SARS-CoV-2
WHAT WE DO
SARS-CoV-2 research services at VRS
At VRS, we work with all SARS-CoV-2 variants of concern (Alpha, Beta, Gamma, Delta, and Omicron), early isolates (Wuhan-like), and various Omicron isolates to support antiviral discovery, vaccine development, and host–virus interaction studies.
Additional historical or current strains can also be sourced upon request.
Our assays
SARS-CoV-2 testing services
Virus quantification assays
TCID₅₀ assay and qRT-PCR are available for quantifying infectious virus (TCID₅₀) or total viral genome copies (qRT-PCR) from biological samples and to evaluate the effect of antiviral compounds or other treatments on virus replication and release.
Our TCID₅₀ and qRT-PCR assays are ISO 17025 accredited.
Antiviral and cytotoxicity assays
Antiviral and cytotoxicity assays are available for evaluating compounds against different variants of SARS-CoV-2.
Our antiviral and cytotoxicity assays are ISO 17025 accredited.
Neutralisation assays
Our microneutralisation assay measures the neutralising activity of antibodies, sera and other test articles against different variants of SARS-CoV-2.
Our microneutralisation assays are ISO 17025 accredited.
Air-liquid interface infection models
For studies requiring a highly physiological in vitro model, we have developed both air–liquid interface (ALI) and organoid systems for SARS-CoV-2 infection (Delta and Omicron). These models are ideal for evaluating antiviral compounds and investigating SARS-CoV-2 biology in a setting that closely mimics the human respiratory tract.
Our ALI cultures are generated using primary human bronchial epithelial cells grown at an air–liquid interface, where they differentiate into a pseudostratified respiratory epithelium comprising ciliated cells, mucus-producing goblet cells, and other specialised cell types found in the human airways. This physiologically relevant model provides a powerful platform for studying virus–host interactions, viral pathogenesis, and antiviral efficacy.
Industrial testing (ISO21702, ISO18184, virucidal activity in suspension)
We offer a range of standardised assays to evaluate the antiviral efficacy of non-porous surfaces, textiles, and disinfectant and virucidal products against SARS-CoV-2.
In addition to our standard assays, we can develop bespoke protocols tailored to specific materials, product applications, and SARS-CoV-2 strains, ensuring testing is aligned with your research or product development requirements.
Our ISO21702, ISO18184 and our suspension test are ISO 17025 accredited.
Bespoke studies
VRS also offers bespoke studies, including customised assay development, mechanism-of-action studies, virus characterisation and fundamental virology research.
Case Study: Characterising antibody resistance across SARS-CoV-2 variants
VRS supported an antibody programme from variant screening to escape characterisation: neutralisation assays across successive SARS-CoV-2 variants, resistance selection under antibody pressure, and fitness analysis of the resulting mutants.
Background
What is SARS-CoV-2?
Severe acute respiratory syndrome coronavirus 2, commonly abbreviated as SARS-CoV-2, is an enveloped, positive-sense, single-stranded RNA virus belonging to the family Coronaviridae, subfamily Orthocoronavirinae, and genus Betacoronavirus.
It is the causative agent of coronavirus disease 2019, also known as COVID-19, and has had a major global impact on public health, healthcare systems, and society.
SARS-CoV-2 enters host cells primarily through interaction between the viral spike glycoprotein and host-cell receptors. The spike protein binds to angiotensin-converting enzyme 2, which is expressed on a range of human cell types, including cells of the respiratory tract. Following receptor binding, the spike protein is activated by host proteases, enabling fusion of the viral envelope with host-cell membranes and release of the viral genome into the cytoplasm. Viral replication then occurs in association with modified intracellular membranes, where replication-transcription complexes synthesise viral RNA.
The SARS-CoV-2 genome is approximately 30 kb in length, making it one of the largest RNA virus genomes. It encodes several non-structural proteins involved in viral replication and immune modulation, as well as structural proteins required for virion formation. The main structural proteins are the spike, envelope, membrane, and nucleocapsid proteins. The spike protein is particularly important because it mediates host-cell entry, is a major target of neutralising antibodies, and has been central to vaccine and therapeutic antibody development.
A key feature of SARS-CoV-2 is its ability to evolve through the accumulation of mutations, particularly in the spike gene. These genetic changes have led to the emergence of multiple variants with altered transmissibility, immune escape potential, and, in some cases, disease characteristics. Variants such as Alpha, Beta, Gamma, Delta, and Omicron have demonstrated the capacity of SARS-CoV-2 to adapt under population-level immune pressure. Continued viral evolution highlights the importance of genomic surveillance, variant characterisation, and ongoing assessment of vaccine and antiviral effectiveness.
