Engineered <i>Bacillus subtilis</i> as Oral Probiotics To Enhance Clearance of Blood Lactate
Elevated lactate concentrations are implicated in various acute and chronic diseases, such as sepsis and mitochondrial dysfunction, respectively. Conversely, ineffective lactate clearance is associated with poor clinical prognoses and high mortality in these diseases. While several groups have proposed using small molecule inhibitors and enzyme replacement to reduce circulating lactate, there are few practical and effective ways to manage this condition. Recent evidence suggests that lactate is exchanged between the systemic circulation and the gut, allowing bidirectional modulation between the gut microbiota and peripheral tissues. Inspired by these findings, this work seeks to engineer spore-forming probiotic <i>Bacillus subtilis</i> strains to enable intestinal delivery of lactate oxidase as a therapeutic enzyme. After strain optimization, we showed that oral administration of engineered <i>B. subtilis</i> spores to the gut of mice reduced the level of blood lactate in two different mouse models involving exogenous challenge or pharmacologic perturbation without disrupting gut microbiota composition, liver function, or immune homeostasis. Taken together, through the oral delivery of engineered probiotic spores to the gastrointestinal tract, our proof-of-concept study offers a practical strategy to aid in the management of disease states with elevated blood lactate and provides a new approach to "knocking down" circulating metabolites to help understand their roles in host physiological and pathological processes.
Authors
- Minmin Yang (ORCID: https://orcid.org/0000-0003-1148-7347)
- Noah Hutchinson
- Peiru Chen (ORCID: https://orcid.org/0009-0006-9369-2377)
- Ningyuan Ye
- Zongqi Wang (ORCID: https://orcid.org/0000-0003-4559-3420)
- Xuesong He (ORCID: https://orcid.org/0000-0002-3333-9188)
- Ming Guan (ORCID: https://orcid.org/0000-0003-0016-2301)
- Jiahe Li
- Ke Zhang (ORCID: https://orcid.org/0000-0001-7982-5758)
- Shaobo Yang (ORCID: https://orcid.org/0009-0006-5257-6775)
- Jianing Yin (ORCID: https://orcid.org/0009-0003-7816-6502)
- Justin D. Crane
- Maria Jennings
- Hania Timek
Institutions
- Northeastern University (US)
- Pfizer (United States) (US)
- University of Michigan (US)
Publication Details
- Journal
- ACS Synthetic Biology
- Published
- 2024-12-31
- DOI
- https://doi.org/10.1021/acssynbio.4c00399
- Citations
- 8
- Primary Topic
- Mitochondrial Function and Pathology
- Type
- article
- Field-Weighted Citation Impact
- 1.87
Funders
- U.S. Department of Health and Human Services
- Nanjing Agricultural University
- Indiana University Bloomington
- National Institute of General Medical Sciences
- National Institute of Biomedical Imaging and Bioengineering
- National Institute of Dental and Craniofacial Research
- Congressionally Directed Medical Research Programs
- DOD Peer Reviewed Cancer Research Program