Abstract
Duck plague (DP) caused by anatid herpesvirus 1, also called duck enteritis virus (DEV), presents one of the most important concerns in mass waterfowl production. Apart from geese and ducks, free-ranging water birds are the most notorious infection carriers. The epidemiology of DEV in Western Europe remains unknown. Therefore, it was reasonable to conduct a study on its occurrence using modern but simple real-time loop-mediated isothermal amplification (LAMP). Analysis of 132 field isolates showed the presence of DEV in 96 birds (72.7 %), and it was found predominantly in wild ducks (Anas platyrhynchos) and mute swans (Cygnus olor). This virus was also found in graylag geese (Anser anser), tundra bean geese (Anser fabalis), and grey herons (Ardea cinerea). The results were recorded as green colour of positive samples, fluorescence under ultraviolet light, and florescent curves in a real-time PCR system. This study indicates the high prevalence of DEV among free-ranging water birds in Poland and the possible transmission to other birds settling in the water environment. This is the first report of DEV detection among free-ranging water birds in Poland.
References
Aravind S, Patil BR, Dey S, Mohan CM (2012) Recombinant UL30 antigen-based single serum dilution ELISA for detection of duck viral enteritis. J Virol Methods 185:234–238
Baudet A (1923) Mortality in ducks in the Netherlands caused by a filtrable virus; fowl plague. Tijdschr Diergeneeskd 50:455–459
Brand CJ, Docherty DE (1984) A survey of North American migratory waterfowl for duck plague (duck virus enteritis) virus. J Wildl Dis 20:261–266
Campagnolo ER, Banerjee M, Panigrahy B, Jones RL (2001) An outbreak of duck viral enteritis (duck plague) in domestic Muscovy ducks (Cairina moschata domesticus) in Illinois. Avian Dis 45:522–528
Gough RE, Alexander DJ (1990) Duck virus enteritis in Great Britain, 1980 to 1989. Vet Rec 126:595–597
Hansen WR, Brown SE, Nashold SW, Knudson DL (1999) Identification of duck plague virus by polymerase chain reaction. Avian Dis 43:106–115
Ji J, Du LQ, Xie QM et al (2009) Rapid diagnosis of duck plagues virus infection by loop-mediated isothermal amplification. Res Vet Sci 87:53–58
Ji J, Xie QM, Chen CY et al (2010) Molecular detection of Muscovy duck parvovirus by loop-mediated isothermal amplification assay. Poult Sci 89:477–483
Kaleta EF (1990) Herpesviruses of birds. Avian Pathol 19:193–211
Kaleta EF, Kuczka A, Kühnhold A et al (2007) Outbreak of duck plague (duck herpesvirus enteritis) in numerous species of captive ducks and geese in temporal conjunction with enforced biosecurity (in-house keeping) due to the threat of avian influenza A virus of the subtype Asia H5N1. Dtsch Tierarztl Wochenschr 114:3–11
King AMQ, Lefkowitz E, Adams MJ, Carstens EB (2012) Virus taxonomy: ninth report of the international committee on taxonomy of viruses. Elsevier, London
Kumar NV, Reddy YN, Rao MVS (2004) Enzyme linked immunosorbent assay for detection of duck plague virus. J Ind Vet 5:481–483
Leibovitz L (1968) Progress report: duck plague surveillance of American Anseriformes. Wildl Dis 4:87–91
Lu X, Li X, Mo Z et al (2012) Rapid identification of Chikungunya and Dengue virus by a real-time reverse transcription-loop-mediated isothermal amplification method. Am J Trop Med Hyg 87:947–953
Murray L, Edwards L, Tuppurainen ES (2013) Detection of capripoxvirus DNA using a novel loop-mediated isothermal amplification assay. BMC Vet Res 9:90
Nagamine K, Hase T, Notomi T (2002) Accelerated reaction by loop-mediated isothermal amplification using loop primers. Mol Cell Probes 16:223–229
Nie K, Zhao X, Ding X et al (2013) Visual detection of human infection with influenza A (H7N9) virus by subtype-specific reverse transcription loop-mediated isothermal amplification with hydroxynaphthol blue dye. Clin Microbiol Infect 19:372–375
Osman HA, Eltom KH, Musa NO et al (2013) Development and evaluation of loop-mediated isothermal amplification assay for detection of Crimean Congo hemorrhagic fever virus in Sudan. J Virol Methods 190:4–10