SARS-CoV-2 is transmitted primarily through respiratory droplets and aerosols produced when infected individuals breathe, talk, cough, or sneeze. Transmission is most efficient in close-contact settings, poorly ventilated indoor environments, and crowded spaces. Infection can cause a wide range of clinical outcomes, from asymptomatic infection to severe respiratory disease and multi-organ complications. Common symptoms include fever, cough, sore throat, fatigue, headache, muscle aches, and loss or alteration of smell or taste, although symptom profiles may vary between individuals and viral variants.
Severe COVID-19 is more likely to occur in older adults, immunocompromised individuals, and people with underlying medical conditions such as cardiovascular disease, chronic respiratory disease, diabetes, obesity, or kidney disease. In severe cases, SARS-CoV-2 infection can lead to viral pneumonia, acute respiratory distress syndrome, thrombo-inflammatory complications, and death. Some individuals also experience prolonged symptoms following acute infection, commonly referred to as long COVID, which may include fatigue, breathlessness, cognitive difficulties, and other persistent health problems.
Since its emergence in late 2019, SARS-CoV-2 has caused hundreds of millions of confirmed infections worldwide and substantial mortality. Beyond its direct clinical impact, the COVID-19 pandemic has placed major pressure on healthcare systems, disrupted economies, and accelerated research into viral diagnostics, vaccines, antivirals, and immune responses. The continuing circulation of SARS-CoV-2 means that it remains an important focus of respiratory virus research and public health surveillance.
Vaccination has played a central role in reducing severe disease, hospitalisation, and death caused by SARS-CoV-2. Several vaccine platforms have been developed, including mRNA vaccines, viral vector vaccines, protein-based vaccines, and inactivated virus vaccines. Antiviral therapies, including polymerase inhibitors and protease inhibitors, are also available for selected patients, particularly those at higher risk of severe disease. However, viral evolution, immune escape, unequal access to interventions, and the persistence of vulnerable populations continue to create challenges for long-term control.
Overall, SARS-CoV-2 is a highly transmissible and adaptable respiratory virus with major clinical, scientific, and public health importance. Its ability to evolve, spread efficiently, and cause disease across diverse populations makes it a continuing priority for antiviral discovery, vaccine development, variant monitoring, and host-virus interaction studies
Frequently Asked Questions
Do you work with live virus?
Yes. All our studies are performed using live, replication-competent wild-type viruses. We maintain a wide range of SARS-CoV-2 isolates, including representatives from all variants of concern.
For SARS-CoV and MERS, we use lentivirus-based pseudotyped reporter virus particles instead, which can be used to study antibodies, sera, or compounds specifically inhibiting virus entry.
Can you work with new virus strains or develop bespoke assays?
Yes. If a required strain is commercially available (or can be supplied by the client), we can acquire, expand and optimise it for your project.
We routinely develop bespoke assays tailored to individual research programmes. We work with both Containment Level 2 (CL2) and Containment Level 3 (CL3) viruses. For new or unusual pathogens, additional biosafety assessments or regulatory approvals may be required before work can begin. We recommend discussing these requirements with us early during project planning to avoid unnecessary delays.
Do you work with other human coronaviruses viruses?
Yes. In addition to SARS-CoV-2, we also work with:
• Human coronavirus NL63
• Human coronavirus 229E
• Human coronavirus OC43
For SARS-CoV and MERS, e use lentivirus-based pseudotyped reporter virus particles instead, which can be used to study antibodies, sera, or compounds specifically inhibiting virus entry.
Why choose VRS for SARS-CoV-2 studies?
VRS has supported SARS-CoV-2 research since the earliest stages of the COVID-19 pandemic, rapidly establishing virus stocks, developing bespoke assays and continuously expanding our capabilities as new variants emerged.
Building on our long-standing expertise with respiratory viruses and seasonal human coronaviruses, we have developed a comprehensive portfolio of assays for SARS-CoV-2, including virus quantification, antiviral and neutralisation assays, resistance studies and bespoke experimental models tailored to specific research objectives.
Our experience extends beyond SARS-CoV-2 to other human coronaviruses, allowing comparative studies and supporting the development of broad-spectrum antiviral and antibody programmes.
Can you adapt existing assays to our specific requirements?
Yes. All experimental work is carried out by our scientific team within our UK laboratories. We do not subcontract laboratory work to third parties.
Where a project requires specialist services outside our scope (for example, peptide synthesis or animal studies), we can coordinate with trusted collaborators while remaining your primary scientific contact throughout the project.
How can I find out more?
You can explore our related resources, including technical articles, case studies and virus-specific services, using the Learn More section above.
If you would like to discuss your project directly, please contact us using our contact form or email vrs@virologyresearchservices.com.
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