Persistent infection of chicken anemia virus (CAV) in chickens has been suspected to result in immunosuppression and exogenous virus contamination within vaccine production. However, no direct evidence for persistent CAV infection has thus far been obtained. In this study, we aimed to establish an in vitro model of persistent CAV infection. CAV-infected MDCC-MSB1 (MSB1) cells, a Marek’s disease virus-transformed continuous cell line, were cultured in the presence of both CAV and CAV neutralizing antibody (NA). Cell viability, expression of viral antigens, viral DNA, and recovery of CAV were examined by acridine orange/propidium iodide staining, immunofluorescence measurement, real-time PCR, and viral isolation, respectively. The results indicated that CAV was maintained and possibly replicated in CAV-infected cells cultured in the presence of NA, without affecting host cell viability. It was also shown that persistently infectious CAV induced cell death again after removing NA. The persistent infection of CAV in MSB1 cells was not related to viral gene mutation. In summary, we have herein established a novel model of persistent CAV infection in MSB1 cells cultured in the presence of NA.

In total, 130 tissue-pooled samples collected from ducks in some provinces/cities in north Vietnam were examined for waterfowl parvovirus genome identification. Twenty-six (20%) samples were positive for the parvovirus infection, based on polymerase chain reaction analysis. Of the 38 farms tested, 14 (36.84%) were positive for the waterfowl parvovirus genome. The rate of the parvovirus genome detection in ducks aged 2–4 weeks (37.04%) was significantly (p < 0.05) higher than that at ages 4 weeks (16.30%). The positive rate on medium-scale farms (9.36%) was significantly (p < 0.05) lower than for small-scale (31.03%) and large-scale (29.73%) farms. The lengths of the four Vietnamese waterfowl parvovirus genomes identified were 4750 nucleotides. Among the four Vietnamese parvovirus genomes, nucleotide identities were from 99.29% to 99.87%. Phylogenetic analysis of the near-complete genomes indicated that the waterfowl circulating in northern Vietnam belonged to the novel goose parvovirus (NGPV) group. The Vietnamese NGPV group was closely related to the Chinese group. Recombination analysis suggested that the Vietnam/VNUA-26/2021 strain was generated by a recombination event. One positive selection site of the capsid protein was detected.

Background and Aim: Newcastle disease (ND) is a major viral disease of poultry worldwide. However, data on the molecular characterization of Newcastle disease virus (NDV) in Vietnam are limited. This study aimed to identify the molecular characteristics of NDV strains from the vaccinated chickens farmed in Northern Vietnam. Materials and Methods: We used reverse-transcription polymerase chain reaction (PCR), sequencing and phylogenetic analysis to characterize NDV strains from vaccinated chicken farms in Northern Vietnam. Results: Seven out of 72 (9.7%) chicken tissue samples collected from seven chicken farms in the four cities/provinces in northern Vietnam were positive for the NDV genome by PCR method. The complete sequences of the fusion (F) and hemagglutinin-neuraminidase (HN) genes of NDVs isolated in the North of Vietnam from 2021 to 2022 were further evaluated. The results indicated that all seven Vietnamese isolates obtained were reported as virulent NDV strains with the amino acid (AA) sequence of the F0 protein proteolytic cleavage site motif (112RRRKRF117). Phylogenetic analysis revealed that they were grouped with other NDV class II from subgenotype VII.2, including the two previous Vietnamese NDV (2015), the Chinese (2017), and Southern African (2013) NDV strains. In addition, some AA substitutions were observed in the neutralizing epitopes of the F and HN proteins of the current Vietnamese NDV strains. Conclusion: The present findings provide useful information for future studies of the evolution of NDVs and improve strategies for ND-controlling programs in Vietnam. Keywords: genetic characterization, Newcastle disease virus, Vietnam, genotype VII.2, virulent strain.

