Jess Alison T, Eskander George Hany, Vu My H, Michail Sonia
Keck School of Medicine, University of Southern California, Los Angeles, CA 90089, USA.
School of Medicine & Health Sciences, George Washington University, Washington, DC 20052, USA.
Metabolites. 2023 Sep 27;13(10):1039. doi: 10.3390/metabo13101039.
Though antibiotics are the mainstay treatment for , a large population of individuals infected will experience recurrence. In turn, fecal microbiota transplantation (FMT) has emerged as a promising treatment for recurrent infection (rCDI). Mechanistically, by providing a healthy, diverse flora to the infected individual, FMT "resets" the underlying gut microbiome dysbiosis associated with rCDI. A proposed mechanism through which this occurs is via microbiome metabolites such as short-chain fatty acids (SCFAs); however, this has not been previously studied in pediatric patients. Using mass spectroscopy, we quantified pre- and post-transplant levels of acetate, isovalerate, butyrate, formate, and propionate in pediatric patients diagnosed with rCDI ( = 9). We compared pre- and post-transplant levels within the rCDI cohort at 1, 3, 6, and 12 months post-transplant and correlated these levels with healthy controls ( = 19). We witnessed a significant difference in the combined SCFA levels and the individual levels of acetate, butyrate, isovalerate, and propionate in the pre-treatment rCDI cohort compared to the healthy controls. In addition, there was a significant increase in combined SCFA levels at 12 months post-transplant within the rCDI group compared to that of their pre-transplant levels, and, more specifically, acetate, propionate, and isovalerate increased from pre-transplant to 12 months post-transplant. The longitudinal aspect of this study allowed us to identify mechanisms that contribute to the durability of responses to FMT, as well as characterize the unique patterns of short-chain fatty acid level recovery in rCDI pediatric patients.
尽管抗生素是[疾病名称]的主要治疗方法,但大量受感染个体仍会复发。相应地,粪便微生物群移植(FMT)已成为复发性[疾病名称]感染(rCDI)的一种有前景的治疗方法。从机制上讲,通过向受感染个体提供健康、多样的菌群,FMT“重置”了与rCDI相关的潜在肠道微生物群失调。一种推测的发生机制是通过微生物群代谢产物,如短链脂肪酸(SCFAs);然而,此前尚未在儿科患者中进行过研究。我们使用质谱法对9例被诊断为rCDI的儿科患者移植前后乙酸盐、异戊酸盐、丁酸盐、甲酸盐和丙酸盐的水平进行了定量。我们比较了rCDI队列在移植后1、3、6和12个月时移植前后的水平,并将这些水平与19名健康对照者进行了关联。我们发现,与健康对照者相比,治疗前rCDI队列中SCFA的综合水平以及乙酸盐、丁酸盐、异戊酸盐和丙酸盐的个体水平存在显著差异。此外,与移植前水平相比,rCDI组在移植后12个月时SCFA的综合水平显著增加,更具体地说,乙酸盐、丙酸盐和异戊酸盐从移植前到移植后12个月有所增加。这项研究的纵向研究使我们能够确定有助于FMT反应持久性 的机制,并描绘rCDI儿科患者短链脂肪酸水平恢复的独特模式。