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  • combat
    COMBAT - Updated biosecurity tool with 4 features
  • Cover Guilty Gilt
    The Guilty Gilt Guide
  • PRRS Ctrl
    PRRS Ctrl 2.0
  • prrs-awards-placeholder
    The 11th European PRRS Research Awards
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Expertise article

Active surveillance and monitoring of PRRSV using carcasses

PRRSv continues to cause economic losses to pig producers. Monitoring herds allows us to evaluate the measures taken to control or eradicate the virus.

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Asian PRRSpective | AS 2022

Asian PRRSpective 2022 - Don't miss the first signals. Early detection

Asian PRRSpective 2022 · Drive the health of your herd with GLOBAL PRRS SOLUTIONS

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Expertise article

Cell-mediated immune response and protective efficacy of porcine reproductive and respiratory syndrome virus modified-live vaccines against co-challenge with PRRSV-1 and PRRSV-2

Cell-mediated immunity (CMI), IL-10, and the protective efficacy of modified-live porcine reproductive and respiratory syndrome virus (PRRSV) vaccines (MLV) against co-challenge with PRRSV-1 and PRRSV-2 (HP-PRRSV) were investigated. Seventy, PRRSV-free, 3-week old, pigs were allocated into 7 groups. Six groups were intramuscularly vaccinated with MLV, including Porcilis (PRRSV-1 MLV, MSD Animal Health, The Netherlands), Amervac (PRRSV-1 MLV, Laboratorios Hipra, Spain), Fostera (PRRSV-2 MLV, Zoetis, USA), Ingelvac PRRS MLV and Ingelvac PRRS ATP (PRRSV-2, Boehringer Ingelheim, USA), and Prime Pac PRRS (PRRSV-2 MLV, MSD Animal Health, The Netherlands). Unvaccinated pigs were left as control. Lymphocyte proliferative response, IL-10 and IFN-γ production were determined. At 35 days post-vaccination (DPV), all pigs were inoculated intranasally with 2 ml of each PRRSV-1 (105.4 TCID50/ml) and PRRSV-2 (105.2 TCID50/ml, HP-PRRSV). Following challenge, sera were quantitatively assayed for PRRSV RNA. Pigs were necropsied at 7 days post-challenge. Viremia, macro- and microscopic lung lesion together with PRRSV antigen presence were evaluated in lung tissues. The results demonstrated that, regardless of vaccine genotype, CMI induced by all MLVs was relatively slow. Increased production of IL-10 in all vaccinated groups was observed at 7 and 14 DPV. Pigs in Amervac, Ingelvac MLV and Ingelvac ATP groups had significantly higher levels of IL-10 compared to Porcilis, Fostera and Prime Pac groups at 7 and 14 DPV. Following challenge, regardless to vaccine genotype, vaccinated pigs had significantly lower lung lesion scores and PRRSV antigens than those in the control group. Both PRRSV-1 and PRRSV-2 RNA were significantly reduced. Prime Pac pigs had lowest PRRSV-1 and PRRSV-2 RNA in serum, and micro- and macroscopic lung lesion scores (p < 0.05) compared to other vaccinated groups. In conclusion, PRRSV MLVs, regardless of vaccine genotype, can reduce viremia and lung lesions following co-challenge with PRRSV-1 and PRRSV-2 (HP-PRRSV). The main difference between PRRSV MLV is the production of IL-10 following vaccination.

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Bite size

For PCR testing, what kind of samples should be used?

Meet the Expert Bite Sizes with Tomasz Trela.

Day 1 - Parvovirus. A remerging pathogen

Day 1 - Parvovirus. A remerging pathogen

Virtual PRRSpective 2020 on demand

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Expertise article

Performance improvement after using Ingelvac PRRS MLV against EU type infection

Two-site production farm with 500 sows located in South Korea.

The efficacy of Ingelvac PRRS MLV administered in 7-week-old piglets was assessed in a grow-finish farm infected with PRRSV1 and secondary bacteria.

The group of pigs vaccinated with Ingelvac PRRS MLV showed better performance and less clinical signs.

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Bite size

Where do we start controlling ASF. Is it with the pigs or the people?

Meet the Expert Bite Sizes with Klaus Depner.

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Expertise article | APVS 2011

Efficacy of Ingelvac®PRRS MLV on HP PRRS control in a farm of Northeast China

In this control case, after confirming PRRS infection, the use of Ingelvac®PRRS MLV proved to be effective in reducing both morbidity and post-weaning mortality as well as days to market