Sacks D L
Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Cell Microbiol. 2001 Apr;3(4):189-96. doi: 10.1046/j.1462-5822.2001.00115.x.
Leishmaniasis is caused by a wide range of parasites that are transmitted by an even wider range of sand fly vectors. The phlebotomine vectors of Leishmaniasis are in some cases only permissive to the complete development of the species of Leishmania that they transmit in nature. The parasite-sand fly interactions that control this specificity are related to differences in the ability of the parasite to inhibit or to resist killing by proteolytic enzymes released into the mid-gut soon after blood feeding, and/or to maintain infection in the mid-gut during excretion of the digested blood meal. In each case, surface expressed or released phosphoglycan-containing molecules appear to promote parasite survival. The evidence that the surface lipophosphoglycan (LPG) mediates promastigote attachment to the mid-gut epithelium so as to prevent their loss during blood-meal excretion is especially strong based on the comparison of development in sand flies using LPG-deficient mutants. LPG displays interspecies polymorphisms in their phosphoglycan domains that in most cases can fully account for species-specific vector competence.
利什曼病由多种寄生虫引起,这些寄生虫通过种类更为繁多的白蛉传播。在某些情况下,利什曼病的白蛉传播媒介仅允许其在自然界传播的利什曼原虫物种完成发育。控制这种特异性的寄生虫与白蛉的相互作用,与寄生虫抑制或抵抗取食血液后不久释放到中肠的蛋白水解酶杀伤的能力差异,和/或在消化后的血餐排泄过程中在中肠维持感染的能力差异有关。在每种情况下,表面表达或释放的含磷酸聚糖分子似乎都能促进寄生虫存活。基于使用缺乏LPG的突变体对白蛉发育的比较,有特别有力的证据表明表面脂磷酸聚糖(LPG)介导前鞭毛体附着于中肠上皮,从而防止它们在血餐排泄过程中丢失。LPG在其磷酸聚糖结构域中表现出种间多态性,在大多数情况下,这些多态性可以充分解释物种特异性的传播媒介能力。