Evolutionary Progenitors of Bracoviruses

Parasitoid Viruses: Symbionts and Pathogens

Volumn , Issue , 2012, Pages 15-31

  Drezen, Jean Michel ^a   Herniou, Elisabeth Anne ^a   Bézier, Annie ^a  

^a UNIVERSITÉ DE TOURS   (France)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 84857990934     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1016/B978-0-12-384858-1.00002-3     Document Type: Chapter

References (86)

1. Abd-Alla A.M., Cousserans F., Parker A.G., Jehle J.A., Parker N.J., Vlak J.M., et al. Genome analysis of a Glossina pallidipes salivary gland hypertrophy virus reveals a novel, large, double-stranded circular DNA virus. J. Virol. 2008, 82:4595-4611.
2. Albrecht U., Wyler T., Pfister-Wilhelm R., Gruber A., Stettler P., Heiniger P., et al. Polydnavirus of the parasitic wasp Chelonus inanitus (Braconidae): characterization, genome organization and time point of replication. J. Gen. Virol. 1994, 75:3353-3363.
3. Arbuckle J.H., Medveczky M.M., Luka J., Hadley S.H., Luegmayr A., Ablashi D., et al. The latent human herpesvirus-6A genome specifically integrates in telomeres of human chromosomes in vivo and in vitro. Proc. Natl. Acad. Sci. U.S.A. 2010, 107:5563-5568.
4. Asgari S., Reineke A., Beck M., Schmidt O. Isolation and characterization of a neprilysin-like protein from Venturia canescens virus-like particles. Insect Mol. Biol. 2002, 11:477-485.
5. Beck M.H., Inman R.B., Strand M.R. Microplitis demolitor bracovirus genome segments vary in abundance and are individually packaged in virions. Virology 2007, 359:179-189.
6. Belle E., Beckage N.E., Rousselet J., Poirié M., Lemeunier F., Drezen J.-M. Visualization of polydnavirus sequences in a parasitoid wasp chromosome. J. Virol. 2002, 76:5793-5796.
7. Belyi V.A., Levine A.J., Skalka A.M. Unexpected inheritance: multiple integrations of ancient bornavirus and ebolavirus/marburgvirus sequences in vertebrate genomes. PLoS Pathog. 2010, 6:e1001030.
8. Bézier A., Annaheim M., Herbinière J., Wetterwald C., Gyapay G., Bernard-Samain S., et al. Polydnaviruses of braconid wasps derive from an ancestral nudivirus. Science 2009, 323:926-930.
9. Bézier A., Herbinière J., Serbielle C., Lesobre J., Wincker P., Huguet E., et al. Bracovirus gene products are highly divergent from insect proteins. Arch. Insect Biochem. Physiol. 2008, 67:172-187.
10. Bibor-Hardy V., Suh M., Pouchelet M., Simard R. Modifications of the nuclear envelope of BHK cells after infection with herpes simplex virus type 1. J. Gen. Virol. 1982, 63:81-94.
11. Bigot Y., Samain S., Augé-Gouillou C., Federici B.A. Molecular evidence for the evolution of ichnoviruses from ascoviruses by symbiogenesis. BMC Evol. Biol. 2008, 8:253.
12. Braunagel S.C., Russell W.K., Rosas-Acosta G., Russell D.H., Summers M.D. Determination of the protein composition of the occlusion-derived virus of Autographa californica nucleopolyhedrovirus. Proc. Natl. Acad. Sci. U.S.A. 2003, 100:9797-9802.
13. Braunagel S.C., Summers M.D. Molecular biology of the baculovirus occlusion-derived virus envelope. Curr. Drug Targets 2007, 8:1084-1095.
14. Chao Y.C., Lee S.T., Chang M.C., Chen H.H., Chen S.S., Wu T.Y., et al. A 2.9-kilobase noncoding nuclear RNA functions in the establishment of persistent Hz-1 viral infection. J. Virol. 1998, 72:2233-2245.
