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rologie i - European Congress of Virology

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5 th <strong>European</strong> <strong>Congress</strong> <strong>of</strong> <strong>Virology</strong>serotypes and the close genetic relationship between them leads to potentialcross species infections. Serotype I canine strain (CCoVI) differs by thepresence <strong>of</strong> a unique open reading frame ORF3, coding for an accessoryglycoprotein gp3, with unknown function. In a phylogenetic study performedto characterize Coronavirus infected cats, structural genes S, M and Nwere sequenced and allowed to detect a new recombinant FCoVI/CCoVIstrain on 5 cats out <strong>of</strong> 26 samples. In these strains, the S gene clusters withFCoVI type, whereas downstream genes ORF3, M and N are grouped withCCoVI genotype. Moreover, ORF3 found in cats samples, displayed oneor two identical deletions, never described in canine samples. In a possiblecross species virus transmission context, our aim is to understand the role<strong>of</strong> gp3 and determine if the deletions observed play a role during the adaptation<strong>of</strong> the recombinant canine strain to the feline species. More globally,this study will give an overall view <strong>of</strong> molecular mechanisms implied inthe inter specific host transmission <strong>of</strong> Coronaviruses.Acute gastroenteritis is one <strong>of</strong> the most common diseases in humans aswell as farm animals. Small, non enveloped RNA viruses are recognizedas important causes <strong>of</strong> this disease. The objective <strong>of</strong> the study was to determinethe prevalence and genetic diversity <strong>of</strong> members <strong>of</strong> genera Sapovirus,Kobuvirus, and Mamastrovirus in asymptomatic pigs in the Czech Republic.A total <strong>of</strong> 196 fecal samples were tested by reverse transcriptionPCR (RT PCR) assay using gene specific primers. Phylogenetic analysiswas carried out using the neighbor joining method with a bootstrap test<strong>of</strong> 1000 replicates using MEGA s<strong>of</strong>tware package v4.0. The most prevalentvirus was kobuvirus (87.3%), followed by astrovirus (34.2%) andsapovirus (10.2%). Statistically significantly highest number <strong>of</strong> positivesamples was detected in the age group <strong>of</strong> post weaning pigs. Consideringthe possible zoonotic potential <strong>of</strong> monitored viruses, their geneticdiversity and degree <strong>of</strong> similarity to human strains was also determined.In conclusion, the circulation <strong>of</strong> porcine sapoviruses, kobuviruses, andastroviruses in the Czech Republic was shown thus extending their <strong>European</strong>distribution. The high prevalence rate <strong>of</strong> gastroenteritis producingviruses in clinically healthy pigs confirmed the role <strong>of</strong> pigs as a reservoir<strong>of</strong> a heterogeneous viral population representing a constant threat tohuman health. The study was supported by the Ministry <strong>of</strong> Agriculture<strong>of</strong> the Czech Republic (Grant No. QH81061) and the Ministry <strong>of</strong> Education,Youth and Sports <strong>of</strong> the Czech Republic (Admirevet; Grant No.CZ.1.05/2.1.00/01.0006, ED0006/01/01).REF 331Prevalence and genetic diversity <strong>of</strong> porcine bocavirus 1 in apparentlyhealthy pigs in the Czech RepublicJana PRODELALOVAVeterinary Research Institute, Brno, CZECH REPUBLICBocaviruses (family Parvoviridae) are pathogens causing various diseasesin both humans and animals. Porcine bocavirus 1 (PBoV1) was firstlyidentified in Sweden in 2009 and it is potentially associated with swinedisease. The virus was detected in pigs suffering from porcine circovirusassociated disease and respiratory disease but also from clinically healthypigs. The aim <strong>of</strong> the present study was to detect and measure the prevalence<strong>of</strong> PBoV1 and analyse partial PBoV1 sequences. Faecal samples were collectedfrom different farms located in the South Moravia region, tested byPCR specific for VP1/VP2 gene <strong>of</strong> PBoV1 and sequenced. Among 179samples obtained from apparently healthy pigs <strong>of</strong> different age groups, theprevalence was 22.4%. Higher infection rate was found in