Your data on MRCVSonline
The nature of the services provided by Vision Media means that we might obtain certain information about you.
Please read our Data Protection and Privacy Policy for details.

In addition, (with your consent) some parts of our website may store a 'cookie' in your browser for the purposes of
functionality or performance monitoring.
Click here to manage your settings.
If you would like to forward this story on to a friend, simply fill in the form below and click send.

Your friend's email:
Your email:
Your name:
 
 
Send Cancel

New modified live vaccine for PRRS
Zoetis said the vaccine is safe to be used as the earliest protection in pigets.
Vaccine is safe to use as earliest piglet protection

A new modified live vaccine has been launched for porcine reproductive and respiratory syndrome (PRRS) virus.

Suvaxyn PRRS MLV has been launched in most EU countries. It contains a European PRRS virus strain (genotype 1) that has been grown and attenuated in a uniquely modified cell line, developed by Zoetis.

Research director Jay Calvert explained: “Suvaxyn PRRS MLV is safe based on true loss of virulence, and not based on a temporary reduction in ability to replicate in macrophage cells in the lung of the pig.”

PRRS causes reproductive losses, lowered birth rates, abortions, stillbirths, mummified foetal pigs, weak live-born piglets and deaths. It also causes respiratory disease in pigs, which impacts growth performance and is often complicated with other bacterial and viral co-infections.

Zoetis said it offers whole herd protection against PRRS and is safe to be used as the earliest protection in piglets. Immunity can therefore be achieved before the risk period, which lasts until the end of fattening. Pig protection is established 28 days after vaccination and lasts for 26 weeks in fattening piglets, or 16 weeks in gilts and sows.

Alvaro Aldaz, director of commercial development and innovation, swine, at Zoetis, said the vaccine has been shown to reduce viremia, nasal shedding and lung lesions in fattening pigs, as well as overcoming maternal immunity, which increases the efficacy of the vaccine when given to piglets during the first days of life.

Monica Balasch, associate director of global biologicals development for Zoetis, added: “In clinical studies conducted with Suvaxyn PRRS MLV, we found excellent results vaccinating pigs from the first day of age. It is safe to be used as the earliest protection in piglets, and to protect the whole herd against PRRS, as it is also safe for use in gilts and sows. The new vaccine represents a flexible alternative to allow for new customised PRRS control programs developed by veterinarians for producers.”

The most common side effects (which may affect more than one in 10 pigs) are: short-lived body temperature increase (0.5°C on average, up to 1.4°C) within four days of vaccination; and local reactions in sows (in the form of swellings which resolve without treatment in five to 32 days).

Become a member or log in to add this story to your CPD history

FIVP launches CMA remedies survey

News Story 1
 FIVP has shared a survey, inviting those working in independent practice to share their views on the CMA's proposed remedies.

The Impact Assessment will help inform the group's response to the CMA, as it prepares to submit further evidence to the Inquiry Group. FIVP will also be attending a hearing in November.

Data will be anonymised and used solely for FIVP's response to the CMA. The survey will close on Friday, 31 October 2025. 

Click here for more...
News Shorts
CMA to host webinar exploring provisional decisions

The Competition and Markets Authority (CMA) is to host a webinar for veterinary professionals to explain the details of its provisional decisions, released on 15 October 2025.

The webinar will take place on Wednesday, 29 October 2025 from 1.00pm to 2.00pm.

Officials will discuss the changes which those in practice may need to make if the provisional remedies go ahead. They will also share what happens next with the investigation.

The CMA will be answering questions from the main parties of the investigation, as well as other questions submitted ahead of the webinar.

Attendees can register here before Wednesday, 29 October at 11am. Questions must be submitted before 10am on 27 October.

A recording of the webinar will be accessible after the event.