Next Article in Journal
Cytomegalovirus Infections in Children with Primary and Secondary Immune Deficiencies
Next Article in Special Issue
Transcriptome Analysis for Genes Associated with Small Ruminant Lentiviruses Infection in Goats of Carpathian Breed
Previous Article in Journal
The Current Evidence Regarding COVID-19 and Pregnancy: Where Are We Now and Where Should We Head to Next?
Previous Article in Special Issue
Analysis of Single Nucleotide Variants (SNVs) Induced by Passages of Equine Influenza Virus H3N8 in Embryonated Chicken Eggs
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Viruses
Volume 13
Issue 10
10.3390/v13101999
viruses-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Phylogenetic Analysis of European Brown Hare Syndrome Virus Strains from Poland (1992–2004)

by
Andrzej Fitzner
1,*,
Ewa Kwit
2,
Wiesław Niedbalski
1,
Ewelina Bigoraj
2,
Andrzej Kęsy
1 and
Artur Rzeżutka
2,*
1
Department of Foot and Mouth Disease, National Veterinary Research Institute, ul. Wodna 7, 98-220 Zduńska Wola, Poland
2
Department of Food and Environmental Virology, National Veterinary Research Institute, Al. Partyzantów 57, 24-100 Puławy, Poland
*
Authors to whom correspondence should be addressed.
Viruses 2021, 13(10), 1999; https://doi.org/10.3390/v13101999
Submission received: 29 July 2021 / Revised: 19 September 2021 / Accepted: 27 September 2021 / Published: 5 October 2021
(This article belongs to the Special Issue State-of-the-Art Animal Virus Research in Poland)
Browse Figures
Versions Notes

Abstract

:
European brown hare syndrome (EBHS) is lethal to several species of free-living hares worldwide. The genetic characterization of its virus (EBHSV) strains in European circulation and epidemiological knowledge of EBHSV infections is not yet complete. The study determined the nucleotide sequences of the genomes of EBHSV strains from Poland and analyzed their genetic and phylogenetic relationships to a group of hare lagoviruses. The genome of five virus strains detected in Poland between 1992 and 2004 was obtained by RT-PCR and sequencing of the obtained amplicons. The genetic relationships of the EBHSV strains were analyzed using the full genome and VP60 gene sequences. Additionally, the amino acid sequence of the VP60 gene was analyzed to identify mutations specific to recognized EBHSV subgroups. Partial amplification of the virus open reading frame (ORF)1 and ORF2 regions obtained nearly complete nucleotide genome sequences of the EBHSV strains. Phylogenetic analysis placed them in a GII.1 cluster with other European strains related to nonpathogenic hare caliciviruses. VP60 gene analysis allocated these EBHSV strains to the G1.2, G2.2–2.3 or G3 virus genetic groups. The amino acid sequence differences in the entire genome ranged from 1.1 to 2.6%. Compared to a reference French EBHSV-GD strain, 22 variable amino acid sites were identified in the VP60 region of the Polish strains, but only six were in VP10. Single amino acid changes appeared in different sequence positions among Polish and other European virus strains from different genetic groups, as well as in VP10 sequences of nonpathogenic hare caliciviruses. The results of the study showed a high genetic homogeneity of EBHSV strains from Poland despite their different location occurrence and initial detection times. These strains are also phylogenetically closely related to other EBHSV strains circulating in Europe, likely confirming the slow evolutionary dynamics of this lagovirus species.

1. Introduction

European brown hare syndrome (EBHS) was recognized for the first time in Sweden in 1980 [1], although it may have appeared earlier in Europe [2,3,4]. Since that time, outbreaks of EBHS have been reported among free-living hares in different European countries [3,5,6,7,8,9,10,11,12,13,14,15], including Poland [16,17,18]. The disease usually has an acute course with nonspecific symptoms typical of generalized viral infections and leads to sudden death [1]. It is caused by the European brown hare syndrome virus (EBHSV) which belongs to the Lagovirus genus within the Caliciviridae family [14,19,20]. Besides EBHSV and rabbit hemorrhagic disease virus (RHDV), the Lagovirus genus also includes nonpathogenic hare caliciviruses (HaCV) [21], which may have an impact on the recombination events and differentiation process of EBHSV [22,23,24]. The non-enveloped capsid of lagoviruses contains a single-stranded RNA of positive polarity, approximately 7.5 kb in length. Unlike other animal caliciviruses, the EBHSV and RHDV genomes contain two open reading frames (ORFs), the first encoding the nonstructural proteins as well as the major capsid virus protein (VP60), and the second encoding the gene of the small structural protein (VP10) [20,25,26,27].
The first genetic and phylogenetic analyses of the EBHS virus strains focused on the short fragments (265–398 bp) of the VP60 gene that encode the capsid structural protein [2,28,29]. They showed the phylogenetic distinctiveness of EBHSV from RHDV and indicated high strain similarity within each calicivirus species. Despite the small number of EBHSV sequences available, phylogenetic variability of EBHSV strains associated with their geographical origin and time of detection has been observed [29]. Analysis of complete VP60 gene sequences also disclosed temporal- and geographic-related differences and revealed the existence of two main genetic groups of EBHSV: group A, encompassing Swedish EBHSV strains detected before 1989, and group B, with virus strains detected after 1989 in the rest of Europe [30]. Contrary to these results, the analyses of partial VP60 gene fragments of approximately 200 bp, have shown at least three independent directions of the virus’ spread from Scandinavia across Europe [1,3,5,8,16,19,25,28]. This finding has confirmed the slow evolutionary dynamics of EBHSV, evidenced by low genetic variability of the strains and formation of new genetic subgroups of limited geographical range [8,28,31,32]. The variability of the EBHSV strains could be related to the evolution of RHDV, in which there have been observed recombination events between different virus types including nonpathogenic hare caliciviruses [23]. No similar type of recombination encompassing the capsid protein gene has been observed among EBHSV strains so far [30]. Nevertheless, it was mapped in the genome region encoding the nonstructural proteins, resulting in the emergence of EBHSV/RHDV2 recombinants [33].
Data on the epidemiology of EBHSV infections and strain virulence circulating in the European hare population are very limited. Gaining full understanding of these aspects of EBHSV is circumscribed by the difficulties in growing it in cell cultures. These difficulties significantly hamper research related to the assessment of the virus’ variability and recognition of the role and functions of particular genes in adaptation of the virus to new hosts.
The purposes of the study were to determine the genome nucleotide sequences of the EBHSV strains from Poland, and to identify conserved or variable single-nucleotide polymorphisms (SNPs). Viral phylogenetic relationships to previously detected EBHSV strains in Europe were also investigated. In order to determine the genetic affiliation of the Polish strains to currently identified EBHSV subgroups, a nucleotide sequence analysis of the VP60 gene was conducted. The amino acid sequences of this gene were also analyzed to identify the presence of mutations specific to the virus subgroups.

