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Coronavirus MHV-A59 infects the lung and causes severe pneumonia in C57BL/6 mice

Identifieur interne : 001D08 ( Main/Exploration ); précédent : 001D07; suivant : 001D09

Coronavirus MHV-A59 infects the lung and causes severe pneumonia in C57BL/6 mice

Auteurs : Zhangsheng Yang [République populaire de Chine] ; Jun Du [République populaire de Chine] ; Gang Chen [République populaire de Chine] ; Jie Zhao [République populaire de Chine] ; Xuanming Yang [République populaire de Chine] ; Lishan Su [États-Unis] ; Genhong Cheng [États-Unis] ; Hong Tang [République populaire de Chine]

Source :

RBID : PMC:7090691

Descripteurs français

English descriptors

Abstract

It remains challenging to develop animal models of lung infection and severe pneumonia by severe acute respiratory syndrome coronavirus (SARS-CoV) and Middle East respiratory syndrome cornavirus (MERS-CoV) without high level of containment. This inevitably hinders understanding of virushost interaction and development of appropriate countermeasures. Here we report that intranasal inoculation of sublethal doses of murine coronavirus mouse hepatitis virus A-59 (MHV-A59), a hepatic and neuronal tropic coronavirus, can induce acute pneumonia and severe lung injuries in C57BL/6 mice. Inflammatory leukocyte infiltrations, hemorrhages and fibrosis of alveolar walls can be observed 2–11 days after MHV-A59 infection. This pathological manifestation is associated with dramatical elevation of tissue IP-10 and IFN-γ and moderate increase of TNF-α and IL-1β, but inability of anti-viral type I interferon response. These results suggest that intranasal infection of MHV-A59 would serve as a surrogate mouse model of acute respiratory distress syndrome by SARS-CoV and MERS-CoV infections.


Url:
DOI: 10.1007/s12250-014-3530-y
PubMed: 25547683
PubMed Central: 7090691


Affiliations:


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<div type="abstract" xml:lang="en">
<p>It remains challenging to develop animal models of lung infection and severe pneumonia by severe acute respiratory syndrome coronavirus (SARS-CoV) and Middle East respiratory syndrome cornavirus (MERS-CoV) without high level of containment. This inevitably hinders understanding of virushost interaction and development of appropriate countermeasures. Here we report that intranasal inoculation of sublethal doses of murine coronavirus mouse hepatitis virus A-59 (MHV-A59), a hepatic and neuronal tropic coronavirus, can induce acute pneumonia and severe lung injuries in C57BL/6 mice. Inflammatory leukocyte infiltrations, hemorrhages and fibrosis of alveolar walls can be observed 2–11 days after MHV-A59 infection. This pathological manifestation is associated with dramatical elevation of tissue IP-10 and IFN-γ and moderate increase of TNF-α and IL-1β, but inability of anti-viral type I interferon response. These results suggest that intranasal infection of MHV-A59 would serve as a surrogate mouse model of acute respiratory distress syndrome by SARS-CoV and MERS-CoV infections.</p>
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</affiliations>
</record>

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