Bovine viral diarrhea virus genomic associations in mucosal disease, enteritis and generalized dermatitis outbreaks in Argentina

被引:28
|
作者
Odeón, AC
Risatti, G
Kaiser, GG
Leunda, MR
Odriozola, E
Campero, CM
Donis, RO
机构
[1] EEA Balcarce, Inst Nacl Tecnol Agropecuaria, RA-7620 Buenos Aires, DF, Argentina
[2] Univ Nebraska, Dept Vet & Biomed Sci, Lincoln, NE 68583 USA
关键词
cattle; viruses; enteritis; dermatitis; bovine viral diarrhea virus; genotyping; pathology; Argentina;
D O I
10.1016/S0378-1135(03)00210-4
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The objective of the present work is the description outbreaks caused by bovine viral diarrhea virus (BVDV) in commercial beef cattle ranches in Argentina. Genetic affiliation and their association with the clinical manifestation were carried out with five BVDV isolates from an outbreak of mucosal disease (MD) (Outbreak #1), acute enteritis (Outbreaks #2 and #3) and generalized dermatitis (Outbreaks #4 and #5). Upon genetic analysis CP BVDV isolate of Outbreak #1 clustered to closely to BVDV Oregon (Genotype 1). BVDV isolates from the outbreaks of generalized dermatitis (Outbreaks #4 and #5) were located close to BVDV Osloss within Genotype 1. The identification by immunohistochemistry of BVDV in exudative dermatitis indicates the epithelial cell tropism of the virus. Phylogenic characterization of BVDV from Outbreaks #2 and #3 locate them as BVDV-2. 5'UTR sequence of these viruses revealed a homology of 88 and 90% to BVDV-890 (Genotype 2) and a 77 and 75% to BVDV-SDI (Genotype 1), respectively. The association of BVDV-2 with severe disease indicates the presence of highly virulent strains. Data from natural outbreaks where BVDV-1 and BVDV-2 were isolated revealed that pathology overlaps and not clearly allows the differentiation between genotypes based on gross or microscopic lesions. Thus, for a definitive diagnosis, further virology and molecular studies are necessary. Additionally, the results of this work focused on the origin and consequences of genetic variations of BVDV with regard to pathogenesis and suggest the association between genotype and a defined clinical syndrome. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:133 / 144
页数:12
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