Antigen distribution of porcine reproductive and respiratory syndrome virus (PRRSV) in Thai crossbred pigs using immunohistochemistry

Twenty, 3-week-old, crossbred pigs from a herd free from porcine reproductive and respiratory syndrome virus (PRRSV) were inoculated intranasally and intramusculary (1 ml each 10**(2.5) TCID sub(50)/ml) with Thai PRRSV isolates of the US genotype (0NP1) (n=9) or the EU genotype (02SB3) (n=8). Three...

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Veröffentlicht in:Wētchasān sattawaphāet 2004-03
Hauptverfasser: Porntip Laohasittikul(Chulalongkorn University, Bangkok (Thailand). Faculty of Veterinary Sciences), Nuttapon Boonarpha(Chulalongkorn University, Bangkok (Thailand). Faculty of Veterinary Sciences), Yongyut Pongprapachuen(Chulalongkorn University, Bangkok (Thailand). Faculty of Veterinary Sciences), Sawang Kesdangsakonwut(Chulalongkorn University, Bangkok (Thailand). Faculty of Veterinary Sciences. Department of Veterinary Pathology. Veterinary Pathology Unit), Supradit Wangnaitham(Chulalongkorn University, Bangkok (Thailand). Faculty of Veterinary Sciences. Department of Veterinary Pathology. Veterinary Pathology Unit), Roongroje Thanawongnuwech(Chulalongkorn University, Bangkok (Thailand). Faculty of Veterinary Sciences. Department of Veterinary Pathology. Veterinary Pathology Unit)
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Zusammenfassung:Twenty, 3-week-old, crossbred pigs from a herd free from porcine reproductive and respiratory syndrome virus (PRRSV) were inoculated intranasally and intramusculary (1 ml each 10**(2.5) TCID sub(50)/ml) with Thai PRRSV isolates of the US genotype (0NP1) (n=9) or the EU genotype (02SB3) (n=8). Three pigs were used as negative controls. Three infected and one control group pig were euthanatized 5, 9 or 15 days postinoculation (DPI) to detect and to compare the location and the amount of PRRSV-antigen present. Immunohistochemical evaluation of formalin-fixed tissues revealed PRRSV-antigen in the pulmonary macrophages of the lungs (6/9, 8/8 and 0/3 of the 01NP1-infected, 02SB3-infected and control pigs, respectively). Macrophages staining for PRRSV-antigen in the spleen were seen in 1/9, 4/8 and 0/3 of the 01NP1-infected, 02SB3-infected and control groups. Other tissues and cells in which PRRSV-antigen was detected included follicular macrophages in the lymph nodes, macrophages in the liver, Peyeris patches, kidney, tonsil, turbinate bones, and heart. No PRRSV-antigen was detected in the brain of any PRRSV-inoculated pigs. Significantly, more PRRSV-antigen was detected in the spleen (P LT 0.05) of the 02SB3-infected pigs than in the spleen of 01NP1-infected pigs. The results suggested that PRRSV-antigen of the EU genotype was seen in a greater proportion of tissues despite showing less clinical signs. It could be that the EU genotype is well adapted to the pigs and may persist in the pigs for a longer period of time.
ISSN:0125-6491