Thursday, April 11, 2019

Comparison of four commercial PRRSV MLV vaccines in herds with co-circulation of PRRSV-1 and PRRSV-2


 2019 Apr;63:66-73. doi: 10.1016/j.cimid.2018.12.010. Epub 2019 Jan 9.

Comparison of four commercial PRRSV MLV vaccines in herds with co-circulation of PRRSV-1 and PRRSV-2.

Author information

1
Seoul National University, College of Veterinary Medicine, Department of Veterinary Pathology, 1 Gwanak-ro, Gwanak-gu, Seoul 08826, Republic of Korea.
2
Seoul National University, College of Veterinary Medicine, Department of Veterinary Pathology, 1 Gwanak-ro, Gwanak-gu, Seoul 08826, Republic of Korea. Electronic address: swine@snu.ac.kr.

Abstract

The efficacy of four commercial porcine reproductive and respiratory syndrome virus (PRRSV) modified-live virus (MLV) vaccines against respiratory disease was evaluated and compared in pig farms suffering from co-infection with PRRSV-1 and PRRSV-2. All vaccinated groups on average exhibited improved growth rate compared to the unvaccinated pigs. Interestingly, the two groups vaccinated with either of the PRRSV-2 MLV vaccines had a better overall growth rate compared to the pigs vaccinated with either of the PRRSV-1 MLV vaccines. Vaccination of pigs with either of the PRRSV-1 MLV vaccines did not result in reduction of PRRSV-1 or PRRSV-2 viremia whereas vaccination of pigs with either of the PRRSV-2 MLV vaccines resulted in the reduction of PRRSV-2 viremia only. Taken together, the results of this field study demonstrate that a PRRSV-2 MLV vaccine can be efficacious against respiratory disease caused by co-infection with PRRSV-1 and PRRSV-2.

KEYWORDS: 

Co-infection; Porcine reproductive and respiratory syndrome; Vaccine; Virus
PMID:
 
30961820
 
DOI:
 
10.1016/j.cimid.2018.12.010

Thursday, March 14, 2019

Cellular Innate Immunity against PRRSV (and IAV)


 2019 Mar 11;6(1). pii: E26. doi: 10.3390/vetsci6010026.

Cellular Innate Immunity against PRRSV and Swine Influenza Viruses.

Author information

1
Department of Population Health and Pathobiology, College of Veterinary Medicine, North Carolina State University, Raleigh, NC 27607, USA. ecrisci@ncsu.edu.
2
Comparative Medicine Institute, North Carolina State University, Raleigh, NC 27607, USA. ecrisci@ncsu.edu.
3
Universitat de Lleida, 25198 Lleida, Spain. lorenzo.fraile@ca.udl.cat.
4
Centro de Investigaciones Biológicas, Consejo Superior de Investigaciones Científicas (CIB-CSIC), 28040 Madrid, Spain. maria.montoya@cib.csic.es.

Abstract

Porcine respiratory disease complex (PRDC) is a polymicrobial syndrome that results from a combination of infectious agents, such as environmental stressors, population size, management strategies, age, and genetics. PRDC results in reduced performance as well as increased mortality rates and production costs in the pig industry worldwide. This review focuses on the interactions of two enveloped RNA viruses-porcine reproductive and respiratory syndrome virus (PRRSV) and swine influenza virus (SwIV)-as major etiological agents that contribute to PRDC within the porcine cellular innate immunity during infection. The innate immune system of the porcine lung includes alveolar and parenchymal/interstitial macrophages, neutrophils (PMN), conventional dendritic cells (DC) and plasmacytoid DC, natural killer cells, and γδ T cells, thus the in vitro and in vivo interactions between those cells and PRRSV and SwIV are reviewed. Likewise, the few studies regarding PRRSV-SwIV co-infection are illustrated together with the different modulation mechanisms that are induced by the two viruses. Alterations in responses by natural killer (NK), PMN, or γδ T cells have not received much attention within the scientific community as their counterpart antigen-presenting cells and there are numerous gaps in the knowledge regarding the role of those cells in both infections. This review will help in paving the way for future directions in PRRSV and SwIV research and enhancing the understanding of the innate mechanisms that are involved during infection with these viruses.

KEYWORDS: 

PRRSV; innate immunity; pig; swine influenza virus
PMID:
 
30862035
 
DOI:
 
10.3390/vetsci6010026

Monday, March 4, 2019

Influence of age, group size, and presence of PRRSv on oral fluids collection

 2019 Feb;244:13-15. doi: 10.1016/j.tvjl.2018.12.005. Epub 2018 Dec 7.

Influence of age, group size and the presence of porcine reproductive and respiratory syndrome virus on the collection of oral fluids.

