Abstract
Inflammatory bowel disease (IBD) is a spectrum of autoimmune diseases affecting the gastrointestinal tract characterized by a relapsing and remitting course of gut mucosal inflammation. Disease flares can be difficult to predict, and the current practice of IBD disease activity surveillance through endoscopy is invasive and requires medical expertise. Recent advancements in synthetic biology raise the possibility that symbiotic microbes can be engineered to selectively detect disease biomarkers used in current clinical practice. Here, we introduce an engineered probiotic capable of detecting the clinical gold standard IBD biomarker, calprotectin, with sensitivity and specificity in IBD patients. Specifically, we identified a bacterial promoter in the probiotic strain Escherichia coli Nissle 1917 (EcN) which exhibits a specific expression increase in the presence of calprotectin. Using murine models of colitis, we show that the reporter signal is activated in vivo during transit of the GI tract following oral delivery. Furthermore, our engineered probiotic can successfully discriminate human patients with active IBD from those in remission and without IBD using patient stool samples, where the intensity of reporter signal quantitatively tracks with clinical laboratory-measured levels of calprotectin. Our pilot study sets the stage for probiotics that can be engineered to detect fecal calprotectin for precise noninvasive disease activity monitoring in IBD patients.
Original language | English (US) |
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Article number | e2221121120 |
Journal | Proceedings of the National Academy of Sciences of the United States of America |
Volume | 120 |
Issue number | 32 |
DOIs | |
State | Published - 2023 |
Funding
ACKNOWLEDGMENTS. We thank Dr. Walter Chazin at Vanderbilt University for his generous gift of supplying the recombinant human calprotectin used in our studies. We thank the Northwestern University Research Histology and Phenotyping Laboratory for providing histology services by which is supported by NCI P30-CA060553 awarded to the Robert H Lurie Comprehensive Cancer Center. We thank the Shilatifard Laboratory for providing assistance with RNA-seq. We thank the Hope Laboratory and for support provided by Third Coast Center for AIDS Research,an NIH-funded center (P30AI117943),for their assistance with in vivo live animal imagingstudies.We apologizetoourmanycolleagueswhoseworkwecould not include due to space constraints. J.Y.X. is supported by the American Society of Gastrointestinal Endoscopy Research Award (AMGT 3-24-22). A.P. is supported by NIH National Institute of General Medical Sciences grant R35GM147170, NSF CAREER grant MCB-2239567, the Army Research Office (W911NF-19-1-0136), the David and Lucile Packard Foundation (2018-68055), and the Pew Charitable Trusts (2019-A-06953). J.B. is supported by NIH National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) grants R01DK127800, R01DK113011, R01DK090625,R01DK132647,and P30DK020595 and National Institute on Aging grants R01AG065988 and P01AG011412 (to J.B.); C.H.is supported by NIDDKgrant F32DK122675; N.J.W. is supported by NIDDK grant F31DK130589.
Keywords
- inflammatory bowel disease
- microbiome
- probiotics
- synthetic biology
ASJC Scopus subject areas
- General