Evidence map›Paper›PMID 17898156›Full record

ArticleJournal of clinical microbiology2007

Discovery of a novel Mycobacterium tuberculosis lineage that is a major cause of tuberculosis in Rio de Janeiro, Brazil.

Luiz Claudio Oliveira Lazzarini, Richard C Huard, Neio L Boechat, Harrison M Gomes, Maranibia C Oelemann, Natalia Kurepina, Elena Shashkina, Fernanda C Q Mello, Andrea L Gibson, Milena J Virginio and 6 more

Abstract read
In one paragraph

Article in Journal of clinical microbiology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 1 pooled it
–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

57 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. A systematic review of East African-Indian family of Mycobacterium tuberculosis in Brazil.The Brazilian journal of infectious diseases : an official publication of the Brazilian Society of Infectious Diseases
    Pooled it
  2. Article
  3. Molecular epidemiology ofJournal of clinical tuberculosis and other mycobacterial diseases · 2024
    Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Identification of gene fusion events inNAR genomics and bioinformatics · 2020
    Article
  12. Article
  13. Global Distribution and Evolution ofFrontiers in microbiology · 2020
    Article
  14. Circulation ofPathogens and global health · 2019
    Review
  15. Article
  16. Frequency of the Mycobacterium tuberculosis RDBMC infectious diseases · 2019
    Article
  17. Article
  18. Article
  19. Review
  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

16 authors.

Luiz Claudio Oliveira LazzariniDepartment of Medicine, Division of International Medicine and Infectious Diseases, Cornell University, Joan and Sanford I Weill Medical College, New York, NY 10021, USA.
Richard C Huard
Neio L Boechat
Harrison M Gomes
Maranibia C Oelemann
Natalia Kurepina
Elena Shashkina
Fernanda C Q Mello
Andrea L Gibson
Milena J Virginio
Ana Grazia Marsico
W Ray Butler
Barry N Kreiswirth
Philip N Suffys
Jose Roberto Lapa E Silva
John L Ho

Funding

TUBERCULOSIS INTERNATIONAL TRAINING AND RESEARCH PROGRAMD43TW000018 · FIC · WEILL MEDICAL COLL OF CORNELL UNIV · PI JOHNSON, WARREN DOUGLAS · 1988 to 2012
$16.1M
Innovative Approaches for Tuberculosis Control in BrazilU2RTW006885 · FIC · JOHNS HOPKINS UNIVERSITY · PI GOLUB, JONATHAN E. · 2005 to 2014
$2.3M
MOLECULAR MECHANISMS IN ENDOTHELIAL DYSFUNCTION IN HIV 1R01HL061960 · NHLBI · WEILL MEDICAL COLLEGE OF CORNELL UNIV · PI HO, JOHN LAP · 1998 to 2004
$1.2M
Large-scale Gene Deletion in Infectious M. tuberculosisR21AI063147 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI HO, JOHN LAP · 2005 to 2006
$390k
MOLECULAR MECHANISMS FOR VASCULAR CELL DEACTIVATIONR01AI039606 · NIAID · WEILL MEDICAL COLLEGE OF CORNELL UNIV · PI JOHNSON, WARREN D. · 1996 to 2000
$258k
FIC NIH HHS D43 TW000018FIC NIH HHS D43 TW00018FIC NIH HHS U2R TW006885NHLBI NIH HHS R01 HL61960NIAID NIH HHS R01 AI39606NIAID NIH HHS R21 AI063147
6 · The paper itself

Abstract

The current study evaluated Mycobacterium tuberculosis isolates from Rio de Janeiro, Brazil, for genomic deletions. One locus in our panel of PCR targets failed to amplify in approximately 30% of strains. A single novel long sequence polymorphism (>26.3 kb) was characterized and designated RD(Rio). Homologous recombination between two similar protein-coding genes is proposed as the mechanism for deleting or modifying 10 genes, including two potentially immunogenic PPE proteins. The flanking regions of the RD(Rio) locus were identical in all strains bearing the deletion. Genetic testing by principal genetic group, spoligotyping, variable-number tandem repeats of mycobacterial interspersed repetitive units (MIRU-VNTR), and IS6110-based restriction fragment length polymorphism analysis cumulatively support the idea that RD(Rio) strains are derived from a common ancestor belonging solely to the Latin American-Mediterranean spoligotype family. The RD(Rio) lineage is therefore the predominant clade causing tuberculosis (TB) in Rio de Janeiro and, as indicated by genotypic clustering in MIRU-VNTR analysis, the most significant source of recent transmission. Limited retrospective reviews of bacteriological and patient records showed a lack of association with multidrug resistance or specific risk factors for TB. However, trends in the data did suggest that RD(Rio) strains may cause a form of TB with a distinct clinical presentation. Overall, the high prevalence of this genotype may be related to enhanced virulence, transmissibility, and/or specific adaptation to a Euro-Latin American host population. The identification of RD(Rio) strains outside of Brazil points to the ongoing intercontinental dissemination of this important genotype. Further studies are needed to determine the differential strain-specific features, pathobiology, and worldwide prevalence of RD(Rio) M. tuberculosis.

Indexed as

Polymorphism, GeneticAnimalsBrazilCluster AnalysisDNA, BacterialDNA FingerprintingDNA Transposable ElementsGenotypeHumansMinisatellite RepeatsMycobacterium tuberculosisPhylogenyPolymerase Chain ReactionPolymorphism, Restriction Fragment LengthRecombination, GeneticSequence DeletionDNA, BacterialDNA Transposable Elements

Identifiers

PMID17898156
PMCPMC2168543

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.