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Archives of Virology

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01.11.2014 | Brief Review

Luteovirus: insights into pathogenicity

verfasst von: Muhammad Ali, Shahid Hameed, Muhammad Tahir

Erschienen in: Archives of Virology | Ausgabe 11/2014

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Abstract

Luteoviruses are economically important plant viruses, infecting almost all cereals throughout the world. Idiosyncrasies related to this virus group may be a strategic consequence of viral genome compression. However, many fundamental questions have yet to be resolved. This review summarizes selected findings covering molecular aspects of pathogenesis relating to plant-infecting RNA viruses in general, and luteoviruses in specific. These studies enhance our understanding of the replication structures and the virus infection pathways.

Ahlquist P (2006) Parallels among positive-strand RNA viruses, reverse-transcribing viruses and double-stranded RNA viruses. Nat Rev Microbiol 4:371–382PubMedCrossRef

Ali M, Tahir M, Hameed S, Ashraf M (2013) Coat protein based molecular characterization of Barley yellow dwarf virus isolates identified on oat plants in Pakistan. Acta Virol 57:383–385PubMed

Allen E, Wang S, Miller WA (1999) Barley yellow dwarf virus RNA requires a cap-independent translation sequence because it lacks a 5′ cap. Virology 253:139–144PubMedCrossRef

Andret-Link P, Fuchs M (2005) Transmission specificity of plant viruses by vectors. J Plant Pathol 87:153–165

Barry JK, Miller WA (2002) A −1 ribosomal frameshift element that requires base pairing across four kilobases suggests a mechanism of regulating ribosome and replicase traffic on a viral RNA. Proc Natl Acad Sci 99:11133–11138PubMedCrossRefPubMedCentral

Baulcombe D (2002) Viral suppression of systemic silencing. Trends Microbiol 10:306–308PubMedCrossRef

Brown J (2000) Molecular markers for the identification and global tracking of whitefly vector—Begomovirus complexes. Virus Res 71:233–260PubMedCrossRef

Callaway A, Giesman-Cookmeyer D, Gillock E, Sit T, Lommel S (2001) The multifunctional capsid proteins of plant RNA viruses. Annu Rev Phytopathol 39:419–460PubMedCrossRef

Caplan JL, Mamillapalli P, Burch-Smith TM, Czymmek K, Dinesh-Kumar S (2008) Chloroplastic protein NRIP1 mediates innate immune receptor recognition of a viral effector. Cell 132:449–462PubMedCrossRefPubMedCentral

10.

Chay CA, Gunasinge UB, Dinesh-Kumar SP, Miller WA, Gray SM (1996) Aphid transmission and systemic plant infection determinants of barley yellow dwarf luteovirus-PAV are contained in the coat protein readthrough domain and 17-kDa protein, respectively. Virology 219:57–65PubMedCrossRef

11.

Cheng Z, He X, Wu M, Zhou G, Keese P, Waterhouse P (1996) Nucleotide sequence of coat protein gene for GPV isolate of barley yellow dwarf virus and construction of expression plasmid for plant. Sci China Ser C Life Sci (English Edition) 39:534–543

12.

Coudriet D, Kishaba A, Bohn G (1981) Inheritance of resistance to muskmelon necrotic spot virus in a melon aphid-resistant breeding line of muskmelon [Cucumis melo, Aphis gossypii]. J Am Soc Hortic Sci 106:789–791

13.

D’Arcy CJ, Burnett PA (1995) Barley yellow dwarf virus: 40 years of progress. APS Press, St Paul, MN

14.

den Boon JA, Diaz A, Ahlquist P (2010) Cytoplasmic viral replication complexes. Cell Host Microbe 8:77–85CrossRef

15.

Di R, Dinesh-Kumar SP, Miller WA (1993) Translational frameshifting by barley yellow dwarf virus RNA (PAV serotype) in Escherichia coli and in eukaryotic cell-free extracts. Mol Plant Microbe Interact MPMI 6:444–452CrossRef

16.

Dinesh-Kumar S, Miller WA (1993) Control of start codon choice on a plant viral RNA encoding overlapping genes. Plant Cell Online 5:679–692CrossRef

17.

