G2P-UK; A National Virology Consortium to address phenotypic consequences of SARSCoV-2 genomic variation

Lead Research Organisation: Imperial College London
Department Name: Infectious Disease

Abstract

There have been almost 100 million cases of SARS-CoV-2 infections world-wide, with more than two million deaths to date. It seems certain that this virus will permanently establish itself in the human population and become endemic, meaning that multiple strategies and measures will be needed to prevent, control and treat SARS-CoV-2 infections for the foreseeable future.
For all viral infections, the outcomes in terms of disease, recovery, viral persistence or onward transmission are dictated by the balance between virus replication and the immune responses of the infected individuals. As SARS-CoV-2 continues to circulate in people this balance will change over time; On one hand the virus that emerged from an animal source may further adapt to its new human host and on the other hand the acquired immune response in the human population will accumulate potentially limiting viral spread.
New variants of SARS CoV-2 with mutations in the genome (different 'genotype') will emerge and some may have altered biological properties ("phenotype"): including transmitting between humans more readily, exacerbating or attenuating disease and mortality, spreading to other animal species (to establish non-human reservoirs) or evading human immunity that is acquired through natural infection or vaccination. The latter is a particular concern at this moment in time given that population-level immunity is increasing as a result of high virus circulation and vaccination programs. Many variants of SARS-CoV-2 are now appearing globally, and the rational assessment of the risks they pose to society requires an evidence-based scientific understanding of any causative changes in biological properties.

The Genotype-to-Phenotype UK National Virology Consortium (G2P-UK) will address this critical knowledge gap by leveraging the combined virological expertise of ten leading research centres to undertake a suite of directed and complementary experimental tests that will link SARS-CoV-2 sequence variation to virus behaviour and function. Tests will include the detailed assessments of virus growth using a series of laboratory models of infection, susceptibility of viruses to inhibition by human immune mechanisms including antibodies, evaluations of the functionality of individual virus proteins, and virus propagation and transmissibility using established small animal models. Co-ordination within G2P will be achieved through upfront agreed methodologies and standards, the free exchange of materials, specimens and know-how, regular scientific meetings and a dedicated consortium website.

SARS-CoV-2 variants of concern that warrant focused investigation will be prioritised through co-ordinated workings with scientists at another consortium, COG-UK, who are responsible for virus surveillance and keeping track of emerging virus variants. Variants of concern will be selected on criteria that include altered disease outcomes, rapid emergence or spread, infections in the context of pre-existing immunity, apparent or inferred escape from immunity, or resistance to anti-viral drugs.G2P will also engage closely with other key UK organisations and scientific consortia including UK-wide Public Health laboratories and UK-CIC (Coronavirus Immunology Consortium), as well as other leading groups working in the UK and internationally, to gather the most holistic and incisive evaluation of the biological phenotypes of variants of concern and the associated risks they carry. These conclusions will be shared rapidly and openly with key groups such as NERVTAG and SAGE to inform national pandemic management and strategies for patient treatment, diagnostics, population-level surveillance, infection control and vaccination.

Technical Summary

SARS-CoV-2 has caused 1.4 million deaths and has devastated economies worldwide. As SARS-CoV-2 replicates and spreads, its RNA genome inevitably mutates. Mutations may confer altered properties of potential concern to human health, such as increased pathogenicity or transmissibility, or reduced sensitivity to prior immunity or antiviral drugs. Importantly, the imminent roll out of vaccination campaigns could provide strong selection pressure for escape from vaccine-induced immunity.

We are a consortium ("G2P-UK") of UK virologists who will work openly with COG-UK and UK-CiC, to establish an experimental pipeline and shared resources (reagents, methodologies and model systems) to rapidly define the phenotypic impacts of SARS-CoV-2 mutations as they emerge. With three interconnected work packages we will obtain and distribute clinical isolates and engineered SARS-CoV-2 mutants (WP1), test the functional properties of the mutations in in vitro assays (WP2) and characterise their phenotype in culture and animal model systems (WP3).

The choice of strains and mutations will be informed by a joint working group that includes COG-UK members. Current virus strains will be immediately introduced into the pipeline, to accumulate a baseline of underpinning knowledge about SARS-CoV-2 behaviour, to validate the consortium working relationships and to seed mechanistic studies suitable for further research. Then, as variants of concern are detected, they will be prioritized for co-ordinated investigation in real time.

By interpreting the biological consequences of SARS-CoV-2 mutations we will inform on the associated risks and vulnerabilities related to public health policy and clinical practice, including treatment strategies, diagnostics and infection control, and vaccination.

Publications

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Carabelli AM (2023) SARS-CoV-2 variant biology: immune escape, transmission and fitness. in Nature reviews. Microbiology

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Dicks MDJ (2022) Modular capsid decoration boosts adenovirus vaccine-induced humoral immunity against SARS-CoV-2. in Molecular therapy : the journal of the American Society of Gene Therapy

 
Title False coloured SEM images of virus infected cells 
Description Multiple false coloured SEM images taken by Dr Steve Gschmeissner of SARS-CoV-2, HIV-1, Hep C and other virus infected cell samples produced and fixed in the Towers lab. 
Type Of Art Image 
Year Produced 2022 
Impact These images are available for sale to the press and often are used in news articles and as illustrations in books. https://sciencephotogallery.com/art/gschmeissner 
 
Description As horizon scanning identifies emerging new SARS-CoV-2 variants of concern (VOC) such as Delta, Lambda and Mu and the Delta subvariant AY4.2 and Omicron, G2P-UK have isolated virus from clinical swabs, generated spike plasmids and Reverse Genetics mutant viruses which have been distributed at speed throughout the consortium for phenotypic analysis. Data is then shared with UKHSA as part of their risk assessment.
We have shown in small animal models that the Delta variant is more severe than the Alpha variant and that is shows 100% transmission. Delta shows increased replication in primary human airway epithelial (HAE) cells. Data from neutralisation tests using sera from vaccinated cohorts have shown that Beta variant is less neutralised than Alpha and Delta. Preliminary Omicron studies have shown that vaccination ( 2 doses and 3 doses) can neutralise Omicron, but not that well compared to Alpha and Delta variants. Omicron can replicate faster than Delta in nasal epithelium.
Exploitation Route The outcomes of this funding are currently being used by UKHSA to risk assess new and emerging SARS-CoV-2 variants
Sectors Government, Democracy and Justice

