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Potato leafroll virus (PLRV) and Potato virus Y (PVY) influence vegetative growth, physiological metabolism, and microtuber production of in vitro-grown shoots of potato (Solanum tuberosum L.)

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Abstract

Effects of Potato leafroll virus (PLRV) and Potato virus Y (PVY) on vegetative growth, physiological metabolism and microtuber production were investigated using in vitro shoot cultures. The results showed that parameters of shoot growth including bud break percentage, shoot length, and node number and length were markedly reduced in the diseased shoots. These negative effects were much more pronounced in shoots co-infected with PLRV and PVY than in those singly infected with either PLRV or PVY. The inhibitive effects on root developments measured by root number and length were observed only in shoots co-infected with PLRV and PVY. Significantly lower contents of chl-a, chl-b and total chl were found in virus infected shoots than in healthy ones. There were striking differences in contents of total soluble protein observed between healthy shoots and PLVR and PVY co-infected ones. The content of total soluble sugar was highest in shoots co-infected with PLRV and PVY, and lowest in healthy shoots. Furthermore, there were no significant differences found in the level of endogenous indole-acetic acid among healthy shoots verses virus infected shoots. However, the level of zeatin-ribosome was much higher in healthy shoots than in virus infected ones. Yet, both healthy and single PLRV infected shoots produced similar levels of gibberillic acid 3, which were much higher than those of PVY single-infected shoots and PLRV and PVY co-infected shoots. Also, there were no significant differences in the number of microtubers among healthy shoots, PLVR single or PVY single infected shoots, but shoots co-infected with PLRV and PVY produced the lowest number of microtubers. Overall, the healthy shoots produced the largest size of microtubers and the highest percentage of microtubers ≥5 mm in diameter.

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Abbreviations

BM:

Basal medium

Chl-a:

Chlorophyll a

Chl-b:

Chlorophyll b

D:

Density

DAS-ELISA:

Sandwich enzyme-linked immunological assay

FV:

Final volume

FW:

Fresh weight

GA3 :

Gibberillic acid 3

IAA:

Indole-acetic acid

JA:

Jasmonic acid

KT:

Kinetin

MS:

Murashige and Skoog medium

MTPM:

Microtuber production medium

PLRV:

Potato leafroll virus

PVA:

Potato virus A

PVM:

Potato virus M

PVPP:

Polyvinylpolypyrolidone

PVS:

Potato virus S

PVX:

Potato virus X

PVY:

Potato virus Y

RT-PCR:

Reverse-transcript polymerase chain reaction

ScYLV:

Sugarcane yellow leaf virus

T chl:

Total chlorophyll

TFW:

Total fresh weight

ZR:

Zeatin-ribosome

References

  • Abdala G, Milrad S, Vigliocco A, Pharis R, Wanner G (1999) Hyperauxinity in diseased leaves affected by Mal de Ri Cuarto Virus (MRCV). Biocell 23:13–18

    Google Scholar 

  • Anžlovar S, Kovac M, Ravnikar M (1996) Photosynthetic pigments in healthy and virus-infected potato plantlets (Solanum tuberosum L.) grown in vitro. Phyton 36:221–230

    Google Scholar 

  • Bailiss KW (1974) The relationship of gibberellin content to cucumber mosaic virus infection of cucumber. Physiol Plant Pathol 4:73–79

    Article  CAS  Google Scholar 

  • Bradford MM (1976) A rapid and sensitive method for the quantization of microgram quantities of protein utilizing the principle of protein–dye binding. Anal Biochem 72:248–254

    Article  PubMed  CAS  Google Scholar 

  • Bugary L, Isac M (1988) Some biochemical changes induced by plum pox in plum. Acta Hortic 235:125–129

    Google Scholar 

  • Cheong EJ, Mock R, Li RH (2012) Elimination of five viruses from sugarcane using in vitro culture of axillary buds and apical meristems. Plant Cell Tissue Organ Cult 109:439–445

    Article  Google Scholar 

  • Clack FM, Adams AN (1997) Characteristic of the microplate and method of enzyme-linked immunosorbent detection of plant viruses. J Gen Virol 34:475–483

    Google Scholar 

  • De Vries-Paterson RM, Evans TA, Stephens CT (1992) The effect of asparagus virus infection on asparagus tissue culture. Plant Cell Tissue Organ Cult 31:31–35