2. Materials and Methods

2.1. EBHSV Strains and Lagovirus Sequences

Five EBHSV strains (NP1192, L98, K501, G104, and K204) detected in hares from 1992 to 2004 were used for the genetic analysis. These virus strains now belong to the strain collection of the National Reference Laboratory for Rabbit Myxomatosis at the National Veterinary Research Institute in Puławy, Poland. Infected animals were found dead in different geographical locations across Poland and liver and spleen samples were taken from the carcasses. The presence of EBHSV in the animals was confirmed by testing the tissue samples using an RHDV–EBHSV CR Mab ELISA kit (IZSLER, Brescia, Italy).
For the phylogenetic analysis, 10 full EBHSV genome sequences, 46 VP60 complete EBHSV sequences, and 10 VP10 complete EBHSV sequences, available in GenBank, were used. These comprised virus strains of particular EBHSV genogroups detected in Sweden (KC832838–39, KJ679513–14, KJ679522, KJ679534–35, KJ679547–48, KJ679553, KJ679558–59, and KJ679562–63), France (AJ971301, AJ971304–06, AJ971311, AJ971315, AM408588, AM887765, AM933648–50, FN689419–21, HF571039–40, KY801206, LT168848, and Z69620), Italy (X98002, KF591083, KJ923230, KU961677–78, and MF356366) and Germany (U09199, LR899140, LR899152, LR899171, LR899182, LR899185, and LR899188). Additionally, six sequences of nonpathogenic HaCV and rabbit calicivirus (RCV) lagoviruses from France (MH204883), Italy (KR230102) and Australia (EU871528 and MK138383–85), as well as RHDV (genotype GI.1b, M67473), and two EBHSV/RHDV2 (LR899142 and LR899187) recombinant strains were also included.

2.2. Amplification of the EBHSV Genome

To determine the genome sequences of Polish virus strains, amplification of the overlapping genome fragments was conducted using primers specific to the EBHSV genome (Supplementary Table S1). Additionally, several sets of primers were designed based on the reference EBHSV-GD89 (Z69620) sequence to cover the missing regions of the virus genome using the primer-BLAST tool (https://www.ncbi.nlm.nih.gov, accessed on 22 September 2018). Primers were synthesized by Genomed S.A. (Warsaw, Poland). EBHSV RNA was extracted from animal tissues using an RNeasy Mini Kit (Qiagen, Hilden, Germany), according to the manufacturer’s instructions. Subsequently, for amplification of individual EBHSV genome fragments, the OneStep RT-PCR Kit, (Qiagen, Hilden, Germany) was employed. The reactions were conducted in 50 µL of PCR mixture containing 2 µL of enzyme mix, 1 × buffer, 400 µM of dNTPs, 0.6 µM of the appropriate forward and reverse primer pair, 10 U of RNAsin (Invitrogen, Waltham, MA, USA), 5 µL of RNA template and redistilled water to the required reaction volume. The following amplification protocol was used: reverse transcription at 50 °C for 30 min and initial denaturation at 94 °C for 30 s followed by 35 cycles consisting of denaturation at 94 °C for 30 s, primer annealing (from 54 °C to 58 °C depending on the primer set) (Supplementary Table S1) for 45 s, extension at 72 °C for 1 min, and a final elongation step at the same temperature but for 10 min. PCRs yielded products varying in length from 265 to 858 bp.

2.3. Sequencing and Phylogenetic Analyzis

PCR amplicons were visualized in 1.5% agarose gel, purified and directly sequenced in both directions using the ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kit on an ABI 3730XL DNA sequencer (Life Technologies, Carlsbad, CA, USA) at the Genomed S.A. sequencing service. For comparative analysis of nucleotide sequences of EBHSV strains, BLASTn software was used (accessed on 22 January 2021) [34,35]. The sequences were aligned using Clustal W [36]. The phylogenetic trees were constructed based on 15 full genome, 51 VP60 and 15 VP10 complete gene sequences of EBHSV using a Maximum Likelihood method with the Tamura–Nei model with uniform rates, and Nearest-Neighbor-Interchange (NNI) method for topology searching in MEGA version 7.0.26 [37]. This tool has also been employed in recent studies on lagovirus phylogeny [38,39]. A branch support was estimated using 1000 bootstrap replicates. The phylogenetic relationship among the sequences analyzed was considered reliable when the bootstrap value was ≥70%. The obtained genome sequences of Polish virus strains were deposited in GenBank under accession numbers MK440613–MK440617.

3. Results

3.1. Sequence Analyzis of EBHSV Strains from Poland

The amplicons’ sequences were merged to the nearly complete genome sequences of the EBHSV L98 (7424 bp), NP1192 (7422 bp), G104 (7414 bp), K204 (7409 bp) and K501 (7330 bp) lacking only the initial twenty-nucleotide fragment upstream of the 5ʹ untranslated region. Only the K501 sequence did not contain the 3ʹUTR fragment. The highest sequence similarities in the entire genome (97.6%), the VP60 gene (97.8%), and in the nonstructural protein (NSP) gene (97.6%) were observed between the K501 and L98 strains. However, the lowest genetic resemblances corresponding to 93%, 93.4%, and 92.8% nucleotide identity in similar genome fragments were between the K204 and NP1192 strains. In the ORF2 region encoding the structural VP10 protein, 98.8% sequence similarity between EBHSV K501 and NP1192 was found despite the nine-year difference between their first detections. Although detected at similar times, K204 and G104 revealed the lowest percentage of identical nucleotides in their VP10 genome fragments at 93.6%. The similarity of the genomic nucleotide sequences of the analyzed virus strains and their fragments encoding structural and nonstructural proteins are presented in Table 1. At 98%, the highest nucleotide sequence similarity of the whole virus genome was observed between NP1192 and the GD89 (Z696290) reference EBHSV strain. When each genome fragment was analyzed separately, the sequence genetic resemblances were 99.4% (VP60), 99.4% (RNA-dependent RNA polymerase), 97.0% (NSP), and 99.1% (VP10). The other Polish virus strains were 93–94% similar to EBHSV GD89 in the whole genome. The comparison of the NP1192 ORF1–ORF2 sequence with the Swedish O4022-10 reference virus strain gave 94% sequence similarity. It ranged from 91 to 92.5% for other Polish strains, although the individual NSP, VP60, and VP10 virus segments showed a relatively higher (91–94%) sequence identity.

