82 research outputs found
Elective Cancer Surgery in COVID-19-Free Surgical Pathways During the SARS-CoV-2 Pandemic: An International, Multicenter, Comparative Cohort Study.
- Author
- Aawsaj Y.
- Abad Gurumeta A.
- Abad-Motos A.
- Abate E.
- Abatini C.
- Abbadessa F.
- Abbas A. M.
- Abbassi-Ghadi N.
- Abbott D.
- Abbott T.
- Abd Elazeem H. A. S.
- Abdalla M.
- Abdallah M.
- Abdel Al S.
- Abdel Jalil R.
- Abdeldayem H.
- Abdelkader Salama I.
- Abdelkarem M. M.
- Abdelkarim M.
- Abdelmajeed A.
- Abdelrahman A.
- Abdelrahman S.
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- Abdulkareem A.
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- J Clin Oncol
- Publication date
- 01/01/2020
- Field of study
PURPOSE: As cancer surgery restarts after the first COVID-19 wave, health care providers urgently require data to determine where elective surgery is best performed. This study aimed to determine whether COVID-19-free surgical pathways were associated with lower postoperative pulmonary complication rates compared with hospitals with no defined pathway. PATIENTS AND METHODS: This international, multicenter cohort study included patients who underwent elective surgery for 10 solid cancer types without preoperative suspicion of SARS-CoV-2. Participating hospitals included patients from local emergence of SARS-CoV-2 until April 19, 2020. At the time of surgery, hospitals were defined as having a COVID-19-free surgical pathway (complete segregation of the operating theater, critical care, and inpatient ward areas) or no defined pathway (incomplete or no segregation, areas shared with patients with COVID-19). The primary outcome was 30-day postoperative pulmonary complications (pneumonia, acute respiratory distress syndrome, unexpected ventilation). RESULTS: Of 9,171 patients from 447 hospitals in 55 countries, 2,481 were operated on in COVID-19-free surgical pathways. Patients who underwent surgery within COVID-19-free surgical pathways were younger with fewer comorbidities than those in hospitals with no defined pathway but with similar proportions of major surgery. After adjustment, pulmonary complication rates were lower with COVID-19-free surgical pathways (2.2% v 4.9%; adjusted odds ratio [aOR], 0.62; 95% CI, 0.44 to 0.86). This was consistent in sensitivity analyses for low-risk patients (American Society of Anesthesiologists grade 1/2), propensity score-matched models, and patients with negative SARS-CoV-2 preoperative tests. The postoperative SARS-CoV-2 infection rate was also lower in COVID-19-free surgical pathways (2.1% v 3.6%; aOR, 0.53; 95% CI, 0.36 to 0.76). CONCLUSION: Within available resources, dedicated COVID-19-free surgical pathways should be established to provide safe elective cancer surgery during current and before future SARS-CoV-2 outbreaks
Elective cancer surgery in COVID-19-free surgical pathways during the SARS-CoV-2 pandemic: An international, multicenter, comparative cohort study
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- Aawsaj Y.
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- Publication venue
- 'American Society of Clinical Oncology (ASCO)'
- Publication date
- 01/01/2021
- Field of study
PURPOSE As cancer surgery restarts after the first COVID-19 wave, health care providers urgently require data to determine where elective surgery is best performed. This study aimed to determine whether COVID-19–free surgical pathways were associated with lower postoperative pulmonary complication rates compared with hospitals with no defined pathway. PATIENTS AND METHODS This international, multicenter cohort study included patients who underwent elective surgery for 10 solid cancer types without preoperative suspicion of SARS-CoV-2. Participating hospitals included patients from local emergence of SARS-CoV-2 until April 19, 2020. At the time of surgery, hospitals were defined as having a COVID-19–free surgical pathway (complete segregation of the operating theater, critical care, and inpatient ward areas) or no defined pathway (incomplete or no segregation, areas shared with patients with COVID-19). The primary outcome was 30-day postoperative pulmonary complications (pneumonia, acute respiratory distress syndrome, unexpected ventilation). RESULTS Of 9,171 patients from 447 hospitals in 55 countries, 2,481 were operated on in COVID-19–free surgical pathways. Patients who underwent surgery within COVID-19–free surgical pathways were younger with fewer comorbidities than those in hospitals with no defined pathway but with similar proportions of major surgery. After adjustment, pulmonary complication rates were lower with COVID-19–free surgical pathways (2.2% v 4.9%; adjusted odds ratio [aOR], 0.62; 95% CI, 0.44 to 0.86). This was consistent in sensitivity analyses for low-risk patients (American Society of Anesthesiologists grade 1/2), propensity score–matched models, and patients with negative SARS-CoV-2 preoperative tests. The postoperative SARS-CoV-2 infection rate was also lower in COVID-19–free surgical pathways (2.1% v 3.6%; aOR, 0.53; 95% CI, 0.36 to 0.76). CONCLUSION Within available resources, dedicated COVID-19–free surgical pathways should be established to provide safe elective cancer surgery during current and before future SARS-CoV-2 outbreaks
The impact of viral mutations on recognition by SARS-CoV-2 specific T cells.
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- Publication venue
- iScience
- Publication date
- 01/01/2021
- Field of study
We identify amino acid variants within dominant SARS-CoV-2 T cell epitopes by interrogating global sequence data. Several variants within nucleocapsid and ORF3a epitopes have arisen independently in multiple lineages and result in loss of recognition by epitope-specific T cells assessed by IFN-γ and cytotoxic killing assays. Complete loss of T cell responsiveness was seen due to Q213K in the A∗01:01-restricted CD8+ ORF3a epitope FTSDYYQLY207-215; due to P13L, P13S, and P13T in the B∗27:05-restricted CD8+ nucleocapsid epitope QRNAPRITF9-17; and due to T362I and P365S in the A∗03:01/A∗11:01-restricted CD8+ nucleocapsid epitope KTFPPTEPK361-369. CD8+ T cell lines unable to recognize variant epitopes have diverse T cell receptor repertoires. These data demonstrate the potential for T cell evasion and highlight the need for ongoing surveillance for variants capable of escaping T cell as well as humoral immunity.This work is supported by the UK Medical Research Council (MRC); Chinese Academy of Medical Sciences(CAMS) Innovation Fund for Medical Sciences (CIFMS), China; National Institute for Health Research (NIHR)Oxford Biomedical Research Centre, and UK Researchand Innovation (UKRI)/NIHR through the UK Coro-navirus Immunology Consortium (UK-CIC). Sequencing of SARS-CoV-2 samples and collation of data wasundertaken by the COG-UK CONSORTIUM. COG-UK is supported by funding from the Medical ResearchCouncil (MRC) part of UK Research & Innovation (UKRI),the National Institute of Health Research (NIHR),and Genome Research Limited, operating as the Wellcome Sanger Institute. T.I.d.S. is supported by a Well-come Trust Intermediate Clinical Fellowship (110058/Z/15/Z). L.T. is supported by the Wellcome Trust(grant number 205228/Z/16/Z) and by theUniversity of Liverpool Centre for Excellence in Infectious DiseaseResearch (CEIDR). S.D. is funded by an NIHR GlobalResearch Professorship (NIHR300791). L.T. and S.C.M.are also supported by the U.S. Food and Drug Administration Medical Countermeasures Initiative contract75F40120C00085 and the National Institute for Health Research Health Protection Research Unit (HPRU) inEmerging and Zoonotic Infections (NIHR200907) at University of Liverpool inpartnership with Public HealthEngland (PHE), in collaboration with Liverpool School of Tropical Medicine and the University of Oxford.L.T. is based at the University of Liverpool. M.D.P. is funded by the NIHR Sheffield Biomedical ResearchCentre (BRC – IS-BRC-1215-20017). ISARIC4C is supported by the MRC (grant no MC_PC_19059). J.C.K.is a Wellcome Investigator (WT204969/Z/16/Z) and supported by NIHR Oxford Biomedical Research Centreand CIFMS. The views expressed are those of the authors and not necessarily those of the NIHR or MRC
Recurrent SARS-CoV-2 mutations in immunodeficient patients
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- Sanderson R.
- Sanderson T.
- Sang F.
- Sass T.
- Scher E.
- Scott C.
- Scott G.
- Sehmi J.
- Shaaban S.
- Shah D.
- Shaw J.
- Shelest E.
- Shepherd J. G.
- Sheridan L. A.
- Sheriff N.
- Shirley L.
- Sillitoe J.
- Silviera S.
- Simpson D. A.
- Singh A.
- Singleton D.
- Skvortsov T.
- Sloan T. J.
- Sluga G.
- Smith C. P.
- Smith D. L.
- Smith K.
- Smith K. S.
- Smith L.
- Smith N.
- Smith P.
- Smollett K. L.
- Snell L. B.
- Somassa T.
- Southgate J.
- Sparks N.
- Spellman K.
- Spencer Chapman M. H.
- Spurgin L. G.
- Spyer M. J.
- Stanley R.
- Stanley W.
- Stanton T. D.
- Starinskij I.
- Stockton J.
- Stonehouse S.
- Storey N.
- Studholme D. J.
- Sudhanva M.
- Swindells E.
- Taha Y.
- Tan N. K.
- Tang J. W.
