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Genetic relatedness analysis reveals the cotransmission of genetically related Plasmodium falciparum parasites in Thiès, Senegal

机译:遗传相关性分析揭示了塞内加尔蒂斯遗传相关的恶性疟原虫的共传播

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BackgroundAs public health interventions drive parasite populations to elimination, genetic epidemiology models that incorporate population genomics can be powerful tools for evaluating the effectiveness of continued intervention. However, current genetic epidemiology models may not accurately simulate the population genetic profile of parasite populations, particularly with regard to polygenomic (multi-strain) infections. Current epidemiology models simulate polygenomic infections via superinfection (multiple mosquito bites), despite growing evidence that cotransmission (a single mosquito bite) may contribute to polygenomic infections. MethodsHere, we quantified the relatedness of strains within 31 polygenomic infections collected from patients in Thiès, Senegal using a hidden Markov model to measure the proportion of the genome that is inferred to be identical by descent. ResultsWe found that polygenomic infections can be composed of highly related parasites and that superinfection models drastically underestimate the relatedness of strains within polygenomic infections. ConclusionsOur findings suggest that cotransmission is a major contributor to polygenomic infections in Thiès, Senegal. The incorporation of cotransmission into existing genetic epidemiology models may enhance our ability to characterize and predict changes in population structure associated with reduced transmission intensities and the emergence of important phenotypes like drug resistance that threaten to undermine malaria elimination activities.
机译:背景技术随着公共卫生干预措施驱使寄生虫种群消灭,结合了人口基因组学的遗传流行病学模型可以成为评估持续干预措施有效性的有力工具。但是,当前的遗传流行病学模型可能无法准确地模拟寄生虫种群的种群遗传概况,尤其是在多基因组(多株)感染方面。尽管越来越多的证据表明共传播(单次蚊子叮咬)可能会导致多基因组感染,但当前的流行病学模型通过重复感染(多次叮咬)模拟多基因组感染。方法在这里,我们使用隐马尔可夫模型对从塞内加尔提耶斯的患者收集的31种多基因组感染中的菌株之间的相关性进行了量化,以测量通过后代推断为相同的基因组的比例。结果我们发现多基因组感染可以由高度相关的寄生虫组成,并且超级感染模型严重低估了多基因组感染中菌株的相关性。结论我们的发现表明,共传播是塞内加尔提耶斯多基因组感染的主要因素。将共传播纳入现有的遗传流行病学模型可能会增强我们表征和预测与降低的传播强度以及可能危害破坏疟疾消除活动的耐药性等重要表型有关的人口结构变化的能力。

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