Loss of virulence in Leishmania donovani deficient in an amastigote-specific protein, A2

被引:128
作者
Zhang, WW [1 ]
Matlashewski, G [1 ]
机构
[1] MCGILL UNIV,INST PARASITOL,ST ANNE BELLEVUE,PQ H9X 3V9,CANADA
关键词
D O I
10.1073/pnas.94.16.8807
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Leishmania donovani is the etiologic agent of fatal visceral leishmaniasis in man, During their life cycle, Leishmania exist as flagellated promastigotes within the sandfly vector and as nonflagellated amastigotes in the macro phage phagolysosomal compartment of the mammalian host, The transformation from promastigotes to amastigotes is a critical step for the establishment of infection, and the molecular basis for this transformation is poorly understood. To define the molecular basis for amastigote survival in the mammalian host, we previously identified an amastigote stage-specific gene family termed ''A2.'' In the present study, we have inhibited the expression of A2 mRNA and A2 protein in amastigotes using antisense RNA and show that the resulting A2-deficient amastigotes are severely compromised with respect to virulence in mice. Amastigotes that did survive in the mice had restored A2 protein expression, These data demonstrate that A2 protein is required for L. donovani survival in a mammalian host, and this represents the first identified amastigote-specific virulence factor identified in Leishmania. This study also reveals that it is possible to study gene function in Leishmania through the expression of antisense RNA.
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页码:8807 / 8811
页数:5
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