15. Choi J.Y., Roh J.Y., Kang J.N., Shim H.J., Woo S.D., Jin B.R., et al. Genomic segments cloning and analysis of Cotesia plutellae polydnavirus using plasmid capture system. Biochem. Biophys. Res. Commun. 2005, 332:487-493.
16. Conord C., Despres L., Vallier A., Balmand S., Miquel C., Zundel S., et al. Long-term evolutionary stability of bacterial endosymbiosis in curculionoidea: additional evidence of symbiont replacement in the dryophthoridae family. Mol. Biol. Evol. 2008, 25:859-868.
17. Crawford A.M., Sheehan C. Replication of Oryctes baculovirus in cell culture: viral morphogenesis, infectivity and protein synthesis. J. Gen. Virol. 1985, 66:529-539.
18. De Buron I., Beckage N.E. Characterization of a polydnavirus (PDV) and virus-like filamentous particle (VLFP) in the braconid wasp Cotesia congregata (Hymenoptera: Braconidae). J. Invertebr. Pathol. 1992, 59:315-327.
19. Deng L., Stoltz D.B., Webb B.A. A gene encoding a polydnavirus structural polypeptide is not encapsidated. Virology 2000, 269:440-450.
20. Deng L., Webb B.A. Cloning and expression of a gene encoding a Campoletis sonorensis polydnavirus structural protein. Arch. Insect Biochem. Physiol. 1999, 40:30-40.
21. Desjardins C.A., Gundersen-Rindal D.E., Hostetler J.B., Tallon L.J., Fadrosh D.W., Fuester R.W., et al. Comparative genomics of mutualistic viruses of Glyptapanteles parasitic wasps. Genome Biol. 2008, 9:R183.
22. Drezen J.-M., Bézier A., Lesobre J., Huguet E., Cattolico L., Periquet G., et al. The few virus-like genes of Cotesia congregata bracovirus. Arch. Insect Biochem. Physiol. 2006, 61:110-122.
23. Dupuy C., Huguet E., Drezen J.-M. Unfolding the evolutionary story of polydnaviruses. Virus Res. 2006, 117:81-89.
24. Dupuy C., Periquet G., Serbielle C., Bézier A., Louis F., Drezen J.-M. Transfer of a chromosomal Maverick to endogenous bracovirus in a parasitoid wasp. Genetica 2011, 139:489-496.
25. Espagne E., Dupuy C., Huguet E., Cattolico L., Provost B., Martins N., et al. Genome sequence of a polydnavirus: insights into symbiotic virus evolution. Science 2004, 306:286-289.
26. Falabella P., Varricchio P., Gigliotti S., Tranfaglia A., Pennacchio F., Malva C. Toxoneuron nigriceps polydnavirus encodes a putative aspartyl protease highly expressed in parasitized host larvae. Insect Mol. Biol. 2003, 12:9-17.
27. Falabella P., Varricchio P., Provost B., Espagne E., Ferrarese R., Grimaldi A., et al. Characterization of the IkB-like gene family in polydnaviruses associated with wasps belonging to different Braconid subfamilies. J. Gen. Virol. 2007, 88:92-104.
28. Federici B.A., Bigot Y. Origin and evolution of polydnaviruses by symbiogenesis of insect DNA viruses in endoparasitic wasps. J. Insect Physiol. 2003, 49:419-432.
29. Fleming J.A.G.W., Summers M.D. Polydnavirus DNA is integrated in the DNA of its parasitoid wasp host. Proc. Natl. Acad. Sci. U.S.A. 1991, 88:9770-9774.
30. Francino M.P. An adaptive radiation model for the origin of new gene functions. Nat. Genet. 2005, 37:573-577.
31. Garcia-Maruniak A., Maruniak J.E., Farmerie W., Boucias D.G. Sequence analysis of a non-classified, non-occluded DNA virus that causes salivary gland hypertrophy of Musca domestica, MdSGHV. Virology 2008, 377:184-196.
32. Gayral P., Noa-Carrazana J.C., Lescot M., Lheureux F., Lockhart B.E., Matsumoto T., et al. A single banana streak virus integration event in the banana genome as the origin of infectious endogenous pararetrovirus. J. Virol. 2008, 82:6697-6710.
