New Disease Reports (2012) 26, 13. [http://dx.doi.org/10.5197/j.2044-0588.2012.026.013]
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First record of Ceratocystis fimbriata on Carapa guianensis

B.A. Halfeld-Vieira 1*, J.E. Zilli 2, K.L. Nechet 1, G.M.D. Pereira 3 and G.R. Souza 4

*halfeld@cnpma.embrapa.br

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Received: 04 May 2012; Published: 19 Sep 2012

Keywords: crabwood, forest pathology

Crabwood or andiroba (Carapa guianensis) is a medium to large tree belonging to the family Meliaceae, widespread in tropical South America, used for timber, furniture, and oil from seeds for cosmetic and ethnomedicinal purposes. Despite its economic importance only one disease caused by Pestalotiopsis macrochaeta has been reported (Halfeld-Vieira & Nechet, 2006). In August 2008, during the course of surveys in a native forest in São João da Baliza municipality in Roraima state, Brazil, dying seedlings of C. guianensis were observed with symptoms of a fungal infection on stems (Fig. 1) and petioles.

Only one fungus species was isolated from perithecia present in infected tissue, forming olive brown cultures on potato dextrose agar (PDA). The following morphological features were observed. Perithecia were dark brown, globose, 112-200 μm, neck erect, 431-680 μm, with divergent ostiolar hyphae (Fig. 2A, 2B); perithecial width at the base was 27-34 μm and 20 μm at the apex. Acospores were “hat” shaped, hyaline, 5-7 x 4-5 μm (Fig. 2C). The anamorph corresponded to Chalara with hyaline, cylindrical, catenulate endoconidia with truncate ends, 10-20 x 3.7-5 µm; chlamydospores were pale to dark brown, ovoid, thick-walled, 10-15 x 10-12 µm (Fig. 2D). Based on these morphological characteristics the fungus was identified as Ceratocystis fimbriata (Wingfield et al., 1993). To confirm the identity of the pathogen, the internal transcribed spacer (ITS) region of a representative isolate was amplified using ITS 1 and ITS 4 universal primers and sequenced (GenBank Accession No. JN051277). Ribosomal DNA-ITS sequence data were found to have up to 98% identity with C. fimbriata. To fulfil Koch’s postulates, pathogenicity tests were performed in a greenhouse on two-month-old C. guianensis seedlings. Stems were wounded with one superficial puncture with a needle tip, a mycelium plug inserted and the wound covered with Parafilm. A PDA disk was used as control and each treatment consisted of six plants kept under greenhouse conditions. Seven days later the Parafilm was removed and the progress of the symptoms was evaluated. After 10 days, the pathogen was re-isolated from the stem lesions only on plants inoculated with mycelium plugs, presenting symptoms and signs similar to those occurring in the original infection. The culture of C. fimbriata was deposited in the fungal collection of Embrapa Roraima, a unit of the Brazilian Agricultural Research Corporation (access number CPAFRR515).

Ceratocystis fimbriata is a native soilborne pathogen in some parts of Brazil and causes mortality in many economically important plants. In recent years, significant damage on Eucalyptus and Tectona grandis (teak) by this pathogen has been reported (Ferreira et al., 2010; Firmino et al., 2012). These exotic species are commonly planted in agroforestry systems with C. guianensis in Brazil. The high number of seedlings of C. guianensis affected by this pathogen observed in the field indicates its potential to have a significant impact on natural populations of this host and to be a threat to this species in agroforestry systems.

 

Figure1+
Figure 1: Seedling of Carapa guianensis showing symptoms of infection with Ceratocystis fimbriata.
Figure 1: Seedling of Carapa guianensis showing symptoms of infection with Ceratocystis fimbriata.
Figure2+
Figure 2: Ceratocystis fimbriata perithecia in diseased tissue (A), perithecium in detail (B), “hat” shaped ascospores (C), chlamydospores, conidiophore and conidia of the anamorphic state (D). Bar=30 μm.
Figure 2: Ceratocystis fimbriata perithecia in diseased tissue (A), perithecium in detail (B), “hat” shaped ascospores (C), chlamydospores, conidiophore and conidia of the anamorphic state (D). Bar=30 μm.

References

  1. Ferreira EM, Harrington TC, Thorpe DJ, Alfenas AC, 2010. Genetic diversity and interfertility among highly differentiated populations of Ceratocystis fimbriata in Brazil. Plant Pathology 59, 721-735. [http://dx.doi.org/10.1111/j.1365-3059.2010.02275.x ]
  2. Firmino AC, Tozze Jr HJ, Furtado EL, 2012. First report of Ceratocystis fimbriata causing wilt in Tectona grandis in Brazil. New Disease Reports [http://ndrs.org.uk] 25, 24. [http://dx.doi.org/10.5197/j.2044-0588.2012.025.024]
  3. Halfeld-Vieira BA, Nechet KL, 2006. First report of Pestalotiopsis macrochaeta on Carapa guianensis. Plant Pathology 55, 304. [http://dx.doi.org/10.1111/j.1365-3059.2005.01274.x ]
  4. Wingfield MJ, Seifert KA, Webber, JF, eds, 1993. Ceratocystis and Ophiostoma: taxonomy, ecology, and pathogenicity. St. Paul, MN, USA: The American Phytopathological Society.

To cite this report: Halfeld-Vieira BA, Zilli JE, Nechet KL, Pereira GMD, Souza GR, 2012. First record of Ceratocystis fimbriata on Carapa guianensis. New Disease Reports 26, 13. [http://dx.doi.org/10.5197/j.2044-0588.2012.026.013]

©2012 The Authors