Agronomy and Crop Science


Publications
763

<scp>PM</scp> 7/62 (2) ‘Candidatus Phytoplasma mali’, ‘Ca. P. pyri’ and ‘Ca. P. prunorum’

Citation
Anonymous (2017). EPPO Bulletin 47 (2)
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. Revised in 2017‐02 as a single Standard as PM 7/62 (2) with the addition of ‘Ca. P. prunorum’.

Molecular identification of diverse ‘Candidatus Phytoplasma’ species associated with grapevine decline in Iran

Citation
Ghayeb Zamharir et al. (2017). Journal of Phytopathology 165 (7-8)
Names
Ca. Phytoplasma
Abstract
AbstractGrapevine (Vitis vinifera) is one of the most important fruits in Iran where the provinces of Qazvin, Lorestan and Markazi are main producers. During 2013–2015, vineyards located in these provinces were surveyed to verify the presence of phytoplasma. The sample collection was based on symptomatology including decline, leaf yellowing and shortening of internodes. Total DNA was extracted from symptomatic and symptomless grapevine samples and used in nested‐polymerase chain reaction (PCR) a
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Metabolomic Response to Huanglongbing: Role of Carboxylic Compounds in Citrus sinensis Response to ‘Candidatus Liberibacter asiaticus’ and Its Vector, Diaphorina citri

Citation
Killiny, Nehela (2017). Molecular Plant-Microbe Interactions® 30 (8)
Names
Ca. Liberibacter asiaticus
Abstract
Huanglongbing, a destructive disease of citrus, is caused by the fastidious bacterium ‘Candidatus Liberibacter asiaticus’ and transmitted by Asian citrus psyllid, Diaphorina citri. The impact of ‘Ca. L. asiaticus’ infection or D. citri infestation on Valencia sweet orange (Citrus sinensis) leaf metabolites was investigated using gas chromatography mass spectrometry, followed by gene expression analysis for 37 genes involved in jasmonic acid (JA), salicylic acid (SA), and proline-glutamine pathw
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PHLOEM PROMOTERS IN TRANSGENIC SWEET ORANGE ARE DIFFERENTIALLY TRIGGERED BY Candidatus Liberibacter asiaticus

Citation
Miyata et al. (2017). Revista Brasileira de Fruticultura 39 (3)
Names
Ca. Liberibacter asiaticus
Abstract
ABSTRACT The use of promoters preferentially expressed in specific plant tissues is a desirable strategy to search for resistance for pathogens that colonize these tissues. The bacterium Candidatus Liberibacter asiaticus (Las), associated with huanglongbing disease (HLB) of citrus, colonizes phloem vessels. Some promoters, besides conferring tissue-specific expression, can also respond to the presence of the pathogen. The objective of the present study was to verify if the presence of Las could
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One Target, Two Mechanisms: The Impact of ‘Candidatus Liberibacter asiaticus’ and Its Vector, Diaphorina citri, on Citrus Leaf Pigments

Citation
Killiny, Nehela (2017). Molecular Plant-Microbe Interactions® 30 (7)
Names
Ca. Liberibacter asiaticus
Abstract
Huanglongbing (HLB) is currently the largest threat to global citrus production. We examined the effect of HLB pathogen ‘Candidatus Liberibacter asiaticus’ infection or infestation by its vector, Diaphorina citri, on ‘Valencia’ sweet orange leaf pigments using high-performance liquid chromatography, followed by gene expression analysis for 46 involved genes in carotenoid and chlorophyll biosynthesis pathways. Both ‘Ca. L. asiaticus’ and D. citri alter the total citrus leaf pigment balance with
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Molecular identification of Candidatus Phytoplasma spp. associated with Sophora yellow stunt in Iran

Citation
Allahverdi et al. (2017). Journal of Plant Protection Research 57 (2)
Names
Ca. Phytoplasma Ca. Phytoplasma phoenicium Ca. Phytoplasma solani
Abstract
Abstract In the spring of 2012, sophora (Sophora alopecuroides L.) plants showing symptoms of leaf yellowing, little leaves and stunting were observed in Firooz-kuh (Tehran province), Sari (Mazandaran province) and Urmia (West Azerbaijan province) in Iran. Symptomatic plants from the three locations were subjected to nested polymerase chain reaction (PCR) to amplify 16SrRNA using primer pair P1/P7 followed by primer pair R16F2n/R16R2. The amplicons were purified, sequenced and the nucleotide seq
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