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Canine Coronavirus Activates Aryl Hydrocarbon Receptor during In Vitro Infection
by
Cerracchio, Claudia
, Serra, Francesco
, Amoroso, Maria Grazia
, Fiorito, Filomena
in
A72 cells
/ ACE2
/ AhR
/ Angiotensin
/ Angiotensin-converting enzyme 2
/ Animals
/ Antagonists
/ Antiviral agents
/ Antiviral drugs
/ CCoV
/ Cell death
/ Cell receptors
/ Cell viability
/ CH223191
/ Coronavirus infections
/ Coronavirus, Canine
/ Coronaviruses
/ COVID-19
/ Dengue fever
/ Development and progression
/ Disease transmission
/ Diseases
/ Dogs
/ Fibrosarcoma
/ Genotype
/ Genotypes
/ Health aspects
/ Hydrocarbons
/ Infections
/ Laboratories
/ Ligands
/ Mammalian cells
/ Mammals
/ Metabolites
/ Microscopy
/ Morphology
/ Peptidyl-dipeptidase A
/ Process controls
/ Receptors, Aryl Hydrocarbon - genetics
/ Receptors, Aryl Hydrocarbon - metabolism
/ Respiratory diseases
/ SARS-CoV-2
/ Severe acute respiratory syndrome coronavirus 2
/ virus yield
/ Viruses
2022
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Canine Coronavirus Activates Aryl Hydrocarbon Receptor during In Vitro Infection
by
Cerracchio, Claudia
, Serra, Francesco
, Amoroso, Maria Grazia
, Fiorito, Filomena
in
A72 cells
/ ACE2
/ AhR
/ Angiotensin
/ Angiotensin-converting enzyme 2
/ Animals
/ Antagonists
/ Antiviral agents
/ Antiviral drugs
/ CCoV
/ Cell death
/ Cell receptors
/ Cell viability
/ CH223191
/ Coronavirus infections
/ Coronavirus, Canine
/ Coronaviruses
/ COVID-19
/ Dengue fever
/ Development and progression
/ Disease transmission
/ Diseases
/ Dogs
/ Fibrosarcoma
/ Genotype
/ Genotypes
/ Health aspects
/ Hydrocarbons
/ Infections
/ Laboratories
/ Ligands
/ Mammalian cells
/ Mammals
/ Metabolites
/ Microscopy
/ Morphology
/ Peptidyl-dipeptidase A
/ Process controls
/ Receptors, Aryl Hydrocarbon - genetics
/ Receptors, Aryl Hydrocarbon - metabolism
/ Respiratory diseases
/ SARS-CoV-2
/ Severe acute respiratory syndrome coronavirus 2
/ virus yield
/ Viruses
2022
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Canine Coronavirus Activates Aryl Hydrocarbon Receptor during In Vitro Infection
by
Cerracchio, Claudia
, Serra, Francesco
, Amoroso, Maria Grazia
, Fiorito, Filomena
in
A72 cells
/ ACE2
/ AhR
/ Angiotensin
/ Angiotensin-converting enzyme 2
/ Animals
/ Antagonists
/ Antiviral agents
/ Antiviral drugs
/ CCoV
/ Cell death
/ Cell receptors
/ Cell viability
/ CH223191
/ Coronavirus infections
/ Coronavirus, Canine
/ Coronaviruses
/ COVID-19
/ Dengue fever
/ Development and progression
/ Disease transmission
/ Diseases
/ Dogs
/ Fibrosarcoma
/ Genotype
/ Genotypes
/ Health aspects
/ Hydrocarbons
/ Infections
/ Laboratories
/ Ligands
/ Mammalian cells
/ Mammals
/ Metabolites
/ Microscopy
/ Morphology
/ Peptidyl-dipeptidase A
/ Process controls
/ Receptors, Aryl Hydrocarbon - genetics
/ Receptors, Aryl Hydrocarbon - metabolism
/ Respiratory diseases
/ SARS-CoV-2
/ Severe acute respiratory syndrome coronavirus 2
/ virus yield
/ Viruses
2022
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Canine Coronavirus Activates Aryl Hydrocarbon Receptor during In Vitro Infection
Journal Article
Canine Coronavirus Activates Aryl Hydrocarbon Receptor during In Vitro Infection
2022
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Overview
The aryl hydrocarbon receptor (AhR) is a ligand-activated transcription factor that interacts with substrates, including microbial metabolites. Recent advances reveal that AhR is involved in the host response to coronaviruses (CoVs) infection. Particularly, AhR antagonists decrease the expression of angiotensin-converting enzyme 2 (ACE2) via AhR up-regulation, resulting in suppression of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection in mammalian cells. Herein, we report that AhR is expressed in canine fibrosarcoma (A72) cells, where it is considerably activated by infection with genotype II of canine coronavirus (CCoV-II). The pharmacological inhibition of AhR, by CH223191, suppressed cell death signs and increased cell viability. Furthermore, the AhR antagonist induced a meaningful decline in virus yield, accompanied by the inhibition of the expression of viral nuclear protein (NP). Fascinatingly, during CCoV infection, a novel co-expression of NP and AhR expression was found. Taken together, our preliminary findings show that infection with CCoV activates AhR, and pharmacologic AhR inhibition reduces CCoV replication, identifying AhR as a possible candidate target for CCoV antiviral therapy.
Publisher
MDPI AG,MDPI
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