Integrative Systems Biology Program, U.S. Army Center for Environmental Health Research, Fort Detrick, Maryland, USA.
Advanced Biomedical Computing Center, Frederick National Laboratory for Cancer Research, Fort Detrick, Maryland, USA.
Appl Environ Microbiol. 2018 Oct 17;84(21). doi: 10.1128/AEM.00978-18. Print 2018 Nov 1.
The experimental pathophysiology of organophosphorus (OP) chemical exposure has been extensively reported. Here, we describe an altered fecal bacterial biota and urine metabolome following intoxication with soman, a lipophilic G class chemical warfare nerve agent. Nonanesthetized Sprague-Dawley male rats were subcutaneously administered soman at 0.8 (subseizurogenic) or 1.0 (seizurogenic) of the 50% lethal dose (LD) and evaluated for signs of toxicity. Animals were stratified based on seizing activity to evaluate effects of soman exposure on fecal bacterial biota and urine metabolites. Soman exposure reshaped fecal bacterial biota by altering , , , , and genera of the and phyla, some of which are known to hydrolyze OP chemicals. However, analogous changes were not observed in the bacterial biota of the ileum, which remained the same irrespective of dose or seizing status of animals after soman intoxication. However, at 75 days after soman exposure, the bacterial biota stabilized and no differences were observed between groups. Interestingly, in considering just the seizing status of animals, we found that the urine metabolomes were markedly different. Leukotriene C, kynurenic acid, 5-hydroxyindoleacetic acid, norepinephrine, and aldosterone were excreted at much higher rates at 72 h in seizing animals, consistent with early multiorgan involvement during soman poisoning. These findings demonstrate the feasibility of using the dysbiosis of fecal bacterial biota in combination with urine metabolome alterations as forensic evidence for presymptomatic OP exposure temporally to enable administration of neuroprotective therapies of the future. The paucity of assays to determine physiologically relevant OP exposure presents an opportunity to explore the use of fecal bacteria as sentinels in combination with urine to assess changes in the exposed host. Recent advances in sequencing technologies and computational approaches have enabled researchers to survey large community-level changes of gut bacterial biota and metabolomic changes in various biospecimens. Here, we profiled changes in fecal bacterial biota and urine metabolome following a chemical warfare nerve agent exposure. The significance of this work is a proof of concept that the fecal bacterial biota and urine metabolites are two separate biospecimens rich in surrogate indicators suitable for monitoring OP exposure. The larger value of such an approach is that assays developed on the basis of these observations can be deployed in any setting with moderate clinical chemistry and microbiology capability. This can enable estimation of the affected radius as well as screening, triage, or ruling out of suspected cases of exposures in mass casualty scenarios, transportation accidents involving hazardous materials, refugee movements, humanitarian missions, and training settings when coupled to an established and validated decision tree with clinical features.
有机磷(OP)化学暴露的实验病理生理学已有广泛报道。在这里,我们描述了沙林(一种亲脂性 G 类化学战神经毒剂)中毒后粪便细菌群和尿液代谢组的变化。非麻醉 Sprague-Dawley 雄性大鼠皮下给予沙林,剂量为 50%致死剂量(LD)的 0.8(无抽搐)或 1.0(抽搐),并评估毒性迹象。根据抽搐活动对动物进行分层,以评估沙林暴露对粪便细菌群和尿液代谢物的影响。沙林暴露通过改变 和 门的 、 、 、 和 属,以及一些已知能水解 OP 化学物质的属,重塑了粪便细菌群。然而,在沙林中毒后,无论动物的剂量或抽搐状态如何,回肠中的细菌群都没有观察到类似的变化。然而,在沙林暴露 75 天后,细菌群稳定下来,各组之间没有差异。有趣的是,仅考虑动物的抽搐状态,我们发现尿液代谢组明显不同。在抽搐动物中,白三烯 C、犬尿氨酸、5-羟吲哚乙酸、去甲肾上腺素和醛固酮在 72 小时时的排泄率更高,这与沙林中毒期间早期多器官受累一致。这些发现表明,使用粪便细菌群的失调以及尿液代谢组的改变作为法医证据来确定 OP 暴露的时间是可行的,这将有助于未来神经保护疗法的应用。目前缺乏用于确定生理相关 OP 暴露的检测方法,这为探索使用粪便细菌作为哨兵与尿液结合来评估暴露宿主的变化提供了机会。测序技术和计算方法的最新进展使研究人员能够在各种生物样本中检测肠道细菌群的大社区水平变化和代谢组变化。在这里,我们研究了化学战神经毒剂暴露后粪便细菌群和尿液代谢组的变化。这项工作的意义在于证明了粪便细菌群和尿液代谢物是两种不同的生物样本,其中富含适合监测 OP 暴露的替代指标。这种方法的更大价值在于,在此基础上开发的检测方法可以在具有中等临床化学和微生物学能力的任何环境中部署。这可以用于估计受影响的半径,以及在大规模伤亡情况下、涉及危险材料的运输事故、难民流动、人道主义任务和训练环境中,对疑似暴露的病例进行筛选、分类或排除,当与具有临床特征的既定和经过验证的决策树结合使用时。