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Mouse Hepatitis Virus Receptor as a Determinant of the Mouse Susceptibility to MHV Infection
In this review, we report that the receptor of mouse hepatitis virus (MHV), carcinoembryonic antigen-related cell adhesion molecule 1 (CEACAM1), is an important determinant of mouse susceptibility to MHV infection. This finding was revealed by using mouse strains with two different allelic forms of...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Research Foundation
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3285771/ https://www.ncbi.nlm.nih.gov/pubmed/22375141 http://dx.doi.org/10.3389/fmicb.2012.00068 |
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author | Taguchi, Fumihiro Hirai-Yuki, Asuka |
author_facet | Taguchi, Fumihiro Hirai-Yuki, Asuka |
author_sort | Taguchi, Fumihiro |
collection | PubMed |
description | In this review, we report that the receptor of mouse hepatitis virus (MHV), carcinoembryonic antigen-related cell adhesion molecule 1 (CEACAM1), is an important determinant of mouse susceptibility to MHV infection. This finding was revealed by using mouse strains with two different allelic forms of the MHV receptor, Ceacam1a and Ceacam1b. Although previous studies indicated that susceptibility is determined by a single gene, Ceacam1, our recent work in gene-replaced mice with chimeric Ceacam1 pointed toward the involvement of other host factors (genes) in the susceptibility. Studies on mouse susceptibility to MHV, as well as the factors involved in their susceptibility, are overviewed. |
format | Online Article Text |
id | pubmed-3285771 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Frontiers Research Foundation |
record_format | MEDLINE/PubMed |
spelling | pubmed-32857712012-02-28 Mouse Hepatitis Virus Receptor as a Determinant of the Mouse Susceptibility to MHV Infection Taguchi, Fumihiro Hirai-Yuki, Asuka Front Microbiol Microbiology In this review, we report that the receptor of mouse hepatitis virus (MHV), carcinoembryonic antigen-related cell adhesion molecule 1 (CEACAM1), is an important determinant of mouse susceptibility to MHV infection. This finding was revealed by using mouse strains with two different allelic forms of the MHV receptor, Ceacam1a and Ceacam1b. Although previous studies indicated that susceptibility is determined by a single gene, Ceacam1, our recent work in gene-replaced mice with chimeric Ceacam1 pointed toward the involvement of other host factors (genes) in the susceptibility. Studies on mouse susceptibility to MHV, as well as the factors involved in their susceptibility, are overviewed. Frontiers Research Foundation 2012-02-24 /pmc/articles/PMC3285771/ /pubmed/22375141 http://dx.doi.org/10.3389/fmicb.2012.00068 Text en Copyright © 2012 Taguchi and Hirai-Yuki. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited. |
spellingShingle | Microbiology Taguchi, Fumihiro Hirai-Yuki, Asuka Mouse Hepatitis Virus Receptor as a Determinant of the Mouse Susceptibility to MHV Infection |
title | Mouse Hepatitis Virus Receptor as a Determinant of the Mouse Susceptibility to MHV Infection |
title_full | Mouse Hepatitis Virus Receptor as a Determinant of the Mouse Susceptibility to MHV Infection |
title_fullStr | Mouse Hepatitis Virus Receptor as a Determinant of the Mouse Susceptibility to MHV Infection |
title_full_unstemmed | Mouse Hepatitis Virus Receptor as a Determinant of the Mouse Susceptibility to MHV Infection |
title_short | Mouse Hepatitis Virus Receptor as a Determinant of the Mouse Susceptibility to MHV Infection |
title_sort | mouse hepatitis virus receptor as a determinant of the mouse susceptibility to mhv infection |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3285771/ https://www.ncbi.nlm.nih.gov/pubmed/22375141 http://dx.doi.org/10.3389/fmicb.2012.00068 |
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