Researchers at the Max Delbrück Center and University Medical Center Hamburg-Eppendorf have traced in skin organoids, how herpes simplex virus 1 infection progresses among neighboring skin cells, deepening our understanding. The work was published in Science Advances.

Low-Res_HSV1

Source: Emanuel Wyler, Max Delbrück Center

A skin organoid infected with herpes simplex virus 1. The virus does not infect all cell types at the same time. Different colors represent different time points of infection by the virus. Dark blue stained cells have just been infected. Yellow indicates cells that were infected at an earlier time point.

Most people think of herpes simplex virus 1 (HSV-1) as a mere cosmetic problem: The virus can cause outbreaks of cold sores on the lips or face, which usually heal on their own within two weeks. But HSV-1 infection can be more sinister. The virus infects sensory nerve cells in the face, where it usually remains dormant. In rare cases, it travels to the central nervous system and causes life-threatening brain inflammation. HSV-1 is also being investigated for potentially playing a role in Alzheimer’s disease — its lifelong persistence in our nervous system may eventually damage nerve cells.

Dr. Emanuel Wyler, a scientist in the RNA Biology and Posttranscriptional Regulation lab at the Max Delbrück Center, has had a longstanding interest in understanding how the virus causes disease. Now he and collaborators at University Medical Center Hamburg-Eppendorf (UKE) have traced step by step how HSV-1 infects the multiple layers of skin cells. Using human hair-bearing skin organoids as a model, the researchers mapped how the virus spreads and which signaling molecules cells release to their neighbors upon being infected.

The research team included Dr. Manja Czech-Sioli, senior author of the paper at the UKE, Dr. Silvia Albertini, co-first author with Wyler, and Dr. Nicole Fischer. Albertini and Fischer are also scientists at UKE.

“It was fascinating to see how the virus spreads through the organoid tissue, from one cell type to another, and also how each cell type responds to it,” adds Czech-Sioli. 

Tracking HSV-1 in 3D skin

Skin is built like a layered sandwich. The protective outermost layer is the epidermis, which primarily consists of keratinocytes. Beneath it sits the dermis, a support layer rich in fibroblasts. Hair follicles pass through these layers, which also contain sensory nerve fibers.

The skin organoids provided by the groups of Manja Czech-Sioli and Nicole Fischer at UKE enabled the team to study infection in a complex, three-dimensional tissue model. While flat cell cultures can reveal how viruses behave in one cell type, these organoids contain many of the features of actual human skin: epidermal cells, dermal cells, hair follicles and nerve-like cells. Consequently, they serve as a better model of how HSV-1 infection progresses. 

The team found that the virus did not infect every type of skin cell in the same way. Fibroblasts in the dermis carried large amounts of virus early during infection. Basal keratinocytes, which sit in the lower epidermis, and several hair follicle cell types carried relatively lower amounts, even when infected cells were nearby. Only later did the virus reach hair follicles and sensory neurons, indicating that both cell types might have some intrinsic resistance to the virus. 

How neighboring cells react to infection  

The researchers then combined imaging with spatial transcriptomics, which measures gene activity in individual cells while preserving their place in tissues. This allowed them to study the leading edge of infection — the zone where HSV-1 had just reached new cells — and identify which genes were switched on. 

At the infection front, dermal fibroblasts switched on IER3, a gene known to respond to HSV-1, for example, and basal keratinocytes increased expression of IRF3, a regulator of antiviral defenses. They also found that members of the Tumor Necrosis Factor (TNF) family of signaling molecules are activated in a spatially coordinated manner. 

“TNFs activate the immune system and may prove to be a major player in determining how well our bodies can control the infection,” explains Wyler. 

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Future organoid models that include immune cells and blood vessels could help researchers study how the body controls HSV-1 before it reaches nerves, why some cells slow the virus while others support replication, and how the infection and the subsequent inflammation damage tissue. 

This study was carried out within the DFG-funded Research Unit 5200, “DEEP-DV: Disrupt–Evade–Exploit – Gene Expression and Host Response Programming in DNA Virus Infection.

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