- Tang M.
- Taylor B. E. W.
- Taylor J. F.
- Taylor S.
- Temperton B.
- Templeton K. E.
- Thomas C.
- Thomson E. C.
- Thomson L.
- Thornton A.
- Thurston S. A. J.
- Todd J. A.
- Tomb R.
- Tong L.
- Tonkin-Hill G.
- Tovar-Corona J. M.
- Trebes A.
- Trotter A. J.
- Tsatsani I.
- Turnbull R.
- Turtle L.
- Twohig K. A.
- Umpleby H.
- Underwood A. P.
- Vamos E. E.
- Vasylyeva T. I.
- Vattipally S.
- Vernet G.
- Vipond B. B.
- Volz E. M.
- Walsh S.
- Wang D.
- Warne B.
- Warwick-Dugdale J.
- Wastnedge E.
- Watkins J.
- Watson L. K.
- Waugh S.
- Webster H. J.
- Weldon D.
- Westwick E.
- Whalley T.
- Wheeler H.
- Whitehead M.
- Whiteley M.
- Whitwham A.
- Wierzbicki C.
- Wilkinson S. A. J.
- Willford N. J.
- Williams C.
- Williams C.
- Williams C.
- Williams C. A.
- Williams L. A.
- Williams R.
- Williams R. J.
- Williams T.
- Williamson K. A.
- Wilson-Davies E.
- Witele E.
- Withell K. T.
- Witney A. A.
- Wolverson P.
- Wong N.
- Workman T.
- Wright D. W.
- Wright V.
- Wyatt T.
- Wyllie S.
- Xu-McCrae L.
- Yavus M.
- Yaze G.
- Yeats C. A.
- Yebra G.
- Yew W. C.
- Young G. R.
- Young J.
- Zamudio M. E.
- Zarebski A. E.
- Zhang P.
- Publication venue
- 'Oxford University Press (OUP)'
- Publication date
- 11/08/2022
- Field of study
Long-term severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections in immunodeficient patients are an important source of variation for the virus but are understudied. Many case studies have been published which describe one or a small number of long-term infected individuals but no study has combined these sequences into a cohesive dataset. This work aims to rectify this and study the genomics of this patient group through a combination of literature searches as well as identifying new case series directly from the COVID-19 Genomics UK (COG-UK) dataset. The spike gene receptor-binding domain and N-terminal domain (NTD) were identified as mutation hotspots. Numerous mutations associated with variants of concern were observed to emerge recurrently. Additionally a mutation in the envelope gene, T30I was determined to be the second most frequent recurrently occurring mutation arising in persistent infections. A high proportion of recurrent mutations in immunodeficient individuals are associated with ACE2 affinity, immune escape, or viral packaging optimisation.There is an apparent selective pressure for mutations that aid cell–cell transmission within the host or persistence which are often different from mutations that aid inter-host transmission, although the fact that multiple recurrent de novo mutations are considered defining for variants of concern strongly indicates that this potential source of novel variants should not be discounted. © The Author(s) 2022. Published by Oxford University Press
Spatial growth rate of emerging SARS-CoV-2 lineages in England, September 2020-December 2021
- Author
- Aanensen DM
- Abudahab K
- Adams A
- Adams H
- Afifi S
- Aggarwal D
- Ahmad SSY
- Aigrain L
- Alcolea-Medina A
- Alikhan N - F
- Allara E
- Amato R
- Angyal A
- Annett T
- Aplin S
- Ariani CV
- Asad H
- Ash A
- Ashfield P
- Ashford F
- Atkinson L
- Attwood SW
- Auckland C
- Aydin A
- Baker DJ
- Baker P
- Balcazar CE
- Ball J
- Barrett JC
- Barrow M
- Barton E
- Bashton M
- Bassett AR
- Batra R
- Baxter C
- Bayzid N
- Beaver C
- Beckett AH
- Beckwith SM
- Bedford L
- Beer R
- Beggs A
- Bellis KL
- Berry L
- Bertolusso B
- Best A
- Betteridge E
- Bibby D
- Bicknell K
- Binns D
- Birchley A
- Bird PW
- Bishop C
- Blacow R
- Blakey V
- Blane B
- Bolt F
- Bonfield J
- Bonner S
- Bonsall D
- Boswell T
- Bosworth A
- Bourgeois Y
- Boyd O
- Bradley DT
- Breen C
- Bresner C
- Breuer J
- Bridgett S
- Bronner IF
- Brooks E
- Broos A
- Brown JR
- Bucca G
- Buchan SL
- Buck D
- Bull M
- Burns PJ
- Burton-Fanning S
- Byaruhanga T
- Byott M
- Campbell S
- Carabelli AM
- Cargill JS
- Carlile M
- Carvalho SF
- Casey A
- Castigador A
- Catalan J
- Chalker V
- Chaloner NJ
- Chand M
- Chappell JG
- Charalampous T
- Chatterton W
- Chaudhry Y
- Churcher CM
- Clark G
- Clarke P
- Cliff AD
- Cogger BJ
- Cole K
- Collins J
- Colquhoun R
- Connor TR
- Cook KF
- Coombes J
- Corden S
- Cormie C
- Cortes N
- Cotic M
- Cotton S
- Cottrell S
- Coupland L
- Cox A
- Cox M
- Craine N
- Crawford L
- Cross A
- Crown MR
- Crudgington D
- Cumley N
- Curran MD
- Curran T
- da Silva Filipe A
- Dabrera G
- Darby AC
- Davidson RK
- Davies A
- Davies RM
- Davis T
- de Angelis D
- De Lacy E
- de Oliveira Martins L
- de Silva TI
- Debebe J
- Denton-Smith R
- Dervisevic S
- Dewar R
- Dey J
- Dias J
- Dobie D
- Dorman MJ
- Downing F
- Driscoll M
- du Plessis L
- Duckworth N
- Durham J
- Eastick K
- Easton LJ
- Eccles R
- Edgeworth J
- Edwards S
- El Bouzidi K
- Eldirdiri S
- Ellaby N
- Elliott S
- Eltringham G
- Ensell L
- Erkiert MJ
- Essex S
- Evans C
- Evans JM
- Everson W
- Fairley DJ
- Fallon K
- Fanaie A
- Farr BW
- Fearn C
- Feltwell T
- Ferguson L
- Fina L
- Flaviani F
- Fleming VM
- Forrest S
- Foster-Nyarko E
- Foulkes BH
- Foulser L
- Fragakis M
- Frampton D
- Francois S
- Fraser C
- Freeman TM
- Fryer H
- Fuchs M
- Fuller W
- Gajee K
- Galai K
- Gallagher A
- Gallagher E
- Gallagher MD
- Gallis M
- Gaskin A
- Gatica-Wilcox B
- Geidelberg L
- Gemmell M
- Georgana I
- George RP
- Gifford L
- Gilbert L
- Girgis ST
- Glaysher S
- Goldstein EJ
- Golubchik T
- Gomes AN
- Gonçalves S
- Goodfellow IG
- Goodwin S
- Goudarzi S
- Gourtovaia M
- Graham C
- Graham L
- Grant PR
- Green A
- Green LR
- Greenaway J
- Gregory R
- Guest M
- Gunson RN
- Gupta RK
- Gutierrez B
- Haldenby ST
- Hamilton WL
- Hansford SE
- Haque T
- Harris KA
- Harrison EM
- Harrison I
- Hart J
- Hartley JA
- Harvey M
- Harvey WT
- Hassan-Ibrahim MO
- Heaney J
- Helmer T
- Henderson JH
- Hesketh AR
- Hey J
- Heyburn D
- Higginson EE
- Hill JD
- Hill V
- Hilson RA
- Hilvers E
- Holden MTG
- Hollis A
- Holmes AH
- Holmes CW
- Holmes N
- Hopes R
- Hornsby HR
- Hosmillo M
- Houlihan C
- Howson-Wells HC
- Hsu SN
- Hubb J
- Huckson H
- Hughes J
- Hughes M
- Hughes W
- Hutchings S
- Idle G
- Illingworth CJ
- Impey R
- Irish-Tavares D
- Iturriza-Gomara M
- Izuagbe R
- Jackson B
- Jackson C
- Jackson DK
- Jackson KA
- Jackson LM
- Jahun AS
- James K
- James V
- Jeanes C
- Jeffries AR
- Jeremiah S
- Jermy A
- John M
- Johnson K
- Johnson R
- Johnston I
- Jones CR
- Jones H
- Jones N
- Jones O
- Jones S
- Joseph A
- Judges S
- Kay GL
- Kay S
- Keatley J - P
- Keeley AJ
- Kenyon A
- Kermack LM
- Khakh M
- Kidd SP
- Kimuli M
- Kirk S
- Kitchen C
- Kitchman K
- Knight BA
- Koshy C
- Kraemer MUG
- Kumziene-Summerhayes S
- Kwiatkowski D
- Lackenby A
- Laing KG
- Lampejo T
- Langford CF
- Lavin D
- Lawton AI
- Le-Viet T
- Lee D
- Lee JCD
- Lensing SV
- Leonard S
- Levett LJ
- Lewis J
- Lewis K
- Liddle J
- Liggett S
- Lillie PJ
- Lindsey BB
- Lister MM
- Livett R
- Lo S
- Loman NJ
- Loose MW
- Louka SF
- Loveson KF
- Lowdon S
- Lowe H
- Lowe HL
- Lucaci AO
- Ludden C
- Lynch J
- Lyons RA
- Lythgoe K
- Machin NW
- MacIntyre-Cockett G
- Mack A
- Macklin B
- Maclean A
- Macnaughton E
- Madona P
- Maes M
- Maftei L
- Mahanama AIK
- Mahungu TW
- Mair D
- Maksimovic J
- Malone CS
- Maloney D
- Manesis N
- Manley R
- Mantzouratou A
- Marchbank A
- Mariappan A
- Martincorena I
- Martinez Nunez RT
- Mather AE
- Maxwell P
- Mayhew M
- Mbisa T
