Differential virological and immunological outcome of severe acute respiratory syndrome coronavirus infection in susceptible and resistant transgenic mice expressing human angiotensin-converting enzyme 2

We previously reported that transgenic (Tg) mice expressing human angiotensin-converting enzyme 2 (hACE2), the receptor for severe acute respiratory syndrome coronavirus (SARS-CoV), were highly susceptible to SARS-CoV infection, which resulted in the development of disease of various severity and ev...

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Veröffentlicht in:Journal of virology Jg. 83; H. 11; S. 5451
Hauptverfasser: Yoshikawa, Naoko, Yoshikawa, Tomoki, Hill, Terence, Huang, Cheng, Watts, Douglas M, Makino, Shinji, Milligan, Gregg, Chan, Tehsheng, Peters, Clarence J, Tseng, Chien-Te K
Format: Journal Article
Sprache:Englisch
Veröffentlicht: United States 01.06.2009
Schlagworte:
Angiotensin-Converting Enzyme 2
Animals
Brain Diseases - virology
Cell Proliferation - drug effects
Concanavalin A - pharmacology
Cytokines - immunology
Gene Expression Regulation, Enzymologic
Genetic Predisposition to Disease - genetics
Humans
Kinetics
Lung Diseases - virology
Lymphocytes - cytology
Lymphocytes - drug effects
Lymphocytes - immunology
Mice
Mice, Transgenic
Organ Specificity
Peptidyl-Dipeptidase A - genetics
Peptidyl-Dipeptidase A - metabolism
Severe Acute Respiratory Syndrome - immunology
Severe Acute Respiratory Syndrome - metabolism
Severe Acute Respiratory Syndrome - pathology
Severe Acute Respiratory Syndrome - virology
Severe acute respiratory syndrome-related coronavirus - immunology
Spleen - cytology
Spleen - drug effects
Spleen - immunology
Virus Replication
ISSN:1098-5514, 1098-5514
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Zusammenfassung:We previously reported that transgenic (Tg) mice expressing human angiotensin-converting enzyme 2 (hACE2), the receptor for severe acute respiratory syndrome coronavirus (SARS-CoV), were highly susceptible to SARS-CoV infection, which resulted in the development of disease of various severity and even death in some lineages. In this study, we further characterized and compared the pathogeneses of SARS-CoV infection in two of the most stable Tg lineages, AC70 and AC22, representing those susceptible and resistant to the lethal SARS-CoV infection, respectively. The kinetics of virus replication and the inflammatory responses within the lungs and brains, as well as the clinical and pathological outcomes, were assessed in each lineage. In addition, we generated information on lymphocyte subsets and mitogen-mediated proliferation of splenocytes. We found that while both lineages were permissive to SARS-CoV infection, causing elevated secretion of many inflammatory mediators within the lungs and brains, viral infection appeared to be more intense in AC70 than in AC22 mice, especially in the brain. Moreover, such infection was accompanied by a more profound immune suppression in the former, as evidenced by the extensive loss of T cells, compromised responses to concanavalin A stimulation, and absence of inflammatory infiltrates within the brain. We also found that CD8(+) T cells were partially effective in attenuating the pathogenesis of SARS-CoV infection in lethality-resistant AC22 mice. Collectively, our data revealed a more intense viral infection and immunosuppression in AC70 mice than in AC22 mice, thereby providing us with an immunopathogenic basis for the fatal outcome of SARS-CoV infection in the AC70 mice.
Bibliographie:ObjectType-Article-1
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ISSN:1098-5514
1098-5514
DOI:10.1128/JVI.02272-08