Malaria

A. Jayakumar, Zahir Osman Eltahir Babiker
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Abstract

Malaria is a tropical parasitic infection of the red blood cells caused by the protozoal species Plasmodium falciparum, P. vivax, P. ovale, P. malariae, and P. knowlesi. It is transmitted through the bite of the female Anopheles mosquito. The average incubation period is twelve to fourteen days. Congenital and blood-borne transmissions can also occur. P. falciparum and P. vivax account for most human infections but almost all deaths are caused by P. falciparum, with children under five years of age bearing the brunt of morbidity and mortality in endemic countries. P. falciparum is dominant in sub-Saharan Africa whereas P. vivax predominates in Southeast Asia and the Western Pacific. P. ovalae and P. malaria are less common and are mainly found in sub-Saharan Africa. P. knowlesi primarily causes malaria in macaques and is geographically restricted to southeast Asia. While taking a blood meal, the female anopheline mosquito injects motile sporozoites into the bloodstream. Within half an hour, the sporozoites invade the hepatocytes and start dividing to form tissue schizonts. In P. vivax and P. ovale, some of the sporozoites that reach the liver develop into hypnozoites and stay dormant within the hepatocytes for months to years after the original infection. The schizonts eventually rupture releasing daughter merozoites into the bloodstream. The merozoites develop within the red blood cells into ring forms, trophozoites, and eventually mature schizont. This part of the life cycle takes twenty-four hours for P. knowlesi; forty-eight hours for P. falciparum, P. vivax, P. ovale; and seventy-two hours for P. malariae. In P. vivax and P. ovale, some of the sporozoites that reach the liver develop into hypnozoites and stay dormant within the hepatocytes for months to years after the original infection. The hallmark of malaria pathogenesis is parasite sequestration in major organs leading to cytoadherence, endothelial injury, coagulopathy, vascular leakage, pro-inflammatory cytokine production, and tissue inflammation. Malaria is the most frequently imported tropical disease in the UK with an annual case load of around 2000. P. falciparum is the predominant imported species, and failure to take chemoprophylaxis is the commonest risk factor.
疟疾
疟疾是由恶性疟原虫、间日疟原虫、卵形疟原虫、疟疾疟原虫和诺氏疟原虫等原生动物引起的一种热带红细胞寄生虫感染。它通过雌性按蚊的叮咬传播。平均潜伏期为12至14天。先天性和血源性传播也可能发生。大多数人类感染是由恶性疟原虫和间日疟原虫引起的,但几乎所有死亡都是由恶性疟原虫造成的,在流行国家,五岁以下儿童在发病率和死亡率方面首当其冲。恶性疟原虫在撒哈拉以南非洲占主导地位,而间日疟原虫在东南亚和西太平洋占主导地位。卵形疟原虫和疟疾疟原虫不太常见,主要分布在撒哈拉以南非洲。诺氏疟原虫主要在猕猴中引起疟疾,地理上仅限于东南亚。在吸食血液的同时,雌性按蚊将可运动的孢子体注射到血液中。半小时内,孢子子侵入肝细胞并开始分裂形成组织分裂体。在间日疟原虫和卵形疟原虫中,到达肝脏的一些孢子虫发育成催眠孢子,并在最初感染后在肝细胞内休眠数月至数年。分裂体最终破裂,释放子分裂子进入血液。分生体在红细胞内发育成环状、滋养体和最终成熟的分殖体。诺氏疟原虫生命周期的这一阶段需要24小时;恶性疟原虫、间日疟原虫、卵形疟原虫48小时;疟疾疟原虫则为72小时。在间日疟原虫和卵形疟原虫中,到达肝脏的一些孢子虫发育成催眠孢子,并在最初感染后在肝细胞内休眠数月至数年。疟疾发病机制的标志是主要器官中的寄生虫隔离,导致细胞粘附、内皮损伤、凝血功能障碍、血管渗漏、促炎细胞因子产生和组织炎症。疟疾是英国最常见的输入性热带疾病,每年大约有2000例病例。恶性疟原虫是主要的输入性病种,未采取化学预防是最常见的危险因素。
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