- McCann CM
- McCarthy SA
- McCluggage K
- McClure PC
- McCrone JT
- McHugh MP
- McKenna JP
- McKerr C
- McManus GM
- McMurray CL
- McNally A
- Meadows L
- Medd N
- Megram O
- Menegazzo M
- Merrick I
- Michell SL
- Michelsen ML
- Mirfenderesky M
- Mirza J
- Miskelly J
- Moles-Garcia E
- Moll RJ
- Molnar Z
- Monahan IM
- Mondani M
- Mookerjee S
- Moore C
- Moore C
- Moore J
- Moore N
- Morcrette H
- Morgan M
- Morgan S
- Mori M
- Morriss A
- Moses S
- Mower C
- Muir P
- Mukaddas A
- Munemo F
- Munn R
- Murray A
- Murray DR
- Murray LJ
- Mutingwende M
- Myers R
- Nastouli E
- Nebbia G
- Nelson A
- Nelson C
- Nicholls S
- Nichols J
- Nicodemi R
- Nomikou K
- O'Brien S
- O'Grady J
- O'Toole Á
- Odedra M
- Ohemeng-Kumi N
- Oliver K
- Orton RJ
- Osman H
- Pacchiarini N
- Padgett D
- Page AJ
- Park EJ
- Park NR
- Parker MD
- Parmar S
- Partridge DG
- Pascall D
- Patel A
- Patel B
- Paterson S
- Payne BAI
- Peacock SJ
- Pearson C
- Pelosi E
- Percival B
- Perkins J
- Perry M
- Pinckert ML
- Platt S
- Podplomyk O
- Pohare M
- Pond M
- Pope CF
- Poplawski R
- Powell J
- Poyner J
- Prestwood L
- Price A
- Price JR
- Prieto JA
- Pritchard DT
- Prosolek SJ
- Pugh G
- Pusok M
- Pybus OG
- Pymont HM
- Quail MA
- Quick J
- Radulescu C
- Raghwani J
- Ragonnet-Cronin M
- Rainbow L
- Rajan D
- Rajatileka S
- Ramadan NA
- Rambaut A
- Ramble J
- Randell PA
- Ratcliffe L
- Raviprakash V
- Raza M
- Redshaw NM
- Rey S
- Reynolds N
- Richter A
- Robertson DL
- Robinson E
- Robson SC
- Rogan F
- Rooke S
- Rowe W
- Roy S
- Rudder S
- Ruis C
- Rushton S
- Saeed K
- Samaraweera B
- Sambles CM
- Sanderson R
- Sanderson T
- Sang F
- Sass T
- Scher E
- Scott C
- Scott G
- Sehmi J
- Shaaban S
- Shah D
- Shaw J
- Shelest E
- Shepherd JG
- Sheridan LA
- Sheriff N
- Shirley L
- Sillitoe J
- Silviera S
- Simpson DA
- Singh A
- Singleton D
- Skvortsov T
- Sloan TJ
- Sluga G
- Smallman-Raynor MR
- Smith CP
- Smith DL
- Smith K
- Smith KS
- Smith L
- Smith N
- Smith P
- Smollett KL
- Snell LB
- Somassa T
- Southgate J
- Spellman K
- Spencer Chapman MH
- Spurgin LG
- Spyer MJ
- Stanley R
- Stanley W
- Stanton TD
- Starinskij I
- Stockton J
- Stonehouse S
- Storey N
- Studholme DJ
- Sudhanva M
- Swindells E
- Taha Y
- Tan NK
- Tang JW
- Tang M
- Taylor BEW
- Taylor JF
- Taylor S
- Temperton B
- Templeton KE
- Thomas C
- Thomson EC
- Thomson L
- Thornton A
- Thurston SAJ
- Todd JA
- Tomb R
- Tong L
- Tonkin-Hill G
- Torok ME
- Tovar-Corona JM
- Trebes A
- Trotter AJ
- Tsatsani I
- Turnbull R
- Turtle L
- Twohig KA
- Umpleby H
- Underwood AP
- Vamos EE
- Vasylyeva TI
- Vattipally S
- Vernet G
- Vipond BB
- Volz EM
- Walsh S
- Wang D
- Warne B
- Warwick-Dugdale J
- Wastnedge E
- Watkins J
- Watson LK
- Waugh S
- Webster HJ
- Weldon D
- Westwick E
- Whalley T
- Wheeler H
- Whitehead M
- Whiteley M
- Whitwham A
- Wierzbicki C
- Willford NJ
- Williams C
- Williams C
- Williams C
- Williams CA
- Williams L - A
- Williams R
- Williams RJ
- Williams T
- Williamson KA
- Wilson-Davies E
- Witele E
- Withell KT
- Witney AA
- Wolverson P
- Wong N
- Workman T
- Wright DW
- Wright V
- Wyatt T
- Wyllie S
- Xu-McCrae L
- Yavus M
- Yaze G
- Yeats CA
- Yebra G
- Yew WC
- Young GR
- Young J
- Zamudio ME
- Zarebski AE
- Zhang P
- Publication venue
- Publication date
- 20/07/2022
- Field of study
This paper uses a robust method of spatial epidemiological analysis to assess the spatial growth rate of multiple lineages of SARS-CoV-2 in the local authority areas of England, September 2020–December 2021. Using the genomic surveillance records of the COVID-19 Genomics UK (COG-UK) Consortium, the analysis identifies a substantial (7.6-fold) difference in the average rate of spatial growth of 37 sample lineages, from the slowest (Delta AY.4.3) to the fastest (Omicron BA.1). Spatial growth of the Omicron (B.1.1.529 and BA) variant was found to be 2.81× faster than the Delta (B.1.617.2 and AY) variant and 3.76× faster than the Alpha (B.1.1.7 and Q) variant. In addition to AY.4.2 (a designated variant under investigation, VUI-21OCT-01), three Delta sublineages (AY.43, AY.98 and AY.120) were found to display a statistically faster rate of spatial growth than the parent lineage and would seem to merit further investigation. We suggest that the monitoring of spatial growth rates is a potentially valuable adjunct to outbreak response procedures for emerging SARS-CoV-2 variants in a defined population
SARS-CoV-2 lineage dynamics in England from September to November 2021: high diversity of Delta sub-lineages and increased transmissibility of AY.4.2
- Author
- Aanensen DM
- Abudahab K
- Adams A
- Adams H
- Afifi S
- Aggarwal D
- Ahmad SSY
- Aigrain L
- Alcolea-Medina A
- Alikhan N - F
- Allara E
- Amato R
- Angyal A
- Annett T
- Aplin S
- Ariani CV
- Asad H
- Ash A
- Ashby D
- Ashfield P
- Ashford F
- Atchison C
- Atkinson L
- Attwood SW
- Auckland C
- Aydin A
- Baker DJ
- Baker P
- Balcazar CE
- Ball J
- Barclay W
- Barrett JC
- Barrow M
- Barton E
- Bashton M
- Bassett AR
- Batra R
- Baxter C
- Bayzid N
- Beaver C
- Beckett AH
- Beckwith SM
- Bedford L
- Beer R
- Beggs A
- Bellis KL
- Berry L
- Bertolusso B
- Best A
- Betteridge E
- Bibby D
- Bicknell K
- Binns D
- Birchley A
- Bird PW
- Bishop C
- Blacow R
- Blakey V
- Blane B
- Bodinier B
- Bolt F
- Bonfield J
- Bonner S
- Bonsall D
- Boswell T
- Bosworth A
- Bourgeois Y
- Bouzidi KE
- Boyd O
- Bradley DT
- Breen C
- Bresner C
- Breuer J
- Bridgett S
- Bronner IF
- Brooks E
- Broos A
- Brown JR
- Bucca G
- Buchan SL
- Buck D
- Bull M
- Burns PJ
- Burton-Fanning S
- Byaruhanga T
- Byott M
- Campbell S
- Carabelli AM
- Cargill JS
- Carlile M
- Carvalho SF
- Casey A
- Castigador A
- Catalan J
- Chadeau-Hyam M
- Chalker V
- Chaloner NJ
- Chand M
- Chapman MHS
- Chappell JG
- Charalampous T
- Chatterton W
- Chaudhry Y
- Churcher CM
- Clark G
- Clarke P
- Cogger BJ
- Cole K
- Collins J
- Colquhoun R
- Connor TR
- Cook KF
- Cooke G
- Coombes J
- Corden S
- Cormie C
- Cortes N
- Cotic M
- Cotton S
- Cottrell S
- Coupland L
- Cox A
- Cox MG
- Craine N
- Crawford L
- Cross A
- Crown MR
- Crudgington D
- Cumley N
- Curran MD
- Curran T
- da Silva Filipe A
- Dabrera G
- Darby AC
- Darzi A
- Davidson RK
- Davies A
- Davies RM
- Davis T
- de Angelis D
- De Lacy E
- de Oliveira Martins L
- de Silva TI
- Debebe J
- Denton-Smith R
- Dervisevic S
- Dewar R
- Dey J
- Dias J
- Dobie D
- Donnelly CA
- Dorman MJ
- Downing F
- Driscoll M
- du Plessis L
- Duckworth N
- Durham J
- Eales O
- Eastick K
- Easton LJ
- Eccles R
- Edgeworth J
- Edwards S
- Eldirdiri S
- Ellaby N
- Elliott P
- Elliott S
- Eltringham G
- Ensell L
- Erkiert MJ
- Essex S
- Evans C
- Evans JM
- Everson W
- Fairley DJ
- Fallon K
- Fanaie A
- Farr BW
- Fearn C
- Feltwell T
- Ferguson L
- Fina L
- Flaviani F
- Fleming VM
- Forrest S
- Foster-Nyarko E
- Foulkes BH
- Foulser L
- Fragakis M
- Frampton D
- Francois S
- Fraser C
- Freeman TM
- Fryer H
- Fuchs M
- Fuller W
- Gajee K
- Galai K
- Gallagher A
- Gallagher E
- Gallagher MD
- Gallis M
- Gaskin A
- Gatica-Wilcox B
- Geidelberg L
- Gemmell M
- Georgana I
- George RP
- Gifford L
- Gilbert L
- Girgis ST
- Glaysher S
- Goldstein EJ
- Golubchik T
- Gomes AN
- Gonçalves S
- Goodfellow IG
- Goodwin S
- Goudarzi S
- Gourtovaia M
- Graham C
- Graham L
- Grant PR
- Green A
- Green LR
- Greenaway J
