Veterinary Research

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PRRSV, the virus p. 11

Janneke J.M. Meulenberg

DOI: https://doi.org/10.1051/vetres:2000054

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Biochemical and molecular analysis of structural proteins of porcine reproductive and respiratory syndrome virus p. 22

S. Dea, C.A. Gagnon, H. Mardassi, B. Pirzadeh and D. Rogan

DOI: https://doi.org/10.1051/vetres:2000013

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PRRSV-macrophage interaction and putative receptors p. 22

H. Nauwynck, X. Duan and M. Pensaert

DOI: https://doi.org/10.1051/vetres:2000035

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Expression of a foreign epitope by porcine reproductive and respiratory syndrome virus p. 23

M.H. Groot Bramel-Verheije, P.J.M. Rottier and J.J.M. Meulenberg

DOI: https://doi.org/10.1051/vetres:2000020

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Structure-function of the nucleocapsid protein of PRRSV North American genotype p. 24

D. Yoo and S. Wootton

DOI: https://doi.org/10.1051/vetres:2000073

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A review of evidence for immunosuppression due to Porcine Reproductive and Respiratory Syndrome Virus p. 27

Trevor W. Drew

DOI: https://doi.org/10.1051/vetres:2000055

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Pig defences against respiratory viruses p. 40

M. Bailey, M.A. Birchall, K. Haverson, K. Gorti and S. Wilson

DOI: https://doi.org/10.1051/vetres:2000006

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Characteristics of the immune response of pigs to PRRS virus p. 41

W. Meier, J. Wheeler, R.J. Husmann, F. Osorio and F.A. Zuckermann

DOI: https://doi.org/10.1051/vetres:2000032

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New strategies in the development of PRRS vaccines. Subunit vaccines and self-limiting vectors, based on defective coronaviruses p. 41

J. Plana-Durán, M. Mourino, E. Viaplana, M. Balasch, I. Casal, M.J. Rodríguez, L. Enjuanes, A. Izeta, S. Alonso and I. Solá

DOI: https://doi.org/10.1051/vetres:2000041

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Phenotypical and functional analysis of macrophages infected with PRRS virus p. 42

L. López-Fuertes, E. Campos, N. Doménech, A. Ezquerra, J.M. Castro, J. Domínguez and F. Alonso

DOI: https://doi.org/10.1051/vetres:2000029

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Passive immunity due to PRRS in vaccinated and unvaccinated sow herds p. 44

C. Dewey and A. Rajic

DOI: https://doi.org/10.1051/vetres:2000016

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Direct cytolytic activity of pbmc from pigs infected with porcine reproductive and respiratory syndrome p. 44

J.N. Samsom, J.J.M. Voermans, M.G.M. de Bruin, E.M.A. van Rooij, J.M.A. Pol and A.T.J. Bianchi

DOI: https://doi.org/10.1051/vetres:2000046

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Ultrastructural pathogenesis of the PRRS virus p. 47

Paloma Suárez

DOI: https://doi.org/10.1051/vetres:2000056

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Pathogenesis of porcine reproductive and respiratory syndrome virus (PRRSV) in gestating sows p. 56

C. Prieto and J.M. Castro

DOI: https://doi.org/10.1051/vetres:2000043

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The pathogenesis of Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) in the boar p. 57

J. Christopher-Hennings

DOI: https://doi.org/10.1051/vetres:2000012

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PRRSV: Study of in vivo cell tropism and virus-induced apoptosis by in situ detection techniques p. 58

J.H. Sur, A.R. Doster, J. Galeota, R.W. Wills and F.A. Osorio

DOI: https://doi.org/10.1051/vetres:2000051

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Virulence of vABV 414, the virus derived from the infectious cDNA clone of the Lelystad virus, for third trimester pregnant gilts p. 59

P.J.G.M. Steverink, J.M.A. Pol, J.N.A. Bos-de Ruijter and J.J.M. Meulenberg

DOI: https://doi.org/10.1051/vetres:2000050

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Effect of vaccination on dual infection with Mycoplasma hyopneumoniae and PRRSV p. 60

E.L. Thacker, P.G. Halbur and B.J. Thacker

DOI: https://doi.org/10.1051/vetres:2000053

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A brief review of procedures and potential problems associated with the diagnosis of porcine reproductive and respiratory syndrome p. 61

