Literature DB >> 35170959

Rapid Inhibitor Discovery by Exploiting Synthetic Lethality.

Jacob D Muscato1, Heidi G Morris1, Aaron Mychack1, Mithila Rajagopal1,2, Vadim Baidin2, Anthony R Hesser1, Wonsik Lee1, Kemal İnecik1, Laura J Wilson3, Christina M Kraml3, Timothy C Meredith1, Suzanne Walker1,2.   

Abstract

Synthetic lethality occurs when inactivation of two genes is lethal but inactivation of either single gene is not. This phenomenon provides an opportunity for efficient compound discovery. Using differential growth screens, one can identify biologically active compounds that selectively inhibit proteins within the synthetic lethal network of any inactivated gene. Here, based purely on synthetic lethalities, we identified two compounds as the only possible inhibitors of Staphylococcus aureus lipoteichoic acid (LTA) biosynthesis from a screen of ∼230,000 compounds. Both compounds proved to inhibit the glycosyltransferase UgtP, which assembles the LTA glycolipid anchor. UgtP is required for β-lactam resistance in methicillin-resistant S. aureus (MRSA), and the inhibitors restored sensitivity to oxacillin in a highly resistant S. aureus strain. As no other compounds were pursued as possible LTA glycolipid assembly inhibitors, this work demonstrates the extraordinary efficiency of screens that exploit synthetic lethality to discover compounds that target specified pathways. The general approach should be applicable not only to other bacteria but also to eukaryotic cells.

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Year:  2022        PMID: 35170959      PMCID: PMC9012225          DOI: 10.1021/jacs.1c12697

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   16.383


  58 in total

1.  Essential Bacillus subtilis genes.

Authors:  K Kobayashi; S D Ehrlich; A Albertini; G Amati; K K Andersen; M Arnaud; K Asai; S Ashikaga; S Aymerich; P Bessieres; F Boland; S C Brignell; S Bron; K Bunai; J Chapuis; L C Christiansen; A Danchin; M Débarbouille; E Dervyn; E Deuerling; K Devine; S K Devine; O Dreesen; J Errington; S Fillinger; S J Foster; Y Fujita; A Galizzi; R Gardan; C Eschevins; T Fukushima; K Haga; C R Harwood; M Hecker; D Hosoya; M F Hullo; H Kakeshita; D Karamata; Y Kasahara; F Kawamura; K Koga; P Koski; R Kuwana; D Imamura; M Ishimaru; S Ishikawa; I Ishio; D Le Coq; A Masson; C Mauël; R Meima; R P Mellado; A Moir; S Moriya; E Nagakawa; H Nanamiya; S Nakai; P Nygaard; M Ogura; T Ohanan; M O'Reilly; M O'Rourke; Z Pragai; H M Pooley; G Rapoport; J P Rawlins; L A Rivas; C Rivolta; A Sadaie; Y Sadaie; M Sarvas; T Sato; H H Saxild; E Scanlan; W Schumann; J F M L Seegers; J Sekiguchi; A Sekowska; S J Séror; M Simon; P Stragier; R Studer; H Takamatsu; T Tanaka; M Takeuchi; H B Thomaides; V Vagner; J M van Dijl; K Watabe; A Wipat; H Yamamoto; M Yamamoto; Y Yamamoto; K Yamane; K Yata; K Yoshida; H Yoshikawa; U Zuber; N Ogasawara
Journal:  Proc Natl Acad Sci U S A       Date:  2003-04-07       Impact factor: 11.205

Review 2.  Wall teichoic acids of gram-positive bacteria.

Authors:  Stephanie Brown; John P Santa Maria; Suzanne Walker
Journal:  Annu Rev Microbiol       Date:  2013       Impact factor: 15.500

Review 3.  Targeting virulence: a new paradigm for antimicrobial therapy.

Authors:  Anne E Clatworthy; Emily Pierson; Deborah T Hung
Journal:  Nat Chem Biol       Date:  2007-09       Impact factor: 15.040

Review 4.  Structure-function relationships of membrane-associated GT-B glycosyltransferases.

Authors:  David Albesa-Jové; David Giganti; Mary Jackson; Pedro M Alzari; Marcelo E Guerin
Journal:  Glycobiology       Date:  2013-11-18       Impact factor: 4.313

5.  Murgocil is a highly bioactive staphylococcal-specific inhibitor of the peptidoglycan glycosyltransferase enzyme MurG.

Authors:  Paul A Mann; Anna Müller; Li Xiao; Pedro M Pereira; Christine Yang; Sang Ho Lee; Hao Wang; Joanna Trzeciak; Jonathan Schneeweis; Margarida Moreira Dos Santos; Nicholas Murgolo; Xinwei She; Charles Gill; Carl J Balibar; Marc Labroli; Jing Su; Amy Flattery; Brad Sherborne; Richard Maier; Christopher M Tan; Todd Black; Kamil Onder; Stacia Kargman; Frederick J Monsma; Mariana G Pinho; Tanja Schneider; Terry Roemer
Journal:  ACS Chem Biol       Date:  2013-09-05       Impact factor: 5.100

6.  Staphylococcus aureus subverts cutaneous defense by D-alanylation of teichoic acids.

Authors:  Maren Simanski; Regine Gläser; Bente Köten; Ulf Meyer-Hoffert; Stefanie Wanner; Christopher Weidenmaier; Andreas Peschel; Jürgen Harder
Journal:  Exp Dermatol       Date:  2013-04       Impact factor: 3.960

7.  Synthesis of glycerol phosphate lipoteichoic acid in Staphylococcus aureus.

Authors:  Angelika Gründling; Olaf Schneewind
Journal:  Proc Natl Acad Sci U S A       Date:  2007-05-03       Impact factor: 11.205

8.  Lipoteichoic acid polymer length is determined by competition between free starter units.

Authors:  Anthony R Hesser; Kaitlin Schaefer; Wonsik Lee; Suzanne Walker
Journal:  Proc Natl Acad Sci U S A       Date:  2020-11-10       Impact factor: 11.205

9.  Discovery of a small molecule that blocks wall teichoic acid biosynthesis in Staphylococcus aureus.

Authors:  Jonathan G Swoboda; Timothy C Meredith; Jennifer Campbell; Stephanie Brown; Takashi Suzuki; Tobias Bollenbach; Amy J Malhowski; Roy Kishony; Michael S Gilmore; Suzanne Walker
Journal:  ACS Chem Biol       Date:  2009-10-16       Impact factor: 5.100

10.  Structure-based mechanism of lipoteichoic acid synthesis by Staphylococcus aureus LtaS.

Authors:  Duo Lu; Mirka E Wörmann; Xiaodong Zhang; Olaf Schneewind; Angelika Gründling; Paul S Freemont
Journal:  Proc Natl Acad Sci U S A       Date:  2009-01-23       Impact factor: 11.205

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