Evidence map›Paper›PMID 29269769›Full record

ArticleNature communications2017

Lipid moieties on lipoproteins of commensal and non-commensal staphylococci induce differential immune responses.

Minh-Thu Nguyen, Julia Uebele, Nimerta Kumari, Hiroshi Nakayama, Lena Peter, Olga Ticha, Anne-Kathrin Woischnig, Mathias Schmaler, Nina Khanna, Naoshi Dohmae and 3 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

53 citing papers in PubMed, 65 citations in OpenAlex.

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  10. Journal of bacteriology · 2025
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  11. Metabolites · 2025
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  15. Fatty acids ofMicrobiology spectrum · 2024
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  17. Essential role ofInfection and immunity · 2023
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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

13 authors at 5 institutions in 5 countries.

Minh-Thu NguyenMicrobial Genetics, Interfaculty Institute of Microbiology and Infection Medicine Tübingen (IMIT), University of Tübingen, Tübingen, 72076, Germany.
Julia UebelePaul-Ehrlich-Institute, Federal Regulatory Agency for Vaccines and Biomedicines, Langen, 63225, Germany.
Nimerta KumariMicrobial Genetics, Interfaculty Institute of Microbiology and Infection Medicine Tübingen (IMIT), University of Tübingen, Tübingen, 72076, Germany.
Hiroshi NakayamaBiomolecular Characterization Unit, RIKEN Center for Sustainable Resource Science, Saitama, 351-0198, Japan.
Lena PeterPaul-Ehrlich-Institute, Federal Regulatory Agency for Vaccines and Biomedicines, Langen, 63225, Germany.
Olga TichaPaul-Ehrlich-Institute, Federal Regulatory Agency for Vaccines and Biomedicines, Langen, 63225, Germany.
Anne-Kathrin WoischnigLaboratory of Infection Biology, Department of Biomedicine, University Hospital Basel, Basel, CH-4031, Switzerland.
Mathias SchmalerLaboratory of Infection Biology, Department of Biomedicine, University Hospital Basel, Basel, CH-4031, Switzerland.ORCID http://orcid.org/0000-0003-3687-8088
Nina KhannaLaboratory of Infection Biology, Department of Biomedicine, University Hospital Basel, Basel, CH-4031, Switzerland.
Naoshi DohmaeBiomolecular Characterization Unit, RIKEN Center for Sustainable Resource Science, Saitama, 351-0198, Japan.
Bok Luel LeeNational Research Laboratory of Defense Proteins, College of Pharmacy, Pusan National University, Pusan, 609-735, South Korea.
Isabelle Bekeredjian-DingPaul-Ehrlich-Institute, Federal Regulatory Agency for Vaccines and Biomedicines, Langen, 63225, Germany.ORCID http://orcid.org/0000-0001-6646-5888
Friedrich GötzMicrobial Genetics, Interfaculty Institute of Microbiology and Infection Medicine Tübingen (IMIT), University of Tübingen, Tübingen, 72076, Germany. friedrich.goetz@uni-tuebingen.de.
Paul Ehrlich Institut · DEUniversity Hospital of Basel · CHUniversity of Tübingen · DERIKEN Center for Sustainable Resource Science · JPPusan National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lipoproteins (Lpp) of Gram-positive bacteria are major players in alerting our immune system. Here, we show that the TLR2 response induced by commensal species Staphylococcus aureus and Staphylococcus epidermidis is almost ten times lower than that induced by noncommensal Staphylococcus carnosus, and this is at least partially due to their different modifications of the Lpp lipid moieties. The N terminus of the lipid moiety is acylated with a long-chain fatty acid (C17) in S. aureus and S. epidermidis, while it is acylated with a short-chain fatty acid (C2) in S. carnosus. The long-chain N-acylated Lpp, recognized by TLR2-TLR1 receptors, silences innate and adaptive immune responses, while the short-chain N-acetylated Lpp, recognized by TLR2-TLR6 receptors, boosts it.

Indexed as

Adaptation, PhysiologicalBacterial ProteinsFatty AcidsHEK293 CellsHumansImmunity, InnateLipidsLipoproteinsSignal TransductionStaphylococcus aureusStaphylococcus epidermidisTh1 CellsToll-Like ReceptorsTumor Necrosis Factor-alphaBacterial ProteinsFatty AcidsLipidsLipoproteinsToll-Like ReceptorsTumor Necrosis Factor-alpha

Identifiers

PMID29269769
PMCPMC5740139
OpenAlexW2773316504

What OpenQuestion holds

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LicenceCC BY
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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.