Ensiling technology shows promise for preserving and providing high-quality forage. However, the high polymeric content and compact properties of fiber result in low biodigestibility. This study aimed to evaluate the use of ensiling technology for storing wheat straw. It also analyzed changes in fermentation-related products, chemical components, bacterial communities, and metabolite profiles of wheat straw ensiled with or without cellulase or Lactiplantibacillus plantarum (L. plantarum). The results showed that inoculation with L. plantarum, either alone or with cellulase, produced abundant organic acids, degraded fiber, suppressed most microbes, and increased certain metabolites in wheat straw silage. Wheat straw inoculated with L. plantarum, either alone or with cellulase, exhibited significantly lower neutral detergent fiber and acid detergent fiber contents compared to the control treatment. Additionally, higher lactic acid and acetic acid contents were observed in these treatments. The microbiome analysis revealed that Lactobacillus was dominant, while Kosakonia was suppressed. Metabolic analysis showed a significant increase in amino acids, peptides, analogues, and organic acid derivatives. Overall, wheat straw inoculated with L. plantarum, either alone or with cellulase, produced well-preserved silage, providing new insights into recycling and utilizing wheat straw through bacterial-enzyme synergy.

This study aimed to evaluate the effects of cellulase or Lactobacillus plantarum (L. plantarum) on the fermentation characteristics and microbial community structure of the sorghum straw silage. Sorghum straw was treated with the following four experimental conditions: distilled water (control, CK), cellulase (CEL), Lactobacillus plantarum (LP), and a combined treatment of Lactobacillus plantarum with cellulase (LPCEL). These results indicated that the LP treatment could markedly (p < 0.05) preserve the crude protein content compared to that in other treatments, whereas the CEL significantly (p < 0.05) reduced the acid detergent fiber content, while the LPCEL had the highest lactic acid content and lowest pH value. Proteobacteria and Pantoea were identified as the dominant phylum and genus in fresh materials, respectively. This phylum level dominance transitioned to Firmicutes post-treatment, while at the genus level, the community shifted from Pantoea to co-dominance of Lactobacillus and Prevotella, with Lactobacillus being the most abundant in both the CEL and LPCEL treatments. In conclusion, adding L. plantarum and cellulase to sorghum straw can significantly improve the fermentation quality of sorghum straw silage, and improve the nutritional value of silage by affecting the microbial community structure and metabolic pathways. • The physicochemical properties of sorghum straw silage were improved by L. plantarum or cellulase. • Microbiomic analyses revealed a progressive reduction after ensiling progress. • The ensiling parameters were influenced by the microbial communities and functions.

This study aimed to investigate the effects of lactic acid bacteria (LAB) inoculants on the fermentation quality, microbial compositions, and predicted functional profiles of forage oat. The forage oat was inoculated with distilled water, Lentilactobacillus buchneri (LB), and Lactiplantibacillus plantarum (LP) as the control (CON), LB and LP treatments, respectively, and the addition of Lentilactobacillus buchneri (LB) or Lactiplantibacillus plantarum (LP) resulted in 1 × 10⁶ colony-forming units/g of fresh weight. After 30 days of fermentation, the lowest pH (4.23) and the lowest content of ammoniacal nitrogen (NH₃-N) in dry matter (DM, 4.39%) were observed in the LP treatment. Interestingly, there was a significant (p < 0.05) difference in lactic acid (LA) concentration among the three treatments. The LP treatment had the highest lactate concentration (7.49% DM). At the same time, a markedly (p < 0.05) elevated acetic acid (AA) concentration (2.48% DM) was detected in the LB treatment. The Shannon and Chao1 indexes of bacterial and fungal communities in all the silage samples decreased compared to those in the fresh materials (FM). Proteobacteria was the dominant phylum in the FM group and shifted from Proteobacteria to Firmicutes after ensiling. Lactobacillus (64.87%) and Weissella (18.93%) were the predominant genera in the CON, whereas Lactobacillus dominated the fermentation process in the LB (94.65%) and LP (99.60%) treatments. For the fungal community structure, the major genus was Apiotrichum (21.65% and 60.66%) in the FM and CON groups after 30 days of fermentation. Apiotrichum was the most predominant in the LB and LP treatments, accounting for 52.54% and 34.47%, respectively. The genera Lactococcus, Pediococcus, and Weissella were negatively associated with the LA content. The genus Ustilago and Bulleromyces were positively associated with the LA content. These results suggest that the addition of LAB regulated the microbial community in oat silage, which influenced the ensiling products, and LP was more beneficial for decreasing the pH and NH₃-N and increasing the LA concentration than LB in forage oat silage.

