: Extracellular serine protease cascades modulate protective responses to bleeding and infection in both mammals and arthropods. Experiments in this proposal are designed to investigate the roles of plasma serine proteases in innate immune responses, including activation of phenoloxidase, synthesis of antimicrobial proteins, and adhesion of hemocytes in a lepidopteran insect, Manduca sexta. The work will test a hypothesis that an initial interaction of a serine protease zymogen with one of several pattern recognition proteins in plasma bound to a pathogen surface triggers a conformational change that activates the protease and triggers a protease cascade in which the final protease in the pathway activates prophenoloxidase or a cytokine-like protein. Such immune responses are likely to affect the outcome of infections of insect vectors with the pathogens and parasites they transmit. The long-term goals of the research are to gain a thorough understanding of the protease cascades that mediate innate immune responses in M. sexta, to apply this knowledge to insect vectors of human diseases, and to apply advantages of the M. sexta system for fundamental studies on the regulation of serine protease activity.
The specific aims of the project are: 1. Investigate the regulation of expression and activity of two plasma serine proteases: Pro-phenoloxidase activating proteinase activator and pro-plasmatocyte spreading peptide activator. 2. Identify proteases that activate signaling molecules, which stimulate expression of antimicrobial genes in fat body. 3. Identify proteases that can self-activate in the presence of a pattern recognition protein and a microbial polysaccharide, and begin to characterize the resulting proteinase cascade pathways. 4. Analyze the regulation of plasma proteinases by M. sexta serine protease inhibitors (serpins). ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM041247-14
Application #
6579685
Study Section
Special Emphasis Panel (ZRG1-TMP (01))
Program Officer
Jones, Warren
Project Start
1991-07-01
Project End
2006-12-31
Budget Start
2003-01-01
Budget End
2003-12-31
Support Year
14
Fiscal Year
2003
Total Cost
$310,090
Indirect Cost
Name
Kansas State University
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
929773554
City
Manhattan
State
KS
Country
United States
Zip Code
66506
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Li, Miao; Christen, Jayne M; Dittmer, Neal T et al. (2018) The Manduca sexta serpinome: Analysis of serpin genes and proteins in the tobacco hornworm. Insect Biochem Mol Biol 102:21-30
Al Souhail, Qasim; Hiromasa, Yasuaki; Rahnamaeian, Mohammad et al. (2016) Characterization and regulation of expression of an antifungal peptide from hemolymph of an insect, Manduca sexta. Dev Comp Immunol 61:258-68
Kanost, Michael R; Arrese, Estela L; Cao, Xiaolong et al. (2016) Multifaceted biological insights from a draft genome sequence of the tobacco hornworm moth, Manduca sexta. Insect Biochem Mol Biol 76:118-147
Cao, Xiaolong; Jiang, Haobo (2015) Integrated modeling of protein-coding genes in the Manduca sexta genome using RNA-Seq data from the biochemical model insect. Insect Biochem Mol Biol 62:2-10
Cao, Xiaolong; He, Yan; Hu, Yingxia et al. (2015) Sequence conservation, phylogenetic relationships, and expression profiles of nondigestive serine proteases and serine protease homologs in Manduca sexta. Insect Biochem Mol Biol 62:51-63
Takahashi, Daisuke; Garcia, Brandon L; Kanost, Michael R (2015) Initiating protease with modular domains interacts with ?-glucan recognition protein to trigger innate immune response in insects. Proc Natl Acad Sci U S A 112:13856-61
Koenig, Christopher; Hirsh, Ariana; Bucks, Sascha et al. (2015) A reference gene set for chemosensory receptor genes of Manduca sexta. Insect Biochem Mol Biol 66:51-63
Kanost, Michael R; Jiang, Haobo (2015) Clip-domain serine proteases as immune factors in insect hemolymph. Curr Opin Insect Sci 11:47-55
Peng, Zeyu; Dittmer, Neal T; Lang, Minglin et al. (2015) Multicopper oxidase-1 orthologs from diverse insect species have ascorbate oxidase activity. Insect Biochem Mol Biol 59:58-71

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