Evidence map›Paper›PMID 31234780›Full record

ArticleBMC infectious diseases2019

Genomic characterization of MDR/XDR-TB in Kazakhstan by a combination of high-throughput methods predominantly shows the ongoing transmission of L2/Beijing 94-32 central Asian/Russian clusters.

B J Klotoe, S Kacimi, E Costa-Conceicão, H M Gomes, R B Barcellos, S Panaiotov, D Haj Slimene, N Sikhayeva, S Sengstake, A R Schuitema and 7 more

Open access · goldAbstract read
In one paragraph

Article in BMC infectious diseases, 2019. 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
1.7field-weighted citation impact, top 16% 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, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Draft genome sequence of a multidrug-resistantMicrobiology resource announcements · 2023
    Article
  5. Genomic Characterization of Drug-ResistantAntibiotics (Basel, Switzerland) · 2023
    Article
  6. Whole-Genome Sequence-Based Characterization of Pre-XDRDiagnostics (Basel, Switzerland) · 2023
    Article
  7. Article
  8. Article
  9. Article
  10. 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

17 authors at 4 institutions in 7 countries.

B J KlotoeInstitute for Integrative Biology of the Cell (I2BC), CEA, CNRS, Univ. Paris-Sud, Université Paris-Saclay, 91198, Gif-sur-Yvette cedex, France.
S KacimiInstitute for Integrative Biology of the Cell (I2BC), CEA, CNRS, Univ. Paris-Sud, Université Paris-Saclay, 91198, Gif-sur-Yvette cedex, France.
E Costa-ConceicãoInstitute for Integrative Biology of the Cell (I2BC), CEA, CNRS, Univ. Paris-Sud, Université Paris-Saclay, 91198, Gif-sur-Yvette cedex, France.
H M GomesInstitute for Integrative Biology of the Cell (I2BC), CEA, CNRS, Univ. Paris-Sud, Université Paris-Saclay, 91198, Gif-sur-Yvette cedex, France.
R B BarcellosInstitute for Integrative Biology of the Cell (I2BC), CEA, CNRS, Univ. Paris-Sud, Université Paris-Saclay, 91198, Gif-sur-Yvette cedex, France.
S PanaiotovInstitute for Integrative Biology of the Cell (I2BC), CEA, CNRS, Univ. Paris-Sud, Université Paris-Saclay, 91198, Gif-sur-Yvette cedex, France.
D Haj SlimeneInstitute for Integrative Biology of the Cell (I2BC), CEA, CNRS, Univ. Paris-Sud, Université Paris-Saclay, 91198, Gif-sur-Yvette cedex, France.
N SikhayevaNational Centre for Biotechnology, Astana, Kazakhstan.
S SengstakeRoyal Tropical Institute (KIT), Amsterdam, The Netherlands.
A R SchuitemaRoyal Tropical Institute (KIT), Amsterdam, The Netherlands.
M AkhalaiaFoundation for Innovative New Diagnostics (FIND), Geneva, Switzerland.
A AlenovaNational Centre for Tuberculosis Problems, Almaty, Kazakhstan.
E ZholdybayevaNational Centre for Biotechnology, Astana, Kazakhstan.
P TarlykovNational Centre for Biotechnology, Astana, Kazakhstan.
R AnthonyRoyal Tropical Institute (KIT), Amsterdam, The Netherlands.
G RefrégierInstitute for Integrative Biology of the Cell (I2BC), CEA, CNRS, Univ. Paris-Sud, Université Paris-Saclay, 91198, Gif-sur-Yvette cedex, France.
C SolaInstitute for Integrative Biology of the Cell (I2BC), CEA, CNRS, Univ. Paris-Sud, Université Paris-Saclay, 91198, Gif-sur-Yvette cedex, France. christophe.sola@i2bc.paris-saclay.fr.ORCID http://orcid.org/0000-0003-4672-2140
Université Paris-Sud · FRNational Center for Biotechnology · KZRoyal Tropical Institute · NLFIND · CH

Funding

Agence Nationale de la Recherche et de la Technologie 2015-1177Ministry of Research and Technology AP05130238Ministry of Research and Technology Priority area: 439 «Life Science» «Development of biomedicine and genetic engineering
6 · The paper itself

Abstract

backgroundKazakhstan remains a high-burden TB prevalence country with a concomitent high-burden of multi-drug resistant tuberculosis. For this reason, we performed an in depth genetic diversity and population structure characterization of Mycobacterium tuberculosis complex (MTC) genetic diversity in Kazakhstan with both patient and community benefit.

methodsA convenience sample of 700 MTC DNA cultures extracts from 630 tuberculosis patients recruited from 12 out of 14 regions in Kazakhstan, between 2010 and 2015, was independently studied by high-throughput hybridization-based methods, TB-SPRINT (59-Plex, n = 700), TB-SNPID (50-Plex, n = 543). DNA from 391 clinical isolates was successfully typed by two methods. To resolve the population structure of drug-resistant clades in more detail two complementary assays were run on the L2 isolates: an IS6110-NTF insertion site typing assay and a SigE SNP polymorphism assay.

resultsStrains belonged to L2/Beijing and L4/Euro-American sublineages; L2/Beijing prevalence totaled almost 80%. 50% of all samples were resistant to RIF and to INH., Subtyping showed that: (1) all L2/Beijing were "modern" Beijing and (2) most of these belonged to the previously described 94-32 sublineage (Central Asian/Russian), (3) at least two populations of the Central Asian/Russian sublineages are circulating in Kazakhstan, with different evolutionary dynamics.

conclusionsFor the first time, the global genetic diversity and population structure of M. tuberculosis genotypes circulating in Kazakhstan was obtained and compared to previous local studies. Results suggest a region-specific spread of a very limited number of L2/Beijing clonal complexes in Kazakhstan many strongly associated with an MDR phenotype.

Indexed as

AdultAgedAntitubercular AgentsDNA, BacterialDrug Resistance, Multiple, BacterialEvolution, MolecularGenetic VariationGenotypeHumansKazakhstanMaleMiddle AgedMycobacterium tuberculosisNucleic Acid Amplification TechniquesNucleic Acid HybridizationPhenotypeAntitubercular AgentsDNA, BacterialGenomicsHigh-throughput diagnostics methodsKazakhstanMDR-TBMolecular evolutionPublic healthTuberculosisXDR-TB

Identifiers

PMID31234780
PMCPMC6592005
OpenAlexW2950700742

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.