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Proof of concept for the reduction of classical swine fever infection in pigs by a novel viral polymerase inhibitor.

Vrancken, Robert
Paeshuyse, Jan
Puerstinger, Gerhard
Rozenski, Jef
Wright, Matthew
Le Potier, Marie-Frédérique
Neyts, Johan
Koenen, F.
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Abstract

5-[(4-bromophenyl)methyl]-2-phenyl-5H-imidazo[4,5-c]pyridine (BPIP) is a representative of a class of imidazopyridines with potent in vitro antiviral activity against pestiviruses including classical swine fever virus (CSFV). This study analysed whether the lead compound, BPIP, was able to reduce virus replication in infected piglets. The compound, administered in feed, was readily bioavailable and was well tolerated. Eight specific-pathogen-free pigs received a daily dose of 75 mg kg(-1) (mixed in feed) for a period of 15 consecutive days, starting 1 day before infection with the CSFV field isolate Wingene. BPIP-treated pigs developed a short, transient viraemia (one animal remained negative) and leukopenia (three animals did not develop leukopenia). Virus titres at peak viraemia (7 days post-infection) were markedly lower (approximately 1000-fold) than in untreated animals (P=0.00005) and the viral genome load in blood was also significantly lower (P

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2009-06-01
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Peer reviewed scientific article
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Administration, Oral, Animals, Antiviral Agents, Classical Swine Fever, Classical swine fever virus, Imidazoles, Leukopenia, Palatine Tonsil, Pyridines, Swine, Viral Load, Viremia
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