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

被引:44
|
作者
Weesendorp, Eefke [1 ]
Rebel, Johanna M. J. [1 ]
Popma-De Graaf, Ditta J. [1 ]
Fijten, Helmi P. D. [1 ]
Stockhofe-Zurwieden, Norbert [1 ]
机构
[1] Cent Vet Inst, Dept Infect Biol, NL-8200 AB Lelystad, Netherlands
关键词
Porcine reproductive and respiratory syndrome virus; Pathogenesis; Immune response; Genetic subtypes; EXPERIMENTALLY INFECTED-PIGS; LELYSTAD VIRUS; IMMUNOLOGICAL RESPONSES; IMMUNE-RESPONSES; SWINE; CELLS; DISEASE; EXPRESSION; CYTOKINES; VIRULENCE;
D O I
10.1016/j.vetmic.2014.09.010
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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-1 alpha 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-gamma 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. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:127 / 138
页数:12
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