Volume 14, Number 4—April 2008
Natural Coinfection with 2 Parvovirus Variants in Dog
Highlight and copy the desired format.
|EID||Vieira MJ, Silva E, Desario C, Decaro N, Carvalheira J, Buonavoglia C, et al. Natural Coinfection with 2 Parvovirus Variants in Dog. Emerg Infect Dis. 2008;14(4):678-679. https://dx.doi.org/10.3201/eid1404.071461|
|AMA||Vieira MJ, Silva E, Desario C, et al. Natural Coinfection with 2 Parvovirus Variants in Dog. Emerging Infectious Diseases. 2008;14(4):678-679. doi:10.3201/eid1404.071461.|
|APA||Vieira, M. J., Silva, E., Desario, C., Decaro, N., Carvalheira, J., Buonavoglia, C....Thompson, G. (2008). Natural Coinfection with 2 Parvovirus Variants in Dog. Emerging Infectious Diseases, 14(4), 678-679. https://dx.doi.org/10.3201/eid1404.071461.|
To the Editor: Canine parvovirus (CPV) emerged in the late 1970s, presumably by mutations in feline panleukopenia virus, and became a major viral pathogen of dogs worldwide (1). Between 1979 and 1981, the original type 2 virus (CPV-2) was replaced by a new genetic and antigenic variant, type 2a (CPV-2a). Between 1983 and 1984, CPV-2a was replaced by type 2b (CPV-2b), which differs from type 2a by only 1 epitope located at residue 426 of the VP2 capsid protein (2). CPV-2 does not replicate in cats, but the new variants replicate in dogs and cats (3). Recently, an antigenic change has been observed in a new strain, CPV-2c, isolated from domestic dogs in Italy (4). This variant was also detected in Vietnam (5), other countries in Europe (6), and the United States (7). CPV-2c was recently detected in cats (8) and is characterized by a replacement of aspartic acid with glutamic acid at residue 426 of the VP2 capsid protein.
To identify CPV types 2, 2a, and 2b, PCR methods were developed (9). However, these methods could not distinguish type 2c from type 2b (4). Consequently, we used a PCR–restriction fragment-length polymorphism (RFLP) assay with endonuclease MboII. This enzyme can distinguish type 2c from other CPVs (4). Recently, a real-time PCR assay based on minor groove binder (MGB) probe technology was developed for rapid identification and characterization of the antigenic variants. This assay is based on 1 nucleotide polymorphism in the VP2 gene (10).
In June 2006, a 10-week-old female dog (PT-32/07) was brought to the veterinary clinic in Figueira da Foz, Portugal, with clinical signs of parvovirus infection, after an episode of gastrointestinal disease in her littermates. Three littermates, also brought to the clinic, showed no signs of infection. None of the dogs were vaccinated against CPV. Clinical signs in dog PT-32/07 were lethargy, anorexia, vomiting, diarrhea, and a temperature of 39.3°C. Identical signs were observed in 1 littermate 3 days later; the 2 other dogs did not show any signs other than lethargy and loose stools.
Rectal swab samples from all dogs were screened for CPV by using an immunomigration rapid test (Synbiotics Corporation, Lyon, France). Two of the dogs showed negative results, and 2 showed positive results. Feces, serum, and lingual swab samples were positive for parvovirus DNA. DNA was quantified by using a real-time PCR with TaqMan technology performed in an i-Cycler iQ (Bio-Rad Laboratories, Milan, Italy).
CPV variants were characterized by using MGB probe technology. This technology uses type-specific probes labeled with different fluorophores (FAM and VIC) that can detect single nucleotide polymorphisms between CPV types 2a/2b and 2b/2c (10). MGB probes specific for type 2b were labeled with FAM in both type 2a/2b and 2b/2c assays, and MGB probes specific for type 2a (type 2a/2b assay) and type 2c (type 2b/2c assay) were labeled with VIC.
All specimens from 1 dog (PT-32/07) were positive for the 2 variants of CPV type 2 (CPV 2b and CPV 2c). Conversely, of the 3 littermates, 2 were positive for CPV type 2b and 1 was positive for CPV type 2c in all samples (Table).
