Wendy A Stirk, Bernadett Pap, Gergely Maróti, Johannes van Staden, Vince Ördög
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The fungal co-partners were isolated from the Cyanobacterial stock cultures and identified as Purpureocillium lilacinum and Sarocladium sp., respectively. The cultures were tested against seven phytopathogens. The phytopathogenic fungi were grown on potato dextrose agar plates and suspension cultures of the Cyanobacteria-fungi and isolated fungal co-partners were placed in the centre of the plate. Antifungal effects were assessed semi-quantitatively after 10 days of incubation. The Cyanobacteria-fungal co-cultures had antifungal activity against Monilinia fructigena and Aspergillus sp. with the N. muscorum/P. lilacinum culture being the most effective. The fungal isolates inhibited M. fructigena with P. lilacinum having a dose-dependent response but did not inhibit Aspergillus sp. This suggested that the antifungal effect of the Cyanobacterial cultures on M. fructigena was due to the fungal partner rather than the cyanobacterium while the antifungal effect on Aspergillus sp. was due to the cyanobacterium partner. As it was not possible to maintain living axenic N. muscorum and N. linckia cultures, this could not be conclusively confirmed. 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引用次数: 0
摘要
蓝藻能合成具有抗真菌活性的次生代谢物,是可持续生态友好型农业的潜在生物杀虫剂。鉴定具有有效生物活性的蓝藻菌株的计划通常会对培养物中的菌株进行筛选。这些菌株通常是单克隆但非轴向的,这可能会影响生成的生物质的生物活性。本研究调查了与真菌共伴侣共分离并保存在 Mosonmagyaróvár 藻类培养物保藏中心(MACC)的 Nostoc muscorum MACC-189 和 N. linckia MACC-612 菌株的体外抗真菌活性。从蓝藻种群培养物中分离出的真菌共伴菌分别被鉴定为紫丁香真菌和 Sarocladium sp.。这些培养物针对七种植物病原菌进行了测试。植物病原真菌生长在马铃薯葡萄糖琼脂平板上,蓝细菌-真菌悬浮培养物和分离出的真菌共伴菌被放置在平板中央。培养 10 天后,对抗真菌效果进行半定量评估。蓝藻-真菌共培养物对果酸单胞菌和曲霉菌具有抗真菌活性,其中 N. muscorum/P. lilacinum 培养物最有效。这表明蓝藻培养物对果核霉菌的抗真菌作用是由真菌伙伴而非蓝藻引起的,而对曲霉菌的抗真菌作用则是由蓝藻伙伴引起的。由于无法维持活的轴生 N. muscorum 和 N. linckia 培养物,因此无法对此进行最终确认。这些结果突出表明,在测试蓝藻培养物的抗真菌生物活性时,使用轴向培养物或鉴定共分离物非常重要。
Cyanobacteria-Fungi Co-Cultures: Which Partner Contributes to Antifungal Activity?
Cyanobacteria synthesize secondary metabolites with antifungal activity, making them potential biopesticide agents for sustainable, eco-friendly agriculture. Programmes to identify Cyanobacterial strains with effective bioactivity generally screen strains maintained in culture collections. These strains are often monoclonal but non-axenic and this may potentially influence the bioactivity of the generated biomass. The present study investigated in vitro antifungal activity of Nostoc muscorum MACC-189 and N. linckia MACC-612 strains co-isolated with fungal co-partners and maintained in the Mosonmagyaróvár Algal Culture Collection (MACC). The fungal co-partners were isolated from the Cyanobacterial stock cultures and identified as Purpureocillium lilacinum and Sarocladium sp., respectively. The cultures were tested against seven phytopathogens. The phytopathogenic fungi were grown on potato dextrose agar plates and suspension cultures of the Cyanobacteria-fungi and isolated fungal co-partners were placed in the centre of the plate. Antifungal effects were assessed semi-quantitatively after 10 days of incubation. The Cyanobacteria-fungal co-cultures had antifungal activity against Monilinia fructigena and Aspergillus sp. with the N. muscorum/P. lilacinum culture being the most effective. The fungal isolates inhibited M. fructigena with P. lilacinum having a dose-dependent response but did not inhibit Aspergillus sp. This suggested that the antifungal effect of the Cyanobacterial cultures on M. fructigena was due to the fungal partner rather than the cyanobacterium while the antifungal effect on Aspergillus sp. was due to the cyanobacterium partner. As it was not possible to maintain living axenic N. muscorum and N. linckia cultures, this could not be conclusively confirmed. These results highlight the importance of either using axenic cultures or identifying the co-isolates when testing Cyanobacteria cultures for antifungal bioactivity.