Detection of rabbit hemorrhagic disease virus (RHDV), genotype GI.1 and GI.2 with a new multiplex real-time RT-qPCR protocol, using the minor capsid VP10 gene

Keywords: rabbit hemorrhagic disease virus, validation, analytical sensitivity, specificity, molecular detection, primers

Abstract

Aim. This study aimed to develop a specific and sensitive multiplex real-time reverse transcription PCR (RT-qPCR) method for the detection and differentiation of rabbit hemorrhagic disease virus (RHDV) genotypes GI.1 and GI.2 circulating in Ukraine, using primers and probes based on the ORF2 gene, encoding the minor capsid protein VP10. Furthermore, to perform an initial validation of this PCR. Methods. The assay was designed to amplify a conserved 101-bp ORF2 sequence, encoding the minor capsid protein VP10, assuming that it would be a less variable region compared to that of the traditionally targeted ORF1 sequence encoding the major capsid protein VP60. Sequence alignment was performed using 38 full-genome sequences of RHDV isolates of various geographic origins present in GenBank. Specific primers to RHDV and two genotype-specific hydrolysis probes (FAM for genotype GI.1 and HEX for genotype GI.2) were designed and partially validated both in silico (BLAST) and in vitro. RNA was extracted from 6 tissue samples (contaminated with RHDV and negative control), and two virus reference strains using the IndiSpin Pathogen Kit, followed by RT-qPCR using a one-step protocol. Analytical sensitivity and specificity were assessed by a 10-fold RNA serial dilution (from 10⁶ to 10⁰ copies). For specificity testing, non-target organisms were included: Myxoma virus, Staphylococcus aureus, Pasteurella multocida, Escherichia coli, and Streptococcus agalactiae. Results. After optimization, the developed RT-qPCR assay demonstrated high analytical sensitivity, detecting as few as 100 RNA copies/reaction with consistent amplification across three replicates. The limit of detection (LOD) was established at 1.0×10² RNA copies for both genotypes. Standard curves yielded slopes of -3.44 (GI.1) and -3.38 (GI.2), corresponding to amplification efficiencies of 95.4% and 97.5%, respectively. The assay showed excellent linearity (R² = 0.925 for GI.1, R² = 0.881 for GI.2) and intra-assay variability (%CV) below 3.5%. No cross-reactivity was observed with non-target pathogens. Conclusions. The developed multiplex RT-qPCR assay demonstrated promising analytical performance for detecting and differentiating RHDV genotypes GI.1 and GI.2. These results provide partial validation of the method. However, limitations include testing only two genotypes, no internal amplification control, and lack of inter-laboratory comparison with WOAH-recommended VP60-based RT-PCR. Future studies should expand validation scope, incorporate internal controls, and perform multi-center validation before routine implementation.

 

References

Abade Dos Santos FA, Pinto A, Burgoyne T, Dalton KP, Carvalho CL, Ramilo DW, Carneiro C, Carvalho T, Peleteiro MC, Parra F, Duarte MD (2022) Spillover events of rabbit haemorrhagic disease virus 2 (recombinant GI.4P-GI.2) from Lagomorpha to Eurasian badger. Transbound Emerg Dis 69(3):1030-1045. https://doi.org/10.1111/tbed.14059

Abrantes J, Lopes AM (2021) A review on the methods used for the detection and diagnosis of rabbit hemorrhagic disease virus (RHDV). Microorganisms 9(5):972. https://doi.org/10.3390/microorganisms9050972

Abrantes J, Droillard C, Lopes AM, et al. (2020) Recombination at the emergence of the pathogenic rabbit haemorrhagic disease virus Lagovirus europaeus/GI.2. Sci Rep 10:14502. https://doi.org/10.1038/s41598-020-71303-4

Aguayo-Adan JA, Rouco C, Delibes-Mateos M, Santoro S (2021) Lack of evidence for differences in the spread of classic (Lagovirus europaeus/GI.1) and novel (Lagovirus europaeus/GI.2) rabbit haemorrhagic disease viruses in Europe and North Africa. Vet Rec 189(8):e1067. https://doi.org/10.1002/vetr.1067

Asin J, Rejmanek D, Clifford DL, Mikolon AB, Henderson EE, Nyaoke AC, Macias-Rioseco M, Streitenberger N, Beingesser J, Woods LW, Lavazza A, Capucci L, Crossley B, Uzal FA (2022) Early circulation of rabbit haemorrhagic disease virus type 2 in domestic and wild lagomorphs in southern California, USA (2020-2021). Transbound Emerg Dis 69(4):e394-e405. https://doi.org/10.1111/tbed.14315

