Characterization of an Emerging Recombinant Duck Circovirus in Northern Vietnam, 2023–2024
by
, and
Hieu Van Dong
1,†
,
Dai Quang Trinh
2,†, 
Giang Huong Thi Tran
1,
Thanh Thi Vu
1,2,
Thinh Hung Ba Nguyen
1,
Amonpun Rattanasrisomporn
3,
Dao Anh Tran Bui
1 and
Jatuporn Rattanasrisomporn
4,*
1
Faculty of Veterinary Medicine, Vietnam National University of Agriculture, Trau Quy Town, Gia Lam District, Hanoi 131000, Vietnam
2
Central Veterinary Medicine JSC No. 5, Ha Binh Phuong Industrial Zone, Hanoi 131000, Vietnam
3
Interdisciplinary of Genetic Engineering and Bioinformatics, Graduate School, Kasetsart University, Bangkok 10900, Thailand
4
Department of Companion Animal Clinical Sciences, Faculty of Veterinary Medicine, Kasetsart University, Bangkok 10900, Thailand
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Viruses 2025, 17(5), 732; https://doi.org/10.3390/v17050732
Submission received: 11 April 2025
/
Revised: 16 May 2025
/
Accepted: 16 May 2025
/
Published: 20 May 2025
(This article belongs to the Special Issue Animal Models in Emerging/Re-Emerging Infectious Diseases)
Abstract
:This study aimed to characterize the duck circovirus circulating in Northern Vietnam based on complete genome sequences. Between 2023 and 2025, 45 pooled tissue samples were collected from nine duck flocks in several provinces in Northern Vietnam. Of the 45 samples tested, 16 (35.56%) were positive for the DuCV genome, as determined using conventional polymerase chain reaction. Nine representative strains were selected for viral genome sequencing. The results indicated that the complete Vietnamese DuCV genomes were from 1992 to 1995 bp in length, and the degree of nucleotide identity shared among them ranged from 96.88% to 99.84%. Phylogenetic analysis of the complete genomes showed that the nine Vietnamese DuCV strains belonged to genotype I, subgenotypes Ia (two strains), Ib (four strains), and Ic (three strains). These viral strains were genetically related to viruses reported in China from 2019 to 2023. Recombination events occurred on the Cap gene sequences of three Vietnamese DuCV strains (Vietnam/VNUA-102/2023, Vietnam/VNUA-225/2023, and Vietnam/VNUA-318/2024). One positive selection was detected on the Rep protein sequence.
1. Introduction
Duck circovirus (DuCV) belongs to the Circoviridae family and includes two genera, Cyclovirus and Circovirus, according to a report by the International Committee on Taxonomy of Viruses (ICTV) released in 2022. The Circovirus genus consists of porcine circovirus types 1–4, canine circovirus, and some strains in bats. Regarding avian hosts, the Circovirus genus includes psittacine beak and feather disease virus, goose circovirus, and DuCV. DuCV is a small, non-enveloped virus that contains single-stranded circular DNA [1,2].
DuCV is a contagious immunosuppressive virus; it harms many duck species and has caused several outbreaks in the poultry industry worldwide. DuCV-infected ducks show stunted growth, abnormal feathering, weakened immune systems, and a susceptibility to other diseases, such as Riemerella anatipestifer, avian pathogenic Escherichia coli, Pastereulla multocida, and Salmonella. Therefore, DuCV poses a significant economic challenge to the duck industry [3,4].
DuCV is described as having icosahedral symmetry and ranges from approximately 15 to 16 nm in diameter. It is considered to be the smallest duck virus. The DuCV genome ranges from 1988 to 1996 nucleotides (nt) in length [5,6]. It contains three open reading frames (ORFs) and two intergenic noncoding regions [2]. In detail, ORF1 encodes the Rep protein, which is needed for viral replication. It is stated that the Rep protein sequence is highly conserved among various DuCV genotypes. ORF2 encodes the Cap protein, which is the viral structural and virulence-associated protein involved in the host immune response. The remaining viral non-structural protein is encoded by the DuCV ORF3 gene. The protein is regarded as the source of DuCV’s apoptotic activity, depending on the cell line [2,7,8].
DuCV is divided into two main genotypes, DuCV-1 and DuCV-2, depending on the phylogenetic tree of the full-length genome and the cap gene [9,10]. In brief, the DuCV-1 genotype is classified into DuCV-1a and DuCV-1b, while the DuCV-2 genotype contains DuCV-2a, DuCV-2b, and DuCV-2c. Furthermore, DuCV-3, as a new type, was reported in laying ducks in Hunan Province in China in 2022. The DuCV-3 genome is about 1755 nt in length. Its shared nt identity with other DuCV genotypes ranges from 62.3% to 63.7% [5].
DuCV was first reported in a six-week-old duck flock in Germany in 2003. Clinical symptoms, including disheveled plumage, emaciation, immunosuppression, and weight loss, were observed in the diseased ducks. Afterward, DuCV surveillance was carried out in many countries in the world, such as Hungary, Taiwan (China), the United States, China, Thailand, etc. [6,8,11,12,13,14,15,16]. It is worth noting that DuCV has been reported to be highly infectious among Chinese breeder flocks and leads to viral persistence in these flocks [17,18].
