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在体外可控条件下彭亨布鲁线虫微丝蚴的脱鞘

The exsheathment of Brugia pahangi microfilariae under controlled conditions in vitro.

作者信息

Devaney E, Howells R E

出版信息

Ann Trop Med Parasitol. 1979 Jun;73(3):227-33. doi: 10.1080/00034983.1979.11687252.

Abstract

Two reproducible techniques for the exsheathment in vitro of microfilariae of Brugia pahangi, and other sheathed microfilariae, are described. Microfilariae were isolated from infected cat blood by filtration and suspended in Hank's Balanced Salt Solution. The first technique involved the incubation of isolated microfilariae for one hour in 20 mM CaCl2 in a phosphate-free Balanced Salt Solution, during which time approximately 90% of the microfilariae lost their sheaths. The second method of exsheathing microfilariae of B. pahangi involved exposure of microfilariae to solutions of endopeptidase (5.8 units/ml) or papaya extract protease (3.0 units/ml) in Ca2+-free HBSS. Exsheathment rates of 95--100% occurred within 30 minutes in both enzyme solutions. Both the Ca2+ ion and the endopeptidase technique have proven equally effective in stimulating exsheathment of microfilariae of Brugia malayi, Wuchereria bancrofti and Litomosoides carinii. Such artificially exsheathed microfilariae are used for in vitro cultivation studies. The viability of Ca2+- and endopeptidase-exsheathed microfilariae of B. pahangi has been confirmed by inoculation of exsheathed larvae into susceptible female mosquitoes.

摘要

本文描述了两种可重复的体外脱去彭亨布鲁线虫及其他带鞘微丝蚴鞘膜的技术。微丝蚴通过过滤从感染猫的血液中分离出来,并悬浮于汉克斯平衡盐溶液中。第一种技术是将分离出的微丝蚴在无磷酸盐平衡盐溶液中的20 mM氯化钙中孵育一小时,在此期间约90%的微丝蚴失去其鞘膜。第二种脱去彭亨布鲁线虫微丝蚴鞘膜的方法是将微丝蚴暴露于无钙的汉克斯平衡盐溶液中的内肽酶(5.8单位/毫升)或木瓜提取物蛋白酶(3.0单位/毫升)溶液中。在两种酶溶液中,30分钟内脱鞘率达95% - 100%。钙离子和内肽酶技术在刺激马来布鲁线虫、班氏吴策线虫和卡里尼丝虫微丝蚴脱鞘方面已被证明同样有效。这种人工脱鞘的微丝蚴用于体外培养研究。通过将脱鞘幼虫接种到易感雌蚊体内,已证实彭亨布鲁线虫经钙离子和内肽酶脱鞘后的微丝蚴的活力。

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