Limited genetic diversity of the Plasmodium falciparum aquaglyceroporin gene

被引:9
作者
Bahamontes-Rosa, Noemi
Wu, Binghua
Beitz, Eric
Kremsner, Peter G.
Kun, Juergen F. J.
机构
[1] Univ Tubingen, Inst Trop Med, Dept Parasitol, D-72074 Tubingen, Germany
[2] Univ Kiel, Dept Pharmaceut Chem, D-24118 Kiel, Germany
[3] Albert Schweitzer Hosp, Med Res Unit, Lambarene, Gabon
关键词
malaria; aquaglyceroporin; polymorphism; methylamine efflux assay;
D O I
10.1016/j.molbiopara.2007.08.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In Plasmodium falciparum small solutes like water, ammonium, glycerol and others are transported by a parasite-encoded channel into the parasite. The gene encoding this channel is termed P. falciparum aquaglyceroporin (PfAQP) and is a single-copy gene and highly homologous to other aquaporins from other protozoa. Aquaporins are considered to be attractive targets for drug treatment and more so since the human and parasite aquaporins show considerable sequence differences. To investigate whether PfAQP may be suitable as a conserved target for potential aquaporin blocking agents we determined the DNA sequences of PfAQP from 65 parasite strains, either from in vitro cultured laboratory strains or from parasites obtained in an malaria-endemic region of Gabon. Only two non-synonymous mutations were found and functionally tested by a methylamine efflux assay. The efflux activity of all variants tested was similar. The lack of functionally variability suggests an invariable protein core, which may restrict parasite populations from evading therapeutic pressure if PfAQP inhibitors will be found. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:255 / 257
页数:3
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