Evaluación del proceso de infección por Lecanicillium fungicola en Agaricus bisporus por microscopia electrónica de barrido

Background Lecanicillium fungicola causes dry bubble disease in Agaricus bisporus mushrooms leading to significant economic losses in commercial production. Aims To monitor the infection process of L. fungicola in Brazilian strains of A. bisporus. Methods The interaction between the mycelium of L. f...

ver descrição completa

Detalhes bibliográficos
Autores: Santana Nunes, Janaira, Rocha de Brito, Manuela, Cunha Zied, Diego [UNESP], Aparecida das Graças Leite, Eloisa, Souza Dias, Eustáquio, Alves, Eduardo
Formato: artículo
Estado:Versión publicada
Fecha de publicación:2017
País:Brasil
Recursos:Universidade Estadual Paulista (UNESP)
Repositorio:Repositório Institucional da UNESP
Idioma:inglés
español
OAI Identifier:oai:repositorio.unesp.br:11449/178614
Acesso em linha:http://dx.doi.org/10.1016/j.riam.2016.04.006
http://hdl.handle.net/11449/178614
Access Level:acceso abierto
Palavra-chave:Mushroom
Mycopathogen
Scanning electron microscopy
X-ray microanalyses
Descrição
Resumo:Background Lecanicillium fungicola causes dry bubble disease in Agaricus bisporus mushrooms leading to significant economic losses in commercial production. Aims To monitor the infection process of L. fungicola in Brazilian strains of A. bisporus. Methods The interaction between the mycelium of L. fungicola (LF.1) and three strains of A. bisporus (ABI 7, ABI 11/14 and ABI 11/21) was studied. Electron microscopy and X-ray microanalyses of vegetative growth and basidiocarp infection were evaluated. Results Micrographs show that the vegetative mycelium of the Brazilian strains of A. bisporus is not infected by the parasite. The images show that the pathogen can interlace the hyphae of A. bisporus without causing damage, which contributes to the presence of L. fungicola during the substrate colonization, allowing their presence during primordial formation of A. bisporus. In the basidiocarp, germ tubes form within 16 h of infection with L. fungicola and the beginning of penetration takes place within 18 h, both without the formation of specialized structures. Conclusions Scanning electron microscopy enabled the process of colonization and reproduction to be observed within the formation of phialides, conidiophores and verticils of L. fungicola. The formation of calcium oxalate crystals by the pathogen was also visible using the X-ray microanalysis, both at the hyphae in the Petri plate and at basidiocarp infection site.