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Modulating bacterial and gut mucosal interactions with engineered biofilm matrix proteins.
Duraj-Thatte, Anna M; Praveschotinunt, Pichet; Nash, Trevor R; Ward, Frederick R; Nguyen, Peter Q; Joshi, Neel S.
Afiliación
  • Duraj-Thatte AM; Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, United States.
  • Praveschotinunt P; John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, United States.
  • Nash TR; Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, United States.
  • Ward FR; John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, United States.
  • Nguyen PQ; Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, United States.
  • Joshi NS; John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, United States.
Sci Rep ; 8(1): 3475, 2018 02 22.
Article en En | MEDLINE | ID: mdl-29472619
Extracellular appendages play a significant role in mediating communication between bacteria and their host. Curli fibers are a class of bacterial fimbria that is highly amenable to engineering. We demonstrate the use of engineered curli fibers to rationally program interactions between bacteria and components of the mucosal epithelium. Commensal E. coli strains were engineered to produce recombinant curli fibers fused to the trefoil family of human cytokines. Biofilms formed from these strains bound more mucins than those producing wild-type curli fibers, and modulated mucin rheology as well. When treated with bacteria producing the curli-trefoil fusions mammalian cells behaved identically in terms of their migration behavior as when they were treated with the corresponding soluble trefoil factors. Overall, this demonstrates the potential utility of curli fibers as a scaffold for the display of bioactive domains and an untapped approach to rationally modulating host-microbe interactions using bacterial matrix proteins.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Ingeniería de Proteínas / Fimbrias Bacterianas / Escherichia coli / Interacciones Huésped-Patógeno Límite: Humans Idioma: En Revista: Sci Rep Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Ingeniería de Proteínas / Fimbrias Bacterianas / Escherichia coli / Interacciones Huésped-Patógeno Límite: Humans Idioma: En Revista: Sci Rep Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido