Molecular characterization of a prophenoloxidase cDNA from the malaria mosquito Anopheles stephensi

Citation
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
Citations number
48
Language
INGLESE
art.tipo
Article
Categorie Soggetti
Entomology/Pest Control","Molecular Biology & Genetics
Journal title
INSECT MOLECULAR BIOLOGY
ISSN journal
0962-1075 → ACNP
Volume
9
Issue
2
Year of publication
2000
Pages
127 - 137
Database
ISI
SICI code
0962-1075(200004)9:2<127:MCOAPC>2.0.ZU;2-T
Abstract
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.