3.2. Analysis of the Lagovirus Phylogenetic Relationships Based on ORF1–ORF2 Genome Sequences

The phylogenetic analysis of genome sequences of EBHSV strains encompassing the ORF1 and ORF2 region (nucleotide positions 21–7350 according to the reference EBHSV-GD (Z69620) strain) assigned them to one common cluster including strains from group A and group B (Figure 1). In the group of EBHSV strains from Poland, NP1192 clusters together with the French reference EBHSV-GD. The L98, K501, K204 and G104 EBHSV strains form one genetic cluster (bootstrap value 100%) jointly with the Italian Wolf17–2016 EBHSV sequence. Within this virus group, two subclusters are formed, one containing the three Polish strains L98, K501, and K204 and the other the G104 strain and virus sequences detected in 2019–2020 in Germany. The results of phylogenetic analysis of the whole virus genome (ORF1–ORF2) and its segments encoding the VP60 and VP10 structural proteins indicates the distinctiveness of G104 from the group of the other EBHSV strains from Poland. Nevertheless, some relatedness was observed to younger European virus strains originating from France and Germany. In the VP60 region, the nucleotide sequence differences between G104 and the other virus strains from the G1.3 and G1.1 subgroups including EBHSVs from group A did not exceed 9.7%, while they were 5% for strains clustered to the G2 group. The highest nucleotide sequence similarity of 99.4% was found between G104 and the 0836 (HF571040) French strain detected in 2008. In the case of the EBHSV strains from France, Sweden, Italy, and Germany clustered together in the G3 group, the nucleotide sequence differences were in the range of 1.3–3.5% (Supplementary Table S2).

3.3. Nucletide and Amino Acid Sequence Analysis of the Structural Genes of EBHSV Strains from Poland and Elsewhere in Europe

The phylogenetic analysis conducted based on the VP60 and VP10 sequences showed that the EBHSV strains from Poland belonged to the G1, G2, or G3 virus genetic groups (Figure 2 and Figure 3). NP1192 and the virus strains from France and Sweden detected in a similar time span are clustered together in the G1.2 subgroup of the G1 cluster. The L98, K501 and K204 Polish strains are related to other French EBHSV strains first detected between 2000 and 2006, which are classified to the G2.2 and G2.3 subgroups. In the case of the G104 strain, it belongs to a large group of G3 EBHSV strains detected in Europe at different times and geographical locations.
The differences in the amino acid sequences between the Polish virus strains range from 1.1 to 2.6% in the entire two-open-reading-frame genome. For the genome fragment encoding the VP60 protein, the variability of the amino acid sequence is 0.9–2.7%; however, for the VP10 fragment it is higher than those observed for the entire genome, at 0.9–5.5%. In comparison to the VP60 region of the reference EBHSV-GD strain, this region of the Polish virus strains’ sequences identified 22 variable amino acids sites, i.e., 58 (A/V), 66 (V/A), 231 (D/E), 270 (S/C), 291 (I/F), 302 (S/T), 327 (I/V), 343 (T/S), 383 (S/N), 410 (T/A/S), 415 (I/L), 417 (L/M), 427 (V/T), 461 (A/S), 476 (A/S), 522 (V/I), 524 (M/L), 536 (A/T), 542 (D/E), 544 (T/A), 565 (L/F), and 566 (A/T) (Table 2). Substitutions at positions 427, 522, and 524 for NP1192 are consistent with the changes observed with EBHSV sequences from the G1 group, whereas the TIL pattern of amino acids of the remaining Polish strains corresponds to the G2 virus group. In the sequences of the Polish L98, K501, G104, and K204 strains, identical amino acid substitutions occur at eight positions, i.e., 58, 66, 302, 327, 383, 427, 522, and 524. The T410A amino acid change was present in the sequences of the L98, K501, and K204 strains, and in the T/S form also in the G104 sequence. The substitutions at positions D542E and A566T are common to the L98, G104, and K204 strains. Two other substitutions, T343S and A476S, appeared in the K501 and K204 sequences. The remaining amino acid changes occur in sequences of Polish virus strains. Analysis of the VP60 amino acid profile of the NP1192 strain at sites 302 (S), 383 (S), 406 (A), 407 (Q), 427 (V), and 469 (V) affiliate this strain to the G1.2 subgroup with the French EBHSV GD89 and B-EBHSV-6 strains. Furthermore, the analysis of codons 383, 410, and 476 located in the C-terminal part of the VP60 gene of EBHSV strains from Poland revealed concordance of the amino acid profile of the L98 strain with that of the Swedish V171 and French 0102 strains from the G2.2 subgroup. The amino acid substitutions at positions 383, 410, and 476 found in K501 and K204 are similar to those of other strains belonging to the G2.3 subgroup. A VP60 amino acid profile is observed for G104, which differs at positions 410, 417, and 476 from other Polish strains, but is consistent with the profile of the 0330 French strain from 2003 and other European EBHSV strains from Sweden, France, and Italy in the 2005–2014 period, as well as from strains detected in recent years in Germany belonging to the G3 group.
In comparison to the Z69620 VP10 reference amino acid sequence, EBHSV strains from Poland and elsewhere in Europe were characterized by changes in six amino acids. Substitutions were identified at four amino acid positions (3, 64, 94, and 113). The E3D substitution was found in the three strains L98, G104, and K204, the N64S change appeared in the pair L98 and G104, and in the N64G form also in K204. The N94S change occurred in the L98, G104, and K204 strain sequences, whereas the N113D change was present in the K501 and G104 strains. Amino acid changes in positions G60S and L85F were present in the Polish G104 strain; however, they also appeared in EBHSV strains detected in 2019 and 2020 in Germany. Analysis of the genome of nonpathogenic GII.2, GII.3, and GII.4 hare caliciviruses proved that the same change at position 60 was also present in the HaCV Bs12-1 sequence and in the G/N form also in the HaCV-A1 sequence. The L85F substitution occurred in all sequences of analyzed nonpathogenic hare caliciviruses.

