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      Immune responses in pigs infected with porcine reproductive and respiratory syndrome virus (PRRSV)

      research-article
      * , , , ,
      Veterinary Immunology and Immunopathology
      Elsevier Science B.V.
      Porcine reproductive and respiratory syndrome, Antibody, Pig, Lymphocytes, Delayed type hypersensitivity, DMEM, Dubelcco's modified Eagle's medium, DTH, delayed type hypersensitivity, EDTA, ethylene diamine tetra-acetic, ELISA, enzyme-linked immunosorbent assay, FCS, foetal calf serum, FITC, fluorescein isothiocyanate, IPMA, immunoperoxydase monolayer assay, LDH, lactate dehydrogenase, MAbs, monoclonal antibodies, PBMC, peripheral blood mononuclear cells, PBS, phosphate buffer saline, PHA, phytohemagglutinine, PI, post-infection, PRRSV, porcine reproductive and respiratory syndrome, PRV, pseudorabies (Aujesky's disease) virus, RNA, ribonucleotide acid, RPMI, Rosewell Park Memorial Institute, SPF, specific pathogen free, LDV, lactate dehydrogenase-elevating virus, CTLs, cytotoxic T lymphocytes, TCID, tissue culture infective doses, IU, international unit, WBC, white blood cells

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          Abstract

          In three successive experiments, the immune functions of pigs persistently infected with the porcine reproductive and respiratory syndrome virus (PRRSV) have been evaluated. Non-specific immune responses were analyzed over a period of 12 weeks post-infection (PI). In addition, the capacity of PRRSV-infected pigs to develop an efficient immune response against pseudorabies virus (PRV) glycoproteins and to resist to a subsequent virulent challenge was investigated. Our results demonstrate that PRRSV produced minor effects on the immune system of pigs. The skin delayed type hypersensitivity (DTH) in response to phytohemagglutinine injection was slightly diminished one week after challenge, but was restored thereafter. However, three weeks after the infection, the total white blood cell count, and the number of CD2 +, CD8 + and IgM + cells were enhanced. The increase in numbers of CD8 + cells persisted for three consecutive weeks. Serum immunoglobulins in infected pigs also increased by week 3 PI and up to 8 weeks PI. These results show that PRRSV may have stimulating effects on the pig immune system during the phase of long-lasting infection. After immunization with PRV glycoproteins, the production of anti-PRV antibodies and skin DTH response against PRV glycoproteins were not affected. On the contrary, following a virulent PRV challenge, PRRSV-infected pigs developed a better secondary antibody response and their resistance to the infection was as effective as in control pigs. Taken together, our data do not support a systemic immunosuppressive effect of PRRSV, during the persistent phase of infection. Other mechanisms may therefore apply to explain the emergence of secondary infections in endemically infected herds.

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          Most cited references23

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          Molecular Characterization of Porcine Reproductive and Respiratory Syndrome Virus, a Member of the Arterivirus Group

          Porcine reproductive and respiratory syndrome virus (PRRSV)-specific cDNA clones spanning the 3′ terminal 5 kb of the genomic RNA were isolated, sequenced, and used as probes for identification of PRRSV-specific RNAs. The PRRSV genome is a positive-stranded polyadenylated RNA of about 15 kb. In infected cells, a 3′ coterminal nested set of six major subgenomic mRNAs could be demonstrated. Within the 3′ terminal 3.5 kb of the PRRSV genome, six overlapping reading frames (ORFs) were identified, each most likely expressed by one of the subgenomic mRNAs. Amino acid sequence comparisons revealed that the most 3′ terminal ORF (ORF7) encodes the PRRSV nucleocapsid protein with a calculated molecular weight of 14 kDa. It displays 44.8% amino acid identity with the capsid protein of lactate dehydrogenase-elevating virus (LDV) and 23.6% with that of equine arteritis virus (EAV). The product of ORF6, the second 3′ terminal ORF, represents a putative membrane protein and exhibits 53.2 and 27.2% amino acid identity with the corresponding LDV and EAV polypeptides, respectively. Similar to EAV, ORFs 2 through 5 might encode glycosylated viral proteins. The polypeptide deduced from the most 5′ ORF (ORF1b) contains two conserved domains common to EAV and coronavirus polymerases. Genome organization, strategy of gene expression, and the sequence of deduced proteins show that PRRSV belongs to the Arterivirus group of viruses.
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            Antibody-dependent enhancement (ADE) of porcine reproductive and respiratory syndrome virus (PRRSV) infection in pigs.

