Engineering tumor-colonizing E. coli Nissle 1917 for detection and treatment of colorectal neoplasia

Candice R. Gurbatri(Columbia University), Georgette Radford(The University of Adelaide), Laura Vrbanac(The University of Adelaide), Jongwon Im(Columbia University), E Thomas(The University of Adelaide), Courtney Coker(Columbia University), Samuel Taylor(Cornell University), YoungUk Jang(Columbia University), Ayelet Sivan(Columbia University), Kyu Y. Rhee(Cornell University), Anas A. Saleh(Cornell University), Tiffany Chien(Columbia University), Fereshteh Zandkarimi(Columbia University), Ioana Lia(Columbia University), Tamsin R.M. Lannagan(The University of Adelaide), Tongtong Wang(South Australian Health and Medical Research Institute), Josephine A. Wright(South Australian Health and Medical Research Institute), Hiroki Kobayashi(South Australian Health and Medical Research Institute), Jia Q. Ng(The University of Adelaide), Matt Lawrence(Royal Adelaide Hospital), Tarik Sammour(Royal Adelaide Hospital), Michelle Thomas(Royal Adelaide Hospital), Mark Lewis(Royal Adelaide Hospital), Lito E. Papanicolas(Flinders University), Joanne Perry(Royal Adelaide Hospital), Tracy Fitzsimmons(Royal Adelaide Hospital), Patricia Kaazan(The University of Adelaide), Amanda Lim(The University of Adelaide), Alexandra M. Stavropoulos(The University of Adelaide), Dion A. Gouskos(The University of Adelaide), Julie Marker, Cheri Ostroff(University of South Australia), Geraint B. Rogers(Flinders University), Nicholas Arpaia(Columbia University Irving Medical Center), Daniel L. Worthley(Brisbane Hand & Upper Limb Research Institute), Susan L. Woods(South Australian Health and Medical Research Institute), Tal Danino(Columbia University Irving Medical Center)
Nature Communications
January 20, 2024
Cited by 161Open Access
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Abstract

Bioengineered probiotics enable new opportunities to improve colorectal cancer (CRC) screening, prevention and treatment. Here, first, we demonstrate selective colonization of colorectal adenomas after oral delivery of probiotic E. coli Nissle 1917 (EcN) to a genetically-engineered murine model of CRC predisposition and orthotopic models of CRC. We next undertake an interventional, double-blind, dual-centre, prospective clinical trial, in which CRC patients take either placebo or EcN for two weeks prior to resection of neoplastic and adjacent normal colorectal tissue (ACTRN12619000210178). We detect enrichment of EcN in tumor samples over normal tissue from probiotic-treated patients (primary outcome of the trial). Next, we develop early CRC intervention strategies. To detect lesions, we engineer EcN to produce a small molecule, salicylate. Oral delivery of this strain results in increased levels of salicylate in the urine of adenoma-bearing mice, in comparison to healthy controls. To assess therapeutic potential, we engineer EcN to locally release a cytokine, GM-CSF, and blocking nanobodies against PD-L1 and CTLA-4 at the neoplastic site, and demonstrate that oral delivery of this strain reduces adenoma burden by ~50%. Together, these results support the use of EcN as an orally-deliverable platform to detect disease and treat CRC through the production of screening and therapeutic molecules.


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