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Biology subjects

Hojo, A.

Publications and source records attributed to Hojo, A..

2 recordsLinked to original sources
bioRxiv2026

Fermented Botanical Product Modulates Soil Bacterial Communities and Enhances Plant-Growth-Promoting Activity for Sustainable Agriculture

Although biostimulants have attracted attention for sustainable agricultural systems, their efficacy remains poorly understood. In this study, we evaluated the effects of fermented botanical product (FBP) produced by fermenting and aging 41 types of fruits, grains, seaweed, and root vegetables with brown sugar for more than three years. Three crops, tomato, rice, and komatsuna (Brassica rapa), were cultivated with the application of 5,000- or 10,000-fold diluted FBP in greenhouses or fields. Application of diluted FBP promoted plant growth, as indicated by increased fresh weights of shoots, leaves, and roots, fruit production in tomato, and rice husk yield. As diluted FBP contained low nutrient levels, an indirect mechanism of plant growth promotion was suggested. Bacterial community structure analysis indicated changes in alpha diversity, beta diversity, and the predominant phyla in FBP-applied soils without plants and in soils cultivated with tomato, rice, and komatsuna. In addition, the abundance of plant-growth-promoting bacteria, such as Arthrobacter, Pseudomonas, Paraburkholderia, and Planifilum, increased in soils treated with diluted FBP. Furthermore, ammonium formation activity was observed in komatsuna cultivation soils treated with diluted FBP, whereas phosphate-solubilizing activity was enhanced in soils from all three crop cultivation systems treated with diluted FBP. These results suggest that diluted FBP influences bacterial communities and promotes crop growth through indirect effects, including increases in plant-growth-promoting bacteria, ammonium production, and phosphate solubilization. Alternatively, FBP may directly stimulate plant growth. Therefore, FBP may be a useful biostimulant for sustainable agricultural systems. HighlightsO_LIDiluted FBP promoted the growth of tomato, rice, and komatsuna (Brassica rapa). C_LIO_LIDiluted FBP altered the bacterial community structure in cultivated soils. C_LIO_LIFBP increased the abundance of plant-growth-promoting bacteria in cultivated soils. C_LIO_LIFBP stimulated ammonium formation and phosphate solubilization in cultivated soils. C_LIO_LIFBP may be a useful biostimulant for sustainable agricultural systems. C_LI Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=112 SRC="FIGDIR/small/728655v1_ufig1.gif" ALT="Figure 1"> View larger version (36K): org.highwire.dtl.DTLVardef@4772dorg.highwire.dtl.DTLVardef@12c40e8org.highwire.dtl.DTLVardef@594513org.highwire.dtl.DTLVardef@c5e5a6_HPS_FORMAT_FIGEXP M_FIG C_FIG

microbiology↗
bioRxiv2024

The transcription factor BATF pioneers the differentiation program of cytolytic effector CD8+ T cells through the direct interaction with IRF4

The transcription factor BATF plays critical roles in the differentiation of various immune cells, including CD8+ T cells. Here, we demonstrated that BATF controls epigenomic and transcriptomic reprogramming of CD8+ T cells at an early phase of acute viral infection, thereby promoting the differentiation of cytolytic effector CD8+ T cells. Loss of BATF drastically perturbed gene expression, chromatin accessibility, and the bindings of key transcription factors including Jun, T-bet, and IRF4. The direct interaction with IRF4 was essential for BATF-mediated effector differentiation, as the BATF mutant lacking this interaction failed to induce proper chromatin remodeling and proliferation of antigen-specific CD8+ T cells. Notably, IRF4 binding was exhaustively dependent on BATF, whereas BATF retained binding capacity even in IRF4-deficient CD8+ T cells. Furthermore, BATF initiated chromatin remodeling in the absence of IRF4, whereas subsequent dynamic epigenomic reorganization required IRF4. Our data proposed that BATF serves as a "pioneer transcription factor" spearheading the reorganization of chromatin architecture upon antigen encounter, followed by further rearrangement of epigenomic and transcriptomic landscapes through the cooperation with IRF4.

immunology↗