Dolja VV, Koonin EV (1991) Phylogeny of capsid proteins of small icosahedral RNA plant viruses. J Gen Virol 72:1481–1486PubMedCrossRef

18.

Domier L (2008) Barley yellow dwarf virus. In: Mahy BWJ, Regenmortel MHV (eds) Encyclopedia of virology. Elsevier Ltd, Oxford, pp 279–286

19.

Domier L (2009) Barley yellow dwarf viruses. In: Mahy BWJ, Regenmortel MHV (eds) Desk encyclopedia of plant and fungal virology. Elsevier Ltd, Oxford, pp 100–107

20.

Dreher TW, Miller WA (2006) Translational control in positive strand RNA plant viruses. Virology 344:185–197PubMedCrossRefPubMedCentral

21.

Escaler M, Aranda MA, Thomas CL, Maule AJ (2000) Pea embryonic tissues show common responses to the replication of a wide range of viruses. Virology 267:318–325PubMedCrossRef

22.

Falk B, Tian T, Harrison B (1999) Transcapsidation interactions and dependent aphid transmission among luteoviruses, and luteovirus-associated RNAs. In: Smith HG, Barker H (eds) Luteoviridae. CAB International, Wallingford, UK, pp 125–134

23.

Fan Q, Treder K, Miller WA (2012) Untranslated regions of diverse plant viral RNAs vary greatly in translation enhancement efficiency. BMC Biotechnol 12:22PubMedCrossRef

24.

Fauquet CM, Mayo M, Maniloff J, Desselberger U, Ball LA (2005) Virus taxonomy: VIIIth report of the International Committee on Taxonomy of Viruses. Access Online via Elsevier

25.

Gildow F, Damsteegt V, Stone A, Smith O, Gray S (2000) Virus-vector cell interactions regulating transmission specificity of soybean dwarf luteoviruses. J Phytopathol 148:333–342CrossRef

26.

Gildow FE (1987) Virus—membrane interactions involved in circulative transmission of luteoviruses by aphids. Current topics in vector research. Springer, Berlin, pp 93–120

27.

Gill C, Chong J (1975) Development of the infection in oat leaves inoculated with barley yellow dwarf virus. Virology 66:440–453PubMedCrossRef

28.

Gill C, Chong J (1979) Cytopathological evidence for the division of barley yellow dwarf virus isolates into two subgroups. Virology 95:59–69PubMedCrossRef

29.

Gray S, Gildow FE (2003) Luteovirus-aphid interactions. Annu Review Phytopathol 41:539–566CrossRef

30.

Gray SM, Banerjee N (1999) Mechanisms of arthropod transmission of plant and animal viruses. Microbiol Mol Biol Rev 63:128–148PubMedPubMedCentral

31.

Guo L, Allen EM, Miller WA (2001) Base-pairing between untranslated regions facilitates translation of uncapped, nonpolyadenylated viral RNA. Mol Cell 7:1103–1109PubMedCrossRef

32.

Jones JD, Dangl JL (2006) The plant immune system. Nature 444:323–329PubMedCrossRef

33.

Kawakami S, Watanabe Y, Beachy RN (2004) Tobacco mosaic virus infection spreads cell to cell as intact replication complexes. Proc Natl Acad Sci USA 101:6291–6296PubMedCrossRefPubMedCentral

34.

Koev G, Mohan BR, Dinesh-Kumar SP, Torbert KA, Somers DA, Miller WA (1998) Extreme reduction of disease in oats transformed with the 5’ half of the barley yellow dwarf virus-PAV genome. Phytopathology 88:1013–1019PubMedCrossRef

35.

Koev G, Miller WA (2000) A positive-strand RNA virus with three very different subgenomic RNA promoters. J Virol 74:5988–5996PubMedCrossRefPubMedCentral

36.

Koev G, Liu S, Beckett R, Miller WA (2002) The 3′-terminal structure required for replication of barley yellow dwarf virus RNA contains an embedded 3′ end. Virology 292:114–126PubMedCrossRef

37.