post weaningpigs (75.5%, 34/45) compared with finisher pigs (8.2%, 5/61) and saws(3%, 1/33). No PBoV1 positive samples were detected in nursing piglets(0/40). PBoV1 positive samples were obtained from three out <strong>of</strong> eightfarms. By comparative sequence analysis <strong>of</strong> 496 bp fragments <strong>of</strong> VP1/VP2gene from domestic pigs and sequences available in GenBank we detectedonly minor differences between PBoV1 s. This result indicates thatPBoV1 s circulating within the apparently healthy domestic pig populationin South Moravia region were highly similar. This work was supportedby the Ministry <strong>of</strong> Agriculture <strong>of</strong> the Czech Republic (Grant No. NAZVQH81061) and the Ministry <strong>of</strong> Education, Youth, and Sports <strong>of</strong> the CzechRepublic (Grant No. AdmireVet CZ.1.05/2.1.00/01.006, ED006/01/01).REF 333Serological surveilance for selected viral agents in ROE DEER(Capreolus Capreolus) and RED DERR (Cervus Elaphus) in CroatiaBesi ROIC, Lorena JEMERSIC, Svjetlana TERZIC, Andreja JUNGIC,Dragan BRNIC, Tomislav KEROS, Jelena PRPICCroatian Veterinary Institute, Zagreb, CROATIADuring the hunting season <strong>of</strong> 2009, blood samples from 32 roe deer(Capreolus capreolus) and 55 red deer (Cervus elaphus) were collectedin four Croatian regions. Sera were tested by enzyme linked immunosorbentassay (ELISA) for the presence <strong>of</strong> antibodies against bovine herpesvirus 1 (BHV 1), parainflurnza 3 virus (PI 3), bovine respiratory syncytialvirus (BRSV), bovine viral diarrhea virus (BVDV) and bluetonguevirus (BTV). Specific antibodies were detected for bovine herpes virus1 (BHV 1) in 12.50% (4 positive/32 tested) roe deer and in 25.45% (14positive/55 tested) red deer. Additionally, positive results were obtainedagainst parainfluenza 3 virus (PI 3) in 68.75% roe deer (22 positive/32 tested)and 83.63% red deer (46 positive/55 tested). Most <strong>of</strong> the seropositivesera were recorded among red deer in the eastern part <strong>of</strong> Croatia which isknown as a district with high density populations <strong>of</strong> wildlife species. Noantibodies were detected against any <strong>of</strong> the other viral agents assayed inthis study. The presence <strong>of</strong> BHV 1 and PI 3 virus antibodies indicate thatboth deer species have been exposed and have responded serologically toviral agents which are related or identical to the domestic livestock pathogens.This study provides the first survey for the presence <strong>of</strong> antibodies toviral diseases in cervids from Croatia.Key words: roe deer (Capreolus capreolus), red deer (Cervus elaphus),viral disease, serology, CroatiaREF 332Prevalence and genetic diversity <strong>of</strong> porcine sapoviruses, kobuviruses,and astroviruses in asymptomatic pigs in the Czech RepublicLucie DUFKOVA 1 , Ivana SCIGALKOVA 2 , Romana MOUTELIKOVA 1 ,Hana MALENOVSKA 1 , Jana PRODELALOVA 11 Veterinary Research Institute, Brno, CZECH REPUBLIC; 2 Faculty <strong>of</strong>Science/Masaryk University, Brno, CZECH REPUBLICREF 334Molecular characterization <strong>of</strong> VP2 Gene <strong>of</strong> infectious pancreaticnecrosis virus from Mexican isolatesEdith ROJAS ANAYA 1 , Elizabeth LOZA RUBIO 1 , Celene SALGADOMIRANDA 1,2 , Gary GARCIA ESPINOSA 21 INIFAP, CENID Microbiología Animal, México City, MÉXICO; 2 FMVZ,UNAM, México City, MÉXICOInfectious pancreatic necrosis virus (IPNV), is considered one <strong>of</strong> the mostimportant viral pathogen in salmonids and remains a serious problem inthe aquaculture industry. To better understand the genetic and biologicaldiversity <strong>of</strong> these viruses in Mexico it is necessary to further study thefeatures which include genetic characterization and virulence that mayimpact on the production <strong>of</strong> biologicals. The aim <strong>of</strong> this study was toperform the molecular characterization <strong>of</strong> the VP2 gene Mexican IPNVisolates from different geographical regions. Seven isolates were obtainedfrom rainbow trout hatchery, during 2006 and 2007 <strong>of</strong> the major farmsproducing trout: Michoacan, Puebla and State <strong>of</strong> Mexico. We designedS212 Vi<strong>rologie</strong>, Vol 17, supplément 2, septembre 2013

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