 
Description Members of the G2P-UK consortium have been providing information to expert groups (SAGE, NERVTAG, Variant Technical Group, 'COVID-19 nMABs Access and Policy National Expert Group') and the media on the SARS-CoV-2 variants Information. Data from G2P-UK are presented at the weekly PHE Variant Technical Group which forms part of the risk assessment for emerging VOCs. Media contributions by G2P-UK investigators have enhanced the general public's understanding of the currents risk posed by variants of concern as well as the benefits of vaccination.
First Year Of Impact 2021
Sector Government, Democracy and Justice
Impact Types Societal,Policy & public services

 
Description 1st South African Workshop on SARS-CoV-2 Variants and Evolution St Lucia, 31st October - 3 rd November Talk: Covid-19 Epidemiology: Understanding SARS CoV2 transmission, from hamsters to humans
Geographic Reach Multiple continents/international 
Policy Influence Type Influenced training of practitioners or researchers
Impact Advisory - sharing ideas and giving and receiving information
 
Description APPG Parliamentary reception on 'Tackling COVID-19: Recognising the exceptional research response: 14th March 2022
Geographic Reach National 
Policy Influence Type Participation in a guidance/advisory committee
Impact Recognition from MP's and Govt
 
Description EUROPEAN COVID SCIENTIFIC ADVISORS MEETING COVID-19 European Scientific Council Meeting
Geographic Reach Europe 
Policy Influence Type Influenced training of practitioners or researchers
Impact Advisor
 
Description JCVI COVID-19 vaccines main meeting 12 May 2022
Geographic Reach National 
Policy Influence Type Participation in a guidance/advisory committee
Impact Advisory
 
Description Participation on NICE Panel
Geographic Reach National 
Policy Influence Type Participation in a guidance/advisory committee
 
Description SAGE COVID 19
Geographic Reach National 
Policy Influence Type Participation in a guidance/advisory committee
Impact Advisor on COVID 19
 
Description Technical coordination meeting: Novel Variants
Geographic Reach National 
Policy Influence Type Contribution to a national consultation/review
Impact Techinical Scientifc participant
 
Description The French National Research Agency for AIDS, hepatitis adn emerging infectious disease Talk: Determinants of transmission of respiratory viruses.
Geographic Reach Multiple continents/international 
Policy Influence Type Influenced training of practitioners or researchers
Impact Sharing information
 
Description Vaccine Effectiveness Expert Panel Cabinet office regular meeting
Geographic Reach National 
Policy Influence Type Participation in a guidance/advisory committee
Impact Nationwide Vaccine expert panel organisation and consultation to the Cabnet office
 
Description Vaccine Science Coordination Meeting
Geographic Reach National 
Policy Influence Type Participation in a guidance/advisory committee
Impact Acted as Chair 2021 - 2022
 
Description Weekly reporting to the UKHSA Variant Technical Group
Geographic Reach National 
Policy Influence Type Participation in a guidance/advisory committee
 
Description CONTRIBUTION TO THE NATIONAL CORE STUDY ON TRANSMISSION OF SARS-COV-2 THEME 5 EM39 and EM59
Amount £955,405 (GBP)
Organisation Health and Safety Executive (HSE) 
Sector Public
Country United Kingdom
Start 04/2021 
End 03/2022
 
Description G2P-UK; A National Virology Consortium to address phenotypic consequences of SARSCoV-2 genomic variation- 1 year project extension
Amount £1,524,763 (GBP)
Funding ID MR/W005611/1 
Organisation Medical Research Council (MRC) 
Sector Public
Country United Kingdom
Start 08/2022 
End 07/2023
 
Description Investigation of proven vaccine breakthrough by SARS-CoV-2 variants in established UK healthcare worker cohorts: SIREN consortium & PITCH Plus Pathway
Amount £1,585,765 (GBP)
Funding ID MR/W02067X/1 
Organisation Medical Research Council (MRC) 
Sector Public
Country United Kingdom
Start 08/2021 
End 08/2022
 
Description From Science to Policy: UK and France Symposium on COVID-19 Vaccines 
Organisation Academy of Medical Sciences (AMS)
Country United Kingdom 
Sector Charity/Non Profit 
PI Contribution Vaccination has been central to the response to the COVID-19 pandemic in both the UK and France. In December 2021, the UK Academy of Medical Sciences and the French Académie Nationale de Médecine convened a joint meeting to compare experiences in the two countries. The purpose of the meeting was to discuss the lessons learned from the vaccination policies implemented in both the UK and France and to examine the role of science in influencing policy..
Collaborator Contribution In December 2021, the UK Academy of Medical Sciences and the French Académie Nationale de Médecine jointly convened a workshop to consider responses to the pandemic in the two countries, with a particular focus on vaccination strategies and the role of science in influencing policymaking. The workshop provided an opportunity to share experiences and to learn lessons that could be applied to the next phase of the COVID-19 pandemic or future public health emergencies.
Impact N/A
Start Year 2021
 
