Completed Cells, Biochemistry & Physiology Infection & Immunity

Characterisation of herpes simplex virus morphogenesis by tracking the virus tegument through the secretory pathway

In plain English

AI plain-English summary

Herpes simplex virus particles, each less than a thousandth of a millimetre across, assemble themselves inside human cells by travelling through a hidden cellular highway—and this project will track that journey in real time. The virus causes cold sores and genital herpes, but in transplant patients, people on chemotherapy, and newborns it can lead to fatal brain inflammation or meningitis. No one knows exactly how the virus’s internal structure—its tegument—comes together inside a living cell. Without that knowledge, designing drugs that block assembly at an early stage remains guesswork. The team will use genetically modified viruses carrying fluorescent markers, then follow individual particles with time-lapse microscopy as they move through cultured cells. This will reveal where and in what order the tegument forms. This is fundamental science. It will not produce a new drug tomorrow. But understanding the virus’s assembly line inside a cell is the kind of basic knowledge that, in the past, has allowed researchers to identify weak points in other viruses and design antivirals against them. A clearer picture of HSV morphogenesis could eventually open routes to therapies that stop the virus before it ever becomes infectious.

View original technical description
Herpes simplex virus (HSV) infects humans causing the sporadic appearance of cold sores or genital herpes. Serious complications of HSV infection, including encephalitis and meningitis, are potentially fatal in transplant patients, individuals undergoing chemotherapy, and newborn babies. To understand how HSV infection causes these diseases it is essential to find out how the virus grows in individual cells in the body. This proposal aims to study how single virus particles of HSV, that are less than one thousandth of a millimetre in diameter, assemble themselves inside the cell. The research will be carried out using viruses that have been modified to contain coloured markers that light up under a microscope. This allows individual viruses to be observed and followed in living cells. In this way, the journey that viruses make through the inside of a cell grown in culture in the laboratory can be traced using time-lapse microscopy. This approach will allow us to address the fundamental questions of how and where in a single cell the virus structure comes together. The resulting answers will then be applied to understanding virus infection in the human host.

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Researchers

Gill Elliott (Principal Investigator)

Related Research

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Characterisation of novel virus-host cell interactions essential for herpes simplex virus envelopment
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Differential targeting of the HSV1 vhs endoribonuclease - preferential degradation of cellular transcripts on the endoplasmic reticulum?
Mechanism of HSV-1 pUL51/pUL7 focal adhesion stabilization

Original classification

Fellowship

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