Evidence map›Paper›PMID 26658274›Full record

ArticlePloS one2015

Mycobacterium tuberculosis Type II Toxin-Antitoxin Systems: Genetic Polymorphisms and Functional Properties and the Possibility of Their Use for Genotyping.

Marina V Zaychikova, Natalia V Zakharevich, Maria O Sagaidak, Nadezhda A Bogolubova, Tatiana G Smirnova, Sofya N Andreevskaya, Elena E Larionova, Maria G Alekseeva, Larisa N Chernousova, Valery N Danilenko

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.9field-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

10 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Review
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  10. Draft genome sequence ofGenomics data · 2016
    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

10 authors at 3 institutions in 2 countries.

Marina V ZaychikovaVavilov Institute of General Genetics, Russian Academy of Sciences, Moscow, Russia.
Natalia V ZakharevichVavilov Institute of General Genetics, Russian Academy of Sciences, Moscow, Russia.
Maria O SagaidakVavilov Institute of General Genetics, Russian Academy of Sciences, Moscow, Russia.
Nadezhda A BogolubovaVavilov Institute of General Genetics, Russian Academy of Sciences, Moscow, Russia.
Tatiana G SmirnovaCentral Research Institute of Tuberculosis, Moscow, Russia.
Sofya N AndreevskayaCentral Research Institute of Tuberculosis, Moscow, Russia.
Elena E LarionovaCentral Research Institute of Tuberculosis, Moscow, Russia.
Maria G AlekseevaVavilov Institute of General Genetics, Russian Academy of Sciences, Moscow, Russia.
Larisa N ChernousovaCentral Research Institute of Tuberculosis, Moscow, Russia.
Valery N DanilenkoVavilov Institute of General Genetics, Russian Academy of Sciences, Moscow, Russia.
Vavilov Institute of General Genetics · RUCentral Scientific Research Institute of Tuberculosis Russian Academy of Medical Sciences · RUInstytut Biotechnologii i Antybiotyków · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Various genetic markers such as IS-elements, DR-elements, variable number tandem repeats (VNTR), single nucleotide polymorphisms (SNPs) in housekeeping genes and other groups of genes are being used for genotyping. We propose a different approach. We suggest the type II toxin-antitoxin (TA) systems, which play a significant role in the formation of pathogenicity, tolerance and persistence phenotypes, and thus in the survival of Mycobacterium tuberculosis in the host organism at various developmental stages (colonization, infection of macrophages, etc.), as the marker genes. Most genes of TA systems function together, forming a single network: an antitoxin from one pair may interact with toxins from other pairs and even from other families. In this work a bioinformatics analysis of genes of the type II TA systems from 173 sequenced genomes of M. tuberculosis was performed. A number of genes of type II TA systems were found to carry SNPs that correlate with specific genotypes. We propose a minimally sufficient set of genes of TA systems for separation of M. tuberculosis strains at nine basic genotype and for further division into subtypes. Using this set of genes, we genotyped a collection consisting of 62 clinical isolates of M. tuberculosis. The possibility of using our set of genes for genotyping using PCR is also demonstrated.

Indexed as

AntitoxinsBacterial ToxinsComputational BiologyDatabases, GeneticGenome, BacterialGenotyping TechniquesMycobacterium tuberculosisPolymorphism, GeneticAntitoxinsBacterial Toxins

Identifiers

PMID26658274
PMCPMC4680722
OpenAlexW2211947719

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Registered trials

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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.