Abstract
In the present study, tonsils and hearts from 100 pigs were collected in a German slaughterhouse in 2010 and tested for porcine parvoviruses (PPV, PPV2, PPV3 and PPV4). PPV was observed in 60 of 100 hearts and 61 of 100 tonsils, and PPV2 was observed in 55 of 100 hearts and 78 of 100 tonsils. PPV3 and PPV4 were found in 20 and 7, respectively, of the 100 tonsils tested, but not in the heart samples. Positive samples of PPV, PPV2 and PPV3 were analyzed by nucleotide sequencing, and phylogenetic analysis revealed at least two distinct lineages for each virus in the German samples. The high detection rate of PPV, PPV2 and PPV3 in healthy animals and their genetic diversity highlights the importance of continuous monitoring of these viruses and their zoonotic potential.
Similar content being viewed by others
References
Adlhoch C, Kaiser M, Ellerbrok H, Pauli G (2010) High prevalence of porcine Hokovirus in German wild boar populations. Virol J 7:171
Bergeron J, Hérbert B, Tijssen P (1996) Genome organization of the Kresse strain of porcine parvovirus: identification of the allotropic determinant and comparison with those of NADL-2 and field isolates. J Virol 70:2508–2515
Bolt DM, Häni H, Müller E, Waldvogel AS (1997) Non-suppurative myocarditis in piglets associated with porcine parvovirus infection. J Comp Pathol 117:107–118
Corcioli F, Zakrzewska K, Fanci R, De Giorgi V, Innocenti M, Rotellini M, Di Lollo S, Azzi A (2010) Human parvovirus PARV4 DNA in tissues from adult individuals: a comparison with human parvovirus B19 (B19V). Virol J 7:272
Cheung AK, Wu G, Wang D, Bayles DO, Lager KM, Vincent AL (2010) Identification and molecular cloning of a novel porcine parvovirus. Arch Virol 155:801–806
Drummond AJ, Rambaut A (2007) BEAST: Bayesian evolutionary analysis by sampling trees. BMC Evol Biol 7:214
Edgar RC (2004) MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Res 32:1792–1797
Fernandes S, Tijssen P (2009) Seamless cloning and domain swapping of synthetic and complex DNA. Anal Biochem 385:171–173
Hijikata M, Abe K, Win KM, Shimizu YK, Keicho N, Yoshikura H (2001) Identification of new parvovirus DNA sequence in swine sera from Myanmar. Jpn J Infect 54:244–245
Huang L, Zhai SL, Cheung AK, Zhang HB, Long JX, Yuan SS (2010) Detection of a novel porcine parvovirus, PPV4, in Chinese swine herds. Virol J 7:333
Kuethe F, Lindner J, Matschke K, Wenzel JJ, Norja P, Ploetze K, Schaal S, Kamvissi V, Bornstein SR, Schwanebeck U, Modrow S (2009) Prevalence of parvovirus B19 and human bocavirus DNA in the heart of patients with no evidence of dilated cardiomyopathy or myocarditis. Clin Infect Dis 49:1660–1666
Lau SK, Woo PC, Tse H, Fu CT, Au WK, Chen XC, Tsoi HW, Tsang TH, Chan JS, Tsang DN, Li KS, Tse CW, Ng TK, Tsang OT, Zheng BJ, Tam S, Chan KH, Zhou B, Yuen KY (2008) Identification of novel porcine and bovine parvoviruses closely related to human parvovirus 4. J Gen Virol 89:1840–1848
Lotze U, Egerer R, Glück B, Zell R, Sigusch H, Erhardt C, Heim A, Kandolf R, Bock T, Wutzler P, Figulla HR (2010) Low level myocardial parvovirus B19 persistence is a frequent finding in patients with heart disease but unrelated to ongoing myocardial injury. J Med Virol 82:1449–1457
Rutherford K, Parkhill J, Crook J, Horsnell T, Rice P, Rajandream MA, Barrell B (2000) Artemis: sequence visualization and annotation. Bioinformatics 16:944–945
