Department of Microbiology and Immunology, Columbia University College of Physicians and Surgeons, New York, New York, USA.
PLoS Comput Biol. 2013 Apr;9(4):e1003025. doi: 10.1371/journal.pcbi.1003025. Epub 2013 Apr 18.
Human infection by malarial parasites of the genus Plasmodium begins with the bite of an infected Anopheles mosquito. Current estimates place malaria mortality at over 650,000 individuals each year, mostly in African children. Efforts to reduce disease burden can benefit from the development of mathematical models of disease transmission. To date, however, comprehensive modeling of the parameters defining human infectivity to mosquitoes has remained elusive. Here, we describe a mechanistic within-host model of Plasmodium falciparum infection in humans and pathogen transmission to the mosquito vector. Our model incorporates the entire parasite lifecycle, including the intra-erythrocytic asexual forms responsible for disease, the onset of symptoms, the development and maturation of intra-erythrocytic gametocytes that are transmissible to Anopheles mosquitoes, and human-to-mosquito infectivity. These model components were parameterized from malaria therapy data and other studies to simulate individual infections, and the ensemble of outputs was found to reproduce the full range of patient responses to infection. Using this model, we assessed human infectivity over the course of untreated infections and examined the effects in relation to transmission intensity, expressed by the basic reproduction number R0 (defined as the number of secondary cases produced by a single typical infection in a completely susceptible population). Our studies predict that net human-to-mosquito infectivity from a single non-immune individual is on average equal to 32 fully infectious days. This estimate of mean infectivity is equivalent to calculating the human component of malarial R0 . We also predict that mean daily infectivity exceeds five percent for approximately 138 days. The mechanistic framework described herein, made available as stand-alone software, will enable investigators to conduct detailed studies into theories of malaria control, including the effects of drug treatment and drug resistance on transmission.
人类感染疟原虫属寄生虫 Plasmodium 始于被感染的按蚊叮咬。目前估计,每年有超过 65 万人死于疟疾,其中大多数是非洲儿童。减少疾病负担的努力可以从开发疾病传播的数学模型中受益。然而,迄今为止,对定义人类对蚊子感染性的参数的全面建模仍然难以捉摸。在这里,我们描述了人类恶性疟原虫感染和病原体向蚊子媒介传播的机制性宿主内模型。我们的模型包括寄生虫生命周期的全部内容,包括导致疾病的红细胞内无性形式、症状发作、可传播给按蚊的红细胞内配子体的发育和成熟,以及人类向蚊子的感染性。这些模型组件是从疟疾治疗数据和其他研究中参数化的,以模拟个体感染,并且发现输出的集合再现了患者对感染的全部反应范围。使用该模型,我们评估了未经治疗的感染过程中的人类感染性,并研究了与传播强度(用基本繁殖数 R0 表示,定义为在完全易感人群中由单个典型感染产生的继发病例数)的关系。我们的研究预测,来自单个非免疫个体的净人类向蚊子的感染性平均等于 32 个完全传染性日。这种平均感染性的估计相当于计算疟疾 R0 的人类部分。我们还预测,大约 138 天内,平均每日感染率超过 5%。本文描述的机制框架作为独立软件提供,将使研究人员能够对疟疾控制理论进行详细研究,包括药物治疗和耐药性对传播的影响。