In Vietnam, DuCV was first reported in duck flocks raised in northern areas in 2022 [19]. DuCV strains, including DuCV-1 and DuCV-2, were circulating in commercial flocks. However, there are few reports investigating the evolution of DuCV in Vietnam. In addition, continuous surveillance of the DuCV genotype prevalence in duck flocks is necessary to better understand viral genetic diversity. Therefore, this study aimed to deepen our understanding of the evolutionary dynamics of DuCV circulating in commercial duck flocks in Vietnam.
2. Materials and Methods
2.1. Ethics Statement
The Committee on Animal Research and Ethics of the Vietnam National University of Agriculture (CARE-2023/08) approved this study. All protocols involving animals in this study were used after obtaining ethics approval from the Committee on Animal Research and Ethics of the Vietnam National University of Agriculture. Informed consent was acquired from the duck owners before sampling and data publication.
2.2. Samples
In this study, a total of 9 duck farms in several provinces in Northern Vietnam, including Thainguyen, Bacgiang, Haiduong, Nghean, Phutho, Hanoi, and Hanam, were selected for sampling during 2023 and 2024. Samples were collected from ducks aged 2 to 7 weeks across nine farms, with five ducks sampled from each farm. The selected farms showed signs of increased mortality rates and decreased growth. Selected ducks from each farm were sent to the Faculty of Veterinary Medicine, Vietnam National University of Agriculture. Pooled tissue samples, including the liver, heart, brain, and bursa of Fabricius, were collected and then homogenized in phosphate-buffered saline and stored at −80 °C until use.
2.3. DNA Extraction and Polymerase Chain Reaction (PCR)
DNA was extracted from tissue homogenates using a Viral Gene-spinTM Viral DNA/RNA Extraction Kit (iNtRON Biotechnology, Seoul, Republic of Korea) according to the manufacturer’s directions. The DNA was eluted in 50 µL of distilled water.
For detection, a DuCV-F1/R1 primer set (DuCV-F1, CCC GCC GAA AAC AAG TAT TA-3′; DuCV-R1, 5′-TCG CTC TTG TAC CAA TCA CG-3′) was used to amplify the target 230 bp part of the DuCV Rep gene as described previously [15]. The following thermal conditions were used: an initial denaturation step at 94 °C for 5 min, followed by 35 cycles at 94 °C for 45 s, 45 °C for 30 s, 72 °C for 30 s, and a final extension step at 72 °C for 10 min. PCR products with 230 bp were examined in a 1.2% agarose gel and then detected by UV light [15].
Regarding complete genome sequencing, four primer sets were used to amplify the 887 bp, 997 bp, 492 bp, and 802 bp fragments of the DuCV genome [19,20]. The following thermal conditions were used: an initial denaturation step at 95 °C for 5 min, followed by 34 cycles at 95 °C for 30 s, 55 °C (four pairs of primers) for 30 s, and 72 °C for 40 s and a final extension step at 72 °C for 10 min. The PCR products were examined in a 1.2% agarose gel and then detected by UV light [19,20].
2.4. Nucleotide Sequencing and Analysis
PCR products were purified using GeneClean® II Kits (MP Biomedicals, Santa Ana, CA, USA). Sequencing of the Vietnamese DuCV genomes was performed by 1st BASE, Selangor, Malaysia.
The sequence data were analyzed by GENETYX ver. 10 software (GENETYX Corp., Tokyo, Japan). The multiple DuCV sequences available (Table 1) were compared with the DuCV sequences in this study using BLAST version 1.3 homology searches. The Clustal W algorithm in BioEdit version 7.2 was used to perform the nucleotide identity comparisons of the complete genomes and full-length Rep and Cap genes and to deduce the amino acid substitution of the Rep and Cap proteins [21,22]. Phylogenetic trees were created using the Maximum Likelihood method supported by 1000 bootstrap replicates in MEGA X software “https://www.megasoftware.net/” (accessed on 20 January 2025). The sequence data obtained in this study were deposited into GenBank with accession numbers PV483400 to PV483408.
2.5. Recombination Events and Selection Profiles of Vietnamese DuCV Strains
Putative recombinations were identified using a recombination detection program (RDP) version Beta 4.97 [23] and SimPlot software version 3.5.1 [24]. The elaboration of evolutionary selection profiles was performed using Datamonkey “http://www.datamonkey.org/” (accessed on 28 January 2025) by following the Fast Unconstrained Bayesian AppRoximation (FUBAR) method [25]. The general time-reversible model was selected based on the best-fit evolutionary model test.
3. Results
3.1. Detection of Duck Circovirus in Field Samples
The results indicated that 16 (35.56%) out of 45 samples were positive for the viral genome. All farms tested were positive for DuCV infection. The proportion of positive cases observed across the tested locations/farms ranged from 20% to 60% (Table 2).