Description G2P-UK 
Organisation Francis Crick Institute
Country United Kingdom 
Sector Academic/University 
PI Contribution Prof Wendy Barclay is currently leading and managing the G2P-UK consortium. This involves both project management and financial management of the award. The Barclay lab have generated a library of pseudovirus plasmids of SARS-CoV-2 variants (all pcDNA 3.1, codon optimised, un-tagged, delta 19) and panels of virus isolates representing the main Variants of Concern (VOCs), Variants under Investigation (VUIs) as well as other variants to evaluate neutralising capability. These have been distributed to the G2P-UK consortium and to other research groups in the UK, USA, Spain, Sweden and Italy. The Barclay Lab has also isolated and propagated SARS-CoV-2 viruses from clinical swabs which have been distributed to the G2P consortium for live virus neutralising assays, immune evasions studies and in vivo experiments.
Collaborator Contribution Glasgow University (CVR)-CVR has adopted a reverse genetic system for SARS-CoV-2 and developed a pipeline for the generation of recombinant viruses for the whole consortium. Pirbright Institute- have worked closely with UKHSA to examine the neutralising antibody response to SARS-CoV-2 variants in elderly UK populations, achievable through access to sera from UKHSA's CONSENSUS audit. King's College, London-The KCL team have expertise in viral neutralisation to collect and characterise sera from vaccinees, infected persons and vaccinees who have been infected for their neutralisation capabilities against the Spike proteins of VOCs as they emerge. UCL-have established SARS-CoV-2 replication assays in cell lines and primary airway cultures that recapitulate the innate immune response seen in human disease. The Francis Crick Institute- have gathered >2000 sera from diverse cohorts (general population, healthcare workers, extremely clinically vulnverable) collected longitudinally as vaccine rollout has progressed for assessment using "gold standard" live virus-neutralisation against VOCs as they have emerged (Alpha, Delta, Omicron); Data has been used by PHE/UKHSA, JCVI, and others to inform public heath response and vaccination policy. Cambridge University are using biopsy derived intestinal organoids, expanding to include primary airway epithelial cells, to examine the impact of VOC mutations on viral replication Oxford University-have established polymerase assays using purified recombinant proteins and performed phenotypic characterisation of mutations in non-structural proteins (nsp) of SARS-CoV-2. University of Bristol- are analysing mutations in VOCs using reverse genetics to dissect individual mutations University of Liverpool are evaluating and comparibg the disease profile and transmissibility of future variants in animal models as well as developing software to quantify SARS-CoV-2 (and any other coronavirus) transcription from sequencing data and identify new subgenomic mRNAs
Impact As horizon scanning identifies emerging new SARS-CoV-2 variants of concern (VOC) such as Delta, Lambda and Mu and the Delta subvariant AY4.2 and Omicron, G2P-UK have isolated virus from clinical swabs, generated spike plasmids and Reverse Genetics mutant viruses which have been distributed at speed throughout the consortium for phenotypic analysis. Data is then shared with UKHSA as part of their risk assessment. We have shown in small animal models that the Delta variant is more severe than the Alpha variant and that is shows 100% transmission. Delta shows increased replication in primary human airway epithelial (HAE) cells. Data from neutralisation tests using sera from vaccinated cohorts have shown that Beta variant is less neutralised than Alpha and Delta. Preliminary Omicron studies have shown that vaccination ( 2 doses and 3 doses) can neutralise Omicron, but not that well compared to Alpha and Delta variants. Omicron can replicate faster than Delta in nasal epithelium.
Start Year 2021
 
Description G2P-UK 
Organisation King's College London
Country United Kingdom 
Sector Academic/University 
PI Contribution Prof Wendy Barclay is currently leading and managing the G2P-UK consortium. This involves both project management and financial management of the award. The Barclay lab have generated a library of pseudovirus plasmids of SARS-CoV-2 variants (all pcDNA 3.1, codon optimised, un-tagged, delta 19) and panels of virus isolates representing the main Variants of Concern (VOCs), Variants under Investigation (VUIs) as well as other variants to evaluate neutralising capability. These have been distributed to the G2P-UK consortium and to other research groups in the UK, USA, Spain, Sweden and Italy. The Barclay Lab has also isolated and propagated SARS-CoV-2 viruses from clinical swabs which have been distributed to the G2P consortium for live virus neutralising assays, immune evasions studies and in vivo experiments.
Collaborator Contribution Glasgow University (CVR)-CVR has adopted a reverse genetic system for SARS-CoV-2 and developed a pipeline for the generation of recombinant viruses for the whole consortium. Pirbright Institute- have worked closely with UKHSA to examine the neutralising antibody response to SARS-CoV-2 variants in elderly UK populations, achievable through access to sera from UKHSA's CONSENSUS audit. King's College, London-The KCL team have expertise in viral neutralisation to collect and characterise sera from vaccinees, infected persons and vaccinees who have been infected for their neutralisation capabilities against the Spike proteins of VOCs as they emerge. UCL-have established SARS-CoV-2 replication assays in cell lines and primary airway cultures that recapitulate the innate immune response seen in human disease. The Francis Crick Institute- have gathered >2000 sera from diverse cohorts (general population, healthcare workers, extremely clinically vulnverable) collected longitudinally as vaccine rollout has progressed for assessment using "gold standard" live virus-neutralisation against VOCs as they have emerged (Alpha, Delta, Omicron); Data has been used by PHE/UKHSA, JCVI, and others to inform public heath response and vaccination policy. Cambridge University are using biopsy derived intestinal organoids, expanding to include primary airway epithelial cells, to examine the impact of VOC mutations on viral replication Oxford University-have established polymerase assays using purified recombinant proteins and performed phenotypic characterisation of mutations in non-structural proteins (nsp) of SARS-CoV-2. University of Bristol- are analysing mutations in VOCs using reverse genetics to dissect individual mutations University of Liverpool are evaluating and comparibg the disease profile and transmissibility of future variants in animal models as well as developing software to quantify SARS-CoV-2 (and any other coronavirus) transcription from sequencing data and identify new subgenomic mRNAs
Impact As horizon scanning identifies emerging new SARS-CoV-2 variants of concern (VOC) such as Delta, Lambda and Mu and the Delta subvariant AY4.2 and Omicron, G2P-UK have isolated virus from clinical swabs, generated spike plasmids and Reverse Genetics mutant viruses which have been distributed at speed throughout the consortium for phenotypic analysis. Data is then shared with UKHSA as part of their risk assessment. We have shown in small animal models that the Delta variant is more severe than the Alpha variant and that is shows 100% transmission. Delta shows increased replication in primary human airway epithelial (HAE) cells. Data from neutralisation tests using sera from vaccinated cohorts have shown that Beta variant is less neutralised than Alpha and Delta. Preliminary Omicron studies have shown that vaccination ( 2 doses and 3 doses) can neutralise Omicron, but not that well compared to Alpha and Delta variants. Omicron can replicate faster than Delta in nasal epithelium.
Start Year 2021
 
