J Gen Virol
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Originally published as JGV in Press, 10.1099/vir.0.013219-0 on August 12, 2009 J Gen Virol 90 (2009), 3015-3021; DOI 10.1099/vir.0.013219-0

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The 2b protein of cucumber mosaic virus is essential for viral infection of the shoot apical meristem and for efficient invasion of leaf primordia in infected tobacco plants

Anurag Sunpapao, Takashi Nakai, Fang Dong, Tomofumi Mochizuki and Satoshi T. Ohki

Graduate School of Life and Environmental Sciences, Osaka Prefecture University, Sakai, Osaka 599-8531, Japan

Correspondence
Tomofumi Mochizuki
tomochi{at}plant.osakafu-u.ac.jp

It has been reported previously that a 2b protein-defective mutant of the cucumber mosaic virus (CMV) Pepo strain ({Delta}2b) induces only mild symptoms in systemically infected tobacco plants. To clarify further the role of the 2b protein as an RNA silencing suppressor in mosaic symptom expression during CMV infection, this study monitored the sequential distribution of {Delta}2b in the shoot meristem and leaf primordia (LP) of inoculated tobacco. Time-course histochemical observations revealed that {Delta}2b was distributed in the shoot meristem at 7 days post-inoculation (p.i.), but could not invade shoot apical meristem (SAM) and quickly disappeared from the shoot meristem, whereas wild-type (Pepo) transiently appeared in SAM from 4 to 10 days p.i. In LP, {Delta}2b signals were detected only at 14 and 21 days p.i., whereas dense Pepo signals were observed in LP from 4 to 18 days p.i. Northern blot analysis showed that small interfering RNA (siRNA) derived from {Delta}2b RNA accumulated earlier in the shoot meristem and LP than that of Pepo. However, a similar amount of siRNA was detected in both Pepo- and {Delta}2b-infected plants at late time points. Tissue printing analysis of the inoculated leaves indicated that the areas infected by Pepo increased faster than those infected by {Delta}2b, whereas accumulation of {Delta}2b in protoplasts was similar to that of Pepo. These findings suggest that the 2b protein of the CMV Pepo strain determines virulence by facilitating the distribution of CMV in the shoot meristem and LP via prevention of RNA silencing and/or acceleration of cell-to-cell movement.







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