New Disease Reports (2009) 19, 33.

Flavescence dorée phytoplasma affecting grapevine(Vitis vinifera) newly reported in Portugal

E. de Sousa 1*, P. Casati 2, F. Cardoso 3, C. Baltazar 4, G. Durante 2, F. Quaglino 2 and P.A. Bianco 2

*esmeraldinasousa@dgpc.min-agricultura.pt

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Accepted: 28 Apr 2009

In 2007, during an official Flavescence dorée (FD) survey, typical FD symptoms, associated with desiccation of inflorescences, withering of clusters, irregular maturation of the wood, leaf rolling, typical vein banding, leaf yellowing on white grapevine variety Loureiro (Fig.1A) and leaf reddening on red variety Vinhão (Fig.1B), were observed in vineyards from Amares region in northern Portugal. In 2002, similar but less severe symptoms occurring in the same region were associated with 16SrI phytoplasmas (‘Candidatus Phytoplasma asteris’), subgroup 16SrI-B (De Sousa et al., 2003). Cuttings and leaf samples were collected from plants with and without symptoms. Total DNA was extracted (Angelini et al., 2001) and assayed in a nested polymerase chain reaction (PCR) using primers P1/P7 (Deng & Hiruki, 1991) followed by either R16F2n/R16R2 (F2n/R2) (Gundersen & Lee, 1996) or R16F1(V)/R16V1731r (F1/V1) (Martini et al., 1999). Phytoplasma strains from group 16SrV (‘Ca. Phytoplasma ulmi’), elm yellows (EY1) and rubus stunt (RUS), were used as reference controls. Healthy C. roseus and no template DNA were used as negative controls. All plants with symptoms and reference controls showed PCR products (F2n/R2 and F1/V1), absent from samples from symptomless plants. Two representative F2n/R2 amplicons, were cloned, sequenced and deposited in GenBank (FJ611961 and FJ611962). The phytoplasma 16S rRNA sequences were identical and shared 99-100% identity with those of group 16SrV. FD phytoplasmas from Portugal exhibited the characteristic FD-D TaqI RFLP pattern (Fig.2). To our knowledge, this is the first report of FD-D in grapevine in northern Portugal. Although the current FD outbreak is limited to Amares region, the high pressure of the Scaphoideus titanus vector populations imposes a threat for FD spread, and a current alert for the Ministry of Agriculture (DGADR). The implementation of strategies for effective control of S.titanus and FD have been suggested and included in the Portuguese legislation (Portaria nº 976/2008, 1 September).

Figure1+
Figure 1: FD symptoms on grapevine (A) Loureiro, white variety, and (B) Vinhão, red variety
Figure 1: FD symptoms on grapevine (A) Loureiro, white variety, and (B) Vinhão, red variety
Figure2+
Figure 2: TaqI-RFLP patterns of PCR amplicons primed with 16SrV group-specific primers F1/V1. MW: molecular marker ΦX174 (Invitrogen, Carlsbad, CA, USA); 1-2: Loureiro var; 3-4: Vinhãovar; EY1; RUS.
Figure 2: TaqI-RFLP patterns of PCR amplicons primed with 16SrV group-specific primers F1/V1. MW: molecular marker ΦX174 (Invitrogen, Carlsbad, CA, USA); 1-2: Loureiro var; 3-4: Vinhãovar; EY1; RUS.

Acknowledgements

The authors would like to thank regional technicians (Entre-Douro-e-Minho and Trás-Montes) for supplying grapevine samples.


References

  1. Angelini E, Clair D, Borgo M, Bertaccini A, Boudon-Padieu E, 2001.Flavescence dorée in France and Italy.  Occurrence of closely related phytoplasma isolates and their near relationships to Palatinate grapevine yellows and an alder phytoplasma.Vitis 40, 79-86.
  2. Deng S, Hiruki C, 1991. Amplification of 16S rRNA genes from culturable and non-culturable mollicutes. Journal of Microbiological Methods 25, 53-61.
  3. De Sousa E, Cardoso F, Bianco P, Guimarães M, Pereira V, 2003. Detection and identification of phytoplasmas belonging to 16SrV-D in Scaphoideus titanus adults in Portugal. In: Proceedings 14th Meeting of the International Council for the Study of Virus and Virus-like Diseases of the Grapevine, Locorotondo, Bari, Italy, 78.
  4. Gundersen, D, Lee I-M, 1996. Ultrasensitive detection of phytoplasmas by nested-PCR assays using two universal primer pairs. Phytopathologia Mediterranea 35, 144-151.
  5. Martini M, Murari E, Mori N, Bertaccini A, 1999. Identification and epidemic distribution of two flavescence dorée-related phytoplasmas in Veneto (Italy). Plant Disease 83, 925-930.

This report was formally published in Plant Pathology

©2009 The Authors