    Google Scholar 

  • Dermastia M, Ravnikar M (1996) Altered cytokinin pattern and enhanced tolerance to potato virus YNTN in the susceptible potato cultivar (Solanum tuberosum cv. Igor) grown in vitro. Physiol Mol Plant Pathol 48:65–71

    Article  CAS  Google Scholar 

  • Dermastia M, Ravnikar M, Kovac M (1995) Increased cytokinin-9-glucosylation in roots of susceptible Solanum tuberosum cultivar infected by potato virus YNTN. Mol Plant Microb Inter 8:327–330

    Article  CAS  Google Scholar 

  • Dobrev PIL, Vâgner HM, Malbeck J, Kamínek M (2005) Purification and determination of plant hormones auxin and abscisic acid using solid phase extraction and two-dimensional high performance liquid chromatography. J Chromatogr A 1075:159–166

    Article  PubMed  CAS  Google Scholar 

  • Dolenc J, Deermastia M (1999) Root system of PVY(NTN)-infected potato cultivar ‘Igor’ grown in vitro. Phyton Ann Rei Bot 39:253–257

    Google Scholar 

  • Dolenc J, Vilhar B, Dermastia M (2000) Systemic infection with potato virus YNTN alters the structure and activity of the shoot apical meristem in a susceptible potato cultivar. Physiol Mol Plant Pathol 56:33–38

    Article  Google Scholar 

  • Duran-Vila N, Cambra M, Medina V, Ortega C, Navarro L (1989) Growth and morphogenesis of citrus tissue cultures infected with Citrus tristeza virus and Citrus infectious variegation virus. Phytopathology 79:820–826

    Article  Google Scholar 

  • Duran-Vila N, Medina V, Pina JA, Ortega C, Molins MI, Navarro L (1991) Growth and morphogenesis of citrus tissue cultures infected with psorosis, vein enation, and cachexia. Phytopathology 81:824–831

    Article  Google Scholar 

  • Faccioli G (2001) Control of potato viruses using meirstem culture and stem-cutting cultures, thermotherapy and chemotherapy. In: Loebenstein G, Berger PH, Brunt A, Lawson RH (eds) Virus and virus-like diseases of potatoes and production of seed-potatoes. Kluwer, Dordrecht, pp 365–390

    Google Scholar 

  • Faccioli G, Rubies-Autonell C, Albertini R (1984) Role of cytokinins in the acquired resistance of Chenopodium amaranticolor towards an infection of tobacco necrosis virus. Phytopathol Mediterr 23:15–22

    CAS  Google Scholar 

  • Fraser RSS (1987) Biochemistry of virus infected plants. Research Atudies Press, Wiley, Letchworth, New York

    Google Scholar 

  • Gonçalves MC, Vega J, Jurandi G, Oliveira JG, Gomes MMA (2005) Sugarcane yellow leaf virus infection leads to alterations in photosynthetic efficiency and carbohydrate accumulation in sugarcane leaves. Fitopatol Bras 30:10–16

    Google Scholar 

  • Gong X-Q, Liu J-H (2012) Genetic transformation and genes for resistance to abiotic and biotic stresses in Citrus and its related genera. Plant Cell Tissue Organ Cult. doi:10.1007/s11240-012-0267-x

  • Hamm PB, Hane DC (1999) Effects of seedborne potato leafroll virus on Russet Norkotah potato. Plant Dis 83:1122–1124

    Article  Google Scholar 

  • Hane DC, Hamm PB (1999) Effects of seedborne potato virus Y infection in two potato cultivars expressing mild disease symptoms. Plant Dis 83:43–45

    Article  Google Scholar 

  • Haq IU, Nazia P, Muhammad TR, Muhammad UD (2012) Comparative characteristcs of micropropagated plantlets of banana from BBTV-infected explants to its normal and saline stressed cultures. Pak J Bot 44:1127–1130

    Google Scholar 

  • Hull R (2002) Matthews’ plant virology, 4th edn. Academic Press, London

    Google Scholar 

  • Jacobsen E (2007) The canon of potato science: 6. Genetic modification and cis- and transgenesis. Potato Res 50:227–230

    Article  Google Scholar 

  • Jameson PE, Clarke SF (2002) Hormone–virus interactions in plants. Crit Rev Plant Sci 21:205–228

