Apple ring rot,which is caused by Botryosphaeria dothidea,severely affects apple production.The mechanisms employed in apple cells against B.dothidea remain unknown.In this research,the pathogen infection mode and the...Apple ring rot,which is caused by Botryosphaeria dothidea,severely affects apple production.The mechanisms employed in apple cells against B.dothidea remain unknown.In this research,the pathogen infection mode and the relationship between cell death and disease resistance in‘Fuji’/B.dothidea interaction pathosystem were investigated.By using transmission electron microscopy(TEM),our research showed that the pathogen infects apple cells both intracellularly and extracellularly.However,compared with that in immature fruit,the incidence of hyphae in the interior of mature apple fruit cells increased dramatically,suggesting that cell wall-mediated penetration resistance could be important in apple resistance against B.dothidea.TEM ultrastructural characterization identified the nuclear morphology of programmed cell death induction in both apple fruit and callus cells under B.dothidea infection.Overexpression of MdVDAC2(MDP0000271281),which encodes an outer-membrane localized anion channel protein in mitochondria,significantly promoted cell death under B.dothidea infection and simultaneously inhibited pathogen infection,suggesting that cell death represents a disease resistance mechanism in apple against B.dothidea infection.Furthermore,BdCatalase(KAF4307763),a cytochromeP450 family protein BdCYP52A4(KAF4300696),and subtilisin-domain containing proteinswere identified fromB.dothidea-secreted proteins,which suggested the potential involvement of active oxygen species and phytoalexins in combating B.dothidea infection and triggering or dampening apple resistance.Collectively,our research suggested that cell wall-mediated penetration resistance,programmed cell death machinery and microbial effector-interrelated signaling were among strategies recruited in apple to combat B.dothidea.The current research laid the foundation for further investigations into resistance mechanisms in apple.展开更多
The single spores were isolated from chlamydospores of Ustilaginoidea virens with three different maturities by PSA. The isolated single spores were cultured on different media at different temperatures under natural ...The single spores were isolated from chlamydospores of Ustilaginoidea virens with three different maturities by PSA. The isolated single spores were cultured on different media at different temperatures under natural light for inducing conidia to explore the optimum isolation technique of single spore and optimum culture condition of conidia. The results showed that the successful isolating rate of single spore from yellow rice false smut balls reached 90. 00% . The sporulation quantities of isolated single spores cultured on PSD and PDB media at 22 - 29 ℃ ( variable temperature under natural light) or 28 ℃ ( constant temperature under dark condition) for 12 d were up to 6. 3 × 107 and 1. 1 × 106 spore / mL,respectively. PSA was the most effective method to isolate single spores from yellow rice false smut balls of U. virens. The optimum conidia culture condition included PSD or PDB medium,22 - 29 ℃ or 28 ℃ ,natural light and vibration culture.展开更多
基金supported by the National Key Research and Development Program of China(Grant No.2018YFD1000307)the Natural Science Foundation in China(Grant Nos.31672136 and 31272132).
文摘Apple ring rot,which is caused by Botryosphaeria dothidea,severely affects apple production.The mechanisms employed in apple cells against B.dothidea remain unknown.In this research,the pathogen infection mode and the relationship between cell death and disease resistance in‘Fuji’/B.dothidea interaction pathosystem were investigated.By using transmission electron microscopy(TEM),our research showed that the pathogen infects apple cells both intracellularly and extracellularly.However,compared with that in immature fruit,the incidence of hyphae in the interior of mature apple fruit cells increased dramatically,suggesting that cell wall-mediated penetration resistance could be important in apple resistance against B.dothidea.TEM ultrastructural characterization identified the nuclear morphology of programmed cell death induction in both apple fruit and callus cells under B.dothidea infection.Overexpression of MdVDAC2(MDP0000271281),which encodes an outer-membrane localized anion channel protein in mitochondria,significantly promoted cell death under B.dothidea infection and simultaneously inhibited pathogen infection,suggesting that cell death represents a disease resistance mechanism in apple against B.dothidea infection.Furthermore,BdCatalase(KAF4307763),a cytochromeP450 family protein BdCYP52A4(KAF4300696),and subtilisin-domain containing proteinswere identified fromB.dothidea-secreted proteins,which suggested the potential involvement of active oxygen species and phytoalexins in combating B.dothidea infection and triggering or dampening apple resistance.Collectively,our research suggested that cell wall-mediated penetration resistance,programmed cell death machinery and microbial effector-interrelated signaling were among strategies recruited in apple to combat B.dothidea.The current research laid the foundation for further investigations into resistance mechanisms in apple.
基金Science and Technology Project of Guizhou Province[QKH Major Project( 2012 ) 6012 ]Supported by Science and Technology Fund of Guizhou Province ( QKH J[2009]2103)+1 种基金Science and Technology Research Programof Guizhou Province ( QKH NY[2012]3031)Project of Guizhou Academy of Agricultural Sciences ( [2010]033 and QNKH[Major]07016)
文摘The single spores were isolated from chlamydospores of Ustilaginoidea virens with three different maturities by PSA. The isolated single spores were cultured on different media at different temperatures under natural light for inducing conidia to explore the optimum isolation technique of single spore and optimum culture condition of conidia. The results showed that the successful isolating rate of single spore from yellow rice false smut balls reached 90. 00% . The sporulation quantities of isolated single spores cultured on PSD and PDB media at 22 - 29 ℃ ( variable temperature under natural light) or 28 ℃ ( constant temperature under dark condition) for 12 d were up to 6. 3 × 107 and 1. 1 × 106 spore / mL,respectively. PSA was the most effective method to isolate single spores from yellow rice false smut balls of U. virens. The optimum conidia culture condition included PSD or PDB medium,22 - 29 ℃ or 28 ℃ ,natural light and vibration culture.