, Caroline Hosking, George Christophides and 2 more

Open access · goldAbstract read
In one paragraph

Article in Malaria journal, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
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  3. Transcriptome profiling of intrahepatocyticFrontiers in genetics · 2025
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  7. Single-cell analyses of polyclonalResearch square · 2024
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  12. Band 3-mediatedFrontiers in cellular and infection microbiology · 2022
    Article
  13. Differential Trafficking and Expression of PIR Proteins in Acute and ChronicFrontiers in cellular and infection microbiology · 2022
    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

12 authors at 3 institutions in 2 countries.

Timothy S Little *The Francis Crick Institute, London, UK.
Deirdre A Cunningham *The Francis Crick Institute, London, UK.
Audrey VandommeThe Francis Crick Institute, London, UK.
Carlos Talavera LopezThe Francis Crick Institute, London, UK.
Sarah AmisThe Francis Crick Institute, London, UK.
Christopher AlderThe Francis Crick Institute, London, UK.
John W G AddyThe Francis Crick Institute, London, UK.
Sarah McLaughlinThe Francis Crick Institute, London, UK.
Caroline HoskingThe Francis Crick Institute, London, UK.
George ChristophidesImperial College, London, UK.
Adam J ReidWellcome Sanger Institute, Cambridge, CB10 1SA, UK.
Jean LanghorneThe Francis Crick Institute, London, UK. Jean.Langhorne@crick.ac.uk.ORCID http://orcid.org/0000-0002-2257-9733
The Francis Crick Institute · GBImperial College London · GBWellcome Sanger Institute · GB

Funding

francis crick institute Phd Studentshipimperial college london PhD studentshipWellcome Trust FC001101Wellcome Trust WT 104777/Z/14/ZWellcome Trust WT 206194
6 · The paper itself

Abstract

backgroundPlasmodium interspersed repeat (pir) is the largest multigene family in the genomes of most Plasmodium species. A variety of functions for the PIR proteins which they encode have been proposed, including antigenic variation, immune evasion, sequestration and rosetting. However, direct evidence for these is lacking. The repetitive nature of the family has made it difficult to determine function experimentally. However, there has been some success in using gene expression studies to suggest roles for some members in virulence and chronic infection.

methodsHere pir gene expression was examined across the life cycle of Plasmodium berghei using publicly available RNAseq data-sets, and at high resolution in the intraerythrocytic development cycle using new data from Plasmodium chabaudi.

resultsExpression of pir genes is greatest in stages of the parasite which invade and reside in red blood cells. The marked exception is that liver merozoites and male gametocytes produce a very large number of pir gene transcripts, notably compared to female gametocytes, which produce relatively few. Within the asexual blood stages different subfamilies peak at different times, suggesting further functional distinctions. Representing a subfamily of its own, the highly conserved ancestral pir gene warrants further investigation due to its potential tractability for functional investigation. It is highly transcribed in multiple life cycle stages and across most studied Plasmodium species and thus is likely to play an important role in parasite biology.

conclusionsThe identification of distinct expression patterns for different pir genes and subfamilies is likely to provide a basis for the design of future experiments to uncover their function.

Indexed as

Gene ExpressionGenes, ProtozoanMultigene FamilyLife Cycle StagesPlasmodium bergheiPlasmodium chabaudi

Identifiers

PMID34823519
PMCPMC8614022
OpenAlexW3176107779

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.