TarO-specific inhibitors of wall teichoic acid biosynthesis restore β-lactam efficacy against methicillin-resistant staphylococci.

نویسندگان

  • Sang Ho Lee
  • Hao Wang
  • Marc Labroli
  • Sandra Koseoglu
  • Paul Zuck
  • Todd Mayhood
  • Charles Gill
  • Paul Mann
  • Xinwei Sher
  • Sookhee Ha
  • Shu-Wei Yang
  • Mihir Mandal
  • Christine Yang
  • Lianzhu Liang
  • Zheng Tan
  • Paul Tawa
  • Yan Hou
  • Reshma Kuvelkar
  • Kristine DeVito
  • Xiujuan Wen
  • Jing Xiao
  • Michelle Batchlett
  • Carl J Balibar
  • Jenny Liu
  • Jianying Xiao
  • Nicholas Murgolo
  • Charles G Garlisi
  • Payal R Sheth
  • Amy Flattery
  • Jing Su
  • Christopher Tan
  • Terry Roemer
چکیده

The widespread emergence of methicillin-resistant Staphylococcus aureus (MRSA) has dramatically eroded the efficacy of current β-lactam antibiotics and created an urgent need for new treatment options. We report an S. aureus phenotypic screening strategy involving chemical suppression of the growth inhibitory consequences of depleting late-stage wall teichoic acid biosynthesis. This enabled us to identify early-stage pathway-specific inhibitors of wall teichoic acid biosynthesis predicted to be chemically synergistic with β-lactams. We demonstrated by genetic and biochemical means that each of the new chemical series discovered, herein named tarocin A and tarocin B, inhibited the first step in wall teichoic acid biosynthesis (TarO). Tarocins do not have intrinsic bioactivity but rather demonstrated potent bactericidal synergy in combination with broad-spectrum β-lactam antibiotics against diverse clinical isolates of methicillin-resistant staphylococci as well as robust efficacy in a murine infection model of MRSA. Tarocins and other inhibitors of wall teichoic acid biosynthesis may provide a rational strategy to develop Gram-positive bactericidal β-lactam combination agents active against methicillin-resistant staphylococci.

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عنوان ژورنال:
  • Science translational medicine

دوره 8 329  شماره 

صفحات  -

تاریخ انتشار 2016