09/15/2022
Dr. Jae Jung will study the natural course of infection and viral reassortment of the emerging pathogen, Severe Fever with Thrombocytopenia Syndrome Virus (SFTSV).
Cleveland Clinic has been awarded a five-year, $2.9 million grant from the National Institute of Allergy and Infectious Diseases (NIAID) at the National Institutes of Health (NIH) to study Severe Fever with Thrombocytopenia Syndrome Virus (SFTSV).
Led by Jae Jung, PhD, Director of Cleveland Clinic's Global Center for Pathogen & Human Health Research, a team will study the natural course of SFTSV infection and tick-borne virus reassortment, which is the process of genetic recombination that is exclusive to segmented ribonucleic acid (RNA) viruses.
SFTSV has been included on a World Health Organization (WHO) list of emerging pathogens most likely to cause a future pandemic. The current fatality rate of SFTSV stands at 12 to 30%, with spread occurring from tick-to-animal/human, human-to-human and animal-to-human contact. Infected Asian longhorned ticks, Haemaphysalis (H.) longicornis, carry the virus, which has been contracted only in Southeast Asia to date.
"We already have a virus similar to SFTSV in the U.S., the heartland virus, which is caused by lonestar ticks. SFTSV itself has not yet been identified in the U.S., but ticks are present, with the first longhorn tick identified in New Jersey in 2018," says Dr. Jung.
In 2020, Dr. Jung pioneered research to develop a vaccine for SFTSV after receiving a $2.8 million grant from the NIAID. His team was able to isolate and sequence 133 different SFTSV strains from 3,000 patients, which helped provide insight into the immunogenicity and protection efficacy in preclinical models. Additionally, in 2021, Dr. Jung used patient samples to discover the possibility of inflammatory biomarkers to help identify patients at the greatest risk for severe disease and death from SFTSV.
Building on his previous work, including a vaccine study that developed a protein nanoparticle vaccine for SFTSV, researchers will now aim to identify the phenotypic changes in the fitness, transmissibility, antigenicity and pathogenicity into progeny reassortants. Once identified, infected models will be treated with the vaccine to see if it effectively blocks infection. This will be done in vitro and in vivo to bridge basic research to clinical application. By identifying the multiple combinations of the three-segment SFTSV reassortment, Dr. Jung and his team can further develop methods to combat the mutations.
The research is occurring within Cleveland Clinic's Global Center for Pathogen & Human Health Research – a cornerstone of the Cleveland Innovation District, offering a home for virus and immune discovery, personalized medicine and diagnostic testing to help multidisciplinary research teams understand the response of the human immune system to viral pathogens. As part of the Cleveland Innovation District, Cleveland Clinic is planning significant expansion of research facilities, including a biosafety level 3 (BSL-3) lab, currently under construction to facilitate research on microbes and pathogens that can cause serious or potentially lethal threats to public health, such as SFTSV.
This team includes Young-Ki Choi, PhD, Chungbuk University, who has extensive expertise in RNA virology and preclinical SFTSV models, and Younho Choi, PhD, Florida Research & Innovation Center, who uses a reverse genetic approach to generate new and mutant viruses of SFTSV to define viral pathogenesis and develop vaccines.
Director, Global Center for Pathogen & Human Health Research
Department Chair, Cancer Biology
Director, Infection Biology
Betsy B. deWindt Endowed Chair in Cancer Biology
Lab Profile
Assistant Staff
Lab Profile
Using patient samples, Dr. Jung and his team uncovered inflammatory biomarkers associated with severe disease and death caused by SFTSV infection, and identified the critical role B cells play in infection.
Dr. Jung's endowed chair will support his research into infectious diseases and virus-induced cancers.
Dr. Jung and his team defined the molecular mechanisms that underlie fetal brain calcification caused by Zika virus infection, most notably identifying the role of the protease NS3 in driving the virus-induced abnormal brain development.
The future of health starts with your support. Donations supply researchers with the tools, space and staff they need to think big.
Give to Cleveland Clinic