Artigo Acesso aberto Revisado por pares

First report of Olive latent virus 2 in wild castor bean ( Ricinus communis ) in Italy

2008; Wiley; Volume: 57; Issue: 2 Linguagem: Inglês

10.1111/j.1365-3059.2007.01722.x

ISSN

1365-3059

Autores

G. Parrella, Angelo De Stradis, C. Vovlas,

Tópico(s)

Plant and Fungal Interactions Research

Resumo

Wild castor bean plants (Ricinus communis), showing bright yellow mosaic leaf symptoms were collected in Vibo Valentia (Calabria region, southern Italy) during spring and summer of 2005 and 2006. Symptoms consisted of yellow speckled leaves with significant mottled areas; some leaves also contained an arabesque line pattern. Electron microscope observations of sap extracts from leaves with symptoms showed semi-spherical to bacilliform particles consistent with Alfamovirus and Oleavirus. Using a range of herbaceous plants and mechanical inoculation, a virus was isolated from castor bean; symptoms, in particular in Nicotiana benthamiana, N. clevelandii, N. occidentalis, N. glutinosa, Chenopodium quinoa, Phaseolus vulgaris cv. La Victorie and Gomphrena globosa, were comparable with those previously described for a castor bean isolate of Olive latent virus 2 (Grieco et al., 2002). The virus was identified serologically by particle decoration with an OLV2 antiserum, raised against an Italian OLV2 isolate (fig. 2; Grieco et al., 1992), and by sequencing the movement gene (MP) and the coat protein gene (CP), as described previously (Grieco et al., 2002). The nucleotide sequence of a 1696 bp amplicon, encompassing the MP and CP genes, was determined (GenBank Acc. AM600639). BLAST analysis showed 97% nucleotide identity with an OLV2/CB castor bean isolate from Greece (GenBank Acc. AJ439450) and 93% with the type isolate (GenBank Acc. X76993). Deduced amino acid sequences identities for MP protein were 98% with OLV2/CB and 94% with the type isolate and 97% and 96% for the CP protein respectively. In both proteins, amino acid substitutions were mostly concentrated in the N terminus region. Most aspects of the eco-biology of OLV2 are still unclear (e.g. vector transmission, isolate variability, natural host range). OLV2 was previously detected in wild castor bean in Greece (Vovlas et al., 2002). This new finding of a disease caused by another OLV2 isolate in the same host might suggest a potential role of castor bean in the epidemiology of OLV2, by acting as a natural virus reservoir. The authors would like to thank Ms Daniela Sorrentino for her excellent technical assistance.

Referência(s)
Altmetric
PlumX