From left, Uddhav Timilsina, PhD; Thomas Melendy, PhD; and Rama Dey-Rao, PhD; are the key developers of the new screening method. 

Easing Screening Process for COVID-19 Antiviral Drugs

Published November 30, 2021

A team of researchers in the Jacobs School of Medicine and Biomedical Sciences has developed a new, high-throughput screening method designed to quickly screen antiviral candidates against the SARS-CoV2 virus.

“Our contribution was to create this screening method so that many, even thousands, of compounds with activity against SARS-CoV2 can be screened rapidly in just hours or days versus weeks or months using other methods. ”
Professor of microbiology and immunology and senior author on paper
Print

Described in a paper published in October in Antiviral Research, the screening method is designed to identify a certain class of antiviral drugs that inhibit the main protease (Mpro), a specific SARS-CoV2 target.

Developing a Faster Way to Screen Antiviral Drugs

Twenty months into the pandemic, the need for antiviral drugs targeted against COVID-19 is clear, given the global persistence of the virus, its ability to rapidly mutate into new variants and the possibility that it could potentially develop strains resistant to existing drugs or vaccines.

But developing antivirals can take many years; the examples of hepatitis C, HIV and human papilloma virus (HPV) all illustrate the myriad difficulties involved with such efforts. The combination of antivirals that eventually proved effective in curing hepatitis C virus, for example, were under development for decades.

The new study was developed by a team of University at Buffalo scientists led by Rama Dey-Rao, PhD, first author and research assistant professor, and Thomas Melendy, PhD, senior author and professor, both in the Department of Microbiology and Immunology.

The Jacobs School researchers reported that their screening assay fulfilled several important goals:

  • it expresses fully mature, functional SARS-CoV-2 Mpro, whereas most other efforts have expressed slightly altered forms, which are not optimal for drug screening
  • it can evaluate Mpro function in living human cells
  • the system is designed so that inhibition of the Mpro produces a positive signal in a living cell; systems that produce a negative signal require further screening to identify false-positives caused by cell toxicity

Sharing Resources During Global Pandemic

“Our contribution was to create this screening method so that many, even thousands, of compounds with activity against SARS-CoV2 can be screened rapidly in just hours or days versus weeks or months using other methods,” says Melendy, who also has an appointment in the Department of Biochemistry.

He adds that UB, like most research universities, has agreed to make resources like this for the pandemic easily available to others to utilize. 

The new screening method identifies antivirals that inhibit an enzyme called the main protease, which is necessary in order for SARS-CoV2 to replicate. Once the virus gets into a cell, the Mpro is critical to being able to produce the other viral enzymes required to function inside the infected cell in order to create more virus and viral spread.

Quicker Searching for Protease Inhibitors

The advantage of the UB screening method is that it eliminates several steps usually involved in screening for antiviral drugs.

Melendy explains that in most cases, inhibitors of viral enzymes are developed by finding and designing molecules that first target the viral enzyme in a test tube. From there, additional testing must be done to determine its toxicity, its ability to get inside human cells and, once inside them, its effectiveness.

After that, he continues, the drug candidates need to be tested against viral infection of human cells, which requires a biosafety level-3 facility requiring high-level containment because of the dangers involved in working with live virus. Because testing against live virus is dangerous, it is very expensive and more time-consuming. As a result, it is not amenable to rapid screening of large collections of compounds.

“By contrast, the system we’ve developed uses just the viral Mpro, not the whole infectious virus expressed in human cells, so it ‘isolates’ that one viral target,” Melendy says.  “When the Mpro is functional, the cells will express a biosensor that is cleaved by the Mpro. But if an effective inhibitor of the viral Mpro (a potential antiviral drug) is added to these cells, the biosensor is not cleaved, and the cells will fluoresce red.”

“Since there is no live virus involved in the high-throughput screening, the system does not require the expensive and risky BSL-3 bio-containment,” Dey-Rao notes.

“And since the entire process occurs inside the living cultured cells, it demonstrates that any inhibitors identified must be functional in living cells,” Melendy adds.  

Advantageous to Treat With Drug ‘Cocktails’

Once an inhibitor is identified, the next steps would be to test it against viral infection of human cells, in animal models, and then in clinical trials.

Uddhav Timilsina, PhD, a postdoctoral associate working in a group headed by Spyridon Stavrou, PhD, assistant professor of microbiology and immunology, verified that this cell-based system works and that the one drug tested that did inhibit the Mpro in the UB assay showed similar inhibition of SARS-CoV2 infection of human lung cells.

The ability to screen thousands of compounds efficiently is key, because a single antiviral drug usually isn’t effective enough. As has been seen with HIV and HCV, the SARS-CoV2 virus will likely also require combinations or “cocktails” of antivirals.

“Antivirals are not ‘perfect,’ and viruses can mutate and become resistant to antivirals,” Melendy explains. “Therefore, it is more effective to develop more than one drug against specific viral target proteins. It’s also highly advantageous to treat individuals with a ‘cocktail’ of more than one antiviral drug.”

He adds that patients with persistent infections with some strains of HCV are now effectively cured using a combination of antivirals, inhibitors of the hepatitis C viral genome replicase — another type of viral enzyme — and the hepatitis C viral protease.

Melendy notes that the Merck SARS-CoV2 antiviral that has been submitted to the U.S. Food and Drug Administration is an inhibitor of the SARS-CoV2 genome replicase.

“Combining it with an inhibitor of the SARS-CoV-2 Mpro would likely provide a more effective therapy,” he says.

SARS-CoV2 Expected to Become Endemic

Melendy adds that with most public health experts expecting SARS-CoV2 to become endemic in the global population, continuing to circulate, causing disease and death; then antiviral drugs, along with vaccines, will be a key part of dealing with this pandemic.

“Having more than one antiviral drug that works against more than one viral target will be critical in dealing with outbreaks especially if  drug-resistant variants emerge, because such viruses would only be resistant to one class of antivirals,” he says.

Along with Dey-Rao, Melendy, Stavrou and Timilsina, additional co-authors in the Jacobs School are:

The work was funded in part by the National Institutes of Health, a SUNY Research Foundation COVID research seed grant award, the Jacobs School, the Department of Microbiology and Immunology and contributions by donors to the UB Foundation’s Papillomavirus Research Fund (which has been redirected to research on SARS-CoV2 during the ongoing pandemic).