Bebnowska D, Hrynkiewicz R, Niedzwiedzka-Rystwej P (2021) Real-time PCR confirms infection with Lagovirus europaeus. Appl Sci 11(2):656. https://doi.org/10.3390/app11020656

Brinkmann A, Ergunay K, Radonic A, Tufan ZK, Domingo C, Nitsche A (2017) Development and preliminary evaluation of a multiplexed amplification and next-generation sequencing method for viral hemorrhagic fever diagnostics. PLoS Negl Trop Dis 11(11):e0006075. https://doi.org/10.1371/journal.pntd.0006075

Byrne AW, Marnell F, Barrett D, Reid N, Hanna REB, McElroy MC, Casey M (2022) Rabbit haemorrhagic disease virus 2 (RHDV2; GI.2) in Ireland focusing on wild Irish hares (Lepus timidus hibernicus): an overview of the first outbreaks and contextual review. Pathogens 11(3):288. https://doi.org/10.3390/pathogens11030288

Calvete C, Sarto MP, Iguacel L, Calvo JH (2021) Infectivity of rabbit haemorrhagic disease virus excreted in rabbit faecal pellets. Vet Microbiol 257:109079. https://doi.org/10.1016/j.vetmic.2021.109079

Calvete C, Capucci L, Lavazza A, Sarto MP, Calvo AJ, Monroy F, Calvo JH (2022) Changes in European wild rabbit population dynamics and the epidemiology of rabbit haemorrhagic disease in response to artificially increased viral transmission. Transbound Emerg Dis 69(5):2682-2696. https://doi.org/10.1111/tbed.14421

Capucci L, Fallacara F, Grazioli S, Lavazza A, Pacciarini ML, Brocchi E (1998) A further step in the evolution of rabbit hemorrhagic disease virus: the appearance of the first consistent antigenic variant. Virus Res 58(1-2):115-126. https://doi.org/10.1016/S0168-1702(98)00106-3

Cavadini P, Trogu T, Velarde R, Lavazza A, Capucci L (2024) Recombination between non-structural and structural genes as a mechanism of selection in lagoviruses: the evolutionary dead-end of an RHDV2 isolated from European hare. Virus Res 339:199257. https://doi.org/10.1016/j.virusres.2023.199257

Chen W, Tu T, Luo Y, Yang Z, Yao X, Wu X, Wang Y (2022) Detection of a new emerging strain of rabbit haemorrhagic disease virus 2 (GI.2) in China. J Vet Res 66(3):289-295. https://doi.org/10.2478/jvetres-2022-0048

Cooke B (2024) Practical suggestions for assessing rabbit haemorrhagic disease virus 2 risk to endangered native lagomorphs in North America and Southern Africa. Viruses 16(8):1299. https://doi.org/10.3390/v16081299

Dalton KP, Podadera A, Granda V, Nicieza I, del Llano D, Gonzalez R, de los Toyos JR, Garcia Ocana M, Vazquez F, Martin Alonso JM, et al. (2018) ELISA for detection of variant rabbit haemorrhagic disease virus RHDV2 antigen in liver extracts. J Virol Methods 251:38-42. https://doi.org/10.1016/j.jviromet.2017.09.019

Erfan AM, Shalaby AG (2020) Genotyping of rabbit hemorrhagic disease virus detected in diseased rabbits in Egyptian provinces by VP60 sequencing. Vet World 13(6):1098-1107. https://doi.org/10.14202/VETWORLD.2020.1098-1107

Esteves PJ, Abrantes J, Lopes AM, et al. (2015) Emergence of pathogenicity in lagoviruses: evolution from pre-existing non-pathogenic strains or through a species jump? PLoS Pathog 11:e1005087. https://doi.org/10.1371/journal.ppat.1005087

Fitzner A, Kesy A, Bulenger K, Niedbalski W (2021) Evidence of independent introductions of RHDV2 strains in Poland based on the genome analysis of viral isolates from 2016-2018. Acta Biochim Pol 68(2):255-263. https://doi.org/10.18388/ABP.2020_5547

