Evidence map›Paper›PMID 19193842›Full record

ArticleJournal of clinical microbiology2009

Use of spoligotyping and large sequence polymorphisms to study the population structure of the Mycobacterium tuberculosis complex in a cohort study of consecutive smear-positive tuberculosis cases in The Gambia.

Bouke C de Jong, Martin Antonio, Timothy Awine, Kunle Ogungbemi, Ype P de Jong, Sebastien Gagneux, Kathryn DeRiemer, Thierry Zozio, Nalin Rastogi, Martien Borgdorff and 2 more

Abstract read
In one paragraph

Article in Journal of clinical microbiology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
–field-weighted citation impact
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

33 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Article
  4. Article
  5. A multiplex PCR assay for the differentiation ofFrontiers in cellular and infection microbiology · 2023
    Article
  6. Review
  7. Exploring the usefulness of molecular epidemiology of tuberculosis in Africa: a systematic review.International journal of molecular epidemiology and genetics · 2020
    Review
  8. Frequency of the Mycobacterium tuberculosis RDBMC infectious diseases · 2019
    Article
  9. Article
  10. Article
  11. First insights into circulating Mycobacterium tuberculosis complex lineages and drug resistance in Guinea.Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases · 2015
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Deciphering the growth behaviour of Mycobacterium africanum.PLoS neglected tropical diseases · 2013
    Article
  19. Article
  20. 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

12 authors.

Bouke C de JongMRC Laboratories, P.O. Box 273, Banjul, The Gambia. bdejong@mrc.gm.
Martin Antonio
Timothy Awine
Kunle Ogungbemi
Ype P de Jong
Sebastien Gagneux
Kathryn DeRiemer
Thierry Zozio
Nalin Rastogi
Martien Borgdorff
Philip C Hill
Richard A Adegbola

Funding

Mycobacterial Determinants of Cavitation &TransmissionK01TW006083 · FIC · STANFORD UNIVERSITY · PI DE JONG, BOUKE C · 2002 to 2010
$780k
FIC NIH HHS K01 TW006083FIC NIH HHS TW006083Medical Research Council MC_U117588500Medical Research Council MC_U190071468Medical Research Council MC_U190081982
6 · The paper itself

Abstract

Mycobacterium africanum, first described in Senegal in 1968, causes up to half of the smear-positive pulmonary tuberculosis cases in West Africa, but it has not been found in other geographical areas except among recent West African migrants. The reasons for the geographic restriction of M. africanum are unknown. We used molecular tools to determine the population structure of the Mycobacterium tuberculosis complex in a cohort study of consecutive smear-positive tuberculosis cases in The Gambia. We collected and genotyped 386 clinical isolates using spoligotype analysis and PCRs for large sequence polymorphisms (LSPs) and compared the genotype patterns to the patterns in an international database. The results of spoligotyping and LSP analysis for the study population were also compared to determine the correlation between them. The main lineages within the Mycobacterium tuberculosis complex identified in The Gambia included M. africanum type I (38.4%), characterized by an LSP in region of difference 702 (RD702; West African type 2). Among the M. tuberculosis sensu stricto isolates, lineages characterized by RD182 and by RD174 were the most common. We also detected a gradient in the prevalence of M. africanum that extended from neighboring Guinea-Bissau. The genotypic diversity of the spoligotype patterns was greater among the isolates of M. africanum than among the isolates of M. tuberculosis. We postulate that M. africanum became endemic in West Africa first, before the introduction of different lineages within M. tuberculosis sensu stricto.

Indexed as

Polymorphism, GeneticAdolescentAdultAgedAged, 80 and overBacterial Typing TechniquesCluster AnalysisCohort StudiesDNA, BacterialDNA FingerprintingFemaleGambiaGenotypeGuinea-BissauHumansMaleDNA, Bacterial

Identifiers

PMID19193842
PMCPMC2668362

What OpenQuestion holds

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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.