33. Govindarajan R., Federici B.A. Ascovirus infectivity and effects of infection on the growth and development of noctuid larvae. J. Invertebr. Pathol. 1990, 56:291-299.
34. Guarino L.A., Dong W., Jin J. In vitro activity of the baculovirus late expression factor LEF-5. J. Virol. 2002, 76:12663-12675.
35. Guarino L.A., Xu B., Jin J., Dong W. A virus-encoded RNA polymerase purified from baculovirus-infected cells. J. Virol. 1998, 72:7985-7991.
36. Harwood S.H., Li L., Ho P.S., Preston A.K., Rohrmann G.F. AcMNPV late expression factor-5 interacts with itself and contains a zinc ribbon domain that is required for maximal late transcription activity and is homologous to elongation factor TFIIS. Virology 1998, 250:118-134.
37. Herniou E.A., Olszewski J.A., Cory J.S., O'Reilly D.R. The genome sequence and evolution of baculoviruses. Annu. Rev. Entomol. 2003, 48:211-234.
38. Hong T., Braunagel S.C., Summers M.D. Transcription, translation, and cellular localization of ODV-E66: a structural protein of the PDV envelope of Autographa californica nuclear polyhedrosis virus. Virology 1994, 204:210-222.
39. Hong T., Summers M.D., Braunagel S.C. N-terminal sequences from Autographa californica nuclear polyhedrosis virus envelope proteins ODV-E66 and ODV-E25 are sufficient to direct reporter proteins to the nuclear envelope, intranuclear microvesicles and the envelope of occlusion-derived virus. Proc. Natl. Acad. Sci. U.S.A. 1997, 94:4050-4055.
40. Hughes A.L., Friedman R. Genome-wide survey for genes horizontally transferred from cellular organisms to baculoviruses. Mol. Biol. Evol. 2003, 20:979-987.
41. Iyer L.M., Aravind L., Koonin E.V. Common origin of four diverse families of large eukaryotic DNA viruses. J. Virol. 2001, 75:11720-11734.
42. Jehle J.A., Blissard G.W., Bonning B.C., Cory J.S., Herniou E.A., Rohrmann G.F., et al. On the classification and nomenclature of baculoviruses: a proposal for revision. Arch. Virol. 2006, 151:1257-1266.
43. Katzourakis A., Gifford R.J. Endogenous viral elements in animal genomes. PLoS Genet. 2010, 6:e1001191.
44. Kim K.S., Kitajima E.W. Nonoccluded Baculovirus and filamentous virus-like particles in the spotted cucumber beetle, Diabrotica undecipunctata (coleoptera: chrysomelid). J. Invertebr. Pathol. 1984, 43:234-241.
45. Krell P.J., Stoltz D.B. Unusual baculovirus of the parasitic wasp Apanteles melanoscelus: isolation and primary characterization. J. Virol. 1979, 29:1118-1130.
46. Lapointe R., Tanaka K., Barney W.E., Whitfield J.B., Banks J.C., Béliveau C., et al. Genomic and morphological features of a banchine polydnavirus: comparison with bracoviruses and ichnoviruses. J. Virol. 2007, 81:6491-6501.
47. Li Y., Wang J., Deng R., Zhang Q., Yang K., Wang X. vlf-1 deletion brought AcMNPV to defect in nucleocapsid formation. Virus Genes 2005, 31:275-284.
48. Lin C.L., Lee J.C., Chen S.S., Wood H.A., Li M.L., Li C.F., et al. Persistent Hz-1 virus infection in insect cells: evidence for insertion of viral DNA into host chromosomes and viral infection in a latent status. J. Virol. 1999, 73:128-139.
49. McLachlin J.R., Miller L.K. Identification and characterization of vlf-1, a baculovirus gene involved in very late gene expression. J. Virol. 1994, 68:7746-7756.
50. Moran N.A. Symbiosis as an adaptive process and source of phenotypic complexity. Proc. Natl. Acad. Sci. U.S.A. 2007, 104:8627-8633.
