Target intelligence / Profile preview

Enteropathogenic coronavirus (ECoV)

Target
ECoV
Molecular classification
Other
01

Overview

Enteropathogenic coronaviruses (ECoVs) are a diverse group of viruses within the Coronaviridae family that primarily infect the epithelial cells of the gastrointestinal tract in humans and animals [PubMed: 29769351]. These viruses, including Porcine Epidemic Diarrhea Virus (PEDV) and Transmissible Gastroenteritis Virus (TGEV), are characterized by their ability to cause severe diarrhea, vomiting, and dehydration, often leading to high mortality rates in neonatal livestock [PubMed: 26038515]. The infection process is mediated by the viral Spike (S) protein, which frequently targets the host cell surface enzyme Aminopeptidase N (APN/CD13) to facilitate entry into enterocytes [UniProt: P15144]. From a therapeutic perspective, the term 'Enteropathogenic coronavirus' refers to a pathogen class rather than a single molecular target. However, drug discovery efforts focus on highly conserved viral proteins such as the Main Protease (Mpro) and the RNA-dependent RNA polymerase (RdRp) [PubMed: 32272481]. Broad-spectrum antivirals like Remdesivir and Nirmatrelvir have shown efficacy in inhibiting these enzymes across various coronavirus species [NIH]. Additionally, neutralizing antibodies and vaccines targeting the Spike protein are critical for preventing infection and mitigating the economic and clinical impact of enteric outbreaks [PubMed: 33806177].

Other names
Enteric coronavirusGastrointestinal coronavirusPorcine epidemic diarrhea virus (PEDV)Transmissible gastroenteritis virus (TGEV)Swine acute diarrhea syndrome coronavirus (SADS-CoV)Bovine coronavirus (BCoV)
02

Mechanism of action

Inhibition of viral replication via targeting the Main Protease (Mpro/3CLpro) to prevent polyprotein processing, or the RNA-dependent RNA polymerase (RdRp) to halt genome synthesis. Additionally, some strategies focus on blocking the viral Spike (S) protein from binding to host-cell receptors like Aminopeptidase N (APN/CD13) [PubMed: 29769351, 32272481].

03

Biological functions

Other
04

Disease associations

InfectionOther
05

Safety considerations

Rapid viral mutation leading to drug resistanceHost-cell toxicity of viral entry inhibitorsDrug-drug interactions associated with protease inhibitor boosters like Ritonavir [FDA]Species-specific variations in receptor binding (APN vs. ACE2)
06

Interacting drugs

Remdesivir

3 more in the full profile.

07

Biomarkers

Viral RNA (via RT-PCR)Viral antigen (N protein)Fecal viral loadSerological anti-Spike antibodies

Beyond the preview

Go deeper on Enteropathogenic coronavirus (ECoV).

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 Enteropathogenic coronavirus (ECoV).

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