在炎症性肠道疾病中发现生物活性微生物基因产物
Yancong Zhang1,2,3, Amrisha Bhosle1,2,3, Sena Bae2,3,4
1Infectious Disease and Microbiome Program, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
研究人员确定了超过34万个可能与炎症性肠道疾病 (IBD) 相关的微生物蛋白家族. 这一发现扩大了对微生物组的理解
科学领域:
- 微生物组研究
- 免疫学
- 生物信息学
背景情况:
- 在炎症性肠道疾病 (IBD) 中,微生物群落及其生物活性化合物受到干扰.
- 很大一部分微生物蛋白质,特别是在肠道中,仍然没有特征,但可能具有生物活性.
研究的目的:
- 系统地确定与IBD肠道炎症相关的潜在生物活性微生物蛋白家族.
- 在功能上描述之前未注释的IBD相关的微生物蛋白质.
主要方法:
- 使用元基因组学,元转录组学和元蛋白组学的组合来识别和优先考虑生物活性微生物蛋白.
- 开发并使用MetaWIBELE工作流程来识别微生物组中的新生物活性元素.
- 通过有针对性的实验验证实预测,包括评估免疫性和生物膜形成.
主要成果:
- 在IBD的背景下确定了超过34万个潜在的生物活性蛋白家族,其中大约一半以前没有被描述.
- 提供了参与宿主微生物相互作用的特定蛋白质的生物活性证据,例如粘附因子和·维尔布兰德样因子.
- 证明了Enterobacteriaceae菌株的差异性免疫性,并确定了von Willebrand因子对象在Bacteroides生物膜形成中的作用.
结论:
- 在多种社区和表型中发现新生物活性元素的MetaWIBELE方法是一种可通用的方法.
- 成千上万的候选微生物蛋白可能与IBD的宿主免疫系统相互作用,提供潜在的治疗点.
- 这项工作扩大了对慢性病中的生物活性基因产品的理解,并为治疗开发提供了一个摘要.
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