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SARS-CoV-2 Variants Associated with Vaccine Breakthrough in the Delaware Valley through Summer 2021.
Marques, Andrew D; Sherrill-Mix, Scott; Everett, John K; Reddy, Shantan; Hokama, Pascha; Roche, Aoife M; Hwang, Young; Glascock, Abigail; Whiteside, Samantha A; Graham-Wooten, Jevon; Khatib, Layla A; Fitzgerald, Ayannah S; Moustafa, Ahmed M; Bianco, Colleen; Rajagopal, Swetha; Helton, Jenna; Deming, Regan; Denu, Lidiya; Ahmed, Azad; Kitt, Eimear; Coffin, Susan E; Newbern, Claire; Mell, Josh Chang; Planet, Paul J; Badjatia, Nitika; Richards, Bonnie; Wang, Zi-Xuan; Cannuscio, Carolyn C; Strelau, Katherine M; Jaskowiak-Barr, Anne; Cressman, Leigh; Loughrey, Sean; Ganguly, Arupa; Feldman, Michael D; Collman, Ronald G; Rodino, Kyle G; Kelly, Brendan J; Bushman, Frederic D.
Afiliación
  • Marques AD; Department of Microbiology, Perelman School of Medicine, University of Pennsylvaniagrid.25879.31, Philadelphia, Pennsylvania, USA.
  • Sherrill-Mix S; Department of Microbiology, Perelman School of Medicine, University of Pennsylvaniagrid.25879.31, Philadelphia, Pennsylvania, USA.
  • Everett JK; Department of Microbiology, Perelman School of Medicine, University of Pennsylvaniagrid.25879.31, Philadelphia, Pennsylvania, USA.
  • Reddy S; Department of Microbiology, Perelman School of Medicine, University of Pennsylvaniagrid.25879.31, Philadelphia, Pennsylvania, USA.
  • Hokama P; Department of Microbiology, Perelman School of Medicine, University of Pennsylvaniagrid.25879.31, Philadelphia, Pennsylvania, USA.
  • Roche AM; Department of Microbiology, Perelman School of Medicine, University of Pennsylvaniagrid.25879.31, Philadelphia, Pennsylvania, USA.
  • Hwang Y; Department of Microbiology, Perelman School of Medicine, University of Pennsylvaniagrid.25879.31, Philadelphia, Pennsylvania, USA.
  • Glascock A; Department of Microbiology, Perelman School of Medicine, University of Pennsylvaniagrid.25879.31, Philadelphia, Pennsylvania, USA.
  • Whiteside SA; Pulmonary, Allergy and Critical Care Division, Department of Medicine, University of Pennsylvaniagrid.25879.31 Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
  • Graham-Wooten J; Pulmonary, Allergy and Critical Care Division, Department of Medicine, University of Pennsylvaniagrid.25879.31 Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
  • Khatib LA; Pulmonary, Allergy and Critical Care Division, Department of Medicine, University of Pennsylvaniagrid.25879.31 Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
  • Fitzgerald AS; Pulmonary, Allergy and Critical Care Division, Department of Medicine, University of Pennsylvaniagrid.25879.31 Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
  • Moustafa AM; Division of Infectious Diseases, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Bianco C; Division of Gastroenterology, Hepatology & Nutrition, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Rajagopal S; Division of Infectious Diseases, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Helton J; Division of Infectious Diseases, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Deming R; Division of COVID-19 Containment, Philadelphia Department of Public Health, Philadelphia, Pennsylvania, USA.
  • Denu L; Division of Infectious Diseases, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Ahmed A; Division of Infectious Diseases, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Kitt E; Department of Microbiology & Immunology, Center for Genomic Sciences, Drexel Universitygrid.166341.7 College of Medicine, Philadelphia, Pennsylvania, USA.
  • Coffin SE; Division of Infectious Diseases, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Newbern C; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvaniagrid.25879.31, Philadelphia, Pennsylvania, USA.
  • Mell JC; Division of Infectious Diseases, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Planet PJ; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvaniagrid.25879.31, Philadelphia, Pennsylvania, USA.
  • Badjatia N; Division of COVID-19 Containment, Philadelphia Department of Public Health, Philadelphia, Pennsylvania, USA.
  • Richards B; Department of Microbiology & Immunology, Center for Genomic Sciences, Drexel Universitygrid.166341.7 College of Medicine, Philadelphia, Pennsylvania, USA.
  • Wang ZX; Division of Infectious Diseases, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Cannuscio CC; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvaniagrid.25879.31, Philadelphia, Pennsylvania, USA.
