Evidence map›Paper›PMID 25280815›Full record

ArticleEukaryotic cell2014

Hammondia hammondi harbors functional orthologs of the host-modulating effectors GRA15 and ROP16 but is distinguished from Toxoplasma gondii by a unique transcriptional profile.

Katelyn A Walzer, Gregory M Wier, Rachel A Dam, Ananth R Srinivasan, Adair L Borges, Elizabeth D English, Daland C Herrmann, Gereon Schares, Jitender P Dubey, Jon P Boyle

Abstract readComparative Study
In one paragraph

Article in Eukaryotic cell, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Toxoplasma gondii and the Brain: Frenemies? Or Just Outright Foes?Journal of the Pediatric Infectious Diseases Society · 2025
    Review
  2. Immunomagnetic separation ofFrontiers in veterinary science · 2022
    Article
  3. Article
  4. Article
  5. Article
  6. Dissection of theeLife · 2018
    Article
  7. Review
  8. Article
  9. Review
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.

Katelyn A WalzerDietrich School of Arts and Sciences, Department of Biological Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Gregory M WierDietrich School of Arts and Sciences, Department of Biological Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Rachel A DamDietrich School of Arts and Sciences, Department of Biological Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Ananth R SrinivasanDietrich School of Arts and Sciences, Department of Biological Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Adair L BorgesDietrich School of Arts and Sciences, Department of Biological Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Elizabeth D EnglishDietrich School of Arts and Sciences, Department of Biological Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Daland C HerrmannFederal Research Institute for Animal Health, Institute of Epidemiology, Greifswald-Isle of Riems, Germany.
Gereon ScharesFederal Research Institute for Animal Health, Institute of Epidemiology, Greifswald-Isle of Riems, Germany.
Jitender P DubeyAnimal Parasitic Diseases Laboratory, Beltsville Agricultural Research Center, Agricultural Research Service, U.S. Department of Agriculture, Beltsville, Maryland, USA.
Jon P BoyleDietrich School of Arts and Sciences, Department of Biological Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania, USA boylej@pitt.edu.

Funding

Howard Hughes Medical Institute
6 · The paper itself

Abstract

Toxoplasma gondii and its nearest extant relative, Hammondia hammondi, are phenotypically distinct despite their remarkable similarity in gene content, synteny, and functionality. To begin to identify genetic differences that might drive distinct infection phenotypes of T. gondii and H. hammondi, in the present study we (i) determined whether two known host-interacting proteins, dense granule protein 15 (GRA15) and rhoptry protein 16 (ROP16), were functionally conserved in H. hammondi and (ii) performed the first comparative transcriptional analysis of H. hammondi and T. gondii sporulated oocysts. We found that GRA15 and ROP16 from H. hammondi (HhGRA15 and HhROP16) modulate the host NF-κB and STAT6 pathways, respectively, when expressed heterologously in T. gondii. We also found the transcriptomes of H. hammondi and T. gondii to be highly distinct. Consistent with the spontaneous conversion of H. hammondi tachyzoites into bradyzoites both in vitro and in vivo, H. hammondi high-abundance transcripts are enriched for genes that are of greater abundance in T. gondii bradyzoites. We also identified genes that are of high transcript abundance in H. hammondi but are poorly expressed in multiple T. gondii life stages, suggesting that these genes are uniquely expressed in H. hammondi. Taken together, these data confirm the functional conservation of known T. gondii virulence effectors in H. hammondi and point to transcriptional differences as a potential source of the phenotypic differences between these species.

Indexed as

Base SequenceCell NucleusCells, CulturedGene Expression RegulationGenes, ProtozoanHost-Parasite InteractionsHumansMolecular Sequence DataNF-kappa BPhylogenyPromoter Regions, GeneticRNA, MessengerSTAT6 Transcription FactorToxoplasmaTranscriptomeNF-kappa BRNA, MessengerSTAT6 protein, humanSTAT6 Transcription Factor

Identifiers

PMID25280815
PMCPMC4248688

What OpenQuestion holds

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Registered trials

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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.