ABSTRACT
Clinical signs of a winter dysentery-like syndrome in 6- to 9-month-old cattle in 3 feedlots included acute onset of diarrhea with high morbidity and low mortality, respiratory tract problems that included dyspnea, coughing, and nasal discharge, and high rectal temperatures. Bovine coronavirus was detected by use of an ELISA and immune electron microscopy in fecal and nasal swab samples and by immunohistochemical analysis of intestinal sections collected from calves during necropsy. Bovine coronavirus should be considered in the differential diagnoses for diseases that cause acute onset of bloody diarrhea in feedlot cattle.
Subject(s)
Cattle Diseases/virology , Coronavirus Infections/veterinary , Coronavirus, Bovine/isolation & purification , Dysentery/veterinary , Feces/virology , Animals , Antigens, Viral/analysis , Cattle , Cattle Diseases/diagnosis , Cattle Diseases/epidemiology , Cells, Cultured , Coronavirus Infections/diagnosis , Coronavirus Infections/virology , Coronavirus, Bovine/immunology , Coronavirus, Bovine/ultrastructure , Diagnosis, Differential , Disease Outbreaks/veterinary , Dysentery/diagnosis , Dysentery/virology , Enzyme-Linked Immunosorbent Assay/veterinary , Female , Intestine, Large/pathology , Intestine, Large/virology , Lung/virology , Lymph Nodes/virology , Male , Microscopy, Immunoelectron/veterinary , Rectal Neoplasms , Respiratory Tract Infections/diagnosis , Respiratory Tract Infections/veterinary , Respiratory Tract Infections/virology , Tumor Cells, CulturedABSTRACT
Prior to the recent discovery of the swine hepatitis E virus (swine HEV) in pigs from the midwestern United States, HEV was not considered endemic to this country. Since swine HEV is antigenically and genetically related to human strains of HEV, it was important to characterize this new virus further. The infectivity titer of a pool of swine HEV in pigs was determined in order to prepare a standardized reagent and to evaluate the dose response in pigs. Although the sequence of swine HEV varied extensively from those of most human strains of HEV, it was very closely related to the two strains of human HEV (US-1 and US-2) isolated in the United States. The U.S. strains which were recently recovered from two patients with clinical hepatitis E in the United States shared >/=97% amino acid identity with swine HEV in open reading frames 1 and 2. Phylogenetic analyses of different regions of the genome revealed that swine HEV and the U.S. strains grouped together and formed a distinct branch. These results suggested that swine HEV may infect humans. When we inoculated rhesus monkeys and a chimpanzee, experimental surrogates of humans, with swine HEV, the primates became infected. Furthermore, in a reciprocal experiment, specific-pathogen-free pigs were experimentally infected with the US-2 strain of human HEV that is genetically similar to swine HEV. These results provided experimental evidence for cross-species infection by the swine virus. Thus, humans appear to be at risk of infection with swine HEV or closely related viruses.
Subject(s)
Hepatitis E virus/genetics , Hepatitis E virus/pathogenicity , Swine/virology , Animals , Base Sequence , DNA Primers/genetics , Genome, Viral , Genotype , Hepatitis E/veterinary , Hepatitis E/virology , Hepatitis E virus/isolation & purification , Hepatitis, Viral, Animal/virology , Humans , Macaca mulatta , Molecular Sequence Data , Open Reading Frames , Sequence Homology, Nucleic Acid , Species Specificity , Swine Diseases/virology , United States , Virulence/genetics , Zoonoses/transmission , Zoonoses/virologyABSTRACT
A novel virus of pigs, swine hepatitis E virus (swine HEV), was recently identified and shown to be antigenically and genetically related to human HEV. In the present study, we attempted to infect specific-pathogen-free (SPF) pigs experimentally with swine HEV or with human strains of HEV. Serum samples collected from naturally infected pigs were used as the source of swine HEV. Pigs inoculated intravenously with serum samples containing swine HEV seroconverted to anti-HEV 4 to 8 weeks postinoculation, and the virus spread to an uninoculated pig. Swine HEV was detected in nasal and rectal swab materials as early as 2 weeks postinoculation and for 4 to 8 weeks thereafter. Viremia appeared 4 to 6 weeks postinoculation and lasted 1 to 3 weeks. The inoculated pigs appeared clinically normal and serum liver enzymes were not significantly elevated. In contrast, pigs were not infected when inoculated intravenously with about 10(5) monkey infectious doses of one of two human strains of HEV (Sar-55 or Mex-14).
