Dual engineered bacteria improve inflammatory bowel disease in mice.

Yong-Qi Wu, Zhen-Ping Zou, Ying Zhou, Bang-Ce Ye
Author Information
  1. Yong-Qi Wu: Laboratory of Biosystems and Microanalysis, State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai, 200237, China.
  2. Zhen-Ping Zou: Laboratory of Biosystems and Microanalysis, State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai, 200237, China.
  3. Ying Zhou: Laboratory of Biosystems and Microanalysis, State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai, 200237, China. zhouying@ecust.edu.cn. ORCID
  4. Bang-Ce Ye: Laboratory of Biosystems and Microanalysis, State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai, 200237, China. bcye@ecust.edu.cn.

Abstract

Currently, there are many different therapies available for inflammatory bowel disease (IBD), including engineered live bacterial therapeutics. However, most of these studies focus on producing a single therapeutic drug using individual bacteria, which may cause inefficacy. The use of dual drugs can enhance therapeutic effects. However, expressing multiple therapeutic drugs in one bacterial chassis increases the burden on the bacterium and hinders good secretion and expression. Therefore, a dual-bacterial, dual-drug expression system allows for the introduction of two probiotic chassis and enhances both therapeutic and probiotic effects. In this study, we constructed a dual bacterial system to simultaneously neutralize pro-inflammatory factors and enhance the anti-inflammatory pathway. These bacteria for therapy consist of Escherichia coli Nissle 1917 that expressed and secreted anti-TNF-α nanobody and IL-10, respectively. The oral administration of genetically engineered bacteria led to a decrease in inflammatory cell infiltration in colon and a reduction in the levels of pro-inflammatory cytokines. Additionally, the administration of engineered bacteria did not markedly aggravate gut fibrosis and had a moderating effect on intestinal microbes. This system proposes a dual-engineered bacterial drug combination treatment therapy for inflammatory bowel disease, which provides a new approach to intervene and treat IBD. KEY POINTS: • The paper discusses the effects of using dual engineered bacteria on IBD • Prospects of engineered bacteria in the clinical treatment of IBD.

Keywords

References

  1. PLoS Pathog. 2010 Jul 22;6(7):e1001010 [PMID: 20661475]
  2. Crit Rev Food Sci Nutr. 2019;59(19):3227-3236 [PMID: 30373382]
  3. Infect Immun. 2004 Oct;72(10):5750-8 [PMID: 15385474]
  4. Cell Host Microbe. 2023 Apr 12;31(4):634-649.e8 [PMID: 37003258]
  5. Clin Transl Gastroenterol. 2016 Jan 07;7:e135 [PMID: 26741065]
  6. Clin Exp Immunol. 1995 Jun;100(3):452-6 [PMID: 7774055]
  7. BMC Microbiol. 2021 Oct 16;21(1):279 [PMID: 34654370]
  8. Nat Commun. 2019 Dec 6;10(1):5580 [PMID: 31811125]
  9. Nat Biotechnol. 2022 Aug;40(8):1259-1269 [PMID: 35301496]
  10. Carbohydr Polym. 2022 Aug 1;289:119410 [PMID: 35483832]
  11. Infect Immun. 2006 Jul;74(7):4075-82 [PMID: 16790781]
  12. Gut. 2004 Nov;53(11):1617-23 [PMID: 15479682]
  13. Biomed Pharmacother. 2023 Jan;157:114081 [PMID: 36481399]
  14. FEMS Microbiol Lett. 2016 Oct;363(19): [PMID: 27619890]
  15. Adv Mater. 2020 Aug;32(34):e2002406 [PMID: 32686247]
  16. Lancet Gastroenterol Hepatol. 2023 Apr;8(4):307-320 [PMID: 36738762]
  17. Curr Opin Biotechnol. 2020 Aug;64:199-209 [PMID: 32603961]
  18. Clin Gastroenterol Hepatol. 2006 May;4(5):621-30 [PMID: 16678077]
  19. ACS Synth Biol. 2021 May 21;10(5):1132-1142 [PMID: 33908255]
  20. Adv Mater. 2021 Sep;33(38):e2102580 [PMID: 34347325]
  21. Cell Host Microbe. 2023 Feb 8;31(2):199-212.e5 [PMID: 36758520]
  22. Science. 2000 Aug 25;289(5483):1352-5 [PMID: 10958782]
  23. Mol Syst Biol. 2017 Apr 3;13(4):923 [PMID: 28373240]
  24. Free Radic Biol Med. 2006 Jul 1;41(1):106-19 [PMID: 16781459]
  25. Trends Pharmacol Sci. 2022 Sep;43(9):772-786 [PMID: 35232591]
  26. Gastroenterology. 2017 Dec;153(6):1504-1516.e2 [PMID: 28827067]
  27. Lancet. 2002 May 4;359(9317):1541-9 [PMID: 12047962]
  28. Annu Rev Immunol. 2001;19:683-765 [PMID: 11244051]
  29. Semin Immunol. 2021 Feb;52:101425 [PMID: 33272897]
  30. Mucosal Immunol. 2010 Jan;3(1):49-56 [PMID: 19794409]
  31. Anat Rec (Hoboken). 2012 Jun;295(6):922-7 [PMID: 22539421]
  32. Biotechnol J. 2020 Oct;15(10):e2000155 [PMID: 32770635]

Grants

  1. 22134003/National Natural Science Foundation of China
  2. 2020YFA0908800/Key Technologies Research and Development Program
  3. 2021YFC2101500/Key Technologies Research and Development Program
  4. 2023YFF1204500/the National Key R&D Program of China
  5. 2023M741176/the China Postdoctoral Science Foundation

MeSH Term

Animals
Inflammatory Bowel Diseases
Mice
Escherichia coli
Probiotics
Interleukin-10
Tumor Necrosis Factor-alpha
Disease Models, Animal
Genetic Engineering
Gastrointestinal Microbiome
Mice, Inbred C57BL
Colon
Cytokines
Anti-Inflammatory Agents

Chemicals

Interleukin-10
Tumor Necrosis Factor-alpha
Cytokines
IL10 protein, mouse
Anti-Inflammatory Agents

Word Cloud

Created with Highcharts 10.0.0bacteriaengineeredinflammatoryboweldiseaseIBDbacterialtherapeuticdualeffectssystemHoweverdrugusingdrugsenhancechassisexpressionprobioticpro-inflammatorytherapycoliNissle1917nanobodyIL-10administrationtreatmentCurrentlymanydifferenttherapiesavailableincludinglivetherapeuticsstudiesfocusproducingsingleindividualmaycauseinefficacyusecanexpressingmultipleoneincreasesburdenbacteriumhindersgoodsecretionThereforedual-bacterialdual-drugallowsintroductiontwoenhancesstudyconstructedsimultaneouslyneutralizefactorsanti-inflammatorypathwayconsistEscherichiaexpressedsecretedanti-TNF-αrespectivelyoralgeneticallyleddecreasecellinfiltrationcolonreductionlevelscytokinesAdditionallymarkedlyaggravategutfibrosismoderatingeffectintestinalmicrobesproposesdual-engineeredcombinationprovidesnewapproachintervenetreatKEYPOINTS:paperdiscussesProspectsclinicalDualimprovemiceEAnti-TNF-αEngineeredInflammatory

Similar Articles

Cited By