Author information

1
Department for Farm Animals and Veterinary Public Health, University Clinic for Swine, University of Veterinary Medicine Vienna, Vienna Vetertinaerplatz 1, A-1220 Vienna, Austria. Electronic address: rgraage@vetclinics.uzh.ch.
2
Department for Farm Animals and Veterinary Public Health, University Clinic for Swine, University of Veterinary Medicine Vienna, Vienna Vetertinaerplatz 1, A-1220 Vienna, Austria.
3
Clinic for Swine at the Centre for Clinical Veterinary Medicine, Ludwig-Maximilians-University Munich, Sonnenstrasse 16, D-85764 Oberschleißheim, Germany.

Abstract

Pen-based oral fluid (OF) samples have been approved for detecting porcine reproductive and respiratory syndrome virus (PRRSV) RNA and antibodies. The aim of the study was to investigate the influence of age, group size and the presence of PRRSV infection on sampling using pen-based OF collected by presenting pigs with a rope to chew. Samples were collected from pigs of 4/5 weeks of age, 7/8 weeks of age and 12/14 weeks of age. Subsequent PRRSV-PCR and ELISA analyses of OF and serum samples were performed. In this study, 76.5-81.9% of pigs chewed the rope. The group size had significant impact on the pig-rope-interaction (P=0.047). OF and serum had an almost perfect and significant agreement for the detection of antibodies (κ=0.829, P<0.001) and a fair and not significant agreement (κ=0.347, P=0.75) for the detection PRRSV-genome.

KEYWORDS: 

ELISA; Oral fluid; PCR; PRRSV; Rope; Surveillance
PMID:
 
30825888
 
DOI:
 
10.1016/j.tvjl.2018.12.005

Litter oral fluid testing was more sensitive than bleeding the weakest pig in the litter (for PRRSV detection in suckling pigs)

 2019 Feb 19;5:8. doi: 10.1186/s40813-019-0115-z. eCollection 2019.

Monitoring PRRSV-1 in suckling piglets in an endemic herd using reverse transcriptase quantitative real time polymerase chain reaction: comparison of the rate of detection in serum and oral fluid samples and evaluation of pooling.

Author information

1
Porc. Spective Swine Vet Pratice, Chene Vert Conseil veterinary group, ZA du Gohélève, 56920 Noyal-Pontivy, France.
2
Labofarm Finalab Veterinary Laboratory Group, 4 rue Théodore Botrel, 22600 Loudéac, France.
3
Ekipaj, 22 rue d'Assas, 49000 Angers, France.

Abstract

BACKGROUND: 

Defining shedding and exposure status for PRRSV is essential in herd stabilisation protocols and weaning-age pigs is a key subpopulation. Oral fluid (OF) sampling is a welfare-friendly and cost saving promising alternative to blood sampling. The first objective of our study was to compare the rate of detection of PRRSV-1 in individual serum sample, individual OF sample, litter-based OF sample, collected the day before weaning. The second objective was to evaluate the interest of pooling samples.

RESULTS: 

The study was performed on a 210-sows, PRRSV-1 exposed, with confirmed shedding, non-vaccinated against PRRSV, herd. 80 litters were sampled and 26 were viropositive and therefore included. The rate of detection of PRRSV-1 with RT-qrtPCR in blood samples, iOF and cOF was 67, 23 and 77%, respectively. The Ct values from RT-qrtPCR on collective OF were statistically lower if the serum of the piglet of the litter was positive. The lower the Cycle threshold (Ct) value of RT-qrtPCR on collective OF, the higher the probability that the serum sampled in the same litter was positive. Ability to detect PRRSV RNA after pooling was 67% for sera and 58% for cOF.

CONCLUSIONS: 

The rate of detection of PRRSV-1 was about the same in cOF and blood samples. Virus sequencing, if required, should be performed on individual serum samples. The smaller the Ct of a cOF sample from a litter, the greater the likelihood that the serum sample from a piglet of that litter is positive.A cost-effective and representative sampling protocol to monitor sow herds stabilisation of a sow batch could be: to collect both cOF and one serum sample per litter; to perform firstly RT-qrtPCR on pooled cOF; in case of negative results to consider the batch negative; in case of positive results in a unvaccinated herd or a killed vaccine vaccinated one to consider the batch positive; in case of positive result in a herd vaccinated with a modified live vaccine serum samples of litters with positive cOF should be tested for sequencing (selecting the litters with the lowest Ct for cOF).