A conventional PCR and RFLP analyses were performed by using the method of Buonavoglia et al. (4) with known positive CPV-2b and CPV-2c samples as controls to confirm our findings. The 583-bp PCR product obtained from the coinfected dog by using primer pair 555for/555rev was digested with MboII. Digestion generated 2 fragments (≈500 and 80 bp) in all dog samples. The CPV-2c control sample showed 2 fragments (≈500 and 80 bp), and CPV-2b control sample was not digested with MboII.
We report CPV-2b and CPV-2c variants in samples from a dog with littermates that were positive for CPV-2b or CPV-2c during an episode of gastrointestinal disease. Coinfection with multiple CPV variants that showed high genetic diversity in the VP2 gene has recently been reported in a domestic cat (8). Continuous and rapid evolution of CPV may cause serious problems in diagnostic testing and vaccine efficacy. Antigenic variation may negatively affect vaccine efficacy if changes occur at major antigenic sites. Thus, continuous monitoring for novel genetic and antigenic virus types is needed. Additional studies are in progress to characterize nucleotide sequences of all CPV isolates from this case.
We thank the Laboratório Nacional de Investigação Veterinária, Porto, Portugal, for infrastructural support.
This work was supported by a course formation research fellowship of the Fundação para a Ciência e Tecnologia of the Ministry of Science and Technology, Portugal, and by Intervet Portugal.
- Truyen U. Evolution of canine parvovirus: a need for new vaccines? Vet Microbiol. 2006;117:9–13.
- Parrish CR, Aquandro CF, Strassheim ML, Evermann JF, Sgro JY, Mohammed HO. Rapid antigenic-type replacement and DNA and sequence evolution of canine parvovirus. J Virol. 1991;65:6544–52.
- Truyen U, Evermann JF, Vieler E, Parrish CR. Evolution of canine parvovirus involved loss and gain of feline host range. Virology. 1996;215:186–9.
- Buonavoglia C, Martella V, Pratelli A, Tempesta M, Cavalli A, Buonavoglia D, Evidence for evolution of canine parvovirus type 2 in Italy. J Gen Virol. 2001;82:3021–5.
- Nakamura M, Tohya Y, Miyazawa T, Mochizuki M, Phung HT, Nguyen NM, A novel antigenic variant of canine parvovirus from a Vietnamese dog. Arch Virol. 2004;149:2261–9.
- Decaro N, Desario C, Addie D, Martella V, Vieira MJ, Elia G, Molecular epidemiology of canine parvovirus, Europe. Emerg Infect Dis. 2007;13:1222–4.
- Hong C, Decaro N, Desario C, Tanner P, Pardo MC, Sanchez S, Occurrence of canine parvovirus type 2c in the United States. J Vet Diagn Invest. 2007;19:535–9.
- Battilani M, Scagliarini A, Ciulli S, Morganti L, Prosperi S. High genetic diversity of the VP2 gene of a canine parvovirus strain detected in a domestic cat. Virology. 2006;352:22–6.
- Senda M, Parrish CR, Harasawa R, Gamoh K, Muramatsu M, Hirayama N, Detection by PCR of wild-type canine parvovirus which contaminates dog vaccines. J Clin Microbiol. 1995;33:110–3.
- Decaro N, Elia G, Martella V, Campolo M, Desario C, Camero M, Characterisation of the canine parvovirus type 2 variants using minor groove binder probe technology. J Virol Methods. 2006;133:92–9.
- Table. Detection by minor groove binder probe assay of CPV antigenic variants in different specimens from dogs from the same litter (10 weeks old), Portugal, 2006
Please use the form below to submit correspondence to the authors or contact them at the following address:
Gertrude Thompson, Department of Veterinary Clinics, Instituto de Ciências Biomédicas de Abel Salazar, Rua Padre Armando Quintas, 4485-661 Vairão, Porto, Portugal;
Comment submitted successfully, thank you for your feedback.
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
- Page created: July 15, 2010
- Page last updated: July 15, 2010
- Page last reviewed: July 15, 2010
- Centers for Disease Control and Prevention,
National Center for Emerging and Zoonotic Infectious Diseases (NCEZID)
Office of the Director (OD)