Determination of pig immunity status after porcine reproductive and respiratory syndrome (PRRS) modified live virus (MLV) vaccination with ELISA and PCR technique

Porcine reproductive and respiratory syndrome (PRRS) is a disease characterised by late-term reproductive failure in sows and gilts, and respiratory problems in piglets and growing pigs. In this study, 240 sera were collected from four farms that had been practicing different PRRS vaccination regime...

Full description

Bibliographic Details
Main Author: Chua, Vi Vian
Format: Project Paper Report
Language:English
Published: 2016
Online Access:http://psasir.upm.edu.my/id/eprint/83662/
http://psasir.upm.edu.my/id/eprint/83662/1/FPV%202016%2065%20IR.pdf
_version_ 1848859601765662720
author Chua, Vi Vian
author_facet Chua, Vi Vian
author_sort Chua, Vi Vian
building UPM Institutional Repository
collection Online Access
description Porcine reproductive and respiratory syndrome (PRRS) is a disease characterised by late-term reproductive failure in sows and gilts, and respiratory problems in piglets and growing pigs. In this study, 240 sera were collected from four farms that had been practicing different PRRS vaccination regime for more a year and vaccinations were done at 2 months before sampling. 15 sera from four age groups: sows, growers, weaners and piglets were collected from each farm and analysed using IDEXX PRRS X3 ELISA for PRRSV antibodies. Pooled serum samples were tested by using nested-PCR that enable the differentiation of Type I and Type II PRRSV. Out of 80 pooled serum samples, none were positive for PRRSV indicating all age groups were not viraemic after vaccination. As for ELISA, results showed all the farms were seropositive for PRRS. Mean S/P ratios of piglets, growers and sows of all four farms were higher than 0.4 which was the cut off value of positive ELISA result but there were no significant difference between the farms except for Farm B which practiced whole herd US MLV vaccination. Farm B showed significantly lower (p<0.05) S/P ratio in their piglet, grower and sow groups which suggest there was low virus circulation in herd. Farm A which practiced US MLV on sow was the only farm found to have seronegative status in their weaners. Thus, these data indicate PRRS MLV vaccination will not cause viraemia and whole herd MLV vaccination may help to reduce virus circulation in PRRS endemic farm.
first_indexed 2025-11-15T12:31:56Z
format Project Paper Report
id upm-83662
institution Universiti Putra Malaysia
institution_category Local University
language English
last_indexed 2025-11-15T12:31:56Z
publishDate 2016
recordtype eprints
repository_type Digital Repository
spelling upm-836622020-10-08T08:16:45Z http://psasir.upm.edu.my/id/eprint/83662/ Determination of pig immunity status after porcine reproductive and respiratory syndrome (PRRS) modified live virus (MLV) vaccination with ELISA and PCR technique Chua, Vi Vian Porcine reproductive and respiratory syndrome (PRRS) is a disease characterised by late-term reproductive failure in sows and gilts, and respiratory problems in piglets and growing pigs. In this study, 240 sera were collected from four farms that had been practicing different PRRS vaccination regime for more a year and vaccinations were done at 2 months before sampling. 15 sera from four age groups: sows, growers, weaners and piglets were collected from each farm and analysed using IDEXX PRRS X3 ELISA for PRRSV antibodies. Pooled serum samples were tested by using nested-PCR that enable the differentiation of Type I and Type II PRRSV. Out of 80 pooled serum samples, none were positive for PRRSV indicating all age groups were not viraemic after vaccination. As for ELISA, results showed all the farms were seropositive for PRRS. Mean S/P ratios of piglets, growers and sows of all four farms were higher than 0.4 which was the cut off value of positive ELISA result but there were no significant difference between the farms except for Farm B which practiced whole herd US MLV vaccination. Farm B showed significantly lower (p<0.05) S/P ratio in their piglet, grower and sow groups which suggest there was low virus circulation in herd. Farm A which practiced US MLV on sow was the only farm found to have seronegative status in their weaners. Thus, these data indicate PRRS MLV vaccination will not cause viraemia and whole herd MLV vaccination may help to reduce virus circulation in PRRS endemic farm. 2016-03 Project Paper Report NonPeerReviewed text en http://psasir.upm.edu.my/id/eprint/83662/1/FPV%202016%2065%20IR.pdf Chua, Vi Vian (2016) Determination of pig immunity status after porcine reproductive and respiratory syndrome (PRRS) modified live virus (MLV) vaccination with ELISA and PCR technique. [Project Paper Report]
spellingShingle Chua, Vi Vian
Determination of pig immunity status after porcine reproductive and respiratory syndrome (PRRS) modified live virus (MLV) vaccination with ELISA and PCR technique
title Determination of pig immunity status after porcine reproductive and respiratory syndrome (PRRS) modified live virus (MLV) vaccination with ELISA and PCR technique
title_full Determination of pig immunity status after porcine reproductive and respiratory syndrome (PRRS) modified live virus (MLV) vaccination with ELISA and PCR technique
title_fullStr Determination of pig immunity status after porcine reproductive and respiratory syndrome (PRRS) modified live virus (MLV) vaccination with ELISA and PCR technique
title_full_unstemmed Determination of pig immunity status after porcine reproductive and respiratory syndrome (PRRS) modified live virus (MLV) vaccination with ELISA and PCR technique
title_short Determination of pig immunity status after porcine reproductive and respiratory syndrome (PRRS) modified live virus (MLV) vaccination with ELISA and PCR technique
title_sort determination of pig immunity status after porcine reproductive and respiratory syndrome (prrs) modified live virus (mlv) vaccination with elisa and pcr technique
url http://psasir.upm.edu.my/id/eprint/83662/
http://psasir.upm.edu.my/id/eprint/83662/1/FPV%202016%2065%20IR.pdf