KEYWORDS: 

Diagnostic; Oral fluid; PCR; PRRS; Pig; Pooling; Serum; Suckling piglets
PMID:
 
30820335
 
PMCID:
 
PMC6381726
 
DOI:
 
10.1186/s40813-019-0115-z

Monday, December 10, 2018

Factors affecting PRRSV time-to-stability in US breeding herds

 2018 Dec 6. doi: 10.1111/tbed.13091. [Epub ahead of print]

Factors affecting Porcine Reproductive and Respiratory Syndrome virus time-to-stability in breeding herds in the Midwestern United States.

Abstract

The time needed to wean porcine reproductive and respiratory syndrome (PRRS) virus negative pigs consistently from a breeding herd after an outbreak is referred to as time-to-stability (TTS). TTS is an important measure to plan herd closure as well as to manage economic expectations. Weekly PRRS incidence data from 82 sow farms in six production systems located in the Midwestern United States were used for the analysis. The objective of this study was to evaluate the effect of recorded predictors on TTS in participant sow farms. The median TTS was 41.0 weeks (1st quartile 31.0 weeks-3rd quartile 55.0 weeks). In the final multivariable mixed-effects Cox model, farms that experienced winter (hazard ratio (HR) 2.46, 95% confidence interval (CI) 1.37-4.43) and autumn (HR 1.73, 95% CI 1.00-2.99) PRRS outbreaks achieved stability sooner than farms that experienced PRRS outbreaks during summer. No statistically significant difference (p=0.76) was observed between the TTS of farms that had a PRRS outbreak during spring and summer (HR 1.09, 95% CI 0.59-1.88). Additionally, farms that had a PRRS outbreak associated with a 1-7-4 restriction fragment length polymorphism (RFLP) cut pattern took significantly longer to achieve stability (HR 0.4, 95% CI 0.3-0.7) compared to farms which had a non-1-7-4 PRRS outbreak. Finally, farms that had a previous PRRS outbreak within a year achieved stability sooner (HR 2.18, 95% CI 1.23-3.86) than farms that did not have a previous PRRS outbreak within a year. This study provides information that may result useful for planning herd closure and managing expectations about the time needed to wean PRRS virus negative pigs in breading herds according to the season of the year when the outbreak occurred and the RFLP cut pattern associated with the outbreak virus. This article is protected by copyright. All rights reserved.

KEYWORDS: 

PRRS ; RFLP ; season; swine; time-to-stability
PMID:
 
30520570
 
DOI:
 
10.1111/tbed.13091

Monday, November 26, 2018

Vaccination of neonatal pigs with MLV PRRSV vaccine is able to overcome maternal immunity

 2018 Nov 15;4:25. doi: 10.1186/s40813-018-0101-x. eCollection 2018.

Vaccination of 1-day-old pigs with a porcine reproductive and respiratory syndrome virus (PRRSV) modified live attenuated virus vaccine is able to overcome maternal immunity.

Abstract

BACKGROUND: 

The objective of the study was to evaluate the influence of maternally derived antibodies (MDA) on the efficacy of a PRRSV-1 based attenuated vaccine, when administered in 1 day-old piglets by the intramuscular route. The protective immunity of the modified live virus vaccine was evaluated in pigs born from seropositive sows, vaccinated at 1 day of age, upon inoculation with a PRRSV-1 isolate. The animals were challenged when the levels of MDAs detected by seroneutralization test (SNT) in the non-vaccinated control group became undetectable (10 weeks after vaccination).

RESULTS: 

A protective effect of vaccination was observed since a significant reduction of viral load in serum compared to the control group was detected in all sampling days after challenge; efficacy was supported by the significant reduction of nasal and oral shedding as well as in rectal temperatures. Clinical signs were not expected after the inoculation of a PRRSV-1 subtype 1 challenge strain. However, the challenge virus was able to develop fever in 61% of the control pigs. Vaccination had a positive impact on rectal temperatures since the percentage of pigs that had fever at least once after challenge was reduced to 31% in vaccinated animals, and control pigs had significantly higher rectal temperatures than vaccinated pigs 3 days post-challenge. The lack of a vaccination effect in body weight gain was probably due to the short evaluation period after challenge (10 days). In the vaccinated group, 9/16 pigs (56%) experienced an increase in ELISA S/P ratio from the day of vaccination to 67 days post-vaccination. All vaccinated pigs were seropositive before challenge, indicating the development of an antibody response following vaccination even in the face of MDAs. In contrast to ELISA results, only 2/16 vaccinated pigs developed neutralizing antibodies detectable by a SNT that used a subtype 1 MA-104 adapted strain. Even in the absence of SN antibodies, vaccinated pigs were protected from challenge with a heterologous strain. The role of cell-mediated immunity should be considered, if protection was not mediated by SN antibodies only.

