Target intelligence / Profile preview

Canine mastadenovirus A (CAdV-1)

Target
CAdV-1
Molecular classification
Virus, Double-stranded DNA virus, Mastadenovirus, Adenoviridae family
01

Overview

Canine mastadenovirus A (commonly known as canine adenovirus type 1 or CAdV-1, occasionally referred to as infectious canine hepatitis virus or Rubarth’s disease virus) is a non-enveloped, icosahedral double-stranded DNA virus in the Mastadenovirus genus of the Adenoviridae family[1][3][5]. It has a genome of approximately 32 kb and infects both domestic and wild canids, causing infectious canine hepatitis (ICH), a severe and often fatal systemic disease characterized by acute hepatitis, vascular damage, and multi-organ involvement[5][7][8]. CAdV-1 primarily targets hepatic and endothelial cells, where viral replication leads to tissue damage and clinical disease. The virus possesses structural proteins including hexon, penton base, and fiber, with the fiber protein mediating attachment to host cell receptors, specifically the coxsackievirus and adenovirus receptor (CAR)[2][9]. Disease prevention relies on vaccination with live attenuated CAdV-2 vaccine, which cross-protects against CAdV-1 without inducing adverse events associated with CAdV-1-based vaccines[1][5]. There are no direct-acting antiviral drugs against this virus; diagnostics rely on molecular and serological tests. CAdV-1 is not a therapeutic target in the sense of a single molecular entity (like a receptor, enzyme, or transporter) suited for pharmacological modulation, but it is a target of preventive vaccination and diagnostic surveillance[1][3][5].

Other names
Canine adenovirus type 1Infectious canine hepatitis virusCAV-1CAdV-1Rubarth's disease virus
02

Mechanism of action

Not applicable (vaccines are preventive, not directly therapeutic against a molecular target on the virus)

03

Biological functions

Infection of host cellsCauses acute and systemic hepatitis in dogs and other canidsReplicates primarily in hepatocytes and vascular endothelial cellsImmune evasion
04

Disease associations

InfectionAcute viral hepatitis (infectious canine hepatitis)Canine hepatic dysfunctionNeurological and systemic infections in dogs and wild canids
05

Safety considerations

Live attenuated vaccines based on CAdV-2 can rarely cause mild vaccine-associated adverse events; CAdV-1-based vaccines are avoided due to adverse effects[1][5].
06

Interacting drugs

None (no approved small molecule drugs; prevention through vaccination, not therapeutic inhibition)
07

Biomarkers

Viral DNA detection (PCR for CAdV-1 DNA)Serological testing for antibodies (ELISA or serum neutralization)Histopathological lesions in liver (diagnostic, not therapeutic)

Beyond the preview

Go deeper on Canine mastadenovirus A (CAdV-1).

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Drug pipeline

Full profile access

Explore the programs pursuing this target and their development progress.

  • Drug candidates
  • Developers
  • Development stage

Clinical trials

Full profile access

Follow the clinical studies evaluating therapies directed at this target.

  • Trial design
  • Status
  • Readouts

Competitive landscape

Full profile access

Compare approaches across drug candidates, modalities, and indications.

  • Programs
  • Modalities
  • Indications

Literature & evidence

Full profile access

Investigate the research and source evidence behind target biology and development.

  • Publications
  • Sources
  • Analysis

Patents

Full profile access

Explore patent activity around therapies and technologies addressing this target.

  • Patents
  • Assignees
  • Technologies

Research & analysis

Full profile access

Connect target biology, drug development, and emerging evidence in your research.

  • Biology
  • Development news
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on Canine mastadenovirus A (CAdV-1).

Explore the full profile

Gosset Free

Get started with Gosset.

Enter your work email and we’ll be in touch with next steps.

Work email preferred.

Book a call