Abstract
As a zoonotic infectious disease, orf outbreaks have been reported in China in recent years. However, molecular epidemiology analysis has not been performed for Chinese orf virus (ORFV) strains. Here, we have identified 13 ORFVs from goats and sheep in China between 2009 and 2011. Thirty-four complete B2L sequences were used to construct a phylogenetic tree to elucidate the molecular epidemiology of ORFV in China. Nucleotide sequences of B2L genes of clinical samples and attenuated vaccine strains were aligned and compared. Three genotypes were found by molecular epidemiology analysis. Amino acid substitutions were dispersed among B2 polypeptides from wild and attenuated ORFV strains.
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Ovine contagious pustular dermatitis (orf) is an infectious viral zoonosis. Diseases caused by orf virus (ORFV) occur worldwide and have been reported in many countries [13]. ORFV causes a common viral skin disease that infects a range of wild ruminant species [10] as well as humans [6, 15, 23], especially immunodeficient individuals [3]. It often infects farmers, abattoir workers, veterinarians, and sheep shearers, who are considered to be at the greatest risk due to their professions; others at high risk are those engaged in the religious slaughter of animals [10, 12, 19, 24]. Thus, orf is a serious health threat to the sheep industry as well as to humans.
ORFV belongs to the genus Parapoxvirus of the family Poxviridae [14] and has an approximately 134–139-kb linear double-stranded DNA genome [8]; the whole genome has a high GC content of approximately 63.5 % [33]. The B2L gene of ORFV encodes a highly immunogenic envelope protein that induces a strong antibody response [8, 26]. A polymerase chain reaction (PCR) method based on the B2L gene is typically used to detect ORFV [1, 13, 17, 22, 30]. Complete or partial B2L sequences have often been used in phylogenetic analysis in India [13], Korea [22], China [7, 20, 34, 36], Brazil [1], and Turkey [18].
Orf was first reported in China in 1955. From the 1980s to the 1990s, orf was detected in eight Chinese provinces including Qinghai, Gansu, Tibet, Xinjiang, Liaoning, Jiangxi, Heilongjiang, and Hebei. In recent years, orf outbreaks have occurred in 17 Chinese provinces and within the city of Beijing [34]. Furthermore, seven women and four men were infected with the ORFV in Fujian Province in 2005. Thus, orf is a nationally important zoonosis in China. Several field cases have been reported [7], but little is known about the molecular epidemiology of the ORFV isolates from China. Thus, a phylogenetic analysis of ORFV in China is urgently needed to evaluate its molecular epidemiology and distribution characteristics. A total of 14 ORFV isolates were identified in clinical samples (one from a vaccine strain) from 10 provinces between 2009 and 2011. Phylogenetic analysis of the ORFV strains was performed based on the complete B2L gene sequence data from China and other countries deposited in GenBank (Table 1). We aligned and compared the deduced B2L amino acid sequences from the ORFV strains isolated from the clinical samples and attenuated vaccine strains. This is the first systematic phylogenetic analysis of orf virus in China, and the results may help to elucidate the molecular characteristics of ORFV in China or even worldwide.
Between 2009 and 2011, clinical samples were collected from 13 cities in 10 Chinese provinces (Fig. 1). Detailed information about the samples is provided in Table 1. In a case from GuangXi (GX/YB), we observed and recorded the clinical symptoms of hoof-type orf, vulva-type orf, and lip-type orf. Scrapings collected from infected goats were suspended in 0.1 M phosphate-buffered saline (1:10 V/V), freeze-thawed twice between −20 °C and 37 °C, and stored overnight at 4 °C. After centrifugation at 5000 rpm for 20 min at 4 °C, DNA was isolated from the supernatant using a genomic DNA purification kit (Promega, USA) and was used as the template in the PCR procedures [13]. Based on the published B2L gene sequence, a pair of primers was designed and synthesized (Sangon, China). The PCR products of B2L were visualized under ultraviolet light after 1 % agarose gel electrophoresis and ethidium bromide staining. Tissue scrapings from healthy goats were treated the same way and used as negative controls.