4. Discussion

The population of hares has decreased sixfold over the last 30 years in Poland. Among the factors responsible for the significant reduction in animal numbers are heavy predation, poaching, and the occurrence of infectious diseases, with EBHSV infections being considered the main cause of death [40]. Additionally, over the whole continent of Europe, a constant decline in the populations of hares and other related species has been observed due to EBHSV outbreaks [1]. A new threat is the RHDV 2 rabbit lagovirus, which crossed the species barrier causing infections in hares with a similar course to RHD [41,42,43,44,45,46].
Although in this study a phylogenetic analysis of EBHSV strains utilizing the complete sequences of the virus genome was carried out, only the VP60-based analyses revealed deep phylogenetic relationships among EBHSV strains. In this context, EBHSV strains from Poland were clustered to the G1, G2, and G3 lineages within the larger virus group B, together with other virus strains from Europe detected in similar time spans [32]. In contrast to virus group A, which encompasses the oldest strains from the Scandinavian Peninsula which disappeared in the late 1980s, group B covers strains detected in Europe more recently [30]. These findings are consistent with previous partial VP60 sequence analyses of Polish EBHSV strains [18,47,48]. Subsequent deeper analysis of the VP60 sequence of the NP1192 strain (G1 group) confirmed its evolutionary relationships with the phylogenetically older French EBHSV-GD89 and B-EBHSV-6 strains as well as with the Swedish V58 strain belonging to the G1.2 subgroup. However, the NP1192 strain did not reveal mutations in codons 406, 407, or 469, which are characteristic of EBHSV strains in the closely related G1.3 subgroup. The four EBHSV strains L98, K501, K204, and G104 belong to the G2 and G3 groups together with French and other European EBHSVs detected since 1999. The phylogeny of these Polish virus strains was also confirmed by analysis of the amino acid sequences of the VP60 gene at the mutational hot spots (aa 427 V/T, 522 V/I, and 524 M/L) specific to G2 viruses [32]. The fifth strain, G104, is related to a much younger virus lineage consisting of Swedish and French strains discovered from 2008 to 2014, as well as to the newer German strains from 2019 to 2020. The close genetic relationships between EBHSV strains from Poland and Germany may have resulted from the geographical proximity of their detection sites and could indicate the common routes of virus spread in a given geographical area.
The profile of amino acid sequences deduced from the nucleotide sequences of the EBHSV strains from Poland in the mutational hot spot positions of VP60 reflects the division of EBHSV strains into the genetic groups previously identified among French strains [32]. The V427, V522, and M524 amino acids characteristic of the G1 group are present in the NP1192 strain. The remaining Polish strains, L98, K501, K204, and G104, contain T, I, and L amino acids in their sequences, which are typical of French, Swedish, and Italian EBHSV strains forming the G2 group as well as strains of the G3 group [30]. Despite the Polish strains described in this study belonging to different genetic virus groups, they seem to represent the same serotype, which can still be detected using currently available ELISA kits (data not shown). Although in other studies distinct antigenic profiles of EBHSV strains have been observed, which could mirror changes in VP60 physiochemical properties, the phenotypic effect was still uncertain [30]. Analysis of the ORF2 genome sequences of EBHSV strains from Poland and elsewhere in Europe from 2016 to 2020, and of nonpathogenic HaCV GII.2–4 caliciviruses, indicates the presence of mutations at amino acid positions 60 and 85 in the VP10 structural protein gene. Among the EBHSV strains from Poland, the amino acid substitutions G60S and L85F occur only in the G104 sequence from 2004. They are also characteristic of much younger EBHSV strains from Germany from 2019 to 2020, although they did not appear in the sequence of the Wolf-17 strain from Italy from 2016. These mutations reflect changes observed in the structural part of the virus genome and can be considered as indirect evidence for the evolutionary processes related to the emergence and spread of a new genetic lineage of the virus strains in the hare population in Poland. The observed variability of the amino acid sequence and results of the phylogenetic analysis of the ORF2 region, supported by the phylogeny of VP60 and the entire genome, confirm G104’s relationship to EBHSV strains circulating in Europe between 2008 and 2020. Moreover, these results support the assumption that the ORF2 region can be employed in tracking the evolution of EBHSV strains to a greater extent than previously thought.
The analysis of the shared phylogenetic resemblance of the Polish virus strains indicates their low genetic variability and likely slow evolutionary dynamics compared with other lagovirus species such as RHDV. Low genetic diversity among the European EBHSV strains has previously been observed [28,29,31,32]. The virus seems to be more conservative; however, the evolutionary process still occurs and has resulted in the disappearance of the oldest group A strains and the emergence of several virus lineages within the new genetic group B [30]. Evidence for the slow evolutionary dynamics of the virus could be the presence of only a relatively small number of new virus variants within the existing genetic subgroups. A possible slow evolution mechanism may be also supported by the close phylogenetic relationships observed between Polish strains from 2001 to 2004 and a much younger Italian EBHSV strain detected in 2016. The close genetic relationship of EBHSV strains is mainly determined by their geographical origin rather than the time span in which their first isolation was achieved [32]. Another factor which may have an impact on evolution dynamics and the emergence of new EBHSV variants are infections of hares with nonpathogenic HaCV and RHDV2, which are phylogenetically related to EBHSV. Nevertheless, the observed lower genetic variability among EBHSV strains in comparison to RHDV could also be associated with the smallness of the hare population limiting the frequency of events of interspecies transmission of the virus and could be associated with the possible natural resistance of those species to EBHSV infection [1,10,15,31,32,40]. It must be noted that based on ORF1-ORF2 sequence analysis of Polish RHDV variants and EBHSV strains, there were no recombination events observed between these two virus species (unpublished data). Likewise, the analyses of the VP60 and VP10 EBHSV sequences, as well as available full genome sequences of lagoviruses, did not reveal any evidence confirming this recombination phenomenon in the group of Polish EBHSV strains. Furthermore, they formed a separate phylogenetic branch in relation to pathogenic RHDV (GI.1) and RHDV2 (GI.2), as well as to nonpathogenic RCV-A1 (GI.4), which were clustered as outgroup sequences.
In addition, there is no vaccine available against EBHSV infection, so mutation is not driven by vaccine-related selective pressure on the population of wild virus strains [1,32]. This situation significantly diminishes the risk of the appearance of virus variants able to evade the host’s immune system. Nevertheless, the detection of new genetic subtypes of nonpathogenic hare and rabbit caliciviruses in Europe and Australia emphasizes the role of asymptomatic infections in fostering the genetic variability of lagoviruses [38,39], and it can be assumed that these infections could enhance the further differentiation of EBHSV strains. A recombination mechanism analogous to that previously observed for nonpathogenic RCV and RHDV2 could also differentiate EBHSV [23,38,42]. The main limitation of each study aiming to analyze the genetic variability of EBHSV is the small number of full genome sequences of the virus available. It also hinders the assessment of their phylogenetic relationships and the investigation of lagovirus evolutionary paths. Nevertheless, a certain degree of genetic diversity among Polish strains was established, allowing for their classification to the G1, G2 or G3 genetic group.

5. Conclusions

EBHSV strains from Poland confirmed their close phylogenetic relationship to other EBHSV strains circulating in Europe. The results of this retrospective study also provide evidence that they show high genetic resemblance despite their different occurrence locations and detection time spans.

Supplementary Materials

The following are available online at https://www.mdpi.com/article/10.3390/v13101999/s1, Table S1: Primers used for amplification and sequencing of the overlapping EBHSV genome fragments. Nucleotide positions (5′–3′) refer to the genome sequence of EBHSV-GD89 strain (GenBank accession no. Z69620). Table S2: Evolutionary divergence between VP60 sequences of EBHSV, nonpathogenic HaCV, RHDV, and RHDV2 including EBHSV/RHDV2 recombinant strains. Evolutionary analyses were conducted in MEGA7 [37].

Author Contributions

Conceptualization, A.F. and A.R.; methodology, A.F., E.K.; investigation, A.F., W.N., E.K. and E.B.; formal analysis, A.F., W.N. and A.R.; writing—original draft preparation, A.F., W.N., E.K. and A.R.; writing—review and editing, A.F., W.N., A.K. and A.R.; visualization, A.F. and E.B.; supervision, A.F. and A.R. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the Ministry of Science and Higher Education of Poland (Research Project No. S/276).