Microbial and enzyme additives can improve silage performance, but there is limited comparative research on the effects of microbial and enzyme additives on improving silage fermentation quality, and the underlying microbial and metabolic pathways remain unclear. This study investigated the effects without inoculants (CK treatment) or with Lactiplantibacillus plantarum (LP treatment), xylanase (XY treatment) and their combination (LPXY treatment) on the fermentation quality, as well as on the microbial communities and metabolite profiles of the wheat straw silage. The results demonstrated that the LP treatment has a better effect on improving the fermentation quality of wheat straw silage compared to other treatments, as evidenced by markedly (p < 0.05) decreased the pH (4.06), acid and neutral fiber (ANF, NDF, 23.43 and 31.69%DM), and increased the lactic acid (LA, 965.89 mg/L) and acetic acid (AA, 656.10 mg/L) concentrations. After the fermentation process, the LP treatment significantly (p < 0.05) enhanced the abundance of Lactobacillus, reduced bacterial Shannon (p < 0.05) and increased some key metabolites content. The structural equation models (SEMs) and Pearson’s correlation results proved that the LP treatment improved the wheat straw silage fermentation quality via increasing the abundance of Lactobacillus, decreasing the diversity of bacterial community and enriching the content of certain key metabolites. The present study provides mechanistic evidence that Lactiplantibacillus plantarum additive is superior to xylanase additive and their combination on improving fermentation quality of wheat straw silage, that is, by enriching certain key metabolites to increase AA and LA concentrations, providing a reference for the cross study of silage feed fermentation microbiome and metabolome.

This study utilized rapeseed straw as the raw material and employed a completely randomized design with four treatments: a distilled water control (CK), individual supplementation of Lactiplantibacillus plantarum (1.0 × 10⁶ CFU/g fresh weight) (Lp), individual supplementation of xylanase (50,000 U/g fresh weight) (XY), and a combined bacterium–enzyme treatment (XYLp). Each treatment was replicated five times, vacuum-sealed, and fermented at 25 °C for 60 days to systematically evaluate the effects of different treatments on the fermentation quality, nutritional composition, and microbial community structure of rapeseed straw silage. The results demonstrated that, compared with the CK group, all additive treatments significantly decreased pH and increased lactic acid (LA) content (p < 0.05). Among them, the Lp group exhibited the lowest pH value (4.27), which was significantly lower than all other treatments except XYLp (p < 0.05). Both the Lp and XYLp groups showed significantly higher LA content than the other groups (p < 0.05). Crude protein (CP) content was significantly higher in all additive treatments than in the CK group (p < 0.05). The XYLp group exhibited the most substantial fiber degradation, with acid detergent fiber (ADF) and neutral detergent fiber (NDF) contents being significantly lower than CK and reaching the lowest values among all treatments (p < 0.05). Both the XY and XYLp groups showed significantly lower hemicellulose and holocellulose contents compared to the CK and Lp groups (p < 0.05). Microbial community analysis revealed that the synergistic bacterium–enzyme treatment significantly enriched fibrolytic genera, including Kosakonia and Pediococcus, and upregulated the expression of key fibrolytic enzymes such as cellulase (EC: 3.2.1.4), β-glucosidase (EC: 3.2.1.21), and endo-1,4-β-xylanase (EC: 3.2.1.8). Functional prediction further indicated that the bacterial–enzyme synergy enhanced fibrous structure degradation and fermentable substrate release by activating carbohydrate metabolism pathways and bacterial secretion systems. These findings suggest that the combined application of Lactiplantibacillus plantarum and xylanase has the potential to be a promising strategy for enhancing fiber degradation and overall fermentation quality in rapeseed straw silage.

This study investigated the distinct effects of Lentilactobacillus buchneri (LB) and Lactiplantibacillus plantarum (LP) inoculants on the fermentation characteristics and bacterial community succession of Leymus chinensis silage. Treatments included distilled water (CON), LB, and LP, applied at a concentration of 1 × 10 ⁶ cfu/g of fresh matter (FM). Compared with the CON group, the fermentation quality was improved by the inoculations, the markedly ( p < 0.05) lower pH and NH ₃ –N were found in the LB and LP treatments. The significantly ( p < 0.05) highest LA and AA contents were detected in the LP and LB treatments, respectively. The bacterial diversity, reflected by Shannon and Chao1 indices, decreased throughout the ensiling process, with the LP group exhibiting the most pronounced reduction. Furthermore, beta‐diversity analysis revealed distinct microbial community structures among the treatments. While fresh L. chinensis was dominated by Proteobacteria (48.03%), Firmicutes (26.23%), and Actinobacteriota (23.72%), the microbiome shifted dramatically after 60 days of ensiling to be predominantly Firmicutes (94.96%–99.79%), the genus Rhodococcus , Microbacterium , Enterococcus and Leuconostoc , Weissella , and Enterococcus were markedly ( p < 0.05) enriched in the CK treatment during fermentation from 3 to 14 days, while from 30 days, the genus Lactobacillus as the dominant genus, especially in the LB and LP treatments. In conclusion, both additives facilitate L. chinensis ensiling by regulating the microbiome, yet L. plantarum demonstrates superior efficacy in optimizing fermentation quality.