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The Roles of Two Clip Domain Serine Proteases in Innate Immune Responses of the Malaria Vector Anopheles gambiae
- Source :
- Journal of Biological Chemistry. 280:40161-40168
- Publication Year :
- 2005
- Publisher :
- Elsevier BV, 2005.
-
Abstract
- The malaria vector Anopheles gambiae is capable of multiple immune responses against Plasmodium ookinetes. Accumulating evidence in several insect species suggests the involvement of serine protease cascades in the initiation and coordination of immune responses. We report molecular and reverse genetic characterization of two mosquito clip domain serine proteases, CLIPB14 and CLIPB15, which share structural similarity to proteases involved in prophenoloxidase activation in other insects. Both CLIPs are expressed in mosquito hemocytes and are transcriptionally induced by bacterial and Plasmodium challenges. Functional studies applying RNA interference revealed that both CLIPs are involved in the killing of Plasmodium ookinetes in Anopheles. Studies on parasite melanization demonstrated an additional role for CLIPB14 in the prophenoloxidase cascade. We further report that both CLIPs participate in defense toward Gram-negative bacteria. Our findings strongly suggest that clip domain serine proteases serve multiple functions and play distinctive roles in several immune pathways of A. gambiae.
- Subjects :
- Plasmodium
Proteases
Hemocytes
Time Factors
Anopheles gambiae
Immunoblotting
Molecular Sequence Data
Biochemistry
Serine
Anopheles
parasitic diseases
Animals
Amino Acid Sequence
Cloning, Molecular
Molecular Biology
RNA, Double-Stranded
Serine protease
Enzyme Precursors
Innate immune system
biology
Reverse Transcriptase Polymerase Chain Reaction
Serine Endopeptidases
Temperature
Gene Expression Regulation, Developmental
Sequence Analysis, DNA
Cell Biology
Prophenoloxidase
biology.organism_classification
Virology
Malaria
Protein Structure, Tertiary
Cell biology
Enzyme Activation
biology.protein
RNA
RNA Interference
Catechol Oxidase
Subjects
Details
- ISSN :
- 00219258
- Volume :
- 280
- Database :
- OpenAIRE
- Journal :
- Journal of Biological Chemistry
- Accession number :
- edsair.doi.dedup.....4b77d2fcdcbe14a6582e648ec29a2616
- Full Text :
- https://doi.org/10.1074/jbc.m506191200