Fresco-Taboada A, Monton M, Tapia I, Soria E, Barcena J, Guillou-Cloarec C, Gall-Recule GL, Blanco E, Rueda P (2022) Development and evaluation of a duplex lateral flow assay for the detection and differentiation between rabbit haemorrhagic disease virus Lagovirus europaeus/GI.1 and /GI.2. Biology 11(3):401. https://doi.org/10.3390/biology11030401

Gall A, Hoffmann B, Teifke JP, Lange B, Schirrmeier H (2007) Persistence of viral RNA in rabbits which overcome an experimental RHDV infection detected by a highly sensitive multiplex real-time RT-PCR. Vet Microbiol 120(1-2):17-32. https://doi.org/10.1016/j.vetmic.2006.10.006

Hall RN, Mahar JE, Read A, Mourant RG, Piper M, Huang N, Strive T (2018) 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 65(2):444-456. https://doi.org/10.1111/tbed.12779

Hall R, Trought K, Strive T, Duckworth JA, Jenckel M (2024) First detection and circulation of RHDV2 in New Zealand. Viruses 16(4):519. https://doi.org/10.3390/v16040519

Harcourt-Brown FM, Harcourt-Brown N, Joudou LM (2020) RHDV2 epidemic in UK pet rabbits. Part 2: PCR results and correlation with vaccination status. J Small Anim Pract 61(8):487-493. https://doi.org/10.1111/jsap.13180

Hougs L, Gatto F, Goerlich O, Grohmann L, Lieske K, Mazzara M, Narendja F, Ovesna J, Papazova N, Scholtens I, Zel J. (2017) Verification of analytical methods for GMO testing when implementing interlaboratory validated methods. EUR 29015 EN, Publications Office of the European Union, Luxembourg, 30 pp. doi:10.2760/645114, JRC 109940.

Hu B, Wei H, Fan Z, Song Y, Chen M, Qiu R, Zhu W, Xu W, Xue J, Wang F (2021) Emergence of rabbit haemorrhagic disease virus 2 in China in 2020. Vet Med Sci 7(1):236-239. https://doi.org/10.1002/vms3.332

Hu B, Fan Z, Qiu R, Chen M, Wei H, Song Y, Liu W, Xu W, Wang F (2023) Novel recombinant rabbit hemorrhagic disease virus 2 (RHDV2) is circulating in China within 12 months after original RHDV2 arrival. Transbound Emerg Dis:1-9. https://doi.org/10.1155/2023/4787785

Hu B, Dong W, Song Y, Fan Z, Cavadini P, Wang F (2025) Detection of a new recombinant rabbit hemorrhagic disease virus 2 in China and development of virus-like particle-based vaccine. Viruses 17(5):710. https://doi.org/10.3390/v17050710

ISO (International Organization for Standardization) (2018) ISO/IEC 17025:2018. General requirements for the competence of testing and calibration laboratories. Geneva: ISO. https://www.iso.org/standard/66912.html

Korovin IA, Rusanova A, Gerilovych A (2024) The laboratory testing of the PCR-based protocol of detection of the rabbit haemorrhagic disease virus RNA. One Health J 2(III):39-44. https://doi.org/10.31073/onehealthjournal2024-III-05

Krytsia YP, Tarasov OA, Mezhenskyi AA, Mezhenskyi AO (2022) Zastosuvannia polimeraznoi lantsiuhovoi reaktsii v rezhymi realnoho chasu dlia detektsii RNK virusu hemorahichnoi khvoroby kroliv: metodychni rekomendatsii (Application of real-time polymerase chain reaction for the detection of RHDV RNA: Guidelines). Kyiv: IVM NAAS. http://ivm.kiev.ua/wp-content/uploads/4_MR-RHD_PCR.pdf

Kwit E, Rzezutka A (2019) Molecular methods in detection and epidemiologic studies of rabbit and hare viruses: a review. J Vet Diagn Invest 31(4):497-508. https://doi.org/10.1177/1040638719852374

Le Gall-Recule G, Lavazza A, Marchandeau S, Bertagnoli S, Zwingelstein F, Cavadini P, Martinelli N, Lombardi G, Guerin JL, Lemaitre E, Decors A, Boucher S, Le Normand B, Capucci L (2013) Emergence of a new lagovirus related to rabbit haemorrhagic disease virus. Vet Res 44:81. https://doi.org/10.1186/1297-9716-44-81

Le Pendu J, Abrantes J, Bertagnoli S, Guitton JS, Le Gall-Recule G, Lopes AM, Marchandeau S, Alda F, Almeida T, Celio AP, et al. (2017) Proposal for a unified classification system and nomenclature of lagoviruses. J Gen Virol 98(7):1658-1666. https://doi.org/10.1099/jgv.0.000840

Liu SJ, Xue HP, Pu BQ, Qian NH (1984) A new viral disease in rabbits. Anim Husb Vet Med (China) 16(9):253-255.