3.2. Characterization of Vietnamese DuCV Genomes
A total of nine representative DuCV-positive samples were selected for viral genome sequencing. Complete genome sequences of DuCV strains were successfully sequenced and characterized. The nine strains were designated as Vietnam/VNUA-102/2023, -114/2023, -137/2023, -225/2023, -251/2023, -318/2024, -322/2024, -315/2024, and -331/2024. The length of the Vietnamese complete genomes ranged from 1992 to 1995 nucleotides. Neither deletion nor insertion mutations were found in the coding regions of the viral genomes in this study.
The nucleotide identities of the complete genomes among the Vietnamese DuCV strains obtained in this study and previous Vietnamese strains are indicated in Table 3 and Table 4. Among current DuCV strains, nucleotide identity ranged from 96.88% to 99.84% (Vietnam/VNUA-137/2023 vs. Vietnam/VNUA-315/2024) (Table 3). The nucleotide identity between the strains in this study and previously reported strains ranged from 83.40% (Vietnam/VNUA-315/2024 vs. Vietnam/OM176556.1/VNUA-HD89/2021) to 99.79% (Vietnam/VNUA-318/2024 vs. Vietnam/OM176555.1/VNUA-TN85/2021) (Table 4).
The nine Vietnamese DuCV strains in this study were compared with strains from other countries found in GenBank. The Vietnamese DuCV genome sequences shared the highest nucleotide identities with those of Chinese strains (DY01, GX05, GX11, GX25, GX39, GX51, and CN/GD/1092), ranging from 99.24% to 99.74% (Table 5).
Phylogenetic analysis indicated that the nine DuCV strains obtained belonged to genotype I. Among the nine strains, several subgenotype viruses were found, including subgenotype Ia (2 strains), Ib (4 strains), and Ic (3 strains) (Figure 1).
Analysis of Cap gene and protein sequences: Among the Vietnamese DuCV strains obtained in this study, nucleotide identity ranged from 93.28% (VNUA-102/2023 vs. VNUA-137/2023) to 99.61% (VNUA-225/2023 vs. VNUA-102/202) (Supplementary Table S1). A phylogenetic tree (Figure 2A) was established based on the full-length Cap gene (780 bp) and indicated that the nine Vietnamese DuCV strains in this study clustered into Genotype I.
The deduced amino acids of the Cap protein were also predicted and analyzed. The results indicated that 14 amino acid substitutions were found in the Vietnamese DuCV strains (Table 6). The motif of the amino acid substitutions was 12G/S/A-47N/H-55S/N-82Q/R-106N/S/G-107K/T-155T/S-156T/A-177V/I-183V/I-194T/G-197Y/H-205R/K-236D/N/E. The substitution at residue 156 (T to A) was unique in that it was only detected in two Vietnamese DuCV strains (VNUA-102/2023 and VNUA-225/2023).
Analysis of Rep gene and protein sequences: Among the Vietnamese DuCV strains in this study, nucleotide identity ranged from 99.08% (Vietnam/VNUA-114/2023 vs. Vietnam/VNUA-102/2023) to 100% (Vietnam/VNUA-137/2023 vs. Vietnam/VNUA-315/2024). Analysis of the phylogenetic tree based on the full-length Rep gene sequences showed that the nine Vietnamese DuCV strains in this study belonged to Genotype I.
3.3. Recombination Analysis of Vietnamese DuCV Strains
Recombination analysis was performed using the nine Vietnamese DuCV strains in this study, six previous Vietnamese strains, and other strains from GenBank. The results indicated that three recombination events had occurred in the Cap gene sequences of the Vietnamese DuCV strains circulating in Northern Vietnam, whereas no recombination events were found in the remaining gene sequences. The three recombination events were Vietnam/VNUA-102/2023, Vietnam/VNUA-225/2023, and Vietnam/VNUA-318/2024, as determined with the five methods supplemented in RDP 5 software (p-value < 0.05) (Table 7 and Table 8). The major parents were the Vietnamese DuCV strains circulating in Vietnam in 2021 (Vietnam/OM176552.1/VNUA-HY40/2021) and 2023 (Vietnam/VNUA-114/2023) (Figure 3), while the minor parent was Germany/NC_005053.1/2003.
To confirm the recombination events, the Vietnam/VNUA-225/2023 or Vietnam/VNUA318/2024 strains were used as a query. Simplot software confirmed that these two strains were recombination events. The breakpoint was at site 619 when the chi-square value changed from 0.2 to 0.5 (Figure 4).
3.4. Analysis of Natural Selection Profile of DuCV Gene Sequences
In a previous study, we reported the detection of positive selection at site 106 in the Cap protein. In this study, the same result was found in the Cap protein sequences of the Vietnamese DuCV strains. For Rep protein sequences, evolutionary analysis indicated that one positive selection was found at residue 112 (Table 9), while 87 negative selections were identified (Supplementary Table S3).
4. Discussion
In this study, DuCV genomes were detected in 16 (35.56%) samples collected from suspected ducks in Northern Vietnam. Nine DuCV complete genomes were characterized. The nine Vietnamese DuCV strains shared a high degree of nucleotide identity (96.88% to 99.84%), belonged to genotype I, and clustered with Chinese strains. In the present study, we reported recombination events in Vietnamese DuCV strains for the first time. The recombination events among Vietnamese DuCV strains circulating in Northern Vietnam from 2023 to 2024 were seen in the Cap gene sequence, and one positive selection was seen on the Rep protein sequence.
