Lung pathogenicity of European genotype 3 strain porcine reproductive and respiratory syndrome virus (PRRSV) differs from that of subtype 1 strains

•We studied pathological responses after infection with EU PRRSV subtype 3 or 1.•EU subtype 3 PRRSV is more pneumovirulent that subtype 1.•EU subtype 3 induced a stronger early inflammatory response than subtype 1.•EU subtype 3 was cleared faster from tissues than subtype 1. Porcine reproductive and...

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Veröffentlicht in:Veterinary microbiology 2014-11, Vol.174 (1-2), p.127-138
Hauptverfasser: Weesendorp, Eefke, Rebel, Johanna M.J., Popma-De Graaf, Ditta J., Fijten, Helmi P.D., Stockhofe-Zurwieden, Norbert
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container_end_page 138
container_issue 1-2
container_start_page 127
container_title Veterinary microbiology
container_volume 174
creator Weesendorp, Eefke
Rebel, Johanna M.J.
Popma-De Graaf, Ditta J.
Fijten, Helmi P.D.
Stockhofe-Zurwieden, Norbert
description •We studied pathological responses after infection with EU PRRSV subtype 3 or 1.•EU subtype 3 PRRSV is more pneumovirulent that subtype 1.•EU subtype 3 induced a stronger early inflammatory response than subtype 1.•EU subtype 3 was cleared faster from tissues than subtype 1. Porcine reproductive and respiratory syndrome (PRRS) is difficult to control due to a high mutation rate of the PRRS virus (PRRSV) and the emergence of virulent strains. The objective of this study was to analyse early and late pathological responses in the respiratory tract after infection with the European PRRSV subtype 3 strain Lena in comparison to two European PRRSV subtype 1 strains: Belgium A and Lelystad-Ter Huurne (LV). For each virus strain, groups of twelve pigs were inoculated, and four pigs per group were euthanized at days 3, 7 and 35 post-infection (p.i.) for consecutive examination. Infection with strain Lena resulted in a more severe disease than with the subtype 1 strains, an inflammatory response within the first week of infection with expression of IL-1α in the lung and lymph node, and an influx of neutrophils and monocytes in bronchoalveolar lavage fluid (BALF). Infection with strain Belgium A or LV resulted in mild or no pathology within the first week of infection, but inflammatory cell influx in the lung interstititium was increased at the end of the experiment at day 35 p.i. At five weeks p.i., all strains induced a higher percentage of cytotoxic T cells and higher levels of IFN-γ producing cells in BALF. This might have contributed to clearance of virus. In general, subtype 3 strain Lena induced a stronger early inflammatory response which led to more severe clinical disease and pathology. On the other hand, this may have supported an enhanced or faster clearance of virus in tissues, compared to subtype 1 strains.
doi_str_mv 10.1016/j.vetmic.2014.09.010
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Porcine reproductive and respiratory syndrome (PRRS) is difficult to control due to a high mutation rate of the PRRS virus (PRRSV) and the emergence of virulent strains. The objective of this study was to analyse early and late pathological responses in the respiratory tract after infection with the European PRRSV subtype 3 strain Lena in comparison to two European PRRSV subtype 1 strains: Belgium A and Lelystad-Ter Huurne (LV). For each virus strain, groups of twelve pigs were inoculated, and four pigs per group were euthanized at days 3, 7 and 35 post-infection (p.i.) for consecutive examination. Infection with strain Lena resulted in a more severe disease than with the subtype 1 strains, an inflammatory response within the first week of infection with expression of IL-1α in the lung and lymph node, and an influx of neutrophils and monocytes in bronchoalveolar lavage fluid (BALF). Infection with strain Belgium A or LV resulted in mild or no pathology within the first week of infection, but inflammatory cell influx in the lung interstititium was increased at the end of the experiment at day 35 p.i. At five weeks p.i., all strains induced a higher percentage of cytotoxic T cells and higher levels of IFN-γ producing cells in BALF. This might have contributed to clearance of virus. In general, subtype 3 strain Lena induced a stronger early inflammatory response which led to more severe clinical disease and pathology. 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Infection with strain Belgium A or LV resulted in mild or no pathology within the first week of infection, but inflammatory cell influx in the lung interstititium was increased at the end of the experiment at day 35 p.i. At five weeks p.i., all strains induced a higher percentage of cytotoxic T cells and higher levels of IFN-γ producing cells in BALF. This might have contributed to clearance of virus. In general, subtype 3 strain Lena induced a stronger early inflammatory response which led to more severe clinical disease and pathology. 