Department of Agricultural Sciences, Faculty of Agriculture and Forestry, FI-00014 University of Helsinki, Finland.
Malar J. 2011 Apr 16;10:90. doi: 10.1186/1475-2875-10-90.
Plasmodium vivax is the most widespread malaria parasite. It has a dormant stage in the human liver, which makes it difficult to eradicate. It is proposed that a relapse of vivax malaria, besides being genetically determined by the specific strain, is induced by the bites of uninfected vectors.
The dormant stage maximizes the possibility for the parasite to reach the vector for sexual reproduction. The advantage would increase if the parasite was able to detect the presence of a new generation of vectors. The sporozoites function both in the vector and in the human hosts. They invade the cells of the salivary gland in the vector and the hepatocytes in the human. Some of the sporozoites develop into hypnozoites in the human liver. It is suggested that the hypnozoite activates when it recognizes the same Anopheles specific protein, which it had previously recognized as a sporozoite to invade the salivary gland in the vector. Another possibility is that the hypnozoite activates upon the bodily reaction by the human on a bite by an Anopheles female.
The connection between the relapse and a new generation of vectors can be documented by simultaneous monitoring of both parasitaemia in humans and the presence of uninfective/infective vectors in the same area with seasonal malaria transmission. Experimental studies are needed to find the saliva components, which trigger the relapse. Although P. cynomolgi in monkeys also has hypnozoites and relapses, testing with monkeys might be problematical. These live in a reasonably stable tropical environment where relapses cannot easily be linked to vectors. The importance of the trigger increases in unpredictable variations in the vector season.
Artificial triggering of hypnozoites would make the medication more effective and resistance against a protein that the parasite itself uses during its life cycle would not develop. In areas with seasonal vivax malaria it could be used locally for eradication.
间日疟原虫是分布最广泛的疟原虫。它在人体肝脏中有一个休眠阶段,这使得它难以根除。有人提出,除了由特定菌株的遗传决定外,间日疟的复发还会被未感染的媒介叮咬所诱导。
休眠阶段最大限度地提高了寄生虫到达媒介进行有性繁殖的可能性。如果寄生虫能够检测到新一代媒介的存在,优势将会增加。子孢子在媒介和人类宿主中都有功能。它们侵入媒介的唾液腺细胞和人类的肝细胞。一些子孢子在人类肝脏中发育成休眠子。有人建议,当休眠子识别到它以前作为子孢子入侵媒介唾液腺的同种按蚊特异性蛋白时,它会被激活。另一种可能性是,当人体对雌性按蚊的叮咬产生反应时,休眠子会被激活。
通过同时监测人类的寄生虫血症和同一地区具有季节性疟疾传播的非感染性/感染性媒介的存在,可以记录复发与新一代媒介之间的联系。需要进行实验研究以找到触发复发的唾液成分。尽管恒河猴中的疟原虫也有休眠子和复发,但用猴子进行测试可能会有问题。这些猴子生活在一个相对稳定的热带环境中,复发不容易与媒介联系起来。在不可预测的媒介季节变化中,触发因素的重要性会增加。
人工触发休眠子将使药物更有效,并且不会对寄生虫在其生命周期中使用的蛋白质产生抗药性。在具有季节性间日疟的地区,可以局部使用该药物进行根除。