Abstract |
The host range of most poliovirus (PV) strains is restricted to simians. This host range specificity is believed to be determined by the interaction between PV and its receptor molecule. To elucidate the molecular basis of this species-specific infection of PV, we cloned orthologs of the PV receptor (PVR) gene ( pvr) as well as those of PV receptor-related genes 1 and 2 ( prr1 and prr2) from various mammalian species. These three genes are widely present in mammalian genomes including those of non-susceptible species. Comparison of the deduced amino acid sequences of PVR orthologs revealed that the NH(2)-terminal immunoglobulin-like domain (domain 1), which is the virus binding site in the human PVR, is highly variable among species, whereas that of PRR1 is highly conserved. Domain 1 of the PVR orthologs for the ring-tailed lemur and rabbit, which are not susceptible to PV, show only 51 and 61% amino acid sequence identity to that of human PVR, respectively. Chimeric PVR proteins that have the domain 1 of the ring-tailed lemur and rabbit PVRs failed to serve as receptors for PV. These results suggest that rapid changes in the domain 1 sequence during mammalian evolution determined the host range restriction of PV.
|
Authors | M Ida-Hosonuma, Y Sasaki, H Toyoda, A Nomoto, O Gotoh, H Yonekawa, S Koike |
Journal | Archives of virology
(Arch Virol)
Vol. 148
Issue 1
Pg. 29-44
(Jan 2003)
ISSN: 0304-8608 [Print] Austria |
PMID | 12536294
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
|
Chemical References |
- Membrane Proteins
- Receptors, Virus
- poliovirus receptor
|
Topics |
- Amino Acid Sequence
- Animals
- Base Sequence
- Biological Evolution
- Callithrix
- Cebus
- Chlorocebus aethiops
- Hominidae
- Lemur
- Membrane Proteins
- Molecular Sequence Data
- Phylogeny
- Poliovirus
(chemistry)
- Receptors, Virus
(genetics)
- Saimiri
- Sequence Homology, Amino Acid
- Species Specificity
|