Bovine viral diarrhea virus subgenotype 1a in a mummified fetus from a Brazilian dairy cattle herd

2021 ◽  
pp. 104063872110220
Author(s):  
Juliana T. T. Fritzen ◽  
Arthur B. Morettin ◽  
Elis Lorenzetti ◽  
Alice F. Alfieri ◽  
Amauri A. Alfieri

We describe the molecular analysis of a wild-type field strain of bovine viral diarrhea virus (BVDV) identified in a mummified fetus from a small Brazilian dairy cattle herd. Nucleic acids extracted from samples of the lung, liver, heart, spleen, and kidney were tested by PCR assays for bovine alphaherpesvirus 1, Neospora caninum, Leptospira spp., Histophilus somni, and Brucella abortus, a nested PCR assay for Mycoplasma bovigenitalium and Ureaplasma diversum, and a RT-PCR assay for BVDV. Amplicons were only obtained in the RT-PCR assay for the partial amplification of the BVDV 5′UTR (288 bp) in kidney and spleen samples and the Npro (438 bp) gene in the kidney sample. Nucleotide sequencing of the amplified products and phylogenetic analyses based on the 2 BVDV genomic regions enabled the BVDV strain to be classified as subgenotype 1a.

2016 ◽  
Vol 229 ◽  
pp. 1-7 ◽  
Author(s):  
Viviana Mari ◽  
Michele Losurdo ◽  
Maria Stella Lucente ◽  
Eleonora Lorusso ◽  
Gabriella Elia ◽  
...  

2016 ◽  
Vol 48 (6) ◽  
pp. 1201-1208 ◽  
Author(s):  
Theerakul Nilnont ◽  
Suneerat Aiumlamai ◽  
Kwankate Kanistanont ◽  
Chaidate Inchaisri ◽  
Jaruwan Kampa

2020 ◽  
Vol 0 (0) ◽  
Author(s):  
Aleksandra Antos ◽  
Jerzy Rola ◽  
Michał Bednarski ◽  
Michał Konrad Krzysiak ◽  
Julia Kęsik-Maliszewska ◽  
...  

AbstractIn this report, we describe the detection of bovine viral diarrhea virus (BVDV) contamination in commercial animal-derived sera and vaccines against animal viral pathogens on the market in Poland. Antibodies against BVDV were detected in 4/45 sera samples (8.9%) using an ELISA test. The presence of BVDV antigen using ELISA was found using ELISA in 3/45 serum samples (6.6%) and 18/172 vaccine samples (10.5%). An RT-PCR was conducted using primers targeting two genome regions, the five prime untranslated region (5’UTR) and N-terminal protease (Npro). BVDV RNA was detected in 33/45 (73.3%) of sera, and 11/172 samples (6.4%) of collected vaccines, of which one vaccine did not declare BVDV strain in its composition. A single serum showed the presence of an infectious virus and only one was contaminated with all 3 species of BVDV. The most frequent species in sera was BVDV-3 (75.5%), whereas in vaccines only BVDV-1 was identified. Sequence analysis showed that the tested commercial sera and one vaccine were contaminated by six genotypes of BVDV: -1a, -1b, -1c, -1d, -2a, and -3. Identification of BVDV and its genetic material in animal-derived products is important due to the possibility of pestivirus transmission as well as the chance of falsifying the results of a diagnostic test. It also demonstrates the necessity of rigorous monitoring of the bioproducts used in the laboratory and industry level.


2011 ◽  
Vol 21 (6) ◽  
pp. 1183-1185
Author(s):  
Mohammad Khalili ◽  
Mohammad Mehdi Molaei ◽  
Ali Asghar Mozaffari ◽  
Fatemeh Dorreh Giraei ◽  
Nasiri-far Ehsan

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