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Cloning, Expression, and Immunological Characterization of Formosan Subterranean Termite (Blattodea: Rhinotermitidae) Arginine Kinase.
Mattison, Christopher P; Tungtrongchitr, Anchalee; Tille, Katherine S; Cottone, Carrie B; Riegel, Claudia.
Afiliação
  • Mattison CP; Southern Regional Research Center, Agricultural Research Service, United States Department of Agriculture, New Orleans, LA.
  • Tungtrongchitr A; Center of Research Excellence on Therapeutic Proteins and Antibody Engineering, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
  • Tille KS; Department of Parasitology, Mahidol University, Bangkok, Thailand.
  • Cottone CB; Malcolm Grow Medical Clinics and Surgical Center, Joint Base Andrews, MD.
  • Riegel C; New Orleans Mosquito, Termite and Rodent Control Board, New Orleans, LA.
J Insect Sci ; 20(4)2020 Jul 01.
Article em En | MEDLINE | ID: mdl-32706873
ABSTRACT
Several parts of the world regularly consume termites. Arthropod arginine kinase proteins often cross-react with human immunoblobulin E (IgE) antibodies and they are considered pan-allergens. The Formosan subterranean termite Coptotermes formosanus (C. formosanus (Shiraki) [Isoptera Rhinotermitidae]), along with cockroaches, belong to the order Blattodea and they are common household pests in tropical and subtropical parts of the world. An sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) band migrating at approximately 37 kDa in C. formosanus termite extracts cross-reacted with IgE from five cockroach allergic patient samples by immunoblot. Liquid chromatography-mass spectrometry analysis of gel slices from the corresponding region of a gel indicated several peptides from the excised region were identical to the American cockroach arginine kinase allergen, Per a 9. The sequence of the full-length C. formosanus arginine kinase gene indicates the protein it encodes is 96% identical to American cockroach Per a 9, 94% identical to German cockroach Bla g 9, and 82-84% identical to shrimp arginine kinase proteins Pen m 2, Lit v 2, and Cra c 2. Full-length C. formosanus arginine kinase was fused to a glutathione S-transferase tag and recombinantly expressed and purified from Escherichia coli by affinity chromatography. The recombinant protein was recognized by IgE from 11 of 12 cockroach or shrimp allergic samples, but did not cross-react with dust mite allergic or peanut/tree nut allergic samples. The results of this study indicate the C. formosanus arginine kinase cross-reacts with cockroach and shrimp allergic IgE, and if consumed would likely act as an allergen.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Arginina Quinase / Expressão Gênica / Proteínas de Insetos / Isópteros Limite: Animals Idioma: En Revista: J Insect Sci Assunto da revista: BIOLOGIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Laos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Arginina Quinase / Expressão Gênica / Proteínas de Insetos / Isópteros Limite: Animals Idioma: En Revista: J Insect Sci Assunto da revista: BIOLOGIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Laos