Identifying the Key Protein for Tick-Borne Encephalitis Virus Infection: A Major Step Forward

Understanding Tick-Borne Encephalitis Virus Infection



Recent research has revealed critical information regarding the mechanism of infection caused by tick-borne encephalitis virus (TBEV), a pathogen transmitted primarily by ticks. Scientists from the Albert Einstein College of Medicine, in collaboration with the Karolinska Institutet and the United States Army Medical Research Institute of Infectious Diseases (USAMRIID), have successfully identified a key protein on human cells that facilitates this viral entry. This groundbreaking discovery not only adds to our understanding of how TBEV causes neurological ailments but also charts a promising course toward the development of antiviral drugs.

The Study Findings



The paper detailing these findings was published in Nature and represents a significant advancement in the understanding of flavivirus infections, including other known viruses such as dengue, Zika, and yellow fever. According to Dr. Kartik Chandran, one of the study's co-leaders, this research is pivotal because it identifies essential protein receptors that flaviviruses exploit to initiate infection.

Understanding the role of these proteins is crucial for designing targeted therapies against not only TBEV but also other related viruses that pose significant health risks across the globe.

Growing Threat of TBEV



TBEV is prevalent in Northern, Central and Eastern Europe, and parts of Central and East Asia, where it causes approximately 10,000 documented cases each year, resulting in severe neurological diseases. The increasing geographical spread of ticks—carriers of this virus—heightens the potential for TBEV infections as they move into new territories. Despite the availability of some vaccines, accessibility remains a challenge in lower-income countries where TBEV is endemic, and no specific treatment exists for infected individuals.

Research Approach



To pinpoint the receptor for TBEV, researchers employed a methodology involving a human cell line. They developed a

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