首页> 外文期刊>Parasitology >Population genetics of concurrent selection with albendazole and ivermectin or diethylcarbamazine on the possible spread of albendazole resistance in Wuchereria bancrofti.
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Population genetics of concurrent selection with albendazole and ivermectin or diethylcarbamazine on the possible spread of albendazole resistance in Wuchereria bancrofti.

机译:同时使用阿苯达唑和伊维菌素或二乙基卡巴他嗪进行选择的种群遗传学对班克氏假单胞菌对阿苯达唑耐药性的可能传播。

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摘要

The Global Program for the Elimination of Lymphatic Filariasis (GPELF) intends to achieve its aims through yearly mass treatments with albendazole (ABZ) combined with ivermectin (IVM) or diethylcarbamazine (DEC). The use of ABZ and IVM separately to combat parasites of veterinary importance has, on many occasions, resulted in widespread drug resistance. In order to help predict the spread of potential ABZ resistance alleles through a population of Wuchereria bancrofti, we have developed a mathematical model that incorporates population genetics into EPIFIL, a model which examines the transmission dynamics of the parasite. Our model considers the effect of the combined treatments on the frequency of a recessive allele, which confers ABZ resistance. The model predicts that after 10 yearly treatments with ALB and DEC, 85% coverage and an initial resistance allele frequency of 5%, the frequency of the resistance genotype will increase from 0.25 to 12.7%. If non-random mating is assumed, the initial genotype frequency will be 2.34% and will increase to 62.7%. ABZ and IVM combination treatment may lead to weaker selection for this genotype. Treatment coverage, initial allele frequencies and number of treatments also affect the rate of selection.
机译:全球消除淋巴丝虫病计划(GPELF)计划通过每年使用阿苯达唑(ABZ)联合伊维菌素(IVM)或二乙基氨基甲嗪(DEC)进行大规模治疗来实现其目标。在许多情况下,分别使用ABZ和IVM对抗具有重要兽医作用的寄生虫已导致广泛的耐药性。为了帮助预测潜在的ABZ抗性等位基因在班氏Wuchereria bancrofti种群中的扩散,我们开发了一种数学模型,将种群遗传学纳入了EPIFIL中,该模型检查了寄生虫的传播动态。我们的模型考虑了联合治疗对隐性等位基因频率的影响,从而赋予了ABZ抗性。该模型预测,经过10年的ALB和DEC治疗,85%的覆盖率和5%的初始抗性等位基因频率,抗性基因型的频率将从0.25增加到12.7%。如果假定非随机交配,则初始基因型频率将为2.34%,并将增加至62.7%。 ABZ和IVM联合治疗可能导致对该基因型的选择较弱。治疗范围,初始等位基因频率和治疗次数也会影响选择率。

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