Differences in Humoral Immune Response against the Type 2 Porcine Reproductive and Respiratory Syndrome Virus via Different Immune Pathways

The intramuscular vaccine is the principal strategy to protect pigs from porcine reproductive and respiratory syndrome virus (PRRSV), However, it is still difficult to control PRRSV effectively. This study infected piglets with PRRSV through intramuscular and intranasal inoculation. Subsequently, vi...

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Bibliographic Details
Main Authors: Chen, J. (Author), Chen, Y. (Author), Cui, Z. (Author), Li, W. (Author), Sun, Y. (Author), Xia, P. (Author), Xu, P. (Author), Zhang, Y. (Author), Zhao, S. (Author)
Format: Article
Language:English
Published: MDPI 2022
Subjects:
IgG
NAs
Online Access:View Fulltext in Publisher
LEADER 02186nam a2200313Ia 4500
001 10.3390-v14071435
008 220718s2022 CNT 000 0 und d
020 |a 19994915 (ISSN) 
245 1 0 |a Differences in Humoral Immune Response against the Type 2 Porcine Reproductive and Respiratory Syndrome Virus via Different Immune Pathways 
260 0 |b MDPI  |c 2022 
856 |z View Fulltext in Publisher  |u https://doi.org/10.3390/v14071435 
520 3 |a The intramuscular vaccine is the principal strategy to protect pigs from porcine reproductive and respiratory syndrome virus (PRRSV), However, it is still difficult to control PRRSV effectively. This study infected piglets with PRRSV through intramuscular and intranasal inoculation. Subsequently, viral loads, anti-PRRSV antibody levels, and neutralizing antibodies (NAs) titers in both serum and saliva were monitored for 43 days. Meanwhile, tissues were obtained through necropsy at 43 days post-inoculation (dpi) to detect viral loads. The results indicated that viremia lasted from 3 to 31 dpi in both the inoculation groups, but the viruses survived in the lungs and lymph nodes after viremia clearance. The antibody response was detected from 11 dpi, but the response of NAs was delayed until 3–4 weeks. Furthermore, intranasal inoculation induced lower viral load levels than injection inoculation. In addition, positive SIgA and NAs levels were produced early, with higher levels through intranasal inoculation. Therefore, our data indicated that a more robust antibody response and lower virus loads could be induced by intranasal inoculation, and mucosal inoculation could be a suitable pathway for PRRSV vaccines. © 2022 by the authors. Licensee MDPI, Basel, Switzerland. 
650 0 4 |a IgG 
650 0 4 |a in vivo 
650 0 4 |a mucosal immunity 
650 0 4 |a NAs 
650 0 4 |a PRRSV-2 
650 0 4 |a SIgA 
650 0 4 |a viremia 
700 1 |a Chen, J.  |e author 
700 1 |a Chen, Y.  |e author 
700 1 |a Cui, Z.  |e author 
700 1 |a Li, W.  |e author 
700 1 |a Sun, Y.  |e author 
700 1 |a Xia, P.  |e author 
700 1 |a Xu, P.  |e author 
700 1 |a Zhang, Y.  |e author 
700 1 |a Zhao, S.  |e author 
773 |t Viruses