Evidence map›Paper›PMID 10368149›Full record

ArticleJournal of bacteriology1999

Insertional inactivation of Treponema denticola tap1 results in a nonmotile mutant with elongated flagellar hooks.

R J Limberger, L L Slivienski, J Izard, W A Samsonoff

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Journal of bacteriology, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

35 citing papers in PubMed, 60 citations in OpenAlex.

  1. Article
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  7. The Role ofFrontiers in cellular and infection microbiology · 2019
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  13. Dioxygen and nitric oxide scavenging by Treponema denticola flavodiiron protein: a mechanistic paradigm for catalysis.Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry · 2015
    Article
  14. Article
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  18. Treponema denticola interactions with host proteins.Journal of oral microbiology · 2012
    Article
  19. 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

4 authors at 2 institutions in 1 country.

R J LimbergerDavid Axelrod Institute for Public Health, Wadsworth Center, New York State Department of Health, Albany, New York 12201-2002, USA. Ron.Limberger@wadsworth.org
L L Slivienski
J Izard
W A Samsonoff
New York State Department of Health · USWadsworth Center · US

Funding

MOLECULAR ANALYSIS OF TREPONEMAL MOTILITY GENESR01AI034354 · NIAID · WADSWORTH CENTER · PI LIMBERGER, RONALD J · 1999 to 2002
$618k
MOLECULAR ANALYSIS OF TREPONEMAL MOTILITY GENESR29AI034354 · NIAID · WADSWORTH CENTER · PI LIMBERGER, RONALD J · 1993 to 1997
–
NIAID NIH HHS AI34354
6 · The paper itself

Abstract

The treponemal fla operon is comprised of numerous motility-related genes; however, the initial gene of this operon, tap1, has no known function. A recently developed system to generate specific mutants in Treponema denticola was utilized to determine if Tap1 was essential for motility. T. denticola tap1 and flanking DNA were identified, cloned, and sequenced, and a suicide plasmid that contained tap1 interrupted with an erythromycin resistance cassette (ermF and ermAM) was constructed. Because of potential polar effects from this cassette, a second plasmid that contained tap1 interrupted with a modified erythromycin resistance cassette that lacked the putative ermF transcription terminator was constructed. Electroporation-mediated allelic exchange incorporated the interrupted tap1 genes into the T. denticola chromosome, creating Tap1-deficient mutants. Reverse transcriptase PCR revealed that the erythromycin resistance cassette within tap1 did not terminate fla operon transcription in either mutant. Moreover, the phenotypes of the two mutants were indistinguishable. These mutants lacked motion in liquid culture, were unable to spread on agar plates, and lacked flagellar filaments as determined by electron microscopy. Immunoblots revealed a marked reduction in detectable FlaB flagellar filament protein compared to that of wild type; however, flaB RNA was easily detectable, and transcription levels did not appear to be altered. The basis for the lack of filament protein expression is unknown. Immunoblotting also showed that the flagellar hook protein (FlgE) was synthesized in the Tap1-deficient mutant; however, electron microscopy revealed that the mutant possessed unusual elongated hooks of variable lengths. We propose that treponemal Tap1 is analogous to FliK, which is involved in monitoring the flagellar hook length of Salmonella typhimurium.

Indexed as

Promoter Regions, GeneticAmino Acid SequenceBacterial ProteinsBase SequenceConsensus SequenceFlagellaMolecular Sequence DataMovementOperonSequence AlignmentSequence Homology, Amino AcidSequence Homology, Nucleic AcidTreponemaBacterial ProteinsTap1 protein, Treponema

Identifiers

PMID10368149
PMCPMC93852
OpenAlexW2128033049

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.