Institute of Ensiling and Processing of Grass, College of Agro-Grassland Science, Nanjing Agricultural University, Nanjing 210095, China.
Institute of Ensiling and Processing of Grass, College of Agro-Grassland Science, Nanjing Agricultural University, Nanjing 210095, China.
J Dairy Sci. 2020 May;103(5):4288-4301. doi: 10.3168/jds.2019-16961. Epub 2020 Mar 12.
The aim of this study was to reveal the reconstitution dynamics of alfalfa microbiota and their contribution to the fermentation quality of Napier grass silages. Napier grass was harvested at approximately 20% dry matter content, chopped to a theoretical length of cut of 2 to 3 cm, and ensiled in laboratory polyethylene plastic bags (400 × 250 mm) for 30 d. The Napier grass was treated with the following: natural fermentation and distilled water (NG), inoculum of alfalfa microbiota (AM), gamma-ray irradiation and distilled water (IR), and gamma-ray radiation and alfalfa microbiota (IR+AM). Three milliliters of inoculum (containing 8.93 log cfu/mL lactic acid bacteria, 9.76 log cfu/mL Enterobacteriaceae, 5.94 log cfu/mL yeast, and 6.53 log cfu/mL mold) eluted from equivalent fresh alfalfa (450 g) was added to each silo of AM and IR+AM treatments, and 3 mL of distilled water was added to the silo of the NG and IR treatments. Three triplicate silos per treatment were opened on d 1, 3, 5, 7, 14, and 30 for sampling and analysis of fermentation quality and bacterial community. Relative to the NG silages, IR+AM silages exhibited a higher lactic acid concentration. The higher acetic acid concentration in NG than in IR+AM silages after 7 d of ensiling was attributed to the dominant genus of Leuconostoc (64.29-49.04%). Adding alfalfa microbiota to sterile Napier grass could increase ammonia-N concentration compared with NG and IR silages after 3 d of ensiling. Leuconostoc was the most predominant genus in NG silages, followed by Lactobacillus. Pediococcus had a greater relative abundance than the indigenous microorganisms and was exclusively found in AM and IR+AM silages, whereas Lactobacillus exhibited a slight increase after 30 d of ensiling (relative abundance in each silage: 6.29 vs. 3.82%, respectively). Lactobacillus was the predominant genus in IR silages since the onset of the ensiling. These results suggest that alfalfa microbiota affected bacterial community succession in Napier grass silages, which in turn affected the fermentation products. Adding alfalfa microbiota to sterile Napier grass could decrease acetic acid concentration compared with NG silages; however, it increased ammonia-N concentration compared with IR silages after 3 d of ensiling.
本研究旨在揭示紫花苜蓿微生物群落的再构成动态及其对象草青贮发酵品质的贡献。象草在干物质含量约为 20%时收获,切碎至理论长度 2-3cm,并在实验室聚乙烯塑料袋(400×250mm)中青贮 30d。象草经过以下处理:自然发酵和蒸馏水(NG)、紫花苜蓿微生物群落接种物(AM)、γ射线辐射和蒸馏水(IR)以及γ射线辐射和紫花苜蓿微生物群落(IR+AM)。从相当于新鲜紫花苜蓿(450g)洗脱的 3ml 接种物(含有 8.93logcfu/mL 乳酸菌、9.76logcfu/mL 肠杆菌科、5.94logcfu/mL 酵母和 6.53logcfu/mL 霉菌)被添加到 AM 和 IR+AM 处理的每个青贮料中,并且 3ml 蒸馏水被添加到 NG 和 IR 处理的青贮料中。每个处理的 3 个重复青贮料在第 1、3、5、7、14 和 30d 打开,用于取样和分析发酵品质和细菌群落。与 NG 青贮料相比,IR+AM 青贮料表现出更高的乳酸浓度。IR+AM 青贮料在青贮后 7d 的乙酸浓度高于 NG 青贮料,这归因于明串珠菌属(64.29-49.04%)的优势属。将紫花苜蓿微生物群落添加到无菌象草中可增加氨态氮浓度,与 NG 和 IR 青贮料相比,在青贮后 3d 时。明串珠菌属是 NG 青贮料中最主要的属,其次是乳酸菌属。肠球菌的相对丰度大于土著微生物,仅存在于 AM 和 IR+AM 青贮料中,而乳酸菌属在青贮 30d 后略有增加(每个青贮料中的相对丰度:6.29%比 3.82%)。乳酸菌属是青贮开始时 IR 青贮料的主要属。这些结果表明,紫花苜蓿微生物群落影响了象草青贮料中细菌群落的演替,进而影响了发酵产物。将紫花苜蓿微生物群落添加到无菌象草中可降低与 NG 青贮料相比的乙酸浓度,但与 IR 青贮料相比,在青贮后 3d 时增加了氨态氮浓度。