Walters L L, Modi G B, Chaplin G L, Tesh R B
Institute of Arctic Biology, University of Alaska Fairbanks.
Am J Trop Med Hyg. 1989 Sep;41(3):295-317.
The development of Leishmania chagasi, etiologic agent of American visceral leishmaniasis, was studied by light and electron microscopy in the gut of the sand fly, Lutzomyia longipalpis, a natural vector. New aspects of suprapylarian Leishmania behavior were elucidated. In the sand fly midgut, amastigotes transformed into promastigotes (division promastigote I) during a first division sequence within the bloodmeal. Secondary division of these promastigotes resulted in a second form (division promastigote II), and these subsequently elongated into nectomonad promastigotes. Nectomonads existed in long and short populations which divided in the bloodmeal and throughout the midgut lumen after escape from the peritrophic membrane. Nectomonads adhered to the midgut cells in a highly organized manner, with their flagella embedded deep into microvilli and cytoplasm. Migration of parasites from the posterior midgut into the cardia/stomodeal valve region at 36 hr was associated with breakdown of the peritrophic membrane anteriorly. Posterior breakdown at 48 hr resulted in a peritrophic tube open at both ends containing some parasites within the digesting bloodmeal for up to 6 days postinfection. At the stomodeal valve, a myriad of slender and rounded promastigotes attached to the intima by flagellar hemidesmosomes; these may represent a transformation sequence from slender nectomonads to pear-shaped haptomonads. Pear-shaped forms appear to be precursors of paramastigotes, which also attached to the valve intima. Both rounded haptomonads and paramastigotes were found in the esophagus, dividing in a complex sequence initiated by posterior cleavage of the cytoplasm producing unique heart-shaped forms. Dividing paramastigotes also colonized the pharynx up to the cibarial valve. The ultrastructure of paramastigotes suggested that they may be infective forms, capable of some motility in the foregut. Free-swimming "infective" promastigotes were observed throughout the midgut and foregut, were attached in the pharynx (armature region), and were associated with the labrum-epipharynx of the proboscis in 3.6% of flies (16 days). The fine structure of hemidesmosomes in the foregut showed regional specializations, including the presence of plasmalemmar bridges in the gap space.
通过光学显微镜和电子显微镜,对美洲内脏利什曼病的病原体恰加斯利什曼原虫在天然传播媒介——长须罗蛉肠道内的发育情况进行了研究。阐明了幽门上利什曼原虫行为的新方面。在罗蛉中肠,无鞭毛体在血餐中的第一次分裂过程中转化为前鞭毛体(分裂前鞭毛体I)。这些前鞭毛体的二次分裂产生了第二种形态(分裂前鞭毛体II),随后它们伸长为游动前鞭毛体。游动前鞭毛体存在长型和短型群体,它们在血餐中分裂,并在从围食膜逸出后在整个中肠腔内分裂。游动前鞭毛体以高度有序的方式附着在中肠细胞上,其鞭毛深深嵌入微绒毛和细胞质中。感染后36小时,寄生虫从中肠后部迁移到贲门/口道瓣膜区域,与围食膜前部的破裂有关。48小时时围食膜后部破裂,形成两端开口的围食管,在消化的血餐中含有一些寄生虫,直至感染后6天。在口道瓣膜处,大量细长和圆形的前鞭毛体通过鞭毛半桥粒附着在内膜上;这些可能代表了从细长的游动前鞭毛体到梨形吸附前鞭毛体的转化序列。梨形形态似乎是副鞭毛体的前体,副鞭毛体也附着在瓣膜内膜上。圆形吸附前鞭毛体和副鞭毛体都出现在食管中,通过细胞质的后部裂解开始复杂的分裂序列,产生独特的心形形态。分裂的副鞭毛体也定殖在咽部直至下咽瓣膜。副鞭毛体的超微结构表明它们可能是感染性形态,在前肠中具有一定的运动能力。在整个中肠和前肠中观察到自由游动的“感染性”前鞭毛体,它们附着在咽部(武装区域),并且在3.6%的苍蝇(16天)中与喙的上唇-下咽相关联。前肠中半桥粒的精细结构显示出区域特化,包括间隙空间中质膜桥的存在。