Go to Top

Researchers at UNM Discover SARS-CoV-2 Coronavirus Interferes with Autophagy Process

A team at the University of New Mexico recently published a paper in the science journal, Cell, which helps explain how autophagy, the fundamental biological process by which cells break down and destroy old or damaged cells, functions in mammalian and human cells and how the SARS-CoV-2 coronavirus can interfere with this process.

The UNM team is led by Dr. Vojo Deretic, a distinguished professor and director of UNM’s Autophagy, Inflammation & Metabolism (AIM) Center of Biomedical Research Excellence. In their paper, “Mammalian hybrid pre-autophagosomal structure HyPAS generates autophagosomes,” they describe how two proteins found on separate cell membranes merge together to form hybrid pre-autophagosomal structures (HyPAS). This process is key in developing autophagosomes, which contain cellular material slated to be degraded by autophagy. Until now, the process of HyPAS formation was not well understood, and their findings help map out key details of how autophagy functions.

Perhaps even more surprising was when the researchers found that the SARS-CoV-2 coronavirus can interfere with the autophagy process. By hiding within a cell membrane, so that the systems within the cell won’t find it, it can inhibit autophagy that would naturally occur when a cell is infected with a virus.

See Michael Haederle’s November 22 article, “Viral Visitation,” on the UNM Health Sciences Newsroom Website here: https://hsc.unm.edu/news/2021/11/autophagy-researchers-covid-infection-hijack-cellular-process.html and reposted below.

See also the research article, “Mammalian hybrid pre-autophagosomal structure HyPAS generates autophagosomes,” on the Cell Website here: https://www.cell.com/cell/fulltext/S0092-8674(21)01233-2

Viral Visitation

By Michael Haederle

UNM Autophagy Researchers Discover SARS-CoV-2 Infection Hijacks Key Cellular Process

The intricate biological process known as autophagy plays a vital role in keeping our cells healthy and functioning by sweeping up and recycling bits of debris and invading micro-organisms.

Until recently, much of what was known about autophagy was based on studies of yeast cells, work that in 2016 led to a Nobel Prize for Japanese researcher Yoshinori Ohsumi.

Now, a team headed by Vojo Deretic, PhD, distinguished professor and director of The University of New Mexico’s Autophagy, Inflammation & Metabolism (AIM) Center of Biomedical Research Excellence, has mapped out key details of how autophagy functions in mammals – including humans.

And, in a startling finding, the researchers provide evidence showing that SARS-CoV-2 infection can disrupt the process.

“This underscores the significance of autophagy as a process,” Deretic says of the new research. “The field is struggling to understand how it works in mammalian and human cells.”

In a paper published this month in the journal Cell, he and his colleagues describe how two proteins – FIP200 and ATG16L1 – that reside on different cell membranes merge to form “hybrid pre-autophagosomal structures” (HyPAS).

This is a key step in the development of autophagosomes, spherical structures that engulf damaged proteins, bacteria, viruses and other debris, and transport them to lysosomes, where enzymes break the material down into molecules that can be reused.

“Autophagy depends on the formation of these membranes inside the cell,” Deretic says. “Until now, we didn’t know where those membranes were coming from. They just magically appeared – so this is the magic.”

Because the process of HyPAS formation had not been well described, the scientists who reviewed the paper prior to its publication were skeptical. “It took a lot of experiments to establish the HyPAS with reviewers,” he says. “It was submitted last year in August, so it takes a while to develop something like that.”

The research team, which included scientists in Norway, Iceland and Finland, as well as at the University of Virginia and University of California, Davis, were surprised to find that the SARS-CoV-2 coronavirus interferes with the autophagy process, Deretic says.

Cells have powerful innate immune mechanisms to recognize viruses trying to replicate in their interior cytoplasm, Deretic says, but the coronavirus has found a sneaky way to reproduce. “SARS-CoV-2 hijacks the cellular membrane. This is its big secret,” he says.

“If the virus is to be successful, it needs to hide inside the membranes, so that these systems that exist inside the cell won’t find it,” he says. “It’s inhibiting autophagy so that it can use the membranes for its own nefarious work. They’re clever little things.”

The project was a team effort, Deretic says, crediting colleagues in the AIM Center, along with Steve Bradfute, PhD, assistant professor in the UNM Center for Global Health, Graham Timmins, PhD, professor in the UNM College of Pharmacy, and members of the UNM Department of Physics & Astronomy.

The AIM Center, which was founded with $11.5 million in Phase 1 funding from the National Institutes of Health (NIH), is seeking nearly $11 million in additional money for Phase 2, he says. Junior faculty supported by the center have brought in another $10 million to fund their individual research projects.

Deretic, who also serves as chair of UNM’s Department of Molecular Genetics & Microbiology, is supported by an NIH R37 Method to Extend Research in Time (MERIT) award, which provided funding for the Cell study.