Parida M, Posadas G, Inoue S et al (2004) Real-Time reverse transcription loop-mediated isothermal amplification for rapid detection of West Nile Virus. J Clin Microbiol 42:257–263
Peiris L, Poon LM (2007) Loop-mediated isothermal amplification for influenza A (H5N1) virus. Emerg Infect Dis 13:899–901
Plummer PJ, Alefantis T, Kaplan S et al (1998) Detection of duck enteritis virus by polymerase chain reaction. Avian Dis 42:554–564
Qi X, Yang X, Cheng A et al (2008) Quantitative analysis of virulent duck enteritis virus loads in experimentally infected ducklings. Avian Dis 52:338–344
Qi X, Yang X, Cheng A et al (2009) Replication kinetics of duck virus enteritis vaccine virus in ducklings immunized by the mucosal or systemic route using real-time quantitative PCR. Res Vet Sci 86:63–67
Qiu X, Li T, Zhang G et al (2012) Development of a loop-mediated isothermal amplification method to rapidly detect porcine circovirus genotypes 2a and 2b. Virol J 9:318
Song C, Wan H, Yu S et al (2012) Rapid detection of duck hepatitis virus type-1 by reverse transcription loop-mediated isothermal amplification. J Virol Methods 182:76–81
Tarasiuk K, Woźniakowski G, Samorek-Salamonowicz E (2013) Loop-mediated isothermal amplification as a simple molecular method for the detection of Derzsy’s disease virus. Bull Vet Inst Pulawy 57:19–23
Wang Y, Yuan X, Li Y et al (2011) Rapid detection of newly isolated Tembusu-related Flavivirus by reverse-transcription loop-mediated isothermal amplification assay. Virol J 8:553
Wobeser G (1987) Experimental duck plague in blue-winged teal and Canada geese. J Wildl Dis 23:368–375
Woźniakowski G, Kozdruń W, Samorek-Salamonowicz E (2012) Loop-mediated isothermal amplification for the detection of goose circovirus. Virol J 9:110
Wu Y, Cheng A, Wang M et al (2011) Serologic detection of duck enteritis virus using an indirect ELISA based on recombinant UL55 protein. Avian Dis 55:626–632
Wu Y, Cheng A, Wang M et al (2011) Establishment of real-time quantitative reverse transcription polymerase chain reaction assay for transcriptional analysis of duck enteritis virus UL55 gene. Virol J 8:266
Yamazaki W, Mioulet V, Murray L et al (2013) Development and evaluation of multiplex RT-LAMP assays for rapid and sensitive detection of foot-and-mouth disease virus. J Virol Methods 192:18–24
Yan L, Peng S, Yan P et al (2012) Comparison of real-time reverse transcription loop-mediated isothermal amplification and real-time reverse transcription polymerase chain reaction for duck Tembusu virus. J Virol Methods 182:50–55
Yang FL, Jia WX, Yue H et al (2005) Development of quantitative real-time polymerase chain reaction for duck enteritis virus DNA. Avian Dis 49:397–400
Yang L, Li J, Bi Y et al (2012) Development and application of a reverse transcription loop-mediated isothermal amplification method for rapid detection of duck hepatitis A virus type 1. Virus Genes 45:585–589
Yang JL, Rui Y, Cheng AC et al (2010) A simple and rapid method for detection of goose parvovirus in the field by loop mediated isothermal amplification. Virol J 7:14
Yoshida H, Sakoda Y, Endo M et al (2011) Evaluation of the reverse transcription loop-mediated isothermal amplification (RT-LAMP) as a screening method for the detection of influenza viruses in the fecal materials of water birds. J Vet Med Sci 73:753–758
Acknowledgments
The authors acknowledge Prof. Zenon Minta and all co-workers of the Department of Poultry Diseases, National Veterinary Research Institute, for sharing the infectious material from wild ducks and swans used in this study. The study was supported by research and development project no. P/020, entitled “The free-living waterfowl as the reservoir and vector of chosen viral infections spreading”.
Conflict of interest
The authors declare that they have no competing interests.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Woźniakowski, G., Samorek-Salamonowicz, E. First survey of the occurrence of duck enteritis virus (DEV) in free-ranging Polish water birds. Arch Virol 159, 1439–1444 (2014). https://doi.org/10.1007/s00705-013-1936-8
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00705-013-1936-8