Institutional Review Board Statement

This study did not require approval of Ethics Committee. The study did not involve humans.

Informed Consent Statement

Not applicable.

Data Availability Statement

Sequences determined in this study were submitted to GenBank database under the accession numbers MK440613–MK440617.

Acknowledgments

The authors are grateful to Marta Chrobocińska for sharing the archive EBHSV strains for genetic analyses.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Gavier-Widén, D.; Mörner, T. Epidemiology and diagnosis of the European brown hare syndrome in Scandinavian countries: A review. Rev. Sci. Tech. 1991, 10, 453–458. [Google Scholar] [CrossRef] [Green Version]
  2. Bascunana, R.C.; Novotny, N.; Belak, S. Detection and differentiation of rabbit hemorrhagic disease and European brown hare syndrome viruses by amplification of VP60 genomic sequences from fresh and fixed tissue specimens. J. Clin. Microbiol. 1997, 35, 2492–2495. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  3. Duff, J.P.; Chasey, D.; Munro, R.; Wooldridge, M. European brown hare syndrome in England. Vet. Rec. 1994, 134, 669–673. [Google Scholar] [CrossRef]
  4. Syrjälä, P.; Nylund, M.; Heinikainen, S. European brown hare syndrome in free-living mountain hares (Lepus timidus) and European brown hares (Lepus europaeus) in Finland 1990–2002. J. Wildl. Dis. 2005, 41, 42–47. [Google Scholar] [CrossRef] [PubMed]
  5. Cancellotti, F.M.; Renzi, M. Epidemiology and current situation of viral haemorrhagic disease of rabbits and the European brown hare syndrome in Italy. Rev. Sci. Tech. 1991, 10, 409–422. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Capucci, L.; Scicluna, M.T.; Lavazza, A. Diagnosis of viral haemorrhagic disease of rabbits and the European brown hare syndrome. Rev. Sci. Tech. 1991, 10, 347–370. [Google Scholar] [CrossRef] [PubMed]
  7. Chasey, D.; Duff, P. European brown hare syndrome and associated virus particles in the UK. Vet. Rec. 1990, 126, 623–624. [Google Scholar] [PubMed]
  8. Frölich, K.; Fickel, J.; Ludwig, A.; Lieckfeldt, D.; Streich, W.J.; Jurčik, R.; Slamečka, J.; Wibbelt, G. New variants of European brown hare syndrome virus strains in free-ranging European brown hares (Lepus Europaeus) from Slovakia. J. Wildl. Dis. 2007, 43, 89–96. [Google Scholar] [CrossRef] [Green Version]
  9. Frölich, K.; Haerer, G.; Bacciarini, L.; Janovsky, M.; Rudolph, M.; Giacometti, M. European brown hare syndrome in free-ranging European brown and mountains hares from Switzerland. J. Wildl. Dis. 2001, 37, 803–807. [Google Scholar] [CrossRef] [Green Version]
  10. Frölich, K.; Meyer, H.; Pielowski, Z.; Ronsholt, L.; von Seck-Lanzendorf, S.; Stolte, M. European brown hare syndrome in free-ranging hares in Poland. J. Wildl. Dis. 1996, 32, 280–285. [Google Scholar] [CrossRef] [Green Version]
  11. Löliger, H.C.; Eskens, U. Incidence, epizootiology and control of viral haemorrhagic disease of rabbits and the European brown hare syndrome in Germany. Rev. Sci. Tech. 1991, 10, 423–434. [Google Scholar] [CrossRef] [Green Version]
  12. Marcato, P.S.; Benazzi, C.; Vecchi, G.; Galeotti, M.; Della Salda, L.; Sarli, G.; Lucidi, P. Clinical and pathological features of rabbit hemorrhagic disease virus and of European brown hare syndrome. Rev. Sci. Tech. 1991, 10, 371–392. [Google Scholar] [CrossRef] [PubMed]
  13. Morisse, J.P.; Le Gall, G.; Boilletot, E. Hepatitis of viral origin in Leporidae: Introduction and aetiological hypotheses. Rev. Sci. Tech. 1991, 10, 283–295. [Google Scholar]
  14. Nauwynck, H.; Callebaut, P.; Peeters, J.; Ducatelle, R.; Uyttebroek, E. Susceptibility of hares and rabbits to a Belgian isolate of European brown hare syndrome virus. J. Wildl. Dis. 1993, 29, 203–208. [Google Scholar] [CrossRef] [PubMed]
  15. Zanni, M.L.; Benassi, M.C.; Scicluna, M.T.; Lavazza, A.; Capucci, L. Clinical evolution and diagnosis of an outbreak of European brown hare syndrome in hares reared in captivity. Rev. Sci. Tech. 1993, 12, 931–940. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  16. Chrobocińska, M.; Górski, J. Prevalence of infection with EBHS (European Brown Hare Syndrome) virus in hares in Poland. Bull. Vet. I Pulawy 1995, 39, 17–21. [Google Scholar]
  17. Chrobocińska, M. The case of infection of hare with European brown hare syndrome virus. Med. Weter. 1999, 55, 750–752. [Google Scholar]
  18. Kwit, E.; Chrobocińska, M.; Grądzki, Z.; Jarosz, Ł.; Majer-Dziedzic, B.; Bigoraj, E. The genetic analysis of new Polish strains of European brown hare syndrome virus. Pol. J. Vet. Sci. 2014, 17, 353–355. [Google Scholar] [CrossRef] [Green Version]
  19. Lavazza, A.; Vecchi, G. Osservazioni su alcuni episodi di mortalita nella leper: Evidenziazione al microscopio elettronico di una particella virale. Selez. Vet. 1989, 30, 461–468. [Google Scholar]
  20. Le Pendu, J.; Abrantes, J.; Bertagnoli, S.; Guitton, J.S.; Le Gall-Reculé, G.; Lopes, A.M.; Marchandeau, S.; Alda, F.; Almeida, T.; Celio, A.P.; et al. Proposal for a unified classification system and nomenclature of lagoviruses. J. Gen. Virol. 2017, 98, 1658–1666. [Google Scholar] [CrossRef]
  21. Droillard, C.; Lemaitre, E.; Chatel, M.; Guitton, J.S.; Marchandeau, S.; Eterradossi, N.; Le Gall-Reculé, G. First complete genome sequence of a hare calicivirus strain isolated from Lepus europaeus. Microb. Res. Ann. 2018, 7, e01224-18. [Google Scholar] [CrossRef] [Green Version]