Description G2P-UK 
Organisation The Pirbright Institute
Country United Kingdom 
Sector Academic/University 
PI Contribution Prof Wendy Barclay is currently leading and managing the G2P-UK consortium. This involves both project management and financial management of the award. The Barclay lab have generated a library of pseudovirus plasmids of SARS-CoV-2 variants (all pcDNA 3.1, codon optimised, un-tagged, delta 19) and panels of virus isolates representing the main Variants of Concern (VOCs), Variants under Investigation (VUIs) as well as other variants to evaluate neutralising capability. These have been distributed to the G2P-UK consortium and to other research groups in the UK, USA, Spain, Sweden and Italy. The Barclay Lab has also isolated and propagated SARS-CoV-2 viruses from clinical swabs which have been distributed to the G2P consortium for live virus neutralising assays, immune evasions studies and in vivo experiments.
Collaborator Contribution Glasgow University (CVR)-CVR has adopted a reverse genetic system for SARS-CoV-2 and developed a pipeline for the generation of recombinant viruses for the whole consortium. Pirbright Institute- have worked closely with UKHSA to examine the neutralising antibody response to SARS-CoV-2 variants in elderly UK populations, achievable through access to sera from UKHSA's CONSENSUS audit. King's College, London-The KCL team have expertise in viral neutralisation to collect and characterise sera from vaccinees, infected persons and vaccinees who have been infected for their neutralisation capabilities against the Spike proteins of VOCs as they emerge. UCL-have established SARS-CoV-2 replication assays in cell lines and primary airway cultures that recapitulate the innate immune response seen in human disease. The Francis Crick Institute- have gathered >2000 sera from diverse cohorts (general population, healthcare workers, extremely clinically vulnverable) collected longitudinally as vaccine rollout has progressed for assessment using "gold standard" live virus-neutralisation against VOCs as they have emerged (Alpha, Delta, Omicron); Data has been used by PHE/UKHSA, JCVI, and others to inform public heath response and vaccination policy. Cambridge University are using biopsy derived intestinal organoids, expanding to include primary airway epithelial cells, to examine the impact of VOC mutations on viral replication Oxford University-have established polymerase assays using purified recombinant proteins and performed phenotypic characterisation of mutations in non-structural proteins (nsp) of SARS-CoV-2. University of Bristol- are analysing mutations in VOCs using reverse genetics to dissect individual mutations University of Liverpool are evaluating and comparibg the disease profile and transmissibility of future variants in animal models as well as developing software to quantify SARS-CoV-2 (and any other coronavirus) transcription from sequencing data and identify new subgenomic mRNAs
Impact As horizon scanning identifies emerging new SARS-CoV-2 variants of concern (VOC) such as Delta, Lambda and Mu and the Delta subvariant AY4.2 and Omicron, G2P-UK have isolated virus from clinical swabs, generated spike plasmids and Reverse Genetics mutant viruses which have been distributed at speed throughout the consortium for phenotypic analysis. Data is then shared with UKHSA as part of their risk assessment. We have shown in small animal models that the Delta variant is more severe than the Alpha variant and that is shows 100% transmission. Delta shows increased replication in primary human airway epithelial (HAE) cells. Data from neutralisation tests using sera from vaccinated cohorts have shown that Beta variant is less neutralised than Alpha and Delta. Preliminary Omicron studies have shown that vaccination ( 2 doses and 3 doses) can neutralise Omicron, but not that well compared to Alpha and Delta variants. Omicron can replicate faster than Delta in nasal epithelium.
Start Year 2021
 
Description G2P-UK 
Organisation University College London
Country United Kingdom 
Sector Academic/University 
PI Contribution Prof Wendy Barclay is currently leading and managing the G2P-UK consortium. This involves both project management and financial management of the award. The Barclay lab have generated a library of pseudovirus plasmids of SARS-CoV-2 variants (all pcDNA 3.1, codon optimised, un-tagged, delta 19) and panels of virus isolates representing the main Variants of Concern (VOCs), Variants under Investigation (VUIs) as well as other variants to evaluate neutralising capability. These have been distributed to the G2P-UK consortium and to other research groups in the UK, USA, Spain, Sweden and Italy. The Barclay Lab has also isolated and propagated SARS-CoV-2 viruses from clinical swabs which have been distributed to the G2P consortium for live virus neutralising assays, immune evasions studies and in vivo experiments.
Collaborator Contribution Glasgow University (CVR)-CVR has adopted a reverse genetic system for SARS-CoV-2 and developed a pipeline for the generation of recombinant viruses for the whole consortium. Pirbright Institute- have worked closely with UKHSA to examine the neutralising antibody response to SARS-CoV-2 variants in elderly UK populations, achievable through access to sera from UKHSA's CONSENSUS audit. King's College, London-The KCL team have expertise in viral neutralisation to collect and characterise sera from vaccinees, infected persons and vaccinees who have been infected for their neutralisation capabilities against the Spike proteins of VOCs as they emerge. UCL-have established SARS-CoV-2 replication assays in cell lines and primary airway cultures that recapitulate the innate immune response seen in human disease. The Francis Crick Institute- have gathered >2000 sera from diverse cohorts (general population, healthcare workers, extremely clinically vulnverable) collected longitudinally as vaccine rollout has progressed for assessment using "gold standard" live virus-neutralisation against VOCs as they have emerged (Alpha, Delta, Omicron); Data has been used by PHE/UKHSA, JCVI, and others to inform public heath response and vaccination policy. Cambridge University are using biopsy derived intestinal organoids, expanding to include primary airway epithelial cells, to examine the impact of VOC mutations on viral replication Oxford University-have established polymerase assays using purified recombinant proteins and performed phenotypic characterisation of mutations in non-structural proteins (nsp) of SARS-CoV-2. University of Bristol- are analysing mutations in VOCs using reverse genetics to dissect individual mutations University of Liverpool are evaluating and comparibg the disease profile and transmissibility of future variants in animal models as well as developing software to quantify SARS-CoV-2 (and any other coronavirus) transcription from sequencing data and identify new subgenomic mRNAs
Impact As horizon scanning identifies emerging new SARS-CoV-2 variants of concern (VOC) such as Delta, Lambda and Mu and the Delta subvariant AY4.2 and Omicron, G2P-UK have isolated virus from clinical swabs, generated spike plasmids and Reverse Genetics mutant viruses which have been distributed at speed throughout the consortium for phenotypic analysis. Data is then shared with UKHSA as part of their risk assessment. We have shown in small animal models that the Delta variant is more severe than the Alpha variant and that is shows 100% transmission. Delta shows increased replication in primary human airway epithelial (HAE) cells. Data from neutralisation tests using sera from vaccinated cohorts have shown that Beta variant is less neutralised than Alpha and Delta. Preliminary Omicron studies have shown that vaccination ( 2 doses and 3 doses) can neutralise Omicron, but not that well compared to Alpha and Delta variants. Omicron can replicate faster than Delta in nasal epithelium.
Start Year 2021
 
