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Publication
Featured researches published by V. Savino.
European Journal of Plant Pathology | 1997
D. Boscia; H. Zeramdini; Mariano Cambra; O. Potere; M.T. Gorris; A. Myrta; B. Di Terlizzi; V. Savino
A monoclonal antibody to an Albanian isolate of plum pox potyvirus (PPV) was obtained (MAbAL), that specifically recognized strain M of this virus. The specificity of MAbAL, assessed by comparative ELISA on 130 PPV isolates of different geographical origin, 22 of which were also tested by comparative IC-PCR, gave consistent and highly reproducible results. MAbAL seems to be elicited by a stable surface determinant that makes it particularly suitable for successful use under a wide range of conditions. MAbAL is an useful addition to the panel of PPV-specific MAbs available to date.
Journal of Plant Pathology | 2014
M. Saponari; D. Boscia; Giuliana Loconsole; Francesco Palmisano; V. Savino; O. Potere; G. P. Martelli
In the course of surveys carried out in June 2014 in the Salento (Apulia, southern Italy) area affected by an epidemic of a strain of Xylella fastidiosa subsp. pauca (Cariddi et al., 2014) denoted CoDiRO (abbreviation from the Italian name “Complesso del Disseccamento Rapido dell’Olivo”), the following symptomatic plants were observed: (i) cherry (Prunus avium), 13 trees showing scanty vegetation and bud failure, but no leaf scorching; (ii) myrtle-leaf milkwort (Polygala myrtifolia), three shrubs showing extensive desiccation of twigs and scorched leaves; (iii) coastal rosemary (Westringia fruticosa), one shrub with extensive chlorosis and desiccation of the leaves. Samples collected from all these hosts (except for two of the 13 cherry plants) were ELISA- and PCR-positive upon testing with the protocols described by Loconsole et al. (2014). Sequencing of the amplified products from five housekeeping genes (gyrB, 16S rRNA, dnaK, tonB, RNA polymerase sigma factor) and of the PCR products obtained using the X. fastidiosa strain- specific primers 272-1int/272-2int, showed that all these amplicons, regardless of the host of origin, had 100% sequence identity with the homologous products amplified from diseased olive trees (Cariddi et al., 2014). These results provide evidence that all the analyzed positive samples contain the same X. fastidiosa strain infecting olives in the same area. With the exception of cherry, for which there is a recorded infection by X. fastidiosa subsp. fastidiosa in California (Hernandez- Martinez et al., 2007), to the best of our knowledge P. myrtifolia and W. fruticosa are hitherto unreported hosts of this bacterium.
Phytopathology | 1993
R. E. Davis; E. L. Dally; A. Bertaccini; I. M. Lee; R. Credi; R. Osler; V. Savino; L. Carraro; B. Di Terlizzi; M. Barba
Vitis: Journal of Grapevine Research | 2015
A. Minafra; P. Casati; V. Elicio; A. Rowhani; P. Saldarelli; V. Savino; G. P. Martelli
Journal of Plant Pathology | 2001
N. Abou Ghanem-Sabanadzovic; M. Mahboubi; B. Di Terlizzi; Sead Sabanadzovic; V. Savino; J.K. Uyemoto; G. P. Martelli
Journal of Plant Pathology | 1999
O. Potere; D. Boscia; K. Djelouah; V. Elicio; V. Savino
Eppo Bulletin | 1996
J. Jawhar; B. Di Terlizzi; W. Khourym; V. Savino
Journal of Phytopathology | 1990
M. Boulila; D. Boscia; B. Di Terlizzi; M. A. Castellano; A. Minafra; V. Savino; G.P. Martelli
Journal of Plant Pathology | 2001
F. Ismaeil; N. A. Ghanem-Sabanadzovic; A. Myrta; B. Di Terlizzi; V. Savino
Eppo Bulletin | 2001
F. Ismaeil; A. Myrta; N. Abou Ghanem‐Sabanadzovic; S. Al Chaabi; V. Savino