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01-12-2016 | Brief Report

Some like it hot: citrus tristeza virus strains react differently to elevated temperature

Authors: S. J. Cowell, S. J. Harper, W. O. Dawson

Published in: Archives of Virology | Issue 12/2016

Abstract

Viruses often infect plants as a mixed population. The dynamics of viral populations dictate the success of the infection, yet there is little understanding of the factors that influence them. It is known that temperature can affect individual viruses; could it also affect a virus population? In order to study this, we observed citrus tristeza virus (CTV) populations in different hosts under winter and summer conditions (25 versus 36 °C). We found that only some CTV strains were affected by a higher summer temperature, which lead to a change in CTV population structure, and that this effect was host dependent.

Al Rwahnih M, Daubert S, Golino D, Rowhani A (2009) Deep sequencing analysis of RNAs from a grapevine showing Syrah decline symptoms reveals a multiple virus infection that includes a novel virus. Virology 387(2):395–401PubMedCrossRef

Moreno P, Ambros S, Albiach-Marti MR, Guerri J, Pena L (2008) Citrus tristeza virus: a pathogen that changed the course of the citrus industry. Mol Plant Pathol 9(2):251–268PubMedCrossRef

García-Arenal F, Fraile A, Malpica JM (2001) Variability and genetic structure of plant virus populations. Annu Rev Phytopathol 39(1):157–186PubMedCrossRef

Syller J (2012) Facilitative and antagonistic interactions between plant viruses in mixed infections. Mol Plant Pathol 13(2):204–216PubMedCrossRef

Alizon S, de Roode JC, Michalakis Y (2013) Multiple infections and the evolution of virulence. Ecol Lett 16(4):556–567PubMedCrossRef

Li S, Wang H, Zhou G (2014) Synergism between Southern rice black-streaked dwarf virus and Rice ragged stunt virus enhances their insect vector acquisition. Phytopathology 104(7):794–799PubMedCrossRef

Karyeija RF, Kreuze JF, Gibson RW, Valkonen JPT (2000) Synergistic interactions of a potyvirus and a phloem-limited crinivirus in sweet potato plants. Virology 269(1):26–36PubMedCrossRef

Untiveros M, Fuentes S, Salazar LF (2007) Synergistic interaction of Sweet potato chlorotic stunt virus (Crinivirus) with carla-, cucumo-, ipomo-, and potyviruses infecting sweet potato. Plant Dis 91:669–676CrossRef

Moreno IM, Malpica JM, Rodríguez-Cerezo E, Garcia-Arenal F (1997) A mutation in tomato aspermy cucumovirus that abolishes cell-to-cell movement is maintained to high levels in the viral RNA population by complementation. J Virol 71(12):9157–9162PubMedPubMedCentral

10.

Harper SJ, Cowell SJ, Dawson WO (2015) With a little help from my friends: Complementation as a survival strategy for viruses in a long-lived host system. Virology 478:123–128PubMedCrossRef

11.

Mansky LM, Durand DP, Hill JH (1995) Evidence for complementation of plant potyvirus pathogenic strains in mixed infection. J Phytopathol 143(4):247–250CrossRef

12.

García-Cano E, Resende RO, Fernández-Muñoz R, Moriones E (2006) Synergistic interaction between Tomato chlorosis virus and Tomato spotted wilt virus results in break down of resistance in tomato. Phytopathology 96(11):1263–1269PubMedCrossRef

13.

Scheets K (1998) Maize chlorotic mottle machlomovirus and Wheat streak mosaicrymovirus concentrations increase in the synergistic disease corn lethal necrosis. Virology 242(1):28–38PubMedCrossRef

14.

Fondong VN, Pita JS, Rey MEC, De Kochko A, Beachy RN, Fauquet CM (2000) Evidence of synergism between African cassava mosaic virus and a new double-recombinant geminivirus infecting cassava in Cameroon. J Gen Virol 8:287–297CrossRef

15.

Syller J, Grupa A (2014) The effects of co-infection by different Potato virus Y (PVY) isolates on concentration in solanaceous hosts and efficiency of transmission. Plant Pathol 63:466–475CrossRef

16.

Harper SJ, Cowell SJ, Dawson WO (2015) Finding balance: virus populations reach equilibrium during the infection process. Virology 485:205–212PubMedCrossRef

17.

