Role of dopachrome conversion enzyme in the melanization of filarial worms in mosquitoes

被引:16
作者
Huang, CY
Christensen, BM
Chen, CC
机构
[1] Natl Yang Ming Univ, Dept Trop Med, Taipei 112, Taiwan
[2] Univ Wisconsin, Dept Anim Hlth & Biomed Sci, Madison, WI USA
关键词
dopachrome conversion enzyme; parasite melanization; RNAi; mosquito; Armigeres subalbatus;
D O I
10.1111/j.1365-2583.2005.00597.x
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
Melanization is an effective defence reaction of mosquito hosts against invading parasites. In mosquitoes, the biosynthesis of melanin is initiated by the hydroxylation of tyrosine to DOPA by phenoloxidase (PO). DOPA is a branch point of the melanization reaction; it may be oxidized to dopaquinone by PO or be decarboxylated to dopamine by dopa decarboxylase. Further oxidation of dopaquinone by PO produces dopachrome. Dopachrome is then converted to 5, 6-dihydroxyindole by dopachrome conversion enzyme (DCE) to produce melanin. The conversion of dopachrome is a rate-limiting step of the melanization reaction, and the presence of PO and DCE significantly accelerates melanization reactions. In this study, a cDNA encoding DCE was cloned from the mosquito Armigeres subalbatus. Real-time PCR analysis revealed increased transcripts from haemocytes in microfilariae (mf)-inoculated mosquitoes. Gene silencing using double-stranded RNA was used to elucidate the role of DCE in the melanization reaction of parasites in Ar. subalbatus. The levels of both DCE transcripts and protein in gene knockdown mosquitoes were dramatically reduced. Compared with controls, the degree of melanization of mf in DCE-knockdown mosquitoes was significantly decreased. These results suggest that DCE is a critical enzyme that is required for effective melanization immune responses.
引用
收藏
页码:675 / 682
页数:8
相关论文
共 45 条
[1]  
ASHIDA M, 1995, P NATL ACAD SCI USA, V92, P10689
[2]   FURTHER-STUDIES ON DOPA QUINONE IMINE CONVERSION FACTOR FROM CUTICLES OF MANDUCA-SEXTA (L) [J].
ASO, Y ;
IMAMURA, Y ;
YAMASAKI, N .
INSECT BIOCHEMISTRY, 1989, 19 (04) :401-407
[3]  
ASO Y, 1984, INSECT BIOCHEM, V14, P463, DOI 10.1016/0020-1790(84)90103-3
[4]   Reassessing the role of defensin in the innate immune response of the mosquito, Aedes aegypti [J].
Bartholomay, LC ;
Fuchs, JF ;
Cheng, LL ;
Beck, ET ;
Vizioli, J ;
Lowenberger, C ;
Christensen, BM .
INSECT MOLECULAR BIOLOGY, 2004, 13 (02) :125-132
[5]   Description of the transcriptomes of immune response-activated Hemocytes from the mosquito vectors Aedes aegypti and Armigeres subalbatus [J].
Bartholomay, LC ;
Cho, WL ;
Rocheleau, TA ;
Boyle, JP ;
Beck, ET ;
Fuchs, JF ;
Liss, P ;
Rusch, M ;
Butler, KM ;
Wu, RCC ;
Lin, SP ;
Kuo, FY ;
Tsao, IY ;
Huang, CY ;
Liu, TT ;
Hsiao, KJ ;
Tsai, SF ;
Yang, UC ;
Nappi, AJ ;
Perna, NT ;
Chen, CC ;
Christensen, BM .
INFECTION AND IMMUNITY, 2004, 72 (07) :4114-4126
[6]   Genetics of mosquito vector competence [J].
Beerntsen, BT ;
James, AA ;
Christensen, BM .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2000, 64 (01) :115-+
[7]   BRUGIA-MALAYI AND BRUGIA-PAHANGI - INHERENT DIFFERENCE IN IMMUNE ACTIVATION IN THE MOSQUITOS ARMIGERES-SUBALBATUS AND AEDES-AEGYPTI [J].
BEERNTSEN, BT ;
LUCKHART, S ;
CHRISTENSEN, BM .
JOURNAL OF PARASITOLOGY, 1989, 75 (01) :76-81
[8]   Reverse genetics in the mosquito Anopheles gambiae:: targeted disruption of the Defensin gene [J].
Blandin, S ;
Moita, LF ;
Köcher, T ;
Wilm, M ;
Kafatos, FC ;
Levashina, EA .
EMBO REPORTS, 2002, 3 (09) :852-856
[9]   Assessing the cost of mounting an immune response [J].
Bonneaud, C ;
Mazuc, J ;
Gonzalez, G ;
Haussy, C ;
Chastel, O ;
Faivre, B ;
Sorci, G .
AMERICAN NATURALIST, 2003, 161 (03) :367-379
[10]   INVITRO STUDY ON HUMORAL ENCAPSULATION OF MICROFILARIAE - ESTABLISHMENT OF TECHNIQUE AND DESCRIPTION OF REACTION [J].
CHEN, CC ;
LAURENCE, BR .
INTERNATIONAL JOURNAL FOR PARASITOLOGY, 1987, 17 (03) :781-787