TY - JOUR
T1 - Discovery of a New Antibiotic Demethoxytetronasin Using a Dual-Sided Agar Plate Assay (DAPA)
AU - Lee, Jung Ho
AU - Ma, Rui
AU - Nguyen, Linh
AU - Khan, Shahebraj
AU - Qader, Mallique
AU - Mpofu, Enock
AU - Shetye, Gauri
AU - Krull, Nyssa K.
AU - Augustinović, Mario
AU - Omarsdottir, Sesselja
AU - Cho, Sanghyun
AU - Franzblau, Scott G.
AU - Murphy, Brian T.
N1 - Publisher Copyright: © 2023 The Authors. Published by American Chemical Society.
PY - 2023/8/11
Y1 - 2023/8/11
N2 - For over a century, researchers have cultured microorganisms together on solid support─typically agar─in order to observe growth inhibition via antibiotic production. These simple bioassays have been critical to both academic researchers that study antibiotic production in microorganisms and to the pharmaceutical industry’s global effort to discover drugs. Despite the utility of agar assays to researchers around the globe, several limitations have prevented their widespread adoption in advanced high-throughput compound discovery and dereplication campaigns. To address a list of specific shortcomings, we developed the dual-sided agar plate assay (DAPA), which exists in a 96-well plate format, allows microorganisms to compete through opposing sides of a solid support in individual wells, is amenable to high-throughput screening and automation, is reusable, and is low-cost. Herein, we validate the use of DAPA as a tool for drug discovery and show its utility to discover new antibiotic natural products. From the screening of 217 bacterial isolates on multiple nutrient media against 3 pathogens, 55 hits were observed, 9 known antibiotics were dereplicated directly from agar plugs, and a new antibiotic, demethoxytetronasin (1), was isolated from a Streptomyces sp. These results demonstrate that DAPA is an effective, accessible, and low-cost tool to screen, dereplicate, and prioritize bacteria directly from solid support in the front end of antibiotic discovery pipelines.
AB - For over a century, researchers have cultured microorganisms together on solid support─typically agar─in order to observe growth inhibition via antibiotic production. These simple bioassays have been critical to both academic researchers that study antibiotic production in microorganisms and to the pharmaceutical industry’s global effort to discover drugs. Despite the utility of agar assays to researchers around the globe, several limitations have prevented their widespread adoption in advanced high-throughput compound discovery and dereplication campaigns. To address a list of specific shortcomings, we developed the dual-sided agar plate assay (DAPA), which exists in a 96-well plate format, allows microorganisms to compete through opposing sides of a solid support in individual wells, is amenable to high-throughput screening and automation, is reusable, and is low-cost. Herein, we validate the use of DAPA as a tool for drug discovery and show its utility to discover new antibiotic natural products. From the screening of 217 bacterial isolates on multiple nutrient media against 3 pathogens, 55 hits were observed, 9 known antibiotics were dereplicated directly from agar plugs, and a new antibiotic, demethoxytetronasin (1), was isolated from a Streptomyces sp. These results demonstrate that DAPA is an effective, accessible, and low-cost tool to screen, dereplicate, and prioritize bacteria directly from solid support in the front end of antibiotic discovery pipelines.
KW - Streptomyces sp
KW - antibiotic bioassay
KW - demethoxytetronasin
KW - dual-sided agar plate assay (DAPA)
KW - tetronasin
UR - https://www.scopus.com/pages/publications/85166773368
U2 - 10.1021/acsinfecdis.3c00171
DO - 10.1021/acsinfecdis.3c00171
M3 - Article
C2 - 37450563
SN - 2373-8227
VL - 9
SP - 1593
EP - 1601
JO - ACS Infectious Diseases
JF - ACS Infectious Diseases
IS - 8
ER -