- Gregory R
- Guest M
- Gunson RN
- Gupta RK
- Gutierrez B
- Haldenby ST
- Hamilton WL
- Hansford SE
- Haque T
- Harris KA
- Harrison EM
- Harrison I
- Hart J
- Hartley JA
- Harvey M
- Harvey WT
- Hassan-Ibrahim MO
- Haw D
- Heaney J
- Helmer T
- Henderson JH
- Hesketh AR
- Hey J
- Heyburn D
- Higginson EE
- Hill JD
- Hill V
- Hilson RA
- Hilvers E
- Holden MTG
- Hollis A
- Holmes AH
- Holmes CW
- Holmes N
- Hopes R
- Hornsby HR
- Hosmillo M
- Houlihan C
- Howson-Wells HC
- Hsu SN
- Hubb J
- Huckson H
- Hughes J
- Hughes M
- Hughes W
- Hutchings S
- Idle G
- Illingworth CJ
- Impey R
- Irish-Tavares D
- Iturriza-Gomara M
- Izuagbe R
- Jackson B
- Jackson C
- Jackson DK
- Jackson KA
- Jackson LM
- Jahun AS
- James K
- James V
- Jeanes C
- Jeffries AR
- Jeremiah S
- Jermy A
- John M
- Johnson K
- Johnson R
- Johnston I
- Jones CR
- Jones H
- Jones N
- Jones O
- Jones S
- Jonnerby J
- Joseph A
- Judges S
- Kay GL
- Kay S
- Keatley J - P
- Keeley AJ
- Kenyon A
- Kermack LM
- Khakh M
- Kidd SP
- Kimuli M
- Kirk S
- Kitchen C
- Kitchman K
- Knight BA
- Koshy C
- Kraemer MUG
- Kumziene-Summerhayes S
- Kwiatkowski D
- Lackenby A
- Laing KG
- Lampejo T
- Langford CF
- Lavin D
- Lawton AI
- Le-Viet T
- Lee D
- Lee JCD
- Lensing SV
- Leonard S
- Levett LJ
- Lewis J
- Lewis K
- Liddle J
- Liggett S
- Lillie PJ
- Lindsey BB
- Lister MM
- Livett R
- Lo S
- Loman NJ
- Loose MW
- Louka SF
- Loveson KF
- Lowdon S
- Lowe H
- Lowe HL
- Lucaci AO
- Ludden C
- Lynch J
- Lyons RA
- Lythgoe K
- Machin NW
- MacIntyre-Cockett G
- Mack A
- Macklin B
- Maclean A
- Macnaughton E
- Madona P
- Maes M
- Maftei L
- Mahanama AIK
- Mahungu TW
- Mair D
- Maksimovic J
- Malone CS
- Maloney D
- Manesis N
- Manley R
- Mantzouratou A
- Marchbank A
- Mariappan A
- Martincorena I
- Mather AE
- Maxwell P
- Mayhew M
- Mbisa T
- McCann CM
- McCarthy SA
- McCluggage K
- McClure PC
- McCrone JT
- McHugh MP
- McKenna JP
- McKerr C
- McManus GM
- McMurray C
- McMurray CL
- McNally A
- Meadows L
- Medd N
- Megram O
- Menegazzo M
- MEng BEWT
- Merrick I
- Michell SL
- Michelsen ML
- Mirfenderesky M
- Mirza J
- Miskelly J
- Moles-Garcia E
- Moll RJ
- Molnar Z
- Monahan IM
- Mondani M
- Mookerjee S
- Moore C
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- Moore J
- Moore N
- Morcrette H
- Morgan M
- Morgan S
- Mori M
- Morriss A
- Moses S
- Mower C
- Muir P
- Mukaddas A
- Munemo F
- Munn R
- Murray A
- Murray DR
- Murray LJ
- Mutingwende M
- Myers R
- Nastouli E
- Nebbia G
- Nelson A
- Nelson C
- Nicholls S
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- Nicodemi R
- Nomikou K
- Nunez RTM
- Odedra M
- Ohemeng-Kumi N
- Oliver K
- Orton RJ
- Osman H
- O’Brien PS
- O’Grady J
- O’Toole Á
- Pacchiarini N
- Padgett D
- Page AJ
- Park EJ
- Park NR
- Parker MD
- Parmar S
- Partridge DG
- Pascall D
- Patel A
- Patel B
- Paterson S
- Payne BAI
- Peacock SJ
- Pearson C
- Pelosi E
- Percival B
- Perkins J
- Perry M
- Pinckert ML
- Platt S
- Podplomyk O
- Pohare M
- Pond M
- Pope CF
- Poplawski R
- Powell J
- Poyner J
- Prestwood L
- Price A
- Price JR
- Prieto JA
- Pritchard DT
- Prosolek SJ
- Pugh G
- Pusok M
- Pybus OG
- Pymont HM
- Quail MA
- Quick J
- Radulescu C
- Raghwani J
- Ragonnet-Cronin M
- Rainbow L
- Rajan D
- Rajatileka S
- Ramadan NA
- Rambaut A
- Ramble J
- Randell P
- Randell PA
- Ratcliffe L
- Raviprakash V
- Raza M
- Redshaw NM
- Rey S
- Reynolds N
- Richter A
- Riley S
- Robertson DL
- Robinson E
- Robson SC
- Rogan F
- Rooke S
- Rowe W
- Roy S
- Rudder S
- Ruis C
- Rushton S
- Saeed K
- Samaraweera B
- Sambles CM
- Sanderson R
- Sanderson T
- Sang F
- Sass T
- Scher E
- Scott C
- Scott G
- Sehmi J
- Shaaban S
- Shah D
- Shaw J
- Shelest E
- Shepherd JG
- Sheridan LA
- Sheriff N
- Shirley L
- Sillitoe J
- Silviera S
- Simpson DA
- Singh A
- Singleton D
- Skvortsov T
- Sloan TJ
- Sluga G
- Smith CP
- Smith DL
- Smith K
- Smith KS
- Smith L
- Smith N
- Smith P
- Smollett KL
- Snell LB
- Somassa T
- Southgate J
- Spellman K
- Spurgin LG
- Spyer MJ
- Stanley R
- Stanley W
- Stanton TD
- Starinskij I
- Stockton J
- Stonehouse S
- Storey N
- Studholme DJ
- Sudhanva M
- Swindells E
- Taha Y
- Tan NK
- Tang JW
- Tang M
- Taylor G
- Taylor JF
- Taylor S
- Temperton B
- Templeton KE
- The COVID-19 Genomics UK (COG-UK) Consortium
- Thomas C
- Thomson EC
- Thomson L
- Thornton A
- Thurston SAJ
- Todd JA
- Tomb R
- Tong L
- Tonkin-Hill G
- Torok ME
- Tovar-Corona JM
- Trebes A
- Trotter AJ
- Tsatsani I
- Turnbull R
- Turtle L
- Twohig KA
- Umpleby H
- Underwood AP
- Vamos EE
- Vasylyeva TI
- Vattipally S
- Vernet G
- Vipond BB
- Volz EM
- Walsh S
- Wang D
- Wang H
- Ward H
- Warne B
- Warwick-Dugdale J
- Wastnedge E
- Watkins J
- Watson LK
- Waugh S
- Webster HJ
- Weldon D
- Westwick E
- Whalley T
- Wheeler H
- Whitehead M
- Whiteley M
- Whitwham A
- Wierzbicki C
- Willford NJ
- Williams C
- Williams C
- Williams C
- Williams CA
- Williams L - A
- Williams R
- Williams RJ
- Williams T
- Williamson KA
- Wilson-Davies E
- Witele E
- Withell KT
- Witney AA
- Wolverson P
- Wong N
- Workman T
- Wright DW
- Wright V
- Wyatt T
- Wyllie S
- Xu-McCrae L
- Yavus M
- Yaze G
- Yeats CA
- Yebra G
- Yew WC
- Young GR
- Young J
- Zamudio ME
- Zarebski AE
- Zhang P
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 27/07/2022
- Field of study
Background: Since the emergence of SARS-CoV-2, evolutionary pressure has driven large increases in the transmissibility of the virus. However, with increasing levels of immunity through vaccination and natural infection the evolutionary pressure will switch towards immune escape. Genomic surveillance in regions of high immunity is crucial in detecting emerging variants that can more successfully navigate the immune landscape. Methods: We present phylogenetic relationships and lineage dynamics within England (a country with high levels of immunity), as inferred from a random community sample of individuals who provided a self-administered throat and nose swab for rt-PCR testing as part of the REal-time Assessment of Community Transmission-1 (REACT-1) study. During round 14 (9 September–27 September 2021) and 15 (19 October–5 November 2021) lineages were determined for 1322 positive individuals, with 27.1% of those which reported their symptom status reporting no symptoms in the previous month. Results: We identified 44 unique lineages, all of which were Delta or Delta sub-lineages, and found a reduction in their mutation rate over the study period. The proportion of the Delta sub-lineage AY.4.2 was increasing, with a reproduction number 15% (95% CI 8–23%) greater than the most prevalent lineage, AY.4. Further, AY.4.2 was less associated with the most predictive COVID-19 symptoms (p = 0.029) and had a reduced mutation rate (p = 0.050). Both AY.4.2 and AY.4 were found to be geographically clustered in September but this was no longer the case by late October/early November, with only the lineage AY.6 exhibiting clustering towards the South of England. Conclusions: As SARS-CoV-2 moves towards endemicity and new variants emerge, genomic data obtained from random community samples can augment routine surveillance data without the potential biases introduced due to higher sampling rates of symptomatic individuals. © 2022, The Author(s)
Genomic reconstruction of the SARS-CoV-2 epidemic in England.
