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First Report of Orchid fleck virus in Costa Rica

December 2002 , Volume 86 , Number  12
Pages  1,402.4 - 1,402.4

Juliana Freitas-Astúa , Empresa Brasileira de Pesquisa Agropecuária/Centro Apta Citros ‘Sylvio Moreira’, CP 4, 13490-970, Cordeirópolis, SP, Brazil ; Lisela Moreira and Carmen Rivera , Centro de Investigación en Biología Celular y Molecular, Universidad de Costa Rica, San José, Costa Rica ; Carlos M. Rodríguez , Instituto del Café, Apartado 131-30009, San José, Costa Rica ; and Elliot W. Kitajima , Departamento de Entomologia, Fitopatologica e Zoologia Agrícola, Escola Superior de Agricultura ‘Luiz de Queiroz’, Universidade de São Paulo, CP 9, 13418-900, Piracicaba, SP, Brazil



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Accepted for publication 5 September 2002.

Orchid fleck virus (OFV), a tentative member of the family Rhabdoviridae, infects orchids in several countries. The virus is vectored worldwide by the mite Brevipalpus californicus (Banks) (Acari: Tenuipalpidae). Eleven plants of Oncidium spp. and one plant each of the genera Cymbidium and Maxillaria exhibiting numerous yellow flecks and necrotic ringspot lesions on leaves were collected in two private orchid collections in Costa Rica. Presence of OFV was assessed by plate-trapped antigen enzyme-linked immunosorbent assay (PTA-ELISA) using an antiserum developed against an OFV isolate in Japan (2), analyses of ultrathin sections of the host cell with transmission electron microscopy (TEM), and reverse transcription-polymerase chain reaction (RT-PCR) amplification using specific primers for the viral nucleocapsid gene (1). Eight of eleven Oncidium samples, and both Cymbidium and Maxillaria samples tested positive for OFV with PTA-ELISA having A405 values ranging from 3.9 to 14.6 times higher than negative controls. Thin sections from individual samples of Cymbidium, Oncidium, and Maxillaria revealed electron-lucent intranuclear viroplasm and short, rodlike particles (40 to 50 × 100 nm) in the nucleus or cytoplasm typical of OFV-infected cells. RT-PCR amplifications from one sample of each genera resulted in PCR-product bands of approximately 800 bp. The Cymbidium RT-PCR product was cloned into a pGEM-T-Easy expression vector and sequenced using an ABI 3700 sequencer. The 619-bp nucleocapsid gene consensus sequence had 98% homology with the OFV isolate 0023 identified in Germany (GenBank Accession No. AF343870) (1). However, it had only approximately 85% nucleocapsid gene homology with other OFV isolates available through GenBank, including those from countries geographically closer to Costa Rica, such as Brazil (1). To our knowledge, this is the first report of OFV infecting orchids in Costa Rica.

References: (1) A. L. Blanchfield et al. J. Phytopathol. 149:713, 2001. (2) H. Kondo et al. Bull. Res. Inst. Bioresour. Okayama Univ. 4:149, 1996.



© 2002 The American Phytopathological Society