Department of Biological Sciences, Idaho State University, Pocatello, ID, USA.
Microbiologyopen. 2021 Mar;10(2):e1185. doi: 10.1002/mbo3.1185.
LGM2605 is a synthetic version of the naturally occurring flaxseed lignan secoisolariciresinol diglucoside (SDG), with known anti-inflammatory and antioxidant properties; however, its effects on gut microbial composition have not previously been evaluated. In the present study, we sought to determine how the 10-day oral administration of LGM2605 alters the gut microbiota of mice. Eight-week-old female C57BL/6 mice were treated with either LGM2605 or saline, administered daily via oral gavage over a 10-day treatment period. Upon termination of treatment, mouse cecums (n = 31) were collected, and cecal DNA was isolated. 16S rRNA genes were sequenced and analyzed in Mothur to identify changes in gut microbial composition induced by LGM2605 treatment (v. saline control). We then assessed community composition, performed indicator taxa analysis, and measured alpha and beta diversity. Overall, LGM2605 significantly altered the gut microbiota of mice; we reported alterations in 3 bacterial phyla and 22 genera as a result of treatment. The study here identifies for the first time significant alterations in the gut microbiota of mice following oral administration of LGM2605, in general shifting toward a more anti-inflammatory composition. These findings lay the foundation for future investigations utilizing LGM2605 to control gut dysbiosis and, by extension, systemic inflammation.
LGM2605 是天然亚麻籽木脂素 secoisolariciresinol diglucoside(SDG)的合成版本,具有已知的抗炎和抗氧化特性;然而,其对肠道微生物组成的影响尚未得到评估。在本研究中,我们试图确定 LGM2605 的 10 天口服给药如何改变小鼠的肠道微生物群。8 周龄雌性 C57BL/6 小鼠用 LGM2605 或生理盐水处理,通过口服灌胃在 10 天的治疗期间每天给药。在治疗结束时,收集小鼠盲肠(n=31),并分离盲肠 DNA。使用 Mothur 对 16S rRNA 基因进行测序和分析,以确定 LGM2605 处理(v. 盐水对照)引起的肠道微生物组成变化。然后,我们评估了群落组成,进行了指示性分类群分析,并测量了 alpha 和 beta 多样性。总体而言,LGM2605 显著改变了小鼠的肠道微生物群;我们报告了由于治疗导致的 3 个细菌门和 22 个属的改变。本研究首次确定了 LGM2605 口服给药后小鼠肠道微生物群的显著改变,总体上向更抗炎的组成转变。这些发现为利用 LGM2605 控制肠道菌群失调以及由此引发的全身炎症的未来研究奠定了基础。