key: cord-0776798-stb209eh
authors: Decaro, Nicola; Desario, Costantina; Addie, Diane D.; Martella, Vito; Vieira, Maria João; Elia, Gabriella; Zicola, Angelique; Davis, Christopher; Thompson, Gertrude; Thiry, Ethienne; Truyen, Uwe; Buonavoglia, Canio
title: Molecular Epidemiology of Canine Parvovirus, Europe
date: 2007-08-03
journal: Emerg Infect Dis
DOI: 10.3201/eid1308.070505
sha: b69fe5e231d41629e4620b18e90999022c72474d
doc_id: 776798
cord_uid: stb209eh

Canine parvovirus (CPV), which causes hemorrhagic enteritis in dogs, has 3 antigenic variants: types 2a, 2b, and 2c. Molecular method assessment of the distribution of the CPV variants in Europe showed that the new variant CPV-2c is widespread in Europe and that the viruses are distributed in different countries.

A total of 232 fecal samples or CPV isolates were obtained from dogs with diarrhea in Italy (n = 107), Germany (n = 37), the United Kingdom (n = 41), Portugal (n = 31), Belgium (n = 13), Spain (n = 1), Switzerland (n = 1), and the Czech Republic (n = 1). The fecal samples collected in Italy, the United Kingdom, Portugal, and Belgium were CPV-positive according to PCRs performed in local laboratories. Samples were collected during [2005] [2006] , with the exception of samples from Italy that were collected only in 2006 because other studies had assessed the molecular epidemiology of CPV in the previous decade (5) . All samples from Germany consisted of cell-culture-adapted CPV strains isolated from dogs with diarrhea in Germany during 1996-2005. Samples were homogenized (10% w/v) in phosphatebuffered saline (pH 7.2) and subsequently clarifi ed by centrifuging at 1,500× g for 15 min. Viral DNA was extracted from the supernatants of fecal homogenates or from the viral suspensions by boiling for 10 min and chilling on ice.

To reduce residual inhibitors of DNA polymerase activity to ineffective concentrations, the DNA extracts were diluted 1:10 in distilled water (10) . CPV DNA titers were calculated by using a real-time PCR, based on TaqMan technology and able to recognize all CPV strains (10) , whereas characterization of the viral type was obtained by means of MGB probe assays specifi c for types 2a/2b and 2b/2c (5) . To rule out the presence of CPV strains of vaccine origin, which are usually type 2 or less frequently type 2b, we subsequently tested samples recognized as types 2/2a and 2b by MGB probe assays that discriminate between vaccine and fi eld strains of CPV (11, 12) .

All samples that had CPV-positive results from laboratories located in the countries of sample origin were confi rmed by TaqMan assay to contain CPV DNA. CPV infection was also demonstrated in the single samples from Spain, Switzerland, and the Czech Republic (Figure) . In Italy, a nearly complete substitution of CPV-2b by CPV-2c was noted; CPV-2a strains were found at low frequency, which confi rmed the progressive decrease noted during the past 5 years (3) (4) (5) . In contrast, CPV-2b is still prevalent in Germany and Portugal, although CPV-2c is also widespread in these countries. Retrospective analysis of archival samples showed that CPV-2c has been circulating in Germany since 1996. An equivalent distribution of types 2a and 2b was assessed in the United Kingdom, where a single CPV-2c strain was detected. In Portugal, no CPV-2a strain was detected, whereas in Belgium all CPVs were type 2a. The single samples from Switzerland and the Czech Republic were CPV-2a, whereas the sample from Spain was CPV-2c. The original type CPV-2 was detected in 1 sample from the United Kingdom and 4 from Italy, but the latter samples had been collected from dogs shortly after vaccination with a classic type-2-based vaccine (12) . 

Despite its DNA genome, CPV possesses a high genetic substitution rate, similar to that observed for RNA viruses, which is responsible for continuous antigenic evolution and rapid displacement of old types by new antigenic variants (13) . CPV-2c, which emerged in Italy in 2000 (2), is spreading with high effi ciency in the dog population of Italy and progressively replacing the antigenic variants 2a and 2b (3) (4) (5) . Such a variant has been detected in Vietnam also (6) , but no information is available on its presence and distribution in other European countries, except for a single case report from Spain (14) .

Our study shows that the new variant 2c is widespread in some European countries (Italy, Portugal, and Germany) and that it could be detected sporadically in the United Kingdom. In contrast with previous studies of CPV-2a in Europe, our study showed that CPV-2a is most frequent in Belgium, whereas in the United Kingdom, Germany, and Italy, it has been overtaken by CPV-2b or CPV-2c. In Portugal, CPV-2a was not detected at all, but types 2b and 2c were equally distributed. To our knowledge, this is the fi rst report of the new variant 2c in Portugal, the United Kingdom, and Germany. In Germany, CPV-2c was detected in archival samples collected in 1996; thus, it was circulating in Europe 4 years before its fi rst offi cial report in Italy. Such a variable geographic distribution of the CPV variants in Europe may be related to different commercial fl ows of dogs imported from foreign countries rather than to different vaccination protocols.

The progressive spreading of CPV-2c in the world or, less probably, its independent emergence in different countries, suggests that the Glu-426 mutation provides a certain advantage in viral replication. The replacement of CPV-2 by types 2a and 2b has been associated with increased ability to bind canine transferrin receptors, although it might not rule out the possibility of mutations at residue 426 of the VP2 protein being selected also for their antigenic effects (1) . Whether the Glu-426 mutation confers benefi t in receptor-binding activity is of interest. Another question is whether the CPV vaccines currently used provide full protection against the new variant or whether they should be replaced by homologous vaccines. This work was supported by grants from the University of Bari (Ricerca di Ateneo 2006: "Caratterizzazione delle varianti di campo del parvovirus del cane mediante real-time PCR con sonde minor groove binding").

Dr Decaro is an associate professor at the Faculty of Veterinary Medicine of Bari, Italy. His research interests include the study of viral pathogens of dogs, with particular emphasis on canine parvovirus and canine coronavirus.

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