Description G2P-UK 
Organisation University of Bristol
Country United Kingdom 
Sector Academic/University 
PI Contribution Prof Wendy Barclay is currently leading and managing the G2P-UK consortium. This involves both project management and financial management of the award. The Barclay lab have generated a library of pseudovirus plasmids of SARS-CoV-2 variants (all pcDNA 3.1, codon optimised, un-tagged, delta 19) and panels of virus isolates representing the main Variants of Concern (VOCs), Variants under Investigation (VUIs) as well as other variants to evaluate neutralising capability. These have been distributed to the G2P-UK consortium and to other research groups in the UK, USA, Spain, Sweden and Italy. The Barclay Lab has also isolated and propagated SARS-CoV-2 viruses from clinical swabs which have been distributed to the G2P consortium for live virus neutralising assays, immune evasions studies and in vivo experiments.
Collaborator Contribution Glasgow University (CVR)-CVR has adopted a reverse genetic system for SARS-CoV-2 and developed a pipeline for the generation of recombinant viruses for the whole consortium. Pirbright Institute- have worked closely with UKHSA to examine the neutralising antibody response to SARS-CoV-2 variants in elderly UK populations, achievable through access to sera from UKHSA's CONSENSUS audit. King's College, London-The KCL team have expertise in viral neutralisation to collect and characterise sera from vaccinees, infected persons and vaccinees who have been infected for their neutralisation capabilities against the Spike proteins of VOCs as they emerge. UCL-have established SARS-CoV-2 replication assays in cell lines and primary airway cultures that recapitulate the innate immune response seen in human disease. The Francis Crick Institute- have gathered >2000 sera from diverse cohorts (general population, healthcare workers, extremely clinically vulnverable) collected longitudinally as vaccine rollout has progressed for assessment using "gold standard" live virus-neutralisation against VOCs as they have emerged (Alpha, Delta, Omicron); Data has been used by PHE/UKHSA, JCVI, and others to inform public heath response and vaccination policy. Cambridge University are using biopsy derived intestinal organoids, expanding to include primary airway epithelial cells, to examine the impact of VOC mutations on viral replication Oxford University-have established polymerase assays using purified recombinant proteins and performed phenotypic characterisation of mutations in non-structural proteins (nsp) of SARS-CoV-2. University of Bristol- are analysing mutations in VOCs using reverse genetics to dissect individual mutations University of Liverpool are evaluating and comparibg the disease profile and transmissibility of future variants in animal models as well as developing software to quantify SARS-CoV-2 (and any other coronavirus) transcription from sequencing data and identify new subgenomic mRNAs
Impact As horizon scanning identifies emerging new SARS-CoV-2 variants of concern (VOC) such as Delta, Lambda and Mu and the Delta subvariant AY4.2 and Omicron, G2P-UK have isolated virus from clinical swabs, generated spike plasmids and Reverse Genetics mutant viruses which have been distributed at speed throughout the consortium for phenotypic analysis. Data is then shared with UKHSA as part of their risk assessment. We have shown in small animal models that the Delta variant is more severe than the Alpha variant and that is shows 100% transmission. Delta shows increased replication in primary human airway epithelial (HAE) cells. Data from neutralisation tests using sera from vaccinated cohorts have shown that Beta variant is less neutralised than Alpha and Delta. Preliminary Omicron studies have shown that vaccination ( 2 doses and 3 doses) can neutralise Omicron, but not that well compared to Alpha and Delta variants. Omicron can replicate faster than Delta in nasal epithelium.
Start Year 2021
 
Description G2P-UK 
Organisation University of Cambridge
Country United Kingdom 
Sector Academic/University 
PI Contribution Prof Wendy Barclay is currently leading and managing the G2P-UK consortium. This involves both project management and financial management of the award. The Barclay lab have generated a library of pseudovirus plasmids of SARS-CoV-2 variants (all pcDNA 3.1, codon optimised, un-tagged, delta 19) and panels of virus isolates representing the main Variants of Concern (VOCs), Variants under Investigation (VUIs) as well as other variants to evaluate neutralising capability. These have been distributed to the G2P-UK consortium and to other research groups in the UK, USA, Spain, Sweden and Italy. The Barclay Lab has also isolated and propagated SARS-CoV-2 viruses from clinical swabs which have been distributed to the G2P consortium for live virus neutralising assays, immune evasions studies and in vivo experiments.
Collaborator Contribution Glasgow University (CVR)-CVR has adopted a reverse genetic system for SARS-CoV-2 and developed a pipeline for the generation of recombinant viruses for the whole consortium. Pirbright Institute- have worked closely with UKHSA to examine the neutralising antibody response to SARS-CoV-2 variants in elderly UK populations, achievable through access to sera from UKHSA's CONSENSUS audit. King's College, London-The KCL team have expertise in viral neutralisation to collect and characterise sera from vaccinees, infected persons and vaccinees who have been infected for their neutralisation capabilities against the Spike proteins of VOCs as they emerge. UCL-have established SARS-CoV-2 replication assays in cell lines and primary airway cultures that recapitulate the innate immune response seen in human disease. The Francis Crick Institute- have gathered >2000 sera from diverse cohorts (general population, healthcare workers, extremely clinically vulnverable) collected longitudinally as vaccine rollout has progressed for assessment using "gold standard" live virus-neutralisation against VOCs as they have emerged (Alpha, Delta, Omicron); Data has been used by PHE/UKHSA, JCVI, and others to inform public heath response and vaccination policy. Cambridge University are using biopsy derived intestinal organoids, expanding to include primary airway epithelial cells, to examine the impact of VOC mutations on viral replication Oxford University-have established polymerase assays using purified recombinant proteins and performed phenotypic characterisation of mutations in non-structural proteins (nsp) of SARS-CoV-2. University of Bristol- are analysing mutations in VOCs using reverse genetics to dissect individual mutations University of Liverpool are evaluating and comparibg the disease profile and transmissibility of future variants in animal models as well as developing software to quantify SARS-CoV-2 (and any other coronavirus) transcription from sequencing data and identify new subgenomic mRNAs
Impact As horizon scanning identifies emerging new SARS-CoV-2 variants of concern (VOC) such as Delta, Lambda and Mu and the Delta subvariant AY4.2 and Omicron, G2P-UK have isolated virus from clinical swabs, generated spike plasmids and Reverse Genetics mutant viruses which have been distributed at speed throughout the consortium for phenotypic analysis. Data is then shared with UKHSA as part of their risk assessment. We have shown in small animal models that the Delta variant is more severe than the Alpha variant and that is shows 100% transmission. Delta shows increased replication in primary human airway epithelial (HAE) cells. Data from neutralisation tests using sera from vaccinated cohorts have shown that Beta variant is less neutralised than Alpha and Delta. Preliminary Omicron studies have shown that vaccination ( 2 doses and 3 doses) can neutralise Omicron, but not that well compared to Alpha and Delta variants. Omicron can replicate faster than Delta in nasal epithelium.
Start Year 2021
 
