IkB genes encoded in Cotesia plutellae bracovirus suppress an antiviral response and enhance baculovirus pathogenicity against the diamondback moth, Plutella xylostella

Journal of Invertebrate Pathology

Volumn 102, Issue 1, 2009, Pages 79-87

  Bae, Sungwoo ^a   Kim, Yonggyun ^a  

^a Andong National University   (South Korea)

Author keywords

Antiviral activity; Baculovirus; Cotesia plutellae; IkB; Melanotic response; NF kB; Plutella xylostella; Polydnavirus

Indexed keywords

I KAPPA B KINASE; VIRUS DNA;

AMINO ACID SEQUENCE; ANIMAL; ARTICLE; BACULOVIRUS; ENZYMOLOGY; GENE EXPRESSION; GENETICS; HOST PARASITE INTERACTION; IMMUNOLOGY; INSECT VIRUS; LARVA; METABOLISM; MOLECULAR GENETICS; MOTH; PATHOGENICITY; PHYLOGENY; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; VIROLOGY; WASP;

AMINO ACID SEQUENCE; ANIMALS; BACULOVIRIDAE; DNA, VIRAL; GENE EXPRESSION; HOST-PARASITE INTERACTIONS; I-KAPPA B KINASE; INSECT VIRUSES; LARVA; MOLECULAR SEQUENCE DATA; MOTHS; PHYLOGENY; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; WASPS;

BRACOVIRUS; CACTACEAE; COTESIA PLUTELLAE; DROSOPHILA MELANOGASTER; HEXAPODA; LEPIDOPTERA; PLUTELLA XYLOSTELLA; PLUTELLIDAE;

EID: 68349111829     PISSN: 00222011     EISSN: 10960805     Source Type: Journal    
DOI: 10.1016/j.jip.2009.06.007     Document Type: Article

References (34)