  22. Forrester, N.L.; Moss, S.R.; Turner, S.L.; Schirrmeier, H.; Gould, E.A. Recombination in rabbit haemorrhagic disease virus: Possible impact on evolution and epidemiology. Virology 2008, 376, 390–396. [Google Scholar] [CrossRef] [PubMed]
  23. Lopes, A.M.; Dalton, K.P.; Magalhaes, M.J.; Parra, F.; Esteves, P.J.; Holmes, E.C.; Abrantes, J. Full genomic analysis of new variant rabbit hemorrhagic disease virus (RHDVb) revealed multiple recombination events. J. Gen. Virol. 2015, 96, 1309–1319. [Google Scholar] [CrossRef] [PubMed]
  24. Silvério, D.; Lopes, A.M.; Mel-Ferreira, J.; Magalhaes, M.J.; Monterosso, P.; Serronha, A.; Maio, E.; Alves, P.C.; Esteves, P.J. Insights into the evolution of the new variant rabbit haemorrhagic disease virus (GI.2) and the identification of novel recombinant strains. Transbound Emerg. Dis. 2018, 65, 983–992. [Google Scholar] [CrossRef] [PubMed]
  25. Le Gall, G.; Huguet, S.; Vende, P.; Vautherot, J.F.; Rasschaert, D. European brown hare syndrome virus: Molecular cloning and sequencing of the genome. J. Gen. Virol. 1996, 77, 1693–1697. [Google Scholar] [CrossRef]
  26. Wirblich, C.; Meyers, G.; Ohlinger, V.F.; Capucci, L.; Eskens, U.; Haas, B.; Thiel, H.J. European brown hare syndrome virus—Relationship to rabbit hemorrhagic disease virus and other caliciviruses. J. Virol. 1994, 68, 5164–5173. [Google Scholar] [CrossRef] [Green Version]
  27. Wirblich, C.; Thiel, H.J.; Meyers, G. Genetic map of the calicivirus rabbit hemorrhagic disease virus as deduced from in vitro translation studies. J. Virol. 1996, 70, 7974–7983. [Google Scholar] [CrossRef] [Green Version]
  28. Billinis, C.; Knowles, N.J.; Spyrou, V.; Sofianidis, G.; Psychas, V.; Birtsas, P.K.; Sofia, M.; Maslarinou, O.M.; Tontis, D.K.; Kanteres, D. Genetic analysis of the first European brown hare syndrome virus isolates from Greece. Wildl. Biol. Pract. 2005, 1, 118–127. [Google Scholar] [CrossRef]
  29. Novotny, N.; Bascunana, C.R.; Uhlén, M.; Belák, S. Phylogenetic analysis of rabbit haemorrhagic disease and European brown hare syndrome viruses by comparison of sequences from the capsid protein gene. Arch. Virol. 1997, 142, 657–673. [Google Scholar] [CrossRef]
  30. Lopes, A.M.; Capucci, L.; Gaviér-Widen, D.; Le Gall-Reculé, G.; Brocchi, E.; Barbieri, I.; Quéméner, A.; Le Pendu, J.; Geoghegan, J.L.; Holmes, E.C.; et al. Molecular evolution and antigenic variation of European brown hare syndrome virus (EBHSV). Virology 2014, 468–470, 104–112. [Google Scholar] [CrossRef] [Green Version]
  31. Drews, B.; Szentiks, C.A.; Roellig, K.; Fickel, J.; Schroeder, K.; Duff, J.P.; Lavazza, A.; Hildebrandt, T.B.; Goeritz, F. Epidemiology, control and management of an EBHS outbreak in captive hares. Vet. Microbiol. 2011, 154, 37–48. [Google Scholar] [CrossRef] [PubMed]
  32. Le Gall-Reculé, G.; Zwingelstein, F.; Laurent, S.; Portejoie, Y.; Rasschaert, D. Molecular epidemiology of European brown hare syndrome virus in France between 1989 and 2003. Arch. Virol. 2006, 151, 1713–1721. [Google Scholar] [CrossRef] [PubMed]
  33. Szillat, K.P.; Höper, D.; Beer, M.; König, P. Full-genome sequencing of German rabbit haemorrhagic disease virus uncovers recombination between RHDV (GI.2) and EBHSV (GII.1). Virus Evol. 2020, 6, veaa080. [Google Scholar] [CrossRef] [PubMed]
  34. Altschul, S.F.; Gish, W.; Miller, W.; Myers, E.W.; Lipman, D.J. Basic local alignment search tool. J. Mol. Biol. 1990, 215, 403–410. [Google Scholar] [CrossRef]
  35. Zhang, Z.; Schwartz, S.; Wagner, L.; Miller, W. A greedy algorithm for aligning DNA sequences. J. Comput. Biol. 2000, 7, 203–214. [Google Scholar] [CrossRef]
  36. Thompson, J.D.; Higgins, D.G.; Gibson, T.J. CLUSTAL W: Improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res. 1994, 22, 4673–4680. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  37. Kumar, S.; Stecher, G.; Tamura, K. MEGA7: Molecular Evolutionary Genetics Analysis version 7.0 for bigger datasets. Mol. Biol. Evol. 2016, 33, 1870–1874. [Google Scholar] [CrossRef] [Green Version]
  38. Hall, R.N.; Mahar, J.E.; Read, A.J.; Mourant, R.; Piper, M.; Huang, N.; Strive, T. A strain-specific multiplex RT-PCR for Australian Rabbit haemorrhagic disease viruses uncovers a new recombinant virus variant in rabbits and hares. Transbound Emerg. Dis. 2018, 65, e444–e456. [Google Scholar] [CrossRef]
  39. Mahar, J.E.; Hall, R.N.; Shi, M.; Mourant, R.; Huang, N.; Strive, T.; Holmes, E.C. The discover of three new hare lagoviruses reveals unexplored viral diversity in this genus. Virus Evol. 2019, 5, vez005. [Google Scholar] [CrossRef] [Green Version]
  40. Panek, M. Current situation of hares and partridges and the management of their populations. In Animal Population Management; Polski Związek Łowiecki: Nowy Świat, Poland, 2016; pp. 99–109. Available online: www.czempin.pzlow.pl (accessed on 29 January 2021). (In Polish)
  41. Camarda, A.; Pugliese, N.; Cavadini, P.; Circella, E.; Capucci, L.; Caroli, A.; Legretto, M.; Malia, E.; Lavazza, A. Detection of the new emerging rabbit haemorrhagic disease type 2 virus (RHDV2) in Sicily from rabbit (Oryctolagus cuniculus) and Italian hare (Lepus corsicanus). Res. Vet. Sci. 2014, 97, 642–645. [Google Scholar] [CrossRef]
  42. Le Gall-Reculé, G.; Lemaitre, E.; Bertagnoli, S.; Hubert, C.; Top, S.; Decors, A.; Marchandeau, S.; Guitton, J.S. Large-scale lagovirus disease outbreaks in European brown hares (Lepus europaeus) in France caused by RHDV2 strains spatially shared with rabbits (Oryctolagus cuniculus). Vet. Res. 2017, 48, 70. [Google Scholar] [CrossRef] [Green Version]
