Neuropathogenesis of a mouse-adapted porcine epidemic diarrhea virus infection in suckling mice
A mouse-adapted porcine epidemic diarrhea virus, MK-p10, showed higher neurovirulence in suckling mice than a non-adapted MK strain. There was no difference in virus growth, whereas clear differences between these two virus infections existed in the type of target cells infected, the spread of virus...
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Published in | Journal of general virology Vol. 94; no. 4; pp. 831 - 836 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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England
01.04.2013
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Abstract | A mouse-adapted porcine epidemic diarrhea virus, MK-p10, showed higher neurovirulence in suckling mice than a non-adapted MK strain. There was no difference in virus growth, whereas clear differences between these two virus infections existed in the type of target cells infected, the spread of virus and the cytokine levels produced in the brain. In the early phase of infection, neurons, astrocytes and neural progenitor cells were infected by MK-p10, whereas neural progenitor cells were the only target cells infected by MK. On days 4–5 post-inoculation, MK-p10 antigens were distributed in a number of neurons in a wide area of the brain; however, antigens were restricted in MK infection. In moribund mice in both infection groups, viral antigens were found in a wide area of the brain. The wide spectrum of initial target cells following MK-p10 infection, as well as its faster spread in the brain, may be evidence of enhanced virulence in suckling mice. |
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AbstractList | A mouse-adapted porcine epidemic diarrhea virus, MK-p10, showed higher neurovirulence in suckling mice than a non-adapted MK strain. There was no difference in virus growth, whereas clear differences between these two virus infections existed in the type of target cells infected, the spread of virus and the cytokine levels produced in the brain. In the early phase of infection, neurons, astrocytes and neural progenitor cells were infected by MK-p10, whereas neural progenitor cells were the only target cells infected by MK. On days 4–5 post-inoculation, MK-p10 antigens were distributed in a number of neurons in a wide area of the brain; however, antigens were restricted in MK infection. In moribund mice in both infection groups, viral antigens were found in a wide area of the brain. The wide spectrum of initial target cells following MK-p10 infection, as well as its faster spread in the brain, may be evidence of enhanced virulence in suckling mice. A mouse-adapted porcine epidemic diarrhea virus, MK-p10, showed higher neurovirulence in suckling mice than a non-adapted MK strain. There was no difference in virus growth, whereas clear differences between these two virus infections existed in the type of target cells infected, the spread of virus and the cytokine levels produced in the brain. In the early phase of infection, neurons, astrocytes and neural progenitor cells were infected by MK-p10, whereas neural progenitor cells were the only target cells infected by MK. On days 4-5 post-inoculation, MK-p10 antigens were distributed in a number of neurons in a wide area of the brain; however, antigens were restricted in MK infection. In moribund mice in both infection groups, viral antigens were found in a wide area of the brain. The wide spectrum of initial target cells following MK-p10 infection, as well as its faster spread in the brain, may be evidence of enhanced virulence in suckling mice.A mouse-adapted porcine epidemic diarrhea virus, MK-p10, showed higher neurovirulence in suckling mice than a non-adapted MK strain. There was no difference in virus growth, whereas clear differences between these two virus infections existed in the type of target cells infected, the spread of virus and the cytokine levels produced in the brain. In the early phase of infection, neurons, astrocytes and neural progenitor cells were infected by MK-p10, whereas neural progenitor cells were the only target cells infected by MK. On days 4-5 post-inoculation, MK-p10 antigens were distributed in a number of neurons in a wide area of the brain; however, antigens were restricted in MK infection. In moribund mice in both infection groups, viral antigens were found in a wide area of the brain. The wide spectrum of initial target cells following MK-p10 infection, as well as its faster spread in the brain, may be evidence of enhanced virulence in suckling mice. |
Author | Ikeda, Hidetoshi Kotani, Osamu Nagata, Noriyo Taguchi, Fumihiro Shirato, Kazuya Takahashi, Kimimasa |
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Cites_doi | 10.1016/0166-2236(96)10049-7 10.1016/0166-2236(90)90107-L 10.1292/jvms.54.313 10.1371/journal.ppat.0030005 10.1016/j.virol.2005.11.044 10.1128/JVI.74.19.8913-8921.2000 10.1523/JNEUROSCI.23-21-07922.2003 10.1006/viro.2002.1551 10.1016/S0042-6822(03)00323-4 10.1002/jmv.1890060309 10.1007/s00705-010-0790-1 10.1007/978-1-4615-1899-0_19 10.1128/JVI.00432-06 10.1128/JVI.79.18.11892-11900.2005 10.1016/j.virusres.2011.07.019 10.2460/ajvr.1981.42.12.2036 10.1016/j.virol.2003.09.023 10.1128/JVI.00464-11 10.1007/BF01317606 |
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SubjectTerms | Animals Animals, Newborn Astrocytes - virology Brain - pathology Brain - virology Mice Nervous System Diseases - pathology Nervous System Diseases - virology Neural Stem Cells - virology Neurons - virology Porcine epidemic diarrhea virus - pathogenicity Virulence |
Title | Neuropathogenesis of a mouse-adapted porcine epidemic diarrhea virus infection in suckling mice |
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