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Dominique Mahe

Researcher at Zoetis

Publications -  19
Citations -  1138

Dominique Mahe is an academic researcher from Zoetis. The author has contributed to research in topics: Porcine circovirus & Circovirus. The author has an hindex of 9, co-authored 18 publications receiving 1108 citations.

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Differential recognition of ORF2 protein from type 1 and type 2 porcine circoviruses and identification of immunorelevant epitopes.

TL;DR: In order to discriminate between common and type-specific antigens, an immunocytological approach was used following transfections with cloned circovirus DNAs, as well as recombinant proteins expressed by either baculovirus or plasmid vectors.
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Protection of swine against post-weaning multisystemic wasting syndrome (PMWS) by porcine circovirus type 2 (PCV2) proteins.

TL;DR: In this paper, a prime-boost protocol was used to immunize pigs against post-weaning multisystemic wasting syndrome (PMWS), a recently described disease of young pigs.

Protection of swine against Post-weaning Multisystemic Wasting Syndrome (PMWS) by Porcine Circovirus Type 2 (PCV2) proteins.

TL;DR: A specific PCV2 vaccine candidate has been developed, and protection induced by a subunit vaccine was even better than the one induced by DNA vaccine, sincePCV2 replication was completely inhibited.
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Post-weaning multisystemic wasting syndrome (PMWS) in pigs in France: Clinical observations from follow-up studies on affected farms.

TL;DR: A disease affecting weaned pigs and known as Postweaning Multisystemic Wasting Syndrome (PMWS) is described on French farms with a strong litter effect on disease susceptibility and the environment was suspected as an important determining factor for the effect of PMWS in the herds.
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An ORF2 protein-based ELISA for porcine circovirus type 2 antibodies in post-weaning multisystemic wasting syndrome.

TL;DR: The specificity of the ELISA for detection ofPCV2 antibodies was demonstrated in sera from pigs experimentally infected with PCV1, PCV2 and other swine viruses, and the semi-quantitative nature of the test was evaluated versus an immunoperoxidase monolayer assay.