4.1 Article

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

Journal

MOLECULAR AND BIOCHEMICAL PARASITOLOGY
Volume 120, Issue 1, Pages 33-40

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/S0166-6851(01)00432-7

Keywords

parasitic protozoan; leishmanolysin; complement; transgenic knockout

Funding

  1. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [ZIAAI000256, Z01AI000256] Funding Source: NIH RePORTER

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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.

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