结肠活体诊断的多层安全框架

Sonia Mecacci, Lucía Torregrosa-Barragán, Enrique Asin-Garcia, Robert W. Smith
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摘要

导读:结直肠癌是全球第二大致命癌症。目前的筛查方法检出率低,经常出现假阳性结果,导致漏诊或不必要的结肠镜检查。为了解决这个问题,瓦赫宁根大学iGEM团队从2022年开始开发了“结肠直肠”,这是一种结肠直肠癌的活体诊断工具。根据合成生物学方法,该项目使用了一种工程大肠杆菌Nissle 1917菌株,该菌株能够与肿瘤细胞结合,检测两种不同的癌症生物标志物,并在粪便中分泌可观察到的彩色蛋白质。由于在体内使用转基因细菌,预防性生物安全措施包括在三级安全设计策略中。结果:第一个遗传保障通过对结肠内膜中丰富的粘蛋白实施营养不良,确保了对结肠环境的活体诊断。为此,合成的嵌合受体被生成,以确保必需基因在粘蛋白存在下的表达。第二种策略限制了工程细菌在人体中的生存能力,防止在开放环境中增殖。在低于37℃的温度下,使用温度敏感的灭活开关诱导细菌细胞死亡。第三种生物控制策略是作为紧急终止开关安装的,以便在任何时候停止结肠直肠试验。通过crispr - cas介导的DNA降解诱导高度基因毒性反应,触发大肠杆菌尼瑟尔细胞死亡。讨论:虽然工程微生物在人类中的应用尚未成为现实,但我们多层策略的安全性考虑为未来生活诊断工具的发展提供了一个框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multilayered safety framework for living diagnostics in the colon
Introduction: Colorectal cancer is the second most deadly cancer worldwide. Current screening methods have low detection rates and frequently provide false positive results, leading to missed diagnoses or unnecessary colonoscopies. To tackle this issue, the Wageningen UR iGEM team from 2022 developed “Colourectal”, a living diagnostic tool for colorectal cancer. Following a synthetic biology approach, the project used an engineered Escherichia coli Nissle 1917 strain capable of binding to tumour cells that detects two distinct cancer biomarkers, and secretes a coloured protein observable in stool. Due to the utilization of genetically modified bacteria in vivo , precautionary biosafety measures were included within a three level safe-by-design strategy. Results: The first genetic safeguard ensured confinement of the living diagnostic to the colon environment by implementing auxotrophy to mucin that is abundant in the colon lining. For this, a synthetic chimeric receptor was generated to ensure expression of essential genes in the presence of mucin. The second strategy limited the viability of the engineered bacteria to the human body, preventing proliferation in open environments. The use of a temperature sensitive kill switch induced bacterial cell death at temperatures below 37°C. The third biocontainment strategy was installed as an emergency kill switch to stop the Colourectal test at any point. By inducing a highly genotoxic response through CRISPR-Cas-mediated DNA degradation, cell death of E. coli Nissle is triggered. Discussion: While the use of engineered microorganisms in human applications is not yet a reality, the safety considerations of our multi-layered strategy provide a framework for the development of future living diagnostic tools.
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