New progress in research into malignant catarrhal fever in cattle

In 2013, the research team had already demonstrated* that malignant catarrhal fever (MCF), which is fatal in cattle, only develops if the AlHV-1 virus can maintain a latent state replicating its viral genome in CD8+ T lymphocytes without producing viral particles.

In this new study, we used high-throughput sequencing approaches on CD8+ T lymphocytes from sick cattle, compared with healthy animals," explains Benjamin Dewals, a researcher and lecturer at the University of Liège. We were able to characterise the T lymphocyte repertoire (TCR sequencing) as well as the expression of cellular and viral genes specifically regulated during infection."

Discovery of a crucial viral gene

Thanks to these analyses, the team identified a viral gene coding for a protein, called A10, potentially involved in the intracellular signalling of infected cells. This protein turned out to be essential for the development of the disease without affecting viral replication in cell culture," explains Meijiao Gong, PhD student at ULiège and first author of the article published in PNAS (2). In addition, we have shown that phosphorylation of A10 alters the phenotype of T lymphocytes, causing their proliferation and the development of MCF."

The results obtained provide an in-depth description of the reprogramming of CD8+ T cells during infection with AlHV-1 and identify A10 as a key element in the development of MCF. This discovery opens up new perspectives for understanding the mechanisms of malignant lymphoproliferation induced by herpesviruses and provides a promising basis for the development of an effective vaccine against this bovine disease.

"This study represents a significant step forward in our understanding of malignant catarrhal fever and offers hope for the development of a vaccine capable of protecting cattle against this devastating disease," concludes Benjamin Dewals.

* Palmeira et al., An essential role for gamma-herpesvirus latency-associated nuclear antigen homolog in an acute lymphoproliferative disease of cattle, Proceedings of the National Academy of Sciences of the United States of America (PNAS) 2013.