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Rebel, Johanna M.J. ; Popma-De Graaf, Ditta J. ; Fijten, Helmi P.D. ; Stockhofe-Zurwieden, Norbert</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c566t-b6346e4e9aec416f30deb082732ba408a802c3fc81b590d2255400cd6f0721b73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>Belgium</topic><topic>Body Temperature</topic><topic>Bronchoalveolar Lavage Fluid - virology</topic><topic>Flow Cytometry - veterinary</topic><topic>Genetic subtypes</topic><topic>Genotype</topic><topic>Immune response</topic><topic>Immunohistochemistry - veterinary</topic><topic>Immunophenotyping - veterinary</topic><topic>Inflammation - pathology</topic><topic>Lung - pathology</topic><topic>Lung - virology</topic><topic>Monocytes - immunology</topic><topic>Pathogenesis</topic><topic>Porcine Reproductive and Respiratory Syndrome - immunology</topic><topic>Porcine Reproductive and Respiratory Syndrome - pathology</topic><topic>Porcine reproductive and respiratory syndrome virus</topic><topic>Porcine respiratory and reproductive syndrome virus</topic><topic>Porcine respiratory and reproductive syndrome virus - genetics</topic><topic>Porcine respiratory and reproductive syndrome virus - pathogenicity</topic><topic>Reverse Transcriptase Polymerase Chain Reaction - veterinary</topic><topic>Species Specificity</topic><topic>Statistics, Nonparametric</topic><topic>Swine</topic><topic>Viremia - veterinary</topic><topic>Virulence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Weesendorp, Eefke</creatorcontrib><creatorcontrib>Rebel, Johanna M.J.</creatorcontrib><creatorcontrib>Popma-De Graaf, Ditta J.</creatorcontrib><creatorcontrib>Fijten, Helmi P.D.</creatorcontrib><creatorcontrib>Stockhofe-Zurwieden, Norbert</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Veterinary microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Weesendorp, Eefke</au><au>Rebel, Johanna M.J.</au><au>Popma-De Graaf, Ditta J.</au><au>Fijten, Helmi P.D.</au><au>Stockhofe-Zurwieden, Norbert</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lung pathogenicity of European genotype 3 strain porcine reproductive and respiratory syndrome virus (PRRSV) differs from that of subtype 1 strains</atitle><jtitle>Veterinary microbiology</jtitle><addtitle>Vet Microbiol</addtitle><date>2014-11-07</date><risdate>2014</risdate><volume>174</volume><issue>1-2</issue><spage>127</spage><epage>138</epage><pages>127-138</pages><issn>0378-1135</issn><eissn>1873-2542</eissn><abstract>•We studied pathological responses after infection with EU PRRSV subtype 3 or 1.•EU subtype 3 PRRSV is more pneumovirulent that subtype 1.•EU subtype 3 induced a stronger early inflammatory response than subtype 1.•EU subtype 3 was cleared faster from tissues than subtype 1. Porcine reproductive and respiratory syndrome (PRRS) is difficult to control due to a high mutation rate of the PRRS virus (PRRSV) and the emergence of virulent strains. The objective of this study was to analyse early and late pathological responses in the respiratory tract after infection with the European PRRSV subtype 3 strain Lena in comparison to two European PRRSV subtype 1 strains: Belgium A and Lelystad-Ter Huurne (LV). For each virus strain, groups of twelve pigs were inoculated, and four pigs per group were euthanized at days 3, 7 and 35 post-infection (p.i.) for consecutive examination. Infection with strain Lena resulted in a more severe disease than with the subtype 1 strains, an inflammatory response within the first week of infection with expression of IL-1α in the lung and lymph node, and an influx of neutrophils and monocytes in bronchoalveolar lavage fluid (BALF). Infection with strain Belgium A or LV resulted in mild or no pathology within the first week of infection, but inflammatory cell influx in the lung interstititium was increased at the end of the experiment at day 35 p.i. At five weeks p.i., all strains induced a higher percentage of cytotoxic T cells and higher levels of IFN-γ producing cells in BALF. This might have contributed to clearance of virus. In general, subtype 3 strain Lena induced a stronger early inflammatory response which led to more severe clinical disease and pathology. On the other hand, this may have supported an enhanced or faster clearance of virus in tissues, compared to subtype 1 strains.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>25301281</pmid><doi>10.1016/j.vetmic.2014.09.010</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Access via ScienceDirect (Elsevier)
subjects Animals
Belgium
Body Temperature
Bronchoalveolar Lavage Fluid - virology
Flow Cytometry - veterinary
Genetic subtypes
Genotype
Immune response
Immunohistochemistry - veterinary
Immunophenotyping - veterinary
Inflammation - pathology
Lung - pathology
Lung - virology
Monocytes - immunology
Pathogenesis
Porcine Reproductive and Respiratory Syndrome - immunology
Porcine Reproductive and Respiratory Syndrome - pathology
Porcine reproductive and respiratory syndrome virus
Porcine respiratory and reproductive syndrome virus
Porcine respiratory and reproductive syndrome virus - genetics
Porcine respiratory and reproductive syndrome virus - pathogenicity
Reverse Transcriptase Polymerase Chain Reaction - veterinary
Species Specificity
Statistics, Nonparametric
Swine
Viremia - veterinary
Virulence
title Lung pathogenicity of European genotype 3 strain porcine reproductive and respiratory syndrome virus (PRRSV) differs from that of subtype 1 strains
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