Targeted gene deletion in Leishmania major identifies leishmanolysin (GP63) as a virulence factor

被引:196
作者
Joshi, PB
Kelly, BL
Kamhawi, S
Sacks, DL
McMaster, WR
机构
[1] Univ British Columbia, Jack Bell Res Ctr, Dept Med Genet, Vancouver, BC V6H 3Z6, Canada
[2] Vancouver Hosp, Immun & Infect Res Ctr, Vancouver, BC V6H 3Z6, Canada
[3] NIAID, Parasit Dis Lab, NIH, Bethesda, MD 20892 USA
基金
加拿大健康研究院;
关键词
parasitic protozoan; leishmanolysin; complement; transgenic knockout;
D O I
10.1016/S0166-6851(01)00432-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Leishmanolysin, the Leishmania surface metalloproteinase of 63 kDa (GP63) has been described as a parasite virulence factor and is involved in the direct interaction of promastigotes and host macrophage receptors and interaction with the complement cascade. To study the role of leishmanolysin in the pathogenesis and virulence of Leishmania major, targeted gene replacement was used to delete the entire 20 kb region containing all seven leishmanolysin genes (gp63 genes 1-7). The resulting L. major leishmanolysin deficient mutants showed normal development inside the sand fly vector, however, promastigotes recovered from sand flies or from culture showed an increase in sensitivity to complement-mediated lysis and a delay in lesion formation in BALB/c animals. The phenotypic differences could be significantly improved by expression of a cloned leishmanolysin gene. These results demonstrate that leishmanolysin is a vital virulence factor in Leishmania pathogenesis. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:33 / 40
页数:8
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