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1. 西南医科大学药学院 药理系细胞治疗与细胞药物泸州市重点实验室,泸州,646000
2. 川南医学转化研究院,泸州,646000
纸质出版日期:2023,
网络出版日期:2023-7-20,
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杨翼飞, 徐桂瑶, 王, 等. 芒柄花黄素对小鼠肠道菌群结构和丰度的影响[J]. 西南医科大学学报, 2023,46(4):342-347.
The impact of formononetin on the structure and abundance of gut microbiota in mice[J]. Journal of Southwest Medical University, 2023,46(4):342-347.
杨翼飞, 徐桂瑶, 王, 等. 芒柄花黄素对小鼠肠道菌群结构和丰度的影响[J]. 西南医科大学学报, 2023,46(4):342-347. DOI: 10.3969/j.issn.2096-3351.2023.04.013.
The impact of formononetin on the structure and abundance of gut microbiota in mice[J]. Journal of Southwest Medical University, 2023,46(4):342-347. DOI: 10.3969/j.issn.2096-3351.2023.04.013.
目的 研究芒柄花黄素(formononetin,FMN)对小鼠肠道菌群结构与丰度的影响。 方法 将12只无特定病原体(specific pathogen free
SPF)级C57BL/6J雄性小鼠随机分为对照组和FMN组,每组6只。FMN组每天灌胃1次FMN,5 mg·kg-1d-1,连续10 d,对照组灌胃相同体积的磷酸盐缓冲溶液(phosphate buffer saline,PBS)。于第11天收集小鼠新鲜粪便,用DNA提取试剂盒提取粪便菌群DNA,使用引物338F (5´-ACTCCTACGGGAGGCAGCAG-3´) 和806R (5´-GGACTACHVGGGTWTCTAAT-3´)对16S rRNA基因V3-V4可变区进行PCR扩增。最后利用Illumina公司的Miseq PE300平台进行测序(上海美吉生物医药科技有限公司)并对测序结果进行分析。 结果 小鼠灌胃FMN 后,肠道菌群丰富度与多样性指数Sobs、Chao、Ace和Shannon明显升高。PCoA和Venn分析结果显示,摄入FMN后小鼠肠道菌群结构明显改变。在门水平上,FMN组拟杆菌门(Bacteroidetes)丰度显著增加,厚壁菌门(Bacteroidetes)和变形菌门(Proteobacteria)丰度显著减少,脱铁杆菌门(Deferribacteres)有上升趋势;在属水平上,FMN组的粪球菌属(Coprococcus)、瘤胃球菌属(Ruminococcus)、unclassified_o__Clostridiales、norank_o__Clostridiales、Odoribacter和norank_o__Bacteroidales丰度显著增加,unclassified_f__Lachnospiraceae丰度显著降低。结论 芒柄花黄素可提高小鼠肠道菌群丰富度与多样性,并改变菌群结构、增加有益菌优势。
Objective The aim of research was to study the effects of formononetin (FMN) on the structure and abundance of intestinal microbiota in mice. Methods A total of 12 specific pathogen-free male C57BL/6J mice were randomly divided into control group and FMN group
with 6 mice in each group. The FMN group was given FMN by gavage once daily at a dose of 5 mg/kg for 10 consecutive days
while the control group was given an equal volume of phosphate buffer saline (PBS). On 11th day
fresh feces of mice were collected in each group
and microbial DNA was extracted using the E.Z.N.A.® soil DNA Kit (Omega Bio-tek
USA)
with the 16S rRNA (V3-V4 region) amplificated using the primers of 338F (5´-ACTCCTACGGGAGGCAGCAG-3´) and 806R (5´-GGACTACHVGGGTWTCTAAT-3´). Finally
Illumina MiSeq sequencing was performed through using PE300 chemical at Majorbio Bio-Pharm Technology Co.
Ltd. (Shanghai
China)
and the sequencing results were analyzed. Results FMN administration significantly increased the gut microbial richness and diversity in mice
with the Sobs
Chao
Ace and Shannon indices obviously increased. PCoA and Venn analysis demonstrated that the FMN intervention significantly changed the structure of gut microbiota. At the phylum level
the abundance of Bacteroidetes was evidently increased in FMN group
while the abundance of Firmicutes and Proteobacteria was significantly decreased. The abundance of Deferribacteres showed an increasing trend. At the genus level
the FMN treatment group showed significantly increased abundance of Coprococcus
Ruminococcus
unclassified_o__Clostridiales
norank_o__Clostridiales
Odoribacter and norank_o__Bacteroidales
and the abundance of unclassified_f__Lachnospiraceae was remarkably decreased.Conclusion FMN could increase the richness and diversity of gut microbiota in mice and promote the abundance of beneficial bacteria.
芒柄花黄素肠道菌群16S rRNA测序
FormononetinGut microbiota16S rRNA sequencing
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