Literature detail

Cross-species infections of cultured cells by hepatitis E virus and discovery of an infectious virus-host recombinant.

Priyanka Shukla1 Hanh T Nguyen Udana Torian Ronald E Engle Kristina Faulk Harry R Dalton Richard P Bendall Frances E Keane Robert H Purcell Suzanne U Emerson
Affiliations 1 institutions
  1. Section of Molecular Hepatitis, Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
PMID 21262830 2011 Proc Natl Acad Sci U S A eng ppublish
PubMed DOI Browse context

Article

Publication summary

The RNA virus, hepatitis E virus (HEV) is the most or second-most important cause of acute clinical hepatitis in adults throughout much of Asia, the Middle East, and Africa. In these regions it is an important cause of acute liver failure, especially in pregnant women who have a mortality rate of 20-30%. Until recently, hepatitis E was rarely identified in industrialized countries, but Hepatitis E now is reported increasingly throughout Western Europe, some Eastern European countries, and Japan. Most of these cases are caused by genotype 3, which is endemic in swine, and these cases are thought to be zoonotically acquired. However, transmission routes are not well understood. HEV that infect humans are divided into nonzoonotic (types 1, 2) and zoonotic (types 3, 4) genotypes. HEV cell culture is inefficient and limited, and thus far HEV has been cultured only in human cell lines. The HEV strain Kernow-C1 (genotype 3) isolated from a chronically infected patient was used to identify human, pig, and deer cell lines permissive for infection. Cross-species infections by genotypes 1 and 3 were studied with this set of cultures. Adaptation of the Kernow-C1 strain to growth in human hepatoma cells selected for a rare virus recombinant that contained an insertion of 174 ribonucleotides (58 amino acids) of a human ribosomal protein gene.

Mutagenesis, Insertional Recombination, Genetic Animals Base Sequence Caco-2 Cells Deer Female Genotype Hepatitis E Hepatitis E virus Humans Male Middle Aged Molecular Sequence Data Pregnancy Pregnancy Complications, Infectious Ribosomal Proteins Species Specificity

Structured evidence records

Evidence records

4 total
1 records
Extraction confidence 0.95
Key finding

Hepatitis E virus genotypes 1 and 3 were capable of infecting both pig and deer cells, showing cross-species infectivity among non-human animal cells.

Virus
Location
Not specified
Supporting text

The HEV strain Kernow-C1 (genotype 3) isolated from a chronically infected patient was used to identify human, pig, and deer cell lines permissive for infection. Cross-species infections by genotypes 1 and 3 were studied with this set of cultures.

Method
cell culture infection
Study design
animal experiment
Transmission direction
animal-to-animal
1 records
Extraction confidence 0.95
Key finding

Hepatitis E virus genotypes 1 and 3 demonstrated cross-species infection in human, pig, and deer cell lines, indicating experimental evidence of host-range permissiveness in vitro.

Virus
Location
Not specified
Supporting text

The HEV strain Kernow-C1 (genotype 3) isolated from a chronically infected patient was used to identify human, pig, and deer cell lines permissive for infection. Cross-species infections by genotypes 1 and 3 were studied with this set of cultures.

Method
experimental infection; cell culture infection assay
Experimental system
in vitro cell culture
1 records
Extraction confidence 0.80
Key finding

The hepatitis E virus genotype 3 strain Kernow-C1 adapted to human hepatoma cells by acquiring an insertion derived from a human ribosomal protein gene, indicating molecular adaptation through recombination.

Virus
Host
Not specified
Location
Not specified
Supporting text

Adaptation of the Kernow-C1 strain to growth in human hepatoma cells selected for a rare virus recombinant that contained an insertion of 174 ribonucleotides (58 amino acids) of a human ribosomal protein gene.

Genes or proteins
ribosomal protein gene
Mechanism types
recombination; replication_efficiency
1 records
Extraction confidence 0.90
Key finding

An infectious recombinant hepatitis E virus (Kernow-C1 genotype 3) was generated during adaptation to human hepatoma cells, acquiring a 174-nt insertion from a human ribosomal protein gene.

Virus
Host
Not specified
Location
Not specified
Supporting text

Adaptation of the Kernow-C1 strain to growth in human hepatoma cells selected for a rare virus recombinant that contained an insertion of 174 ribonucleotides (58 amino acids) of a human ribosomal protein gene.

Event type
recombination
Genes or segments
ribosomal protein gene insertion