Description G2P-UK 
Organisation University of Glasgow
Department MRC - University of Glasgow Centre for Virus Research
Country United Kingdom 
Sector Academic/University 
PI Contribution Prof Wendy Barclay is currently leading and managing the G2P-UK consortium. This involves both project management and financial management of the award. The Barclay lab have generated a library of pseudovirus plasmids of SARS-CoV-2 variants (all pcDNA 3.1, codon optimised, un-tagged, delta 19) and panels of virus isolates representing the main Variants of Concern (VOCs), Variants under Investigation (VUIs) as well as other variants to evaluate neutralising capability. These have been distributed to the G2P-UK consortium and to other research groups in the UK, USA, Spain, Sweden and Italy. The Barclay Lab has also isolated and propagated SARS-CoV-2 viruses from clinical swabs which have been distributed to the G2P consortium for live virus neutralising assays, immune evasions studies and in vivo experiments.
Collaborator Contribution Glasgow University (CVR)-CVR has adopted a reverse genetic system for SARS-CoV-2 and developed a pipeline for the generation of recombinant viruses for the whole consortium. Pirbright Institute- have worked closely with UKHSA to examine the neutralising antibody response to SARS-CoV-2 variants in elderly UK populations, achievable through access to sera from UKHSA's CONSENSUS audit. King's College, London-The KCL team have expertise in viral neutralisation to collect and characterise sera from vaccinees, infected persons and vaccinees who have been infected for their neutralisation capabilities against the Spike proteins of VOCs as they emerge. UCL-have established SARS-CoV-2 replication assays in cell lines and primary airway cultures that recapitulate the innate immune response seen in human disease. The Francis Crick Institute- have gathered >2000 sera from diverse cohorts (general population, healthcare workers, extremely clinically vulnverable) collected longitudinally as vaccine rollout has progressed for assessment using "gold standard" live virus-neutralisation against VOCs as they have emerged (Alpha, Delta, Omicron); Data has been used by PHE/UKHSA, JCVI, and others to inform public heath response and vaccination policy. Cambridge University are using biopsy derived intestinal organoids, expanding to include primary airway epithelial cells, to examine the impact of VOC mutations on viral replication Oxford University-have established polymerase assays using purified recombinant proteins and performed phenotypic characterisation of mutations in non-structural proteins (nsp) of SARS-CoV-2. University of Bristol- are analysing mutations in VOCs using reverse genetics to dissect individual mutations University of Liverpool are evaluating and comparibg the disease profile and transmissibility of future variants in animal models as well as developing software to quantify SARS-CoV-2 (and any other coronavirus) transcription from sequencing data and identify new subgenomic mRNAs
Impact As horizon scanning identifies emerging new SARS-CoV-2 variants of concern (VOC) such as Delta, Lambda and Mu and the Delta subvariant AY4.2 and Omicron, G2P-UK have isolated virus from clinical swabs, generated spike plasmids and Reverse Genetics mutant viruses which have been distributed at speed throughout the consortium for phenotypic analysis. Data is then shared with UKHSA as part of their risk assessment. We have shown in small animal models that the Delta variant is more severe than the Alpha variant and that is shows 100% transmission. Delta shows increased replication in primary human airway epithelial (HAE) cells. Data from neutralisation tests using sera from vaccinated cohorts have shown that Beta variant is less neutralised than Alpha and Delta. Preliminary Omicron studies have shown that vaccination ( 2 doses and 3 doses) can neutralise Omicron, but not that well compared to Alpha and Delta variants. Omicron can replicate faster than Delta in nasal epithelium.
Start Year 2021
 
