From the Department of Surgery and Sepsis and Critical Illness Research Center (J.A.M., L.S.K., E.E.P., K.B.K., P.S.C., G.S.G., P.A.E., A.M.M.), University of Florida College of Medicine, Gainesville, Florida; Pathogenesis, LLC (E.M.W.), Gainesville, Florida; and Department of Nutrition and Integrative Physiology (R.N.), Florida State University College of Health and Human Sciences, Tallahassee, Florida.
J Trauma Acute Care Surg. 2023 Jan 1;94(1):15-22. doi: 10.1097/TA.0000000000003803. Epub 2022 Oct 7.
Previous animal models have demonstrated altered gut microbiome after mild traumatic injury; however, the impact of injury severity and critical illness is unknown. We hypothesized that a rodent model of severe multicompartmental injuries and chronic stress would demonstrate microbiome alterations toward a "pathobiome" characterized by an overabundance of pathogenic organisms, which would persist 1 week after injury.
Male Sprague-Dawley rats (n = 8 per group) were subjected to either multiple injuries (PT) (lung contusion, hemorrhagic shock, cecectomy, and bifemoral pseudofractures), PT plus daily chronic restraint stress for 2 hours (PT/CS), or naive controls. Fecal microbiome was measured on days 0, 3, and 7 using high-throughput 16S rRNA sequencing and Quantitative Insights Into Microbial Ecology 2 bioinformatics analysis. Microbial α diversity was assessed using Chao1 and Shannon indices, and β diversity with principle coordinate analysis. Intestinal permeability was evaluated by plasma occludin; ileum and descending colon tissues were reviewed for injury. Analyses were performed in GraphPad (GraphPad Software, La Jolla, CA) and R (R Foundation for Statistical Computing, Vienna, Austria), with significance defined as p < 0.05.
There were significant alterations in β diversity at day 3 and between all groups. By day 3, both PT and PT/CS demonstrated significantly depleted bacterial diversity (Chao1) ( p = 0.01 and p = 0.001, respectively) versus naive, which persisted up to day 7 in PT/CS only ( p = 0.001). Anaerostipes and Rothia dominated PT and Lactobacillus bloomed in PT/CS cohorts by day 7. Plasma occludin was significantly elevated in PT/CS compared with naive ( p = 0.04), and descending colon of both PT and PT/CS showed significantly higher injury compared with naive ( p = 0.005, p = 0.006).
Multiple injuries with and without chronic stress induces significant alterations in microbiome diversity and composition within 3 days; these changes are more prominent and persist for 1 week postinjury with stress. This rapid and persistent transition to a "pathobiome" phenotype represents a critical phenomenon that may influence outcomes after severe trauma and critical illness.
先前的动物模型表明,轻度创伤后肠道微生物组会发生改变;然而,受伤严重程度和危重病的影响尚不清楚。我们假设,严重多部位损伤和慢性应激的啮齿动物模型会表现出微生物组向以过度丰富的病原体为特征的“病理生物组”的改变,这种改变在受伤后 1 周内仍然存在。
雄性 Sprague-Dawley 大鼠(每组 8 只)分别接受多处损伤(PT)(肺挫伤、失血性休克、盲肠切除术和双侧股骨假性骨折)、PT 加每日慢性束缚应激 2 小时(PT/CS)或未受伤对照。使用高通量 16S rRNA 测序和定量微生物生态系统分析(Quantitative Insights Into Microbial Ecology 2,QIIME2)在第 0、3 和 7 天测量粪便微生物组。使用 Chao1 和 Shannon 指数评估微生物 α 多样性,用主坐标分析评估 β 多样性。通过血浆闭合蛋白评估肠道通透性;评估回肠和降结肠组织损伤。使用 GraphPad(GraphPad Software,La Jolla,CA)和 R(R 基金会,维也纳,奥地利)进行分析,定义显著性为 p < 0.05。
第 3 天和所有组之间的β多样性均有显著改变。第 3 天,PT 和 PT/CS 两组的细菌多样性(Chao1)明显减少(p = 0.01 和 p = 0.001),与未受伤组相比,PT/CS 组直到第 7 天仍保持减少(p = 0.001)。Anaerostipes 和 Rothia 在 PT 中占主导地位,Lactobacillus 在 PT/CS 组中在第 7 天大量繁殖。PT/CS 组的血浆闭合蛋白明显高于未受伤组(p = 0.04),PT 和 PT/CS 的降结肠与未受伤组相比均显示出更高的损伤(p = 0.005,p = 0.006)。
伴有或不伴有慢性应激的多发性损伤在 3 天内引起微生物组多样性和组成的显著改变;这些变化在应激后 1 周内更为明显且持续存在。这种快速而持久的向“病理生物组”表型的转变是一个关键现象,可能会影响严重创伤和危重病的结局。