Practical aspects of PRRSV RNA detection in processing fluids collected in commercial swine farms.


Journal

Preventive veterinary medicine
ISSN: 1873-1716
Titre abrégé: Prev Vet Med
Pays: Netherlands
ID NLM: 8217463

Informations de publication

Date de publication:
Jul 2020
Historique:
received: 23 01 2020
revised: 22 04 2020
accepted: 24 04 2020
pubmed: 20 5 2020
medline: 16 2 2021
entrez: 20 5 2020
Statut: ppublish

Résumé

Processing fluid samples are easily collected under field conditions and provide the means to test more piglets more frequently in a practical way, thereby improving PRRSV surveillance. However, a deeper understanding of the diagnostic characteristics of this newly described sample type is still required. Therefore, the objective of this field-based study was to determine the relationship between viremic piglets and the detection of PRRSV RNA in processing fluid samples. In two PRRSV-positive breeding herds, processing fluids (n = 77) and individual piglet serum samples (n = 834) were collected from 77 litters in three sampling events and tested for PRRSV RNA. Among the 77 litters in the study, 55 litters (71.4%) contained no viremic piglets and processing fluids tested negative for PRRSV RNA. Among the 22 (28.6%) litters with ≥1 viremic piglets, 10 litters contained a single viremic piglet and 5 of the 10 processing fluids from this group tested positive for PRRSV RNA. Based on a fitted mixed effects logistic regression model, the probability of detecting PRRSV RNA in processing fluids was highly dependent on the number of viremic piglets contributing to the sample. When the within-litter prevalence was ≥39%, the probability of detecting PRRSV RNA in processing fluids was ≥95%. By extension, the results suggest that pooling processing fluids from several litters increases the probability of PRRSV RNA detection because of the greater likelihood of including multiple litters each with ≥1 viremic piglets. In contemporary breeding herds that use processing fluid samples for PRRSV surveillance, the diagnostic costs associated with testing 100% of the processing-age piglet population can be estimated at €0.077 ($0.086 USD) per pig weaned. In contrast, to achieve an equivalent testing coverage with the use of individual piglet serum samples, the diagnostic costs associated would be €4.48 ($5.00 USD) per pig weaned. Processing fluid represents a practical, reliable and efficient method to surveil breeding herds for PRRSV because it allows for continuous surveillance at a low cost.

Identifiants

pubmed: 32428814
pii: S0167-5877(20)30067-2
doi: 10.1016/j.prevetmed.2020.105021
pii:
doi:

Substances chimiques

RNA, Viral 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

105021

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare no conflicts of interest with respect to the conduct, authorship, and/or publication of this study. Co-author JZ has served as a consultant to IDEXX Laboratories, Inc. on areas of diagnostic medicine independent of this research. The terms of the consulting arrangement have been reviewed and approved by Iowa State University in accordance with its conflict of interest policies.

Auteurs

Will A López (WA)

Veterinary Diagnostic and Production Animal Medicine Department, College of Veterinary Medicine, Iowa State University, Lloyd Veterinary Medical Center, 1809 S Riverside Dr., Ames, IA 50011-3619, United States; PIC North America, 100 Bluegrass Commons Blvd #2200, Hendersonville, TN 37075, United States.

Jeffrey J Zimmerman (JJ)

Veterinary Diagnostic and Production Animal Medicine Department, College of Veterinary Medicine, Iowa State University, Lloyd Veterinary Medical Center, 1809 S Riverside Dr., Ames, IA 50011-3619, United States.

Phillip C Gauger (PC)

Veterinary Diagnostic and Production Animal Medicine Department, College of Veterinary Medicine, Iowa State University, Lloyd Veterinary Medical Center, 1809 S Riverside Dr., Ames, IA 50011-3619, United States.

Karen M Harmon (KM)

Veterinary Diagnostic and Production Animal Medicine Department, College of Veterinary Medicine, Iowa State University, Lloyd Veterinary Medical Center, 1809 S Riverside Dr., Ames, IA 50011-3619, United States.

Laura Bradner (L)

Veterinary Diagnostic and Production Animal Medicine Department, College of Veterinary Medicine, Iowa State University, Lloyd Veterinary Medical Center, 1809 S Riverside Dr., Ames, IA 50011-3619, United States.

Min Zhang (M)

Department of Statistics, College of Liberal Arts and Sciences, Iowa State University, Ames, Iowa 50011, United States.

Luis Giménez-Lirola (L)

Veterinary Diagnostic and Production Animal Medicine Department, College of Veterinary Medicine, Iowa State University, Lloyd Veterinary Medical Center, 1809 S Riverside Dr., Ames, IA 50011-3619, United States.

Alejandro Ramirez (A)

Veterinary Diagnostic and Production Animal Medicine Department, College of Veterinary Medicine, Iowa State University, Lloyd Veterinary Medical Center, 1809 S Riverside Dr., Ames, IA 50011-3619, United States.

Jean Paul Cano (JP)

Veterinary Diagnostic and Production Animal Medicine Department, College of Veterinary Medicine, Iowa State University, Lloyd Veterinary Medical Center, 1809 S Riverside Dr., Ames, IA 50011-3619, United States; PIC North America, 100 Bluegrass Commons Blvd #2200, Hendersonville, TN 37075, United States.

Daniel C L Linhares (DCL)

Veterinary Diagnostic and Production Animal Medicine Department, College of Veterinary Medicine, Iowa State University, Lloyd Veterinary Medical Center, 1809 S Riverside Dr., Ames, IA 50011-3619, United States. Electronic address: linhares@iastate.edu.

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