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Targeting of Pseudomonas aeruginosa cell surface via GP12, an Escherichia coli specific bacteriophage protein.
Ongwae, George M; Chordia, Mahendra D; Cawley, Jennie L; Dalesandro, Brianna E; Wittenberg, Nathan J; Pires, Marcos M.
Afiliación
  • Ongwae GM; Department of Chemistry, Lehigh University, Bethlehem, PA, 18015, USA.
  • Chordia MD; Department of Chemistry, University of Virginia, Charlottesville, VA, 22904, USA.
  • Cawley JL; Department of Chemistry, Lehigh University, Bethlehem, PA, 18015, USA.
  • Dalesandro BE; Department of Chemistry, University of Virginia, Charlottesville, VA, 22904, USA.
  • Wittenberg NJ; Department of Chemistry, Lehigh University, Bethlehem, PA, 18015, USA.
  • Pires MM; Department of Chemistry, University of Virginia, Charlottesville, VA, 22904, USA. mpires@virginia.edu.
Sci Rep ; 12(1): 721, 2022 01 14.
Article en En | MEDLINE | ID: mdl-35031652
Bacteriophages are highly abundant molecular machines that have evolved proteins to target the surface of host bacterial cells. Given the ubiquity of lipopolysaccharides (LPS) on the outer membrane of Gram-negative bacteria, we reasoned that targeting proteins from bacteriophages could be leveraged to target the surface of Gram-negative pathogens for biotechnological applications. To this end, a short tail fiber (GP12) from the T4 bacteriophage, which infects Escherichia coli (E. coli), was isolated and tested for the ability to adhere to whole bacterial cells. We found that, surprisingly, GP12 effectively bound the surface of Pseudomonas aeruginosa cells despite the established preferred host of T4 for E. coli. In efforts to elucidate why this binding pattern was observed, it was determined that the absence of the O-antigen region of LPS on E. coli improved cell surface tagging. This indicated that O-antigens play a significant role in controlling cell adhesion by T4. Probing GP12 and LPS interactions further using deletions of the enzymes involved in the biosynthetic pathway of LPS revealed the inner core oligosaccharide as a possible main target of GP12. Finally, we demonstrated the potential utility of GP12 for biomedical applications by showing that GP12-modified agarose beads resulted in the depletion of pathogenic bacteria from solution.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Pseudomonas aeruginosa / Proteínas Estructurales Virales / Escherichia coli Idioma: En Revista: Sci Rep Año: 2022 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: Pseudomonas aeruginosa / Proteínas Estructurales Virales / Escherichia coli Idioma: En Revista: Sci Rep Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido