Research Centre for Plant Growth and Development, School of Life Sciences, University of KwaZulu-Natal Pietermaritzburg Campus, P/Bag X01, Scottsville, Pietermaritzburg, 3209, South Africa.
Institute of Plant Biology, HUN-REN Biological Research Centre, Temesvári Krt, 62, 6726, Szeged, Hungary.
Curr Microbiol. 2024 Oct 10;81(11):401. doi: 10.1007/s00284-024-03914-3.
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.
蓝藻合成具有抗真菌活性的次生代谢物,使它们成为可持续、环保农业的潜在生物农药。识别具有有效生物活性的蓝藻菌株的计划通常会筛选保存在培养物库中的菌株。这些菌株通常是单克隆的,但不是无菌的,这可能会潜在地影响产生的生物量的生物活性。本研究调查了与真菌共生体共同分离并保存在莫松马乔罗瓦尔藻类培养物收集(MACC)中的蓝藻 Nostoc muscorum MACC-189 和 N. linckia MACC-612 菌株的体外抗真菌活性。真菌共生体从蓝藻库存培养物中分离出来,并分别鉴定为 Purpureocillium lilacinum 和 Sarocladium sp.。将培养物针对七种植物病原体进行了测试。植物病原菌在土豆葡萄糖琼脂平板上生长,将蓝藻-真菌悬浮培养物和分离的真菌共生体置于平板中央。在孵育 10 天后,半定量评估抗真菌效果。蓝藻-真菌共培养物对 Monilinia fructigena 和 Aspergillus sp.具有抗真菌活性,其中 N. muscorum/P. lilacinum 培养物的效果最显著。真菌分离物抑制了 M. fructigena,P. lilacinum 具有剂量依赖性反应,但不抑制 Aspergillus sp.这表明蓝藻培养物对 M. fructigena 的抗真菌作用是由于真菌伙伴而不是蓝藻,而对 Aspergillus sp.的抗真菌作用是由于蓝藻伙伴。由于不可能维持活的无菌 N. muscorum 和 N. linckia 培养物,因此无法得出明确的结论。这些结果强调了在测试蓝藻培养物的抗真菌生物活性时,使用无菌培养物或鉴定共分离物的重要性。