Guo Yi-Syuan, Liber Julian A, Morrell-Falvey Jennifer L, Bonito Gregory, Retterer Scott T
Environmental Molecular Sciences Division, Pacific Northwest National Laboratory, Richland, Washington, United States of America.
Biosciences Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee, United States of America.
PLoS One. 2024 Dec 30;19(12):e0312855. doi: 10.1371/journal.pone.0312855. eCollection 2024.
Through their expansive mycelium network, soil fungi alter the physical arrangement and chemical composition of their local environment. This can significantly impact bacterial distribution and nutrient transport and can play a dramatic role in shaping the rhizosphere around a developing plant. However, direct observation and quantitation of such behaviors is extremely difficult due to the opacity and complex porosity of the soil microenvironment. In this study, we demonstrate the development and use of an engineered microhabitat to visualize fungal growth in response to varied levels of confinement. Microfluidics were fabricated using photolithography and conventional soft lithography, assembled onto glass slides, and prepared to accommodate fungal cultures. Selected fungal strains across three phyla (Ascomycota: Morchella sextalata, Fusarium falciforme; Mucoromycota: Linnemannia elongata, Podila minutissima, Benniella; Basidiomycota: Laccaria bicolor, and Serendipita sp.) were cultured within microhabitats and imaged using time-lapse microscopy to visualize development at the mycelial level. Fungal hyphae of each strain were imaged as they penetrated through microchannels with well-defined pore dimensions. The hyphal penetration rates through the microchannels were quantified via image analysis. Other behaviors, including differences in the degree of branching, peer movement, and tip strength were also recorded for each strain. Our results provide a repeatable and easy-to-use approach for culturing fungi within a microfluidics platform and for visualizing the impact of confinement on hyphal growth and other fungal behaviors pertinent to their remodeling of the underground environment.
通过其庞大的菌丝网络,土壤真菌改变了其局部环境的物理结构和化学成分。这会显著影响细菌分布和养分运输,并在塑造发育中植物周围的根际环境方面发挥重要作用。然而,由于土壤微环境的不透明性和复杂的孔隙率,直接观察和定量这些行为极其困难。在本研究中,我们展示了一种工程微生境的开发和应用,以可视化真菌在不同限制水平下的生长情况。微流控装置采用光刻和传统软光刻技术制造,组装在载玻片上,并准备好用于容纳真菌培养物。从三个门中挑选出的真菌菌株(子囊菌门:六棱羊肚菌、镰状镰刀菌;毛霉门:细长林奈霉、微小波迪拉菌、本尼菌;担子菌门:双色蜡蘑、Serendipita属)在微生境中培养,并使用延时显微镜成像,以在菌丝水平上观察其发育情况。每个菌株的真菌菌丝在穿透具有明确孔径尺寸的微通道时进行成像。通过图像分析对菌丝穿过微通道的穿透速率进行定量。还记录了每个菌株的其他行为,包括分支程度、菌丝移动和菌丝尖端强度的差异。我们的结果提供了一种可重复且易于使用的方法,用于在微流控平台上培养真菌,并可视化限制对菌丝生长以及与它们对地下环境重塑相关的其他真菌行为的影响。