Evidence map›Paper›PMID 16299270›Full record

ArticleInfection and immunity2005

Haemophilus ducreyi targets Src family protein tyrosine kinases to inhibit phagocytic signaling.

Jason R Mock, Merja Vakevainen, Kaiping Deng, Jo L Latimer, Jennifer A Young, Nicolai S C van Oers, Steven Greenberg, Eric J Hansen

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Mammalian Pragmin regulates Src family kinases via the Glu-Pro-Ile-Tyr-Ala (EPIYA) motif that is exploited by bacterial effectors.Proceedings of the National Academy of Sciences of the United States of America · 2011
    Article
  9. Host-pathogen interplay of Haemophilus ducreyi.Current opinion in infectious diseases · 2010
    Review
  10. Article
  11. Article
  12. 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

8 authors at 2 institutions in 1 country.

Jason R MockDepartment of Microbiology, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390-9048, USA.
Merja Vakevainen
Kaiping Deng
Jo L Latimer
Jennifer A Young
Nicolai S C van Oers
Steven Greenberg
Eric J Hansen
The University of Texas Southwestern Medical Center · USColumbia University · US

Funding

MOLECULAR MICROBIOLOGY TRAINING GRANTT32AI007520 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI Julie K Pfeiffer · 1997 to 2026
$7.0M
Haemophilus ducreyi Inhibits PhagocytosisR37AI032011 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI HANSEN, ERIC JOHN · 2006 to 2015
$3.8M
MOLECULAR PATHOGENESIS OF CHANCROIDR01AI032011 · NIAID · UNIVERSITY OF TEXAS SW MED CTR/DALLAS · PI HANSEN, ERIC JOHN · 1992 to 2004
$1.7M
Haemophilus ducreyi Inhibits PhagocytosisR56AI032011 · NIAID · UNIVERSITY OF TEXAS SW MED CTR/DALLAS · PI HANSEN, ERIC JOHN · 2005 to 2005
$390k
NIAID NIH HHS 5-T32-AI007520-08NIAID NIH HHS AI32011NIAID NIH HHS R01 AI032011NIAID NIH HHS R37 AI032011NIAID NIH HHS R56 AI032011NIAID NIH HHS T32 AI007520
6 · The paper itself

Abstract

Haemophilus ducreyi, the etiologic agent of the sexually transmitted disease chancroid, has been shown to inhibit phagocytosis of both itself and secondary targets in vitro. Immunodepletion of LspA proteins from H. ducreyi culture supernatant fluid abolished this inhibitory effect, indicating that the LspA proteins are necessary for the inhibition of phagocytosis by H. ducreyi. Fluorescence microscopy revealed that macrophages incubated with wild-type H. ducreyi, but not with a lspA1 lspA2 mutant, were unable to complete development of the phagocytic cup around immunoglobulin G-opsonized targets. Examination of the phosphotyrosine protein profiles of these two sets of macrophages showed that those incubated with wild-type H. ducreyi had greatly reduced phosphorylation levels of proteins in the 50-to-60-kDa range. Subsequent experiments revealed reductions in the catalytic activities of both Lyn and Hck, two members of the Src family of protein tyrosine kinases that are known to be involved in the proximal signaling steps of Fcgamma receptor-mediated phagocytosis. Additional experiments confirmed reductions in the levels of both active Lyn and active Hck in three different immune cell lines, but not in HeLa cells, exposed to wild-type H. ducreyi. This is the first example of a bacterial pathogen that suppresses Src family protein tyrosine kinase activity to subvert phagocytic signaling in hostcells.

Indexed as

PhagocytosisAnimalsAntibodies, BacterialBacterial ProteinsCatalysisCell LineChancroidHaemophilus ducreyiHumansLectinsMacrophagesMiceMutationPhosphoproteinsProto-Oncogene Proteins c-hckReceptors, IgGAntibodies, BacterialBacterial ProteinsLectinsLspA1 protein, Haemophilus ducreyiLspA2 protein, Haemophilus ducreyilyn protein-tyrosine kinasePhosphoproteinsProto-Oncogene Proteins c-hckReceptors, IgGsrc-Family Kinases

Identifiers

PMID16299270
PMCPMC1307070
OpenAlexW2109822117

What OpenQuestion holds

Textmetadata
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.