Partial characterization of a bipartite begomovirus infecting yellow passion flower in Brazil

Plant Pathology

Volumn 52, Issue 5, 2003, Pages 648-654

  Novaes, Q S ^a   Freitas Astua, J ^b   Yuki, V A ^c   Kitajima, E W ^a   Camargo, L E A ^a   Rezende, J A M ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

^b EMBRAPA CERRADOS   (Brazil)

^c INSTITUTO AGRONÔMICO   (Brazil)

Author keywords

Diagnosis; Electron microscopy; Indirect DAS ELISA; Passiflora edulis f. flavicarpa; PCR

Indexed keywords

PHYLOGENETICS; SYMPTOM; VIRUS; WHITEFLY;

BRAZIL;

ALEYRODIDAE; BEGOMOVIRUS; BEMISIA TABACI; DIPTERA; HEMIPTERA; PASSIFLORA; PASSIFLORA EDULIS; PASSIFLORA EDULIS F. FLAVICARPA; PASSION FRUIT WOODINESS VIRUS;

EID: 0142027934     PISSN: 00320862     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-3059.2003.00878.x     Document Type: Article

References (17)

1. Abouzid AM, Freitas-Astúa J, Purcifull DE, Polston JE, Beckham KA, Crawford WE, Petersen MA, Peyser B, Patte C, Hiebert E, 2002. Serological studies using polyclonal antisera prepared against the viral coat protein of four begomoviruses expressed in Escherichia coli. Plant Disease 86, 1109-14.
2. Brown JK, Bird J, Fletcher DC, 1993. First report of passiflora leaf mottle disease caused by a whitefly-transmitted geminivirus in Puerto Rico. Plant Disease 77, 1264.
3. Brown JK, Idris AM, Torres-Jerez I, Banks GK, Wyatt SD, 2001. The core region of the coat protein gene is highly useful for establishing the provisional identification and classification of begomoviruses. Archives of Virology 146, 1581-98.
4. Fernandes AV, Galvac̃o RM, Andrade EC, Zerbini FM, Fontes EPB, 1999a. Biological and functional characterization of new Brazilian geminiviruses which infect Lycopersicon esculentum and Sida sp. Anais Da 28a Reunião Anual da Sociedade Brasileira de Bioquímica e Biologia Molecular, 49 (abstract).
5. Fernandes AV, Galvão RM, Machado JS, Zerbini FM, Fontes EPB, 1999b. Cloning and molecular characterization of A components of two new Sida rhombifolia-infecting geminiviruses. Virus Reviews and Research 4 (Suppl.), 148 (abstract).
6. FNP Consultoria & Comércio: Agrianual, 2002. Anuário da Agricultura Brasileira. São Paulo, Brazil: FNP Consultoria & Comércio.
7. Francki RIB, Milne RG, Hatta T, 1985. Atlas of Plant Viruses. Boca Raton, FL, USA: CRC Press.
8. Kitajima EW, Nome C, 1999. Microscopía eletrónica en virología vegetal. In: do Campo D, Lenardon S, eds. Métodos para Detectar Patógenos Sistêmicos. Córdoba, Argentina: IFFYVE/INTA, 59-87.
9. Kitajima EW, Rezende JAM, 2001. Enfermidades de etiologia viral. In: Bruckner CH, Picanço MC, eds. Maracujá: Tecnologia de Produção, Pós-Colheita, Agroindústria, Mercado. Porto Alegre, Brazil: Cinco Continentes, 277-82.
10. Lourenção AL, Yuki VA, Alves SB, 1999. Epizootia de Aschersonia cf. goldiana em Bemisia tabaci (Homoptera: Aleyrodidae) Biótipo B no Estado de Sã;o Paulo. Anais da Sociedade Entomológica do Brasil 28, 343-5.
11. Novaes QS, Rezende JAM, 1999. Possível aplicação do DAS-ELISA indireto na seleção de maracujazeiro tolerante ao Passionfruit woodiness virus. Fitopatologia Brasileira 24, 76-9.
12. Rojas MR, Gilbertson RL, Russel DR, Maxwell DP, 1993. Use of degenerate primers in the polymerase chain reaction to detect whitefly-transmitted geminiviruses. Plant Disease 77, 340-7.
13. Sambrook J, Maniatis T, Frisch EF, 1989. Molecular Cloning: A Laboratory Manual, 2nd edn. Cold Spring Harbor, NY, USA: Cold Spring Harbor Laboratory Press.
14. Souza JSI, Meletti LMM, 1997. Maracujá: Espécies, Variedades, Cultivo. Piracicaba, Brazil: FEALQ.
15. Van Regenmortel MHV, Dubs MC, 1993. Serological procedures. In: Matthews REF, ed. Diagnosis of Plant Virus Diseases. Boca Raton, FL, USA: CRC Press, 159-214.
16. Wyatt SD, Brown JK, 1996. Detection of subgroup II geminivirus isolates in leaf extracts by degenerate primers and polymerase chain reaction. Phytopathology 86, 1288-93.
17. Zhang YP, Uyemoto JK, Kirkpatrick BC, 1998. A small-scale procedure for extracting nucleic acids from woody plants infected with various phytopathogens for PCR assay. Journal of Virological Methods 71, 45-50.