- Author
- Aanensen DM
- Abnizova I
- Abudahab K
- Adams A
- Adams H
- Afifi S
- Aggarwal D
- Ahmad SSY
- Aigrain L
- Alcolea A
- Alderton A
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- Alikhan N-F
- Allara E
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- Amato R
- Anderson R
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- Pohare M
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- Poplawski R
- Powell J
- Poyner J
- Preston T
- Prestwood L
- Price A
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- Pritchard DT
- Prosolek SJ
- Puethe C
- Pugh G
- Pusok M
- Pybus OG
- Pymont HM
- Quail M
- Quail MA
- Quick J
- Radulescu C
- Raghwani J
- Ragonnet-Cronin M
- Rainbow L
- Rajan D
- Rajatileka S
- Ramadan NA
- Rambaut A
- Ramble J
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- Ratcliffe L
- Raviprakash V
- Rawlings S
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- Redshaw N
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- Rudder S
- Ruis C
- Rushton S
- Sadri R
- Saeed K
- Saint C
- Salmon N
- Samaraweera B
- Sambles CM
- Sanderson R
- Sanderson T
- Sanderson T
- Sang F
- Sass T
- Saul D
- Scher E
- Schwach F
- Schwach F
- Scott C
- Scott G
- Seekings P
- Sehmi J
- Shaaban S
- Shah D
- Shaw J
- Shelest E
- Shepherd JG
- Sheridan LA
- Sheriff N
- Shirley L
- Sillitoe J
- Silviera S
- Simms A
- Simpson DA
- Singh A
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- Sinnott M
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- Siwek B
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- Skelton J
- Skvortsov T
- Slater-Tunstill J
- Sloan TJ
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- Sluga G
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- Smith KS
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- Smith M
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- Smollett KL
- Sneade L
- Snell LB
- Somassa T
- Soria CD
- Sousa C
- Souster E
- Southgate J
- Sparkes A
- Spellman K
- Spencer Chapman MH
- Spencer-Chapman M
- Spurgin LG
- Spyer MJ
- Squares J
- Stanley R
- Stanley R
- Stanley W
- Stanton TD
- Starinskij I
- Steed C
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- Still I
- Stockton J
- Stonehouse S
- Storey N
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- Studholme DJ
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- Sudhanva M
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- Swiatkowska A
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- Swindells E
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- Taha Y
- Taluy E
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- Tang M
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- Taylor S
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- Templeton KE
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- Thornton A
- Thurston S
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- Todd JA
- Tomb R
- Tong L
- Tonkin-Hill G
- Toombs D
- Topping B
- Torok ME
- Tovar-Corona J
- Tovar-Corona JM
- Trebes A
- Trotter AJ
- Tsatsani I
- Turnbull R
- Turtle L
- Twohig KA
- Umpleby H
- Underwood AP
- Ungureanu D
- Uphill J
- Urbanova J
- Vamos EE
- Van Vuuren PJ
- Vancollie V
- Vasylyeva TI
- Vattipally S
- Verdejo CJ
- Vernet G
- Vipond BB
- Voak P
- Volz E
- Volz EM
- Vöhringer HS
- Walker D
- Walker M
- Waller M
- Walsh S
- Wang D
- Ward G
- Warne B
- Warwick-Dugdale J
- Wastnedge E
- Watkins J
- Watson LK
- Waugh S
- Weatherhogg C
- Webb N
- Webster HJ
- Weldon D
- Wells A
- Wells E
- Westwick E
- Westwood L
- Whalley T
- Wheeler H
- Whipp T
- Whitehead M
- Whiteley M
- Whiteley T
- Whitton G
- Whitwham A
- Widaa S
- Wierzbicki C
- Willford NJ
- Williams C
- Williams C
- Williams C
- Williams CA
- Williams L-A
- Williams M
- Williams R
- Williams RJ
- Williams T
- Williamson KA
- Wilson M
- Wilson-Davies E
- Witele E
- Withell KT
- Witney AA
- Wolverson P
- Wong N
- Workman T
- Wright DW
- Wright S
- Wright V
- Wyatt T
- Wyllie S
- Xu-McCrae L
- Yavus M
- Yaze G
- Yeats CA
- Yebra G
- Yew WC
- Young GR
- Young J
- Zamudio ME
- Zarebski AE
- Zhang P
- Publication venue
- Nature
- Publication date
- 01/01/2021
- Field of study
The evolution of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus leads to new variants that warrant timely epidemiological characterization. Here we use the dense genomic surveillance data generated by the COVID-19 Genomics UK Consortium to reconstruct the dynamics of 71 different lineages in each of 315 English local authorities between September 2020 and June 2021. This analysis reveals a series of subepidemics that peaked in early autumn 2020, followed by a jump in transmissibility of the B.1.1.7/Alpha lineage. The Alpha variant grew when other lineages declined during the second national lockdown and regionally tiered restrictions between November and December 2020. A third more stringent national lockdown suppressed the Alpha variant and eliminated nearly all other lineages in early 2021. Yet a series of variants (most of which contained the spike E484K mutation) defied these trends and persisted at moderately increasing proportions. However, by accounting for sustained introductions, we found that the transmissibility of these variants is unlikely to have exceeded the transmissibility of the Alpha variant. Finally, B.1.617.2/Delta was repeatedly introduced in England and grew rapidly in early summer 2021, constituting approximately 98% of sampled SARS-CoV-2 genomes on 26 June 2021
Investigation of hospital discharge cases and SARS-CoV-2 introduction into Lothian care homes
- Author
- Aanensen DM
- Abudahab K
- Adams A
- Adams H
- Afifi S
- Aggarwal D
- Ahmad SSY
- Aigrain L
- Alcolea-Medina A
- Alikhan N
- Allara E
- Amato R
- Angyal A
- Annett T
- Aplin S
- Ariani CV
- Asad H
- Ash A
- Ashfield P
- Ashford F
- Atkinson L
- Attwood SW
- Auckland C
- Aydin A
- Baker DJ
- Baker P
- Balcazar CE
- Ball J
- Barrett JC
- Barrow M
- Barton E
- Bashton M
- Bassett AR
- Batra R
- Baxter C
- Bayzid N
- Beaver C
- Beckett AH
- Beckwith SM
- Bedford L
- Beer R
- Beggs A
- Bellis KL
- Berry L
- Bertolusso B
- Best A
- Betteridge E
- Bibby D
- Bicknell K
- Binns D
- Birchley A
- Bird PW
- Bishop C
- Blacow R
- Blakey V
- Blane B
- Bolt F
- Bonfield J
- Bonner S
- Bonsall D
- Boswell T
- Bosworth A
- Bourgeois Y
- Boyd O
- Bradley DT
- Breen C
- Bresner C
- Breuer J
- Bridgett S
- Bronner IF
- Brooks E
- Broos A
- Brown JR
- Bucca G
- Buchan SL
- Buck D
- Bull M
- Burns PJ
- Burton-Fanning S
- Byaruhanga T
- Byott M
- Campbell S
- Carabelli AM
- Cargill JS
- Carlile M
- Carvalho SF
- Casey A
- Castigador A
- Catalan J
- Chalker V
- Chaloner NJ
- Chand M
- Chappell JG
