Melon necrotic spot virus newly reported in China

Q.-S. Gu¹*, W.-H. Bao², Y.-P. Tian¹, M. Prins³, H.-X Yang², J. Lu², L.-F. Liu¹ and B. Peng¹

¹ Biotechnology Center, Zhengzhou Fruit Research Institute, Chinese Academy of Agricultural Sciences, Zhengzhou 450009,Henan Province, P.R. China
² Haimen Institute of Agricultural Sciences, Haimen, Jiangsu Province, P.R.China
³ Keygene N.V., Wageningen, The Netherlands.

*guqsh@126.com

Accepted for publication 28/08/07

During April 2007, systemic necrotic spots were observed on melon (Cucumis melo) grown in plastic greenhouses in Haimen city of Jiangsu Province, China. By mid May disease rates in different plastic houses ranged from 19% to 100% with symptoms characteristic of Melon necrotic spot virus (MNSV). These symptoms included many necrotic spots on the young leaves (Fig. 1a) followed by coalescence of spots to form larger irregular lesions on older leaves (Fig. 1b). Necrotic stripes appeared on stems, and the infected leaves also became curled and wilted.

Figure 1:  Necrotic spots on young leaves (a); coalesced spots forming large irregular lesions on older leaves (b)

Sap extracts in 0.01 M phosphate buffer, pH 7.0, from diseased plants were mechanically inoculated to melon, watermelon (Citrullus lanatus ) and cucumber (Cucumis sativus). Melon, watermelon and cucumber all showed local necrotic spots on cotyledons three to five days post inoculation in the greenhouse and six days post inoculation under 20 °C in a growth chamber, but systemic necrotic spots were observed only on melon plants, which began to appear six to seven days post inoculation in the greenhouse and 9-14 days post inoculation at 20°C in a growth chamber (Fig. 2a and Fig. 2b).

Figure 2:  Systemic necrotic spots on muskmelon 7 days post inoculation (a); systemic necrotic spots on honeydew melon 7 days post inoculation (b)

For further confirmation of the causal agent, primers MNSV-CP-5’ (GTGAAGCTTAARCAGGC) and MNSV-CP-3’ (ACRTARAGATCACCRTGGGC) were synthesized (Yakoubi et al., 2007) to amplify a 710 bp region of the MNSV coat protein gene. The expected PCR product was amplified from Trizol extracted total RNA from virus infected fresh leaves, but no PCR products were amplified from healthy plant total RNA. The alignment of a 673 bp nucleotide sequence, which excluded the primer sequences (GenBank EU016217 ), showed 93% and 92% identity to MNSV isolates from Spain (GenBank DQ339157), and the Netherlands (GenBank M29671), respectively.

MNSV has been previously reported in Japan, the Netherlands, USA, UK (Hibi and Furuki 1985), Greece (Avgelis, 1985), Korea (Choi et al., 2003), Spain (Diaz et al.,2003) and other countries (e.g. Yakoubi et al., 2007). To the best of our knowledge, this is first report of MNSV in China.

Acknowledgements

This research was supported by the Special Program for Key Basic Research of the Ministry of Science and Technology, China (Grant No. 2005CCA01700).

References

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