Department of Surgery and Sepsis and Critical Illness Research Center, University of Florida College of Medicine, Gainesville, FL. Electronic address: https://twitter.com/jen_munley.
Department of Surgery and Sepsis and Critical Illness Research Center, University of Florida College of Medicine, Gainesville, FL. Electronic address: https://twitter.com/LaurenKelly_MD.
Surgery. 2023 Dec;174(6):1453-1462. doi: 10.1016/j.surg.2023.08.023. Epub 2023 Oct 11.
Preclinical studies of the gut microbiome after severe traumatic injury have demonstrated severe dysbiosis in males, with sex-specific microbial differences up to 2 days after injury. However, the impact of host sex on injury-driven dysbiosis over time remains unknown. We hypothesized that sex-specific differences in intestinal microbiome diversity and composition after traumatic injury with and without stress would persist after 7 days.
Male and proestrus female Sprague-Dawley rats (n = 8/group) were subjected to either polytrauma (lung contusion, hemorrhagic shock, cecectomy, bifemoral pseudofractures), polytrauma plus chronic restraint stress, or naïve controls. The fecal microbiome was measured on days 0, 3, and 7 using 16S rRNA sequencing and Quantitative Insights into Microbial Ecology bioinformatics analyses. Microbial alpha-diversity (Chao1 and Shannon indices) and beta-diversity were assessed. Analyses were performed in GraphPad and "R," with significance defined as P < .05.
Polytrauma and polytrauma plus chronic restraint stress reduced alpha-diversity (Chao1, Shannon) within 3 days postinjury, which persisted up to day 7 in both sexes; polytrauma and polytrauma plus chronic restraint stress females had significantly decreased Chao1 compared to male counterparts at day 7 (P = .02). At day 7, the microbiome composition in polytrauma females had higher proportion of Mucispirillum, whereas polytrauma plus chronic restraint stress males demonstrated elevated abundance of Ruminococcus and Akkermansia.
Multicompartmental trauma induces intestinal dysbiosis that is sex-specific with persistence of decreased diversity and unique "pathobiome" signatures in females after 1 week. These findings underline sex as an important biological variable that may influence variable host-specific responses and outcomes after severe trauma and critical illness. This underscores the need to consider precision medicine strategies to ameliorate these outcomes.
严重创伤后肠道微生物组的临床前研究表明,男性存在严重的生态失调,损伤后 2 天内存在特定于性别的微生物差异。然而,宿主性别对随时间推移的创伤驱动的生态失调的影响尚不清楚。我们假设,创伤后无论是否存在应激,雄性和发情前期雌性大鼠肠道微生物组多样性和组成的性别特异性差异将在 7 天后持续存在。
雄性和动情前期雌性 Sprague-Dawley 大鼠(n=8/组)分别接受多器官创伤(肺挫伤、失血性休克、盲肠切除术、双侧假骨折)、多器官创伤加慢性束缚应激或对照处理。在 0、3 和 7 天使用 16S rRNA 测序和定量微生物生态分析(QIIME)进行粪便微生物组分析。评估微生物 α-多样性(Chao1 和 Shannon 指数)和 β-多样性。使用 GraphPad 和“R”进行分析,显著性定义为 P <.05。
多器官创伤和多器官创伤加慢性束缚应激在损伤后 3 天内降低了 α-多样性(Chao1、Shannon),这种情况持续到 7 天,两性均如此;与雄性相比,多器官创伤和多器官创伤加慢性束缚应激的雌性在第 7 天的 Chao1 明显降低(P=.02)。在第 7 天,多器官创伤雌性的微生物组中 Mucispirillum 的比例更高,而多器官创伤加慢性束缚应激的雄性则表现出 Ruminococcus 和 Akkermansia 的丰度增加。
多器官创伤导致肠道生态失调,具有性别特异性,女性在 1 周后多样性持续降低,并具有独特的“病理生物组”特征。这些发现强调了性别作为一个重要的生物学变量,可能会影响严重创伤和危重病后宿主特异性反应和结局的变异性。这突显了需要考虑精准医疗策略来改善这些结局。