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Monitoring American plum line pattern virus in plum by ELISA and dot-blot hybridisation throughout the year [Prunus salicina Lindl.; Apulia; Enzyme-linked Immunosorbent Assay]

American plum line pattern virus (APLPV) was monitored monthly throughout a year in a Japanese plum tree by using ELISA and dot-blot hybridisation. Leaf samples were tested from March to November and dormant buds were tested from December to February. Flowers, cortex and fruits, when available, were...

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Published in:Journal of plant pathology 2004-07, Vol.86 (2), p.167-169
Main Authors: Al Rwahnih, M. (Bari Univ. (Italy). Dipartimento di Protezione delle Piante e Microbiologia Applicata), Myrta, A. (Istituto Agronomico Mediterraneo, Valenzano, Bari (Italy)), Herranz, M.C., Pallás, V. (Universidad Politecnica de Valencia (Spain). Inst. de Biologia Molecular y Cellular de Plantas)
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creator Al Rwahnih, M. (Bari Univ. (Italy). Dipartimento di Protezione delle Piante e Microbiologia Applicata)
Myrta, A. (Istituto Agronomico Mediterraneo, Valenzano, Bari (Italy))
Herranz, M.C.
Pallás, V. (Universidad Politecnica de Valencia (Spain). Inst. de Biologia Molecular y Cellular de Plantas)
description American plum line pattern virus (APLPV) was monitored monthly throughout a year in a Japanese plum tree by using ELISA and dot-blot hybridisation. Leaf samples were tested from March to November and dormant buds were tested from December to February. Flowers, cortex and fruits, when available, were also tested. For leaf samples, detection by ELISA and hybridisation was reliable from March to May. For dormant bud samples, detection was reliable from December to February. Detection levels decreased from June to August and were unsatisfactory from September to November. During this latter period, molecular hybridisation was more sensitive than ELISA. Leaves were better sources of APLPV than flowers and cortical tissues in Spring, whereas mature fruits were better sources than leaves in Summer [L'American plum line pattern virus (APLPV) è stato monitorato mensilmente, nel corso di un anno, in una pianta di susino giapponese utilizzando l'ELISA e l'ibridazione dot-blot. I campioni di foglie sono stati saggiati da marzo a novembre e le gemme dormienti da dicembre a febbraio. Sono stati pure studiati i fiori, la corteccia e i frutti, quando disponibili. Per quanto riguarda i campioni di foglie, l'individuazione tramite ELISA e ibridazione risultava attendibile da marzo a maggio. Per le gemme dormienti, l'individuazione era attendibile da dicembre a febbraio. I livelli di individuazione si riducevano da giugno ad agosto e risultavano insoddisfacenti da settembre a novembre. Nel corso di quest'ultimo periodo, l'ibridazione molecolare è risultata più sensibile rispetto all'ELISA. Le foglie costituivano una fonte migliore di APLPV rispetto ai fiori e ai tessuti corticali in primavera, mentre i frutti maturi costituivano una fonte migliore rispetto alle foglie in estate]
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(Bari Univ. (Italy). Dipartimento di Protezione delle Piante e Microbiologia Applicata); Myrta, A. (Istituto Agronomico Mediterraneo, Valenzano, Bari (Italy)); Herranz, M.C.; Pallás, V. (Universidad Politecnica de Valencia (Spain). Inst. de Biologia Molecular y Cellular de Plantas)</creator><creatorcontrib>Al Rwahnih, M. (Bari Univ. (Italy). Dipartimento di Protezione delle Piante e Microbiologia Applicata); Myrta, A. (Istituto Agronomico Mediterraneo, Valenzano, Bari (Italy)); Herranz, M.C.; Pallás, V. (Universidad Politecnica de Valencia (Spain). Inst. de Biologia Molecular y Cellular de Plantas)</creatorcontrib><description>American plum line pattern virus (APLPV) was monitored monthly throughout a year in a Japanese plum tree by using ELISA and dot-blot hybridisation. Leaf samples were tested from March to November and dormant buds were tested from December to February. Flowers, cortex and fruits, when available, were also tested. For leaf samples, detection by ELISA and hybridisation was reliable from March to May. For dormant bud samples, detection was reliable from December to February. Detection levels decreased from June to August and were unsatisfactory from September to November. During this latter period, molecular hybridisation was more sensitive than ELISA. Leaves were better sources of APLPV than flowers and cortical tissues in Spring, whereas mature fruits were better sources than leaves in Summer [L'American plum line pattern virus (APLPV) è stato monitorato mensilmente, nel corso di un anno, in una pianta di susino giapponese utilizzando l'ELISA e l'ibridazione dot-blot. I campioni di foglie sono stati saggiati da marzo a novembre e le gemme dormienti da dicembre a febbraio. Sono stati pure studiati i fiori, la corteccia e i frutti, quando disponibili. Per quanto riguarda i campioni di foglie, l'individuazione tramite ELISA e ibridazione risultava attendibile da marzo a maggio. Per le gemme dormienti, l'individuazione era attendibile da dicembre a febbraio. I livelli di individuazione si riducevano da giugno ad agosto e risultavano insoddisfacenti da settembre a novembre. Nel corso di quest'ultimo periodo, l'ibridazione molecolare è risultata più sensibile rispetto all'ELISA. 