High-throughput screening for novel inhibitors of Neisseria gonorrhoeae penicillin-binding protein 2.

The increasing prevalence of N. gonorrhoeae strains exhibiting decreased susceptibility to third-generation cephalosporins and the recent isolation of two distinct strains with high-level resistance to cefixime or ceftriaxone heralds the possible demise of β-lactam antibiotics as effective treatment...

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Main Authors: Alena Fedarovich, Kevin A Djordjevic, Shauna M Swanson, Yuri K Peterson, Robert A Nicholas, Christopher Davies
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3458020?pdf=render
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spelling doaj-4ab2958792474f6a83da680e8a5b545f2020-11-25T00:23:37ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0179e4491810.1371/journal.pone.0044918High-throughput screening for novel inhibitors of Neisseria gonorrhoeae penicillin-binding protein 2.Alena FedarovichKevin A DjordjevicShauna M SwansonYuri K PetersonRobert A NicholasChristopher DaviesThe increasing prevalence of N. gonorrhoeae strains exhibiting decreased susceptibility to third-generation cephalosporins and the recent isolation of two distinct strains with high-level resistance to cefixime or ceftriaxone heralds the possible demise of β-lactam antibiotics as effective treatments for gonorrhea. To identify new compounds that inhibit penicillin-binding proteins (PBPs), which are proven targets for β-lactam antibiotics, we developed a high-throughput assay that uses fluorescence polarization (FP) to distinguish the fluorescent penicillin, Bocillin-FL, in free or PBP-bound form. This assay was used to screen a 50,000 compound library for potential inhibitors of N. gonorrhoeae PBP 2, and 32 compounds were identified that exhibited >50% inhibition of Bocillin-FL binding to PBP 2. These included a cephalosporin that provided validation of the assay. After elimination of compounds that failed to exhibit concentration-dependent inhibition, the antimicrobial activity of the remaining 24 was tested. Of these, 7 showed antimicrobial activity against susceptible and penicillin- or cephalosporin-resistant strains of N. gonorrhoeae. In molecular docking simulations using the crystal structure of PBP 2, two of these inhibitors docked into the active site of the enzyme and each mediate interactions with the active site serine nucleophile. This study demonstrates the validity of a FP-based assay to find novel inhibitors of PBPs and paves the way for more comprehensive high-throughput screening against highly resistant strains of N. gonorrhoeae. It also provides a set of lead compounds for optimization of anti-gonococcal agents.http://europepmc.org/articles/PMC3458020?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Alena Fedarovich
Kevin A Djordjevic
Shauna M Swanson
Yuri K Peterson
Robert A Nicholas
Christopher Davies
spellingShingle Alena Fedarovich
Kevin A Djordjevic
Shauna M Swanson
Yuri K Peterson
Robert A Nicholas
Christopher Davies
High-throughput screening for novel inhibitors of Neisseria gonorrhoeae penicillin-binding protein 2.
PLoS ONE
author_facet Alena Fedarovich
Kevin A Djordjevic
Shauna M Swanson
Yuri K Peterson
Robert A Nicholas
Christopher Davies
author_sort Alena Fedarovich
title High-throughput screening for novel inhibitors of Neisseria gonorrhoeae penicillin-binding protein 2.
title_short High-throughput screening for novel inhibitors of Neisseria gonorrhoeae penicillin-binding protein 2.
title_full High-throughput screening for novel inhibitors of Neisseria gonorrhoeae penicillin-binding protein 2.
title_fullStr High-throughput screening for novel inhibitors of Neisseria gonorrhoeae penicillin-binding protein 2.
title_full_unstemmed High-throughput screening for novel inhibitors of Neisseria gonorrhoeae penicillin-binding protein 2.
title_sort high-throughput screening for novel inhibitors of neisseria gonorrhoeae penicillin-binding protein 2.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description The increasing prevalence of N. gonorrhoeae strains exhibiting decreased susceptibility to third-generation cephalosporins and the recent isolation of two distinct strains with high-level resistance to cefixime or ceftriaxone heralds the possible demise of β-lactam antibiotics as effective treatments for gonorrhea. To identify new compounds that inhibit penicillin-binding proteins (PBPs), which are proven targets for β-lactam antibiotics, we developed a high-throughput assay that uses fluorescence polarization (FP) to distinguish the fluorescent penicillin, Bocillin-FL, in free or PBP-bound form. This assay was used to screen a 50,000 compound library for potential inhibitors of N. gonorrhoeae PBP 2, and 32 compounds were identified that exhibited >50% inhibition of Bocillin-FL binding to PBP 2. These included a cephalosporin that provided validation of the assay. After elimination of compounds that failed to exhibit concentration-dependent inhibition, the antimicrobial activity of the remaining 24 was tested. Of these, 7 showed antimicrobial activity against susceptible and penicillin- or cephalosporin-resistant strains of N. gonorrhoeae. In molecular docking simulations using the crystal structure of PBP 2, two of these inhibitors docked into the active site of the enzyme and each mediate interactions with the active site serine nucleophile. This study demonstrates the validity of a FP-based assay to find novel inhibitors of PBPs and paves the way for more comprehensive high-throughput screening against highly resistant strains of N. gonorrhoeae. It also provides a set of lead compounds for optimization of anti-gonococcal agents.
url http://europepmc.org/articles/PMC3458020?pdf=render
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