Rao Ramakrishna U
Department of Internal Medicine, Infectious Diseases Division,Washington University School of Medicine, St. Louis, MO 63110, USA.
Indian J Med Res. 2005 Sep;122(3):199-204.
The parasitic nematodes Wuchereria bancrofti, Brugia malayi and B. timori cause a dreadful disease in humans known as lymphatic filariasis, which afflicts more than 120 million people worldwide. As per recent epidemiologic estimates on prevalence of W. bancrofti and B. malayi, about 428 million people are at risk, with 28 million microfilaria carriers and 21 million clinical cases spread out in 13 States and 5 Union Territories of India. The Indian subcontinent that comprises Bangladesh, India, Maldives, Nepal and Sri Lanka harbours 50 per cent of the world's lymphatic filarial disease burden. Recently, an endobacterium of Wolbachia species that belongs to the family Rickettsiaceae was found in all life cycle stages of these nematodes and the transmission is exclusively vertical through the embryonic stages of the female worms. People with filariasis have been exposed to these Wolbachia bacteria or their proteins by the natural killing of parasites. Wolbachia have also been identified occasionally in body fluids of infected patients. Evidence suggests that these Wolbachia are mutualistic symbionts and can be cured from the nematodes by several antibiotics having antirickettsial properties. Treatment of nematodes with tetracyclines affect Wolbachia and they get cleared from worm tissues; and this elimination causes reproductive abnormalities in worms and affect worm's embryogenesis, resulting in sterility. Although it is impractical, prolonged treatment with doxycycline significantly reduces the numbers of microfilaria in circulation, which is an important strategy to control transmission of filariasis by mosquito vectors. In this review, the current knowledge of Wolbachia as a drug target and potential ways to reduce the infection through anti-Wolbachia treatments is discussed.
寄生线虫班氏吴策线虫、马来布鲁线虫和帝汶布鲁线虫可在人类中引发一种可怕的疾病,即淋巴丝虫病,全球有超过1.2亿人受其折磨。根据最近关于班氏吴策线虫和马来布鲁线虫流行情况的流行病学估计,约4.28亿人面临风险,在印度的13个邦和5个联邦属地有2800万微丝蚴携带者和2100万临床病例。包括孟加拉国、印度、马尔代夫、尼泊尔和斯里兰卡在内的印度次大陆承载了全球50%的淋巴丝虫病负担。最近,在这些线虫的所有生命周期阶段都发现了一种属于立克次体科的沃尔巴克氏体属内共生菌,其传播仅通过雌虫的胚胎阶段垂直进行。丝虫病患者因寄生虫的自然死亡而接触到这些沃尔巴克氏体细菌或其蛋白质。在感染患者的体液中偶尔也发现了沃尔巴克氏体。有证据表明,这些沃尔巴克氏体是互利共生体,可用几种具有抗立克次体特性的抗生素从线虫中清除。用四环素治疗线虫会影响沃尔巴克氏体,它们会从虫体组织中清除;这种清除会导致线虫生殖异常并影响其胚胎发育,从而导致不育。尽管不切实际,但用强力霉素进行长期治疗可显著减少循环中的微丝蚴数量,这是控制蚊媒传播丝虫病的一项重要策略。在这篇综述中,讨论了关于沃尔巴克氏体作为药物靶点的现有知识以及通过抗沃尔巴克氏体治疗减少感染的潜在方法。