An outbreak of ORFV infection among dairy goats in 2009 was reported in Korea [12]. Infection with this virus in black goats had not been previously observed in Korea prior to the import of dairy goats from abroad. In the present study, five ORFVs were isolated from Korean black goats and characterized to evaluate the genetic relationships between these ORFVs and other strains of this virus. The complete B2L and VIR genes were sequenced, and phylogenetic trees were subsequently constructed.

Five suspected cases of contagious ecthyma in Korean black goats were reported in different geographic areas of Korea between 2010 and 2011 (Table 1). The affected goats were 6~12 months old. Heavy scabs on the lips were observed in all the animals. Dried scabs were collected from the infected goats and stored at -70℃ until analysis.

PCR with OVS- and OVA-specific primers was performed as previously described [10]. The OVS and OVA primer sequences were 5'-AGGCGGTGGAATGGA AAGA-3' and 5'-CCAGCAGGTATGCCAGGATG-3', respectively. Briefly, total viral DNA was extracted from scab samples using a QIAamp DNA Mini kit (Qiagen, Germany) according to the manufacturer's instructions. Amplification was performed using a GeneAmp PCR System 2700 (Applied Biosystems, USA) under the following conditions: preliminary heating at 94℃ for 5 min; 10 cycles of denaturation at 94℃ for 30 seconds, annealing at 55℃ for 45 seconds, and elongation at 72℃ for 1 min; 20 cycles of denaturation at 94℃ for 30 seconds, annealing at 57℃ for 45 seconds, and elongation at 72℃ for 1 min; and a final elongation step at 72℃ for 5 min.

Virus was isolated from the clinical scab samples of Korean black goats. The scab samples were homogenized mechanically in PBS in a tube using a pellet pestle device (Kimble Chase, USA). Homogenized samples were centrifuged in 4℃ at 3,000 × g for 5 min. The supernatant was then passed through a 0.45-µM filter (Millipore) and used to inoculate ovine testis cells (OA3.Ts) (ATCC). The cell cultures were incubated in Dulbeccos modified Eagles medium (Invitrogen, Carlsbad, CA) at 37℃ in 5% CO₂ and three blind passages were performed until cytopathic effects (CPEs) were observed. The ORFV was isolated in OA3.Ts cells and propagated in Madin-Darby bovine kidney (MDBK) cells (ATCC).

Also, the homogenates were centrifuged in 4℃ at 3,000 × g for 5 min. The supernatant was then collected and negatively stained with 2% phosphotungstic acid for electron microscopy.

PCR for the phylogenetic analysis was performed using previously described primers [4,8]. The amplified products were purified using an Agarose Gel DNA Extraction kit (INtRON, Korea) and cloned into a pGEM-T vector (Promega, USA) according to the manufacturer's instructions. Automated nucleotide sequencing of the VP60 gene insert was performed using an ABI 3130XL Genetic Analyzer (Applied Biosystems, USA) with a BigDye Terminator Cycle Sequencing kit (Applied Biosystems, USA). The sequences were confirmed by three or more independent reactions in both directions. Published parapoxvirus sequences were retrieved from GenBank (National Center for Biotechnology Information, USA) for phylogenetic analyses.

B2L and VIR gene sequences of the Korean ORFV strains were aligned with the corresponding parapoxvirus sequences using Bioedit software (Ibis Biosciences, USA). A phylogenetic analysis was conducted using Bioedit software and Molecular Evolutionary Genetics Analysis (MEGA) 4.0 software with bootstrap values calculated from 1,000 replicates [14]. The neighbor-joining method was used for tree construction.

Cases of ORFV infection at five black goat farms were diagnosed and confirmed by PCR and DNA sequencing. The amplified PCR products were separated by electrophoresis and visualized by ethidium bromide staining. The size of the amplified PCR product was 708 bp. One ORFV strain (ORF/2011) was isolated from clinical samples from the infected black goats. CPEs were first observed 6 days after the cell cultures were passed twice, and typical parapoxvirus CPE patterns, indicated by cell rounding, pyknosis, and cell detachment, were observed.

Negatively stained ORFV particles were examined by electron microscopy. The particles had an oval-shaped morphology characteristic of parapoxviruses. Viral particle size was approximately 150~200 nm (data not shown).

An additional PCR assay was performed to obtain the full-length B2L and partial VIR gene fragments for sequencing. The amplified PCR products were 1206 bp for the full-length B2L gene and 552 bp for the partial VIR gene. The DNA was purified and sequenced for comparative analysis. Sequence comparison of the five Korean ORFV strains (contained one ORFV isolate) identified from Korean black goats demonstrated a high degree of identity between each virus and a previously reported ORF/09/Korea strain [12]. Results of the phylogenetic analysis based on the complete B2L gene (Fig. 1A) demonstrated that the five ORFV strains were most closely related to the ORF/09/Korea strain identified in 2009 and the Taiwan EU327506 strain. The five ORFV strains and ORF/09/Korea strain had a 99.2~99.5% and 98.4~99.2% similarity at the nucleotide and predicted amino acid level, respectively. The phylogenetic analysis based on the partial VIR gene revealed that the five ORFV strains were most closely related to the ORF/09/Korea strain identified in 2009 (Fig. 1B). The five ORFV strains and ORF/09/Korea strain showed a 99.0~99.2% and 98.7% similarity at the nucleotide and amino acid level, respectively.

ORFV is a highly contagious transboundary pathogen. If the virus is introduced into disease-free areas, it infects small ruminants and spreads easily [1]. ORFV infection among the Korean black goat population was not reported until dairy goats were brought into Korea. Dairy goats were initially imported from abroad during the 1990s to produce liquid and powdered milk. The dairy goat population in Korea has increased over the past several years. Several causes for ORFV outbreaks in Korean black goats exist, and a phylogenetic analysis may indicate the hypothetical origin of the viral strains involved.

B2L and VIR gene sequences have been widely used for molecular epidemiological studies of parapoxviruses. These are epidemiologically relevant sequences and a significant quantity of sequence data has been deposited in GenBank [1-4,9,10]. In the present study, the Korean ORFV strains were most closely related to the ORF/09/Korea strain from dairy goats according to the phylogenetic analysis based on the B2L and VIR genes. This result indicates that ORFVs from dairy goats might have been introduced into the Korean black goat population. Based on a molecular analysis alone, it is difficult to determine the precise route by which the ORFV from dairy goats was transmitted to Korean black goats. However, data from the current study suggest that introduction of ORFV into the Korean black goat population might have occurred through dairy goats imported for meat production or improvement of stock genetics.

The vaccine using orf virus isolated from goat may potentially provide better protection for goats than for sheep [11]. We isolated one ORFV as a vaccine candidate from a large-scale outbreak of ORFV infection in Korean goats. A vaccine will be developed in a future study. Additional epidemiological data concerning the distribution of ORFVs among dairy and Korean black goats in Korea will also contribute to the prevention of further ORFV outbreaks.