  43. Lopes, A.M.; Marques, S.; Silva, E.; Magalhães, M.J.; Pinheiro, A.; Alves, P.C.; Le Pendu, J.; Esteves, P.J.; Thompson, G.; Abrantes, J. Detection of RHDV strains in the Iberian hare (Lepus granatensis): Earliest evidence of rabbit lagovirus cross-species infection. Vet. Res. 2014, 45, 94–101. [Google Scholar] [PubMed] [Green Version]
  44. Neimanis, A.; Ahola, H.; Larsson Petersson, U.; Lopes, A.M.; Abrantes, J.; Zohari, S.; Esteves, P.J.; Gavier-Widen, D. Overcoming species barriers: An outbreak of Lagovirus europaeus GI.2/RHDV2 in an isolated population of mountain hares (Lepus timidus). BMC Vet. Res. 2018, 14, 367. [Google Scholar] [CrossRef] [Green Version]
  45. Puggioni, G.; Cavadini, P.; Maestrale, C.; Scivoli, R.; Botti, G.; Ligios, C.; Le Gall-Reculé, G.; Lavazza, A.; Capucci, L. The new French 2010 variant of the rabbit of the hemorrhagic disease virus causes an RHD-like disease in the Sardinian Cape hare (Lepus capensis mediterraneus). Vet. Res. 2013, 44, 96. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  46. Velarde, R.; Cavadini, P.; Neimanis, A.; Cabezon, O.; Chiari, M.; Gaffuri, A.; Lavin, S.; Grilli, G.; Gavier-Widen, D.; Lavazza, A.; et al. Spillover events of infection of Brown hares (Lepus europaeus) with rabbit haemorrhagic disease type 2 virus (RHDV2) caused sporadic cases of an European Brown Hare Syndrome-like disease in Italy and Spain. Transbound Emerg. Dis. 2017, 64, 1750–1761. [Google Scholar] [CrossRef] [PubMed]
  47. Chrobocińska, M. Analysis of the fragment of capsid protein gene sequences of Polish strains of European brown hare syndrome virus. Bull. Vet. Inst. Pulawy 2002, 46, 213–222. [Google Scholar]
  48. Chrobocińska, M. Charakterystyka Fenotypowa i Molekularna Krajowych Szczepów Wirusów Krwotocznej Choroby Zajęcy (EBHSV) i Krwotocznej Choroby Królików (RHDV) (Phenotypic and Molecular Characteristics of Native Strains of European Brown Hare Syndrome Virus (EBHSV) and Rabbit Haemorrhagic Disease Virus (RHDV) (In Polish)). In Habilitation Dissertation; The National Veterinary Research Institute: Puławy, Poland, 2007. [Google Scholar]
Viruses 13 01999 g001 550
Figure 1. The phylogenetic Maximum Likelihood tree constructed using the ORF1–ORF2 (21–7350 bp) nucleotide sequences of European EBHSV strains and other hare and rabbit caliciviruses. Bootstrap values (1000 replicates) greater than 70% are shown at the corresponding tree nodes. The tree is drawn to scale with branch lengths in the same units as those of the evolutionary distances used to infer the phylogenetic tree. Evolutionary analyses were conducted using MEGA7 [37]. The rabbit hemorrhagic disease virus—RHDV (GI.1c), EBHSV GII.1/RHDV2 GI.2 recombinants, and rabbit calicivirus RCV–A1 (GI.4) were used as an outgroup to root the tree. EBHSV strains from Poland are marked by black dots.
Figure 1. The phylogenetic Maximum Likelihood tree constructed using the ORF1–ORF2 (21–7350 bp) nucleotide sequences of European EBHSV strains and other hare and rabbit caliciviruses. Bootstrap values (1000 replicates) greater than 70% are shown at the corresponding tree nodes. The tree is drawn to scale with branch lengths in the same units as those of the evolutionary distances used to infer the phylogenetic tree. Evolutionary analyses were conducted using MEGA7 [37]. The rabbit hemorrhagic disease virus—RHDV (GI.1c), EBHSV GII.1/RHDV2 GI.2 recombinants, and rabbit calicivirus RCV–A1 (GI.4) were used as an outgroup to root the tree. EBHSV strains from Poland are marked by black dots.
Viruses 13 01999 g001
Viruses 13 01999 g002 550
Figure 2. The phylogenetic Maximum Likelihood tree constructed using nucleotide sequences of the VP60 protein gene of European EBHSV strains and other hare and rabbit caliciviruses. Bootstrap values (1000 replicates) greater than 70% are shown at the corresponding tree nodes. The tree is drawn to scale with branch lengths in the same units as those of the evolutionary distances used to infer the phylogenetic tree. Evolutionary analyses were conducted using MEGA7 [37]. The nonpathogenic hare caliciviruses—HaCV (GII.2–4) were used as an outgroup to root the tree. EBHSV strains from Poland are marked by black dots.
Figure 2. The phylogenetic Maximum Likelihood tree constructed using nucleotide sequences of the VP60 protein gene of European EBHSV strains and other hare and rabbit caliciviruses. Bootstrap values (1000 replicates) greater than 70% are shown at the corresponding tree nodes. The tree is drawn to scale with branch lengths in the same units as those of the evolutionary distances used to infer the phylogenetic tree. Evolutionary analyses were conducted using MEGA7 [37]. The nonpathogenic hare caliciviruses—HaCV (GII.2–4) were used as an outgroup to root the tree. EBHSV strains from Poland are marked by black dots.
Viruses 13 01999 g002
Viruses 13 01999 g003 550
Figure 3. The phylogenetic Maximum Likelihood tree constructed using nucleotide sequences of the VP10 protein gene (ORF2) of European EBHSV strains and other hare and rabbit caliciviruses. Bootstrap values (1000 replicates) greater than 70% are shown at the corresponding tree nodes. The tree is drawn to scale with branch lengths in the same units as those of the evolutionary distances used to infer the phylogenetic tree. Evolutionary analyses were conducted using MEGA7 [37]. The rabbit hemorrhagic disease virus—RHDV (GI.1c), EBHSV GII.1/RHDV2 GI.2 recombinants, and rabbit calicivirus RCV-A1 (GI.4) were used as an outgroup to root the tree. EBHSV strains from Poland are marked by black dots.
