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New whole blood test for toxoplasmosis
Toxoplasma gondii can be found in the faeces of infected cats.
Test could improve maternal-child health outcomes

A new low-cost whole blood test for toxoplasmosis has been developed by researchers at the University of Chicago.

In the study, researchers tested 205 people known to be infected with toxoplasmosis, including pregnant women. The blood was tested using reference tests, standard serum tests and the new whole-blood point of care (POC), obtained by finger stick.

They found that the whole blood test had a 100 per cent agreement with conventional testing and proved highly sensitive (100 per cent) and specific (100 per cent).  The scores also held true for women with lower levels of anti-Toxoplasma antibodies.

"Our work establishes a new point of care test in the outpatient setting at very low cost enabling diagnosis and prompt treatment for toxoplasma infections acquired for the first time during pregnancy,” the authors note.  

“This enables life, sight and cognition saving treatments. If combined with multiplexed testing for other congenital infections and markers associated with premature birth, it will markedly improve maternal-child outcomes and save lives."

Toxoplasmosis is a disease caused by the parasite Toxoplasma gondii. The parasite can be found in undercooked contaminated meat or in the faeces of infected cats.

Transmission of toxoplasmosis from a mother to her unborn child can result in severe congenital problems and fetal death. As such, testing for the parasitic infection during pregnancy is critical.

Current tests for toxoplasmosis are serum tests, which require blood samples to be processed using infrastructure and technology. This can be prohibitive, however, in developing countries and unaffordable in developed countries like the United States.

The study, Rapid, inexpensive, fingerstick, whole-blood, sensitive, specific, point-of-care test for anti-Toxoplasma antibodies, is published in PLOS Neglected Tropical Diseases.

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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. 

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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.