Evidence map›Paper›PMID 34906144›Full record

ArticleMalaria journal2021

Assessment of Plasmodium falciparum anti-malarial drug resistance markers in pfcrt and pfmdr1 genes in isolates from Honduras and Nicaragua, 2018-2021.

Gustavo Fontecha, Alejandra Pinto, Osman Archaga, Sergio Betancourth, Lenin Escober, Jessica Henríquez, Hugo O Valdivia, Alberto Montoya, Rosa Elena Mejía

Open access · goldAbstract read
In one paragraph

Article in Malaria journal, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

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  7. A PCR-RFLP Technique to Assess the Geographic Origin ofTropical medicine and infectious disease · 2022
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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

9 authors at 2 institutions in 2 countries.

Gustavo FontechaMicrobiology Research Institute, National Autonomous University of Honduras, Tegucigalpa, Honduras. gustavo.fontecha@unah.edu.hn.ORCID http://orcid.org/0000-0001-9756-4520
Alejandra PintoMicrobiology Research Institute, National Autonomous University of Honduras, Tegucigalpa, Honduras.
Osman ArchagaMicrobiology Research Institute, National Autonomous University of Honduras, Tegucigalpa, Honduras.
Sergio BetancourthMicrobiology Research Institute, National Autonomous University of Honduras, Tegucigalpa, Honduras.
Lenin EscoberNational Malaria Laboratory, National Department of Surveillance, Ministry of Health of Honduras, Tegucigalpa, Honduras.
Jessica HenríquezNational Malaria Laboratory, National Department of Surveillance, Ministry of Health of Honduras, Tegucigalpa, Honduras.
Hugo O ValdiviaDepartment of Parasitology, U.S. Naval Medical Research Unit No, 6 (NAMRU-6), Lima, Peru.
Alberto MontoyaNational Center for Diagnosis and Reference, Health Ministry, Managua, Nicaragua.
Rosa Elena MejíaPan American Health Organization, Tegucigalpa, Honduras.
National Autonomous University of Honduras · HNUnited States Naval Medical Research Unit SOUTH · PE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCentral America and the island of Hispaniola have set out to eliminate malaria by 2030. However, since 2014 a notable upturn in the number of cases has been reported in the Mosquitia region shared by Nicaragua and Honduras. In addition, the proportion of Plasmodium falciparum malaria cases has increased significantly relative to vivax malaria. Chloroquine continues to be the first-line drug to treat uncomplicated malaria in the region. The objective of this study was to evaluate the emergence of chloroquine resistant strains of P. falciparum using a genetic approach. Plasmodium vivax populations are not analysed in this study.

methods205 blood samples from patients infected with P. falciparum between 2018 and 2021 were analysed. The pfcrt gene fragment encompassing codons 72-76 was analysed. Likewise, three fragments of the pfmdr1 gene were analysed in 51 samples by nested PCR and sequencing.

resultsAll samples revealed the CVMNK wild phenotype for the pfcrt gene and the N86, Y184F, S1034C, N1042D, D1246 phenotype for the pfmdr1 gene.

conclusionsThe increase in falciparum malaria cases in Nicaragua and Honduras cannot be attributed to the emergence of chloroquine-resistant mutants. Other possibilities should be investigated further. This is the first study to report the genotype of pfmdr1 for five loci of interest in Central America.

Indexed as

AntimalarialsATP-Binding Cassette, Sub-Family C ProteinsDrug ResistanceGenetic MarkersHondurasMalaria, FalciparumMembrane Transport ProteinsNicaraguaPlasmodium falciparumProtozoan ProteinsAntimalarialsATP-Binding Cassette, Sub-Family C ProteinsGenetic MarkersMdr1 protein, Plasmodium falciparumMembrane Transport ProteinsPfCRT protein, Plasmodium falciparumProtozoan ProteinsDrug resistanceHondurasNicaraguaPfcrtPfmdr1Plasmodium falciparumSurveillance

Identifiers

PMID34906144
PMCPMC8670165
OpenAlexW4225984322

What OpenQuestion holds

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LicenceCC BY
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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.