Lee L, Palukaitis P, Gray SM (2002) Host-dependent requirement for the Potato leafroll virus 17-kDa protein in virus movement. Mol Plant Microbe Interact 15:1086–1094PubMedCrossRef

38.

Liu F, Wang X, Liu Y, Xie J, Gray S, Zhou G, Gao B (2007) A Chinese isolate of barley yellow dwarf virus-PAV represents a third distinct species within the PAV serotype. Arch Virol 152:1365–1373PubMedCrossRef

39.

Liu Y, Zhai H, Zhao K, Wu B, Wang X (2012) Two suppressors of RNA silencing encoded by cereal-infecting members of the family luteoviridae. J Gen Virol 93:1825–1830PubMedCrossRef

40.

Lucas WJ, Lee J-Y (2004) Plasmodesmata as a supracellular control network in plants. Nat Rev Mol Cell Biol 5:712–726PubMedCrossRef

41.

Lucas WJ (2006) Plant viral movement proteins: agents for cell-to-cell trafficking of viral genomes. Virology 344:169–184PubMedCrossRef

42.

Mayo M, D’Arcy C (1999) Family Luteoviridae: a reclassification of luteoviruses. In: Smith HG, Barker H (eds) Luteoviridae. CAB International, Wallingford, UK, pp 15–22

43.

Miller WA, Rasochová L (1997) Barley yellow dwarf viruses. Annu Rev Phytopathol 35:167–190PubMedCrossRef

44.

Miller W, Beckett R, Liu S (2002) Structure, function and variation of the Barley yellow dwarf virus and Cereal yellow dwarf virus genomes. In: Henry M, McNab A (eds) Barley yellow dwarf disease: recent advances and future strategies. CIMMYT, Mexico, DF, pp 1–8

45.

Miller W, Wang Z, Treder K (2007) The amazing diversity of cap-independent translation elements in the 3′-untranslated regions of plant viral RNAs. Biochem Soc Trans 35:1629–1633PubMedCrossRefPubMedCentral

46.

Miller WA, Liu S, Beckett R (2002) Barley yellow dwarf virus: luteoviridae or Tombusviridae? Mol Plant Pathol 3:177–183PubMedCrossRef

47.

Nass PH, Domier LL, Jakstys BP, D’Arcy CJ (1998) In situ localization of barley yellow dwarf virus-PAV 17-kDa protein and nucleic acids in oats. Phytopathology 88:1031–1039PubMedCrossRef

48.

Novoa RR, Calderita G, Arranz R, Fontana J, Granzow H, Risco C (2005) Virus factories: associations of cell organelles for viral replication and morphogenesis. Biol Cell 97:147–172PubMedCrossRef

49.

Paul CP, Barry JK, Dinesh-Kumar SP, Brault V, Miller WA (2001) A sequence required for −1 ribosomal frameshifting located four kilobases downstream of the frameshift site. J Mol Biol 310:987–999PubMedCrossRef

50.

Peter KA, Gildow F, Palukaitis P, Gray SM (2009) The C terminus of the polerovirus p5 readthrough domain limits virus infection to the phloem. J Virol 83:5419–5429PubMedCrossRefPubMedCentral

51.

Plant EP, Jacobs KLM, Harger JW, Meskauskas A, Jacobs JL, Baxter JL, Petrov AN, Dinman JD (2003) The 9-Å solution: How mRNA pseudoknots promote efficient programmed −1 ribosomal frameshifting. RNA 9:168–174PubMedCrossRefPubMedCentral

52.

Pogany J, Fabian MR, White KA, Nagy PD (2003) A replication silencer element in a plus-strand RNA virus. EMBO J 22:5602–5611PubMedCrossRefPubMedCentral

53.

Power A, Gray S (1995) Aphid transmission of barley yellow dwarf viruses: interactions between viruses, vectors, and host plants. In: D’Arcy CJ, Burnett PA (eds) Barley yellow dwarf virus: 40 years of progress. APS Press, St Paul, MN, pp 259–289

54.