    Article  CAS  Google Scholar 

  • Kleinhempel D, Schenk G, Bittner H, Gase G, Kursinger B (1990) Determination of virus resistance under in vitro conditions. Eur Assoc Potato Res 5:341–342

    Google Scholar 

  • Kuriger WE, Agrios GN (1977) Cytokinin levels and kinetin–virus interactions in tobacco ringspot virus infected cowpea plants. Phytopathology 67:604–609

    Article  CAS  Google Scholar 

  • Lalonde S, Tegeder M, Throne-Holst M, Frommer WB, Patrick JW (2003) Phloem loading and unloading of sugars and amino acids. Plant Cell Environ 26:37–56

    Article  CAS  Google Scholar 

  • Loebenstein G, Berger PH, Brunt A, Lawson R (2001) Virus and virus-like diseases of potatoes and production of seed-potatoes. Kluwer, Dordrecht

    Google Scholar 

  • Mederos DC, Martínez RS, Villafaña OP, Alfonso YA, Ramírez JEG, Pérez RH (2009) Alternations induced by Papaya ringspot potyvirus on chlorophyll content in papaya (Carica papaya L.). Fitopatol Bras 13:125–126

    Google Scholar 

  • Muletarova S, Stoikova D, Ivanov K (1995) Changes in the isoenzyme spectrum of peroxidase in potato and tobacco plants inoculated with potato virus A. Rasteniev’dni Nauki 32:118–120

    CAS  Google Scholar 

  • Murashige T, Skoog F (1962) A revised medium for rapid growth and bioassays with tobacco cell cultures. Physiol Plant 15:473–497

    Article  CAS  Google Scholar 

  • Navas-Castillo J, Moreno P, Duran-Vila N (1995) Citrus psorosis, ringspot, cristacortis and concave gum pathogens are maintained in callus culture. Plant Cell Tissue Organ Cult 40:133–137

    Article  Google Scholar 

  • Pandy S, Joshi A (1989) Effect of cucumis virus 3 infection on chlorophyll content, chloroplast mumber and chlorophyllase activity on bitter gourd. Indian Phytopathol 42:549–550

    Google Scholar 

  • Pennazio S, Roggero P (1996) Plant hormones and plant virus diseases. The auxins. Microbiologica 19:369–378

    PubMed  CAS  Google Scholar 

  • Peros IJO, Bonnel E, Reynaud B (1990) In vitro culture of sugarcane infected with maize streak virus (MSV). Plant Cell Tissue Organ Cult 23:145–149

    Google Scholar 

  • Petrovič N, Miersch O, Ravnikar M, Kovac M (1997) Potato virus YNTN alters the distribution and concentration of endogenous jasmonic acid in potato plants grown in vitro. Physiol Mol Plant Pathol 50:237–244

    Article  Google Scholar 

  • Poggi-Pollini C, Masia A, Giunched L (1990) Free indole-3-acetic acidin sugarbeet root of rhizomania susceptible and moderately resistant cutivars. Phytopathol Mediterr 29:191–195

    CAS  Google Scholar 

  • Pruski K (2007) The canon of potato science: 22. In vitro multiplication through nodal cuttings. Potato Res 50:293–296

    Article  Google Scholar 

  • Raju PN (1974) Dolichos enation mosaic virus (DEMV) and symbiotic nitrogen fixation in field bean (Dolicho lablab Linn.). Proc Indian Natl Sci Acad B 40:629–635

    Google Scholar 

  • Ranalli P (2007) The canon of potato science: 24. Microtubers. Potato Res 50:301–304

    Article  Google Scholar 

  • Rao MRK, Narasimham B, Reddy GS, Murthy VD (1977) Effect of mosaic virus infection on the endogenous gibberellin levels of sathgudi leaves (Citrus sinensis Osbeck). Hortic J India 34:196–198

    Google Scholar 

  • Russell SL, Kimmins WC (1971) Growth regulators and the effect of BYDV on barley (Hordeum vulgare L.). Ann Bot 35:1037–1043

    CAS  Google Scholar 

  • Shalitin D, Wolf S (2000) Cucumber mosaic virus infection affects sugar transport in melon plants. Plant Physiol 123:597–604

    Article  PubMed  CAS  Google Scholar 

  • Sinha A, Srivastava M (2010) Biochemical changes in mungbean plants infected by Mungbean yellow mosaic virus. Inter J Virol 6:150–157

