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海藻酶解物对大黄鱼生长和肠道菌群结构的影响

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为明确海藻酶解物饲喂大黄鱼的应用效果及对肠道菌群的影响,2022年11-12月在福建宁德海域使用添加0.5%复合海藻酶解物和0.5%海带酶解物的自配饲料饲养网箱养殖的大黄鱼8周,测定大黄鱼的存活率和平均增重,并采用NovaSeq PE250方案对肠道内容物进行16S rDNA扩增子测序,分析肠道菌群组成和特定菌群的相对丰度.结果显示:0.5%的复合海藻酶解物或0.5%的海带酶解物均可显著提高大黄鱼的存活率和平均增重(P<0.05);肠道菌群分析显示0.5%复合海藻酶解物组大黄鱼肠道中扩增子序列变体(ASVs)达1 353种,以厚壁菌门(Firmicutes)、变形菌门(Proteobacteria)、拟杆菌门(Bacteroidota)、梭杆菌门(Fusobacteriota)和放线菌门(Actinobacteriota)为主,而0.5%海带酶解物组大黄鱼肠道中ASVs仅242种,各样本中以厚壁菌门和脱硫杆菌门(Desulfobacterota)为主,变形菌门相对丰度较低,均与对照组(749个ASVs,各样本中菌门相对丰度无规律)有较大差异;基于KEGG的肠道菌群功能分析显示在淀粉和蔗糖代谢、谷胱甘肽代谢、磷酸转移酶系统、氰基氨基酸代谢、亨廷顿病和其他糖降解上3组存在显著差异(P<0.05);进一步分析发现,0.5%复合海藻酶解物增加了大黄鱼肠道菌群α多样性并提高了拟杆菌属及丁酸合成相关细菌的相对丰度,而0.5%海带酶解物则降低了大黄鱼肠道菌群α多样性,但可抑制肠道中假单胞菌属细菌的生长,且体外培养试验证实褐藻寡糖可极显著抑制变形假单胞菌生长(P<0.01).综上可知,本试验制备的2种海藻酶解物可调节大黄鱼形成不同的肠道菌群结构,并均可促进大黄鱼的健康和生长,该结果可为大黄鱼海藻类饲料添加剂的开发和通过调整大黄鱼肠道菌群改善大黄鱼健康和生长的饲料添加剂研发提供数据参考.
Effects of Seaweed Enzymatic Hydrolysates on Growth and Intestinal Microflora Structure of Larimichthys crocea
This experiment aimed to determine the application effect of seaweeds enzymatic hydrolysate fed La-rimichthys crocea and its impact on host's intestinal microflora.The cage cultured Larimichthys crocea were fed with self-prepared diets supplemented with 0.5%compound seaweeds enzyme hydrolysates and 0.5%kelp enzyme hydrolysates for 8 weeks from November to December 2022 in Ningde sea area,Fujian Province of China,to observe the effects on the survival and weight gain of the Larimichthys crocea and the16S rDNA am-plicon sequencing of intestinal contents was performed using by the NovaSeq PE250 protocol to analyze the composition of the intestinal microflora and the relative abundance of specific microflora.The results showed that 0.5%compound seaweeds enzyme hydrolysates and 0.5%kelp enzyme hydrolysates both could significant-ly increase the survival rate and average weight gain of Larimichthys crocea,and the analysis of intestinal mi-croflora showed that 1 353 amplicon sequence variants(ASVs)were observed in the intestine of Larimichthys crocea in the 0.5%compound seaweeds enzyme hydrolysates group,and they were dominated by Firmicutes,Proteobacteria,Bacteroidota,Fusobacteriota and Actinobacteriota,and only 242 ASVs in the 0.5%kelp en-zyme hydrolysates group,with Firmicutes and Desulfobacterota predominating and Proteobacteria in lower rela-tive abundance in all samples,all of which differed from the 749 ASVs in the control group and the irregular relative abundance of bacterial phyla in all samples;based on the KEGG-based functional analysis of intestinal microflora also showed significant differences in starch and sucrose metabolism,glutathione metabolism,phos-photransferase system,cyanoamino acid metabolism,Huntington's disease and other glycan degradation(P<0.05).Further analysis revealed that 0.5%complex seaweed enzyme hydrolysates significantly increased the α-diversity of intestinal microflora and promoted the relative abundances of the Bacteroides and butyric acid-syn-thesizing bacteria,while 0.5%kelp enzyme hydrolysates decreased the α-diversity of intestinal microflora but inhibited the growth of Pseudomonas bacteria in the intestinal tract,and in vitro culture test confirmed that algal oligosaccharides could extremely significantly inhibit the growth of Pseudomonas plecoglossicida(P<0.01).In conclusion,the two kinds of seaweed enzyme hydrolysis prepared in this experiment can regulate the formation of different intestinal microflora in Larimichthys crocea to promote health and growth,which provides data ref-erence for the development of seaweed feed additives for Larimichthys crocea and the research and development of feed additives that improve the health and growth of Larimichthys crocea by adjusting the intestinal microflo-ra.[Chinese Journal of Animal Nutrition,2024,36(3):1819-1833]

Larimichthys croceaseaweeds enzymatic hydrolysatehealthgrowthintestinal microflora

张露、熊宇明、董黎黎、梁萍、秦志清、王磊、江和基、黄志坚、殷光文、林建斌、王登峰

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福建农林大学动物科学学院(蜂学学院),福州 350002

福建省淡水水产研究所,福州 350002

大黄鱼 海藻酶解物 健康 生长 肠道菌群

福建省海洋服务与渔业高质量发展专项福建省自然科学基金面上项目

FJHY-YYKJ-2022-2-42021J01084

2024

动物营养学报
中国畜牧兽医学会

动物营养学报

CSTPCD北大核心
影响因子:1.297
ISSN:1006-267X
年,卷(期):2024.36(3)
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