November
2003
, Volume
87
, Number
11
Pages
1,317
-
1,321
Authors
Eliane Cristina
Locali
,
Centro APTA Citros ‘Sylvio Moreira’/IAC, Rod. Anhanguera Km 158, CP 4, 13490-970, Cordeirópolis-SP, Brazil
;
Juliana
Freitas-Astua
and
Alessandra Alves
de Souza
,
Centro APTA Citros ‘Sylvio Moreira’/IAC, Rod. Anhanguera Km 158, CP 4, 13490-970, Cordeirópolis-SP, Brazil, and Empresa Brasileira de Pesquisa Agropecuária
;
Marco Aurélio
Takita
,
Gustavo
Astua-Monge
, and
Renata
Antonioli
,
Centro APTA Citros ‘Sylvio Moreira’/IAC, Rod. Anhanguera Km 158, CP 4, 13490-970, Cordeirópolis-SP, Brazil
;
Elliot W.
Kitajima
,
Depto. Entomol., Fitopatol. & Zool. Agríc., Escola Superior de Agricultura ‘Luiz de Queiroz’, Universidade de São Paulo, CP 9, 13418-900, Piracicaba, SP, Brazil
; and
Marcos Antonio
Machado
,
Centro APTA Citros ‘Sylvio Moreira’/IAC, Rod. Anhanguera Km 158, CP 4, 13490-970, Cordeirópolis-SP, Brazil
Affiliations
Go to article:
RelatedArticle
Accepted for publication 30 May 2003.
Abstract
ABSTRACT
Citrus leprosis virus (CiLV), a tentative member of the Rhabdoviridae family, affects citrus trees in Brazil, where it is transmitted by mites Brevipalpus spp. It also occurs in other South American countries and was recently identified in Central America. This northbound spread of CiLV is being considered a serious threat to the citrus industry of the United States. However, despite its importance, difficulties related to the biology of CiLV have hindered much of the progress regarding its accurate detection, leaving both the analyses of symptoms and electron microscopy as the only tools available. An attempt to overcome this problem was made by constructing a cDNA library from double-stranded RNA extracted from leprosis lesions of infected Citrus sinensis (sweet orange) leaves. After cloning and sequencing, specific primers were designed to amplify putative CiLV genome regions with similarity to genes encoding the movement protein and replicase of other plant viruses. RNA from infected citrus plants corresponding to different varieties and locations were amplified by reverse transcription-polymerase chain reaction (RT-PCR) using the two pairs of primers. Amplified products were purified, cloned in pGEM-T, and sequenced. The sequences confirmed the genomic regions previously associated with CiLV. The results demonstrate that RT-PCR was specific, accurate, rapid, and reliable for the detection of CiLV.
JnArticleKeywords
Additional keywords:
Brevipalpus sp.,
citrus diseases,
Citrus leprosis virus,
RT-PCR
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ArticleCopyright
© 2003 The American Phytopathological Society