William L. Mengeling and Kelly M. Lager

DOI: https://doi.org/10.1051/vetres:2000057

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Diagnosing acute infections of porcine reproductive and respiratory syndrome virus in swine p. 70

K.M. Lager and W.L. Mengeling

DOI: https://doi.org/10.1051/vetres:2000027

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Diagnosis of persistent or prolonged porcine reproductive and respiratory syndrome virus infections p. 71

D. Benfield, J. Nelson, K. Rossow, C. Nelson, M. Steffen and R. Rowland

DOI: https://doi.org/10.1051/vetres:2000007

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Distinction between infections with European and American/vaccine type PRRS virus after vaccination with a modified-live PRRS virus vaccine p. 72

A. Bøtner, B. Strandbygaard, K.J. Sørensen, M.B. Oleksiewicz and T. Storgaard

DOI: https://doi.org/10.1051/vetres:2000009

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Detection of antibodies to porcine reproductive and respiratory syndrome virus (PRRSV) in blended sera or in blood samples collected on filter papers p. 73

E. Hutet, S. Chevallier, M. Eloit, A. Touratier, P. Blanquefort and E. Albina

DOI: https://doi.org/10.1051/vetres:2000023

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Monitoring of PRRSV infection status in swine herds based on analysis of antibodies in meat sample drippings p. 74

S. Mortensen, B. Strandbygaard, A. Bøtner, N. Feld and P. Willeberg

DOI: https://doi.org/10.1051/vetres:2000033

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Development of a serological marker system for epidemiological studies of porcine reproductive and respiratory syndrome virus p. 74

L. Yang, E.A. Nelson, T.M. Weller, K.-J. Yoon, W. Wu and K.B. Platt

DOI: https://doi.org/10.1051/vetres:2000072

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The "colorful" epidemiology of PRRS p. 77

Thomas Blaha

DOI: https://doi.org/10.1051/vetres:2000058

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PRRS in North America, Latin America, and Asia p. 84

C. Dewey

DOI: https://doi.org/10.1051/vetres:2000015

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Seroepidemiology of porcine reproductive and respiratory syndrome virus infection on commercial farms p. 85

H.S. Joo, K. Direksin and Ch. Johnson

DOI: https://doi.org/10.1051/vetres:2000024

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History, occurrence, dynamics and current status of PRRS in Europe p. 86

V.F. Ohlinger, S. Pesch and C. Bischoff

DOI: https://doi.org/10.1051/vetres:2000037

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Prevalence and risk factors for infection with Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) in swine herds in Illinois (USA) p. 87

R.M. Weigel, L.D. Firkins and G. Scherba

DOI: https://doi.org/10.1051/vetres:2000069

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A longitudinal study into the interaction between PRRSV and Mycoplasma hyopneumoniae in finishing pigs p. 88

E. Grosse Beilage and Th. Blaha

DOI: https://doi.org/10.1051/vetres:2000021

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Genetic variations among PRRSV strains isolated in Italy and in Russia p. 89

V.G. Andreyev, A.V. Scherbakov, V.A. Pylnov, A.A. Gusev, P. Cordioli and G. Sala

DOI: https://doi.org/10.1051/vetres:2000003

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Experiences with eradication of Porcine Reproductive and Respiratory Syndrome in Danish swine herds p. 91

M. Andreasen

DOI: https://doi.org/10.1051/vetres:2000002

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Control of Porcine Reproductive and Respiratory Syndrome: the challenge of identifying carrier animals p. 91

J.J. Zimmerman, C.-C. Chang, D. Horter and K.-J. Yoon

DOI: https://doi.org/10.1051/vetres:2000075

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Vaccinology of PRRS p. 92

J.M.A. Pol and P.J.G.M. Steverink

DOI: https://doi.org/10.1051/vetres:2000042

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Elimination of PRRS virus in five pig farms using a test and removal procedure in the breeding herd p. 93

S.A. Dee, T.W. Molitor and R.E. Philips

DOI: https://doi.org/10.1051/vetres:2000014

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Eradication of Porcine Reproductive and Respiratory Syndrome virus in 125 herds in “Pays de la Loire" (France) p. 94

P. Blanquefort and F. Benoit

DOI: https://doi.org/10.1051/vetres:2000008

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The production of PRRS negative pigs from multiple PRRS serologically stable herds over time using segregated early weaning (SEW) p. 95

