Literature detail

Investigation of the Role of Healthy and Sick Equids in the COVID-19 Pandemic through Serological and Molecular Testing.

Kaila O Y Lawton1 Rick M Arthur2 Benjamin C Moeller3,4 Samantha Barnum1 Nicola Pusterla1
Affiliations 4 institutions
  1. Department of Medicine and Epidemiology, School of Veterinary Medicine, University of California, Davis, CA 95616, USA.
  2. School of Veterinary Medicine, University of California, Davis, CA 95616, USA.
  3. KL Maddy Equine Analytical Chemistry Laboratory, School of Veterinary Medicine, University of California, Davis, CA 95616, USA.
  4. Department of Molecular Biosciences, School of Veterinary Medicine, University of California, Davis, CA 95616, USA.
PMID 35268183 2022 Animals (Basel) eng epublish
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Article

Publication summary

More and more studies are reporting on the natural transmission of SARS-CoV-2 between humans with COVID-19 and their companion animals (dogs and cats). While horses are apparently susceptible to SARS-CoV-2 infection based on the homology between the human and the equine ACE-2 receptor, no clinical or subclinical infection has yet been reported in the equine species. To investigate the possible clinical role of SARS-CoV-2 in equids, nasal secretions from 667 horses with acute onset of fever and respiratory signs were tested for the presence of SARS-CoV-2 by qPCR. The samples were collected from January to December of 2020 and submitted to a commercial molecular diagnostic laboratory for the detection of common respiratory pathogens (equine influenza virus, equine herpesvirus-1/-4, equine rhinitis A and B virus, <i>Streptococcus equi</i> subspecies <i>equi</i>). An additional 633 serum samples were tested for antibodies to SARS-CoV-2 using an ELISA targeting the receptor-binding domain of the spike protein. The serum samples were collected from a cohort of 587 healthy racing Thoroughbreds in California after track personnel tested qPCR-positive for SARS-CoV-2. While 241/667 (36%) equids with fever and respiratory signs tested qPCR-positive for at least one of the common respiratory pathogens, not a single horse tested qPCR-positive for SARS-CoV-2. Amongst the racing Thoroughbreds, 35/587 (5.9%) horses had detectable antibodies to SARS-CoV-2. Similar to dogs and cats, horses do not seem to develop clinical SARS-CoV-2 infection. However, horses can act as incidental hosts and experience silent infection following spillover from humans with COVID-19. SARS-CoV-2-infected humans should avoid close contact with equids during the time of their illness.

blood ELISA healthy horses horses nasal secretions qPCR SARS-CoV-2 sick equids

Structured evidence records

Evidence records

3 total
1 records
Extraction confidence 0.98
Key finding

SARS-CoV-2 antibodies were detected in 35 of 587 healthy racing Thoroughbred horses in California, suggesting silent equine infection following human spillover.

Virus
Location
Not specified
Supporting text

An additional 633 serum samples were tested for antibodies to SARS-CoV-2 using an ELISA targeting the receptor-binding domain of the spike protein. Amongst the racing Thoroughbreds, 35/587 (5.9%) horses had detectable antibodies to SARS-CoV-2.

Method
ELISA
Sample type
serum
1 records
Extraction confidence 0.90
Key finding

Serology indicated silent SARS-CoV-2 infection in horses following spillover from infected humans.

Virus
Location
Supporting text

Amongst the racing Thoroughbreds, 35/587 (5.9%) horses had detectable antibodies to SARS-CoV-2. ... However, horses can act as incidental hosts and experience silent infection following spillover from humans with COVID-19.

Method
ELISA; qPCR
Study design
serological survey
Transmission direction
human-to-animal
Geographic raw
California
Country inferred
United States
1 records
Extraction confidence 0.85
Key finding

Surveillance found no SARS-CoV-2-positive nasal samples but detected antibodies in 5.9% of racing Thoroughbreds, indicating low-level spillover exposure from infected humans.

Virus
Location
Supporting text

Nasal secretions from 667 horses with acute onset of fever and respiratory signs were tested for the presence of SARS-CoV-2 by qPCR. An additional 633 serum samples were tested for antibodies to SARS-CoV-2 using an ELISA targeting the receptor-binding domain of the spike protein. The serum samples were collected from a cohort of 587 healthy racing Thoroughbreds in California after track personnel tested qPCR-positive for SARS-CoV-2.

Method
qPCR; ELISA
Sample type
nasal secretions; serum
Geographic raw
California
Country inferred
United States