Genome-Wide Association Studies of Drug-Resistance Determinants

被引:13
|
作者
Volkman, Sarah K. [1 ,2 ,3 ]
Herman, Jonathan [1 ,4 ]
Lukens, Amanda K. [1 ,2 ]
Hartl, Daniel L. [2 ,5 ]
机构
[1] Harvard TH Chan Sch Publ Hlth, Dept Immunol & Infect Dis, Boston, MA 02215 USA
[2] Broad Inst MIT & Harvard, Infect Dis Initiat, Cambridge, MA 02142 USA
[3] Simmons Coll, Sch Nursing & Hlth Sci, Boston, MA 02115 USA
[4] Weill Cornell Med Coll, Weill Dept Med, New York, NY USA
[5] Harvard Univ, Organism & Evolutionary Biol, Cambridge, MA 02138 USA
关键词
PLASMODIUM-FALCIPARUM MALARIA; COPY NUMBER VARIATION; RED-BLOOD-CELLS; THYMIDYLATE SYNTHASE GENE; IN-VITRO RESISTANCE; CYTOCHROME-B GENE; ARTEMISININ RESISTANCE; CHLOROQUINE-RESISTANCE; DIHYDROFOLATE-REDUCTASE; PFMDR1; GENE;
D O I
10.1016/j.pt.2016.10.001
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Population genetic strategies that leverage association, selection, and linkage have identified drug-resistant loci. However, challenges and limitations persist in identifying drug-resistance loci in malaria. In this review we discuss the genetic basis of drug resistance and the use of genome-wide association studies, complemented by selection and linkage studies, to identify and understand mechanisms of drug resistance and response. We also discuss the implications of nongenetic mechanisms of drug resistance recently reported in the literature, and present models of the interplay between nongenetic and genetic processes that contribute to the emergence of drug resistance. Throughout, we examine artemisinin resistance as an example to emphasize challenges in identifying phenotypes suitable for population genetic studies as well as complications due to multiple-factor drug resistance.
引用
收藏
页码:214 / 230
页数:17
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