Complementary assays helping to overcome challenges for identifying neuraminidase inhibitors

Author:

Richter Martina1,Schumann Lilia1,Walther Elisabeth1,Hoffmann Anja1,Braun Heike1,Grienke Ulrike23,Rollinger Judith M3,von Grafenstein Susanne4,Liedl Klaus R4,Kirchmair Johannes5,Wutzler Peter1,Sauerbrei Andreas1,Schmidtke Michaela1

Affiliation:

1. Department of Virology & Antiviral Therapy, Jena University Hospital, Hans-Knoell-Strasse 2, Jena, Germany

2. Institute of Pharmacy/Pharmacognosy, Center for Molecular Biosciences Innsbruck, University of Innsbruck, Innrain 80–82, Innsbruck, Austria

3. Department of Pharmacognosy, University of Vienna, Althanstrasse 14, Vienna, Austria

4. Institute of General, Inorganic & Theoretical Chemistry, Center for Molecular Biosciences Innsbruck, University of Innsbruck, Innrain 80–82, Innsbruck, Austria

5. Center for Bioinformatics, University of Hamburg, Bundesstrasse 43, Hamburg, Germany

Abstract

ABSTRACT  Aims: In this study, we analyze the challenges involved in detecting novel neuraminidase inhibitors (NAIs) and offer strategies to overcome them with complementary bioassays. Materials & Methods: We investigated the inhibitory activities of NAIs (oseltamivir, zanamivir, DANA, katsumadain A and remazol) as well as non-NAIs (amantadine, nucleozin and rifampicin) on influenzaviral and bacterial (Streptococcus pneumoniae, Clostridium perfringens and Vibrio cholerae) neuraminidases (NAs) with chemiluminescence (CL)- and fluorescence (FL)-based assays. Furthermore, hemagglutination-based NA inhibition assays were established. Results: Our study shows three types of signal interference affecting the readout of biochemical assays: self-FL (katsumadain A and remazol), FL quenching (rifampicin) and CL quenching (rifampicin, remazol, nucleozin and katsumadain A). These challenges were overcome by hemagglutination-based assays. Conclusion: The latter allow a robust performance in discriminating NAIs and non-NAIs.

Publisher

Future Medicine Ltd

Subject

Virology

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