Evidence map›Paper›PMID 8757862›Full record

ArticleInfection and immunity1996

Biochemical and molecular analysis of phospholipase C and phospholipase D activity in mycobacteria.

K A Johansen, R E Gill, M L Vasil

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Infection and immunity, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

32 citing papers in PubMed, 81 citations in OpenAlex.

  1. Article
  2. Roles of Lipolytic enzymes inFrontiers in microbiology · 2024
    Review
  3. Phospholipase C: underrated players in microbial infections.Frontiers in cellular and infection microbiology · 2023
    Review
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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

3 authors at 1 institution in 1 country.

K A JohansenDepartment of Microbiology, University of Colorado Health Sciences Center, Denver 80262, USA.
R E Gill
M L Vasil
University of Colorado Health · US

Funding

P AERUGINOSA PHOSPHOLIPASE C--MOLECULAR PATHOGENESISR01DK046440 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI VASIL, MICHAEL L. · 1993 to 1997
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REGULATION OF GENE EXPRESSION BY CELL-CELL INTERACTIONSR01GM031900 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI GILL, RONALD E · 1985 to 1995
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NIDDK NIH HHS DK46440NIGMS NIH HHS GM31900
6 · The paper itself

Abstract

Resurgence of mycobacterial infections in the United States has led to an intense effort to identify potential virulence determinants in the genus Mycobacterium, particularly ones that would be associated with the more virulent species (e.g., Mycobacterium tuberculosis). Thin-layer chromatography (TLC) using radiolabeled phosphatidylcholine and sphingomyelin as substrates indicated that cell extracts of M. tuberculosis contain both phospholipase C (PLC) and phospholipase D (PLD) activities. In contrast, only PLD activity was detected in cell extracts of M. smegmatis. Neither activity was detected in cell-free culture supernatants from these organisms. We and others recently identified two open reading frames in M. tuberculosis with the potential to encode proteins which are highly homologous to the nonhemolytic (PlcN) and hemolytic (PlcH) phospholipase C enzymes of Pseudomonas aeruginosa. In contrast to the plc genes in P. aeruginosa, which are considerably distal to each other (min 34 and 64 on the chromosome), the mycobacterial genes, designated mpcA and mpcB, are tandemly arranged in the same relative orientation and separated by only 191 bp. Both the mpcA and the mpcB genes were individually cloned in M. smegmatis, and PLC activity was expressed from each gene in this organism. Hybridization experiments using the mpcA and the mpcB genes as probes under conditions of moderate stringency identified sequences homologous to these genes in M. bovis, M. bovis BCG, and M. marinum but not in several other Mycobacterium species, including M. smegmatis, M. avium, and M. intracellulare. TLC analysis using radiolabeled substrates indicated that M. bovis and M. marinum cell extracts contain PLC and PLD activities, but only PLD activity was detected in M. bovis BCG cell extracts. Sphingomyelinase activity was also detected in whole-cell extracts of M. tuberculosis, M. marinum, M. bovis, and M. bovis BCG, but this activity was not detected in extracts of M. smegmatis. Sphingomyelinase activity was detected in cell extracts from M. smegmatis harboring either recombinant mpcA or mpcB. These data indicate that PLC and sphingomyelinase activities are associated with the most virulent mycobacterial species, while PLD activity was detected in both virulent and saprophytic strains.

Indexed as

Bacterial ProteinsGenes, BacterialAmino Acid SequenceBase SequenceCloning, MolecularGene ExpressionMolecular Sequence DataMycobacteriumMycobacterium tuberculosisPhospholipase DRestriction MappingSequence Analysis, DNASequence Homology, Amino AcidSpecies SpecificitySphingomyelin PhosphodiesteraseType C PhospholipasesBacterial ProteinsMpcA protein, Mycobacterium tuberculosisMpcB protein, Mycobacterium tuberculosisPhospholipase DSphingomyelin PhosphodiesteraseType C Phospholipases

Identifiers

PMID8757862
PMCPMC174216
OpenAlexW1936222408

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.