Lopes AM, Dalton KP, Magalhaes MJ, Parra F, Esteves PJ, Holmes EC, Abrantes J (2015) Full genomic analysis of new variant rabbit hemorrhagic disease virus revealed multiple recombination events. J Gen Virol 96(6):1309-1319. https://doi.org/10.1099/vir.0.000070

Luo Y, Zhou L, Wang X, Li Y, Luo Z, Wang Y (2019) Development of a real-time RT-PCR for rabbit hemorrhagic disease virus detection according to VP10 gene. In: Proc. 3rd Int. Conf. Biol Inf Biomed Eng (BIBE), Hangzhou, China, pp. 1-5.

Mahar JE, Hall RN, Peacock D, Kovaliski J, Piper M, Mourant RG, Huang N, Campbell S, Gu X, Read A, Urakova N, Cox TE, Holmes EC, Strive T (2017) Rabbit hemorrhagic disease virus 2 (RHDV2; GI.2) is replacing endemic strains of RHDV in the Australian landscape within 18 months of its arrival. J Virol 92(2):e01374-17. https://doi.org/10.1128/JVI.01374-17

Mahar JE, Jenckel M, Huang N, Smertina E, Holmes EC, Strive T, Hall RN (2021) Frequent intergenotypic recombination between the non-structural and structural genes is a major driver of epidemiological fitness in caliciviruses. Virus Evol 7(2):veab080. doi:10.1093/ve/veab080

Mezhenskyi AA, Mezhenska NA, Krytsia YP (2023) Indicators of the manifestation of the epizootic process of rabbit hemorrhagic disease (RHDV (GI.1) and RHDV2 (GI.2)) in Ukraine in 2021-2022. Veterinarian biotehnologiia - Veterinary Biotechnology 42:67-80. https://doi.org/10.31073/vet_biotech42-08

Mezhenskyi AA, Mezhenska NA, Mezhenskyi AO, Tarasov OA, Krytsia YP (2024) Poshyrenist ta sezonnist hemorahichnoi khvoroby kroliv v Ukraini u 2021-2023 rokakh (Prevalence and seasonality of rabbit haemorrhagic disease in Ukraine in 2021-2023). Veterynarna biotekhnolohiia - Veterinary Biotechnology 45:48-61. https://doi.org/10.31073/vet_biotech45-05

Niedzwiedzka-Rystwej P, Hukowska-Szematowicz B, Dzialo J, Tokarz-Deptula B, Deptula W (2013) Real-time PCR detection of rabbit haemorrhagic disease virus in rabbits infected with different European strains of RHDV. Pol J Vet Sci 16(1):39-43. https://doi.org/10.2478/pjvs-2013-0006

Neimanis AS, Ahola H, Larsson Pettersson U, et al. (2018) Overcoming species barriers: an outbreak of Lagovirus europaeus GI.2/RHDV2 in an isolated population of mountain hares (Lepus timidus). BMC Vet Res 14:367. https://doi.org/10.1186/s12917-018-1694-7

O'Connor TW, Read AJ, Hall RN, Strive T, Kirkland PD (2022) Immunological cross-protection between different rabbit hemorrhagic disease viruses: implications for rabbit biocontrol and vaccine development. Vaccines 10(5):666. https://doi.org/10.3390/vaccines10050666

Pacioni C, Hall RN, Strive T, Ramsey DSL, Gill MS, Vaughan TG (2022) Comparative epidemiology of rabbit haemorrhagic disease virus strains from viral sequence data. Viruses 15(1):21. https://doi.org/10.3390/v15010021

Peacock DE, Iannella A, Sinclair RG, Kovaliski J (2024) Surveillance of wildlife viruses: insights from South Australia's monitoring of rabbit haemorrhagic disease virus (RHDV GI.1 and GI.2). Viruses 16(10):1553. https://doi.org/10.3390/v16101553

Perera KD, Johnson D, Lovell S, Groutas WC, Chang KO, Kim Y (2022) Potent protease inhibitors of highly pathogenic lagoviruses: rabbit hemorrhagic disease virus and European brown hare syndrome virus. Microbiol Spectr 10(4):e0014222. https://doi.org/10.1128/spectrum.00142-22