Description G2P-UK 
Organisation University of Liverpool
Country United Kingdom 
Sector Academic/University 
PI Contribution Prof Wendy Barclay is currently leading and managing the G2P-UK consortium. This involves both project management and financial management of the award. The Barclay lab have generated a library of pseudovirus plasmids of SARS-CoV-2 variants (all pcDNA 3.1, codon optimised, un-tagged, delta 19) and panels of virus isolates representing the main Variants of Concern (VOCs), Variants under Investigation (VUIs) as well as other variants to evaluate neutralising capability. These have been distributed to the G2P-UK consortium and to other research groups in the UK, USA, Spain, Sweden and Italy. The Barclay Lab has also isolated and propagated SARS-CoV-2 viruses from clinical swabs which have been distributed to the G2P consortium for live virus neutralising assays, immune evasions studies and in vivo experiments.
Collaborator Contribution Glasgow University (CVR)-CVR has adopted a reverse genetic system for SARS-CoV-2 and developed a pipeline for the generation of recombinant viruses for the whole consortium. Pirbright Institute- have worked closely with UKHSA to examine the neutralising antibody response to SARS-CoV-2 variants in elderly UK populations, achievable through access to sera from UKHSA's CONSENSUS audit. King's College, London-The KCL team have expertise in viral neutralisation to collect and characterise sera from vaccinees, infected persons and vaccinees who have been infected for their neutralisation capabilities against the Spike proteins of VOCs as they emerge. UCL-have established SARS-CoV-2 replication assays in cell lines and primary airway cultures that recapitulate the innate immune response seen in human disease. The Francis Crick Institute- have gathered >2000 sera from diverse cohorts (general population, healthcare workers, extremely clinically vulnverable) collected longitudinally as vaccine rollout has progressed for assessment using "gold standard" live virus-neutralisation against VOCs as they have emerged (Alpha, Delta, Omicron); Data has been used by PHE/UKHSA, JCVI, and others to inform public heath response and vaccination policy. Cambridge University are using biopsy derived intestinal organoids, expanding to include primary airway epithelial cells, to examine the impact of VOC mutations on viral replication Oxford University-have established polymerase assays using purified recombinant proteins and performed phenotypic characterisation of mutations in non-structural proteins (nsp) of SARS-CoV-2. University of Bristol- are analysing mutations in VOCs using reverse genetics to dissect individual mutations University of Liverpool are evaluating and comparibg the disease profile and transmissibility of future variants in animal models as well as developing software to quantify SARS-CoV-2 (and any other coronavirus) transcription from sequencing data and identify new subgenomic mRNAs
Impact As horizon scanning identifies emerging new SARS-CoV-2 variants of concern (VOC) such as Delta, Lambda and Mu and the Delta subvariant AY4.2 and Omicron, G2P-UK have isolated virus from clinical swabs, generated spike plasmids and Reverse Genetics mutant viruses which have been distributed at speed throughout the consortium for phenotypic analysis. Data is then shared with UKHSA as part of their risk assessment. We have shown in small animal models that the Delta variant is more severe than the Alpha variant and that is shows 100% transmission. Delta shows increased replication in primary human airway epithelial (HAE) cells. Data from neutralisation tests using sera from vaccinated cohorts have shown that Beta variant is less neutralised than Alpha and Delta. Preliminary Omicron studies have shown that vaccination ( 2 doses and 3 doses) can neutralise Omicron, but not that well compared to Alpha and Delta variants. Omicron can replicate faster than Delta in nasal epithelium.
Start Year 2021
 
Description G2P-UK 
Organisation University of Oxford
Department Oxford Hub
Country United Kingdom 
Sector Academic/University 
PI Contribution Prof Wendy Barclay is currently leading and managing the G2P-UK consortium. This involves both project management and financial management of the award. The Barclay lab have generated a library of pseudovirus plasmids of SARS-CoV-2 variants (all pcDNA 3.1, codon optimised, un-tagged, delta 19) and panels of virus isolates representing the main Variants of Concern (VOCs), Variants under Investigation (VUIs) as well as other variants to evaluate neutralising capability. These have been distributed to the G2P-UK consortium and to other research groups in the UK, USA, Spain, Sweden and Italy. The Barclay Lab has also isolated and propagated SARS-CoV-2 viruses from clinical swabs which have been distributed to the G2P consortium for live virus neutralising assays, immune evasions studies and in vivo experiments.
Collaborator Contribution Glasgow University (CVR)-CVR has adopted a reverse genetic system for SARS-CoV-2 and developed a pipeline for the generation of recombinant viruses for the whole consortium. Pirbright Institute- have worked closely with UKHSA to examine the neutralising antibody response to SARS-CoV-2 variants in elderly UK populations, achievable through access to sera from UKHSA's CONSENSUS audit. King's College, London-The KCL team have expertise in viral neutralisation to collect and characterise sera from vaccinees, infected persons and vaccinees who have been infected for their neutralisation capabilities against the Spike proteins of VOCs as they emerge. UCL-have established SARS-CoV-2 replication assays in cell lines and primary airway cultures that recapitulate the innate immune response seen in human disease. The Francis Crick Institute- have gathered >2000 sera from diverse cohorts (general population, healthcare workers, extremely clinically vulnverable) collected longitudinally as vaccine rollout has progressed for assessment using "gold standard" live virus-neutralisation against VOCs as they have emerged (Alpha, Delta, Omicron); Data has been used by PHE/UKHSA, JCVI, and others to inform public heath response and vaccination policy. Cambridge University are using biopsy derived intestinal organoids, expanding to include primary airway epithelial cells, to examine the impact of VOC mutations on viral replication Oxford University-have established polymerase assays using purified recombinant proteins and performed phenotypic characterisation of mutations in non-structural proteins (nsp) of SARS-CoV-2. University of Bristol- are analysing mutations in VOCs using reverse genetics to dissect individual mutations University of Liverpool are evaluating and comparibg the disease profile and transmissibility of future variants in animal models as well as developing software to quantify SARS-CoV-2 (and any other coronavirus) transcription from sequencing data and identify new subgenomic mRNAs
Impact As horizon scanning identifies emerging new SARS-CoV-2 variants of concern (VOC) such as Delta, Lambda and Mu and the Delta subvariant AY4.2 and Omicron, G2P-UK have isolated virus from clinical swabs, generated spike plasmids and Reverse Genetics mutant viruses which have been distributed at speed throughout the consortium for phenotypic analysis. Data is then shared with UKHSA as part of their risk assessment. We have shown in small animal models that the Delta variant is more severe than the Alpha variant and that is shows 100% transmission. Delta shows increased replication in primary human airway epithelial (HAE) cells. Data from neutralisation tests using sera from vaccinated cohorts have shown that Beta variant is less neutralised than Alpha and Delta. Preliminary Omicron studies have shown that vaccination ( 2 doses and 3 doses) can neutralise Omicron, but not that well compared to Alpha and Delta variants. Omicron can replicate faster than Delta in nasal epithelium.
Start Year 2021
 
Description Contribution to a Nature article Omnicron 
Form Of Engagement Activity A magazine, newsletter or online publication
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Postgraduate students
Results and Impact Prof Wendy Barclay was interviewed for an article in Nature-Omicron's lasting mysteries-four questions scientists are racing to answer
https://www.nature.com/articles/d41586-022-00428-5
Year(s) Of Engagement Activity 2022
 
Description Contribution to a Scientific American article on omicron 
Form Of Engagement Activity A magazine, newsletter or online publication
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Postgraduate students
Results and Impact Prof Wendy Barclay contributed to an article in Scientific American about the SARS-CoV-2 Omicron variant.
https://www.scientificamerican.com/article/omicrons-surprising-anatomy-explains-why-it-is-wildly-contagious/
Year(s) Of Engagement Activity 2022
 
