RGD Reference Report - SARS-coronavirus modulation of myocardial ACE2 expression and inflammation in patients with SARS. - Rat Genome Database

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SARS-coronavirus modulation of myocardial ACE2 expression and inflammation in patients with SARS.

Authors: Oudit, G Y  Kassiri, Z  Jiang, C  Liu, P P  Poutanen, S M  Penninger, J M  Butany, J 
Citation: Oudit GY, etal., Eur J Clin Invest. 2009 Jul;39(7):618-25. doi: 10.1111/j.1365-2362.2009.02153.x. Epub 2009 May 6.
RGD ID: 40818405
Pubmed: PMID:19453650   (View Abstract at PubMed)
PMCID: PMC7163766   (View Article at PubMed Central)
DOI: DOI:10.1111/j.1365-2362.2009.02153.x   (Journal Full-text)


BACKGROUND: Angiotensin converting enzyme 2 (ACE2), a monocarboxylase that degrades angiotensin II to angiotensin 1-7, is also the functional receptor for severe acute respiratory syndrome (SARS) coronavirus (SARS-CoV) and is highly expressed in the lungs and heart. Patients with SARS also suffered from cardiac disease including arrhythmias, sudden cardiac death, and systolic and diastolic dysfunction.
MATERIALS AND METHODS: We studied mice infected with the human strain of the SARS-CoV and encephalomyocarditis virus and examined ACE2 mRNA and protein expression. Autopsy heart samples from patients who succumbed to the SARS crisis in Toronto (Canada) were used to investigate the impact of SARS on myocardial structure, inflammation and ACE2 protein expression.
RESULTS: Pulmonary infection with the human SARS-CoV in mice led to an ACE2-dependent myocardial infection with a marked decrease in ACE2 expression confirming a critical role of ACE2 in mediating SARS-CoV infection in the heart. The SARS-CoV viral RNA was detected in 35% (7/20) of autopsied human heart samples obtained from patients who succumbed to the SARS crisis during the Toronto SARS outbreak. Macrophage-specific staining showed a marked increase in macrophage infiltration with evidence of myocardial damage in patients who had SARS-CoV in their hearts. The presence of SARS-CoV in the heart was also associated with marked reductions in ACE2 protein expression.
CONCLUSIONS: Our data show that SARS-CoV can mediate myocardial inflammation and damage associated with down-regulation of myocardial ACE2 system, which may be responsible for the myocardial dysfunction and adverse cardiac outcomes in patients with SARS.

RGD Manual Disease Annotations    Click to see Annotation Detail View
TermQualifierEvidenceWithReferenceNotesSourceOriginal Reference(s)
Cardiovirus Infections  ISOAce2 (Mus musculus)40818405; 40818405encephalomyocarditis virus more ...RGD 
Cardiovirus Infections  IEP 40818405encephalomyocarditis virus more ...RGD 
severe acute respiratory syndrome  ISOAce2 (Mus musculus)40818405; 40818405mRNA and protein:decreased expression:heart (mouse)RGD 
severe acute respiratory syndrome  IEP 40818405mRNA and protein:decreased expression:heart (mouse)RGD 

Objects Annotated

Genes (Rattus norvegicus)
Ace2  (angiotensin converting enzyme 2)

Genes (Mus musculus)
Ace2  (angiotensin converting enzyme 2)

Genes (Homo sapiens)
ACE2  (angiotensin converting enzyme 2)


Additional Information