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1.
Proc Biol Sci ; 272(1580): 2499-503, 2005 Dec 07.
Artigo em Inglês | MEDLINE | ID: mdl-16271975

RESUMO

Dutch elm disease is caused by the fungal pathogen Ophiostoma novo-ulmi which is transmitted by the native elm bark beetle, Hylurgopinus rufipes. We have found that four semiochemicals (the monoterpene (-)-beta-pinene and the sesquiterpenes (-)-alpha-cubebene, (+)-spiroaxa-5,7-diene and (+)-delta-cadinene) from diseased American elms, Ulmus americana, synergistically attract H. rufipes, and that sesquiterpene emission is upregulated in elm trees inoculated with O. novo-ulmi. The fungus thus manipulates host trees to enhance their apparency to foraging beetles, a strategy that increases the probability of transportation of the pathogen to new hosts.


Assuntos
Ascomicetos , Compostos Bicíclicos com Pontes/metabolismo , Fatores Quimiotáticos/metabolismo , Besouros/fisiologia , Insetos Vetores/fisiologia , Monoterpenos/metabolismo , Doenças das Plantas/microbiologia , Sesquiterpenos/metabolismo , Ulmus/metabolismo , Animais , Monoterpenos Bicíclicos , Cromatografia Gasosa , Besouros/microbiologia , Insetos Vetores/microbiologia , Ulmus/microbiologia
2.
Mycol Res ; 107(Pt 5): 528-36, 2003 May.
Artigo em Inglês | MEDLINE | ID: mdl-12884949

RESUMO

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 beta-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.


Assuntos
Ascomicetos/classificação , Malus/microbiologia , Doenças das Plantas/microbiologia , Reação em Cadeia da Polimerase/métodos , Ascomicetos/genética , Primers do DNA , DNA Fúngico/análise , DNA Fúngico/isolamento & purificação , Técnicas de Tipagem Micológica , Técnicas de Amplificação de Ácido Nucleico , Especificidade da Espécie , Árvores/microbiologia
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