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Effect of In Vitro Culture of Long Shoot Tip on Variant Structure and Titer of Grapevine Viruses

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Journal Plants (Basel)
Date 2022 Jul 27
PMID 35893611
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Abstract

Shoot tip culture is a very effective approach for studying plant viruses. In this study, we evaluated the numbers, diversity, and titer of grapevine viruses in in vitro grapevine plants after long shoot tip culture. Six virus-infected grapevine cultivars (Cabernet Franc, Cabernet Gernischt, Cabernet Sauvignon, Wink, Victoria, and Merlot) collected from six regions of China were used as the research materials. Approximately 1.5 cm long shoot tips were used for meristem culture. The average survival rate of the six grapevine cultivars was 45.7%. Merlot collected from Beijing showed the highest survival rate (80.0%). Regeneration was not achieved in Cabernet Gernischt collected from Liaoning province and Cabernet Sauvignon from Tianjin due to bacterial and fungal contamination. Virus detection conducted in the surviving regenerated plants showed that the virus infection status, including the viral numbers and the species present in plants grown in vitro, was the same as that in corresponding in vivo plants. Moreover, the analysis of sequence diversity and the mutation frequency in grapevine viruses in vitro indicated that the structure of grapevine viruses was stable in long shoot tip culture after four sub-culture passages. Further, the relative viral titer of in vitro grapevine plants was much higher than that of in vivo plants. These results aid in the investigation of viruses in woody plants.

References
1.
Osman F, Leutenegger C, Golino D, Rowhani A . Comparison of low-density arrays, RT-PCR and real-time TaqMan RT-PCR in detection of grapevine viruses. J Virol Methods. 2008; 149(2):292-9. DOI: 10.1016/j.jviromet.2008.01.012. View

2.
Cuevas J, Moya A, Sanjuan R . Following the very initial growth of biological RNA viral clones. J Gen Virol. 2005; 86(Pt 2):435-443. DOI: 10.1099/vir.0.80359-0. View

3.
Beuve M, Sempe L, Lemaire O . A sensitive one-step real-time RT-PCR method for detecting Grapevine leafroll-associated virus 2 variants in grapevine. J Virol Methods. 2007; 141(2):117-24. DOI: 10.1016/j.jviromet.2006.11.042. View

4.
Moya A, Elena S, Bracho A, Miralles R, Barrio E . The evolution of RNA viruses: A population genetics view. Proc Natl Acad Sci U S A. 2000; 97(13):6967-73. PMC: 34371. DOI: 10.1073/pnas.97.13.6967. View

5.
Minafra A, Saldarelli P, Grieco F, Martelli G . Nucleotide sequence of the 3' terminal region of the RNA of two filamentous grapevine viruses. Arch Virol. 1994; 137(3-4):249-61. DOI: 10.1007/BF01309473. View