- Charalampous T
- Chatterton W
- Chaudhry Y
- Churcher CM
- Clark G
- Clarke P
- Cogger BJ
- Cole K
- Collins J
- Colquhoun R
- Connor TR
- Cook KF
- Coombes J
- Corden S
- Cormie C
- Cortes N
- Cotic M
- Cotton S
- Cotton S
- Cottrell S
- Coupland L
- Cox A
- Cox M
- Craine N
- Crawford L
- Cross A
- Crown MR
- Crudgington D
- Cumley N
- Curran MD
- Curran T
- Cutino-Moguel T
- da Silva Filipe A
- Dabrer G
- Darby AC
- Davidson RK
- Davies A
- Davies RM
- Davis T
- de Angelis D
- De Lacy E
- de Oliveira Martins L
- de Silva TI
- Debebe J
- Delgado Callico L
- Denton-Smith R
- Dervisevic S
- Dewar R
- Dewar R
- Dey J
- Dias J
- Dobie D
- Dorman MJ
- Downing F
- Driscoll M
- du Plessis L
- Duckworth N
- Durham J
- Eastick K
- Easton LJ
- Eccles R
- Edgeworth J
- Edwards S
- El Bouzidi K
- Eldirdiri S
- Ellaby N
- Elliott S
- Eltringham G
- Ensell L
- Erkiert MJ
- Essex S
- Evans C
- Evans JM
- Everson W
- Fairley DJ
- Fallon K
- Fanaie A
- Farr BW
- Fearn C
- Feltwell T
- Ferguson L
- Fina L
- Flaviani F
- Fleming VM
- Forrest S
- Foster-Nyarko E
- Foulkes BH
- Foulser L
- Fragakis M
- Frampton D
- Francois S
- Fraser C
- Freeman TM
- Fryer H
- Fuchs M
- Fuller W
- Gajee K
- Galai K
- Gallagher A
- Gallagher E
- Gallagher MD
- Gallis M
- Gaskin A
- Gatica-Wilcox B
- Geidelberg L
- Gemmell M
- Georgana I
- George RP
- Gifford L
- Gilbert L
- Girgis ST
- Glaysher S
- Goldstein EJ
- Golubchik T
- Gomes AN
- Gonçalves S
- Goodwin S
- Goudarzi S
- Gourtovaia M
- Graham C
- Graham L
- Grant PR
- Green A
- Green LR
- Greenaway J
- Gregory R
- Guest M
- Gunson RN
- Gupta RK
- Gutierrez B
- Haas JG
- Haldenby ST
- Hamilton WL
- Hansford SE
- Haque T
- Harris KA
- Harrison EM
- Harrison I
- Hart J
- Hartley JA
- Harvey M
- Harvey WT
- Hassan-Ibrahim MO
- Heaney J
- Helmer T
- Henderson JH
- Hesketh AR
- Hey J
- Heyburn D
- Higginson EE
- Hill JD
- Hill V
- Hilson RA
- Hilvers E
- Holden MTG
- Hollis A
- Holmes AH
- Holmes CW
- Holmes N
- Hopes R
- Hornsby HR
- Hosmillo M
- Houlihan C
- Howson-Wells HC
- Hsu SN
- Hubb J
- Huckson H
- Hughes J
- Hughes M
- Hughes W
- Hutchings S
- Idle G
- Illingworth CJ
- Impey R
- Irish-Tavares D
- Iturriza-Gomara M
- Izuagbe R
- Jackson B
- Jackson C
- Jackson DK
- Jackson KA
- Jackson LM
- Jahun AS
- James K
- James V
- Jeanes C
- Jeffries AR
- Jeremiah S
- Jermy A
- John M
- Johnson K
- Johnson R
- Johnston I
- Jones CR
- Jones H
- Jones N
- Jones O
- Jones S
- Joseph A
- Judges S
- Kay GL
- Kay S
- Keatley J
- Keeley AJ
- Kele B
- Kenyon A
- Kermack LM
- Khakh M
- Kidd SP
- Killough NF
- Kimuli M
- Kirk S
- Kitchen C
- Kitchman K
- Knight BA
- Koshy C
- Kraemer MUG
- Kumziene-Summerhayes S
- Kwiatkowski D
- Lackenby A
- Laing KG
- Lampejo T
- Langford CF
- Lavin D
- Lawton AI
- Le-Viet T
- Lee D
- Lee JCD
- Lensing SV
- Leonard S
- Levett LJ
- Lewis J
- Lewis K
- Liddle J
- Liggett S
- Lillie PJ
- Lindsey BB
- Lister MM
- Livett R
- Lo S
- Loman NJ
- Loose MW
- Louka SF
- Loveson KF
- Lowdon S
- Lowe H
- Lowe HL
- Lucaci AO
- Ludden C
- Lynch J
- Lyons RA
- Machin NW
- MacIntyre-Cockett G
- Mack A
- Macklin B
- Maclean A
- Macnaughton E
- Madona P
- Maes M
- Maftei L
- Mahanama AIK
- Mahungu TW
- Mair D
- Maksimovic J
- Malone CS
- Maloney D
- Manesis N
- Manley R
- Mantzouratou Anna
- Marchbank A
- Mariappan A
- Markov A
- Martincorena I
- Martinez Nunez RT
- Mather AE
- Maxwell P
- Mayhew M
- Mbisa T
- McCann CM
- McCarthy SA
- McCluggage K
- McClure PC
- McCrone JT
- McHugh MP
- McHugh MP
- McKenna JP
- McKerr C
- McManus GM
- McMurray C
- McMurray CL
- McNal A
- Meadows L
- Medd N
- Megram O
- Menegazzo M
- Merrick I
- Michell SL
- Michelsen ML
- Mirfenderesky M
- Mirza J
- Miskelly J
- Moles-Garcia E
- Moll RJ
- Molnar Z
- Monahan IM
- Mondani M
- Mookerjee S
- Moore C
- Moore C
- Moore J
- Moore N
- Morcrette H
- Morgan M
- Morgan S
- Mori M
- Morriss A
- Moses S
- Mower C
- Muir P
- Mukaddas A
- Munemo F
- Munn R
- Murray A
- Murray DR
- Murray LJ
- Mutingwende M
- Myers R
- Nastouli E
- Nebbia G
- Nelson A
- Nelson C
- Nicholls S
- Nichols J
- Nicodemi R
- Nomikou K
- O'Brien S
- O'Toole Á
- Odedra M
- Ohemeng-Kumi N
- Oliver K
- Orton RJ
- Osman H
- O’Grady J
- Pacchiarini N
- Padgett D
- Page AJ
- Park EJ
- Park NR
- Parker MD
- Parmar S
- Partridge DG
- Pascall D
- Patel A
- Patel B
- Paterson S
- Payne BAI
- Peacock SJ
- Pearson C
- Pelosi E
- Percival B
- Perkins J
- Perry M
- Pinckert ML
- Platt S
- Podplomyk Fd O
- Pohare M
- Pond M
- Pope CF
- Poplawski R
- Powell J
- Poyner J
- Prestwood L
- Price A
- Price JR
- Prieto JA
- Pritch DT
- Prosolek SJ
- Pugh G
- Pusok M
- Pybus OG
- Pymont HM
- Quail MA
- Quick J
- Radulescu C
- Raghwani J
- Ragonnet-Cronin M
- Rainbow L
- Rajan D
- Rajatileka S
- Ramadan NA
- Rambaut A
- Ramble J
- Randell P
- Randell PA
- Ratcliffe L
- Raviprakash V
- Raza M
- Redshaw NM
- Rey S
- Reynolds N
- Richter A
- Robertson DL
- Robinson E
- Robson SC
- Rogan F
- Rooke S
- Rowe W
- Roy S
- Rudder S
- Ruis C
- Rushton S
- Saeed K
- Samaraweera B
- Sambles CM
- Sanderson R
- Sanderson T
- Sang F
- Sass T
- Scher E
- Scott C
- Scott G
- Sehmi J
- Shaaban S
- Shah D
- Shaw J
- Shelest E
- Shepherd JG
- Sheridan LA
- Sheriff N
- Shirley L
- Sillitoe J
- Silviera S
- Simpson DA
- Singh A
- Singleton D
- Skvortsov T
- Sloan TJ
- Sluga G
- Smith CP
- Smith DL
- Smith K
- Smith KS
- Smith L
- Smith N
- Smith P
- Smollett KL
- Snell LB
- Somassa T
- Southgate J
- Spellman K
- Spencer Chapman MH
- Spurgin LG
- Spyer MJ
- Stanley R
- Stanley W
- Stanton TD
- Starinskij I
- Stockton J
- Stonehouse S
- Storey N
- Studholme DJ
- Sudhanva M
- Swindells E
- Taha Y
- Tan NK
- Tang JW
- Tang M
- Taylor BEW
- Taylor JF
- Taylor S
- Temperton B
- Templeton K
- Templeton KE
- Thomas C
- Thomas-McEwen PMD
- Thomson EC
- Thomson L
- Thornton A
- Thurston SAJ
- Todd JA
- Tomb R
- Tong L
- Tonkin-Hill G
- Tovar-Corona JM
- Trebes A
- Trotter AJ
- Tsatsani I
- Turnbull R
- Twohig KA
- Umpleby H
- Underwood AP
- Vamos EE
- Vasylyeva TI
- Vattipally S
- Vernet G
- Vipond BB
- Volz EM
- Walsh S
- Wang D
- Warne B
- Warwick-Dugdale J
- Wastnedge E
- Watkins J
- Watson DipHe LK
- Waugh S
- Webster HJ
- Weldon D
- Westwick E
- Whalley T
- Wheeler H
- Whitehead M
- Whiteley M
- Whitwham A
- Wierzbicki C
- Willford NJ
- Williams C
- Williams C
- Williams C
- Williams CA
- Williams L
- Williams R
- Williams RJ
- Williams T
- Williamson KA
- Wilson-Davies E
- Witele E
- Withell KT
- Witney AA
- Wolverson P
- Wong N
- Workma T
- Wright DW
- Wright V
- Wyatt T
- Wyllie S
- Xu-McCrae L
- Yavus M
- Yaze G
- Yeats CA
- Yebra G
- Yew WC
- Young GR
- Young J
- Zarebski AE
- Zhang P
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/05/2023
