Evidence map›Paper›PMID 41173927›Full record

ArticleScientific reports2025

A multiplex real-time PCR assay for detection of equid herpesvirus 1 and 4.

Rebecca L Tallmadge, Melissa Laverack, Manigandan Lejeune, Beate Crossley, Diego G Diel

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Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Rebecca L TallmadgeDepartment of Population Medicine and Diagnostic Sciences, Animal Health Diagnostic Center (AHDC), College of Veterinary Medicine, Cornell University, Ithaca, NY, USA.
Melissa LaverackDepartment of Population Medicine and Diagnostic Sciences, Animal Health Diagnostic Center (AHDC), College of Veterinary Medicine, Cornell University, Ithaca, NY, USA.
Manigandan LejeuneDepartment of Population Medicine and Diagnostic Sciences, Animal Health Diagnostic Center (AHDC), College of Veterinary Medicine, Cornell University, Ithaca, NY, USA.
Beate CrossleyCalifornia Animal Health & Food Safety Laboratory System (CAHFS), University of California, Davis, CA, USA.
Diego G DielDepartment of Population Medicine and Diagnostic Sciences, Animal Health Diagnostic Center (AHDC), College of Veterinary Medicine, Cornell University, Ithaca, NY, USA. dgdiel@cornell.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Equid herpesvirus (EHV) 1 and -4 are common viral pathogens of horses that can cause upper respiratory disease, neurological disease, abortion, and death. As characteristic alphaherpesviruses, both EHV-1 and EHV-4 can establish latency, resulting in a lifelong carrier state in infected animals. Here we describe the development and validation of a rapid and sensitive multiplex real-time PCR assay (EHV1-4MP) that simultaneously detects EHV-1 and EHV-4 and includes an endogenous internal control - melanocortin 1 receptor (MC1R) - targeting the equid genome. The EHV1-4MP assay analytical sensitivity was determined to be approximately two copies for EHV-1, four copies for EHV-4, and 10 copies for the equid MC1R gene per reaction. Analytical specificity was determined using a panel of 28 equine respiratory pathogens and commensal equine microorganisms. The EHV1-4MP assay detected reference and clinical isolates of EHV-1 and EHV-4, and did not detect other equid herpesviruses such as EHV-2, EHV-3, EHV-5, or several other viral and bacterial pathogens of horses. Importantly, the EHV1-4MP assay developed here has improved specificity compared to existing assays and is able to exclude the closely related EHV-3, EHV-8, and EHV-9 viruses. Diagnostic performance was evaluated using 60 clinical samples including upper respiratory swabs and washes, blood, placenta, lung, and brain. The EHV1-4MP assay results were in 100% concordance with singleplex EHV-1 and EHV-4 assays. Our results demonstrate that the EHV1-4MP real-time assay developed here offers rapid, sensitive, and simultaneous detection of EHV-1 and EHV-4.

Indexed as

Herpesviridae InfectionsHerpesvirus 1, EquidHerpesvirus 4, EquidHorse DiseasesMultiplex Polymerase Chain ReactionReal-Time Polymerase Chain ReactionAnimalsHorsesSensitivity and Specificity

Identifiers

PMID41173927
PMCPMC12578806

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.