Evidence map›Paper›PMID 20086092›Full record

ArticleInfection and immunity2010

Haemophilus ducreyi SapA contributes to cathelicidin resistance and virulence in humans.

Kristy L B Mount, Carisa A Townsend, Sherri D Rinker, Xiaoping Gu, Kate R Fortney, Beth W Zwickl, Diane M Janowicz, Stanley M Spinola, Barry P Katz, Margaret E Bauer

Abstract read
In one paragraph

Article in Infection and immunity, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

26 citing papers in PubMed, 42 citations in OpenAlex.

  1. Molecular pathogenesis ofMicrobiology and molecular biology reviews : MMBR · 2025
    Review
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  4. AInfection and immunity · 2024
    Article
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  11. Interactions of the Skin PathogenFrontiers in immunology · 2020
    Review
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  14. Article
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  17. Article
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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

10 authors at 1 institution in 1 country.

Kristy L B MountDepartment of Microbiology and Immunology, Indiana University School of Medicine, 635 Barnhill Dr., Room MS 420, Indianapolis, IN 46202-5124, USA.
Carisa A Townsend
Sherri D Rinker
Xiaoping Gu
Kate R Fortney
Beth W Zwickl
Diane M Janowicz
Stanley M Spinola
Barry P Katz
Margaret E Bauer
Indiana University School of Medicine

Funding

University of Washington STI-TM Cooperative Research CtrU19AI031448 · NIAID · UNIVERSITY OF WASHINGTON · PI HOLMES, KING K. · 1995 to 2010
$15.2M
VIRAL DETERMINANTS OF HSV DISEASE IN MICEU19AI031494 · NIAID · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI SPINOLA, STANLEY M. · 1995 to 2009
$13.6M
Haemophilus ducreyi Resistance to Antimicrobial PeptidesR21AI075008 · NIAID · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI BAUER, MARGARET E · 2007 to 2008
$412k
UNIVERSITY OF WASHINGTON STD COOPERATIVE RESEARCH CENTERU01AI031448 · NIAID · UNIVERSITY OF WASHINGTON · PI HOLMES, KING KENNARD · 1991 to 1994
–
VARIABILITY IN HERPES SIMPLEX VIRUS GLYCOPROTEINS AND INFECTIVITYU01AI031494 · NIAID · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI WILDE, CHARLES E · 1991 to 1994
–
NCRR NIH HHS UL RR052761NIAID NIH HHS AI 31448NIAID NIH HHS AI 31494NIAID NIH HHS R21 AI075008NIAID NIH HHS U19 AI031448NIAID NIH HHS U19 AI031494NIAID NIH HHS U19 AI31494
6 · The paper itself

Abstract

Haemophilus ducreyi is an extracellular pathogen of human epithelial surfaces that resists human antimicrobial peptides (APs). The organism's genome contains homologs of genes sensitive to antimicrobial peptides (sap operon) in nontypeable Haemophilus influenzae. In this study, we characterized the sap-containing loci of H. ducreyi 35000HP and demonstrated that sapA is expressed in broth cultures and H. ducreyi-infected tissue; sapA is also conserved among both class I and class II H. ducreyi strains. We constructed a nonpolar sapA mutant of H. ducreyi 35000HP, designated 35000HPsapA, and compared the percent survival of wild-type 35000HP and 35000HPsapA exposed to several human APs, including alpha-defensins, beta-defensins, and the cathelicidin LL-37. Unlike an H. influenzae sapA mutant, strain 35000HPsapA was not more susceptible to defensins than strain 35000HP was. However, we observed a significant decrease in the survival of strain 35000HPsapA after exposure to LL-37, which was complemented by introducing sapA in trans. Thus, the Sap transporter plays a role in resistance of H. ducreyi to LL-37. We next compared mutant strain 35000HPsapA with strain 35000HP for their ability to cause disease in human volunteers. Although both strains caused papules to form at similar rates, the pustule formation rate at sites inoculated with 35000HPsapA was significantly lower than that of sites inoculated with 35000HP (33.3% versus 66.7%; P = 0.007). Together, these data establish that SapA acts as a virulence factor and as one mechanism for H. ducreyi to resist killing by antimicrobial peptides. To our knowledge, this is the first demonstration that an antimicrobial peptide resistance mechanism contributes to bacterial virulence in humans.

Indexed as

Drug Resistance, BacterialAdultAnti-Bacterial AgentsAntimicrobial Cationic PeptidesBacterial ProteinsCathelicidinsChancroidConserved SequenceFemaleGene DeletionGene Expression ProfilingGenetic Complementation TestHaemophilus ducreyiHuman ExperimentationHumansMaleAnti-Bacterial AgentsAntimicrobial Cationic PeptidesBacterial ProteinsCathelicidinsSapA protein, Haemophilus ducreyiVirulence Factors

Identifiers

PMID20086092
PMCPMC2825904
OpenAlexW2142929394

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.