    Article  CAS  Google Scholar 

  • Smaerea S, Andronic L, Grigorov T, Bujoreanu V (2010) In vitro regenerative genotypic specifity of meristems from virus infected grapevine cultivars. Rom Biotechnol Lett 15:19–25

    Google Scholar 

  • Sridhar R, Mohanty SK, Anjaneyulu A (1978) Physiology of rice tungro virus disease: increased cytokinin activity in tungro-infected rice cultivars. Physiol Plant 43:363–366

    Article  CAS  Google Scholar 

  • Srivastava S, Singh A (2010) Changes in catalase activity and total protein in urdbean [Vigna mungo (L.) Hepper] plants as a result of ULCV infection. Indian J Sci Res 1:67–69

    CAS  Google Scholar 

  • Sulstyarsi A, Supriyadi U (2012) The total protein band profile of the green leafhoppers (Nephotetti irescens) and the leaves of rice (Oryza sativa) infected by tungro virus. Bioscience 1:32–35

    Google Scholar 

  • Sun Q, Zhang CQ (2005) Studies on the methods of detecting PVYN and PVYO by RT-PCR. Sci Agric Sinica 38:213–216

    CAS  Google Scholar 

  • Sutha RMR, Rajappan K (1998) Tomato wilt virus infection on photosynthetic pigments in tomato. Plant Dis Res 13:138–140

    Google Scholar 

  • Tsao CWV, Postman JD, Reed BM (2000) Virus infections reduced in vitro multiplication of ‘Malling Landmark’ raspberry. In Vitro Cell Dev Plant 36:65–68

    Article  Google Scholar 

  • Valkonen JPT (2007) Viruses: economical losses and biotechnological potential. In: Vreugdenhil D (ed) Potato biology and biotechnology advances and perspectives. Elsevier, Amsterdam, pp 619–641

    Chapter  Google Scholar 

  • Wang QC, Mawassi M, Sahar N, Li P, Violeta C-T, Gafny R, Sela I, Tanne E, Perl A (2004) Cryopreservation of grapevine (Vitis spp.) embryogenic cell suspensions by encapsulation–vitrification. Plant Cell Tissue Organ Cult 77:267–275

    Article  CAS  Google Scholar 

  • Wang QC, Liu Y, Xie YH, You M (2006) Cryotherapy of potato shoot tips for efficient elimination of Potato leafroll Virus (PLRV) and Potato virus Y (PVY). Potato Res 49:119–129

    Article  Google Scholar 

  • Wang CX, Hong H, Wang GP, Jiang B, Fan XD (2009) Effects of citrus tristeza virus on the growth of in vitro-cultured citrus. J Plant Pathol 91:357–363

    CAS  Google Scholar 

  • Wang B, Ma YL, Zhang ZB, Wu ZM, Wu YF, Wang QC, Li MF (2011) Potato viruses in China. Crop Prot 30:1117–1123

    Article  Google Scholar 

  • Yan YJ, Wu K, Xie HF, Gao YF (2010) Molecular biological identification of Potato leafroll virus from field samples in Shaanxi. J Northwest A&F Univ 38:88–92

    Google Scholar 

  • Zhang H, Zhu X, Liu H (1997) Effect of banana bunchy top virus (BBTV) on endogenous hormone of banana plant. Acta Phytopathol Sinica 27:79–83

    Google Scholar 

  • Zhang Z-Y, Wang Y-G, Shen X-J, Li L, Zhou S-F, Li W-C, Fu F-L (2013) RNA interference-mediated resistance to maize dwarf mosaic virus. doi:10.1007/s11240-013-0289-z

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Acknowledgments

The authors would like to acknowledge financial supports from Department of Science and Technology of Shaanxi Province through a key project “13115” (2009ZDKG-10), Department of Science and technology of Yulin City (2011KJZX04) and Northwest A&F University through a president foundation.

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Correspondence to Qiao-Chun Wang.

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Jing-Wei Li and Biao Wang contributed equally to the present study.

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Li, JW., Wang, B., Song, XM. et al. Potato leafroll virus (PLRV) and Potato virus Y (PVY) influence vegetative growth, physiological metabolism, and microtuber production of in vitro-grown shoots of potato (Solanum tuberosum L.). Plant Cell Tiss Organ Cult 114, 313–324 (2013). https://doi.org/10.1007/s11240-013-0327-x

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