Competitive Fitness of Essential Gene Knockdowns Reveals a Broad-Spectrum Antibacterial Inhibitor of the Cell Division Protein FtsZ

Author:

Hogan Andrew M.1,Scoffone Viola C.2,Makarov Vadim3,Gislason April S.1,Tesfu Haben1,Stietz Maria S.1,Brassinga Ann Karen C.1,Domaratzki Michael4,Li Xuan5,Azzalin Alberto26,Biggiogera Marco2,Riabova Olga3,Monakhova Natalia3,Chiarelli Laurent R.2ORCID,Riccardi Giovanna2,Buroni Silvia2,Cardona Silvia T.17ORCID

Affiliation:

1. Department of Microbiology, University of Manitoba, Winnipeg, Manitoba, Canada

2. Department of Biology and Biotechnology, University of Pavia, Pavia, Italy

3. Federal Research Center Fundamentals of Biotechnology of the Russian Academy of Sciences, Moscow, Russia

4. Department of Computer Science, University of Manitoba, Winnipeg, Manitoba, Canada

5. Department of Mathematics and Statistics, University of Minnesota-Duluth, Duluth, Minnesota, USA

6. Department of Internal Medicine and Therapeutics, University of Pavia, Fondazione IRCCS San Matteo, Pavia, Italy

7. Department of Medical Microbiology and Infectious Disease, University of Manitoba, Winnipeg, Canada

Abstract

To streamline the elucidation of antibacterial compounds’ mechanism of action, comprehensive high-throughput assays interrogating multiple putative targets are necessary. However, current chemogenomic approaches for antibiotic target identification have not fully utilized the multiplexing potential of next-generation sequencing.

Funder

Italian Cystic Fibrosis Foundation

Cystic Fibrosis Canada

Gouvernement du Canada | Canadian Institutes of Health Research

Research Manitoba

Cystic Fibrosis Foundation

Università degli Studi di Pavia

University of Manitoba

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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