Reavy B, Mayo M (2002) Persistent transmission of luteoviruses by aphids. Adv Bot Res 36:21–46CrossRef

55.

Restrepo-Hartwig MA, Ahlquist P (1996) Brome mosaic virus helicase-and polymerase-like proteins colocalize on the endoplasmic reticulum at sites of viral RNA synthesis. J Virol 70:8908–8916PubMedPubMedCentral

56.

Schaad MC, Jensen PE, Carrington JC (1997) Formation of plant RNA virus replication complexes on membranes: role of an endoplasmic reticulum-targeted viral protein. EMBO J 16:4049–4059PubMedCrossRefPubMedCentral

57.

Shen R, Miller WA (2004) Subgenomic RNA as a riboregulator: negative regulation of RNA replication by Barley yellow dwarf virus subgenomic RNA 2. Virology 327:196–205PubMedCrossRef

58.

Tacke E, Prüfer D, Schmitz J, Rohde W (1991) The potato leafroll luteovirus 17 K protein is a single-stranded nucleic acid-binding protein. J Gen Virol 72:2035PubMedCrossRef

59.

Wang D, Maule AJ (1995) Inhibition of host gene expression associated with plant virus replication. Science 267:229–231PubMedCrossRef

60.

Wang M-B, Cheng Z, Keese P, Graham M, Larkin P, Waterhouse P (1998) Comparison of the coat protein, movement protein and RNA polymerase gene sequences of Australian, Chinese, and American isolates of barley yellow dwarf virus transmitted by Rhopalosiphum padi. Arch Virol 143:1005–1013PubMedCrossRef

61.

Wang S, Browning KS, Miller WA (1997) A viral sequence in the 3′-untranslated region mimics a 5′ cap in facilitating translation of uncapped mRNA. EMBO J 16:4107–4116PubMedCrossRefPubMedCentral

62.

Wang S, Guo L, Allen E, Miller WA (1999) A potential mechanism for selective control of cap-independent translation by a viral RNA sequence in cis and in trans. RNA 5:728–738PubMedCrossRefPubMedCentral

63.

Wang X, Chang S, Jin Z, Li L, Zhou G (2001) Nucleotide sequences of the coat protein and readthrough protein genes of the Chinese GAV isolate of barley yellow dwarf virus. Acta Virol 45:249PubMed

64.

Wang X, Zhou G (2003) Identification of a protein associated with circulative transmission of Barley yellow dwarf virus from cereal aphids, Schizaphis graminum and Sitobion avenae. Chin Sci Bull 48:2083–2087CrossRef

65.

Wang X, Liu Y, Chen L, Zhao D, Wang X, Zhang Z (2013) Wheat resistome in response to barley yellow dwarf virus infection. Funct Integr Genomics 13(2):155–165

66.

Waziri H, El Gaffar MA, Allam E, El Din AG (2002) Coat protein sequence of an Egyptian BYDV-PAV isolate. In: Henry M, McNab A (eds) Barley yellow dwarf disease: recent advances and future strategies. CIMMYT, Mexico, DF, pp 97–99

67.

Xia Z, Cao R, Sun K, Zhang H (2012) The movement protein of barley yellow dwarf virus-GAV self-interacts and forms homodimers in vitro and in vivo. Arch Virol 157:1233–1239PubMedCrossRef

68.

Yoon J-Y, Choi S-K, Palukaitis P, Gray SM (2011) Agrobacterium-mediated infection of whole plants by yellow dwarf viruses. Virus Res 160:428–434PubMedCrossRef

69.

Zvereva AS, Pooggin MM (2012) Silencing and innate immunity in plant defense against viral and non-viral pathogens. Viruses 4:2578–2597PubMedCrossRefPubMedCentral

Titel: Luteovirus: insights into pathogenicity
verfasst von: Muhammad Ali
Shahid Hameed
Muhammad Tahir
Publikationsdatum: 01.11.2014
Verlag: Springer Vienna
Erschienen in: Archives of Virology / Ausgabe 11/2014
Print ISSN: 0304-8608
Elektronische ISSN: 1432-8798
DOI: https://doi.org/10.1007/s00705-014-2172-6

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