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dc.contributor.authorDavies, Mark R
dc.contributor.authorMcIntyre, Liam
dc.contributor.authorMutreja, Ankur
dc.contributor.authorLacey, Jake A
dc.contributor.authorLees, John A
dc.contributor.authorTowers, Rebecca J
dc.contributor.authorDuchêne, Sebastián
dc.contributor.authorSmeesters, Pierre R
dc.contributor.authorFrost, Hannah R
dc.contributor.authorPrice, David J.
dc.contributor.authorHolden, Matthew T G
dc.contributor.authorDavid, Sophia
dc.contributor.authorGiffard, Philip M
dc.contributor.authorWorthing, Kate A
dc.contributor.authorSeale, Anna C
dc.contributor.authorBerkley, James A
dc.contributor.authorHarris, Simon R
dc.contributor.authorRivera-Hernandez, Tania
dc.contributor.authorBerking, Olga
dc.contributor.authorCork, Amanda J
dc.contributor.authorTorres, Rosângela S L A
dc.contributor.authorLithgow, Trevor
dc.contributor.authorStrugnell, Richard A
dc.contributor.authorBergmann, Rene
dc.contributor.authorNitsche-Schmitz, Patric
dc.contributor.authorChhatwal, Gusharan S
dc.contributor.authorBentley, Stephen D
dc.contributor.authorFraser, John D
dc.contributor.authorMoreland, Nicole J
dc.contributor.authorCarapetis, Jonathan R
dc.contributor.authorSteer, Andrew C
dc.contributor.authorParkhill, Julian
dc.contributor.authorSaul, Allan
dc.contributor.authorWilliamson, Deborah A
dc.contributor.authorCurrie, Bart J
dc.contributor.authorTong, Steven Y C
dc.contributor.authorDougan, Gordon
dc.contributor.authorWalker, Mark J
dc.date.accessioned2019-11-27T00:36:50Z
dc.date.available2019-11-27T00:36:50Z
dc.date.issued2019-06
dc.identifier259130243
dc.identifier5a56762a-36bf-4356-9cb0-c753ed597d46
dc.identifier31133745
dc.identifier85066634559
dc.identifier000469996900015
dc.identifier.citationDavies , M R , McIntyre , L , Mutreja , A , Lacey , J A , Lees , J A , Towers , R J , Duchêne , S , Smeesters , P R , Frost , H R , Price , D J , Holden , M T G , David , S , Giffard , P M , Worthing , K A , Seale , A C , Berkley , J A , Harris , S R , Rivera-Hernandez , T , Berking , O , Cork , A J , Torres , R S L A , Lithgow , T , Strugnell , R A , Bergmann , R , Nitsche-Schmitz , P , Chhatwal , G S , Bentley , S D , Fraser , J D , Moreland , N J , Carapetis , J R , Steer , A C , Parkhill , J , Saul , A , Williamson , D A , Currie , B J , Tong , S Y C , Dougan , G & Walker , M J 2019 , ' Atlas of group A streptococcal vaccine candidates compiled using large-scale comparative genomics ' , Nature Genetics , vol. 51 , no. 6 , pp. 1035-1043 . https://doi.org/10.1038/s41588-019-0417-8en
dc.identifier.issn1061-4036
dc.identifier.otherORCID: /0000-0002-4958-2166/work/60196428
dc.identifier.urihttps://hdl.handle.net/10023/19008
dc.descriptionThis work was supported by National Health and Medical Research Council project and program grants for: Protein Glycan Interactions in Infectious Diseases and Cellular Microbiology; the Coalition to Accelerate New Vaccines Against Streptococcus (CANVAS; an Australian and New Zealand joint initiative); and The Wellcome Trust, UK. For part of this study, M.R.D. was supported by a National Health and Medical Research Council postdoctoral training fellowship (635250) and A.M. was a GENDRIVAX fellow funded by the European Union’s Seventh Framework Programme FP7/2007–2013/ under REA grant agreement number 251522.en
dc.description.abstractGroup A Streptococcus (GAS; Streptococcus pyogenes) is a bacterial pathogen for which a commercial vaccine for humans is not available. Employing the advantages of high-throughput DNA sequencing technology to vaccine design, we have analyzed 2,083 globally sampled GAS genomes. The global GAS population structure reveals extensive genomic heterogeneity driven by homologous recombination and overlaid with high levels of accessory gene plasticity. We identified the existence of more than 290 clinically associated genomic phylogroups across 22 countries, highlighting challenges in designing vaccines of global utility. To determine vaccine candidate coverage, we investigated all of the previously described GAS candidate antigens for gene carriage and gene sequence heterogeneity. Only 15 of 28 vaccine antigen candidates were found to have both low naturally occurring sequence variation and high (>99%) coverage across this diverse GAS population. This technological platform for vaccine coverage determination is equally applicable to prospective GAS vaccine antigens identified in future studies.
dc.format.extent5824169
dc.language.isoeng
dc.relation.ispartofNature Geneticsen
dc.subjectQR Microbiologyen
dc.subjectQR180 Immunologyen
dc.subjectDASen
dc.subjectBDCen
dc.subjectR2Cen
dc.subject~DC~en
dc.subjectSDG 3 - Good Health and Well-beingen
dc.subject.lccQRen
dc.subject.lccQR180en
dc.titleAtlas of group A streptococcal vaccine candidates compiled using large-scale comparative genomicsen
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. School of Medicineen
dc.contributor.institutionUniversity of St Andrews. Infection and Global Health Divisionen
dc.contributor.institutionUniversity of St Andrews. Biomedical Sciences Research Complexen
dc.contributor.institutionUniversity of St Andrews. Infection Groupen
dc.identifier.doi10.1038/s41588-019-0417-8
dc.description.statusPeer revieweden
dc.date.embargoedUntil2019-11-27


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