In our previous report on DuCV infection in Northern Vietnam, it was pointed out that the DuCV-positive rate found among ducks in 2021 was high [19]. In this study, we continued to observe DuCV infection among duck flocks in some provinces in Northern Vietnam. In the present study, 35.56% of the tested ducks were positive for the DuCV genome, a number lower than the 43.08% reported in the country in 2021 and the 84% reported in Hungary [15] but higher than the 21.8% observed in the Republic of Korea and the 6.06% seen in the U.S. [8,11]. The low sample size, time constraints, and regional sampling are the main reasons for these differences. The results of this study indicate that DuCV infection remains prevalent in Northern Vietnam, with a detection rate of 35.56%.
Historically, DuCV strains were mainly divided into genotype I (subgenotypes Ia, Ib, Ic, and Id) and genotype II based on the full-length Cap gene sequences and complete genome sequences [5,6,19,26]. A later report confirmed a novel DuCV genotype III virus in mainland China [5]. This finding suggests that DuCV strains worldwide are continuously evolving. Therefore, studies on DuCV infection and genetic characterization are necessary. In this study, we found that DuCV strains circulating in Northern Vietnam belong to genotype I, subgenotypes Ia, Ib, and Ic, which is similar to our previous report from 2021 [19]. Other genotype II and III viruses were not detected in the present study, suggesting that genotype I viruses are the predominant ones in circulation in Northern Vietnam, affecting the duck production industry. The nine Vietnamese DuCV strains in this study and six previously reported strains [19] were genetically close to Chinese DuCV strains. Vietnam and China share a long border, along which live birds, including ducks, are traded daily. The trading of live birds may result in outbreaks of avian influenza in poultry [27,28]. This situation may affect the diversity of DuCV strains in Northern Vietnam.
Recombination is an important pattern of viral evolution. Previously, many researchers reported on recombination events among global DuCV strains, showing that recombination events may occur in both coding and noncoding regions of the viral genome [6,10,11,29]. In our 2021 report on six Vietnamese DuCV strains, we did not find any recombination events. In the present study, three Vietnamese DuCV strains were found to have resulted from recombination events in the Cap gene sequences. Interestingly, the major parents were Vietnamese strains circulating in Northern Vietnam in 2021 and 2023. This finding suggests that recombination plays a critical role in viral evolution, leading to a significant increase in the genetic diversity of DuCV strains.
It was reported that amino acid substitutions occurring in the Cap protein at residues 3–15, 104–124, and 232–238 may have resulted in antigenic changes and viral virulence. In this study, we only detected one positive selection at residue 106, which was similar to our previous report [19]. Rep and ORF3 gene sequences play critical roles in the replication and apoptosis of DuCV strains in host cells [2,7]. Substitutions on the ORF3 protein may result in changes in pathogenesis and immunosuppression [7]. In this study, one positive selection was found at residue 112 on the Rep protein, equivalent to residue 7 on the ORF3 protein, since the ORF3 gene sequence is within the Rep gene sequence, which belongs to one of the immunogenic regions (3–15, 104–124, 232–238) [30]. This finding suggests that virulence gene sequences are under positive selection, in line with a previous report [31]. In addition, 87 negatively selected sites were found among Vietnamese DuCV strains, suggesting that this protein is under purifying selection. In other viruses, virulence genes seem to be under positive selection compared to other genes. Wang et al. pointed out that the Rep gene was more conserved due to strong purifying [30]. This may be due to its critical role in viral replication. Further studies should focus on elucidating the role of natural selection in the Rep and ORF3 genes of DuCV strains.
5. Conclusions
In this study, DuCV infection was continuously detected among duck flocks in Northern Vietnam during 2023–2024, with a positive rate of 35.56%. Nine representative complete genomes, ranging from 1992 to 1995 bp in length, were successfully sequenced and characterized. Neither insertions nor deletions were found in the coding regions of these viral genomes. The Vietnamese DuCV complete genomes in this study shared a high degree of nucleotide identity, ranging from 96.88% to 99.84%. Phylogenetic analysis indicated that the nine Vietnamese DuCV strains belonged to genotype I, subgenotypes Ia, Ib, and Ic, and were genetically close to Chinese viral strains reported in 2019–2023. Recombination events occurred in three of the Vietnamese DuCV strains, and one positive selection was found in the Rep/ORF3 gene.
Supplementary Materials
The following supporting information can be downloaded at https://www.mdpi.com/article/10.3390/v17050732/s1, Table S1: Comparison of nucleotide identity among Vietnamese DuCV strains in this study based on Cap gene sequences; Table S2: Comparison of nucleotide identity among Vitenamse DuCV strains in this study based on Rep gene sequences; Table S3: Negative selection on VP2 protein sequence.
Author Contributions
Conceptualization: H.V.D., D.Q.T. and J.R.; methodology: H.V.D., G.H.T.T., and D.Q.T.; software, H.V.D. and D.Q.T.; formal analysis: H.V.D., G.H.T.T., and J.R.; investigation: H.V.D., D.Q.T. and J.R.; resources: J.R.; data curation: H.V.D., T.T.V., T.H.B.N., and J.R.; original draft preparation: H.V.D., D.Q.T. and J.R.; writing—review and editing: D.A.T.B., A.R. and J.R.; visualization: J.R.; supervision: J.R.; project administration: J.R.; funding management: J.R. All authors have read and agreed to the published version of the manuscript.
