EPIDEMIOLOGICAL ANALYSIS OF BVDV INFECTION IN CATTLE FARMS OF KHARKOV REGION, UKRAINE

Main Authors: ANTON GERILOVYCH, BORYS STEGNIY, STEFAN VILCEK, ERNST PETERHANS, ROMAN KUCHERYAVENKO, IRYNA GORAICHUK, VITALIY BOLOTIN, OLEKSIY SOLODIANKIN, ALEKSANDAR POTKONJAK
Format: Article Journal
Terbitan: , 2013
Subjects:
Online Access: https://zenodo.org/record/6523916
ctrlnum 6523916
fullrecord <?xml version="1.0"?> <dc schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><creator>ANTON GERILOVYCH</creator><creator>BORYS STEGNIY</creator><creator>STEFAN VILCEK</creator><creator>ERNST PETERHANS</creator><creator>ROMAN KUCHERYAVENKO</creator><creator>IRYNA GORAICHUK</creator><creator>VITALIY BOLOTIN</creator><creator>OLEKSIY SOLODIANKIN</creator><creator>ALEKSANDAR POTKONJAK</creator><date>2013-06-15</date><description>Bovine viral diarrhea is a widespread infection of cattle caused by bovine viral diarrhea virus (BVDV),a member of the Pestivirus genus of the Flaviviridae family. The virus persists in the cattle population by a unique combination of transient and persistent infections. Persistently infected (PI)animals may succumb to mucosal disease, which is characterized by lesions in the gastrointestinal tract and its invariably lethal outcome. This study was focused on identification PI animals in cattle farms of Kharkov region, Ukraine. For this reason 1080 blood samples from three different farms were tested for presence BVDV specific antibody by ELISA and viral genetic materials by realtime RT-PCR. In this study 5 PI animals were detected in two farms. Following phylogenetic analysis in 5&#x2019;-UTR (245 bp fragment) was used for the genetic typing of revealed BVDV isolates into subgenotypes. The genetic typing indicated that all 4 viruses from second farm were typed as BVDV-1b and all of them were absolutely identical in 5&#x2019;-UTR. The virus from third farm typed as BVDV-1f.</description><identifier>https://zenodo.org/record/6523916</identifier><identifier>10.5281/zenodo.6523916</identifier><identifier>oai:zenodo.org:6523916</identifier><relation>doi:10.5281/zenodo.6523915</relation><rights>info:eu-repo/semantics/openAccess</rights><rights>https://creativecommons.org/licenses/by/4.0/legalcode</rights><source>Contemporary Agriculture (2013) 62(1-2) 46-52</source><subject>bovine viral diarrhea</subject><subject>real-time RT-PCR</subject><subject>ELISA</subject><subject>genotyping</subject><subject>phylogenetic analysis</subject><subject>cattle</subject><title>EPIDEMIOLOGICAL ANALYSIS OF BVDV INFECTION IN CATTLE FARMS OF KHARKOV REGION, UKRAINE</title><type>Journal:Article</type><type>Journal:Article</type><recordID>6523916</recordID></dc>
format Journal:Article
Journal
Journal:Journal
author ANTON GERILOVYCH
BORYS STEGNIY
STEFAN VILCEK
ERNST PETERHANS
ROMAN KUCHERYAVENKO
IRYNA GORAICHUK
VITALIY BOLOTIN
OLEKSIY SOLODIANKIN
ALEKSANDAR POTKONJAK
title EPIDEMIOLOGICAL ANALYSIS OF BVDV INFECTION IN CATTLE FARMS OF KHARKOV REGION, UKRAINE
publishDate 2013
topic bovine viral diarrhea
real-time RT-PCR
ELISA
genotyping
phylogenetic analysis
cattle
url https://zenodo.org/record/6523916
contents Bovine viral diarrhea is a widespread infection of cattle caused by bovine viral diarrhea virus (BVDV),a member of the Pestivirus genus of the Flaviviridae family. The virus persists in the cattle population by a unique combination of transient and persistent infections. Persistently infected (PI)animals may succumb to mucosal disease, which is characterized by lesions in the gastrointestinal tract and its invariably lethal outcome. This study was focused on identification PI animals in cattle farms of Kharkov region, Ukraine. For this reason 1080 blood samples from three different farms were tested for presence BVDV specific antibody by ELISA and viral genetic materials by realtime RT-PCR. In this study 5 PI animals were detected in two farms. Following phylogenetic analysis in 5’-UTR (245 bp fragment) was used for the genetic typing of revealed BVDV isolates into subgenotypes. The genetic typing indicated that all 4 viruses from second farm were typed as BVDV-1b and all of them were absolutely identical in 5’-UTR. The virus from third farm typed as BVDV-1f.
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