Plasmodium falciparum Falcipain-2a Polymorphisms in Southeast Asia and Their Association With Artemisinin Resistance

被引:26
|
作者
Siddiqui, Faiza A. [1 ]
Cabrera, Mynthia [1 ]
Wang, Meilian [2 ]
Brashear, Awtum [1 ]
Kemirembe, Karen [1 ]
Wang, Zenglei [1 ]
Miao, Jun [1 ]
Chookajorn, Thanat [3 ]
Yang, Zhaoqing [4 ]
Cao, Yaming [2 ]
Dong, Gang [5 ]
Rosenthal, Philip J. [6 ]
Cui, Liwang [1 ]
机构
[1] Penn State Univ, Dept Entomol, 501 ASI Bldg, University Pk, PA 16802 USA
[2] China Med Univ, Coll Basic Med Sci, Shenyang, Liaoning, Peoples R China
[3] Mahidol Univ, Fac Trop Med, Genom & Evolutionary Med Unit, Bangkok, Thailand
[4] Kunming Med Univ, Dept Pathogen Biol & Immunol, Kunming, Yunnan, Peoples R China
[5] Med Univ Vienna, Max F Perutz Labs, Vienna, Austria
[6] Univ Calif San Francisco, Dept Med, San Francisco, CA USA
基金
美国国家卫生研究院; 中国国家自然科学基金;
关键词
ACT; artemisinin resistance; falcipain; 2a; malaria; Plasmodium falciparum; CYSTEINE PROTEASE FALCIPAIN-2; DIHYDROARTEMISININ-PIPERAQUINE FAILURE; IN-VITRO; HEMOGLOBIN; MALARIA; CAMBODIA; PARASITES; PROTEINASE; ASSAYS; LOCI;
D O I
10.1093/infdis/jiy188
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Falcipain-2a ([FP2a] PF3D7_1115700) is a Plasmodium falciparum cysteine protease and hemoglobinase. Functional FP2a is required for potent activity of artemisinin, and in vitro selection for artemisinin resistance selected for an FP2a nonsense mutation. Methods. To investigate associations between FP2a polymorphisms and artemisinin resistance and to characterize the diversity of the enzyme in parasites from the China-Myanmar border, we sequenced the full-length FP2a gene in 140 P falciparum isolates collected during 2004-2011. Results. The isolates were grouped into 8 different haplotype groups. Haplotype group I appeared in samples obtained after 2008, coinciding with implementation of artemisinin-based combination therapy in this region. In functional studies, compared with wild-type parasites, the FP2a haplotypes demonstrated increased ring survival, and all haplotype groups exhibited significantly reduced FP2a activity, with group I showing the slowest protease kinetics and reduced parasite fitness. Conclusions. These results suggest that altered hemoglobin digestion due to FP2a mutations may contribute to artemisinin resistance.
引用
收藏
页码:434 / 442
页数:9
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