4.1 Article

The Tetracycline Destructases: A Novel Family of Tetracycline-Inactivating Enzymes

Journal

CHEMISTRY & BIOLOGY
Volume 22, Issue 7, Pages 888-897

Publisher

CELL PRESS
DOI: 10.1016/j.chembiol.2015.05.017

Keywords

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Funding

  1. NIH Director's New Innovator Award
  2. National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
  3. National Institute of General Medical Sciences of NIH (NIGMS) [DP2DK098089, R01GM099538]
  4. Children's Discovery Institute [MD-II-2011-117]
  5. Washington University in St. Louis
  6. NIGMS [T32HG000045, T32GM007067]
  7. National Science Foundation [DBI-0922879, DGE-1143954]
  8. National Human Genome Research Institute (NHGRI)

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Enzymes capable of inactivating tetracycline are paradoxically rare compared with enzymes that inactivate other natural-product antibiotics. We describe a family of flavoenzymes, previously unrecognizable as resistance genes, which are capable of degrading tetracycline antibiotics. From soil functional metagenomic selections, we discovered nine genes that confer high-level tetracycline resistance by enzymatic inactivation. We also demonstrate that a tenth enzyme, an uncharacterized homolog in the human pathogen Legionella longbeachae, similarly inactivates tetracycline. These enzymes catalyze the oxidation of tetracyclines in vitro both by known mechanisms and via previously undescribed activity. Tetracycline-inactivation genes were identified in diverse soil types, encompass substantial sequence diversity, and are adjacent to genes implicated in horizontal gene transfer. Because tetracycline inactivation is scarcely observed in hospitals, these enzymes may fill an empty niche in pathogenic organisms, and should therefore be monitored for their dissemination potential into the clinic.

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