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1.
Res Vet Sci ; 95(2): 799-801, 2013 Oct.
Article in English | MEDLINE | ID: mdl-23648077

ABSTRACT

Bovine torovirus (BToV) is an established enteric pathogen of cattle, but its occurrence in Brazilian cattle had not been reported until now. This article describes a survey on BToV in Brazil carried out on 80 fecal samples from diarrheic young and adult cattle, using a nested-RT-PCR targeting the nucleocapsid (N) gene. BToV was detected in 6.25% (5/80) of stool samples from three different geographic regions. Sequences analysis showed that Brazilian BToVs have a high degree of identity with European and Japanese BToVs and a lower degree of identity with North American Breda 1 strain. These results show that, albeit its low frequency and the scarce number of research on the field, BToV is still present amongst cattle populations.


Subject(s)
Genetic Variation , Torovirus Infections/veterinary , Torovirus/classification , Animals , Brazil/epidemiology , Cattle , Europe/epidemiology , Japan/epidemiology , Phylogeny , Torovirus/genetics , Torovirus Infections/epidemiology , Torovirus Infections/virology
2.
Infect Genet Evol ; 12(8): 1870-8, 2012 Dec.
Article in English | MEDLINE | ID: mdl-22634277

ABSTRACT

Bovine coronavirus has been associated with diarrhoea in newborn calves, winter dysentery in adult cattle and respiratory tract infections in calves and feedlot cattle. In Cuba, the presence of BCoV was first reported in 2006. Since then, sporadic outbreaks have continued to occur. This study was aimed at deepening the knowledge of the evolution, molecular markers of virulence and epidemiology of BCoV in Cuba. A total of 30 samples collected between 2009 and 2011 were used for PCR amplification and direct sequencing of partial or full S gene. Sequence comparison and phylogenetic studies were conducted using partial or complete S gene sequences as phylogenetic markers. All Cuban bovine coronavirus sequences were located in a single cluster supported by 100% bootstrap and 1.00 posterior probability values. The Cuban bovine coronavirus sequences were also clustered with the USA BCoV strains corresponding to the GenBank accession numbers EF424621 and EF424623, suggesting a common origin for these viruses. This phylogenetic cluster was also the only group of sequences in which no recombination events were detected. Of the 45 amino acid changes found in the Cuban strains, four were unique.


Subject(s)
Cattle Diseases/virology , Coronavirus Infections/veterinary , Coronavirus Infections/virology , Coronavirus, Bovine/classification , Coronavirus, Bovine/genetics , Membrane Glycoproteins/genetics , Viral Envelope Proteins/genetics , Amino Acid Sequence , Animals , Cattle , Cluster Analysis , Coronavirus, Bovine/isolation & purification , Dysentery/veterinary , Dysentery/virology , Evolution, Molecular , Feces/virology , Molecular Sequence Data , Phylogeny , Recombination, Genetic , Sequence Alignment , Sequence Analysis, DNA , Spike Glycoprotein, Coronavirus
3.
J Virol Methods ; 169(2): 375-9, 2010 Nov.
Article in English | MEDLINE | ID: mdl-20723564

ABSTRACT

Neonatal calf diarrhea is a multi-etiology syndrome of cattle and direct detection of the two major agents of the syndrome, group A rotavirus and Bovine coronavirus (BCoV) is hampered by their fastidious growth in cell culture. This study aimed at developing a multiplex semi-nested RT-PCR for simultaneous detection of BCoV (N gene) and group A rotavirus (VP1 gene) with the addition of an internal control (mRNA ND5). The assay was tested in 75 bovine feces samples tested previously for rotavirus using PAGE and for BCoV using nested RT-PCR targeted to RdRp gene. Agreement with reference tests was optimal for BCoV (kappa=0.833) and substantial for rotavirus detection (kappa=0.648). the internal control, ND5 mRNA, was detected successfully in all reactions. Results demonstrated that this multiplex semi-nested RT-PCR was effective in the detection of BCoV and rotavirus, with high sensitivity and specificity for simultaneous detection of both viruses at a lower cost, providing an important tool for studies on the etiology of diarrhea in cattle.


Subject(s)
Cattle Diseases/diagnosis , Coronavirus Infections/veterinary , Coronavirus, Bovine/isolation & purification , Reference Standards , Reverse Transcriptase Polymerase Chain Reaction/methods , Rotavirus Infections/veterinary , Rotavirus/isolation & purification , Animals , Cattle , Cattle Diseases/virology , Coronavirus Infections/diagnosis , Coronavirus Infections/virology , Feces/virology , Molecular Sequence Data , Polymerase Chain Reaction/methods , RNA, Viral/genetics , Reverse Transcriptase Polymerase Chain Reaction/standards , Rotavirus Infections/diagnosis , Rotavirus Infections/virology , Sensitivity and Specificity , Sequence Analysis, DNA
4.
Virology ; 405(2): 352-60, 2010 Sep 30.
Article in English | MEDLINE | ID: mdl-20609456

ABSTRACT

Insectivorous bats are the main reservoirs of rabies virus (RABV) in various regions of the world. The aims of this study were to (a) establish genealogies for RABV strains from different species of Brazilian insectivorous bats based on the nucleoprotein (N) and glycoprotein (G) genes, (b) investigate specific RABV lineages associated with certain genera of bats and (c) identify molecular markers that can distinguish between these lineages. The genealogic analysis of N and G from 57 RABV strains revealed seven genus-specific clusters related to the insectivorous bats Myotis, Eptesicus, Nyctinomops, Molossus, Tadarida, Histiotus and Lasiurus. Molecular markers in the amino acid sequences were identified which were specific to the seven clusters. These results, which constitute a novel finding for this pathogen, show that there are at least seven independent epidemiological rabies cycles maintained by seven genera of insectivorous bats in Brazil.


Subject(s)
Antigens, Viral/genetics , Chiroptera/virology , Glycoproteins/genetics , Molecular Epidemiology , Nucleocapsid Proteins/genetics , Rabies virus/genetics , Rabies/veterinary , Viral Envelope Proteins/genetics , Animals , Brazil/epidemiology , Chiroptera/classification , Genetic Variation , Mice , Polymerase Chain Reaction , Rabies/epidemiology , Rabies/virology , Rabies virus/classification , Sequence Analysis, DNA , Species Specificity
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