A combination screening to identify enhancers of para-aminosalicylic acid against Mycobacterium tuberculosis

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作者
Jinyeong Heo
Dahae Koh
Minjeong Woo
Doyoon Kwon
Virgínia Carla de Almeida Falcão
Connor Wood
Honggun Lee
Kideok Kim
Inhee Choi
Jichan Jang
Priscille Brodin
David Shum
Vincent Delorme
机构
[1] Institut Pasteur Korea,Screening Discovery Platform
[2] Institut Pasteur Korea,Tuberculosis Research Laboratory
[3] Medicinal Chemistry Platform,Molecular Mechanisms of Antibiotics, Division of Life Science, Research Institute of Life Science, Department of Bio & Medical Big Data (BK21 Four Program)
[4] Institut Pasteur Korea,undefined
[5] Gyeongsang National University,undefined
[6] University of Lille,undefined
[7] CNRS,undefined
[8] INSERM,undefined
[9] CHU Lille,undefined
[10] Institut Pasteur de Lille,undefined
[11] U1019 - UMR 9017 - CIIL - Center for Infection and Immunity of Lille,undefined
来源
Scientific Reports | / 12卷
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摘要
Para-aminosalicylic acid (PAS) is an antibiotic that was largely used for the multi-therapy of tuberculosis in the twentieth century. To try to overcome the inconvenience of its low efficacy and poor tolerance, we searched for novel chemical entities able to synergize with PAS using a combination screening against growing axenic Mycobacterium tuberculosis. The screening was performed at a sub-inhibitory concentration of PAS on a library of about 100,000 small molecules. Selected hit compounds were analyzed by dose–response and further probed with an intracellular macrophage assay. Scaffolds with potential additive effect with PAS are reported, opening interesting prospects for mechanism of action studies. We also report here evidence of a yet unknown bio-activation mechanism, involving activation of pyrido[1,2-a]pyrimidin-4-one (PP) derivatives through the Rv3087 protein.
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