51. Murphy N., Banks J.C., Whitfield J.B., Austin A.D. Phylogeny of the parasitic microgastroid subfamilies (Hymenoptera: Braconidae) based on sequence data from seven genes, with an improved time estimate of the origin of the lineage. Mol. Phylogenet. Evol. 2008, 47:378-395.
52. Oppenheimer D.I., Volkman L.E. Evidence for rolling circle replication of Autographa californica M nucleopolyhedrovirus genomic DNA. Arch. Virol. 1997, 142:2107-2113.
53. Parkinson N., Conyers C., Smith I. A venom protein from the endoparasitoid wasp Pimpla hypochondriaca is similar to snake venom reprolysin-type metalloproteases. J. Invertebr. Pathol. 2002, 79:129-131.
54. Pasquier-Barre F., Dupuy C., Huguet E., Monteiro F., Moreau A., Poirié M., et al. Polydnavirus replication: the EP1 segment of the parasitoid wasp Cotesia congregata is amplified within a larger precursor molecule. J. Gen. Virol. 2002, 83:2035-2045.
55. Passarelli A.L., Miller L.K. Identification of genes encoding late expression factors located between 56.0 and 65.4 map units of the Autographa californica nuclear polyhedrosis virus genome. Virology 1993, 197:704-714.
56. Peng K., van Oers M.M., Hu Z., van Lent J.W., Vlak J.M. Baculovirus per os infectivity factors form a complex on the surface of occlusion-derived virus. J. Virol. 2010, 84:9497-9504.
57. Perera O., Green T.B., Stevens S.M., White S., Becnel J.J. Proteins associated with Culex nigripalpus nucleopolyhedrovirus occluded virions. J. Virol. 2007, 81:4585-4590.
58. Poirié M., Carton Y., Dubuffet A. Virulence strategies in parasitoid Hymenoptera as an example of adaptive diversity. C. R. Biol. 2009, 332:311-320.
59. Price D.R., Bell H.A., Hinchliffe G., Fitches E., Weaver R., Gatehouse J.A. A venom metalloproteinase from the parasitic wasp Eulophus pennicornis is toxic towards its host, tomato moth (Lacanobia oleracae). Insect Mol. Biol. 2009, 18:195-202.
60. Raina A.K., Adams J.R., Lupiani B., Lynn D.E., Kim W., Burand J.P., et al. Further characterization of the gonad-specific virus of corn earworm, Helicoverpa zea. J. Invertebr. Pathol. 2000, 76:6-12.
61. Renault S., Petit A., Bénédet F., Bigot S., Bigot Y. Effects of the Diadromus pulchellus ascovirus, DpAV-4, on the hemocytic encapsulation response and capsule melanization of the leek-moth pupa, Acrolepiopsis assectella. J. Insect Physiol. 2002, 48:297-302.
62. Rohrmann, G.F., 2008. Baculovirus Molecular Biology. National Library of Medicine, National Center for Biotechnology Information, Bethesda. (). http://www.ncbi.nlm.gov/books/NBK1736/.
63. Russell R.L., Rohrmann G.F. Characterization of P91, a protein associated with virions of an Orgyia pseudotsugata baculovirus. Virology 1997, 233:210-223.
64. Sklan E.H., Staschke K., Oakes T.M., Elazar M., Winters M., Aroeti B., et al. A Rab-GAP TBC domain protein binds hepatitis C virus NS5A and mediates viral replication. J. Virol. 2007, 81:11096-11105.
65. Sparks W.O., Harrison R.L., Bonning B.C. Autographa californica multiple nucleopolyhedrovirus ODV-E56 is a per os infectivity factor, but is not essential for binding and fusion of occlusion-derived virus to the host midgut. Virology 2010, 409:69-76.
66. Stoltz D.B. Evidence for chromosomal transmission of polydnavirus DNA. J. Gen. Virol. 1990, 71:1051-1056.
67. Stoltz D.B., Vinson S.B. Viruses and parasitsm in insects. Adv. Virus Res. 1979, 183:125-171.
68. Stoltz D.B., Whitfield J.B. Making nice with viruses. Science 2009, 323:884-885.
69. Tilmann P., Styer E., Hamm J. Transmission of ascovirus from Heliothis virescens (Lepidotera: Noctuidae) by three parasitoids and effects of virus on survival of parasitoid Cardiochiles nigriceps (Hymenoptera: Braconidae). Environ. Entomol. 2004, 33:633-643.
