Evidence map›Paper›PMID 34111210›Full record

ArticlePloS one2021

GroEL is an immunodominant surface-exposed antigen of Rickettsia typhi.

Jessica Rauch, Jessica Barton, Marcel Kwiatkowski, Malte Wunderlich, Pascal Steffen, Kristin Moderzynski, Stefanie Papp, Katharina Höhn, Hella Schwanke, Susanne Witt and 7 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 28% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

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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

17 authors at 2 institutions in 1 country.

Jessica RauchBernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.ORCID 0000-0003-4499-7327
Jessica BartonBernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
Marcel KwiatkowskiUniversity Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0002-5804-6031
Malte WunderlichBernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.ORCID 0000-0002-3881-2026
Pascal SteffenUniversity Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0003-3883-699X
Kristin ModerzynskiBernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
Stefanie PappBernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
Katharina HöhnBernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
Hella SchwankeBernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.ORCID 0000-0001-9252-3594
Susanne WittBernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.ORCID 0000-0001-9102-1517
Ulricke RichardtBernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
Ute MehlhoopBernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
Hartmut SchlüterUniversity Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0002-9358-7036
Verena PiankaBernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
Bernhard FleischerBernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
Dennis TappeBernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
Anke OsterlohBernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.ORCID 0000-0002-4078-1070
Bernhard Nocht Institute for Tropical Medicine · DEUniversität Hamburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rickettsioses are neglected and emerging potentially fatal febrile diseases that are caused by obligate intracellular bacteria, rickettsiae. Rickettsia (R.) typhi and R. prowazekii constitute the typhus group (TG) of rickettsiae and are the causative agents of endemic and epidemic typhus, respectively. We recently generated a monoclonal antibody (BNI52) against R. typhi. Characterization of BNI52 revealed that it specifically recognizes TG rickettsiae but not the members of the spotted fever group (SFG) rickettsiae. We further show that BNI52 binds to protein fragments of ±30 kDa that are exposed on the bacterial surface and also present in the periplasmic space. These protein fragments apparently derive from the cytosolic GroEL protein of R. typhi and are also recognized by antibodies in the sera from patients and infected mice. Furthermore, BNI52 opsonizes the bacteria for the uptake by antigen presenting cells (APC), indicating a contribution of GroEL-specific antibodies to protective immunity. Finally, it is interesting that the GroEL protein belongs to 32 proteins that are differentially downregulated by R. typhi after passage through immunodeficient BALB/c CB17 SCID mice. This could be a hint that the rickettsia GroEL protein may have immunomodulatory properties as shown for the homologous protein from several other bacteria, too. Overall, the results of this study provide evidence that GroEL represents an immunodominant antigen of TG rickettsiae that is recognized by the humoral immune response against these pathogens and that may be interesting as a vaccine candidate. Apart from that, the BNI52 antibody represents a new tool for specific detection of TG rickettsiae in various diagnostic and experimental setups.

Indexed as

AnimalsAntibodies, BacterialAntibodies, MonoclonalAntigens, BacterialCell LineChaperonin 60HEK293 CellsHumansMiceMice, Inbred BALB CMice, SCIDPeriplasmRickettsia InfectionsRickettsia typhiXenopus laevisAntibodies, BacterialAntibodies, MonoclonalAntigens, BacterialChaperonin 60

Identifiers

PMID34111210
PMCPMC8191997
OpenAlexW3169597299

What OpenQuestion holds

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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.