The ratooning capacity of sugarcane cultivars represents a crucial agronomic trait that significantly influences the sustainability of crop yields. This study elucidates the physiological and molecular mechanisms underlying the sugarcane ratooning ability observed in ratoon-competent GuiTang 29 (GT29) and ratoon-deficient Badila cultivars following stem excision. Through integrated hormonal profiling and transcriptome analysis, we identified significant differences in hormone levels and gene expression patterns. The quantification of 15 endogenous hormones via HPLC revealed marked reductions in zeatin (ZA) and zeatin riboside (ZR) in both cultivars. Additionally, GT29 exhibited notable reductions in gibberellins (GA3 and GA5) and strigolactone (5-DS) post-stem-excision, while Badila displayed stable or distinct hormonal changes. Additionally, Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analyses indicated that hormone signal transduction, MAPK signaling pathways, phenylpropanoid biosynthesis, flavonoid biosynthesis, and other metabolic pathways were significantly enriched in both GT29 and Badila, with a particularly higher enrichment of plant hormone signal transduction in GT29. Furthermore, several differentially expressed genes (DEGs) had different expression patterns between GT29 and Badila, including the cytokinin receptor B-ARR and transcription factor A-ARR, gibberellin pathway components GID1 and DELLA, and AUX/IAA and SAUR in the auxin pathway. The real-time quantitative PCR (qRT-PCR) validation of 12 DEGs corroborated the RNA-seq data, further supporting the reliability of the transcriptomic analysis. This study delineates a clear molecular framework distinguishing ratoon competence, offers novel insights into the molecular basis of perennial regeneration and provides reliable candidate genes for functional marker development in sugarcane breeding.

Long-term continuous cropping is a prevalent agricultural practice aimed at maximizing land use efficiency and crop yields, yet it often leads to severe soil degradation, nutrient imbalance, and microbial community disruption. Effective soil remediation strategies are urgently needed to restore soil health and ensure sustainable agricultural production. In this study, we investigated the impact of forest soil amendment on microbial community structure, diversity, and functional potential in long-term continuous cropping soils. Using metagenomic sequencing, we analyzed soils from natural forest (BK), forest soil-amended soils (BCP), and fields under continuous cropping for 15 years (CP15) and 30 years (CP30). Forest soil amendment significantly mitigated microbial diversity loss and structural degradation caused by prolonged monoculture. Alpha diversity analysis revealed that BCP restored microbial diversity to levels comparable to BK, while beta diversity and NMDS analyses showed that microbial community composition in BCP closely resembled that of forest soil. Taxonomic profiling indicated that forest soil amendment enriched beneficial taxa such as Actinobacterota and Acidobacteriota, reversing shifts observed in CP15 and CP30. Functionally, COG and KEGG annotations revealed that BCP soils exhibited higher abundances of genes involved in carbohydrate metabolism, energy production, and nutrient cycling. Notably, the amendment reduced antibiotic resistance genes and virulence factors, potentially improving the microbial risk profile of soil communities. These findings demonstrate that forest soil amendment effectively restores microbial community structure and functionality in degraded soils, providing a nature-based solution for sustainable agriculture.