Evidence map›Paper›PMID 37823960›Full record

ArticleJournal, genetic engineering & biotechnology2023

Phylogenetic analysis of prospective M. bovis antigens with the aim of developing candidate vaccines for bovine tuberculosis.

Zhandos Abay, Sandugash Sadikalieva, Kamshat Shorayeva, Bolat Yespembetov, Makpal Sarmykova, Kuanish Jekebekov, Gaukhar Tokkarina, Zharkinay Absatova, Elina Kalimolda, Yeraly Shayakhmetov and 10 more

Open access · diamondAbstract read
In one paragraph

Article in Journal, genetic engineering & biotechnology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. 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

20 authors at 2 institutions in 2 countries.

Zhandos AbayResearch Institute for Biological Safety Problems, Gvardeysky, 080409, Kazakhstan.
Sandugash SadikalievaResearch Institute for Biological Safety Problems, Gvardeysky, 080409, Kazakhstan.
Kamshat ShorayevaResearch Institute for Biological Safety Problems, Gvardeysky, 080409, Kazakhstan. abaizh097@mail.ru.
Bolat YespembetovResearch Institute for Biological Safety Problems, Gvardeysky, 080409, Kazakhstan.
Makpal SarmykovaResearch Institute for Biological Safety Problems, Gvardeysky, 080409, Kazakhstan.
Kuanish JekebekovResearch Institute for Biological Safety Problems, Gvardeysky, 080409, Kazakhstan.
Gaukhar TokkarinaResearch Institute for Biological Safety Problems, Gvardeysky, 080409, Kazakhstan.
Zharkinay AbsatovaResearch Institute for Biological Safety Problems, Gvardeysky, 080409, Kazakhstan.
Elina KalimoldaResearch Institute for Biological Safety Problems, Gvardeysky, 080409, Kazakhstan.
Yeraly ShayakhmetovResearch Institute for Biological Safety Problems, Gvardeysky, 080409, Kazakhstan.
Sabina MoldagulovaResearch Institute for Biological Safety Problems, Gvardeysky, 080409, Kazakhstan.
Aisha IssabekResearch Institute for Biological Safety Problems, Gvardeysky, 080409, Kazakhstan.
Syrym KopeyevResearch Institute for Biological Safety Problems, Gvardeysky, 080409, Kazakhstan.
Alisher OmurtayResearch Institute for Biological Safety Problems, Gvardeysky, 080409, Kazakhstan.
Kainar BarakbayevResearch Institute for Biological Safety Problems, Gvardeysky, 080409, Kazakhstan.
Markhabat KassenovResearch Institute for Biological Safety Problems, Gvardeysky, 080409, Kazakhstan.
Nazym SyrymResearch Institute for Biological Safety Problems, Gvardeysky, 080409, Kazakhstan.
Yergali AbduraimovResearch Institute for Biological Safety Problems, Gvardeysky, 080409, Kazakhstan.
Kunsulu ZakaryaResearch Institute for Biological Safety Problems, Gvardeysky, 080409, Kazakhstan.
Ainur NurpeisovaResearch Institute for Biological Safety Problems, Gvardeysky, 080409, Kazakhstan.
Al-Farabi Kazakh National University · KZInstitute of Informatics Problems · RU

Funding

Ministry of Education and Science of the Republic of Kazakhstan IRN AR09259683
6 · The paper itself

Abstract

backgroundBovine Tuberculosis is a respiratory disease caused by the pathogen Mycobacterium bovis (M. bovis) that infects cattle. Though rare, this disease can also affect humans, as well as domestic and wild animals, making it a serious concern. Therefore, searching for alternative and new vaccines with high efficiency and safety is the main goal in bovine tuberculosis prophylaxis. New vaccines, known as vector vaccines, have the potential to become safe and effective alternatives to the traditional BCG vaccine. In this study, two major immunodominant proteins of M. bovis Esat-6 and TB10.4 were utilized to create a vector vaccine for bovine tuberculosis.

methodsThe Esat-6 and TB10.4 genes were amplified by PCR. The amplified and purified PCR products were sequenced by the Sanger method. Assembly and multiple alignments of amplicon nucleotides were carried out in the MEGA 11 software.

resultTwo genes of the local strain 0078-M. bovis-8/RIBSP were sequenced. The nucleotide sequences were deposited in the GenBank database. Comparative analysis of the nucleotide sequences of the ESAT-6 and TB10.4 genes established 100% identity of the compared strains of Mycobacterium.

conclusionThrough the use of phylogenetic analysis, it has been confirmed that the amplified genes are related to the mycobacteria genus. This discovery allows the development of a vector vaccine against bovine tuberculosis utilising these genes.

Indexed as

Bovine tuberculosisESAT-6M. bovisPCRSengerSequencingTB10.4Vaccine

Identifiers

PMID37823960
PMCPMC10570230
OpenAlexW4387564349

What OpenQuestion holds

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LicenceCC BY
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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.