Funding
This study was supported by the Faculty of Veterinary Medicine, Kasetsart University, Bangkok, Thailand.
Institutional Review Board Statement
The animal study protocol was approved by the Vietnam National University of Agriculture. The University’s Committee on Animal Research and Ethics (CARE-2023/08, 10 January 2023) and the owners of the cats approved the protocol for sampling.
Informed Consent Statement
Informed consent was obtained from all subjects involved in the study.
Data Availability Statement
The data presented in this study are available within the article. Raw data supporting this study are available from the corresponding author.
Conflicts of Interest
No conflicts of interest are declared by the authors.
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Figure 1.
A phylogenetic tree was constructed based on the complete genome sequences of Vietnamese DuCV strains compared with the strains available from GenBank. The maximum likelihood method with the Kimura-2 parameter model was used in MEGA X software to establish the phylogenetic tree (1000 bootstrap replicates). The Vietnamese DuCV strains in this study are marked by solid circles.
Figure 1.
A phylogenetic tree was constructed based on the complete genome sequences of Vietnamese DuCV strains compared with the strains available from GenBank. The maximum likelihood method with the Kimura-2 parameter model was used in MEGA X software to establish the phylogenetic tree (1000 bootstrap replicates). The Vietnamese DuCV strains in this study are marked by solid circles.
Figure 2.
Phylogenetic trees were established based on the full-length (A) Cap sequences and (B) Rep sequences of Vietnamese DuCV strains compared with the strains available from GenBank. The maximum likelihood method with the Kimura-2 parameter model was used in MEGA X software to establish the phylogenetic trees (1000 bootstrap replicates). The Vietnamese DuCV strains in this study are marked by solid circles.
Figure 2.
Phylogenetic trees were established based on the full-length (A) Cap sequences and (B) Rep sequences of Vietnamese DuCV strains compared with the strains available from GenBank. The maximum likelihood method with the Kimura-2 parameter model was used in MEGA X software to establish the phylogenetic trees (1000 bootstrap replicates). The Vietnamese DuCV strains in this study are marked by solid circles.
Figure 3.
Detection of recombination events of full-length Cap gene sequences of the Vietnam/VNUA-114/2023 DuCV strain performed using MaxChi analysis. A pairwise distance model with window size 200, step size 20, and 1000 bootstrap replicates was generated by the RDP 5 program.
Figure 3.
Detection of recombination events of full-length Cap gene sequences of the Vietnam/VNUA-114/2023 DuCV strain performed using MaxChi analysis. A pairwise distance model with window size 200, step size 20, and 1000 bootstrap replicates was generated by the RDP 5 program.
Figure 4.
A distance plot was used for recombination identification. The (A) Vietnam/VNUA-225/2023 and (B) Vietnam/VNUA318/2024 strains were used as a query. Pairwise distance with a window size of 200 bp and step size of 20 bp was applied via the SimPlot program.
Figure 4.
A distance plot was used for recombination identification. The (A) Vietnam/VNUA-225/2023 and (B) Vietnam/VNUA318/2024 strains were used as a query. Pairwise distance with a window size of 200 bp and step size of 20 bp was applied via the SimPlot program.
Table 1.
General information on the sequences used in this study.
| No. | GenBank Accession Number | Strain | Country | Host | Year | Genotype |
|---|---|---|---|---|---|---|
| 1 | OR842553.1 | CN/GD/1092 | China | Duck | 2023 | I |
| 2 | OR842554.1 | CN/GD/1099 | China | Duck | 2023 | I |
| 3 | PP860902.1 | SDLC | China | Duck | 2023 | I |
