Evidence map›Paper›PMID 39621694›Full record

ArticlePloS one2024

Applying a cytochrome c oxidase I barcode for Leishmania species typing.

Carlos Mata-Somarribas, Grazielle Cardoso das Graças, Luiza de Oliveira R Pereira, Mariana Côrtes Boité, Lilian Motta Cantanhêde, Camila Patrício Braga Filgueira, Adrián Fallas, Leana Quirós-Rojas, Karina A Morelli, Gabriel Eduardo Melim Ferreira and 1 more

Abstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

11 authors.

Carlos Mata-SomarribasCentro Nacional de Referencia de Parasitología, Instituto Costarricense de Investigación y Enseñanza en Nutrición y Salud, Cartago, Costa Rica.ORCID 0000-0001-7650-5388
Grazielle Cardoso das GraçasHospital Universitário Gaffrée e Guinle-Universidade Federal do Estado do Rio de Janeiro, Rio de Janeiro, RJ, Brasil.
Luiza de Oliveira R PereiraLaboratório de Pesquisa em Leishmanioses, Fiocruz-Fundação Oswaldo Cruz, Instituto Oswaldo Cruz, Rio de Janeiro, RJ, Brasil.
Mariana Côrtes BoitéLaboratório de Pesquisa em Leishmanioses, Fiocruz-Fundação Oswaldo Cruz, Instituto Oswaldo Cruz, Rio de Janeiro, RJ, Brasil.
Lilian Motta CantanhêdeLaboratório de Pesquisa em Leishmanioses, Fiocruz-Fundação Oswaldo Cruz, Instituto Oswaldo Cruz, Rio de Janeiro, RJ, Brasil.
Camila Patrício Braga FilgueiraLaboratório de Pesquisa em Leishmanioses, Fiocruz-Fundação Oswaldo Cruz, Instituto Oswaldo Cruz, Rio de Janeiro, RJ, Brasil.ORCID 0000-0001-7885-7774
Adrián FallasHospital Escalante Pradilla, Caja Costarricense de Seguro Social, San José, Costa Rica.
Leana Quirós-RojasHospital de Guápiles, Caja Costarricense de Seguro Social, Limón, Costa Rica.
Karina A MorelliDepartamento de Ecologia, Instituto de Biologia Roberto Alcântara Gomes-Universidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ, Brasil.
Gabriel Eduardo Melim FerreiraLaboratório de Epidemiologia Genética, Fundação Oswaldo Cruz Noroeste-Fiocruz Rondônia, Rondônia, RO, Brasil.ORCID 0000-0002-3514-3031
Elisa CupolilloLaboratório de Pesquisa em Leishmanioses, Fiocruz-Fundação Oswaldo Cruz, Instituto Oswaldo Cruz, Rio de Janeiro, RJ, Brasil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Species delimitation has always been a challenge for taxonomists and for Leishmania studies there is no exception. Herein we attempt to display the usefulness of the mitochondrial gene Cytochrome Oxidase I-coI in classical and barcode-based approaches for Leishmania characterization. A total of 228 samples were analyzed, comprising 28 Leishmania related taxa, mainly from cultures of the Oswaldo Cruz Foundation`s Leishmania Collection. Primers were designed for amplification of coI; sequences were analyzed by distance-based indicators and both the Neighbor Joining and NeighborNet as species grouping techniques. Automatic Barcode Gap Discovery was applied to define species delimitation while for the character-based analysis a software for Barcoding with Logic formulas was employed. Final sequences of 486 bp with 238 parsimonious sites were aligned and edited. Robust groups were formed for most of the genus species, distinctive nucleotide positions in the barcode sequence were observed for 11 of them. A good agreement between the techniques applied and the original characterization was observed. Few species were not distinguished by coI: (i) L. (V.) peruviana, L. (V.) lindenbergi, and L. (V.) utingensis; (ii) L. (L.) venezuelensis and (iii) L. colombiensis and L. equatorensis with identical sequences. Some of these taxa have been, at one time or another, classified as controversial and, for most of them, a higher number of isolates should be studied to properly infer their taxonomic status. CoI represents a mitochondrial target that stands out as a taxonomically important asset with multiple advantages over other genes. This paper corresponds to the first report of coI analysis in Leishmania, a potentially advantageous target for the characterization of this parasite.

Indexed as

DNA Barcoding, TaxonomicElectron Transport Complex IVLeishmaniaPhylogenySpecies SpecificityElectron Transport Complex IV

Identifiers

PMID39621694
PMCPMC11611135

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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.