Histopathological characterization of Coffea arabica cultivar IPR 106 resistance to Meloidogyne paranaensis

• Autor(a) principal: Shigueoka, Luciana Harumi
• Data de Publicação: 2019
• Outros Autores: Dorigo, Orazília França, Arita, Lucas Yuuki, Fonseca, Inês Cristina de Batista, Silva, Santino Aleandro da, Sera, Gustavo Hiroshi, Machado, Andressa Cristina Zamboni
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Scientia Agrícola (Online)
• DOI: 10.1590/1678-992x-2018-0002
• Texto Completo: https://www.revistas.usp.br/sa/article/view/160618
• topic: management; root-knot nematodes; giant cells

Meloidogyne species are widely distributed in coffee growing areas in Brazil, where M. paranaensis is responsible to significant losses to the crop. One of the main management strategies is the use of resistant cultivars, such as Apoatã rootstock and cultivars IPR 100 and IPR 106. However, the parasitic relationship between coffee and M. paranaensis in cultivars carrying resistance genes has been poorly understood. The objective of this paper was to characterize the resistance response of Coffea arabica cv. IPR 106 to M. paranaensis. For this, penetration and histopathological studies were carried out using root tissues parasitized by the nematode. ‘IPR 106’ and ‘Mundo Novo’ (susceptible cultivar) seedlings were inoculated with 4,000 eggs of M. paranaensis and, 15 days after inoculation (DAI), roots were stained with fuchsine to verify the penetration rates of the nematode. Histopathological studies were conducted at 15, 30, 45 and 60 DAI and nematode reproduction was calculated at 120 DAI. ‘IPR 106’ did not avoid completely nematode penetration at 15 DAI, although the number of nematodes was 50 % lower than in Mundo Novo, disregarding the hypothesis of a pre-infectional mechanism of resistance that could prevent nematode penetration completely. However, giant cells and collapsed nematodes were observed in ‘IPR 106’ at 30 DAI, suggesting that the resistance mechanism to M. paranaensis in ‘IPR 106’ involves a post-infectional response and could be mediated by a hypersensitive reaction.