Evidence map›Paper›PMID 22701513›Full record

ArticlePloS one2012

In vitro sensitivity of Plasmodium falciparum from China-Myanmar border area to major ACT drugs and polymorphisms in potential target genes.

Zenglei Wang, Daniel Parker, Hao Meng, Lanou Wu, Jia Li, Zhen Zhao, Rongping Zhang, Miao Miao, Qi Fan, Haiyan Wang and 2 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
6.3field-weighted citation impact, top 3% 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

29 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Molecular Surveillance and in vitro Drug Sensitivity Study ofThe American journal of tropical medicine and hygiene · 2020
    Article
  7. Article
  8. Article
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  11. Association between Polymorphisms in the PfAntimicrobial agents and chemotherapy · 2017
    Article
  12. Article
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  15. Article
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  17. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 2 countries.

Zenglei WangDepartment of Entomology, Pennsylvania State University, University Park, Pennsylvania, United States of America.
Daniel Parker
Hao Meng
Lanou Wu
Jia Li
Zhen Zhao
Rongping Zhang
Miao Miao
Qi Fan
Haiyan Wang
Liwang Cui
Zhaoqing Yang
Kunming Medical University · CNPennsylvania State University · USKansas State University · US

Funding

Southeast Asia Malaria Research CenterU19AI089672 · NIAID · UNIVERSITY OF SOUTH FLORIDA · PI CUI, LIWANG · 2010 to 2023
$28.9M
Population biology of malaria drug resistance in YunnanR01AI075429 · NIAID · KUNMING MEDICAL COLLEGE · PI YANG, ZHAOQING · 2007 to 2010
$327k
NIAID NIH HHS 1R01AI075429NIAID NIH HHS R01 AI075429NIAID NIH HHS U19 AI089672NIAID NIH HHS U19AI089672
6 · The paper itself

Abstract

Drug resistance has always been one of the most important impediments to global malaria control. Artemisinin resistance has recently been confirmed in the Greater Mekong Subregion (GMS) and efforts for surveillance and containment are intensified. To determine potential mechanisms of artemisinin resistance and monitor the emergence and spread of resistance in other regions of the GMS, we investigated the in vitro sensitivity of 51 culture-adapted parasite isolates from the China-Myanmar border area to four drugs. The 50% inhibitory concentrations (IC₅₀s) of dihydroartemisinin, mefloquine and lumefantrine were clustered in a relatively narrow, 3- to 6-fold range, whereas the IC₅₀ range of artesunate was 12-fold. We assessed the polymorphisms of candidate resistance genes pfcrt, pfmdr1, pfATP6, pfmdr6 and pfMT (a putative metabolite/drug transporter). The K76T mutation in pfcrt reached fixation in the study parasite population, whereas point mutations in pfmdr1 and pfATP6 had low levels of prevalence. In addition, pfmdr1 gene amplification was not detected. None of the mutations in pfmdr1 and pfATP6 was associated significantly with in vitro sensitivity to artemisinin derivatives. The ABC transporter gene pfmdr6 harbored two point mutations, two indels, and number variations in three simple repeats. Only the length variation in a microsatellite repeat appeared associated with altered sensitivity to dihydroartemisinin. The PfMT gene had two point mutations and one codon deletion; the I30N and N496- both reached high levels of prevalence. However, none of the SNPs or haplotypes in PfMT were correlated significantly with resistance to the four tested drugs. Compared with other parasite populations from the GMS, our studies revealed drastically different genotype and drug sensitivity profiles in parasites from the China-Myanmar border area, where artemisinins have been deployed extensively for over 30 years.

Indexed as

AntimalarialsArtemisininsArtesunateATP-Binding Cassette, Sub-Family C ProteinsCalcium-Transporting ATPasesChinaDrug ResistanceEthanolaminesFluorenesLumefantrineMembrane Transport ProteinsMyanmarPlasmodium falciparumPolymorphism, GeneticProtozoan ProteinsAntimalarialsArtemisininsartenimolArtesunateATP6 protein, Plasmodium falciparumATP-Binding Cassette, Sub-Family C ProteinsCalcium-Transporting ATPasesEthanolaminesFluorenesLumefantrineMdr1 protein, Plasmodium falciparumMembrane Transport ProteinsPfCRT protein, Plasmodium falciparumProtozoan Proteins

Identifiers

PMID22701513
PMCPMC3365119
OpenAlexW2054869324

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.