Shackelton LA, Holmes EC (2006) Phylogenetic evidence for the rapid evolution of human B19 erythrovirus. J Virol 80:3666–3669
Shackelton LA, Parrish CR, Truyen U, Holmes EC (2005) High rate of viral evolution associated with the emergence of carnivore parvovirus. Proc Natl Acad Sci USA 102:379–384
Siegl G (1976) The Parvoviruses. In: Gard S, Hallauer C (eds) Virology Monographs, 15th edn. Springer, Wien, New York, pp 47–52
Söderlund-Venermo M, Hokynar K, Nieminen J, Rautakorpi H, Hedman K (2002) Persistence of human parvovirus B19 in human tissues. Pathol Biol 50:307–316
Streck AF, Bonatto SL, Homeier T, Souza CK, Gonçalves KR, Gava D, Canal CW, Truyen U (2011) High rate of viral evolution in the capsid protein of porcine parvovirus. J Gen Virol 92:2628–2636
Streck AF, Gava D, Souza CK, Gonçalves KR, Bortolozzo FP, Wentz I, Canal CW (2011) Presence of porcine parvovirus in sera from pigs is independent of antibody titers. Berl Munch Tierarztl Wochenschr 124:242–246
Tijssen P, Agbandje-McKenna M, Almendral JM, Bergoin M, Flegel TW, Hedman K, Kleinschmidt JA, Li D, Pintel D, Tattersall P (2011) Parvoviridae. In: King MQ, Adams MJ, Carstens E, Lefkowitz EJ (eds) Virus taxonomy: classification and nomenclature of viruses: ninth report of the international committee on taxonomy of viruses. Elsevier, San Diego
Truyen U, Streck AF (2012) Porcine parvovirus In: Zimmerman J, Karriker L, Ramirez A, Schwartz K, Stevenson G (eds) Diseases of Swine, 10th Ed. John Wiley & Sons Inc, Oxfort, pp 447–455
Waldvogel AS, Hassam S, Weilenmann R, Tratschin JD, Siegl G, Hänichen T, Briner J, Pospischil A (1991) Retrospective study of myocardial canine parvovirus infection by in situ hybridization. Zentralbl Veterinarmed B 38:353–357
Whelan JA, Russell NB, Whelan MA (2003) A method for the absolute quantification of cDNA using real-time PCR. J Immunol Methods 278(1–2):261–269
Xiao CT, Giménez-Lirola LG, Halbur PG, Opriessnig T (2012) Increasing porcine PARV4 prevalence with pig age in the U.S. pig population. Vet Microbiol 160:290–296
Xiao CT, Gerber PF, Giménez-Lirola LG, Halbur PG, Opriessnig T (2013) Characterization of porcine parvovirus type 2 (PPV2) which is highly prevalent in the USA. Vet Microbiol 161:325–330
Zeeuw EJL, Leinecker N, Herwig V, Selbitz HJ, Truyen U (2007) Study of the virulence and cross-neutralization capability recent porcine parvovirus field isolates and vaccine viruses experimentally infected pregnant gilts. J Gen Virol 88:420–427
Zimmermann P, Ritzmann M, Selbitz HJ, Heinritzi K, Truyen U (2006) VP1 sequences of German porcine parvovirus isolates define two genetic lineages. J Gen Virol 87:295–301
Acknowledgments
This research was supported by the Deutscher Akademischer Austausch Dienst (DAAD, Germany) and Coordenação de Aperfeiçoamento Pessoal de Nível Superior (CAPES, Brazil). We thank Dietlinde Woll and Martin Pfeffer for critically reading the manuscript.
Author information
Authors and Affiliations
Corresponding author
Electronic supplementary material
Below is the link to the electronic supplementary material.
Rights and permissions
About this article
Cite this article
Streck, A.F., Homeier, T., Foerster, T. et al. Analysis of porcine parvoviruses in tonsils and hearts from healthy pigs reveals high prevalence and genetic diversity in Germany. Arch Virol 158, 1173–1180 (2013). https://doi.org/10.1007/s00705-013-1603-0
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00705-013-1603-0