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Proc Natl Acad Sci U S A. 2007 July 3; 104(27): 11197–11202.
Published online 2007 June 25. doi: 10.1073/pnas.0704624104.
PMCID: PMC1899193
Applied Biological Sciences
Dispersing biofilms with engineered enzymatic bacteriophage
Timothy K. Lu* and James J. Collins
*Harvard–MIT Division of Health Sciences and Technology, 77 Massachusetts Avenue, Room E25–519, Cambridge, MA 02139; and
Center for BioDynamics and Department of Biomedical Engineering, Boston University, 44 Cummington Street, Boston, MA 02215
To whom correspondence should be addressed. E-mail: jcollins/at/bu.edu
Communicated by Hans Kornberg, Boston University, Boston, MA, May 17, 2007.
Author contributions: T.K.L. and J.J.C. designed research; T.K.L. performed research; T.K.L. contributed new reagents/analytic tools; T.K.L. analyzed data; and T.K.L. and J.J.C. wrote the paper.
Received April 20, 2007.
Abstract
Synthetic biology involves the engineering of biological organisms by using modular and generalizable designs with the ultimate goal of developing useful solutions to real-world problems. One such problem involves bacterial biofilms, which are crucial in the pathogenesis of many clinically important infections and are difficult to eradicate because they exhibit resistance to antimicrobial treatments and removal by host immune systems. To address this issue, we engineered bacteriophage to express a biofilm-degrading enzyme during infection to simultaneously attack the bacterial cells in the biofilm and the biofilm matrix, which is composed of extracellular polymeric substances. We show that the efficacy of biofilm removal by this two-pronged enzymatic bacteriophage strategy is significantly greater than that of nonenzymatic bacteriophage treatment. Our engineered enzymatic phage substantially reduced bacterial biofilm cell counts by ≈4.5 orders of magnitude (≈99.997% removal), which was about two orders of magnitude better than that of nonenzymatic phage. This work demonstrates the feasibility and benefits of using engineered enzymatic bacteriophage to reduce bacterial biofilms and the applicability of synthetic biology to an important medical and industrial problem.
Keywords: phage therapy, synthetic biology