Scanning electron microscopy of Ancylostoma spp. dog infective larvae captured and destroyed by the nematophagous fungus Duddingtonia flagrans

• Autor(a) principal: Maciel, A.S.
• Data de Publicação: 2008
• Outros Autores: Araújo, J.V., Campos, A.K., Benjamin, L.A., Freitas, L.G.
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: LOCUS Repositório Institucional da UFV
• Texto Completo: https://doi.org/10.1016/j.micron.2008.12.007; http://www.locus.ufv.br/handle/123456789/19046
• topic: Nematophagous fungus; Duddingtonia flagrans; Ancylostoma spp.Dogs; Biological control

The interaction between the nematode-trapping fungus Duddingtonia flagrans (isolate CG768) against Ancylostoma spp. dog infective larvae (L3) was evaluated by means of scanning electron microscopy. Adhesive network trap formation was observed 6 h after the beginning of the interaction, and the capture of Ancylostoma spp. L3 was observed 8 h after the inoculation these larvae on the cellulose membranes colonized by the fungus. Scanning electron micrographs were taken at 0, 12, 24, 36 and 48 h, where 0 is the time when Ancylostoma spp. L3 was first captured by the fungus. Details of the capture structure formed by the fungus were described. Nematophagous Fungus Helper Bacteria (NHB) were found at interactions points between the D. flagrans and Ancylostoma spp. L3. The cuticle penetration by the differentiated fungal hyphae with the exit of nematode internal contents was observed 36 h after the capture. Ancylostoma spp. L3 were completely destroyed after 48 h of interaction with the fungus. The scanning electron microscopy technique was efficient on the study of this interaction, showing that the nematode-trapping fungus D. flagrans (isolate CG768) is a potential exterminator of Ancylostoma spp. L3.