Herpes’ commute into nervous system is aided by a sinister trick.
- Scientists discover how herpes kidnaps protein to infect nervous system
- Opens a door to long-needed HSV1 and HSV2 vaccine
- More than half of U.S. adults are carriers of herpes HSV1
- Virus can cause blindness, life-threatening encephalitis and may contribute to dementia
Herpes type 1 is sealed with a kiss for a lifetime. More than half of U.S. adults are carriers of HSV1 (herpes simplex virus type 1) which hibernates in the peripheral nervous system and can never be eradicated.
A new Northwestern Medicine study published in Nature has uncovered the virus’s sneaky strategy for infecting the nervous system, opening a path to long-needed vaccine development for both HSV1 and its close sibling HSV2.
Some carriers will never even experience so much as a cold sore from HSV1. But for others, it can cause blindness or life-threatening encephalitis. There is increasing evidence it contributes to dementia.
And HSV2, which is more commonly transmitted via sexual contact, can be passed from a mother to newborn during the birthing process as neonatal herpes, appearing as lesions all over the body of the infant. Most babies recover, but in the worst cases, it can cause brain damage or disseminate through all the organs and be lethal.
“We desperately need a vaccine to prevent herpes from invading the nervous system,” said Gregory Smith, PhD, professor of Microbiology-Immunology.
The new study from Smith’s lab has uncovered a route to that. The study discovered how herpes kidnaps a protein from epithelial cells and turns it into a defector to help it travel into the peripheral nervous system. They have termed the process “assimilation.” It’s a discovery that may have wide-ranging implications for many viruses, including HIV and SARS-CoV-2Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the official name of the virus strain that causes coronavirus disease (COVID-19). Previous to this name being adopted, it was commonly referred to as the 2019 novel coronavirus (2019-nCoV), the Wuhan coronavirus, or the Wuhan virus.”>SARS-CoV-2, Smith said.
Riding the rails
“The virus needs to inject its genetic code into the nucleus, so it can start making more herpes viruses,” Smith said. “It reprograms the cell to become a virus factory. The big question is how does it get to the nucleus of a neuron?”
Like many viruses, herpes hops on train tracks in the cell called microtubules and uses protein engines called dynein and kinesin to move along the tracks. Smith’s team discovered herpes uses a kinesin engine that it brings with it from other cells to ferry it to the nucleus in the neuron. That kinesin protein becomes a defector to serve the virus’s purpose.
“By learning how the virus is achieving this incredible feat to get into our nervous system, we can now think about how to take away that ability,” Smith said. “If you can stop it from assimilating kinesin, you would have a virus that couldn’t infect the nervous system. And then you have a candidate for a preventive vaccine.”
Herpes takes a ‘cross-country’ trip
Picture the cell as a rail yard. All tracks lead to the hub called the centrosome. There are two types of train engines: proteins dynein and kinesin. One travels toward the hub — say downtown — and the other leads away from it to the suburbs.
When a more typical virus, such as influenza, infects mucosal epithelial cells (cells that line your nose and mouth), it grabs onto both engines and moves back and forth on the microtubule tracts until it eventually arrives at the nucleus more or less by chance. Overall, going from the suburbs to the nucleus, via the centrosome, is a short commute.
But traveling down nerves is the equivalent of a cross-country journey. Herpes jumps on the dynein engine for this trip, but it also makes sure kinesin engines do not take it back the way it came.
“It’s a long way to go,” Smith said. “It probably takes eight hours for it to travel from the end of the neuron to the hub.”
But the dynein engine can’t take it any further than the hub. And herpes needs to reach the nucleus. That’s when it reaches into its ‘pocket’ and pulls out a kinesin engine that it kidnapped from the mucosal epithelial cells and convinced to become part of its team. And in an act of betrayal, that assimilated kinesin ferries it right to the nucleus.
“This is the first discovery of any virus repurposing a cellular protein and using it to drive subsequent rounds of infection,” said Caitlin Pegg, student in the Driskill Graduate Program in Life Sciences (DGP) and lead author of the study.
“We are excited to further uncover the molecular mechanisms that these viruses have evolved that make them arguably the most successful pathogens known to science,” Smith said.
Reference: “Herpesviruses assimilate kinesin to produce motorized viral particles” by Caitlin E. Pegg, Sofia V. Zaichick, Ewa Bomba-Warczak, Vladimir Jovasevic, DongHo Kim, Himanshu Kharkwal, Duncan W. Wilson, Derek Walsh, Patricia J. Sollars, Gary E. Pickard, Jeffrey N. Savas and Gregory A. Smith, 17 November 2021, Nature.
Other Northwestern contributors to the study are Sofia Zaichick, PhD; and the laboratories of Jeffrey Savas, PhD, assistant professor in the Ken and Ruth Davee Department of Neurology Division of Behavioral Neurology; and Derek Walsh, PhD, professor of Microbiology-Immunology. The laboratories of Duncan Wilson, PhD (Albert Einstein College of Medicine) and Patricia Sollars, PhD and Gary Pickard, PhD (University of Nebraska-Lincoln) also contributed to the study.
Smith is a member of the Robert H. Lurie Comprehensive Cancer Center of Northwestern UniversityEstablished in 1851, Northwestern University (NU) is a private research university based in Evanston, Illinois, United States. Northwestern is known for its McCormick School of Engineering and Applied Science, Kellogg School of Management, Feinberg School of Medicine, Pritzker School of Law, Bienen School of Music, and Medill School of Journalism. ”>Northwestern University.
The research was primarily funded by National Institutes of Health AI056346, with added support from AI125244, AI148780, AI141470 and NS106812, the National Science Foundation and the Cellular and Molecular Basis of Disease Training Grant T32GM08061.