70. Vanarsdall A.L., Okano K., Rohrmann G.F. Characterization of the role of very late expression factor 1 in baculovirus capsid structure and DNA processing. J. Virol. 2006, 80:1724-1733.
71. Vigdorovich V., Miller A.D., Strong R.K. Ability of hyaluronidase 2 to degrade extracellular hyaluronan is not required for its function as a receptor for jaagsiekte sheep retrovirus. J. Virol. 2007, 81:3124-3129.
72. Volkoff A.N., Jouan V., Urbach S., Samain S., Bergoin M., Wincker P., et al. Analysis of virion structural components reveals vestiges of the ancestral ichnovirus genome. PLoS Pathog. 2010, 6:e1000923.
73. Wang Y., Bininda-Emonds O.R., van Oers M.M., Vlak J.M., Jehle J.A. The genome of Oryctes rhinoceros nudivirus provides novel insight into the evolution of nuclear arthropod-specific large circular double-stranded DNA viruses. Virus Genes 2011, 42:444-456.
74. Wang Y., Burand J.P., Jehle J.A. Nudivirus genomics: diversity and classification. Virologica Sinica 2007, 22:128-136.
75. Wang Y., Jehle J.A. Nudiviruses and other large, double-stranded circular DNA viruses of invertebrates: New insights on an old topic. J. Invert. Pathol. 2009, 101:187-193.
76. Webb B., Strand M.R. The biology and genomics of polydnaviruses. Comprehensive Molecular Insect Science 2005, Vol. 6:323-360. Elsevier, Amsterdam.
77. Webb B.A., Strand M.R., Dickey S.E., Beck M.H., Hilgarth R.S., Barney W.E., et al. Polydnavirus genomes reflect their dual roles as mutualists and pathogens. Virology 2006, 347:160-174.
78. Weber B., Annaheim M., Lanzrein B. Transcriptional analysis of polydnaviral genes in the course of parasitization reveals segment-specific patterns. Arch. Insect. Biochem. Physiol. 2007, 66:9-22.
79. Wetterwald C., Roth T., Kaeslin M., Annaheim M., Wespi G., Heller M., et al. Identification of bracovirus particle proteins and analysis of their transcript levels at the stage of virion formation. J. Gen. Virol. 2010, 91:2610-2619.
80. Whitfield J.B. Estimating the age of the polydnavirus/braconid wasp symbiosis. Proc. Natl. Acad. Sci. U.S.A. 2002, 21:7508-7513.
81. Wu W., Lin T., Pan L., Yu M., Li Z., Pang Y., et al. Autographa californica multiple nucleopolyhedrovirus nucleocapsid assembly is interrupted upon deletion of the 38K gene. J. Virol. 2006, 80:11475-11485.
82. Wu Y.L., Wu C.P., Lee S.T., Tang H., Chang C.H., Chen H.H., et al. The early gene hhi1 reactivates Heliothis zea nudivirus 1 in latently infected cells. J. Virol. 2010, 84:1057-1065.
83. Wyder S., Tschannen A., Hochuli A., Gruber A., Saladin V., Zumbach S., et al. Characterization of Chelonus inanitus polydnavirus segments: sequences and analysis, excision site and demonstration of clustering. J. Gen. Virol. 2002, 83:247-256.
84. Wyler T., Lanzrein B. Ovary development and polydnavirus morphogenesis in the parasitic wasp Chelonus inanitus. II. Ultrastructural analysis of calyx cell development, virion formation and release. J. Gen. Virol. 2003, 84:1151-1163.
85. Yang S., Miller L.K. Expression and mutational analysis of the baculovirus very late factor 1 (vlf-1) gene. Virology 1998, 245:99-109.
86. Zhang J. Evolution by gene duplication an update. Trends Ecol. Evol. 2003, 18:292-297.