Genetic Diversity and Lack of Artemisinin Selection Signature on the Plasmodium falciparum ATP6 in the Greater Mekong Subregion

被引:12
|
作者
Miao, Miao [1 ]
Wang, Zenglei [1 ]
Yang, Zhaoqing [2 ]
Yuan, Lili [2 ]
Parker, Daniel M. [1 ]
Putaporntip, Chaturong [3 ]
Jongwutiwes, Somchai [3 ]
Xangsayarath, Phonepadith [4 ,5 ]
Pongvongsa, Tiengkham [6 ]
Moji, Hazuhiko [7 ]
Trinh Dinh Tuong [8 ]
Abe, Tomoko [4 ,5 ]
Nakazawa, Shusuke [4 ,5 ]
Kyaw, Myat Phone [9 ]
Yan, Guiyun [10 ]
Sirichaisinthop, Jeeraphat [11 ]
Sattabongkot, Jetsumon [12 ]
Mu, Jianbing [13 ]
Su, Xin-zhuan [13 ]
Kaneko, Osamu [4 ,5 ]
Cui, Liwang [1 ]
机构
[1] Penn State Univ, Dept Entomol, University Pk, PA 16802 USA
[2] Kunming Med Coll, Dept Parasitol, Kunming, Yunnan, Peoples R China
[3] Chulalongkorn Univ, Dept Parasitol, Mol Biol Malaria & Opportunist Parasites Res Unit, Bangkok, Thailand
[4] Nagasaki Univ, Dept Protozool, Inst Trop Med NEKKEN, Nagasaki, Japan
[5] Nagasaki Univ, Global Ctr Excellence Program, Nagasaki, Japan
[6] Stn Malariol Parasitol & Entomol, Kaysone Dist, Savannakhet Pro, Laos
[7] Res Inst Humanity & Nat, Kyoto, Japan
[8] Natl Inst Malariol Parasitol & Entomol, Dept Epidemiol, Hanoi, Vietnam
[9] Dept Med Res Lower Myanmar, Parasitol Res Div, Yangon, Myanmar
[10] Univ Calif Irvine, Program Publ Hlth, Irvine, CA USA
[11] Vector Borne Dis Training Ctr, Sara Buri, Thailand
[12] Mahidol Univ, Fac Trop Med, Bangkok, Thailand
[13] NIAID, Lab Malaria & Vector Res, NIH, Bethesda, MD 20892 USA
来源
PLOS ONE | 2013年 / 8卷 / 03期
基金
美国国家卫生研究院;
关键词
IN-VITRO; MITOCHONDRIAL-DNA; POINT MUTATIONS; S769N MUTATION; SERCA PFATP6; RESISTANCE; MALARIA; POLYMORPHISM; ARTESUNATE; CA2+-ATPASE;
D O I
10.1371/journal.pone.0059192
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 Ca2+-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 (similar to 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 dN/dS 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.
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页数:12
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