In total, 126 tissue-pooled samples were collected from suspected sick chickens showing signs of stunted growth, weakness, and diarrhea in five provinces/cities in Northern Vietnam. The Gyrovirus gala 1 (GyVg1) genome was detected in 26 (20.63%) of the 126 chicken samples based on a polymerase chain reaction assay. The five Vietnamese GyVg1 genomes obtained were all 2.375 nucleotides in length. Among them, the nucleotide identical rates ranged from 94.01% to 100%. Phylogenetic analysis of the complete genomes revealed that the current five GyVg1 strains belonged to different branches at two levels: GyVg1 II (two of five strains) and GyVg1 III (three of five strains). The Vietnamese GyVg1 strains were generically clustered with the Japanese and Chinese strains. Some amino acid substitutions were found in VPs 1, 2, and 3 of the Vietnamese GyVg1 strains. In addition, three and two positive selection sites of VPs 1 and 3 were detected, respectively. A recombination event occurred and generated a recombination Chicken/Vietnam/AGV/VNUA-TN12/2023 strain. These findings indicate the first evidence of GyVg1 viruses circulating in commercial chicken flocks in Vietnam.

Porcine sapovirus (PoSaV) has been reported in many countries over the world, which may cause gastroenteritis symptoms in pigs with all ages. There has been no report on PoSaV infection in Vietnam up to now. In this study, a total of 102 samples were collected from piglets, fattening pigs, and sows with diarrhea in several cities and provinces in northern Vietnam. The PoSaV genome was examined using polymerase chain reaction (PCR). Sequencing of the partial RNA-dependent RNA polymerase (RdRp) gene sequences (324 bp) was performed. Of the 102 tested samples, 10 (9.8%) and 7/20 (35%) were detected as positive for the PoSaV RdRp gene using the PCR method at the individual and farm levels, respectively. Genetic analysis of the partial RdRp gene region of about 324 bp indicated that the nucleotide identity of the current 10 Vietnamese viral strains ranged from 61.39% to 100%. Among the 10 strains obtained, 8 belonged to genotype III and the remaining 2 strains were clustered in genotype VIII. The Vietnamese genotype III viruses formed two sub-clusters. The Vietnamese PoSaV strains were closely related to PoSaVs reported in South Korea, Venezuela, and the Netherlands. This research was the first to describe PoSaV infection in northern Vietnam during 2022–2023.

Background and Aim: Feline bocavirus (FBoV), a member of the Parvoviridae family, has been implicated in gastrointestinal and respiratory conditions in domestic cats. Despite increasing global recognition, the molecular epidemiology of FBoV in Vietnamese animal populations remains largely unexplored. This study aimed to detect and genetically characterize FBoV strains circulating among domestic cats in Northern Vietnam to better understand their genotypic diversity and potential clinical relevance. Materials and Methods: A total of 166 fecal samples were collected from domestic cats of varying age, sex, and clinical status across four provinces in Northern Vietnam between 2022 and 2023. DNA was extracted and screened for FBoV using conventional polymerase chain reaction targeting the non-structural (NS)-1 gene. Positive samples were subjected to Sanger sequencing, and partial NS1 sequences were analyzed using MEGA X for phylogenetic inference. Recombination analysis was performed using RDP 4.0, and statistical significance was assessed using Fisher’s exact test. Results: FBoV DNA was detected in 4 of 166 samples (2.41%), including one from a diarrheic cat and three from healthy cats. Phylogenetic analysis of the partial NS1 gene revealed that three strains belonged to genotype I and one to genotype II, all showing close genetic similarity to Chinese strains. Nucleotide identities among Vietnamese strains ranged from 64.68% to 99.57%. No recombination events were observed among the detected strains. FBoV was detected across age groups and both sexes, without significant associations. Co-infections with other enteric viruses (feline coronavirus, feline panleukopenia virus, feline astrovirus, and feline kobuvirus) were not observed in the FBoV-positive samples. Conclusion: This study provides the first molecular evidence of co-circulating FBoV genotypes I and II in domestic cats in Vietnam, indicating viral genetic diversity and suggesting possible regional transmission routes linked to neighboring countries. While FBoV was present in both symptomatic and asymptomatic cats, its clinical significance remains inconclusive. The findings underscore the need for expanded surveillance, complete genome analyses, and investigation into FBoV’s pathogenic potential and co-infection dynamics in the feline population. These data will be instrumental in shaping future diagnostic and control strategies for feline viral enteritis in Vietnam. Keywords: domestic cats, feline bocavirus, genotype, molecular epidemiology, NS1 gene, Vietnam.