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Development of a Molecular Tool for the Diagnosis of Leprosis, a Major Threat to Citrus Production in the Americas

November 2003 , Volume 87 , Number  11
Pages  1,317 - 1,321

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



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Accepted for publication 30 May 2003.
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.


Additional keywords: Brevipalpus sp., citrus diseases, Citrus leprosis virus, RT-PCR

© 2003 The American Phytopathological Society