Bertaccini, Assunta


Publications
31

Differentiation of ‘Candidatus Phytoplasma cynodontis’ Based on 16S rRNA and groEL Genes and Identification of a New Subgroup, 16SrXIV-C

Citation
Mitrović et al. (2015). Plant Disease 99 (11)
Names
Ca. Phytoplasma cynodontis
Abstract
‘Candidatus Phytoplasma cynodontis’ is widespread in bermudagrass and has only been found in monocotyledonous plants. Molecular studies carried out on strains collected in Italy, Serbia, and Albania enabled verification of molecular variability in the 16S ribosomal RNA (rRNA) gene. Based on restriction fragment length polymorphism and sequence analyses, the strains from Serbia were clearly differentiated from all others and assigned to a new ribosomal DNA (rDNA) subgroup designated as 16SrXIV-C

‘Candidatus Phytoplasma balanitae’ associated with witches’ broom disease of Balanites triflora

Citation
Win et al. (2013). International Journal of Systematic and Evolutionary Microbiology 63 (Pt_2)
Names
Ca. Phytoplasma balanitae
Abstract
A phytoplasma was identified in naturally infected wild Balanites triflora plants exhibiting typical witches’ broom symptoms (Balanites witches’ broom: BltWB) in Myanmar. The 16S rRNA gene sequence revealed that BltWB phytoplasma had the highest similarity to that of ‘Candidatus Phytoplasma ziziphi’ and it was also closely related to that of ‘Candidatus Phytoplasma ulmi ’. Phylogenetic analysis of the 16S rRNA gene sequences indicated th

‘Candidatus Phytoplasma convolvuli’, a new phytoplasma taxon associated with bindweed yellows in four European countries

Citation
Martini et al. (2012). International Journal of Systematic and Evolutionary Microbiology 62 (Pt_12)
Names
Ca. Phytoplasma convolvuli
Abstract
Plants of Convolvulus arvensis exhibiting symptoms of undersized leaves, shoot proliferation and yellowing, collectively defined as bindweed yellows, were sampled in different regions of Europe and assessed for phytoplasma infection by PCR amplification using phytoplasma universal rRNA operon primer pairs. Positive results were obtained for all diseased plants. RFLP analysis of amplicons comprising the16S rRNA gene alone or the16S rRNA gene and 16-23S intergenic spacer region indicated that the