All PCR products were purified using a DNA purification system (Promega) according to the manufacturer’s protocol. The purified PCR products were sequenced using an automated DNA sequencer (Model 3770, Applied Biosystems, USA). The B2L gene sequences of ORFV strains from the other countries were obtained from GenBank (http://www.ncbi.nlm.nih.gov/). Sequence editing was performed using the DNASTAR program (http://www.dnastar.com/) [5, 9]. Multiple alignments were produced using the ClustalW program (http://www.clustal.org/) [28]. A phylogenetic tree was constructed based on the deduced amino acid sequences of the B2L gene using the neighbor-joining method [25, 35]. Bootstrap analysis was performed for 1000 trials, using the maximum-likelihood method in MEGA version 4.0 (http://www.megasoftware.net/) [27].
Thompson et al. [28] used ClustalW software to uncover possible substitutions in amino acid alignments of the B2 envelope proteins in wild-type ORFV and attenuated vaccine strains. The Chinese vaccine (JQ904789) and USA vaccine (AY278209) strains were selected for comparison with isolates from goats (JQ904791, JQ904793, AY278208), sheep (JQ904795, JQ904799, AY424970).
Typical clinical symptoms of orf in goats and sheep that were sampled included papules, pimples, ulceration, and incrustation around the lip, hoof, and vulva (see Supplementary material Figure S1). The expected 1,137-bp PCR products were obtained from DNA extracted from scrapings, but not from the negative controls. The sequencing results showed that the B2L gene was 1,137 bp long, encoded 378 encoded amino acids, had an average G:C ratio of approximately 63.3 %, and had a predicated molecular weight of 41.7 kDa. The B2L gene sequences identified in this study were submitted to NCBI GenBank and assigned accession numbers (JQ904786–JQ904799).
The 14 ORFV isolates from this study and 20 strains downloaded from GenBank were aligned and subjected to phylogenetic analysis. They shared 96.8–98.9 % and 97.5–99.2 % sequence identity at the nucleotide and amino acid level, respectively. The results of neighbor-joining analysis revealed three distinct genotypes (Fig. 2). Genotype I included 17 ORFV strains, 16 of which were from different parts of China and only one of which was from Germany. Genotype II contained nine strains from India (4/9) and China (5/9). Genotype III included eight ORFV isolates from the USA (4/8), New Zealand (1/8), China (2/8), and South Korea (1/8).
In genotype I, 94.1 % (16/17) of the strains were from China; the other (HM133903) was from Germany. Fourteen ORFV strains in genotype I were isolated from Chinese goats. In genotype II, 8/9 (88.9 %) strains (the other was HM466933) were isolated from sheep in India and China. In genotype III, there were two goat strains, two sheep strains, one takin strain, and three host unknown strains.
Multiple alignment of amino acid sequences showed substitutions dispersed all along the length of the protein. Compared with wild ORFV strains, the Chinese vaccine strain JQ904789 had five amino acid substitutions, including A11G, E98A, V101I, S249G, and Q256R (see Supplementary material Figure S2). The USA vaccine strain AY278209 appeared to be divergent from the other strains, as evidenced by substitutions such as S5Y, S6F, V9L, D79N, R111K, and N196D (see Supplementary material Figure S2). For the JS FX goat strain JQ904791, seven unique amino acid substitutions were observed: V16G, A24G, L26R, A27G, N30T, S32T, and T33P. The unique amino acid substitutions V9L and R111K were also found.
It is difficult to differentiate among orf, pox, foot-and-mouth disease, ulcerative dermatosis, dermatophilosis, and staphylococcal dermatitis based on clinical symptoms [31, 32]. The PCR method was able to diagnose ORFV infection in field specimens of the affected animals [16]. It was traditionally believed that clinical symptoms of orf are found around the ovine lips only. Three types (lip, vulva, and hoof) of orf were observed in goats of the GX/YB strain (JQ904793) in this study.
