CLIPB4 Is a Central Node in the Protease Network that Regulates Humoral Immunity in Anopheles gambiae Mosquitoes
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S. Karger AG
Abstract
Insect humoral immune responses are regulated in part by protease cascades, whose components circulate as zymogens in the hemolymph. In mosquitoes, these cascades consist of clip-domain serine proteases (cSPs) and/or their non-catalytic homologs, which form a complex network, whose molecular make-up is not fully understood. Using a systems biology approach, based on a co-expression network of gene family members that function in melanization and co-immunoprecipitation using the serine protease inhibitor (SRPN)2, a key negative regulator of the melanization response in mosquitoes, we identify the cSP CLIPB4 from the African malaria mosquito Anopheles gambiae as a central node in this protease network. CLIPB4 is tightly co-expressed with SRPN2 and forms protein complexes with SRPN2 in the hemolymph of immune-challenged female mosquitoes. Genetic and biochemical approaches validate our network analysis and show that CLIPB4 is required for melanization and antibacterial immunity, acting as a prophenoloxidase (proPO)-activating protease, which is inhibited by SRPN2. In addition, we provide novel insight into the structural organization of the cSP network in An. gambiae, by demonstrating that CLIPB4 is able to activate proCLIPB8, a cSP upstream of the proPO-activating protease CLIPB9. These data provide the first evidence that, in mosquitoes, cSPs provide branching points in immune protease networks and deliver positive reinforcement in proPO activation cascades. © 2023 The Author(s).
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Anopheles gambiae, Clip-domain serine protease, Insect immunity, Melanization, Phenoloxidase, Animals, Anopheles, Female, Immunity, humoral, Insect proteins, Serine endopeptidases, Serine proteases, Serpins, Clipb4 protein, Proteinase, Regulator protein, Unclassified drug, Insect protein, Serine proteinase, Serine proteinase inhibitor, Animal experiment, Article, Biochemical analysis, Coimmunoprecipitation, Complex formation, Controlled study, Gene expression, Gene identification, Hemolymph, Humoral immunity, Imago, Nonhuman, Phenotype, Protein depletion, Protein expression, Protein protein interaction, Systems biology, Animal, Genetics, Metabolism