Document Detail


Neutrophils are needed for an effective immune response against pulmonary rat coronavirus infection, but also contribute to pathology.
MedLine Citation:
PMID:  24323639     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Polymorphonuclear neutrophils (PMN) infiltrate the respiratory tract early after viral infection and can contribute to both host defence and pathology. Coronaviruses are important causes of respiratory tract infections, ranging from mild to severe depending on the viral strain. This study evaluated the role of PMN during a non-fatal pulmonary coronavirus infection in the natural host. Rat coronavirus (RCoV) causes respiratory disease in adult rats, characterized by an early PMN response, viral replication and inflammatory lesions in the lungs, mild weight loss and effective resolution of infection. To determine their role during RCoV infection, PMN were depleted and the effects on disease progression, viral replication, inflammatory response and lung pathology were analysed. Compared with RCoV infection in control animals, PMN-depleted rats had worsened disease with weight loss, clinical signs, mortality and prolonged pulmonary viral replication. PMN-depleted animals had fewer macrophages and lymphocytes in the respiratory tract, corresponding to lower chemokine levels. Combined with in vitro experiments showing that PMN express cytokines and chemokines in response to RCoV-infected alveolar epithelial cells, these findings support a role for PMN in eliciting an inflammatory response to RCoV infection. Despite their critical role in the protection from severe disease, the presence of PMN was correlated with haemorrhagic lesions, epithelial barrier permeability and cellular inflammation in the lungs. This study demonstrated that while PMN are required for an effective antiviral response, they also contribute to lung pathology during RCoV infection.
Authors:
Anoria K Haick; Joanna P Rzepka; Elizabeth Brandon; Onesmo B Balemba; Tanya A Miura
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural     Date:  2013-12-09
Journal Detail:
Title:  The Journal of general virology     Volume:  95     ISSN:  1465-2099     ISO Abbreviation:  J. Gen. Virol.     Publication Date:  2014 Mar 
Date Detail:
Created Date:  2014-02-19     Completed Date:  2014-05-02     Revised Date:  2014-07-16    
Medline Journal Info:
Nlm Unique ID:  0077340     Medline TA:  J Gen Virol     Country:  England    
Other Details:
Languages:  eng     Pagination:  578-90     Citation Subset:  IM    
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MeSH Terms
Descriptor/Qualifier:
Animals
Coronavirus Infections / immunology,  pathology,  veterinary*,  virology
Coronavirus, Rat / immunology*,  physiology
Cytokines / immunology
Male
Neutrophils / immunology*
Pulmonary Alveoli / immunology*,  pathology,  virology
Rats
Rats, Inbred F344
Rodent Diseases / immunology*,  pathology,  virology
Grant Support
ID/Acronym/Agency:
P20 RR015587/RR/NCRR NIH HHS; P20 RR016454/RR/NCRR NIH HHS; U54 AI081680/AI/NIAID NIH HHS
Chemical
Reg. No./Substance:
0/Cytokines

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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