Plasmodium vivax:: Isotopic, PicoGreen, and microscopic assays for measuring chloroquine sensitivity in fresh and cryopreserved isolates

被引:40
作者
Kosaisavee, Varakorn
Suwanarusk, Rossarin
Nosten, Francois
Kyle, Dennis E.
Barrends, Marion
Jones, James
Price, Ric
Russell, Bruce [1 ]
Lek-Uthai, Usa
机构
[1] Menzies Sch Hlth Res, Int Hlth Program, Div Infect Dis, Darwin, NT, Australia
[2] Charles Darwin Univ, Darwin, NT, Australia
[3] USAMC, Armed Forces Res Inst Med Sci, Dept Entomol, Bangkok, Thailand
[4] Mahidol Univ, Fac Publ Hlth, Bangkok 10700, Thailand
[5] Shoklo Malaria Res Unit, Mae Sot, Thailand
[6] Walter Reed Army Inst Res, Div Expt Therapeut, Silver Spring, MD USA
关键词
Plasmodium vivax; chloroquine; antimalarial sensitivity; in vitro; isotopic; PicoGreen; microscopic; cryopreservation;
D O I
10.1016/j.exppara.2006.02.006
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
In vitro susceptibility tests provide information on the intrinsic response of Plasmodium vivax to antimalarials, free from confounding factors such as host immunity or relapse. This study examined the utility of radioisotope and PicoGreen assays as alternatives to the traditional microscopic examination for assessing response of P. vivax to antimalarial drugs. There was no significant difference in the mean chloroquine IC50 of P. vivax (n = 40) as determined by the microscopic (33.4 ng/ml), isotopic (33.6 ng/ml), and PicoGreen (39.1 ng/ml) assays, respectively (F= 0.239, df = 2, 51, and p = 0.788). However measurement of IC(50)s by the microscopic method was slightly more successful in producing valid assays (57%), compared to the isotopic (32.5%) and PicoGreen (45.5%) methods. In a paired comparison of 20 fresh and cryopreserved isolates as examined by the microscopic method, there were no significant differences between the mean IC50 responses (T= 1.58, df = 15, and p = 0.34). Detailed methodologies for the short time culture of field and cryopreserved P. vivax are described. Although the microscopic in vitro assay provides a useful method for characterizing the drug susceptibility phenotype of P. vivax isolates, its utility is limited by a laborious methodology and need for highly skilled microscopists. Future efforts should focus on further development of high throughput assays such as the PicoGreen assay as described in this study. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:34 / 39
页数:6
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