  • Strelau KM; Sackler Institute for Comparative Genomics, American Museum of Natural History, New York, New York, USA.
  • Jaskowiak-Barr A; Molecular & Genomic Pathology Laboratory, Thomas Jefferson Universitygrid.265008.9 Hospital, Philadelphia, Pennsylvania, USA.
  • Cressman L; Jefferson Occupational Health Network for Employees and Students (JOHN), Thomas Jefferson Universitygrid.265008.9, Philadelphia, Pennsylvania, USA.
  • Loughrey S; Molecular & Genomic Pathology Laboratory, Thomas Jefferson Universitygrid.265008.9 Hospital, Philadelphia, Pennsylvania, USA.
  • Ganguly A; Department of Anatomy, Pathology, and Cell Biology, Thomas Jefferson Universitygrid.265008.9 Hospital, Philadelphia, Pennsylvania, USA.
  • Feldman MD; Leonard Davis Institute of Health Economics, University of Pennsylvaniagrid.25879.31, Philadelphia, Pennsylvania, USA.
  • Collman RG; Department of Family Medicine and Community Health, University of Pennsylvaniagrid.25879.31, Philadelphia, Pennsylvania, USA.
  • Rodino KG; Leonard Davis Institute of Health Economics, University of Pennsylvaniagrid.25879.31, Philadelphia, Pennsylvania, USA.
  • Kelly BJ; Department of Family Medicine and Community Health, University of Pennsylvaniagrid.25879.31, Philadelphia, Pennsylvania, USA.
  • Bushman FD; Division of Infectious Diseases, Department of Medicine & Department of Biostatistics, Epidemiology, and Informatics, Perelman School of Medicine, University of Pennsylvaniagrid.25879.31, Philadelphia, Pennsylvania, USA.
mBio ; 13(1): e0378821, 2021 02 22.
Article en En | MEDLINE | ID: mdl-35130727
The severe acute respiratory coronavirus-2 (SARS-CoV-2) is the cause of the global outbreak of COVID-19. Evidence suggests that the virus is evolving to allow efficient spread through the human population, including vaccinated individuals. Here, we report a study of viral variants from surveillance of the Delaware Valley, including the city of Philadelphia, and variants infecting vaccinated subjects. We sequenced and analyzed complete viral genomes from 2621 surveillance samples from March 2020 to September 2021 and compared them to genome sequences from 159 vaccine breakthroughs. In the early spring of 2020, all detected variants were of the B.1 and closely related lineages. A mixture of lineages followed, notably including B.1.243 followed by B.1.1.7 (alpha), with other lineages present at lower levels. Later isolations were dominated by B.1.617.2 (delta) and other delta lineages; delta was the exclusive variant present by the last time sampled. To investigate whether any variants appeared preferentially in vaccine breakthroughs, we devised a model based on Bayesian autoregressive moving average logistic multinomial regression to allow rigorous comparison. This revealed that B.1.617.2 (delta) showed 3-fold enrichment in vaccine breakthrough cases (odds ratio of 3; 95% credible interval 0.89-11). Viral point substitutions could also be associated with vaccine breakthroughs, notably the N501Y substitution found in the alpha, beta and gamma variants (odds ratio 2.04; 95% credible interval of1.25-3.18). This study thus overviews viral evolution and vaccine breakthroughs in the Delaware Valley and introduces a rigorous statistical approach to interrogating enrichment of breakthrough variants against a changing background. IMPORTANCE SARS-CoV-2 vaccination is highly effective at reducing viral infection, hospitalization and death. However, vaccine breakthrough infections have been widely observed, raising the question of whether particular viral variants or viral mutations are associated with breakthrough. Here, we report analysis of 2621 surveillance isolates from people diagnosed with COVID-19 in the Delaware Valley in southeastern Pennsylvania, allowing rigorous comparison to 159 vaccine breakthrough case specimens. Our best estimate is a 3-fold enrichment for some lineages of delta among breakthroughs, and enrichment of a notable spike substitution, N501Y. We introduce statistical methods that should be widely useful for evaluating vaccine breakthroughs and other viral phenotypes.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Vacunas / COVID-19 Tipo de estudio: Risk_factors_studies Límite: Humans País/Región como asunto: America do norte Idioma: En Revista: MBio Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Vacunas / COVID-19 Tipo de estudio: Risk_factors_studies Límite: Humans País/Región como asunto: America do norte Idioma: En Revista: MBio Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos