Lack of antiviral activity of probenecid in vitro and in Syrian golden hamsters

Author:

Box Helen J12,Sharp Joanne12,Pennington Shaun H3ORCID,Kijak Edyta12,Tatham Lee12,Caygill Claire H3,Lopeman Rose C3,Jeffreys Laura N3,Herriott Joanne12,Neary Megan12ORCID,Valentijn Anthony12,Pertinez Henry12,Curley Paul12,Arshad Usman12,Rajoli Rajith K R12ORCID,Jochmans Dirk4,Vangeel Laura4,Neyts Johan4,Chatelain Eric5,Escudié Fanny5ORCID,Scandale Ivan5,Rannard Steve26,Stewart James P7,Biagini Giancarlo A3,Owen Andrew12ORCID

Affiliation:

1. Department of Pharmacology and Therapeutics, Institute of Systems, Molecular and Integrative Biology, University of Liverpool , Liverpool L7 3NY , UK

2. Centre of Excellence in Long-acting Therapeutics (CELT), University of Liverpool , Liverpool L7 3NY , UK

3. Centre for Drugs and Diagnostics, Department of Tropical Disease Biology, Liverpool School of Tropical Medicine , Liverpool L3 5QA , UK

4. KU Leuven, Department of Microbiology, Immunology and Transplantation, Rega Institute, Laboratory of Virology and Chemotherapy , 3000, Leuven, Belgium and the Global Virus Network (GVN), Baltimore, MD , USA

5. Drugs for Neglected Diseases initiative (DNDi), Research and Development, 1202 , Geneva , Switzerland

6. Department of Chemistry, University of Liverpool , Liverpool L7 3NY , UK

7. Department of Infection Biology & Microbiomes, Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool , Liverpool , UK

Abstract

Abstract Objectives Antiviral interventions are required to complement vaccination programmes and reduce the global burden of COVID-19. Prior to initiation of large-scale clinical trials, robust preclinical data to support candidate plausibility are required. This work sought to further investigate the putative antiviral activity of probenecid against SARS-CoV-2. Methods Vero E6 cells were preincubated with probenecid, or control media for 2 h before infection (SARS-CoV-2/Human/Liverpool/REMRQ0001/2020). Probenecid or control media was reapplied, plates reincubated and cytopathic activity quantified by spectrophotometry after 48 h. In vitro human airway epithelial cell (HAEC) assays were performed for probenecid against SARS-CoV-2-VoC-B.1.1.7 (hCoV-19/Belgium/rega-12211513/2020; EPI_ISL_791333, 2020-12-21) using an optimized cell model for antiviral testing. Syrian golden hamsters were intranasally inoculated (SARS-CoV-2 Delta B.1.617.2) 24 h prior to treatment with probenecid or vehicle for four twice-daily doses. Results No observable antiviral activity for probenecid was evident in Vero E6 or HAEC assays. No reduction in total or subgenomic RNA was observed in terminal lung samples (P > 0.05) from hamsters. Body weight of uninfected hamsters remained stable whereas both probenecid- and vehicle-treated infected hamsters lost body weight (P > 0.5). Conclusions These data do not support probenecid as a SARS-CoV-2 antiviral drug.

Funder

COVID-19 supplement to project LONGEVITY

Wellcome Trust

EPSRC

NIH

BBSRC

Medical Research Council

UK Research and Innovation

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology,Microbiology (medical)

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