Limited Functionality Warning

We are currently updating our network. During this time, certain functionality may be unavailable, including online orders. We apologize for any inconvenience this may cause you.

Please contact Customer Service with any questions or comments.
Phone: (608) 274-4330
Toll-Free Phone: (800) 356-9526
Email: custserv@promega.com
Hours: 7am – 6pm, CST, Monday-Friday

 

 

Emmanuel Heilmann

Institute of Virology Medical
University of Innsbruck

Molecular Virology, drug resistance, viral evolution

Help me to win the Young Researcher
Award 2023 from Promega.

Why should you vote for me!

We are developing exiting new technology to avoid gain-of-function research with dangerous viruses. This technology allows us to prepare for the next pandemic and to fight viral resistance against antiviral drugs

Abstract

In viro veritas – how to predict the future of one virus with another virus

To license an antiviral drug and for endemic as well as pandemic preparedness, it is paramount to study resistance mechanisms of currently circulating and potentially emerging viruses. However, studying dangerous pathogens is difficult due to the necessary safety precautions and, even more importantly, possible alterations of the virus in the laboratory that increase its pathogenicity (also called "gain-of-function" research). Currently, two dangerous Coronaviruses, SARS-CoV-2 and MERS-CoV, are circulating in humans and animals. Whereas SARS-CoV-2 is transmitting between humans since already three years, MERS-CoV so far only jumps occasionally from camels to humans in a process called zoonotic infection. Notably, MERS-CoV seems to be very lethal with estimations going up to 30 % mortality. 

SARS-CoV-2 has seen overwhelming attention of the scientific community and pharmaceutical industry, resulting in the swift development of antiviral drugs, most notably Paxlovid, a combination drug aimed at the “main protease”, an enzyme essential for viral replication. However, sooner or later, viruses develop resistances against antivirals as has been studied intensively with viruses such as HIV, HCV and Influenza. To understand the potential resistance mechanisms and guide treatment decisions, a direct approach is using the authentic viruses themselves. However, using a pandemic virus such as SARS-CoV-2 or an endemic, highly lethal virus such as MERS-CoV in research, poses great challenges. In this study we therefore apply new methods with which the effectiveness of protease inhibitors against a range of main proteases can be assessed and more importantly, mutations against these inhibitors can be predicted safely.
Check award description

Describe the activity of your laboratory in a few lines: 
We are an oncolytic virus lab with a focus on vesicular stomatitis virus (VSV). Since the pandemic, we have also adapted SARS-CoV-2 research topics and coronaviruses in general. My projects are at the intersection of VSV and SARS-CoV-2, because I develop method that use VSV to study aspects of SARS-CoV-2 and more recently also MERS-CoV.

image-emmanuel-heilmann

Tell us something about your scientific background :
I studied Molecular Medicine at the Medical University of Innsbruck. For my bachelor thesis, I started working at the Institute of Virology on VSV, continued as a student assistant and completed my master and doctoral thesis there. First, I developed new methods to control viral replication in a therapeutic setting. VSV is used to treat cancer. Therefore, tight control over its replication is crucial. When the SARS-CoV-2 pandemic started, I shifted to developing technology to study the activity of viral enzymes, how to block them and how to predict mutations of dangerous viruses such as SARS-CoV-2 and MERS-CoV against antiviral drugs.

Can you describe yourself in 3 adjectives?
Driven, quiet, pragmatic 

If you were a famous scientist, who would you be?
John von Neumann

What are your other interests outside of science?
Martial arts, Piano, Foodsharing (environmental organization)