Evidence map›Paper›PMID 42014970›Full record

ArticleBMC microbiology2026

Genome characteristics and type IV effector protein repertoire of Coxiella burnetii depend rather on Genomic Groups than on host species.

Hanka Brangsch, Christian Berens, Selina Fuchs, Stephen Fitzgerald, Tom N McNeilly, Anja Lührmann, Katja Mertens-Scholz

Abstract read
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Article in BMC microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

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No citing paper in PubMed yet.

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

7 authors.

Hanka BrangschFriedrich-Loeffler-Institut, Institut für bakterielle Infektionen und Zoonosen, Jena, Germany.
Christian BerensFriedrich-Loeffler-Institut, Institut für molekulare Pathogenese, Jena, Germany.
Selina FuchsFriedrich-Loeffler-Institut, Institut für bakterielle Infektionen und Zoonosen, Jena, Germany.
Stephen FitzgeraldMoredun Research Institute, Penicuik, UK.
Tom N McNeillyMoredun Research Institute, Penicuik, UK.
Anja Lührmann *Mikrobiologisches Institut, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
Katja Mertens-Scholz *Friedrich-Loeffler-Institut, Institut für bakterielle Infektionen und Zoonosen, Jena, Germany. Katja.Mertens-Scholz@fli.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundQ fever is a zoonotic disease with virtually worldwide dissemination. Its bacterial agent, Coxiella burnetii, is primarily found in cattle and small ruminants. Disease manifestation is highly variable, i.e. asymptomatic, acute or chronic in humans, and subclinical or present as reproductive disorders in ruminants. Different genomic lineages of C. burnetii have been recognized and are considered to show host preferences and influence the disease outcome. The virulence of C. burnetii is essentially determined by effector proteins that modulate host cell processes, allowing the bacterium to persist and proliferate in the host. Thus, these effectors have been suggested to play a role in the presumed host specificity and disease manifestation.

resultsIn the present study, a comprehensive set of 140 C. burnetii genomes from ten Genomic Groups (GGs) and various hosts was studied bioinformatically to determine if there was an association between their genomic characteristics, including the effector protein repertoire, and their isolation source. The differences in genome size, IS1111 count, number of coding sequences, accessory genome and others could be attributed to lineage-specific traits. Likewise, the GGs showed conserved sets of effector proteins, although intra-lineage variances were high in GGIV. Several effector proteins, e.g. Cem8 (CBU_1634a) and CBU_0469, were highly conserved, while CBU_2007 showed a remarkably high number of sequence variants.

conclusionsC. burnetii exhibits genomic diversity that aligns with phylotypes rather than host species, suggesting that genomic traits as well as host factors influence disease outcome rather than a host species specific adaptation.

Indexed as

Bacterial ProteinsCoxiella burnetiiGenome, BacterialQ FeverType IV Secretion SystemsAnimalsCattleGenomicsHost SpecificityHumansPhylogenyVirulenceBacterial ProteinsType IV Secretion SystemsCoxiella burnetiiGenomic Groupsgenotypinghost preferencepangenomeSNPT4BSS effector proteinstype IV secretion system

Identifiers

PMID42014970
PMCPMC13104383

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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.