CONCLUSIONS: 

The efficacy of the attenuated PRRSV-1 vaccine in 1-day-old pigs seropositive to PRRSV prior to a PRRSV-1 challenge was demonstrated by improvement of clinical, virological and immunological variables. With the current experimental design, maternal immunity did not interfere with the development of a protective immune response against a PRRSV-1 challenge, after vaccination of 1 day-old pigs. Confirmation of these results under field conditions will be needed.

KEYWORDS: 

Maternal-derived immunity; Modified live vaccine; Porcine reproductive and respiratory syndrome
PMID:
 
30459958
 
PMCID:
 
PMC6237022
 
DOI:
 
10.1186/s40813-018-0101-x

Thursday, November 8, 2018

Biosecurity scoring system for PRRS - measure and benchmark vulnerability to PRRS infection!

 2018 Nov 15;160:116-122. doi: 10.1016/j.prevetmed.2018.10.004. Epub 2018 Oct 10.

Development and validation of a scoring system to assess the relative vulnerability of swine breeding herds to the introduction of PRRS virus.

Author information

1
Veterinary Diagnostic and Production Animal Medicine Department, Iowa State University, Ames, IA, United States; Laboratory of Veterinary Epidemiology (Epilab), Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
2
Laboratory of Veterinary Epidemiology (Epilab), Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
3
Veterinary Diagnostic and Production Animal Medicine Department, Iowa State University, Ames, IA, United States.
4
Veterinary Diagnostic and Production Animal Medicine Department, Iowa State University, Ames, IA, United States. Electronic address: holtkamp@iastate.edu.

Abstract

Biosecurity is defined as the set of practices carried out to prevent the introduction and spread of infectious agents in a herd. These practices are essential in swine production, especially for highly infectious agents such as porcine reproductive and respiratory syndrome virus (PRRSv). Even with years of research and experience over the last three decades, PRRSv is still causing productivity losses and is the major health problem affecting the global swine industry. Despite knowledge of the various ways in which the virus can be transmitted from one herd to another (e.g. animals, semen, truck, air, and people), determining the most frequent ways in which the virus is transmitted in the field is difficult. A systematic approach to assess vulnerabilities at a herd level related to PRRSv transmission could help producers prioritize biosecurity practices to reduce or avoid the occurrence of outbreaks. The aim of this study was to develop a biosecurity vulnerability score that represents the relative vulnerability of swine breeding herds to the introduction of PRRSv. To create the biosecurity vulnerability score (outcome), a multi-criteria decision analysis methodology was used to rank and quantify biosecurity practices based on expert opinion. To validate the biosecurity vulnerability score, a survey of biosecurity practices and PRRS outbreak histories in 125 breed-to-wean herds in the U.S. swine industry was used. Data on the frequency of PRRS outbreaks was used to test the hypothesis that biosecurity vulnerability scores were different between farms that have a low incidence of PRRS outbreaks, compared to farms that have a high incidence. In the two databases used, the scores consistently showed that farms with higher scores have a higher frequency of PRRS outbreaks. In the first validation, farms that had never had an outbreak investigation before had a significant (p < 0.02) lower score (0.29; 0.21-0.37) when compared to farms that had 2 or more outbreaks (0.43; 0.39-0.46). In the second, the farms of the control group also had significant (p < 0.004) lower scores (0.30; 0.27-0.33) compared to the case group (0.35; 0.33-0.38). Also, the results suggest that events related to swine movements, transmission by air and water, and people movements should be prioritized. The biosecurity vulnerability scores may be useful to assess vulnerabilities on biosecurity protocols in order to reduce the frequency of PRRS outbreaks and may help producers and veterinarians prioritize investments in improving biosecurity practices over time.

KEYWORDS: 

Biosecurity; Biosecurity vulnerability score; Carrying agents; PRRS; Risk events; Swine farms
PMID:
 
30388993
 
DOI:
 
10.1016/j.prevetmed.2018.10.004