Department of Surgery, Division of GI, Trauma and Endocrine Surgery, and Burn Research Program, University of Colorado Denver, Anschutz Medical Campus, Aurora, Colorado.
Immunology Graduate Program, University of Colorado Denver, Anschutz Medical Campus, Aurora, Colorado.
Shock. 2020 Jan;53(1):71-77. doi: 10.1097/SHK.0000000000001321.
Maintenance of the commensal bacteria that comprise the gut microbiome is essential to both gut and systemic health. Traumatic injury, such as burn, elicits a number of changes in the gut, including a shift in the composition of the microbiome (dysbiosis), increased gut leakiness, and bacterial translocation into the lymphatic system and bloodstream. These effects are believed to contribute to devastating secondary complications following burn, including pneumonia, acute respiratory distress syndrome, multi-organ failure, and septic shock. Clinical studies demonstrate that advanced age causes a significant increase in mortality following burn, but the role of the gut in this age-dependent susceptibility has not been investigated. In this study, we combined our well-established murine model of scald burn injury with bacterial 16S-rRNA gene sequencing to investigate how burn injury affects the fecal microbiome in aged versus young mice. Of our treatment groups, the most substantial shift in gut microbial populations was observed in aged mice that underwent burn injury. We then profiled antimicrobial peptides (AMPs) in the ileum, and found that burn injury stimulated a 20-fold rise in levels of regenerating islet-derived protein 3 gamma (Reg3γ), a 16-fold rise in regenerating islet-derived protein 3 beta (Reg3β), and an 8-fold rise in Cathelicidin-related antimicrobial peptide (Cramp) in young, but not aged mice. Advanced age alone elicited 5-fold higher levels of alpha defensin-related sequence1 (Defa-rs1) in the ileum, but this increase was lost following burn. Comparison of bacterial genera abundance and AMP expression across treatment groups revealed distinct correlation patterns between AMPs and individual genera. Our results reveal that burn injury drives microbiome dysbiosis and altered AMP expression in an age-dependent fashion, and highlight potential mechanistic targets contributing to the increased morbidity and mortality observed in elderly burn patients.
维持肠道微生物组中的共生细菌对于肠道和全身健康都是至关重要的。创伤性损伤,如烧伤,会引起肠道的多种变化,包括微生物组组成的改变(失调)、肠道通透性增加以及细菌易位到淋巴系统和血液中。这些影响被认为是导致烧伤后毁灭性的继发性并发症的原因,包括肺炎、急性呼吸窘迫综合征、多器官衰竭和感染性休克。临床研究表明,高龄会显著增加烧伤后的死亡率,但肠道在这种年龄依赖性易感性中的作用尚未得到研究。在这项研究中,我们将我们成熟的烫伤烧伤小鼠模型与细菌 16S-rRNA 基因测序相结合,以研究烧伤如何影响老年和年轻小鼠的粪便微生物组。在我们的治疗组中,观察到烧伤对老年小鼠肠道微生物群的影响最大。然后,我们对回肠中的抗菌肽 (AMP) 进行了分析,发现烧伤刺激了年轻小鼠中再生胰岛衍生蛋白 3 伽马 (Reg3γ) 水平升高 20 倍、再生胰岛衍生蛋白 3 贝塔 (Reg3β) 升高 16 倍和 Cathelicidin-related antimicrobial peptide (Cramp) 升高 8 倍,但在老年小鼠中没有观察到这种变化。单独的高龄导致回肠中 alpha 防御素相关序列 1 (Defa-rs1) 的水平升高了 5 倍,但在烧伤后这种增加消失了。对细菌属丰度和 AMP 表达进行比较,揭示了 AMP 与单个属之间存在独特的相关模式。我们的研究结果表明,烧伤损伤以年龄依赖的方式导致微生物组失调和 AMP 表达改变,并突出了导致老年烧伤患者发病率和死亡率增加的潜在机制靶点。