| 4 | PP081932.1 | Xinjiang2023 | China | Duck | 2023 | I |
| 5 | OR134489.1 | DuCV-GX51 | China | Duck | 2022 | I |
| 6 | PP860900.1 | SDHZ | China | Duck | 2022 | I |
| 7 | OQ657184.1 | DZ1116 | China | Duck | 2022 | I |
| 8 | OR134488.1 | GX49 | China | Duck | 2022 | I |
| 9 | OM176552.1 | VNUA-HY40 | Vietnam | Duck | 2021 | I |
| 10 | OM176553.1 | VNUA-HN47 | Vietnam | Duck | 2021 | I |
| 11 | OM176554.1 | VNUA-TB61 | Vietnam | Duck | 2021 | I |
| 12 | OM176555.1 | VNUA-TN85 | Vietnam | Duck | 2021 | I |
| 13 | ON227551.1 | GD/JM/180 | China | Duck | 2021 | I |
| 14 | ON227553.1 | GD/ZQ/188 | China | Duck | 2021 | I |
| 15 | ON227542.1 | GD/QY/129 | China | Duck | 2021 | I |
| 16 | ON227548.1 | GD/ZQ/144 | China | Duck | 2021 | I |
| 17 | OK094642.1 | DY01 | China | Duck | 2020 | I |
| 18 | OR134472.1 | GX25 | China | Duck | 2020 | I |
| 19 | OR134475.1 | GX28 | China | Duck | 2020 | I |
| 20 | OR134505.1 | GX29 | China | Duck | 2020 | I |
| 21 | OR134478.1 | GX33 | China | Duck | 2020 | I |
| 22 | OR134508.1 | GX35 | China | Duck | 2021 | I |
| 23 | OR134510.1 | GX39 | China | Duck | 2021 | I |
| 24 | OR134481.1 | GX41 | China | Duck | 2021 | I |
| 25 | OR134464.1 | GX05 | China | Duck | 2019 | I |
| 26 | OR134467.1 | GX11 | China | Duck | 2019 | I |
| 27 | MW255980.1 | BaodingNO.Du | China | Duck | 2019 | I |
| 28 | MK814581.1 | GX190510 | China | Duck | 2019 | I |
| 29 | MT084134.1 | SDHX1223 | China | Duck | 2018 | I |
| 30 | MT084131.1 | AHHF1109 | China | Duck | 2018 | I |
| 31 | MN928795.1 | HN02 | China | Duck | 2018 | I |
| 32 | MN068356.1 | HZ170301 | China | Duck | 2017 | I |
| 33 | MN068357.1 | YF180401 | China | Duck | 2017 | I |
| 34 | MF627688.1 | JSPX03E | China | Duck | 2016 | I |
| 35 | KY328304.1 | SDFC12 | China | Duck | 2015 | I |
| 36 | GU014543.1 | AQ0901 | China | Duck | 2009 | I |
| 37 | KC460531.1 | NN12/2012 | China | Duck | 2012 | I |
| 38 | HQ180265.1 | LZ/11/09 | China | Muscovy duck | 2009 | I |
| 39 | GU168779.1 | FJzq290 | China | Muscovy duck | 2008 | I |
| 40 | GQ334371.1 | Zhejiang | China | Duck | 2008 | I |
| 41 | EU344803.1 | LJ33 | China | Duck | 2007 | I |
| 42 | EU344806.1 | YS07 | China | Muscovy duck | 2007 | I |
| 43 | MT318126.1 | VC4 | Brasil | Mallard | 2014 | I |
| 44 | KC851819.1 | D12-KD-019 | South Korea | Duck | 2012 | I |
| 45 | KC851821.1 | D12-KD-028 | South Korea | Duck | 2012 | I |
| 46 | DQ100076.1 | 33753-52 | USA | Duck | 2007 | I |
| 47 | AY228555.1 | Germany | Mallard duck | 2003 | I | |
| 48 | NC_005053.1 | Germany | Mallard duck | 2003 | I | |
| 49 | OM176556.1 | VNUA-HD89 | Vietnam | Duck | 2021 | II |
| 50 | OM176557.1 | VNUA-BG135 | Vietnam | Duck | 2021 | II |
| 51 | MK814585.1 | YN180506 | China | Duck | 2018 | II |
| 52 | MN052853.1 | FJ1815 | China | Muscovy duck | 2018 | II |
| 53 | KR491945.1 | YN24-2013 | China | Muscovy duck | 2013 | II |
| 54 | KP229377.1 | CP12021 | Taiwan (China) | Muscovy duck | 2012 | II |
| 55 | GU131343.1 | WF0804 | China | Duck | 2008 | II |
| 56 | EU344805.1 | MH11 | China | Muscovy duck | 2007 | II |
| 57 | EU499309.1 | MH02/07 | China | Mule duck | 2007 | II |
| 58 | EU344802.1 | HZ09 | China | Muscovy duck | 2007 | II |
| 59 | DQ166836.1 | TC2 | Taiwan (China) | Muscovy duck | 2002 | II |
| 60 | DQ166838.1 | TC4 | Taiwan (China) | Muscovy duck | 2002 | II |
| 61 | OP432310.1 | HNU-HYH | China | Duck | 2022 | III |
Table 2.
Diagnosis of duck circovirus in field samples using the PCR method.
| Farm Number | Location | No. of Tested Samples | No. of Positive Samples | Positive Rate |
|---|---|---|---|---|
| 1 | Thainguyen | 5 | 1 | 20 |
| 2 | Bacgiang | 5 | 2 | 40 |
| 3 | Haiduong | 5 | 2 | 40 |
| 4 | Bacgiang | 5 | 2 | 40 |
| 5 | Nghean | 5 | 1 | 20 |
| 6 | Thainguyen | 5 | 1 | 20 |
| 7 | Phutho | 5 | 3 | 60 |
| 8 | Hanoi | 5 | 3 | 60 |
| 9 | Hanam | 5 | 1 | 20 |
| Total | 45 | 16 | 35.56 | |
Table 3.