Orf is currently endemic in China. No commercial orf vaccine is available, so the number of outbreaks in sheep and goats continues to increase. Although there have been phylogenetic analyses conducted of orf cases in China [7, 34, 36], there have been limited numbers of case reports in each region. Understanding the molecular epidemiology of an infectious disease is useful for controlling and even eradicating it [4] . In this paper, we identified 14 ORFV strains in China that were distributed among 10 provinces between 2009 and 2011. We first sequenced and compared the B2L gene sequence from the attenuated Chinese and USA vaccine strains. The phylogenetic analysis was based on 34 complete B2L gene sequences (14 from this study) that had been reported worldwide between 2003 and 2011.
Phylogenetic analysis with 1,000 bootstrap replicates identified three genotypes (Fig. 2). Among the 14 Chinese isolates studied in this paper, 11 belonged to genotype I, two were genotype II, and only the SD/DY (JQ904794) isolate belonged to genotype III. The ORFV strains isolated from one country or nearby regions belonged to similar genotypes, while virus strains from the same species belonged to similar branches (Fig. 2). The middle branch of the phylogenetic tree had a bootstrap value of 41 %. This is a low percentage, and maybe this branch represents a new orf virus genotype (genotype II). The phylogenetic analysis results may indicate the hypothetical source of these viral strains [2, 29], but it is difficult to determine the precise route by which the identified ORFV variants were introduced. This may mean that ORFV strains in China are phylogenetically closely related to the other ORFV strains reported worldwide.
A live attenuated vaccine for orf based on heterologous cells or tissues is effective and popular [14, 21], but its exact attenuated molecular mechanism is obscure. The ORFV glycoprotein is one of the the important target proteins for studying virus-host interactions.
The B2L gene has been reported to encode a highly immunogenic envelope protein and play an important role in ORFV immunity [26]. To uncover the differences between vaccine and wild ORFV strains at the amino acid level, eight ORFV strains were selected, and their B2L genes were compared using ClustalW software. In the current study, some amino acid substitutions were dispersed along the B2L polypeptide of the wild and attenuated vaccine ORFV strains at positions 11, 16, 24, 26, 30, 32, 33, 98, 101, 109, and 313 (see Supplementary material Figure S2). Similar results were reported in India [13] and Brazil [1]. However, no unique amino acid substitutions were observed, which may reflect the fact that ORFV strains are antigenically closely related [11]. The role that these alternative amino acids play in the vaccine strain attenuated process remains to be elucidated. Future studies should produce more detailed epidemiological data about the distribution of ORFV in China and other countries.
