Rotaviruses are important pathogens associated with diarrhoeal diseases in almost all
species of mammals. In the present study, a nested reverse transcriptase‐polymerase chain …

A polymerase chain reaction (PCR) protocol has been developed for identification of bovine
group A rotavirus infection in feces. Primers (20mers) complementary to 3′ ends of double …

Monoclonal antibodies to group A rotavirus Vp6 protein were prepared and used for
verification of three blocking enzyme‐linked immunosorbent assay (ELISA) modifications to …

VP6 protein antigens allow classification of rotaviruses into at least four subgroups,
depending on the presence or absence of SG-specific epitopes: SG I, SG II, SG (I+ II), and …

Fecal samples from rotavirus-infected piglets were characterized by a serotyping enzyme-
linked immunosorbent assay (ELISA) by using monoclonal antibodies (MAbs) specific to …

We adapted the polymerase chain reaction (PCR) to detect the noncultivatable group B and
C rotaviruses and introduced a simple and convenient technique to purify viral RNA from …

The use of the polymerase chain reaction (PCR) for identifying serotypes of human and
bovine rotaviruses was examined. In the identification of 115 human rotavirus samples in …

Feces and serum specimens were collected from three farms in Michigan on which∼ 50-lb
(8-to 9-week-old) pigs experienced diarrhea just after placement into all-in-all-out finishing …

Group A rotaviruses (RVA) are a major cause of acute infantile gastroenteritis. The viral
genome comprises 11 double‐stranded RNA segments and the respective gene segments …

A pair of primers designed from the sequence of genome segment 9 of group B rat rotavirus
(IDIR) were employed to amplify genome segment 9 of a group B bovine rotavirus in a …