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Species specific identification of the Neofabraea pathogen complex associated with pome fruits using PCR and multiplex DNA amplification

Published online by Cambridge University Press:  24 June 2003

Tara D. GARIÉPY
Affiliation:
Department of Biological Sciences, Simon Fraser University, Burnaby, British Columbia V5A 1S6, Canada. E-mail: [email protected] Present address: Saskatoon Research Centre, Agriculture and Agri-Food Canada, Saskatoon, Saskatchewan S7N 0X2, Canada.
C. André LÉVESQUE
Affiliation:
Eastern Cereal and Oilseed Research Centre, Research Branch, Agriculture and Agri-Food Canada, 960 Carling Avenue, Ottawa, Ontario K1A 0C6, Canada.
Sharon N. de JONG
Affiliation:
Eastern Cereal and Oilseed Research Centre, Research Branch, Agriculture and Agri-Food Canada, 960 Carling Avenue, Ottawa, Ontario K1A 0C6, Canada.
James E. RAHE
Affiliation:
Department of Biological Sciences, Simon Fraser University, Burnaby, British Columbia V5A 1S6, Canada. E-mail: [email protected]
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Abstract

Five species of pathogenic fungi belong to Neofabraea. One of these, N. krawtzewii (syn. N. populi), is responsible for bark lesions on poplar (Populus) trees. The other four species cause post-harvest bull's eye rot of pome fruits, and at least two of these also cause bark cankers on pome fruit trees. Morphological variation among these species is slight, and overlap in geographic range sometimes occurs. As a consequence, identification based on conventional criteria can be tenuous. PCR primers with putative species specificity were developed following genetic analysis of the β-tubulin gene for isolates of each of the five species of Neofabraea. PCR conditions required to achieve specificity of the primer sets were determined, and a multiplex PCR protocol was developed to optimize their diagnostic utility on apple fruits. A protocol with higher annealing temperatures in the initial PCR cycles followed by lower temperatures in later cycles gave complete species-specificity when the primer sets were used individually and in multiplex, resulting in successful detection of the pathogens from axenic culture and infected apple fruits.

Type
Research Article
Copyright
© The British Mycological Society 2003

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