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(Bari Univ. (Italy). Dipartimento di Protezione delle Piante e Microbiologia Applicata); Myrta, A. (Istituto Agronomico Mediterraneo, Valenzano, Bari (Italy)); Herranz, M.C.; Pallás, V. (Universidad Politecnica de Valencia (Spain). Inst. de Biologia Molecular y Cellular de Plantas)</creatorcontrib><title>Monitoring American plum line pattern virus in plum by ELISA and dot-blot hybridisation throughout the year [Prunus salicina Lindl.; Apulia; Enzyme-linked Immunosorbent Assay]</title><title>Journal of plant pathology</title><description>American plum line pattern virus (APLPV) was monitored monthly throughout a year in a Japanese plum tree by using ELISA and dot-blot hybridisation. Leaf samples were tested from March to November and dormant buds were tested from December to February. Flowers, cortex and fruits, when available, were also tested. For leaf samples, detection by ELISA and hybridisation was reliable from March to May. For dormant bud samples, detection was reliable from December to February. Detection levels decreased from June to August and were unsatisfactory from September to November. During this latter period, molecular hybridisation was more sensitive than ELISA. Leaves were better sources of APLPV than flowers and cortical tissues in Spring, whereas mature fruits were better sources than leaves in Summer [L'American plum line pattern virus (APLPV) è stato monitorato mensilmente, nel corso di un anno, in una pianta di susino giapponese utilizzando l'ELISA e l'ibridazione dot-blot. I campioni di foglie sono stati saggiati da marzo a novembre e le gemme dormienti da dicembre a febbraio. Sono stati pure studiati i fiori, la corteccia e i frutti, quando disponibili. Per quanto riguarda i campioni di foglie, l'individuazione tramite ELISA e ibridazione risultava attendibile da marzo a maggio. Per le gemme dormienti, l'individuazione era attendibile da dicembre a febbraio. I livelli di individuazione si riducevano da giugno ad agosto e risultavano insoddisfacenti da settembre a novembre. Nel corso di quest'ultimo periodo, l'ibridazione molecolare è risultata più sensibile rispetto all'ELISA. Le foglie costituivano una fonte migliore di APLPV rispetto ai fiori e ai tessuti corticali in primavera, mentre i frutti maturi costituivano una fonte migliore rispetto alle foglie in estate]</description><subject>American plum line pattern virus</subject><subject>apulia</subject><subject>bark</subject><subject>BOURGEON</subject><subject>buds</subject><subject>campionamento</subject><subject>corteccia</subject><subject>CORTEZA</subject><subject>Drupes</subject><subject>ECHANTILLONNAGE</subject><subject>ECORCE</subject><subject>elisa</subject><subject>ENFERMEDADES DE LAS PLANTAS</subject><subject>Enzyme linked immunosorbent assay</subject><subject>FEUILLE</subject><subject>fiori</subject><subject>FLEUR</subject><subject>FLORES</subject><subject>Flower buds</subject><subject>flowers</subject><subject>foglie</subject><subject>fruit</subject><subject>FRUTO</subject><subject>frutto</subject><subject>gemme</subject><subject>HIBRIDACION MOLECULAR</subject><subject>HOJAS</subject><subject>Horticulture</subject><subject>HYBRIDATION MOLECULAIRE</subject><subject>ibridazione molecolare</subject><subject>IDENTIFICACION</subject><subject>identification</subject><subject>identificazione</subject><subject>ilarvirus</subject><subject>ilarviruses</subject><subject>Leaf buds</subject><subject>Leaves</subject><subject>MALADIE DES PLANTES</subject><subject>malattie delle piante</subject><subject>molecular hybridization</subject><subject>MUESTREO</subject><subject>Phytopathology</subject><subject>plant diseases</subject><subject>POUILLES</subject><subject>prunus salicina</subject><subject>puglia</subject><subject>sampling</subject><subject>Short Communication</subject><subject>TEST ELISA</subject><subject>Tissue samples</subject><subject>Viroids</subject><subject>Viruses</subject><subject>YEMA (PLANTA)</subject><issn>1125-4653</issn><issn>2239-7264</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNpFkN1q20AUhEVJoI7bRyicq9wp7K5-VsJXwriNwaWFOlehiCPtyl53tavsT0B9qb5iBQ7kagbmYwbmQ7JiLKtTzsr8JllRyoo0L4vsY3Ln_YWQvOCkXCX_vlujgnXKnKAZpVM9Gph0HEErI2HCEKQz8Kpc9KDeom6G3WH_qwE0AoQNaadtgPPcOSWUx6CsgXB2Np7ONobFSpglOnj-6aJZejxq1SuDcFBG6IcNNFPUCjewM3_nUabL9B8pYD-O0VhvXSdNgMZ7nH9_Sm4H1F5-ftN18vR1d9w-pocf3_bb5pAOjFUhFVwyIfO6oFVWZjkpOGW0JgMdkBa8lJR2GWXIeNd3KLKqkrzsKaGc8HooOpGtk_tr7-TsS5Q-tKPyvdQajbTRt5TzhV7-XCdfruDFLze2k1MjurnNaV1XtOLv-YC2xZNTvt0fGSFFSQjhNPsPh6GCMw</recordid><startdate>200407</startdate><enddate>200407</enddate><creator>Al Rwahnih, M. 