Brlansky RH, Damsteegt VD, Howd DS, Roy A (2003) Molecular analyses of Citrus tristeza virus subisolates separated by aphid transmission. Plant Dis 87(4):397–401CrossRef

18.

Hilf ME, Mavrodieva VA, Garnsey SM (2005) Genetic marker analysis of a global collection of isolates of Citrus tristeza virus : characterization and distribution of CTV genotypes and association with symptoms. Phytopathology 95(8):909–917PubMedCrossRef

19.

Scott KA, Hlela Q, Zablocki O, Read D, Van Vuuren S, Pietersen G (2013) Genotype composition of populations of grapefruit-cross-protecting Citrus tristeza virus strain GFMS12 in different host plants and aphid-transmitted sub-isolates. Arch Virol 158(1):27–37PubMedCrossRef

20.

Harper SJ (2013) Citrus tristeza virus: evolution of complex and varied genotypic groups. Front Microbiol 4:93PubMedPubMedCentralCrossRef

21.

Harper SJ, Cowell SJ, Robertson CJ, Dawson WO (2014) Differential tropism in roots and shoots infected by Citrus tristeza virus. Virology 460:91–99PubMedCrossRef

22.

Szittya G, Silhavy D, Molnár A, Havelda Z, Lovas Á, Lakatos L, Bánfalvi Z, Burgyán J (2003) Low temperature inhibits RNA silencing-mediated defence by the control of siRNA generation. EMBO J 22(3):633–640PubMedPubMedCentralCrossRef

23.

Walkey DGA (1991) Production of virus-free plants. Applied plant virology, 2nd edn. Chapman and Hall, London, pp 270–292CrossRef

24.

Kobyłko T, Nowak B, Urban A (2005) Incidence of Apple mosaic virus (ApMV) on hazelnut in south-east Poland. Folia Hortic 17:153–161

25.

Zotto AD, Nome SF, Di Rienzo JA, Docampo DM (1999) Fluctuations of Prunus necrotic ringspot virus (PNRSV) at various phenological stages in peach cultivars. Plant Dis 83(11):1055–1057CrossRef

26.

Roistacher CN, Blue RL, Nauer EM, Calavan EC (1974) Suppression of tristeza virus symptoms in Mexican lime seedlings grown at warm temperatures. Plant Dis Rep 58(8):757–760

27.

Franck A, Hirth L (1976) Temperature-resistant strains of Alfalfa mosaic virus. Virology 70(2):283–291PubMedCrossRef

28.

Hitchborn JH (1956) The effect of temperature on infection with strains of Cucumber mosaic virus. Ann App Biol 44(4):590–598CrossRef

29.

Glasa M, Labonne G, Quiot JB (2003) Effect of temperature on Plum pox virus infection. Acta Virol 47(1):49–52PubMed

30.

Livak KJ, Schmittgen TD (2001) Analysis of relative gene expression data using real-time quantitative PCR and the 2_ΔΔCT method. Methods 25(4):402–408PubMedCrossRef

31.

Permar TA, Garnsey SM, Gumpf DJ, Lee RF (1990) A monoclonal antibody that discriminates strains of Citrus tristeza virus. Phytopathology 80:224–228CrossRef

32.

Garnsey S, Cambra M (1991) Enzyme-linked immunosorbent assay (ELISA) for citrus pathogens. In: Roistacher CN (ed) Graft transmissible diseases of citrus: handbook for detection and diagnosis. FAO, Rome, pp 193–216

33.

Kassanis B, Lebeurier G (1969) The behavior of Tomato bushy stunt virus and Bromegrass mosaic virus at different temperatures in vivo and in vitro. J Gen Virol 4:385–395CrossRef

34.

Jones RW, Jackson AO, Morris TJ (1990) Defective-interfering RNAs and elevated temperatures inhibit replication of Tomato bushy stunt virus in inoculated protoplasts. Virology 176(2):539–545PubMedCrossRef

Title: Some like it hot: citrus tristeza virus strains react differently to elevated temperature
Authors: S. J. Cowell
S. J. Harper
W. O. Dawson
Publication date: 01-12-2016
Publisher: Springer Vienna
Published in: Archives of Virology / Issue 12/2016
Print ISSN: 0304-8608
Electronic ISSN: 1432-8798
DOI: https://doi.org/10.1007/s00705-016-3083-5

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