Complement-like protein TEP1 is a determinant of vectorial capacity in the malaria vector Anopheles gambiae

Cell. 2004 Mar 5;116(5):661-70. doi: 10.1016/s0092-8674(04)00173-4.


Anopheles mosquitoes are major vectors of human malaria in Africa. Large variation exists in the ability of mosquitoes to serve as vectors and to transmit malaria parasites, but the molecular mechanisms that determine vectorial capacity remain poorly understood. We report that the hemocyte-specific complement-like protein TEP1 from the mosquito Anopheles gambiae binds to and mediates killing of midgut stages of the rodent malaria parasite Plasmodium berghei. The dsRNA knockdown of TEP1 in adults completely abolishes melanotic refractoriness in a genetically selected refractory strain. Moreover, in susceptible mosquitoes this knockdown increases the number of developing parasites. Our results suggest that the TEP1-dependent parasite killing is followed by a TEP1-independent clearance of dead parasites by lysis and/or melanization. Further elucidation of the molecular mechanisms of TEP1-mediated parasite killing will be of great importance for our understanding of the principles of vectorial capacity in insects.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Anopheles / anatomy & histology
  • Anopheles / metabolism*
  • Anopheles / parasitology*
  • Female
  • Humans
  • Insect Proteins / chemistry
  • Insect Proteins / genetics
  • Insect Proteins / metabolism*
  • Insect Vectors / genetics
  • Insect Vectors / parasitology
  • Insect Vectors / physiology*
  • Malaria / epidemiology*
  • Models, Molecular
  • Molecular Sequence Data
  • Plasmodium berghei / cytology
  • Plasmodium berghei / physiology
  • Polymorphism, Genetic
  • Protein Structure, Tertiary
  • RNA / metabolism
  • Sequence Alignment


  • Insect Proteins
  • RNA