Genetic and experimental evidence for cross-species infection by swine hepatitis E virus

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Published inJournal of Virology Vol. 72; no. 12; pp. 9714 - 9721
Main Authors Meng, X.J. (National Institute of Allergy and Infectious Diseases, Bethesda, MD.), Halbur, P.G, Shapiro, M.S, Govindarajan, S, Bruna, J.D, Mushahwar, I.K, Purcell, R.H, Emerson, S.U
Format Journal Article
LanguageEnglish
Published United States American Society for Microbiology 01.12.1998
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ABSTRACT 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.
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.
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 greater than or equal to 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.
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.
Author Govindarajan, S
Shapiro, M.S
Mushahwar, I.K
Bruna, J.D
Emerson, S.U
Purcell, R.H
Halbur, P.G
Meng, X.J. (National Institute of Allergy and Infectious Diseases, Bethesda, MD.)
AuthorAffiliation Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892 1 ; Department of Veterinary Diagnostic and Production Animal Medicine, College of Veterinary Medicine, Iowa State University, Ames, Iowa 50011 2 ; Bioqual, Inc., Rockville, Maryland 20850 3 ; Pathology and Clinical Laboratories, Rancho Los Amigos Medical Center, Downey, California 90242 4 ; and Viral Discovery Group, Abbott Laboratories, North Chicago, Illinois 60064 5
AuthorAffiliation_xml – name: Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892 1 ; Department of Veterinary Diagnostic and Production Animal Medicine, College of Veterinary Medicine, Iowa State University, Ames, Iowa 50011 2 ; Bioqual, Inc., Rockville, Maryland 20850 3 ; Pathology and Clinical Laboratories, Rancho Los Amigos Medical Center, Downey, California 90242 4 ; and Viral Discovery Group, Abbott Laboratories, North Chicago, Illinois 60064 5
Author_xml – sequence: 1
  fullname: Meng, X.J. (National Institute of Allergy and Infectious Diseases, Bethesda, MD.)
– sequence: 2
  fullname: Halbur, P.G
– sequence: 3
  fullname: Shapiro, M.S
– sequence: 4
  fullname: Govindarajan, S
– sequence: 5
  fullname: Bruna, J.D
– sequence: 6
  fullname: Mushahwar, I.K
– sequence: 7
  fullname: Purcell, R.H
– sequence: 8
  fullname: Emerson, S.U
BackLink https://www.ncbi.nlm.nih.gov/pubmed/9811705$$D View this record in MEDLINE/PubMed
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Corresponding author. Mailing address: Laboratory of Infectious Diseases, NIAID, National Institutes of Health, Bldg. 7, Rm. 206, 7 Center Dr. MSC 0740, Bethesda, MD 20892-0740. Phone: (301) 496-6227. Fax: (301) 402-0524. E-mail: xjmeng@atlas.niaid.nih.gov.
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Snippet Article Usage Stats Services JVI Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley...
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...
ABSTRACT 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...
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SourceType Open Access Repository
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StartPage 9714
SubjectTerms Animals
Base Sequence
CERDO
DNA Primers - genetics
EXPERIMENTACION IN VIVO
EXPERIMENTAL INFECTION
EXPERIMENTATION IN VIVO
GENBANK/AF082843
GENOMAS
GENOME
Genome, Viral
GENOMES
Genotype
Hepatitis E - veterinary
Hepatitis E - virology
Hepatitis E virus
Hepatitis E virus - genetics
Hepatitis E virus - isolation & purification
Hepatitis E virus - pathogenicity
Hepatitis, Viral, Animal - virology
Humans
IN VIVO EXPERIMENTATION
INFECCION EXPERIMENTAL
INFECTION EXPERIMENTALE
MACACA MULATTA
MOLECULAR SEQUENCE DATA
MONKEYS
MONO
NUCLEOTIDE SEQUENCE
Open Reading Frames
PHYLOGENETICS
PORCIN
SECUENCIA NUCLEOTIDICA
Sequence Homology, Nucleic Acid
SEQUENCE NUCLEOTIDIQUE
SINGE
Species Specificity
SWINE
Swine - virology
Swine Diseases - virology
United States
Viral Pathogenesis and Immunity
Virulence - genetics
Zoonoses - transmission
Zoonoses - virology
Title Genetic and experimental evidence for cross-species infection by swine hepatitis E virus
URI http://jvi.asm.org/content/72/12/9714.abstract
https://www.ncbi.nlm.nih.gov/pubmed/9811705
https://search.proquest.com/docview/17140806
https://search.proquest.com/docview/70052320
https://pubmed.ncbi.nlm.nih.gov/PMC110481
Volume 72
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