Evidence map›Paper›PMID 23555629›Full record

ArticlePloS one2013

Genetic diversity and lack of artemisinin selection signature on the Plasmodium falciparum ATP6 in the Greater Mekong Subregion.

Miao Miao, Zenglei Wang, Zhaoqing Yang, Lili Yuan, Daniel M Parker, Chaturong Putaporntip, Somchai Jongwutiwes, Phonepadith Xangsayarath, Tiengkham Pongvongsa, Hazuhiko Moji and 11 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

6 citing papers in PubMed, 17 citations in OpenAlex.

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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

21 authors at 11 institutions in 6 countries.

Miao MiaoDepartment of Entomology, Pennsylvania State University, University Park, PA, USA.
Zenglei Wang
Zhaoqing Yang
Lili Yuan
Daniel M Parker
Chaturong Putaporntip
Somchai Jongwutiwes
Phonepadith Xangsayarath
Tiengkham Pongvongsa
Hazuhiko Moji
Trinh Dinh Tuong
Tomoko Abe
Shusuke Nakazawa
Myat Phone Kyaw
Guiyun Yan
Jeeraphat Sirichaisinthop
Jetsumon Sattabongkot
Jianbing Mu
Xin-zhuan Su
Osamu Kaneko
Liwang Cui
Nagasaki University · JPPennsylvania State University · USChulalongkorn University · THSecond Affiliated Hospital of Kunming Medical College · CNMahidol University · THMyanmar Oxford Clinical Research Unit · MMNational Institute of Allergy and Infectious Diseases · USNational Institute of Malariology, Parasitology and Entomology · VNNational Institutes of Health · USResearch Institute for Humanity and Nature · JPUniversity of California, Irvine · US

Funding

Southeast Asia Malaria Research CenterU19AI089672 · NIAID · UNIVERSITY OF SOUTH FLORIDA · PI CUI, LIWANG · 2010 to 2023
$28.9M
Malaria Parasite Sexual Development, Drug Resistance, and EvolutionZIAAI000892 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI SU, XINZHUAN · 2009 to 2025
$23.3M
Population biology of malaria drug resistance in YunnanR01AI075429 · NIAID · KUNMING MEDICAL COLLEGE · PI YANG, ZHAOQING · 2007 to 2010
$327k
Intramural NIH HHSNIAID NIH HHS 1R01AI075429NIAID NIH HHS R01 AI075429NIAID NIH HHS U19 AI089672
6 · The paper itself

Abstract

The recent detection of clinical Artemisinin (ART) resistance manifested as delayed parasite clearance in the Cambodia-Thailand border area raises a serious concern. The mechanism of ART resistance is not clear; but the P. falciparum sarco/endoplasmic reticulum Ca(2+)-ATPase (PfSERCA or PfATP6) has been speculated to be the target of ARTs and thus a potential marker for ART resistance. Here we amplified and sequenced pfatp6 gene (~3.6 Kb) in 213 samples collected after 2005 from the Greater Mekong Subregion, where ART drugs have been used extensively in the past. A total of 24 single nucleotide polymorphisms (SNPs), including 8 newly found in this study and 13 nonsynonymous, were identified. However, these mutations were either uncommon or also present in other geographical regions with limited ART use. None of the mutations were suggestive of directional selection by ARTs. We further analyzed pfatp6 from a worldwide collection of 862 P. falciparum isolates in 19 populations from Asia, Africa, South America and Oceania, which include samples from regions prior to and after deployments ART drugs. A total of 71 SNPs were identified, resulting in 106 nucleotide haplotypes. Similarly, many of the mutations were continent-specific and present at frequencies below 5%. The most predominant and perhaps the ancestral haplotype occurred in 441 samples and was present in 16 populations from Asia, Africa, and Oceania. The 3D7 haplotype found in 54 samples was the second most common haplotype and present in nine populations from all four continents. Assessment of the selection strength on pfatp6 in the 19 parasite populations found that pfatp6 in most of these populations was under purifying selection with an average d(N)/d(S) ratio of 0.333. Molecular evolution analyses did not detect significant departures from neutrality in pfatp6 for most populations, challenging the suitability of this gene as a marker for monitoring ART resistance.

Indexed as

MutationPolymorphism, Single NucleotideAntimalarialsArtemisininsAsia, SoutheasternCalcium-Transporting ATPasesDNA, ProtozoanDrug ResistanceHaplotypesHumansMalaria, FalciparumPhylogeographyPlasmodium falciparumSelection, GeneticAntimalarialsartemisininArtemisininsATP6 protein, Plasmodium falciparumCalcium-Transporting ATPasesDNA, Protozoan

Identifiers

PMID23555629
PMCPMC3608609
OpenAlexW2144315263

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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.