M
Massimo Zaccardelli
Publications - 5
Citations - 420
Massimo Zaccardelli is an academic researcher. The author has contributed to research in topics: Pseudomonas syringae & Gene. The author has an hindex of 5, co-authored 5 publications receiving 380 citations.
Papers
More filters
Journal ArticleDOI
The plant pathogen Pseudomonas syringae pv. tomato is genetically monomorphic and under strong selection to evade tomato immunity.
Rongman Cai,James J. Lewis,Shuangchun Yan,Haijie Liu,Christopher R. Clarke,F. Campanile,Nalvo F. Almeida,Nalvo F. Almeida,Nalvo F. Almeida,David J. Studholme,Magdalen Lindeberg,David J. Schneider,Massimo Zaccardelli,João C. Setubal,João C. Setubal,Nadia P. Morales-Lizcano,Adriana Bernal,Gitta Coaker,Christy Baker,Carol L. Bender,Scotland Leman,Boris A. Vinatzer +21 more
TL;DR: A genome-based micro-evolutionary study of a bacterial plant pathogen, Pseudomonas syringae pv.
Journal ArticleDOI
Role of Recombination in the Evolution of the Model Plant Pathogen Pseudomonas syringae pv. tomato DC3000, a Very Atypical Tomato Strain
Shuangchun Yan,Haijie Liu,Toni J. Mohr,Jenny Jenrette,Rossella Chiodini,Massimo Zaccardelli,João C. Setubal,Boris A. Vinatzer +7 more
TL;DR: A thorough investigation into tomato strain DC3000 and close relatives isolated from Antirrhinum majus, Apium graveolens, and Solanaceae and Brassicaceae species found that PtoDC3000 is located in the same phylogenetic cluster as isolates from several BrassicFamily species and that these isolates have a relatively wide host range that includes tomato, Arabidopsis thaliana, and cauliflower.
Journal ArticleDOI
Identification and in planta detection of Pseudomonas syringae pv. tomato using PCR amplification of hrpZPst.
TL;DR: A rapid detection method based on PCR amplification of Pseudomonas syringae pv.
Journal ArticleDOI
Detection and identification of the crucifer pathogen, Xanthomonas campestris pv. campestris , by PCR amplification of the conserved Hrp/type III secretion system gene hrcC
TL;DR: A diagnostic protocol for the identification/detection of Xcc by PCR amplification of fragments from the pathogenicity-associated gene hrcC is described, which specifically detected Xcc in inoculated leaves, seeds and naturally infected leaves of crucifers.
Journal ArticleDOI
Morphological and Molecular Characterization of Fusarium solani Isolates
TL;DR: Nine of 34 isolates in the FSSC, classified as F.solani var.