Evidence map›Paper›PMID 40460112›Full record

ArticlePloS one2025

Differential expression of host invasion-associated genes by Sarcocystis calchasi in intermediate versus definitive hosts.

Kristina Maier-Sam, Oliver Rupp, Anne Voss, Saskia Nemitz, Tassilo E Wollenweber, Tara Procida-Kowalski, Jochen Wilhelm, Achim D Gruber, Michael Lierz

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Two Decades (2003-2024) of InvestigatingPathogens (Basel, Switzerland) · 2026
    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

9 authors.

Kristina Maier-SamClinic for Birds, Reptiles, Amphibians and Fish, Justus Liebig University, Giessen, Germany.ORCID 0000-0003-2954-4960
Oliver RuppDepartment of Bioinformatics and Systems Biology, Justus Liebig University, Giessen, Germany.ORCID 0000-0003-2755-6458
Anne VossInstitute of Veterinary Pathology, Freie Universität Berlin, Berlin, Germany.
Saskia NemitzClinic for Birds, Reptiles, Amphibians and Fish, Justus Liebig University, Giessen, Germany.
Tassilo E WollenweberBiological and Medical Research Center (BMFZ), Genomics & Transcriptomics Laboratory, Medical Faculty, Heinrich Heine University, Düsseldorf, Germany.
Tara Procida-KowalskiInstitute for Lung Health (ILH), Genomics and Bioinformatics, Justus Liebig University, Giessen, Germany.
Jochen WilhelmInstitute for Lung Health (ILH), Genomics and Bioinformatics, Justus Liebig University, Giessen, Germany.ORCID 0000-0001-5544-9647
Achim D GruberInstitute of Veterinary Pathology, Freie Universität Berlin, Berlin, Germany.ORCID 0000-0002-4502-0393
Michael LierzClinic for Birds, Reptiles, Amphibians and Fish, Justus Liebig University, Giessen, Germany.ORCID 0000-0003-3710-1596

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sarcocystis calchasi is a pathogenic apicomplexan parasite affecting avian species of several orders. To complete its heteroxenous life cycle, S. calchasi infects a wide range of avian intermediate hosts and accipitriform raptors serve as definitive hosts. The mechanism of invasion into host cells is largely understood in other apicomplexan parasites, particularly Toxoplasma gondii, which also belongs to the family of Sarcocystidae. However, Sarcocystis species exhibit several distinguishing features in their life cycles and in their secretory organelles. The composition of secretory pathogenesis determinants, including surface antigens and secretory organelle proteins, has been shown to differ between closely related species, as evidenced by Sarcocystis neurona. In this study, whole-genome sequencing was performed on S. calchasi, and transcriptomes were determined by RNA-seq of S. calchasi sporozoites and bradyzoites derived from intermediate and definitive hosts as well as from merozoites propagated in primary embryonal pigeon liver cells. The S. calchasi genome contains homologs of genes encoding proteins associated with the well-conserved host invasion machinery like AMA1 and rhoptry neck proteins, albeit with a markedly reduced number of genes encoding surface antigens, rhoptry and dense granule proteins in comparison to T. gondii. Our transcriptome analysis revealed different gene expression profiles between S. calchasi sporozoites, merozoites and bradyzoites. Factors associated with host cell attachment (surface antigens and micronemal proteins) were expressed predominantly either in sporozoites and merozoites or in bradyzoites. As sporozoites and merozoites invade various intermediate hosts and cell types whereas bradyzoites enter definitive host intestinal epithelium, their differential expression patterns indicate that S. calchasi utilizes different sets of secretory pathogenesis determinants for host cell attachment and invasion, depending on the type of host and cell.

Indexed as

Host-Parasite InteractionsSarcocystisSarcocystosisAnimalsColumbidaeProtozoan ProteinsTranscriptomeProtozoan Proteins

Identifiers

PMID40460112
PMCPMC12132954

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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.