Nucleotide identities of the Vietnamese complete genomes in this study.
| Virus Strain | Nucleotide Identity (%) | ||||||||
|---|---|---|---|---|---|---|---|---|---|
| Vietnam/ VNUA-102/2023 | Vietnam/ VNUA-114/2023 | Vietnam/ VNUA-137/2023 | Vietnam/ VNUA-225/2023 | Vietnam/ VNUA-251/2023 | Vietnam/ VNUA-318/2024 | Vietnam/ VNUA-322/2024 | Vietnam/ VNUA-315/2024 | Vietnam/ VNUA-331/2024 | |
| Vietnam/VNUA-102/2023 | 100 | ||||||||
| Vietnam/VNUA-114/2023 | 97.03 | 100 | |||||||
| Vietnam/VNUA-137/2023 | 97.03 | 99.19 | 100 | ||||||
| Vietnam/VNUA-225/2023 | 99.44 | 97.18 | 97.08 | 100 | |||||
| Vietnam/VNUA-251/2023 | 96.93 | 99.19 | 99.49 | 97.08 | 100 | ||||
| Vietnam/VNUA-318/2024 | 99.39 | 96.93 | 97.03 | 99.24 | 96.88 | 100 | |||
| Vietnam/VNUA-322/2024 | 97.13 | 99.29 | 99.19 | 97.29 | 99.29 | 97.08 | 100 | ||
| Vietnam/VNUA-315/2024 | 97.08 | 99.24 | 99.84 | 97.13 | 99.54 | 96.98 | 99.24 | 100 | |
| Vietnam/VNUA-331/2024 | 97.29 | 99.34 | 99.44 | 97.34 | 99.44 | 97.19 | 99.34 | 99.49 | 100 |
Table 4.
Comparison of nucleotide identities between current Vietnamese DuCV complete genomes and previous Vietnamese strains in GenBank.
Table 4.
Comparison of nucleotide identities between current Vietnamese DuCV complete genomes and previous Vietnamese strains in GenBank.
| Virus Strain | Nucleotide Identity (%) | |||||
|---|---|---|---|---|---|---|
| Vietnam/OM176553.1/ VNUA-HN47/2021 | Vietnam/OM176554.1/ VNUA-TB61/2021 | Vietnam/OM176552.1/ VNUA-HY40/2021 | Vietnam/OM176555.1/ VNUA-TN85/2021 | Vietnam/OM176556.1/ VNUA-HD89/2021 | Vietnam/OM176557.1/ VNUA-BG135/2021 | |
| Vietnam/VNUA-102/2023 | 96.98 | |||||
| Vietnam/VNUA-114/2023 | 99.14 | 99.04 | ||||
| Vietnam/VNUA-137/2023 | 99.54 | 99.44 | ||||
| Vietnam/VNUA-225/2023 | 97.03 | 97.03 | 97.04 | |||
| Vietnam/VNUA-251/2023 | 99.34 | 99.24 | 97.54 | 96.98 | ||
| Vietnam/VNUA-318/2024 | 96.88 | 96.88 | 97.19 | 99.79 | 83.50 | |
| Vietnam/VNUA-322/2024 | 99.14 | 99.04 | 97.64 | 97.19 | 83.70 | 84.44 |
| Vietnam/VNUA-315/2024 | 99.59 | 99.49 | 97.49 | 97.08 | 83.40 | 84.04 |
| Vietnam/VNUA-331/2024 | 99.39 | 99.29 | 97.79 | 97.29 | 83.65 | 84.19 |
Table 5.
Nucleotide identity between the Vietnamese DuCV complete genomes and other sequences from abroad.
Table 5.
Nucleotide identity between the Vietnamese DuCV complete genomes and other sequences from abroad.
| Strain Name | Virus with the Highest Nucleotide Identity | ||||
|---|---|---|---|---|---|
| GenBank Accession Number | Strain Name | Country | Year | % | |
| Vietnam/VNUA-102/2023 | OK094642.1 | DY01 | China | 2020 | 99.54 |
| Vietnam/VNUA-114/2023 | OR134472.1 | GX25 | China | 2020 | 99.49 |
| Vietnam/VNUA-137/2023 | OR134489.1 | GX51 | China | 2022 | 99.64 |
| OR842553.1 | CN/GD/1092 | China | 2023 | ||
| Vietnam/VNUA-225/2023 | OK094642.1 | DY01 | China | 2020 | 99.24 |
| Vietnam/VNUA-251/2023 | OR134464.1 | GX05 | China | 2019 | 99.59 |
| OR134467.1 | GX11 | China | 2019 | ||
| Vietnam/VNUA-318/2024 | OR134510.1 | GX39 | China | 2021 | 99.64 |
| OK094642.1 | DY01 | China | 2020 | ||
| Vietnam/VNUA-322/2024 | OR134472.1 | GX25 | China | 2020 | 99.49 |
| Vietnam/VNUA-315/2024 | OR134489.1 | GX51 | China | 2022 | 99.69 |
| Vietnam/VNUA-331/2024 | OR134472.1 | GX25 | China | 2020 | 99.74 |
Table 6.
