No abstract

African swine fever (ASF) is a dangerous infectious disease of domestic pigs and wild boar caused by African swine fever virus (ASFV). In Vietnam, the ASF epidemic is gradually turning into an endemic status with several recovered pigs post infection, but there were not many studies evaluating the role of these pigs in the epidemiological context in Vietnam. The aim of this study was to evaluate the viral antigen distribution and lesions in recovered pigs post ASFV infection. Ten pigs recovered from ASF at 6 weeks of age were monitored and assessed for anti-ASFV antibodies and viremia until slaughter. The five major organs (lung, liver, spleen, kidney, and lymph nodes) of these pigs were evaluated for microscopic lesions and viral antigen distribution. Anti-ASFV antibody was consistently observed to be high (S/P% ≥ 80) until slaughter, while viremia levels were very high (7 log 10 copies/mL) at 6 weeks of age and gradually decreased to undetectable levels at 12 weeks of age (6th week post-infection). At slaughter, the ASFV-associated lesions in the organs of these pigs were mild and nonspecific. Seven out of ten pigs recovering from ASF still carried the virus in surveyed organ tissues, although not in the serum. These findings suggest that ASF-recovered pigs may be potential carriers of the virus, contributing to the increased complexity in the current endemic status in Vietnam.

African swine fever virus (ASFV), the causative agent of contagious hemorrhagic disease in domestic pigs and wild boars, has temporally regulated gene expression kinetics. The p30 and p72 major structural proteins are involved in viral entry each with different expression kinetics, but neither of their chronological expressions and distribution have been identified in virus-infected animals. Here, we found that both transcription and translation levels of p30 were significantly higher than those of p72 in target organs during the earlier infection-phase. Lymphocyte apoptosis/necrosis and angiectasia were observed as signs of early infection with acute African swine fever. These results show that the chronologically differential expression of ASFV structural proteins tends to be prominent in infected animals, and the p30 protein could play a role in the indication of acute lesions during early infection compared to the late-expressed p72 protein. In conclusion, we propose to consider the chronological expression dynamics of ASFV structural proteins in infected animals to understand virus pathogenesis and antigen targeting for vaccine development.

No abstract

Porcine circovirus type 3 (PCV3) was rst detected in 2016 and has been recorded in many pig-producing countries around the world. PCV3 was quickly reported in Vietnamese pig farms. PCV3 was found in complex cases with multiple clinical syndromes in swine. This study aimed to investigate the genetic diversity among PCV3 strains circulating in Vietnam, which provide novel insights into molecular characteristics and genetic diversity of these PCV3 isolates. A total of 249 samples were collected from swine farms located in eight provinces of Vietnam. We identi ed 11.65% (29/249) of collected samples with the presence of PCV3. The ORF2 genes of 29 PCV3-positive samples were ampli ed, puri ed, and sequenced. Phylogenetic analysis of these strains showed that 23/29 PCV3 strains belong to PCV3b subtype, while the remaining strains fall into sub-type c and sub-type a (a-1 and a-2). Analysis of the ORF2 genes indicated that the 29 PCV3 strains had high sequence identity (96.90-100% at the genomic level and 96.19-100% at the amino acid level). Fifteen amino acid substitutions were found in the predicted Bcell epitopes in capsid protein of Vietnamese PCV3 strains.