Description Contribution to article in BMJ 
Form Of Engagement Activity A magazine, newsletter or online publication
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Postgraduate students
Results and Impact Prof Wendy Barclay contributed to an article in the BMJ How similar is covid-19 to the flu?
https://www.bmj.com/content/379/bmj.o2625
Year(s) Of Engagement Activity 2022
 
Description Contribution to article on Imperial College Website Two years of COVID 
Form Of Engagement Activity A magazine, newsletter or online publication
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Postgraduate students
Results and Impact Prof Wendy Barclay was interviewed for an article on the Imperial College website-Two years of COVID-19: what's next for the pandemic
https://www.imperial.ac.uk/stories/two-years-of-covid/
Year(s) Of Engagement Activity 2022
 
Description EMBO-EMBL SYMPOSIUM: talk in Heidelberg Innate Immunity in Host-Pathogen Interactions. 
Form Of Engagement Activity A talk or presentation
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Industry/Business
Results and Impact Talk
Year(s) Of Engagement Activity 2022
 
Description Guest speaker at the Australasian Virology Society 
Form Of Engagement Activity A talk or presentation
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Postgraduate students
Results and Impact Prof Barclay was invited to be a guest speaker at the Australasian Virology Society (5-8th December 2022) to give a presentation about Antivirals and Vaccines.
Year(s) Of Engagement Activity 2022
 
Description ICL, UKHSA, & LSHTM and National Institute for Health Research (NIHR) Health Protection Research Unit in Modelling and Health Economics Independent Scientific Advisory Board Meetin 
Form Of Engagement Activity A formal working group, expert panel or dialogue
Part Of Official Scheme? No
Geographic Reach National
Primary Audience Policymakers/politicians
Results and Impact Advisory
Year(s) Of Engagement Activity 2022
 
Description Interview for LBC radio 
Form Of Engagement Activity A press release, press conference or response to a media enquiry/interview
Part Of Official Scheme? No
Geographic Reach National
Primary Audience Media (as a channel to the public)
Results and Impact Omicron and Christmas - Prof Greg Towers was interviewed with Professor Chris Smith from Cambridge University by LBC's Eddie Mair, Dec 2021. This discussion was about Omicron and provided information for the listeners on this new variant of concern.
Year(s) Of Engagement Activity 2021
 
Description Interview with BBC Hugh Pym - Why Omicron is creating so many new cases and what's likely to happen in the future? 
Form Of Engagement Activity A press release, press conference or response to a media enquiry/interview
Part Of Official Scheme? No
Geographic Reach National
Primary Audience Other audiences
Results and Impact Prof Wendy Barclay was interviewed for the BBC by Hugh Pym to discuss "why Omicron is creating so many new
cases and what's likely to happen in the future."
Year(s) Of Engagement Activity 2022
 
Description Interview with NTV 
Form Of Engagement Activity A press release, press conference or response to a media enquiry/interview
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Media (as a channel to the public)
Results and Impact Prof Greg Towers was interview by Russian TV station NTV for his opinions of Omicron and Vaccination. This provided information to the Russian Public.
Year(s) Of Engagement Activity 2022
 
Description Interview with Times Radio 
Form Of Engagement Activity A press release, press conference or response to a media enquiry/interview
Part Of Official Scheme? No
Geographic Reach National
Primary Audience Media (as a channel to the public)
Results and Impact Times Radio interviewed Prof Greg Towers about moving with Omicron into the new year . This interview provided information to listeners about the new variant of concern that was causing an uptick in covid-19 cases.
Year(s) Of Engagement Activity 2021
 
Description Invited speaker to a scientific meeting 
Form Of Engagement Activity A talk or presentation
Part Of Official Scheme? No
Geographic Reach National
Primary Audience Postgraduate students
Results and Impact Prof Wendy Barclay was invited to give a presentation on
Immune responses in COVID-19 and other coronavirus infections at the Royal Society 2 day meeting on The Science of Covid
https://royalsociety.org/science-events-and-lectures/2022/03/tof-covid/
Year(s) Of Engagement Activity 2022
 
Description National Core Studies Immunology Birmingham Talk The Genotype to Phenotype Consortium: "G2P" 
Form Of Engagement Activity A talk or presentation
Part Of Official Scheme? No
Geographic Reach National
Primary Audience Professional Practitioners
Results and Impact Talk
Year(s) Of Engagement Activity 2022
 
Description Participation in Paris Talk COVID-19: European Scientific Councils Meeting 
Form Of Engagement Activity A formal working group, expert panel or dialogue
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Policymakers/politicians
Results and Impact Wendy Barclay participated in the European Scientific Council Meeting in September 2022 to provide advice on COVID-19. Topics discussed:
Lessons learnt on the response to the crisis: Surveillance: how to organize surveillance during the autumn? ° Schools: Vaccination boosters this autumn:for whom, and how ?
Year(s) Of Engagement Activity 2022
 
Description Participation in WHO COVID-19 Global research & innovation forum 
Form Of Engagement Activity A formal working group, expert panel or dialogue
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Policymakers/politicians
Results and Impact Wendy Barclay participated in the WHO COVID-19 Global research & innovation forum. Topics discussed: what the focus for virology research should
be in the coming 6 months (to have the greatest impact on informing disease control) and what fundamental research needs to be
done to enable genotype-to-phenotype predictive virology
Year(s) Of Engagement Activity 2022
 
Description Royal Society conference on the science of COVID Talk SARS-CoV-2 Variants. Evolution in real time 
Form Of Engagement Activity A talk or presentation
Part Of Official Scheme? No
Geographic Reach National
Primary Audience Professional Practitioners
Results and Impact Talk
Year(s) Of Engagement Activity 2022
 
Description Weekly reporting to UKHSA Variant Technical Group 
Form Of Engagement Activity A formal working group, expert panel or dialogue
Part Of Official Scheme? No
Geographic Reach National
Primary Audience Policymakers/politicians
Results and Impact Wendy Barclay presents current data from the G2P-UK consortium at the weekly PHE Variant Technical Group which forms part of the risk assessment for emerging Variants of Concern (VOCs).
Year(s) Of Engagement Activity 2021,2022