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Authors Ágoston

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Ágoston, János


Publications
5

CitationNamesAbstract
Evaluation the Significance of 'Candidatus Phytoplasma Prunorum' Pathogen for Apricot Cultivars Koncz et al. (2024). Universal Journal of Plant Science 11 (1) Ca. Phytoplasma
Detection and molecular identification of 'Candidatus Phytoplasma asteris' associated with muscari virescence of three grape hyacinth species Mergenthaler et al. (2023). Plant Protection Science 59 (4) Ca. Phytoplasma asteris
First Report of ‘Candidatus Phytoplasma asteris’ Associated with Cyclamen Little Leaf in Hungary Viczián et al. (2023). Plant Disease 107 (8) Ca. Phytoplasma asteris
Detection of ‘Candidatus Phythoplasma prunorum’ in Apricot Trees and its Associated Psyllid Samples Koncz et al. (2023). Agronomy 13 (1) Ca. Phythoplasma prunorum Ca. Phytoplasma prunorum
First Report of Lychnis flos-cuculi as a New Host Plant for ‘Candidatus Phytoplasma asteris’ (Subgroup 16SrI-B) Mergenthaler et al. (2020). Plant Disease 104 (4) Ca. Phytoplasma asteris

Detection of ‘Candidatus Phythoplasma prunorum’ in Apricot Trees and its Associated Psyllid Samples
‘Candidatus Phytoplasma prunorum’ is causing ever increasing economic losses through the decline of apricot trees in European countries, e.g., Hungary. In this study, the pathogen was identified from plant tissues and insects by nested-PCR. The insect species were identified via morphology and molecular methods. The incidence of the pathogen was 29.6% in randomly selected apricot trees. Most of the infected trees with symptoms died within a year. These results show that phytoplasma is significantly present and causes damage in the investigated plantations. The only known insect vector of this phytoplasma is the plum psyllid, Cacopsylla pruni, which was regularly encountered in the sampled apricot orchards and in their surroundings. In a two-year study, several adults among the sampled specimens were observed to be infected by the pathogen. This observation further confirms the role of the plum psyllid in vectoring the phytoplasma. All the sampled plum psyllid adults belonged to the ‘B’ biotype. Besides C. pruni, Cacopsylla crataegi was abundant in the samples. Several adults of the latter species were also infected by the pathogen ‘Ca. Phytoplasma prunorum’. The rates of occurrence of this phytoplasma in male and female adults of the two psyllid species appeared to be similar. The examined C. crataegi individuals showed genetic differences from each other and from specimens included in a previous investigation.
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