New Disease Reports (2010) 22, 28. [http://dx.doi.org/10.5197/j.2044-0588.2010.022.028]
Get pdf (413 KB)

First report of Alternaria tomatophila and A. grandis causing early blight on tomato and potato in Brazil

T.T.M.S. Rodrigues 1, M.L. Berbee 2, E.G. Simmons 3, C.R. Cardoso 1, A. Reis 4, L.A. Maffia 1 and E.S.G. Mizubuti 1*

*mizubuti@ufv.br

Show affiliations

Received: 04 May 2010; Published: 01 Nov 2010

Keywords: Alternaria solani, etiology, phylogeny

Strong population subdivision according to the host was revealed in a study designed to assess the genetic variability of Alternaria solani on potato (Solanum tuberosum) and tomato (S. lycopersicum) in Brazil (Lourenço Jr. et al., 2009).We hypothesised that more than one species cause early blight disease on these hosts. We analysed 19 isolates obtained from potato and nine from tomato, sampled from 2005 to 2008 from seven geographic regions. Ex-type and authentic isolates of A. tomatophila (EGS 42-156), A. grandis (EGS 44-106 and 44-108), and a representative isolate of A. solani (EGS 44-098) were used for comparison (Simmons, 2000). Based on morphological characteristics all isolates from tomato were identified as A. tomatophila and those from potato as A. grandis (Simmons, 2007) (Fig. 1; Table 1).A. solani was not detected in the samples. A preliminary report has been previously published (Rodrigues & Mizubuti, 2009).

The pathogenicity of three isolates from tomato and five from potato were tested on susceptible plants in cross inoculation assays. Two drops of a 104conidia/ml suspension were placed on five leaflets in each plant (six plants/isolate). The lesion diameter (mm) was determined using a digital caliper and the formula of the area of a circle was used to estimate the lesion area (LA) four days after inoculation. On potato, the mean LA for A. grandis was 464.1 (SD = 53.0) compared to 345.9 (SD = 48.0) for A. tomatophila. On tomato, the mean LA for A. tomatophila was 64.9 (SD = 5.2) compared to 33.8 (SD = 8.1) for A. grandis. Although larger lesions were formed when A. grandis and A. tomatophila were inoculated on their host of origin, there was no statistical difference between species on a particular host. The isolates were recovered from the lesions to fulfil Koch's Postulates. Additionally, reconstruction of the phylogeny was used to investigate the relationships among the species. The major allergen Alt a1 and glyceraldehyde-3-phosphate (Gpd) genes data set were analysed. The Brazilian isolates from tomato clustered with the ex-type A. tomatophila isolate with strong support from parsimony (MP) and neighbour-joining (NJ) analyses. The A. grandis population clustered most closely with the ex-type isolate of A. grandis in a clade also including A. solani (Fig. 2). Alternaria tomatophila has been recorded to cause early blight on tomato in the United States, Australia, New Zealand, and Venezuela (Simmons, 2000).In Brazil, A. solani has been reported as the causal agent of early blight (Lourenço Jr. et al., 2009). We report here that at least two additional species are widely distributed on tomato and potato fields in Brazil.

Figure1+
Figure 1: Conidia of Alternaria spp.; (A) Alternaria grandis (isolate AS220 – Brazil); (B) A. grandis (isolate EGS 44-106); (C) A. solani (isolate EGS 44-098); (D) A. tomatophila (isolate AS109 - Brazil) (Bars = 20 µm).
Figure 1: Conidia of Alternaria spp.; (A) Alternaria grandis (isolate AS220 – Brazil); (B) A. grandis (isolate EGS 44-106); (C) A. solani (isolate EGS 44-098); (D) A. tomatophila (isolate AS109 - Brazil) (Bars = 20 µm).
Figure2+
Figure 2: Maximum parsimony tree based on the Alt a1/Gpd sequences set. Numbers between slashes indicate bootstrap value in MP and NJ analysis. The topology was rooted with A. alternata. Sequences for ex-type and representative isolates were generated in this study and are marked with * or **, respectively [GenBank Accession Nos.: GQ180093/GQ180077 (EGS 44-106); GQ180096/ GQ180080 (EGS 44-098); GQ180099/GQ180083 (EGS 46-178); GQ180097/GQ180081 (EGS 45-020); GQ180098/GQ180082 (EGS 45-053); and GQ180101/GQ180085 (EGS 42-156)].
Figure 2: Maximum parsimony tree based on the Alt a1/Gpd sequences set. Numbers between slashes indicate bootstrap value in MP and NJ analysis. The topology was rooted with A. alternata. Sequences for ex-type and representative isolates were generated in this study and are marked with * or **, respectively [GenBank Accession Nos.: GQ180093/GQ180077 (EGS 44-106); GQ180096/ GQ180080 (EGS 44-098); GQ180099/GQ180083 (EGS 46-178); GQ180097/GQ180081 (EGS 45-020); GQ180098/GQ180082 (EGS 45-053); and GQ180101/GQ180085 (EGS 42-156)].
Figure3+

Acknowledgements

Research was partially funded by CAPES, FAPEMIG and Canada's NSERC.


References

  1. Lourenço Jr. V, Moya A, González-Candelas F, Carbone I, Maffia LA, Mizubuti ESG, 2009. Molecular diversity and evolutionary processes of Alternaria solani in Brazil inferred using genealogical and coalescent approaches. Phytopathology 99, 765-774. [http://dx.doi.org/10.1094/PHYTO-99-6-0765]
  2. Rodrigues TTMS, Mizubuti ESG, 2009. Pinta preta: surge uma nova espécie. Revista Batata Show 24, 14-16.
  3. Simmons EG, 2000. Alternaria themes and variations (244-286) species on Solanaceae.Mycotaxon 75, 1-115.
  4. Simmons EG, 2007. Alternaria: An Identification Manual. Utrecht, Netherlands: CBS Fungal Biodiversity Centre.

To cite this report: Rodrigues TTMS, Berbee ML, Simmons EG, Cardoso CR, Reis A, Maffia LA, Mizubuti ESG, 2010. First report of Alternaria tomatophila and A. grandis causing early blight on tomato and potato in Brazil. New Disease Reports 22, 28. [http://dx.doi.org/10.5197/j.2044-0588.2010.022.028]

©2010 The Authors