L. Cui et al., Molecular characterization of a prophenoloxidase cDNA from the malaria mosquito Anopheles stephensi, INSEC MOL B, 9(2), 2000, pp. 127-137
Some refractory anopheline mosquitoes are capable of killing Plasmodium, th
e causative agent of malaria, by melanotic encapsulation of invading ookine
tes. Phenoloxidase (PO) appears to be involved in the formation of melanin
and toxic metabolites in the surrounding capsule. A cDNA encoding Anopheles
stephensi prophenoloxidase (Ans-proPO) was isolated from a cDNA library sc
reened with an amplimer produced by reverse transcriptase polymerase chain
reaction (RT-PCR) with degenerate primers designed against conserved proPO
sequences. The 2.4-kb-long cDNA has a 2058 bp open reading frame encoding A
ns-proPO of 686 amino acids. The deduced amino acid sequence shows signific
ant homology to other insect proPO sequences especially at the two putative
copper-binding domains. In A. stephensi, Ans-proPO expression was detected
in larval, pupal and adult stages. The Ans-proPO mRNA was detected by RT-P
CR and in situ hybridization in haemocytes, fat body and epidermis of adult
female mosquitoes. A low level of expression was detected in the ovaries,
whereas no expression was detected in the midguts. Semi-quantitative RT-PCR
analysis of Ans-proPO mRNA showed that its expression was similar in adult
female heads, thoraxes and abdomens. No change in the level of Ans-proPO e
xpression was found in adult females after blood feeding, bacterial challen
ge or Plasmodium berghei infection. However, elevated PO activity was detec
ted in P. berghei-infected mosquitoes, suggesting that in non-selected perm
issive mosquitoes PO may be involved in limiting parasite infection. Genomi
c Southern blot and immunoblots suggest the presence of more than one proPO
gene in the A. stephensi genome, which is consistent with the findings in
other Diptera and Lepidoptera species. The greatest similarity in sequence
and expression profile between Ans-proPO and A. gambiae proPO6 suggests tha
t they might be homologues. Our results demonstrate that Ans-proPO is const
itutively expressed through different developmental stages and under differ
ent physiological conditions, implying that other factors in the proPO acti
vation cascade regulate melanotic encapsulation.