A.M. Rajic, C.E. Dewey, A.E. Deckert, R.M. Friendship, S.W. Martin and D. Yoo

DOI: https://doi.org/10.1051/vetres:2000044

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Vaccination of MDA positive pigs with a live modified PRRSV vaccine p. 96

P.A.M. van Woensel, K. Liefkens and S. Demaret

DOI: https://doi.org/10.1051/vetres:2000066

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Efficacy of an American and a European serotype PRRSV vaccine after challenge with American and European wild–type strains of the virus p. 97

G.G. Labarque, H.J. Nauwynck, P.A.M. van Woensel, N. Visser and M.B. Pensaert

DOI: https://doi.org/10.1051/vetres:2000026

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Aujeszky's disease (pseudorabies) virus: the virus and molecular pathogenesis - State of the art, June 1999 p. 99

Thomas C. Mettenleiter

DOI: https://doi.org/10.1051/vetres:2000059

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Searching for genes of Aujeszky's disease virus required for neurotropism and virulence p. 116

L.W. Enquist and A.D. Brideau

DOI: https://doi.org/10.1051/vetres:2000018

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Functions of viral glycoproteins in the pathogenesis of Aujeszky's disease virus in pigs p. 116

H. Nauwynck, H. Favoreel and M. Pensaert

DOI: https://doi.org/10.1051/vetres:2000036

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Latency of Aujeszky's disease virus p. 117

F.A. Osorio

DOI: https://doi.org/10.1051/vetres:2000039

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Experimental infection of wild boar with pseudorabies virus isolates of different virulence p. 118

T. Müller, J. Teuffert, R. Zellmer and F.J. Conraths

DOI: https://doi.org/10.1051/vetres:2000034

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Development and evaluation of TaqMan-based PCR assays to quantitate PRV latency p. 119

N. Aleman, A. Vilnis, H. Hill, B. Thacker and R. Maes

DOI: https://doi.org/10.1051/vetres:2000001

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Aujeszky's disease virus: opportunities and challenges p. 121

Federico A. Zuckermann

DOI: https://doi.org/10.1051/vetres:2000060

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DNA vaccine coding for glycoprotein B of PRV induces cytotoxic T cell responses in pigs against PRV p. 132

E.M.A. van Rooij, B.L. Haagmans, H.L. Glansbeek, Y.E. de Visser, W. Boersma and A.T.J. Bianchi

DOI: https://doi.org/10.1051/vetres:2000062

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Mechanisms of protective immunity against Aujeszky's disease virus p. 132

F.A. Zuckermann, S. Martin and R. Husmann

DOI: https://doi.org/10.1051/vetres:2000076

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Effects of cytokines upon the immune response of swine to Aujeszky's disease virus p. 133

S. Martin, P.F. Russell, P.M. Jaqua, S. Grimm, D. Lowery, D. Strom and F.A. Zuckermann

DOI: https://doi.org/10.1051/vetres:2000030

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Enhanced protective response and immuno-adjuvant effects of porcine GM-CSF on DNA vaccination of pigs against Aujeszky's disease virus p. 134

C. Somasundaram, H. Takamatsu, F. Lefèvre and B. Charley

DOI: https://doi.org/10.1051/vetres:2000048

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Genetically improved Aujeszky's disease strain MNC+/10a derived from strain K/61 and testing for safety and potency in pigs p. 135

B. Lomniczi, M. Kelemen and E. Wehmann

DOI: https://doi.org/10.1051/vetres:2000028

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Analysis of protective immunity against PRV infection in pigs using attenuated and inactivated PRV vaccines p. 135

E.M.A. van Rooij, M.G.M. de Bruin, Y.E. de Visser, W. Boersma and A.T.J. Bianchi

DOI: https://doi.org/10.1051/vetres:2000063

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Antibody-induced endocytosis of viral glycoproteins, expressed on pseudorabies virus-infected monocytes protects these cells from complement-mediated lysis p. 136

H.W. Favoreel, H.J. Nauwynck, P. Van Oostveldt and M.B. Pensaert

DOI: https://doi.org/10.1051/vetres:2000019

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Phenotype of IL-2 or pseudorabies virus induced cytolytic cells in the pig p. 137

M.G.M. de Bruin, E.M.A. van Rooij, Y.E. de Visser, J.J.M. Voermans and A.T.J. Bianchi

DOI: https://doi.org/10.1051/vetres:2000010

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Increased immunogenicity of a DNA vaccine encoding pseudorabies virus IE180 protein by co-administration of IL-2 or by delivery in liposomes p. 138

