Evidence map›Paper›PMID 33384023›Full record

ArticleMalaria journal2020

Molecular surveillance and temporal monitoring of malaria parasites in focal Vietnamese provinces.

Bui Van Long, Genevieve Allen, Melanie Brauny, Le Thi Kieu Linh, Srinivas Reddy Pallerla, Tran Thi Thu Huyen, Hoang Van Tong, Nguyen Linh Toan, Do Quyet, Ho Anh Son and 1 more

Open access · goldAbstract read
In one paragraph

Article in Malaria journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

  1. Trial
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  5. Review
  6. Genetic Diversity of Circumsporozoite Surface Protein ofPathogens (Basel, Switzerland) · 2022
    Article
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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

11 authors at 2 institutions in 2 countries.

Bui Van LongInstitute of Tropical Medicine, Universitätsklinikum Tübingen, Wilhelmstrasse 27, 72074, Tübingen, Germany.
Genevieve AllenInstitute of Tropical Medicine, Universitätsklinikum Tübingen, Wilhelmstrasse 27, 72074, Tübingen, Germany.
Melanie BraunyInstitute of Tropical Medicine, Universitätsklinikum Tübingen, Wilhelmstrasse 27, 72074, Tübingen, Germany.
Le Thi Kieu LinhInstitute of Tropical Medicine, Universitätsklinikum Tübingen, Wilhelmstrasse 27, 72074, Tübingen, Germany.
Srinivas Reddy PallerlaInstitute of Tropical Medicine, Universitätsklinikum Tübingen, Wilhelmstrasse 27, 72074, Tübingen, Germany.
Tran Thi Thu HuyenInstitute of Biomedicine and Pharmacy, Vietnam Military Medical University, Hanoi, Vietnam.
Hoang Van TongInstitute of Biomedicine and Pharmacy, Vietnam Military Medical University, Hanoi, Vietnam.
Nguyen Linh ToanInstitute of Biomedicine and Pharmacy, Vietnam Military Medical University, Hanoi, Vietnam.
Do QuyetVietnam Military Medical University, Hanoi, Vietnam.
Ho Anh SonInstitute of Biomedicine and Pharmacy, Vietnam Military Medical University, Hanoi, Vietnam. hoanhsonhp@gmail.com.
Thirumalaisamy P VelavanInstitute of Tropical Medicine, Universitätsklinikum Tübingen, Wilhelmstrasse 27, 72074, Tübingen, Germany. velavan@medizin.uni-tuebingen.de.ORCID http://orcid.org/0000-0002-9809-9883
Universitätsklinikum Tübingen · DEVietnam Military Medical University · VN

Funding

Bundesministerium für Bildung und Forschung BMBF01DP17047Deutscher Akademischer Austauschdienst 57445019
6 · The paper itself

Abstract

backgroundWhile the World Health Organization (WHO) Southeast Asia region has the second highest incidence of malaria worldwide, malaria in Vietnam is focal to few provinces, where delayed parasite clearance to anti-malarial drugs is documented. This study aims to understand Plasmodium species distribution and the genetic diversity of msp1 and msp2 of parasite populations using molecular tools.

methodsA total of 222 clinical isolates from individuals with uncomplicated malaria were subjected to Plasmodium species identification by nested real-time PCR. 166 isolates positive for Plasmodium falciparum mono infections were further genotyped for msp1 (MAD20, K1, and RO33), and msp2 allelic families (3D7 and FC27). Amplicons were resolved through capillary electrophoresis in the QIAxcel Advanced system.

resultsMono-infections were high and with 75% P. falciparum, 14% Plasmodium vivax and 9% P. falciparum/P. vivax co-infections, with less than 1% Plasmodium malariae identified. For msp1, MAD20 was the most prevalent (99%), followed by K1 (46%) allelic family, with no sample testing positive for RO33 (0%). For msp2, 3D7 allelic family was predominant (97%), followed by FC27 (10%). The multiplicity of infection of msp1 and msp2 was 2.6 and 1.1, respectively, and the mean overall multiplicity of infection was 3.7, with the total number of alleles ranging from 1 to 7.

conclusionsGiven the increasing importance of antimalarial drugs in the region, the genetic diversity of P. falciparum msp1 and msp2 should be regularly monitored with respect to treatment outcomes and/or efficacy studies in regions, where there are ongoing changes in the malaria epidemiology.

Indexed as

Genetic VariationAntigens, ProtozoanCoinfectionGenotypeMalariaMalaria, FalciparumMalaria, VivaxMerozoite Surface Protein 1Plasmodium falciparumPlasmodium malariaePlasmodium vivaxProtozoan ProteinsVietnamAntigens, ProtozoanMerozoite Surface Protein 1merozoite surface protein 2, PlasmodiumProtozoan ProteinsMalariamsp1msp2Multiplicity of infectionSpeciesVietnam

Identifiers

PMID33384023
PMCPMC7775626
OpenAlexW3114285391

What OpenQuestion holds

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LicenceCC BY
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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.