            Infection of porcine alveolar macrophages by the porcine reproductive and respiratory syndrome virus (PRRSV) was significantly enhanced in vitro by antibody raised against the PRRSV isolate ISU-P (p < 0.01). Increased yields and infection rates were highly correlated (r = 0.95) and the ratio of yield to infection rate was greater than 1.4, suggesting that more than one mechanism was responsible for enhanced infection. Antibody-dependent enhancement (ADE) of infection was also demonstrated in vivo using a completely randomized block design (n = 16). The mean level and duration of viremia were greater (p < 0.05) in pigs injected with subneutralizing amounts of PRRSV-specific IgG prior to virus challenge than in control pigs injected with normal IgG. In contrast, virus replication was significantly (p < 0.01) inhibited in pigs with neutralizing antibody titers of 4 log2. The period of time that subneutralizing levels of antibody can persist and contribute to ADE of PRRSV infection was estimated in 4 pigs injected with PRRSV-specific IgG to yield an initial neutralizing antibody titer of 3.8 log2. Neutralizing activity declined to undetectable levels by day 37 postinjection (PI). ADE activity was first detected in undiluted sera on day 20 PI and persisted through day 62 PI. Western immunoblot analysis of sera collected between days 37 and 62 PI detected antibodies specific for the 15-kDa nucleocapsid and 26-kDa glycosylated envelope proteins. These results strongly suggest that ADE has the potential to contribute to the pathogenesis of PRRSV infection and is mediated by antibody specific for the 26-kDa envelope protein.
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              Interaction between Streptococcus suis serotype 2 and porcine reproductive and respiratory syndrome virus in specific pathogen-free piglets.

              Secondary specific pathogen-free (sSPF) piglets were inoculated intranasally with Streptococcus suis serotype 2 alone, porcine reproductive and respiratory syndrome virus (PRRSV) alone, or with PRRSV followed by S suis. Uninfected piglets were used as controls. Pigs inoculated with PRRSV (ATCC VR-2332) followed by challenge with a virulent strain (87555) of S suis serotype 2 developed clinical signs, suppurative meningitis and large numbers of S suis in their tissues, including the brain and meninges. Pigs inoculated with PRRSV alone, S suis (87555) alone, or with PRRSV and the DH5 strain of S suis serotype 2 (lacking a protein associated with virulence) and the uninfected piglets did not develop clinical signs or lesions or have large numbers of bacteria in their tissues. The results suggest that PRRSV predisposes sSPF pigs to infection and disease caused by virulent S suis serotype 2. Co-infection of piglets with PRRSV and a virulent strain of S suis may provide a useful model for the study of S suis septicaemia and meningitis.
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                Author and article information

                Journal
                Vet Immunol Immunopathol
                Vet. Immunol. Immunopathol
                Veterinary Immunology and Immunopathology
                Elsevier Science B.V.
                0165-2427
                1873-2534
                10 September 1998
                16 February 1998
                10 September 1998
                : 61
                : 1
                : 49-66
                Affiliations
                Centre National d'Etudes Vétérinaires et Alimentaires, Unité de Virologie et Immunologie Porcines, BP 53, F-22440 Ploufragan, France
                Author notes
                [* ]Corresponding author. Tel.: +33 2 96 76 01 30; fax: +33 2 96 78 68 61; e-mail: emmanuel.albina.cneva@zoopole.asso.fr
                Article
                S0165-2427(97)00134-7
                10.1016/S0165-2427(97)00134-7
                7119871
                9613472
                654d1731-630e-49e9-a080-2034e72c3ca4
                Copyright © 1998 Elsevier Science B.V. All rights reserved.

                Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.

                History
                : 22 September 1997
                Categories
                Article

                Veterinary medicine
                porcine reproductive and respiratory syndrome,antibody,pig,lymphocytes,delayed type hypersensitivity,dmem, dubelcco's modified eagle's medium,dth, delayed type hypersensitivity,edta, ethylene diamine tetra-acetic,elisa, enzyme-linked immunosorbent assay,fcs, foetal calf serum,fitc, fluorescein isothiocyanate,ipma, immunoperoxydase monolayer assay,ldh, lactate dehydrogenase,mabs, monoclonal antibodies,pbmc, peripheral blood mononuclear cells,pbs, phosphate buffer saline,pha, phytohemagglutinine,pi, post-infection,prrsv, porcine reproductive and respiratory syndrome,prv, pseudorabies (aujesky's disease) virus,rna, ribonucleotide acid,rpmi, rosewell park memorial institute,spf, specific pathogen free,ldv, lactate dehydrogenase-elevating virus,ctls, cytotoxic t lymphocytes,tcid, tissue culture infective doses,iu, international unit,wbc, white blood cells

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