J. Bu, Y. Song, D.J. Burgess and A.E. Garmendia

DOI: https://doi.org/10.1051/vetres:2000011

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Challenges of the final stages of the ADV eradication program p. 141

Maurice Pensaert and Robert B. Morrison

DOI: https://doi.org/10.1051/vetres:2000061

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Risk factors of new Aujeszky's disease virus infection in swine herds in Brittany (France) p. 146

S. Heliez, V. Auvigne and C. Fourichon

DOI: https://doi.org/10.1051/vetres:2000022

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Non-vaccinated subpopulations play a major role in reinfections during eradication programs based on regular vaccination against Aujeszky's disease virus p. 147

V.F. Ohlinger, S. Pesch and I. Hense

DOI: https://doi.org/10.1051/vetres:2000038

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Aujeszky's disease virus (ADV) in mammalian wildlife on swine farms in Illinois (USA): Potential for transmission to non-infected herds p. 148

R.M. Weigel, E.C. Hahn, B. Paszkiet and G. Scherba

DOI: https://doi.org/10.1051/vetres:2000068

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Spatial-temporal dynamics of pseudorabies virus infections in a wild boar population p. 149

T. Selhorst, T. Müller and C. Staubach

DOI: https://doi.org/10.1051/vetres:2000047

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Modelling pseudorabies virus infection supports eradication p. 149

A. Van Nes, M.C.M. De Jong and J.H.M. Verheijden

DOI: https://doi.org/10.1051/vetres:2000064

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Development of a computerised system for animal health management as a part of an eradication program of Aujeszky's disease p. 150

V. Auvigne, T. Berthe, M. Cadou, G. Laudren, A. Kergourlay and D. Taraud

DOI: https://doi.org/10.1051/vetres:2000005

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Progress in eradication and control programmes against Aujeszky's disease (pseudorabies) in France p. 151

P. Vannier, S. Strugar, J.F. Pansart, A Mesplède and M. Le Gal

DOI: https://doi.org/10.1051/vetres:2000065

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The eradication of Aujeszky's disease from pig production in Sweden p. 152

J.Å. Robertsson and M. Wierup

DOI: https://doi.org/10.1051/vetres:2000045

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No Aujeszky's disease or PRRS in Finland p. 153

P.M.-L. Veijalainen and H. Tapiovaara

DOI: https://doi.org/10.1051/vetres:2000067

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Evaluation of Italian Aujeszky's disease control programme in two regions of northern Italy in 1997 p. 154

G. Zanardi, M. Tamba, C. Macchi, L. Alborali and P. Guadagnini

DOI: https://doi.org/10.1051/vetres:2000074

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Progress of the Aujeszky's disease virus eradication programme in Brittany (France) p. 155

V. Auvigne and C. Bougeard

DOI: https://doi.org/10.1051/vetres:2000004

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Current epizootiological status of the Eastern European countries for Aujeszky's disease p. 155

I. Medveczky

DOI: https://doi.org/10.1051/vetres:2000031

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The results of serological monitoring for Aujeszky's disease in pigs performed during the period of 1991-1997 p. 156

Z. Pejsak, A. Mokrzycka and A. Lipowski

DOI: https://doi.org/10.1051/vetres:2000040

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The eradication of Aujeszky's disease in the United States p. 157

A.C. Taft

DOI: https://doi.org/10.1051/vetres:2000052

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Update of the Aujeszky's disease situation in Argentina p. 158

M.G. Echeverria, C.M. Galosi, J.L. Molfese, M.E. Etcheverrigaray, M.R. Pecoraro and E.O. Nosetto

DOI: https://doi.org/10.1051/vetres:2000017

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Effectiveness and costs of different strategies to eradicate Aujeszky's disease virus p. 158

A. Stegeman

DOI: https://doi.org/10.1051/vetres:2000049

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Aujeszky's disease: the position of the European Commission and regulation perspectives p. 159

J.M. Westergaard

DOI: https://doi.org/10.1051/vetres:2000070

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Terminating Aujeszky vaccination in the Netherlands? p. 160

A. De Koeijer and A. Stegeman

DOI: https://doi.org/10.1051/vetres:2000025

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Immunity survey of vaccinated fattening pigs in the North of France p. 161

F. Wolff, G. Juillard, M. Ledru and J. Guillotin

DOI: https://doi.org/10.1051/vetres:2000071

• Abstract