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Genetic diversity of the Pvk12 gene in Plasmodium vivax from the China-Myanmar border area.
Deng, Shuang; Ruan, Yonghua; Bai, Yao; Hu, Yue; Deng, Zeshuai; He, Yongshu; Ruan, Rui; Wu, Yanrui; Yang, Zhaoqing; Cui, Liwang.
Afiliação
  • Deng S; Department of Pathogen Biology and Immunology, Kunming Medical University, Kunming, 650500, Yunnan Province, China.
  • Ruan Y; Department of Pathology, Kunming Medical University, Kunming, 650500, Yunnan Province, China.
  • Bai Y; Department of Pathology, Kunming Medical University, Kunming, 650500, Yunnan Province, China.
  • Hu Y; Department of Pathogen Biology and Immunology, Kunming Medical University, Kunming, 650500, Yunnan Province, China.
  • Deng Z; Department of Pharmacology, Kunming Medical University, Kunming, 650500, Yunnan Province, China.
  • He Y; Department of Pathogen Biology and Immunology, Kunming Medical University, Kunming, 650500, Yunnan Province, China.
  • Ruan R; Department of Pathology, Kunming Medical University, Kunming, 650500, Yunnan Province, China.
  • Wu Y; Department of Cell Biology and Medical Genetics, Kunming Medical University, Kunming, 650500, Yunnan Province, China.
  • Yang Z; Department of Cell Biology and Medical Genetics, Kunming Medical University, Kunming, 650500, Yunnan Province, China.
  • Cui L; Department of Orthopedics, The First Affiliated Hospital, Kunming Medical University, Kunming, 650500, Yunnan Province, China.
Malar J ; 15(1): 528, 2016 Nov 04.
Article em En | MEDLINE | ID: mdl-27809837
ABSTRACT

BACKGROUND:

Plasmodium falciparum resistance to artemisinin emerged in the Greater Mekong Sub-region has been associated with mutations in the propeller domain of the kelch gene Pfk13.

METHODS:

Here the polymorphisms in Pvk12 gene, the orthologue of Pfk13 in Plasmodium vivax, were determined by PCR and sequencing in 262 clinical isolates collected in recent years (2012-2015) from the China-Myanmar border area.

RESULTS:

Sequencing of full-length Pvk12 genes from these isolates identified three synonymous mutations (N172N, S360S, S697S) and one non-synonymous mutation M124I, all of which were at very low prevalence (2.0-3.1%). Moreover, these mutations were non-overlapping between the two study sites on both sides of the border. Molecular evolutionary analysis detected signature of purifying selection on Pvk12.

CONCLUSIONS:

There is no direct evidence that Pvk12 is involved in artemisinin resistance in P. vivax, but it remains a potential candidate requiring further investigation. Continuous monitoring of potential drug resistance in this parasite is needed in order to facilitate the regional malaria elimination campaign.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Plasmodium vivax / Polimorfismo Genético / Resistência a Medicamentos / Proteínas de Protozoários Tipo de estudo: Risk_factors_studies Limite: Humans País/Região como assunto: Asia Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Plasmodium vivax / Polimorfismo Genético / Resistência a Medicamentos / Proteínas de Protozoários Tipo de estudo: Risk_factors_studies Limite: Humans País/Região como assunto: Asia Idioma: En Ano de publicação: 2016 Tipo de documento: Article