References
Abrahao JS, Campos RK, Trindade GS, Guedes MI, Lobato ZI, Mazur C, Ferreira PC, Bonjardim CA, Kroon EG (2009) Detection and phylogenetic analysis of Orf virus from sheep in Brazil: a case report. Virol J 6:47
Adachi JA, Perego C, Graviss L, Dvorak T, Hachem R, Chemaly RF, Raad II (2009) The role of interventional molecular epidemiology in controlling clonal clusters of multidrug resistant Pseudomonas aeruginosa in critically ill cancer patients. Am J Infect Control 37:442–446
Ara M, Zaballos P, Sanchez M, Querol I, Zubiri ML, Simal E, Horndler C (2008) Giant and recurrent orf virus infection in a renal transplant recipient treated with imiquimod. J Am Acad Dermatol 58:S39–S40
Buller NB, Ashley P, Palmer M, Pitman D, Richards RB, Hampson DJ (2010) Understanding the molecular epidemiology of the footrot pathogen Dichelobacter nodosus to support control and eradication programs. J Clin Microbiol 48:877–882
Burland TG (2000) DNASTAR’s Lasergene sequence analysis software. Methods Mol Biol 132:71–91
Carr RW (1968) A case of orf (ecthyma contagiosum; contagious pustular dermatitis) contracted by a human from a wild Alaskan mountain goat. Alaska Med 10:75–77
Chan KW, Lin JW, Lee SH, Liao CJ, Tsai MC, Hsu WL, Wong ML, Shih HC (2007) Identification and phylogenetic analysis of orf virus from goats in Taiwan. Virus Genes 35:705–712
Chan KW, Yang CH, Lin JW, Wang HC, Lin FY, Kuo ST, Wong ML, Hsu WL (2009) Phylogenetic analysis of parapoxviruses and the C-terminal heterogeneity of viral ATPase proteins. Gene 432:44–53
Clewley JP (1995) Macintosh sequence analysis software. DNAStar’s LaserGene. Mol Biotechnol 3:221–224
Crumbie A (1998) The orf virus: a disease of the farming community. Community Nurse 4:44–45
Fleming SB, Blok J, Fraser KM, Mercer AA, Robinson AJ (1993) Conservation of gene structure and arrangement between vaccinia virus and orf virus. Virology 195:175–184
Ghislain PD, Dinet Y, Delescluse J (2001) Orf in urban surroundings and religious practices: a study over a 3-year period. Ann Dermatol Venereol 128:889–892
Hosamani M, Bhanuprakash V, Scagliarini A, Singh RK (2006) Comparative sequence analysis of major envelope protein gene (B2L) of Indian orf viruses isolated from sheep and goats. Vet Microbiol 116:317–324
Hosamani M, Scagliarini A, Bhanuprakash V, McInnes CJ, Singh RK (2009) Orf: an update on current research and future perspectives. Expert Rev Anti Infect Ther 7:879–893
Hubner G, Loewe KR, Dittmar FK (1974) Human infection by the virus of contagious pustular dermatitis of sheep (author’s transl). Dtsch Med Wochenschr 99:2392–2394
Inoshima Y, Morooka A, Sentsui H (2000) Detection and diagnosis of parapoxvirus by the polymerase chain reaction. J Virol Methods 84:201–208
Inoshima Y, Murakami K, Yokoyama T, Sentsui H (2001) Genetic heterogeneity among parapoxviruses isolated from sheep, cattle and Japanese serows (Capricornis crispus). J Gen Virol 82:1215–1220
Karakas A, Oguzoglu TC, Coskun O, Artuk C, Mert G, Gul HC, Sener K, Ozkul A (2013) First molecular characterization of a Turkish orf virus strain from a human based on a partial B2L sequence. Arch Virol 158:1105–1108
Lederman ER, Austin C, Trevino I, Reynolds MG, Swanson H, Cherry B, Ragsdale J, Dunn J, Meidl S, Zhao H, Li Y, Pue H, Damon IK (2007) ORF virus infection in children: clinical characteristics, transmission, diagnostic methods, and future therapeutics. Pediatr Infect Dis J 26:740–744
Li W, Ning Z, Hao W, Song D, Gao F, Zhao K, Liao X, Li M, Rock DL, Luo S (2012) Isolation and phylogenetic analysis of orf virus from the sheep herd outbreak in northeast China. BMC Vet Res 8:229
Mercante MT, Lelli R, Ronchi GF, Pini A (2008) Production and efficacy of an attenuated live vaccine against contagious ovine ecthyma. Vet Ital 44:537–542 (543-537)
Oem JK, Roh IS, Lee KH, Lee KK, Kim HR, Jean YH, Lee OS (2009) Phylogenetic analysis and characterization of Korean orf virus from dairy goats: case report. Virol J 6:167
