Porcine circovirus-associated disease (PCVAD) is one of the most serious infectious diseases in pigs worldwide. The primary causative agent of PCVAD is porcine circovirus type 2 (PCV2)， which can cause lymphoid depletion and immunosuppression in pigs. Our previous study demonstrated that Laiwu (LW) pigs， a Chinese indigenous pig breed， have stronger resistance to PCV2 infection than Yorkshire × Landrace (YL) pigs. In this study， we found that the YL pigs showed more severe lymphocyte apoptosis and higher viral load in the spleen tissue than LW pigs. To illustrate the differential gene expression between healthy and infected spleens， transcriptome profiling of spleen tissues from PCV2-infected and... More
Porcine circovirus-associated disease (PCVAD) is one of the most serious infectious diseases in pigs worldwide. The primary causative agent of PCVAD is porcine circovirus type 2 (PCV2)， which can cause lymphoid depletion and immunosuppression in pigs. Our previous study demonstrated that Laiwu (LW) pigs， a Chinese indigenous pig breed， have stronger resistance to PCV2 infection than Yorkshire × Landrace (YL) pigs. In this study， we found that the YL pigs showed more severe lymphocyte apoptosis and higher viral load in the spleen tissue than LW pigs. To illustrate the differential gene expression between healthy and infected spleens， transcriptome profiling of spleen tissues from PCV2-infected and control YL pigs was compared by RNA sequencing. A total of 90 differentially expressed genes (DEGs) was identified， including CD207， RSAD2， OAS1， OAS2， MX2， ADRB3， CXCL13， CCR1， and ADRA2C， which were significantly enriched in gene ontology (GO) terms related to the defense response to virus and cell-cell signaling， and another nine DEGs， KLF11， HGF， PTGES3， MAP3K11， XDH， CYCS， ACTC1， HSPH1， and RYR2， which were enriched in GO terms related to regulation of cell proliferation or apoptosis. Among these DEGs， the CXCL13 gene， which can suppress lymphocyte apoptosis during PCV2 infection， was significantly down-regulated in response to PCV2 infection in YL but not in LW pigs. By analysis of the regulatory elements in the promoter and 3'-untranslated region (3'-UTR) of porcine CXCL13， we found that the single nucleotide polymorphism (SNP) -1014 G (LW) > A (YL) and the Sus scrofa microRNA-296-5p (ssc-miR-296-5p) participated in regulating CXCL13 expression during the response to PCV2 infection.