- Field of study
Summary Background The first epidemic wave of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) in Scotland resulted in high case numbers and mortality in care homes. In Lothian, over one-third of care homes reported an outbreak, while there was limited testing of hospital patients discharged to care homes. Aim To investigate patients discharged from hospitals as a source of SARS-CoV-2 introduction into care homes during the first epidemic wave. Methods A clinical review was performed for all patients discharges from hospitals to care homes from 1st March 2020 to 31st May 2020. Episodes were ruled out based on coronavirus disease 2019 (COVID-19) test history, clinical assessment at discharge, whole-genome sequencing (WGS) data and an infectious period of 14 days. Clinical samples were processed for WGS, and consensus genomes generated were used for analysis using Cluster Investigation and Virus Epidemiological Tool software. Patient timelines were obtained using electronic hospital records. Findings In total, 787 patients discharged from hospitals to care homes were identified. Of these, 776 (99%) were ruled out for subsequent introduction of SARS-CoV-2 into care homes. However, for 10 episodes, the results were inconclusive as there was low genomic diversity in consensus genomes or no sequencing data were available. Only one discharge episode had a genomic, time and location link to positive cases during hospital admission, leading to 10 positive cases in their care home. Conclusion The majority of patients discharged from hospitals were ruled out for introduction of SARS-CoV-2 into care homes, highlighting the importance of screening all new admissions when faced with a novel emerging virus and no available vaccine
Tracking SARS-CoV-2 mutations and variants through the COG-UK-Mutation Explorer
- Author
- Aanensen DM
- Abudahab K
- Adams A
- Adams H
- Afifi S
- Aggarwal D
- Ahmad SSY
- Aigrain L
- Alcolea-Medina A
- Alikhan N - F
- Allara E
- Amato R
- Angyal A
- Annett T
- Aplin S
- Ariani CV
- Asad H
- Ash A
- Ashfield P
- Ashford F
- Atkinson L
- Attwood SW
- Auckland C
- Aydin A
- Baker DJ
- Baker P
- Balcazar CE
- Ball J
- Barrett JC
- Barrow M
- Barton E
- Bashton M
- Bassett AR
- Batra R
- Baxter C
- Bayzid N
- Beaver C
- Beckett AH
- Beckwith SM
- Bedford L
- Beer R
- Beggs A
- Bellis KL
- Berry L
- Bertolusso B
- Best A
- Betteridge E
- Bibby D
- Bicknell K
- Binns D
- Birchley A
- Bird PW
- Bishop C
- Blacow R
- Blakey V
- Blane B
- Bolt F
- Bonfield J
- Bonner S
- Bonsall D
- Boswell T
- Bosworth A
- Bourgeois Y
- Boyd O
- Bradley DT
- Breen C
- Bresner C
- Breuer J
- Bridgett S
- Bronner IF
- Brooks E
- Broos A
- Brown JR
- Bucca G
- Buchan SL
- Buck D
- Bull M
- Burns PJ
- Burton-Fanning S
- Byaruhanga T
- Byott M
- Campbell S
- Carabelli AM
- Cargill JS
- Carlile M
- Carvalho SF
- Casey A
- Castigador A
- Catalan J
- Chalker V
- Chaloner NJ
- Chand M
- Chappell JG
- Charalampous T
- Chatterton W
- Chaudhry Y
- Churcher CM
- Clark G
- Clarke P
- Cogger BJ
- Cole K
- Collins J
- Colquhoun R
- Connor TR
- Cook KF
- Coombes J
- Corden S
- Cormie C
- Cortes N
- Cotic M
- Cotton S
- Cottrell S
- Coupland L
- Cox A
- Cox M
- Craine N
- Crawford L
- Cross A
- Crown MR
- Crudgington D
- Cumley N
- Curran MD
- Curran T
- da Silva Filipe A
- Dabrera G
- Darby AC
- Davidson RK
- Davies A
- Davies RM
- Davis T
- de Angelis D
- De Lacy E
- de Oliveira Martins L
- de Silva TI
- Debebe J
- Denton-Smith R
- Dervisevic S
- Dewar R
- Dey J
- Dias J
- Dobie D
- Dorman MJ
- Downing F
- Driscoll M
- du Plessis L
- Duckworth N
- Durham J
- Eastick K
- Easton LJ
- Eccles R
- Edgeworth J
- Edwards S
- El Bouzidi K
- Eldirdiri S
- Ellaby N
- Elliott S
- Eltringham G
- Ensell L
- Erkiert MJ
- Essex S
- Evans C
- Evans JM
- Everson W
- Fairley DJ
- Fallon K
- Fanaie A
- Farr BW
- Fearn C
- Feltwell T
- Ferguson L
- Fina L
- Flaviani F
- Fleming VM
- Forrest S
- Foster-Nyarko E
- Foulkes BH
- Foulser L
- Fragakis M
- Frampton D
- Francois S
- Fraser C
- Freeman TM
- Fryer H
- Fuchs M
- Fuller W
- Gajee K
- Galai K
- Gallagher A
- Gallagher E
- Gallagher MD
- Gallis M
- Gaskin A
- Gatica-Wilcox B
- Geidelberg L
- Gemmell M
- Georgana I
- George RP
- Gifford L
- Gilbert L
- Girgis ST
- Glaysher S
- Goldstein EJ
- Golubchik T
- Gomes AN
- Gonçalves S
- Goodfellow IG
- Goodwin S
- Goudarzi S
- Gourtovaia M
- Graham C
- Graham L
- Grant PR
- Green A
- Green LR
- Greenaway J
- Gregory R
- Guest M
- Gunson RN
- Gupta RK
- Gutierrez B
- Haldenby ST
- Hamilton WL
- Hansford SE
- Haque T
- Harris KA
- Harrison EM
- Harrison EM
- Harrison I
- Hart J
- Hartley JA
- Harvey M
- Harvey WT
- Hassan-Ibrahim MO
- Heaney J
- Helmer T
- Henderson JH
- Hesketh AR
- Hey J
- Heyburn D
- Higginson EE
- Hill JD
- Hill V
- Hilson RA
- Hilvers E
- Holden MTG
- Hollis A
- Holmes AH
- Holmes CW
- Holmes N
- Hopes R
- Hornsby HR
- Hosmillo M
- Houlihan C
- Howson-Wells HC
- Hsu NS
- Hsu SN
- Hubb J
- Huck-Son H
- Hughes J
- Hughes J
- Hughes M
- Hughes W
- Hutchings S
- Idle G
- Illingworth CJ
- Impey R
- Irish-Tavares D
- Iturriza-Gomara M
- Izuagbe R
- Jackson B
- Jackson C
- Jackson DK
- Jackson KA
- Jackson LM
- Jahun AS
- James K
- James V
- Jeanes C
- Jeffries AR
- Jeremiah S
- Jermy A
- John M
- Johnson K
- Johnson R
- Johnston I
- Jones CR
- Jones H
- Jones N
- Jones O
- Jones S
- Joseph A
- Judges S
- Kay GL
- Kay S
- Keatley J - P
- Keeley AJ
- Kenyon A
- Kermack LM
- Khakh M
- Kidd SP
- Kimuli M
- Kirk S
- Kitchen C
- Kitchman K
- Knight BA
- Koshy C
- Kraemer MUG
- Kumziene-Summerhayes S
- Kwiatkowski D
- Lackenby A
- Laing KG
- Lampejo T
- Langford CF
- Lavin D
- Lawton AI
- Le-Viet T
- Lee D
- Lee JCD
- Lensing SV
- Leonard S
- Levett LJ
- Lewis J
- Lewis K
- Liddle J
- Liggett S
- Lillie PJ
- Lindsey BB
- Lister MM
- Livett R
- Lo S
- Loman NJ
- Loose MW
- Louka SF
- Loveson KF
- Lowdon S
- Lowe H
- Lowe HL
- Lucaci AO
- Ludden C
- Lynch J
- Lyons RA
- Lythgoe K
- Machin NW
- MacIntyre-Cockett G
- Mack A
- Macklin B
- Maclean A
- Macnaughton E
- Madona P
- Maes M
- Maftei L
- Mahanama AIK
- Mahungu TW
- Mair D
- Maksimovic J
- Malone CS
- Maloney D
- Manesis N
- Manley R
- Mantzouratou A
- Marchbank A
- Mariappan A
- Martincorena I
- Martinez Nunez RT
- Mather AE
- Maxwell P
- Mayhew M
- Mbisa T
- McCann CM
- McCarthy SA
- McCluggage K
- McClure PC
- McCrone JT
- McHugh MP
- McKenna JP
- McKerr C
- McManus GM
- McMurray CL
- McNally A
- Meadows L
- Medd N
- Megram O
- Menegazzo M
- Merrick I
- Michell SL
- Michelsen ML
- Mirfenderesky M
- Mirza J
- Miskelly J
- Moles-Garcia E
- Moll RJ
- Molnar Z
- Monahan IM
- Mondani M
- Mookerjee S
- Moore C
- Moore C
- Moore J
- Moore N