Amino acid substitutions on the cap protein of Vietnamese DuCV strains.
| Virus Strain | Genotype | Amino Acid Residues on Cap Protein | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 12 | 47 | 55 | 82 | 106 | 107 | 155 | 156 | 177 | 183 | 194 | 197 | 205 | 236 | ||
| Majority | G | N | S | Q | N | K | T | T | V | V | T | Y | R | D | |
| VNUA-102/2023 | I | . | H | . | R | S | T | . | A | . | I | G | H | K | N |
| VNUA-114/2023 | I | . | . | . | . | . | . | . | . | . | . | . | . | . | . |
| VNUA-137/2023 | I | . | . | N | . | . | . | S | . | . | . | . | . | . | . |
| VNUA-225/2023 | I | . | H | S | R | S | T | . | A | . | I | G | H | K | N |
| VNUA-251/2023 | I | . | . | N | . | S | . | . | . | . | . | . | . | ||
| VNUA-318/2024 | I | . | H | . | R | S | T | . | . | . | I | G | H | N | |
| VNUA-322/2024 | I | . | . | . | . | . | . | . | . | I | . | . | . | . | . |
| VNUA-315/2024 | I | . | . | N | . | . | . | S | . | . | . | . | . | . | . |
| VNUA-331/2024 | I | . | . | . | . | . | . | . | . | . | . | . | . | . | . |
| VNUA-HN47/2021 | I | . | . | N | . | . | . | . | . | . | . | . | . | . | . |
| VNUA-TB61/2021 | I | S | . | N | . | . | . | . | . | . | . | . | . | . | . |
| VNUA-HY40/2021 | I | . | . | . | . | S | T | . | . | . | . | . | . | . | . |
| VNUA-TN85/2021 | I | . | H | . | R | S | T | . | . | . | I | G | H | K | N |
| VNUA-HD89/2021 | II | A | H | . | . | . | . | . | . | I | . | G | . | K | E |
| VNUA-BG135/2021 | II | A | H | . | . | G | . | . | . | I | . | G | . | K | E |
Vietnamese DuCV strains in this study are indicated in bold.
Table 7.
Recombination statistics of the Vietnamese DuCV Cap gene sequences using RDP 5.
| Method | Recombination p-Value |
|---|---|
| GENECONV | 3.71 × 10−2 |
| MaxChi | 3.26 × 10−2 |
| Chimaera | 3.16 × 10−2 |
| SiScan | 9.58 × 10−5 |
| PhylPro | 3.42 × 10−2 |
Recombination events having a p-value below 0.05 were deemed reliable.
Table 8.
Recombination analysis of the Vietnamese DuCV Cap gene sequences using RDP 5.
| No. | Recombination Event | Major Parent | Minor Parent |
|---|---|---|---|
| 1 | Vietnam/VNUA-102/2023 | Vietnam/VNUA-114/2023 | Germany/NC_005053.1/2003 |
| 2 | Vietnam/VNUA-225/2023 | Vietnam/OM176552.1/VNUA-HY40/2021 | Germany/NC_005053.1/2003 |
| 3 | Vietnam/VNUA-318/2024 | Vietnam/OM176552.1/VNUA-HY40/2021 | Germany/NC_005053.1/2003 |
Table 9.
Positive selection on Rep protein of DuCV strains.
| Site | α | β | β − α | Prob [α > β] | Prob [α < β] | Bayes Factor [α and β] |
|---|---|---|---|---|---|---|
| 112 | 0.62 | 4.98 | 4.36 | 0.02 | 0.95 | 42.93 |
α indicates posterior synonymous substitution rate at a site; β indicates posterior non-synonymous substitution rate at a site; α > β: negative selection; α < β: positive selection; α = β: neutral selection; Prob [α > β] ≥ 0.9: posterior probability of negative selection at a site; Prob [α < β] ≥ 0.9: posterior probability of positive selection at a site. Eighty-nine negatively selective positions were indicated.
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Dong, H.V.; Trinh, D.Q.; Tran, G.H.T.; Vu, T.T.; Nguyen, T.H.B.; Rattanasrisomporn, A.; Bui, D.A.T.; Rattanasrisomporn, J. Characterization of an Emerging Recombinant Duck Circovirus in Northern Vietnam, 2023–2024. Viruses 2025, 17, 732. https://doi.org/10.3390/v17050732
AMA Style
Dong HV, Trinh DQ, Tran GHT, Vu TT, Nguyen THB, Rattanasrisomporn A, Bui DAT, Rattanasrisomporn J. Characterization of an Emerging Recombinant Duck Circovirus in Northern Vietnam, 2023–2024. Viruses. 2025; 17(5):732. https://doi.org/10.3390/v17050732
Chicago/Turabian StyleDong, Hieu Van, Dai Quang Trinh, Giang Huong Thi Tran, Thanh Thi Vu, Thinh Hung Ba Nguyen, Amonpun Rattanasrisomporn, Dao Anh Tran Bui, and Jatuporn Rattanasrisomporn. 2025. "Characterization of an Emerging Recombinant Duck Circovirus in Northern Vietnam, 2023–2024" Viruses 17, no. 5: 732. https://doi.org/10.3390/v17050732
APA StyleDong, H. V., Trinh, D. Q., Tran, G. H. T., Vu, T. T., Nguyen, T. H. B., Rattanasrisomporn, A., Bui, D. A. T., & Rattanasrisomporn, J. (2025). Characterization of an Emerging Recombinant Duck Circovirus in Northern Vietnam, 2023–2024. Viruses, 17(5), 732. https://doi.org/10.3390/v17050732
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