Evidence map›Paper›PMID 22140447›Full record

ArticlePloS one2011

Modulation of the host interferon response and ISGylation pathway by B. pertussis filamentous hemagglutinin.

Christine Dieterich, David A Relman

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

15 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Filamentous Hemagglutinin ofInternational journal of molecular sciences · 2022
    Article
  6. Review
  7. Emerging Roles of USP18: From Biology to Pathophysiology.International journal of molecular sciences · 2020
    Review
  8. Pertussis vaccines and protective immunity.Current opinion in immunology · 2019
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. 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

2 authors at 2 institutions in 1 country.

Christine DieterichDepartment of Microbiology and Immunology, Stanford University School of Medicine, Stanford, California, United States of America.
David A Relman
Stanford University · USVA Palo Alto Health Care System · US

Funding

Analytical Tools for Comparative Microbial GenomicsR33AI057188 · NIAID · STANFORD UNIVERSITY · PI RELMAN, DAVID ARNOLD · 2005 to 2006
$823k
Analytical Tools for Comparative Microbial GenomicsR21AI057188 · NIAID · STANFORD UNIVERSITY · PI RELMAN, DAVID ARNOLD · 2003 to 2004
$287k
Bordetella Response to Host Cues and Cell SignalsR03AI054970 · NIAID · STANFORD UNIVERSITY · PI RELMAN, DAVID ARNOLD · 2003 to 2004
$130k
NIAID NIH HHS AI057188NIAID NIH HHS AI54970NIAID NIH HHS R03 AI054970NIAID NIH HHS R21 AI057188NIAID NIH HHS R33 AI057188
6 · The paper itself

Abstract

Bordetella pertussis filamentous hemagglutinin (FHA) is a surface-associated and secreted protein that serves as a crucial adherence factor, and displays immunomodulatory activity in human peripheral blood mononuclear cells (PBMCs). In order to appreciate more fully the role of secreted FHA in pathogenesis, we analyzed FHA-induced changes in genome-wide transcript abundance in human PBMCs. Among the 683 known unique genes with greater than 3-fold change in transcript abundance following FHA treatment, 125 (18.3%) were identified as interferon (IFN)-regulated. Among the latter group were genes encoding several members of the IFN type I response, as well as 3 key components of the ISGylation pathway. Using real-time RT-PCR, we confirmed FHA-associated increases in transcript abundance for the genes encoding ubiquitin-like protein, ISG15, and its specific protease USP18. Western-blot analysis demonstrated the presence of both, free ISG15 and several ISGylated conjugates in FHA-stimulated PBMC lysates, but not in unstimulated cells. Intracellular FACS analysis provided evidence that monocytes and a natural killer-enriched cell population were the primary producers of ISG15 in PBMCs after FHA stimulation. Our data reveal previously-unrecognized effects of B. pertussis FHA on host IFN and ISGylation responses, and suggest previously-unsuspected mechanisms by which FHA may alter the outcome of the host-pathogen interaction.

Indexed as

Adhesins, BacterialBordetella pertussisCytokinesGene Expression ProfilingGene Expression RegulationGenome, HumanHost-Pathogen InteractionsHumansInflammation MediatorsInterferonsKiller Cells, NaturalLeukocytes, MononuclearLipopolysaccharidesMonocytesRNA, MessengerSignal TransductionAdhesins, BacterialCytokinesfilamentous hemagglutinin adhesin, Bordetella pertussisInflammation MediatorsInterferonsISG15 protein, humanLipopolysaccharidesRNA, MessengerUbiquitinsVirulence Factors, Bordetella

Identifiers

PMID22140447
PMCPMC3227562
OpenAlexW2094488151

What OpenQuestion holds

Textmetadata
LicenceCC0
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.