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(Bari Univ. (Italy). Dipartimento di Protezione delle Piante e Microbiologia Applicata); Myrta, A. (Istituto Agronomico Mediterraneo, Valenzano, Bari (Italy)); Herranz, M.C.; Pallás, V. (Universidad Politecnica de Valencia (Spain). Inst. de Biologia Molecular y Cellular de Plantas)</creatorcontrib><collection>AGRIS</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Journal of plant pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Al Rwahnih, M. (Bari Univ. (Italy). Dipartimento di Protezione delle Piante e Microbiologia Applicata); Myrta, A. (Istituto Agronomico Mediterraneo, Valenzano, Bari (Italy)); Herranz, M.C.; Pallás, V. (Universidad Politecnica de Valencia (Spain). Inst. de Biologia Molecular y Cellular de Plantas)</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Monitoring American plum line pattern virus in plum by ELISA and dot-blot hybridisation throughout the year [Prunus salicina Lindl.; Apulia; Enzyme-linked Immunosorbent Assay]</atitle><jtitle>Journal of plant pathology</jtitle><date>2004-07</date><risdate>2004</risdate><volume>86</volume><issue>2</issue><spage>167</spage><epage>169</epage><pages>167-169</pages><issn>1125-4653</issn><eissn>2239-7264</eissn><abstract>American plum line pattern virus (APLPV) was monitored monthly throughout a year in a Japanese plum tree by using ELISA and dot-blot hybridisation. Leaf samples were tested from March to November and dormant buds were tested from December to February. Flowers, cortex and fruits, when available, were also tested. For leaf samples, detection by ELISA and hybridisation was reliable from March to May. For dormant bud samples, detection was reliable from December to February. Detection levels decreased from June to August and were unsatisfactory from September to November. During this latter period, molecular hybridisation was more sensitive than ELISA. Leaves were better sources of APLPV than flowers and cortical tissues in Spring, whereas mature fruits were better sources than leaves in Summer [L'American plum line pattern virus (APLPV) è stato monitorato mensilmente, nel corso di un anno, in una pianta di susino giapponese utilizzando l'ELISA e l'ibridazione dot-blot. I campioni di foglie sono stati saggiati da marzo a novembre e le gemme dormienti da dicembre a febbraio. Sono stati pure studiati i fiori, la corteccia e i frutti, quando disponibili. Per quanto riguarda i campioni di foglie, l'individuazione tramite ELISA e ibridazione risultava attendibile da marzo a maggio. Per le gemme dormienti, l'individuazione era attendibile da dicembre a febbraio. I livelli di individuazione si riducevano da giugno ad agosto e risultavano insoddisfacenti da settembre a novembre. Nel corso di quest'ultimo periodo, l'ibridazione molecolare è risultata più sensibile rispetto all'ELISA. Le foglie costituivano una fonte migliore di APLPV rispetto ai fiori e ai tessuti corticali in primavera, mentre i frutti maturi costituivano una fonte migliore rispetto alle foglie in estate]</abstract><pub>An International Journal of the Italian Phytopathological Society</pub><tpages>3</tpages></addata></record>
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subjects American plum line pattern virus
apulia
bark
BOURGEON
buds
campionamento
corteccia
CORTEZA
Drupes
ECHANTILLONNAGE
ECORCE
elisa
ENFERMEDADES DE LAS PLANTAS
Enzyme linked immunosorbent assay
FEUILLE
fiori
FLEUR
FLORES
Flower buds
flowers
foglie
fruit
FRUTO
frutto
gemme
HIBRIDACION MOLECULAR
HOJAS
Horticulture
HYBRIDATION MOLECULAIRE
ibridazione molecolare
IDENTIFICACION
identification
identificazione
ilarvirus
ilarviruses
Leaf buds
Leaves
MALADIE DES PLANTES
malattie delle piante
molecular hybridization
MUESTREO
Phytopathology
plant diseases
POUILLES
prunus salicina
puglia
sampling
Short Communication
TEST ELISA
Tissue samples
Viroids
Viruses
YEMA (PLANTA)
title Monitoring American plum line pattern virus in plum by ELISA and dot-blot hybridisation throughout the year [Prunus salicina Lindl.; Apulia; Enzyme-linked Immunosorbent Assay]
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