Horticulture


Publications
183

PM 9/25 (2) Bactericera cockerelli and ‘Candidatus Liberibacter solanacearum’

Citation
Anonymous (2020). EPPO Bulletin 50 (3)
Names
“Liberibacter solanacearum”
Abstract
Specific scopeThis Standard describes a national regulatory control system for the bacterial pathogen ‘Candidatus Liberibacter solanacearum’ and its vector Bactericera cockerelli when regulated as quarantine pests. It also covers measures to reduce the risk of ‘Ca. L. solanacearum’ spreading to potato production systems when listed as a regulated nonquarantine pest (RNQP) on seed potatoFor the EPPO A1 listed pests recommended for regulation as quarantine pests B. cockerelli and ‘Ca. L. solanacea
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<scp>PM</scp> 7/62 (3) ‘Candidatus Phytoplasma mali’, ‘Ca. P. pyri’ and ‘Ca. P. prunorum’

Citation
Anonymous (2020). EPPO Bulletin 50 (1)
Names
Ca. Phytoplasma mali
Abstract
Specific scopeThis Standard describes a diagnostic protocol for ‘Candidatus Phytoplasma mali’, ‘Ca. P. pyri’ and ‘Ca. P. prunorum’.This Standard should be used in conjunction with PM 7/76 Use of EPPO diagnostic protocolsSpecific approval and amendmentApproved as PM 7/62 Candidatus Phytoplasma mali and PM 7/63 Ca. P. pyri in 2006. First revision in 2017‐02 as a single Standard as PM 7/62 (2) with the addition of ‘Ca. P. prunorum’. Second revision in 2019‐06.

<scp>PM</scp> 9/27 (1) ‘Candidatus Liberibacter’ species that are causal agents of Huanglongbing disease of citrus and their vectors: procedures for official control

Citation
Anonymous (2020). EPPO Bulletin 50 (1)
Names
Liberibacter
Abstract
ScopeThis Standard describes procedures for official control with the aim of detecting, containing and eradicating those ‘Candidatus Liberibacter’ species which are causal agents of Huanglongbing (also known as citrus greening disease) and their vectors Trioza erytreae and Diaphorina citri. NPPOs may draw on this guidance when developing national contingency plans for outbreaks of ‘Candidatus Liberibacter’ species and their vectors.Approval and amendmentFirst approved in 2019‐09.

A novel haplotype of ‘Candidatus Liberibacter solanacearum’ found in Apiaceae and Polygonaceae family plants

Citation
Haapalainen et al. (2020). European Journal of Plant Pathology 156 (2)
Names
“Liberibacter solanacearum”
Abstract
AbstractA previously unknown haplotype of the plant pathogen ‘CandidatusLiberibacter solanacearum’ (Lso) was found in cultivated carrots and parsnips in eastern Finland. That same haplotype was found in western Finland, over 300 km away, in the family Polygonaceae, the speciesFallopia convolvulus(wild buckwheat) andPersicaria lapathifolia(pale persicaria) growing as weeds within carrot and parsnip fields. The infected plants, both apiaceous and polygonaceous, showed symptoms of foliar discoloura
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Huanglongbing, Caused by ‘Candidatus Liberibacter asiaticus,’ Detected in New Locations Across Southern and Coastal Georgia

Citation
Oliver et al. (2020). Plant Health Progress 21 (1)
Names
Ca. Liberibacter asiaticus
Abstract
Huanglongbing (HLB) or citrus greening disease is the most devastating disease of citrus worldwide. This disease, caused by the bacterium ‘Candidatus Liberibacter asiaticus’ (CLas), leads to low fruit quality and unproductive trees. In 2008, HLB was found in a residential citrus tree in Savannah, Georgia, and, as a result, the state has been quarantined for this disease since 2009. Nonetheless, little is known about the distribution of CLas within Georgia, even though the commercial planting of
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MOLECULAR CHARACTERIZATION OF ‘Candidatus PHYTOPLASMA MALI’ STRAINS FROM BULGARIA AND POLAND

Citation
Cieślińska, Borisova (2019). Acta Scientiarum Polonorum Hortorum Cultus 18 (5)
Names
Ca. Phytoplasma mali
Abstract
During 2015, samples from 22 apple trees showing proliferation symptoms were collected in southwest Bulgaria and Central and South Poland and tested for phytoplasma presence. ‘Candidatus Phytoplasma mali’ was identified in 18 samples based on results of restriction fragment length polymorphism (RFLP) analysis of the 16S rRNA gene amplified in nested PCR using primer pair P1/P7 followed by R16F2n/R16R2 and F1/B6 primer pairs. The nitroreductase and rhodonase like genes and ribosomal protein genes
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