- Morcrette H
- Morgan M
- Morgan S
- Mori M
- Morriss A
- Moses S
- Mower C
- Muir P
- Mukaddas A
- Munemo F
- Munn R
- Murray A
- Murray DR
- Murray LJ
- Mutingwende M
- Myers R
- Nastouli E
- Nebbia G
- Nelson A
- Nelson C
- Nicholls S
- Nichols J
- Nicodemi R
- Nielsen M
- Nomikou K
- O'Brien S
- O'Grady J
- O'Toole Á
- Odedra M
- Ohemeng-Kumi N
- Oliver K
- Orton R
- Orton RJ
- Osman H
- Pacchiarini N
- Padgett D
- Page AJ
- Park EJ
- Park NR
- Parker MD
- Parmar S
- Partridge DG
- Pascall D
- Patel A
- Patel B
- Paterson S
- Payne BAI
- Peacock SJ
- Peacock SJ
- Peacock TP
- Pearson C
- Pelosi E
- Percival B
- Perkins J
- Perry M
- Pinckert ML
- Platt S
- Podplomyk O
- Pohare M
- Pond M
- Pope CF
- Poplawski R
- Powell J
- Poyner J
- Prestwood L
- Price A
- Price JR
- Prieto JA
- Pritchard DT
- Prosolek SJ
- Pugh G
- Pusok M
- Pybus OG
- Pymont HM
- Quail MA
- Quick J
- Radulescu C
- Raghwani J
- Ragonnet-Cronin M
- Rainbow L
- Rajan D
- Rajatileka S
- Ramadan NA
- Rambaut A
- Rambaut A
- Ramble J
- Randell PA
- Ratcliffe L
- Raviprakash V
- Raza M
- Redshaw NM
- Rey S
- Reynolds N
- Richter A
- Robertson DL
- Robertson DL
- Robinson E
- Robson SC
- Rogan F
- Rooke S
- Rowe W
- Roy S
- Rudder S
- Ruis C
- Rush-Ton S
- Saeed K
- Samaraweera B
- Sambles CM
- Sanderson R
- Sanderson T
- Sang F
- Sass T
- Scher E
- Scott C
- Scott G
- Sehmi J
- Shaaban S
- Shah D
- Shaw J
- Shelest E
- Shepherd JG
- Sheridan LA
- Sheriff N
- Shirley L
- Sillitoe J
- Silviera S
- Simpson DA
- Singh A
- Singleton D
- Skvortsov T
- Sloan TJ
- Sluga G
- Smith CP
- Smith DL
- Smith K
- Smith KS
- Smith L
- Smith N
- Smith P
- Smollett KL
- Snell LB
- Somassa T
- Southgate J
- Spellman K
- Spencer Chapman MH
- Spurgin LG
- Spyer MJ
- Stanley R
- Stanley W
- Stanton TD
- Starinskij I
- Stockton J
- Stonehouse S
- Storey N
- Studholme DJ
- Sudhanva M
- Swindells E
- Taha Y
- Tan NK
- Tang JW
- Tang M
- Taylor BEW
- Taylor JF
- Taylor S
- Temperton B
- Templeton KE
- Thomas C
- Thomson EC
- Thomson L
- Thornton A
- Thurston SAJ
- Todd JA
- Tomb R
- Tong L
- Tonkin-Hill G
- Torok ME
- Tovar-Corona JM
- Trebes A
- Trotter AJ
- Tsatsani I
- Turnbull R
- Turtle L
- Twohig KA
- Umpleby H
- Underwood AP
- Vamos EE
- Vasylyeva TI
- Vattipally S
- Vernet G
- Vipond BB
- Volz EM
- Walsh S
- Wang D
- Warne B
- Warwick-Dugdale J
- Wastnedge E
- Watkins J
- Watson LK
- Waugh S
- Webster HJ
- Weldon D
- Westwick E
- Whalley T
- Wheeler H
- Whitehead M
- Whiteley M
- Whitwham A
- Wierzbicki C
- Willford NJ
- Williams C
- Williams C
- Williams C
- Williams CA
- Williams L - A
- Williams R
- Williams RJ
- Williams T
- Williamson KA
- Wilson-Davies E
- Witele E
- Withell KT
- Witney AA
- Wolverson P
- Wong N
- Workman T
- Wright DW
- Wright V
- Wyatt T
- Wyllie S
- Xu-McCrae L
- Yavus M
- Yaze G
- Yeats CA
- Yebra G
- Yew WC
- Young GR
- Young J
- Zamudio ME
- Zarebski AE
- Zhang P
- Publication venue
- Publication date
- 01/03/2022
- Field of study
COG-UK Mutation Explorer (COG-UK-ME, https://sars2.cvr.gla.ac.uk/cog-uk/—last accessed date 16 March 2022) is a web resource that displays knowledge and analyses on SARS-CoV-2 virus genome mutations and variants circulating in the UK, with a focus on the observed amino acid replacements that have an antigenic role in the context of the human humoral and cellular immune response. This analysis is based on more than 2 million genome sequences (as of March 2022) for UK SARS-CoV-2 data held in the CLIMB-COVID centralised data environment. COG-UK-ME curates these data and displays analyses that are cross-referenced to experimental data collated from the primary literature. The aim is to track mutations of immunological importance that are accumulating in current variants of concern and variants of interest that could alter the neutralising activity of monoclonal antibodies (mAbs), convalescent sera, and vaccines. Changes in epitopes recognised by T cells, including those where reduced T cell binding has been demonstrated, are reported. Mutations that have been shown to confer SARS-CoV-2 resistance to antiviral drugs are also included. Using visualisation tools, COG-UK-ME also allows users to identify the emergence of variants carrying mutations that could decrease the neutralising activity of both mAbs present in therapeutic cocktails, e.g. Ronapreve. COG-UK-ME tracks changes in the frequency of combinations of mutations and brings together the curated literature on the impact of those mutations on various functional aspects of the virus and therapeutics. Given the unpredictable nature of SARS-CoV-2 as exemplified by yet another variant of concern, Omicron, continued surveillance of SARS-CoV-2 remains imperative to monitor virus evolution linked to the efficacy of therapeutics
The SARS-CoV-2 Alpha variant was associated with increased clinical severity of COVID-19 in Scotland: A genomics-based retrospective cohort analysis
- Author
- Aanensen DM
- Abudahab K
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- Afifi S
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- Wyllie S
- Xu-McCrae L
- Yavus M
- Yaze G
- Yeats CA
- Yebra G
- Yew WC
- Young GR
- Young J
- Zarebski AE
- Zhang P
- Publication venue
- Publication date
- 13/04/2023
- Field of study
Objectives
The SARS-CoV-2 Alpha variant was associated with increased transmission relative to other variants present at the time of its emergence and several studies have shown an association between Alpha variant infection and increased hospitalisation and 28-day mortality. However, none have addressed the impact on maximum severity of illness in the general population classified by the level of respiratory support required, or death. We aimed to do this.
Methods
In this retrospective multi-centre clinical cohort sub-study of the COG-UK consortium, 1475 samples from Scottish hospitalised and community cases collected between 1st November 2020 and 30th January 2021 were sequenced. We matched sequence data to clinical outcomes as the Alpha variant became dominant in Scotland and modelled the association between Alpha variant infection and severe disease using a 4-point scale of maximum severity by 28 days: 1. no respiratory support, 2. supplemental oxygen, 3. ventilation and 4. death.
Results
Our cumulative generalised linear mixed model analyses found evidence (cumulative odds ratio: 1.40, 95% CI: 1.02, 1.93) of a positive association between increased clinical severity and lineage (Alpha variant versus pre-Alpha variants).
Conclusions
The Alpha variant was associated with more severe clinical disease in the Scottish population than co-circulating lineages
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