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SARS-CoV replicates in primary human alveolar type II cell cultures but not in type I-like cells.

Identifieur interne : 003032 ( Main/Exploration ); précédent : 003031; suivant : 003033

SARS-CoV replicates in primary human alveolar type II cell cultures but not in type I-like cells.

Auteurs : Eric C. Mossel [États-Unis] ; Jieru Wang ; Scott Jeffers ; Karen E. Edeen ; Shuanglin Wang ; Gregory P. Cosgrove ; C Joel Funk ; Rizwan Manzer ; Tanya A. Miura ; Leonard D. Pearson ; Kathryn V. Holmes ; Robert J. Mason

Source :

RBID : pubmed:18022664

Descripteurs français

English descriptors

Abstract

Severe acute respiratory syndrome (SARS) is a disease characterized by diffuse alveolar damage. We isolated human alveolar type II cells and maintained them in a highly differentiated state. Type II cell cultures supported SARS-CoV replication as evidenced by RT-PCR detection of viral subgenomic RNA and an increase in virus titer. Virus titers were maximal by 24 h and peaked at approximately 10(5) pfu/mL. Two cell types within the cultures were infected. One cell type was type II cells, which were positive for SP-A, SP-C, cytokeratin, a type II cell-specific monoclonal antibody, and Ep-CAM. The other cell type was composed of spindle-shaped cells that were positive for vimentin and collagen III and likely fibroblasts. Viral replication was not detected in type I-like cells or macrophages. Hence, differentiated adult human alveolar type II cells were infectible but alveolar type I-like cells and alveolar macrophages did not support productive infection.

DOI: 10.1016/j.virol.2007.09.045
PubMed: 18022664


Affiliations:


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<term>Epithelium (virology)</term>
<term>Humans</term>
<term>Pulmonary Alveoli (cytology)</term>
<term>Pulmonary Alveoli (virology)</term>
<term>RNA, Viral (analysis)</term>
<term>Reverse Transcriptase Polymerase Chain Reaction</term>
<term>SARS Virus (genetics)</term>
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<term>Différenciation cellulaire</term>
<term>Effet cytopathogène viral</term>
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<div type="abstract" xml:lang="en">Severe acute respiratory syndrome (SARS) is a disease characterized by diffuse alveolar damage. We isolated human alveolar type II cells and maintained them in a highly differentiated state. Type II cell cultures supported SARS-CoV replication as evidenced by RT-PCR detection of viral subgenomic RNA and an increase in virus titer. Virus titers were maximal by 24 h and peaked at approximately 10(5) pfu/mL. Two cell types within the cultures were infected. One cell type was type II cells, which were positive for SP-A, SP-C, cytokeratin, a type II cell-specific monoclonal antibody, and Ep-CAM. The other cell type was composed of spindle-shaped cells that were positive for vimentin and collagen III and likely fibroblasts. Viral replication was not detected in type I-like cells or macrophages. Hence, differentiated adult human alveolar type II cells were infectible but alveolar type I-like cells and alveolar macrophages did not support productive infection.</div>
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