Efficacy of a canarypox-vectored recombinant vaccine expressing the hemagglutinin gene of equine influenza H3N8 virus in the protection of ponies from viral challenge

Jules M. Minke Merial SAS, 254 rue Marcel Mérieux, Lyon, 69007, France.

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Caroline Edlund Toulemonde Merial SAS, 254 rue Marcel Mérieux, Lyon, 69007, France.

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Hervé Coupier Botswana Vaccine Institute, Broadhurst Industrial Site, Lejara Rd Private Bag 0031, Gaborone, Botswana.

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Pierre-Michel Guigal Merial SAS, 254 rue Marcel Mérieux, Lyon, 69007, France.

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Sonia Dinic Merial SAS, 254 rue Marcel Mérieux, Lyon, 69007, France.

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Tracey Sindle Centre for Preventive Medicine, Animal Health Trust, Lanwades Park, Kentford, Newmarket, Suffolk, CB8 7UU, United Kingdom.

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David Jessett Centre for Preventive Medicine, Animal Health Trust, Lanwades Park, Kentford, Newmarket, Suffolk, CB8 7UU, United Kingdom.

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Linda Black Merial Ltd, 115 Transtech Dr, Athens, GA 30601.

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Michel Bublot Merial SAS, 254 rue Marcel Mérieux, Lyon, 69007, France.

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Maria C. Pardo Merial Ltd, 115 Transtech Dr, Athens, GA 30601.

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Jean-Christophe Audonnet Merial SAS, 254 rue Marcel Mérieux, Lyon, 69007, France.

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Abstract

Objective—To determine onset and duration of immunity provided by a 2- or 3-dose series of a new canarypox-vectored recombinant vaccine for equine influenza virus (rCP-EIV vaccine) expressing the hemagglutinin genes of influenza H3N8 virus strains A/eq/Kentucky/94 and A/eq/Newmarket/2/93 in ponies.

Animals—Forty-nine 1- to 3-year-old male Welsh Mountain Ponies that were seronegative for equine influenza virus.

Procedures—Vaccinated and control ponies were challenged with aerosolized influenza virus A/eq/Sussex/89 (H3N8), representative of the Eurasian lineage of circulating influenza viruses. In trial 1, control ponies and ponies that received rCP-EIV vaccine were challenged 2 weeks after completion of the 2-dose primary vaccination program. In trial 2, ponies were challenged 5 months after 2 doses of rCP-EIV vaccine or 1 year after the first boosting dose of rCP-EIV vaccine, administered 5 months after completion of the primary vaccination program. After challenge, ponies were observed daily for clinical signs of influenza and nasal swab specimens were taken to monitor virus excretion.

Results—The challenge reliably produced severe clinical signs consistent with influenza infection in the control ponies, and virus was shed for up to 7 days. The vaccination protocol provided clinical and virologic protection to vaccinates at 2 weeks and 5 months after completion of the primary vaccination program and at 12 months after the first booster.

Conclusion and Clinical Relevance—The rCP-EIV vaccine provided protection of ponies to viral challenge. Of particular importance was the protection at 5 months after the second dose, indicating that this vaccine closes an immunity gap between the second and third vaccination.

Abstract

Objective—To determine onset and duration of immunity provided by a 2- or 3-dose series of a new canarypox-vectored recombinant vaccine for equine influenza virus (rCP-EIV vaccine) expressing the hemagglutinin genes of influenza H3N8 virus strains A/eq/Kentucky/94 and A/eq/Newmarket/2/93 in ponies.

Animals—Forty-nine 1- to 3-year-old male Welsh Mountain Ponies that were seronegative for equine influenza virus.

Procedures—Vaccinated and control ponies were challenged with aerosolized influenza virus A/eq/Sussex/89 (H3N8), representative of the Eurasian lineage of circulating influenza viruses. In trial 1, control ponies and ponies that received rCP-EIV vaccine were challenged 2 weeks after completion of the 2-dose primary vaccination program. In trial 2, ponies were challenged 5 months after 2 doses of rCP-EIV vaccine or 1 year after the first boosting dose of rCP-EIV vaccine, administered 5 months after completion of the primary vaccination program. After challenge, ponies were observed daily for clinical signs of influenza and nasal swab specimens were taken to monitor virus excretion.

Results—The challenge reliably produced severe clinical signs consistent with influenza infection in the control ponies, and virus was shed for up to 7 days. The vaccination protocol provided clinical and virologic protection to vaccinates at 2 weeks and 5 months after completion of the primary vaccination program and at 12 months after the first booster.

Conclusion and Clinical Relevance—The rCP-EIV vaccine provided protection of ponies to viral challenge. Of particular importance was the protection at 5 months after the second dose, indicating that this vaccine closes an immunity gap between the second and third vaccination.

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