Figure 3. The phylogenetic Maximum Likelihood tree constructed using nucleotide sequences of the VP10 protein gene (ORF2) of European EBHSV strains and other hare and rabbit caliciviruses. Bootstrap values (1000 replicates) greater than 70% are shown at the corresponding tree nodes. The tree is drawn to scale with branch lengths in the same units as those of the evolutionary distances used to infer the phylogenetic tree. Evolutionary analyses were conducted using MEGA7 [37]. The rabbit hemorrhagic disease virus—RHDV (GI.1c), EBHSV GII.1/RHDV2 GI.2 recombinants, and rabbit calicivirus RCV-A1 (GI.4) were used as an outgroup to root the tree. EBHSV strains from Poland are marked by black dots.
Viruses 13 01999 g003
Table
Table 1. The nucleotide sequence analysis of the genomes of Polish, reference and other European EBHSV strains.
Table 1. The nucleotide sequence analysis of the genomes of Polish, reference and other European EBHSV strains.
EBHSV Strain/Acc. NumberNP1192L98K501G104K204
ORF1-ORF2NSPVP60VP10ORF1-ORF2NSPVP60VP10ORF1-ORF2NSPVP60VP10ORF1-ORF2NSPVP60VP10ORF1-ORF2NSPVP60VP10
* 21–733021–52825282–70137006–733021–733021–52825282–70137006–733021–733021–52825282–70137006–733021–733021–52825282–70137006–733021–733021–52825282–70137006–7330
NP1192/MK440617
L98/MK44061694.794.694.896.5
K501/MK44061594.193.794.398.897.697.697.895.9
G104/MK44061394.594.494.794.296.596.696.495.495.595.595.794.8
K204/MK44061493.092.893.494.896.095.896.695.997.096.997.594.894.594.495.293.6
EBHSV-GD **/Z6962097.797.199.499.194.394.094.996.293.793.194.299.794.093.794.994.592.792.393.595.1
O4022-10 **/KC83283893.793.793.694.292.592.692.192.891.791.791.394.291.992.291.491.391.091.090.792.2
WOLF17/MF35636693.593.294.096.495.094.895.595.794.393.994.896.794.894.795.394.293.493.094.295.8
L03596/2019/LR89914093.593.294.394.295.295.395.494.294.394.294.594.297.597.398.397.793.493.194.692.5
L03594/2020/LR89915292.792.593.692.294.694.695.192.293.893.694.692.396.496.397.195.792.992.694.290.7
L03613/2019/LR89917193.693.494.093.695.495.495.693.994.594.395.293.697.497.398.097.493.493.194.592.8
L03475/2019/LR89918292.892.693.792.294.694.695.392.293.893.694.892.396.596.397.295.792.992.594.390.7
L03476/2019/LR89918593.893.694.393.695.695.895.893.994.694.595.493.697.897.598.597.493.693.394.992.8
L03477/2019/LR89918894.294.194.594.596.096.495.695.195.095.194.994.598.598.498.798.694.094.094.593.3
* nucleotide positions according to EBHSV-GD (Z69620); ** reference EBHSV strains. ORF1-ORF2—open reading frame 1 and 2; NSP—nonstructural protein genes; VP60—capsid structural protein; VP10—minor capsid structural protein.
Table
Table 2. Amino acid substitutions in the VP60 region of EBHSV strains from Poland (compared to the reference EBHSV-GD 89 strain and representatives of the EBHSV genetic groups).
Table 2. Amino acid substitutions in the VP60 region of EBHSV strains from Poland (compared to the reference EBHSV-GD 89 strain and representatives of the EBHSV genetic groups).
EBHSV StrainAccession NumberOriginGenetic Group/SubgroupPosition of Amino Acids in Particular Regions of VP60 Gene
bcdef
5866231270291302327343383410415417427461476522524536542544565566
EBHSV-GDZ69620FranceB/G1.2AVDSISITSTILVAAVMADTLA
NP1192MK440617Poland 1992B/G1.2AVDSISITSTILVAAVMADTLA
L98MK440616Poland 1998B/G2.2VADSFTVTNAILTAAILAEALT
K501MK440615Poland 2001B/G2.3VADSITVSNAILTASILADTLA
K204MK440614Poland 2004B G2.3VADSITVSNALLTSSILTETFT
G104MK440613Poland 2004B/G3VAECITVTNSIMTAAILAETLT
BS89X98002Italy 1989B/G1.1AVDSITITSSILVAVVMADTLA
V58KJ679553Sweden 1994B/G1.2AVDSITITNTIMVAVVMADTLA
A0256AJ971306France 2002B/G1.3AVDSITVSNTLLVASVMTETFT
V171KJ679558Sweden 2001B/G2.2AADSITVTNAILTAAILTETLT
V715KJ679559Sweden 2002B/G2.3VADSITVSNAILTASILAETLA
O516AM933650France 2005B/G3AVECITITNSIMTAAILAETLA
MI09KF591083Italy 2009B/G3AVECITITNSLLTAAILAETLT
BS15-1KU961677Italy 2015B/-undefinedAADSITVSNSIMVAAILAETLT
WOLFMF356366Italy 2016B/-undefinedAADSITVSNSIMVAAILAETLT
0330AM408588France 2003B/G3VAECITITNSIMTAAILAETLT
E14-40/2LT168848France 2014B/G3AAECITVTNSIMTAAILAETLT
08-36HF571040SwedenB/G3VAECITVTNSIMTAAILAETLT
L03596/2019LR899140GermanyB/G3AAECITVSNSIMTAAILAETLT
L03594/2020LR899152GermanyB/G3AAECITVTNSIMTAAILAETLT
L03613/2019LR899171GermanyB/G3AAECITVSNSIMTAAILTETLT
L03475/2019LR899182GermanyB/G3AAECITVTNSIMTAAILAETLT
L03476/2019LR899185GermanyB/G3AAECITVSNSIMTAAILAETLT
L03477/2019LR899188GermanyB/G3AAECITVTNSIMTAAILAETLT
O4021-9KC832839Sweden 1982AAMDSINITNSILVADVMADTLA
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Fitzner, A.; Kwit, E.; Niedbalski, W.; Bigoraj, E.; Kęsy, A.; Rzeżutka, A. Phylogenetic Analysis of European Brown Hare Syndrome Virus Strains from Poland (1992–2004). Viruses 2021, 13, 1999. https://doi.org/10.3390/v13101999

AMA Style

Fitzner A, Kwit E, Niedbalski W, Bigoraj E, Kęsy A, Rzeżutka A. Phylogenetic Analysis of European Brown Hare Syndrome Virus Strains from Poland (1992–2004). Viruses. 2021; 13(10):1999. https://doi.org/10.3390/v13101999

Chicago/Turabian Style

Fitzner, Andrzej, Ewa Kwit, Wiesław Niedbalski, Ewelina Bigoraj, Andrzej Kęsy, and Artur Rzeżutka. 2021. "Phylogenetic Analysis of European Brown Hare Syndrome Virus Strains from Poland (1992–2004)" Viruses 13, no. 10: 1999. https://doi.org/10.3390/v13101999

APA Style

Fitzner, A., Kwit, E., Niedbalski, W., Bigoraj, E., Kęsy, A., & Rzeżutka, A. (2021). Phylogenetic Analysis of European Brown Hare Syndrome Virus Strains from Poland (1992–2004). Viruses, 13(10), 1999. https://doi.org/10.3390/v13101999

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop