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A high-content image-based drug screen of clinical compounds against cell transmission of adenovirus.


ABSTRACT: Human adenoviruses (HAdVs) are fatal to immuno-suppressed individuals, but no effective anti-HAdV therapy is available. Here, we present a novel image-based high-throughput screening (HTS) platform, which scores the full viral replication cycle from virus entry to dissemination of progeny and second-round infections. We analysed 1,280 small molecular weight compounds of the Prestwick Chemical Library (PCL) for interference with HAdV-C2 infection in a quadruplicate, blinded format, and performed robust image analyses and hit filtering. We present the entire set of the screening data including all images, image analyses and data processing pipelines. The data are made available at the Image Data Resource (IDR, idr0081). Our screen identified Nelfinavir mesylate as an inhibitor of HAdV-C2 multi-round plaque formation, but not single round infection. Nelfinavir has been FDA-approved for anti-retroviral therapy in humans. Our results underscore the power of image-based full cycle infection assays in identifying viral inhibitors with clinical potential.

SUBMITTER: Georgi F 

PROVIDER: S-EPMC7423605 | biostudies-literature | 2020 Aug

REPOSITORIES: biostudies-literature

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A high-content image-based drug screen of clinical compounds against cell transmission of adenovirus.

Georgi Fanny F   Kuttler Fabien F   Murer Luca L   Andriasyan Vardan V   Witte Robert R   Yakimovich Artur A   Turcatti Gerardo G   Greber Urs F UF  

Scientific data 20200812 1


Human adenoviruses (HAdVs) are fatal to immuno-suppressed individuals, but no effective anti-HAdV therapy is available. Here, we present a novel image-based high-throughput screening (HTS) platform, which scores the full viral replication cycle from virus entry to dissemination of progeny and second-round infections. We analysed 1,280 small molecular weight compounds of the Prestwick Chemical Library (PCL) for interference with HAdV-C2 infection in a quadruplicate, blinded format, and performed  ...[more]

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