Literature DB >> 33310196

Assessing the litter level agreement of RT-PCR results for porcine reproductive and respiratory syndrome virus in testicles, tails and udder wipes diagnostic samples relative to serum from piglets.

Carles Vilalta1, Juan M Sanhueza2, Mark Schwartz3, Mariana Kikuti4, Montserrat Torremorell4, Cesar A Corzo4.   

Abstract

Porcine reproductive and respiratory syndrome (PRRS) is currently the most detrimental disease in the U.S swine industry. Clinical signs of PRRS virus (PRRSv) infection in breeding herds include reproductive failure with abortions, stillbirths, premature farrowings and increased pre-weaning mortality. Serum from due-to-wean piglets is considered the most suitable specimen to monitor PRRSv infection and stability in breeding herds. However, processing fluids (PF - the serosanguinous exudate resultant of the collection of tails and testicles during processing) are a new specimen proposed to monitor piglets at processing (3-5 days of age) and udder wipes (UW) of lactating sows is yet another specimen to monitor infection status of suckling piglets indirectly. Here, we assessed which specimen type (e.g. sera, testicles, tails or UW) should be used to accurately establish the PRRSv status of a litter. Twenty-four litters were conveniently selected on a farm at 10 weeks post PRRSv outbreak. Blood samples, tails and testicles from every piglet in a litter, and an udder skin wipe from the sow were collected at processing (3-5 days). Individual litter testicles and tails as well as the udder wipe were placed each in a reclosable bag to prevent cross-contamination. Sensitivity (Se), specificity (Sp), negative predictive value (NPV), positive predictive value (PPV) and global agreement at the litter level were calculated using the sera results of the litter as the gold standard. The optimum cycle threshold (Ct) value to classify a sample as negative was ≥35 for serum and ≥36 for the aggregated samples (testicles, tails, and UW) based on the ROC curve analysis. Using those thresholds, the fluid collected from the testicles showed the best overall performance (Se = 92 % [62-100]; Sp = 82 % [48-98], NPV = 90 % [55-100], PPV = 85 % [55-98], global agreement = 87 %) compared to tail fluid and UW. Sensitivity of the tail fluid was 62 % (32-86) and the UW was 23 % (5-54), both of which yielded a 100 % specificity and PPV. This study provides information on the contribution of each of the tissues collected at processing on the detection of PRRSv, which becomes relevant in countries were castration and/or tail docking is banned.
Copyright © 2020 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Castration; Monitoring; PRRSv; Processing fluids; Swine health; Tail docking; Udder wipes

Mesh:

Year:  2020        PMID: 33310196     DOI: 10.1016/j.prevetmed.2020.105211

Source DB:  PubMed          Journal:  Prev Vet Med        ISSN: 0167-5877            Impact factor:   2.670


  1 in total

1.  Considerations in the use of processing fluids for the detection of PRRSV RNA and antibody.

Authors:  Will López; Jeff Zimmerman; Phil Gauger; Karen Harmon; Ronaldo Magtoto; Laura Bradner; Derald Holtkamp; Min Zhang; Jianqiang Zhang; Alejandro Ramirez; Daniel Linhares; Luis Giménez-Lirola
Journal:  J Vet Diagn Invest       Date:  2022-08-10       Impact factor: 1.569

  1 in total

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