Evidence map›Paper›PMID 11500438›Full record

ArticleInfection and immunity2001

Characterization of Haemophilus ducreyi cdtA, cdtB, and cdtC mutants in in vitro and in vivo systems.

D A Lewis, M K Stevens, J L Latimer, C K Ward, K Deng, R Blick, S R Lumbley, C A Ison, E J Hansen

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2001. 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
2.5field-weighted citation impact, top 11% 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, 52 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

9 authors at 2 institutions in 3 countries.

D A LewisDepartment of Microbiology, University of Texas Southwestern Medical Center, Dallas, Texas 75235-9048, USA.
M K Stevens
J L Latimer
C K Ward
K Deng
R Blick
S R Lumbley
C A Ison
E J Hansen
The University of Texas Southwestern Medical Center · USImperial College London · GB

Funding

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
FHA-LIKE PROTEIN OF HAEMOPHILUS DUCREYIF32AI009845 · NIAID · UNIVERSITY OF TEXAS SW MED CTR/DALLAS · PI WARD, CHISTINE K · 1997 to 1999
–
NIAID NIH HHS AI32011NIAID NIH HHS F32 AI009845NIAID NIH HHS F32-AI09845NIAID NIH HHS R01 AI032011NIAID NIH HHS R37 AI032011NIAID NIH HHS R56 AI032011Wellcome Trust
6 · The paper itself

Abstract

Haemophilus ducreyi expresses a soluble cytolethal distending toxin (CDT) that is encoded by the cdtABC gene cluster and can be detected in culture supernatant fluid by its ability to kill HeLa cells. The cdtA, cdtB, and cdtC genes of H. ducreyi were cloned independently into plasmid vectors, and their encoded proteins expressed singly or in various combinations in an Escherichia coli background. All three gene products had to be expressed in order for E. coli-derived culture supernatant fluids to demonstrate cytotoxicity for HeLa cells. Isogenic H. ducreyi cdtA and cdtB mutants were constructed and used in combination with the wild-type parent strain and a previously described H. ducreyi cdtC mutant (M. K. Stevens, J. L. Latimer, S. R. Lumbley, C. K. Ward, L. D. Cope, T. Lagergard, and E. J. Hansen, Infect. Immun. 67:3900-3908, 1999) to determine the relative contributions of the CdtA, CdtB, and CdtC proteins to CDT activity. Expression of CdtA, CdtB, and CdtC appeared necessary for H. ducreyi-derived culture supernatant fluid to exhibit cytotoxicity for HeLa cells. Whole-cell sonicates and periplasmic extracts from the cdtB and cdtC mutants had no effect on HeLa cells, whereas these same fractions from a cdtA mutant had a very modest cytotoxic effect on these same human cells. CdtA appeared to be primarily associated with the H. ducreyi cell envelope, whereas both CdtB and CdtC were present primarily in the soluble fraction from sonicated cells. Both the cdtA mutant and the cdtB mutant were found to be fully virulent in the temperature-dependent rabbit model for experimental chancroid.

Indexed as

AnimalsBacterial ToxinsChancroidCulture Media, ConditionedEscherichia coliGenetic Complementation TestHaemophilus ducreyiHeLa CellsHumansMutationRabbitsReverse Transcriptase Polymerase Chain ReactionSubcellular FractionsVirulenceBacterial ToxinsCulture Media, Conditionedcytolethal distending toxin

Identifiers

PMID11500438
PMCPMC98678
OpenAlexW2163990236

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.