Buss Marjorie T, Zhu Lian, Kwon Jamie H, Tabor Jeffrey J, Shapiro Mikhail G
Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA, USA.
Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, USA.
Nat Commun. 2025 Aug 25;16(1):7931. doi: 10.1038/s41467-025-62569-1.
Inflammatory bowel diseases (IBD) affect millions of people globally, result in severe symptoms, and are difficult to diagnose and monitor - often necessitating the use of invasive and costly methods such as colonoscopies or endoscopies. Engineered gut bacteria offer a promising alternative due to their ability to persist in the gastrointestinal (GI) tract and sense and respond to specific environmental signals. However, probiotics that have previously been engineered to report on inflammatory and other disease biomarkers in the Gl tract rely on fluorescent or bioluminescent reporters, whose signals cannot be resolved in situ due to the poor penetration of light in tissue, or on colorimetric reporters which rely on plating feces. To overcome this limitation, we introduce probiotic biosensors that can be imaged in situ using ultrasound - a widely available, inexpensive imaging modality providing sub-mm spatial resolution deep inside the body. These biosensors are based on the clinically approved probiotic bacterium E. coli Nissle, which we engineered to transiently colonize the GI tract, sense inflammatory biomarkers, and respond by expressing air-filled sound-scattering protein nanostructures called gas vesicles. After optimizing biomolecular signaling circuits to respond sensitively to the biomarkers thiosulfate and tetrathionate and produce strong and stable ultrasound contrast, we validated our living biosensors in vivo by noninvasively imaging antibiotic-induced inflammation in mice. By connecting cell-based diagnostic agents to ultrasound, these probiotic biosensors will potentially make it easier and cheaper to diagnose and monitor IBD or other GI conditions.
炎症性肠病(IBD)在全球影响着数百万人,会导致严重症状,且难以诊断和监测——通常需要使用侵入性且昂贵的方法,如结肠镜检查或内窥镜检查。工程化肠道细菌是一种有前景的替代方案,因为它们能够在胃肠道(GI)中持续存在,并感知和响应特定的环境信号。然而,以前设计用于报告胃肠道中炎症和其他疾病生物标志物的益生菌依赖于荧光或生物发光报告基因,由于光在组织中的穿透性差,其信号无法在原位解析,或者依赖于粪便平板培养的比色报告基因。为了克服这一限制,我们引入了可以使用超声进行原位成像的益生菌生物传感器——超声是一种广泛可用、价格低廉的成像方式,可在身体内部提供亚毫米级的空间分辨率。这些生物传感器基于临床批准的益生菌大肠杆菌Nissle,我们对其进行工程改造,使其能够短暂定殖于胃肠道,感知炎症生物标志物,并通过表达称为气体囊泡的充满空气的声音散射蛋白纳米结构做出反应。在优化生物分子信号传导回路以对生物标志物硫代硫酸盐和连四硫酸盐敏感响应并产生强烈且稳定的超声造影后,我们通过对小鼠抗生素诱导的炎症进行无创成像,在体内验证了我们的活体生物传感器。通过将基于细胞的诊断试剂与超声连接起来,这些益生菌生物传感器可能会使炎症性肠病或其他胃肠道疾病的诊断和监测变得更容易、更便宜。