Evidence map›Paper›PMID 32958854›Full record

ArticleScientific reports2020

The anti-apoptotic Coxiella burnetii effector protein AnkG is a strain specific virulence factor.

Walter Schäfer, Teresa Schmidt, Arne Cordsmeier, Vítor Borges, Paul A Beare, Julian Pechstein, Jan Schulze-Luehrmann, Jonas Holzinger, Nicole Wagner, Christian Berens and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
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  3. TFEB and MCOLN1 are important forFrontiers in cellular and infection microbiology · 2026
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  5. Bacterial Puppeteering: How the Stealth BacteriumPathogens (Basel, Switzerland) · 2025
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  6. Frontiers in immunology · 2025
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  9. Caspase-8 activity mediates TNFα production and restrictsbioRxiv : the preprint server for biology · 2024
    Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Frontiers in cellular and infection microbiology · 2022
    Article
  17. Idiosyncratic Biogenesis of Intracellular Pathogens-Containing Vacuoles.Frontiers in cellular and infection microbiology · 2021
    Review
  18. Recent Advances on the Innate Immune Response toFrontiers in cellular and infection microbiology · 2021
    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

13 authors at 5 institutions in 3 countries.

Walter SchäferMikrobiologisches Institut - Klinische Mikrobiologie, Immunologie und Hygiene, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Wasserturmstraße 3/5, 91054, Erlangen, Germany.
Teresa SchmidtMikrobiologisches Institut - Klinische Mikrobiologie, Immunologie und Hygiene, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Wasserturmstraße 3/5, 91054, Erlangen, Germany.
Arne CordsmeierMikrobiologisches Institut - Klinische Mikrobiologie, Immunologie und Hygiene, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Wasserturmstraße 3/5, 91054, Erlangen, Germany.
Vítor BorgesDepartment of Infectious Diseases, National Institute of Health, Lisbon, Portugal.
Paul A BeareCoxiella Pathogenesis Section, Laboratory of Bacteriology, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT, USA.
Julian PechsteinMikrobiologisches Institut - Klinische Mikrobiologie, Immunologie und Hygiene, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Wasserturmstraße 3/5, 91054, Erlangen, Germany.
Jan Schulze-LuehrmannMikrobiologisches Institut - Klinische Mikrobiologie, Immunologie und Hygiene, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Wasserturmstraße 3/5, 91054, Erlangen, Germany.
Jonas HolzingerMikrobiologisches Institut - Klinische Mikrobiologie, Immunologie und Hygiene, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Wasserturmstraße 3/5, 91054, Erlangen, Germany.
Nicole WagnerInstitut für Molekulare Pathogenese, Friedrich-Loeffler-Institut, 07743, Jena, Germany.
Christian BerensInstitut für Molekulare Pathogenese, Friedrich-Loeffler-Institut, 07743, Jena, Germany.ORCID http://orcid.org/0000-0002-7500-5864
Carsten HeydelInstitut für Hygiene und Infektionskrankheiten der Tiere, Justus Liebig Universität Gießen, Frankfurter Straße 85-89, 35392, Gießen, Germany.ORCID http://orcid.org/0000-0003-2507-3778
João Paulo GomesDepartment of Infectious Diseases, National Institute of Health, Lisbon, Portugal.
Anja LührmannMikrobiologisches Institut - Klinische Mikrobiologie, Immunologie und Hygiene, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Wasserturmstraße 3/5, 91054, Erlangen, Germany. anja.luehrmann@uk-erlangen.de.
Friedrich-Alexander-Universität Erlangen-Nürnberg · DEFriedrich-Loeffler-Institut · DENational Institute of Health Dr. Ricardo Jorge · PTJustus-Liebig-Universität Gießen · DENational Institutes of Health · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ability to inhibit host cell apoptosis is important for the intracellular replication of the obligate intracellular pathogen Coxiella burnetii, as it allows the completion of the lengthy bacterial replication cycle. Effector proteins injected into the host cell by the C. burnetii type IVB secretion system (T4BSS) are required for the inhibition of host cell apoptosis. AnkG is one of these anti-apoptotic effector proteins. The inhibitory effect of AnkG requires its nuclear localization, which depends on p32-dependent intracellular trafficking and importin-α1-mediated nuclear entry of AnkG. Here, we compared the sequences of ankG from 37 C. burnetii isolates and classified them in three groups based on the predicted protein size. The comparison of the three different groups allowed us to identify the first 28 amino acids as essential and sufficient for the anti-apoptotic activity of AnkG. Importantly, only the full-length protein from the first group is a bona fide effector protein injected into host cells during infection and has anti-apoptotic activity. Finally, using the Galleria mellonella infection model, we observed that AnkG from the first group has the ability to attenuate pathology during in vivo infection, as it allows survival of the larvae despite bacterial replication.

Indexed as

AnimalsApoptosisBacterial ProteinsCell DeathCoxiella burnetiiHost-Pathogen InteractionsHumansProtein TransportSequence AlignmentVirulence FactorsAnkG protein, Coxiella burnetiiBacterial ProteinsVirulence Factors

Identifiers

PMID32958854
PMCPMC7506536
OpenAlexW3087085633

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.