Search bioRxiv⌕ Search

Biology subjects

Metzen, I. E.

Publications and source records attributed to Metzen, I. E..

2 recordsLinked to original sources

Ethylene signal-driven plant-multitrophic synergy boosts crop performance

Efficient nutrient use in agriculture depends on the dynamic interplay between plant roots, soil, and microbial communities. The root-rhizosphere interface is central to nutrient uptake and serves as a key hub for interactions with beneficial microbes. Arbuscular mycorrhizal (AM) fungi, positioned at the nexus between plant roots and soil microbiota, play a critical role in enhancing crop performance under nutrient-limited conditions. In this study, we dissected the genetic and molecular basis of AM fungi-induced lateral root development in maize (Zea mays), focusing on the role of ethylene-responsive transcription factors (ERFs). We identified ERF genes as essential regulators of pericycle cell division, acting downstream of ethylene biosynthesis genes (ACS6 and ACS7) and AM fungal signaling. Our findings reveal that AM fungi promote lateral root initiation by activating ERF expression and reprogramming flavonoid metabolism, particularly reducing the accumulation of flavonols such as kaempferol and quercetin, which otherwise inhibit root development when over-accumulated. Furthermore, we demonstrated that Massilia, a beneficial rhizobacterium, synergizes with AM fungi to enhance lateral root formation by colonizing fungal hyphae, degrading flavonoids, and contributing to auxin production. Together, our results uncover a tripartite signaling network linking ethylene signaling, flavonoid-mediated microbial recruitment, and AM symbiosis. This study highlights ERFs as central integrators of plant-microbe interactions and provides a molecular framework for engineering root architecture and microbiome assembly to improve nutrient acquisition and support sustainable crop productivity.

plant biology↗

Streamlining the isolation of fungal hyphae: A semi-automated approach for soil substrates

Extracting fungal hyphae with their natural associated microbiota from soil samples presents a significant challenge due to their small size, typically in the micrometer range, and the formation of dynamic fungal networks. Previous methods, which involved supplementing soil substrates with sand or glass beads, have proven technically challenging for large-scale field applications and tend to create artificial conditions that disrupt the plant-microbe-soil continuum. In this study, we introduce a semi-automated approach for efficiently extracting fungal hyphae from a variety of soil types, including natural loamy soils. The Sieving and Sucrose Centrifugation (SSC) technique enables the enrichment of fungal hyphae, spores, and their surface-associated bacteria, with subsequent analysis of hyphal length density and the identification of tightly attached surface bacteria via next-generation sequencing (NGS). A comparison of different hyphal extraction techniques revealed that the SSC method yielded maximal hyphal length density. Furthermore, the SSC approach effectively enriched fungal hyphae from a highly diverse community, establishing a dependable method for advancing soil microbial research.

plant biology↗