1. Bae S., and Kim Y. Host physiological changes due to parasitism of a braconid wasp, Cotesia plutellae, on diamondback moth, Plutella xylostella. Comp. Biochem. Physiol. 138A (2004) 39-44
2. Baeuerle P.A. Ikappa B-NF-kappa B structures: at the interface of inflammation control. Cell 95 (1998) 729-731
3. Basio N.A., and Kim Y. Additive effect of teratocytes and calyx fluid from Cotesia plutellae on immunosuppression of Plutella xylostella. Physiol. Entomol. 31 (2006) 341-347
4. Beck M.H., and Strand M.R. A novel polydnaviral protein inhibits the insect prophenoloxidase activating pathway. Proc Natl. Acad. Sci. USA 104 (2008) 19267-19272
5. Choi J.Y., Roh J.Y., Kang J.N., Shim H.J., Woo S.D., Jin B.R., Li M.S., and Je Y.H. Genomic segments cloning and analysis of Cotesia plutellae polydnavirus using plasmid capture system. Biochem. Biophys. Res. Commun. 332 (2005) 487-493
6. Engelhard E.K., Kam-Morgan L.N.W., Washburn J.O., and Volkman L.E. The insect tracheal system: a conduit for the systemic spread of Autographa californica. Proc. Natl. Acad. Sci. USA 91 (1994) 3224-3227
7. Espagne E., Dupuy C., Huguet E., Cattolico L., Provost B., Martin N., Poirié M., Periquet G., and Drezen J.M. Genome sequence of a polydnavirus: insights into symbiotic virus evolution. Science 306 (2004) 286-289
8. Falabella P., Varricchio P., Provost B., Espagne E., Ferrarese R., Grimaldi A., Eguileor M., Fimiani G., Ursini M.V., Malva C., Drezen J.M., and Pennacchio F. Characterization of the IkB-like gene family in polydnaviruses associated with wasps belonging to different braconid subfamilies. J. Gen. Virol. 88 (2007) 92-104
9. Fath-Goodin A., Gill T.A., Martin S.B., and Webb B.A. Effect of Campoletis sonorensis ichnovirus cys-motif proteins on Heliothis virescens larval development. J. Insect Physiol. 52 (2006) 576-585
10. Ghosh S., May M.J., and Kopp E.B. NF-κB and Rel proteins: evolutionarily conserved mediators of immune responses. Annu. Rev. Immunol. 16 (1998) 225-260
11. Huxford T., Huang D.B., Malek S., and Ghosh G. The crystal structure of the IkappaBalpha/NF-kappaB complex reveals mechanisms of NF-kappaB inactivation. Cell 95 (1998) 729-731
12. Ibrahim A.M., and Kim Y. Transient expression of protein tyrosine phosphatases encoded in Cotesia plutellae bracovirus inhibits insect cellular immune responses. Naturwissenschaften 95 (2008) 25-32
13. Ibrahim A.M., Choi J.Y., Je Y.H., and Kim Y. Protein tyrosine phosphatases encoded in Cotesia plutellae bracovirus: sequence analysis, expression profile, and a possible biological role in host immunosuppression. Dev. Comp. Immunol. 31 (2007) 978-990
14. Je Y.H., Chang J.H., Kim M.H., Roh J.Y., Jin B.R., and O''Reilly D.R. The use of defective Bombyx mori nucleopolyhedrovirus genomes maintained in Escherichia coli for the rapid generation of occlusion-positive and occlusion-negative expression vectors. Biotechnol. Lett. 23 (2001) 1809-1817
15. Karin M., and Ben-Neriah Y. Phosphorylation meets ubiquitination: the control of NF-κB activity. Annu. Rev. Immunol. 18 (2000) 621-663
16. Kim Y., Basio N.A., Ibrahim A.M., and Bae S. Gene structure of Cotesia plutellae bracovirus (CpBV)-IKB and its expression pattern in diamondback moth, Plutella xylostella, parasitized by Cotesia plutellae. Kor. J. Appl. Entomol. 45 (2006) 1-10
17. Krell P.J., Summers M.D., and Vinson S.B. Virus with a multipartite superhelical DNA genome from the ichneumonid parasitoid, Campoletis sonorensis. J. Virol. 43 (1982) 859-870
18. Kroemer J.A., and Webb B.A. Polydnavirus genes and genomes: emerging gene families and new insights into polydnavirus replication. Annu. Rev. Entomol. 49 (2004) 431-456
19. Le NT., Asgari S., Amaya K., Tan E.F., and Beckage N.E. Persistence and expression of Cotesia congregata polydnavirus in host larvae of the tobacco hornworm, Manduca sexta. J. Insect Physiol. 49 (2003) 533-543
20. Lee S., and Kim Y. Two homologous parasitism-specific proteins encoded in Cotesia plutellae bracovirus and their expression profiles in parasitized Plutella xylostella. Arch. Insect. Biochem. Physiol. 67 (2008) 157-171
21. Lee K., Cho S., Lee H., Choi J.Y., Je Y.H., and Kim Y. Gene expression of Cotesia plutellae bracovirus EP1-like protein (CpBV-ELP1) in parasitized diamondback moth, Plutella xylostella. J. Asia-Pac. Entomol. 8 (2005) 249-255
22. Lee S., Nalini M., and Kim Y. A viral lectin encoded in Cotesia plutellae bracovirus and its immunosuppressive effect on host hemocytes. Comp. Biochem. Physiol. 149 (2008) 351-361
23. Lemaitre B., Nicolas E., Michaout L., Reichhart J.M., and Hoffmann J.A. The dorsoventral regulatory gene cassette spätzle/Toll/cactus controls the potent antifungal response in Drosophila adults. Cell 86 (1996) 973-983
24. Lemaitre B., Reichhart J.M., and Hoffmann J.A. Drosophila host defense: differential induction of antimicrobial peptide genes after infection by various classes of microorganisms. Proc. Natl. Acad. Sci. USA 94 (1997) 14614-14619
25. Ligoxygakis P., Pelte N., Ji C., Leclerc V., Duvic B., Belvin M., Jiang H., Hoffmann J.A., and Reichhart J.M. A serpin mutant links Toll activation to melanization in the host defence of Drosophila. EMBO J. 21 (2002) 6330-6337
26. Popham H.J.R., Shelby K.S., Brandt S.L., and Coudron T.A. Potent virucidal activity against HzSNPV in larval Heliothis virescens plasma. J. Gen. Virol. 85 (2004) 2225-2261
27. Rivkin H., Kroemer J.A., Bronshtein A., Belausov E., Webb B.A., and Chejanovsky N. Response of immunocompetent and immunosuppressed Spodoptera littoralis larvae to baculovirus infection. J. Gen. Virol. 87 (2006) 2217-2225
28. Shi M., Chen Y.F., Huang F., Liu P.C., Zhou X.P., and Chen X.X. Characterization of a novel gene encoding ankyrin repeat domain from Cotesia vestalis polydnavirus (CvBV). Virology 375 (2008) 374-382
29. Thoetkiattikul H., Beck M.H., and Strand M.R. Inhibitor kappaB-like proteins from a polydnavirus inhibit NF-kappaB activation and suppress the insect immune response. Proc. Natl. Acad. Sci. USA 102 (2005) 11426-11431
30. Washburn J.O., Kirkpatrick B.A., and Volkman L.E. Comparative pathogenesis of Autographa californica nuclear polyhedrosis virus in larvae of Trichoplusia ni and Heliothis virescens. Virology 209 (1995) 561-568
31. Webb B.A. Polydnavirus biology, genome structure and evolution. In: Miller L.K., and Ball L.A. (Eds). The Insect Viruses (1998), Plenum Press, New York. 105-139
32. Webb B.A., and Summers M.D. Stimulation of polydnavirus replication by 20-hydroxyecdysone. Experientia 48 (1992) 1018-1022
33. Webb B.A., Strand M.R., Dickey S.E., Beck M.H., Hilgarth R.S., Barney W.E., Kadash K., Kroemer J.A., Lindstrom K.G., Rattanadechakul W., Shelby K.S., Thoetkiattikul H., Turnbull M.W., and Witherell R.A. Polydnavirus genomes reflect their dual roles as mutualists and pathogens. Virology 347 (2006) 160-174
34. Zambon R.A., Nandakumar M., Vakharia V.N., and Wu L.P. The Toll pathway is important for an antiviral response in Drosophila. Proc. Natl. Acad. Sci. USA 20 (2005) 7257-7262