Evidence map›Paper›PMID 26360617›Full record

ArticlePLoS neglected tropical diseases2015

Human Genetic Ancestral Composition Correlates with the Origin of Mycobacterium leprae Strains in a Leprosy Endemic Population.

Nora Cardona-Castro, Edwin Cortés, Camilo Beltrán, Marcela Romero, Jaime E Badel-Mogollón, Gabriel Bedoya

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

5 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Cutaneous Mycobacterial Infections.Clinical microbiology reviews · 2018
    Review
  5. Unsolved matters in leprosy: a descriptive review and call for further research.Annals of clinical microbiology and antimicrobials · 2016
    Review
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

6 authors at 2 institutions in 1 country.

Nora Cardona-CastroInstituto Colombiano de Medicina Tropical-Universidad CES, Sabaneta, Antioquia, Colombia.
Edwin CortésGrupo GENMOL, Instituto de Biología Universidad de Antioquia, Medellín, Colombia.
Camilo BeltránInstituto Colombiano de Medicina Tropical-Universidad CES, Sabaneta, Antioquia, Colombia.
Marcela RomeroInstituto Colombiano de Medicina Tropical-Universidad CES, Sabaneta, Antioquia, Colombia.
Jaime E Badel-MogollónSkandha EIT S.A.S., Medellin, Colombia.
Gabriel BedoyaGrupo GENMOL, Instituto de Biología Universidad de Antioquia, Medellín, Colombia.
Instituto Colombiano de Medicina Tropical · COUniversidad de Antioquia · CO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent reports have suggested that leprosy originated in Africa, extended to Asia and Europe, and arrived in the Americas during European colonization and the African slave trade. Due to colonization, the contemporary Colombian population is an admixture of Native-American, European and African ancestries. Because microorganisms are known to accompany humans during migrations, patterns of human migration can be traced by examining genomic changes in associated microbes. The current study analyzed 118 leprosy cases and 116 unrelated controls from two Colombian regions endemic for leprosy (Atlantic and Andean) in order to determine possible associations of leprosy with patient ancestral background (determined using 36 ancestry informative markers), Mycobacterium leprae genotype and/or patient geographical origin. We found significant differences between ancestral genetic composition. European components were predominant in Andean populations. In contrast, African components were higher in the Atlantic region. M. leprae genotypes were then analyzed for cluster associations and compared with the ancestral composition of leprosy patients. Two M. leprae principal clusters were found: haplotypes C54 and T45. Haplotype C54 associated with African origin and was more frequent in patients from the Atlantic region with a high African component. In contrast, haplotype T45 associated with European origin and was more frequent in Andean patients with a higher European component. These results suggest that the human and M. leprae genomes have co-existed since the African and European origins of the disease, with leprosy ultimately arriving in Colombia during colonization. Distinct M. leprae strains followed European and African settlement in the country and can be detected in contemporary Colombian populations.

Indexed as

Endemic DiseasesRacial GroupsAdolescentAdultAgedCluster AnalysisColombiaFemaleHaplotypesHumansLeprosyMaleMiddle AgedMycobacterium lepraePhylogenySequence Homology

Identifiers

PMID26360617
PMCPMC4567314
OpenAlexW1436127467

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.