Shah PT, Bahoussi AN, Yang C, Yao G, Dong L, Wu C, Xing L (2023) Genetic characteristics and phylogeographic dynamics of lagoviruses, 1988-2021. Viruses 15(4):815. https://doi.org/10.3390/v15040815

Shi L, Liu Y, Chang C, Wang J, Zhang Z, Wang S, Zhang Z (2024) Report on simultaneous infection of rabbit haemorrhagic disease virus type 1 and type 2 in kits in China. Preprint. https://doi.org/10.21203/rs.3.rs-3823446/v1

Sun Z, An Q, Li Y, Gao X, Wang H (2024) Epidemiological characterization and risk assessment of rabbit haemorrhagic disease virus 2 (RHDV2/b/GI.2) in the world. Vet Res 55:12. https://doi.org/10.1186/s13567-024-01286-x

Toh X, Ong J, Chan C, Teo XH, Toh S, Fernandez CJ, Huangfu T (2022) First detection of rabbit haemorrhagic disease virus (RHDV2) in Singapore. Transbound Emerg Dis 69(3):1521-1528. https://doi.org/10.1111/tbed.14116

Tokarz-Deptula B, Kulus J, Baraniecki L, Stosik M, Deptula W (2024) Characterisation of Lagovirus europaeus GI-RHDVs (rabbit haemorrhagic disease viruses) in terms of their pathogenicity and immunogenicity. Int J Mol Sci 25(10):5342. https://doi.org/10.3390/ijms25105342

Tung HY, Chen WC, Ou BR, Yeh JY, Cheng YH, Tsng PH, Hsu MH, Tsai M, Liang Y (2018) Simultaneous detection of multiple pathogens by multiplex PCR coupled with DNA biochip hybridization. Lab Anim 52(2):186-195. https://doi.org/10.1177/0023677217718864

Tu T, Zhou Y, Jiang D, et al. (2022) The pathogenicity comparison of Lagovirus europaeus GI.1 and GI.2 strains in China by using relative quantitative assay. Sci Rep 12:20518. https://doi.org/10.1038/s41598-022-25118-0

Velarde R, Cavadini P, Neimanis A, Cabezon O, Chiari M, Gaffuri A, Lavin S, Grilli G, Gavier-Widen D, Lavazza A, Capucci L (2017) 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 64(6):1750-1761. https://doi.org/10.1111/tbed.12562

Velarde R, Abrantes J, Lopes AM, Estruch J, Corte-Real JV, Esteves PJ, Garcia-Bocanegra I, Ruiz-Olmo J, Rouco C (2021) Spillover event of recombinant Lagovirus europaeus/GI.2 into the Iberian hare (Lepus granatensis) in Spain. Transbound Emerg Dis 68(6):3187-3193. https://doi.org/10.1111/tbed.14264

WOAH (World Organisation for Animal Health) (2023) Rabbit haemorrhagic disease. In: Manual of Diagnostic Tests and Vaccines for Terrestrial Animals, Chapter 3.7.2. (Accessed 2025-08-22). https://www.woah.org/en/disease/rabbit-haemorrhagic-disease/

Wu M, Chen M, Qiu R, Ge L, Fan Z, Hu B, Wei H, Li Y, Wang F (2024) Specific detection of RHDV GI.1 and GI.2 by RT-LAMP-CRISPR/Cas12a platform. Transbound Emerg Dis 2024:3881457. https://doi.org/10.1155/tbed/3881457

Zhang L, Zhao Q, Tian Y, Tang YK, Wang Y, Huang B (2023) A novel reverse-transcription recombinase polymerase amplification assay for rapid detection of GI.1 genotype of rabbit hemorrhagic disease virus. Front Vet Sci 10:1056601. https://doi.org/10.3389/fvets.2023.1056601

Published
2025-10-03
How to Cite
Mezhenskyi, A., Tarasov, O., Mezhenska, N., Borovkov, S., & Mezhenskyi, A. (2025). Detection of rabbit hemorrhagic disease virus (RHDV), genotype GI.1 and GI.2 with a new multiplex real-time RT-qPCR protocol, using the minor capsid VP10 gene. Agricultural Science and Practice, 12(2), 28-41. https://doi.org/10.15407/agrisp12.02.028