Churcher Thomas S, Sinden Robert E, Edwards Nick J, Poulton Ian D, Rampling Thomas W, Brock Patrick M, Griffin Jamie T, Upton Leanna M, Zakutansky Sara E, Sala Katarzyna A, Angrisano Fiona, Hill Adrian V S, Blagborough Andrew M
MRC Centre for Outbreak Analysis and Modelling, Infectious Disease Epidemiology, Imperial College London, London, United Kingdom.
Department of Life Sciences, Imperial College London, South Kensington, London, United Kingdom.
PLoS Pathog. 2017 Jan 12;13(1):e1006108. doi: 10.1371/journal.ppat.1006108. eCollection 2017 Jan.
Over a century since Ronald Ross discovered that malaria is caused by the bite of an infectious mosquito it is still unclear how the number of parasites injected influences disease transmission. Currently it is assumed that all mosquitoes with salivary gland sporozoites are equally infectious irrespective of the number of parasites they harbour, though this has never been rigorously tested. Here we analyse >1000 experimental infections of humans and mice and demonstrate a dose-dependency for probability of infection and the length of the host pre-patent period. Mosquitoes with a higher numbers of sporozoites in their salivary glands following blood-feeding are more likely to have caused infection (and have done so quicker) than mosquitoes with fewer parasites. A similar dose response for the probability of infection was seen for humans given a pre-erythrocytic vaccine candidate targeting circumsporozoite protein (CSP), and in mice with and without transfusion of anti-CSP antibodies. These interventions prevented infection more efficiently from bites made by mosquitoes with fewer parasites. The importance of parasite number has widespread implications across malariology, ranging from our basic understanding of the parasite, how vaccines are evaluated and the way in which transmission should be measured in the field. It also provides direct evidence for why the only registered malaria vaccine RTS,S was partially effective in recent clinical trials.
自罗纳德·罗斯发现疟疾是由感染性蚊子叮咬所致已过去一个多世纪,但目前仍不清楚注入的寄生虫数量如何影响疾病传播。目前人们认为,所有带有唾液腺子孢子的蚊子,无论其携带的寄生虫数量多少,都具有同等的传染性,尽管这从未得到过严格验证。在此,我们分析了1000多例人体和小鼠的实验性感染情况,并证明了感染概率和宿主潜伏期长度存在剂量依赖性。吸血后唾液腺中含有较多子孢子的蚊子比含有较少寄生虫的蚊子更有可能引发感染(且感染速度更快)。对于接种了针对环子孢子蛋白(CSP)的红细胞前期候选疫苗的人,以及接受和未接受抗CSP抗体输血的小鼠,也观察到了类似的感染概率剂量反应。这些干预措施对较少寄生虫蚊子叮咬导致的感染预防效果更佳。寄生虫数量的重要性在疟疾学领域具有广泛影响,涵盖了我们对寄生虫的基本认识、疫苗评估方式以及现场传播测量方法等方面。这也为唯一已注册的疟疾疫苗RTS,S在近期临床试验中部分有效的原因提供了直接证据。