Paiba GA, Thomas DR, Morgan KL, Bennett M, Salmon RL, Chalmers R, Kench SM, Coleman TJ, Meadows D, Morgan-Capner P, Softley P, Sillis M, Green LE (1999) Orf (contagious pustular dermatitis) in farmworkers: prevalence and risk factors in three areas of England. Vet Rec 145:7–11
Robinson AJ, Petersen GV (1983) Orf virus infection of workers in the meat industry. N Z Med J 96:81–85
Saitou N, Nei M (1987) The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol Biol Evol 4:406–425
Sullivan JT, Mercer AA, Fleming SB, Robinson AJ (1994) Identification and characterization of an orf virus homologue of the vaccinia virus gene encoding the major envelope antigen p37K. Virology 202:968–973
Tamura K, Dudley J, Nei M, Kumar S (2007) MEGA4: molecular evolutionary genetics analysis (MEGA) software version 4.0. Mol Biol Evol 24:1596–1599
Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG (1997) The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res 25:4876–4882
Thompson RC, Constantine CC, Morgan UM (1998) Overview and significance of molecular methods: what role for molecular epidemiology? Parasitology 117(Suppl):S161–S175
Tikkanen MK, McInnes CJ, Mercer AA, Buttner M, Tuimala J, Hirvela-Koski V, Neuvonen E, Huovilainen A (2004) Recent isolates of parapoxvirus of Finnish reindeer (Rangifer tarandus tarandus) are closely related to bovine pseudocowpox virus. J Gen Virol 85:1413–1418
Watson P (2001) Clinical diagnosis of FMD in sheep. Vet Rec 149:499
Wilson DJ, Scott PR, Sargison ND, Bell G, Rhind SM (2002) Effective treatment of severe facial dermatitis in lambs. Vet Rec 150:45–46
Wittek R, Kuenzle CC, Wyler R (1979) High C+G content in parapoxvirus DNA. J Gen Virol 43:231–234
Zhang K, Shang Y, Jin Y, Wang G, Zheng H, He J, Lu Z, Liu X (2010) Diagnosis and phylogenetic analysis of Orf virus from goats in China: a case report. Virol J 7:78
Zhang W, Sun Z (2008) Random local neighbor joining: a new method for reconstructing phylogenetic trees. Mol Phylogenet Evol 47:117–128
Zhao K, Song D, He W, Lu H, Zhang B, Li C, Chen K, Gao F (2010) Identification and phylogenetic analysis of an Orf virus isolated from an outbreak in sheep in the Jilin province of China. Vet Microbiol 142:408–415
Acknowledgments
This work was supported by the National Natural Science Foundation of China (Grant No. 31201914), the China Agriculture Research System (CARS-39) and China Postdoctoral Science Foundation funded project (2013M530683). We thank Professor Gangyi Xu of Sichuan Agricultural University, Professor Zijun Zhang of Anhui Agricultural University, and Professor Xunping Jiang of Huazhong Agricultural University for their contributions. The authors wish to thank the journal editors and anonymous reviewers for editing and revising the manuscript.
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Supplementary material 1 (PDF 54 kb) Figure S1. Representative clinical symptoms of orf virus (ORFV) infection. (A) Goat with severe proliferative ecthyma lesions around the hoof. (B) Severe proliferative ecthyma lesions around the testis and urethral orifice. (C) Wart-like multiple nodules on the upper and lower labia. The arrows indicate the lesion positions
705_2013_1946_MOESM2_ESM.pdf
Supplementary material 2 (PDF 29 kb) Figure S2. Multiple sequence alignment of the B2L amino acid sequences derived from clinical samples and attenuated vaccine orf virus (ORFV) strains using ClustalW. The dots represent identity among all sequences. The numbers indicate the amino acid positions of the B2 envelope protein
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Zhang, K., Liu, Y., Kong, H. et al. Comparison and phylogenetic analysis based on the B2L gene of orf virus from goats and sheep in China during 2009-2011. Arch Virol 159, 1475–1479 (2014). https://doi.org/10.1007/s00705-013-1946-6
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DOI: https://doi.org/10.1007/s00705-013-1946-6