Your browser doesn't support javascript.
loading
SARS-CoV-2 variants associated with vaccine breakthrough in the Delaware Valley through summer 2021.
Marques, Andrew D; Sherrill-Mix, Scott; Everett, John; 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 Pennsylvania, Philadelphia, PA.
  • Sherrill-Mix S; Department of Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Everett J; Department of Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Reddy S; Department of Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Hokama P; Department of Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Roche AM; Department of Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Hwang Y; Department of Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Glascock A; Department of Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Whiteside SA; Pulmonary, Allergy and Critical Care Division; Department of Medicine; University of Pennsylvania Perelman School of Medicine; Philadelphia, PA.
  • Graham-Wooten J; Pulmonary, Allergy and Critical Care Division; Department of Medicine; University of Pennsylvania Perelman School of Medicine; Philadelphia, PA.
  • Khatib LA; Pulmonary, Allergy and Critical Care Division; Department of Medicine; University of Pennsylvania Perelman School of Medicine; Philadelphia, PA.
  • Fitzgerald AS; Pulmonary, Allergy and Critical Care Division; Department of Medicine; University of Pennsylvania Perelman School of Medicine; Philadelphia, PA.
  • Moustafa AM; Division of Infectious Diseases, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Bianco C; Division of Gastroenterology, Hepatology & Nutrition, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Rajagopal S; Division of Infectious Diseases, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Helton J; Division of Infectious Diseases, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Deming R; Division of COVID-19 Containment, Philadelphia Department of Public Health, Philadelphia, PA.
  • Denu L; Division of Infectious Diseases, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Ahmed A; Division of Infectious Diseases, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Kitt E; Department of Microbiology & Immunology, Center for Genomic Sciences, Drexel University College of Medicine. Philadelphia, PA.
  • Coffin SE; Division of Infectious Diseases, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Newbern C; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Mell JC; Division of Infectious Diseases, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Planet PJ; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Badjatia N; Division of COVID-19 Containment, Philadelphia Department of Public Health, Philadelphia, PA.
  • Richards B; Department of Microbiology & Immunology, Center for Genomic Sciences, Drexel University College of Medicine. Philadelphia, PA.
  • Wang ZX; Division of Infectious Diseases, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Cannuscio CC; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Strelau KM; Sackler Institute for Comparative Genomics, American Museum of Natural History, New York, NY.
  • Jaskowiak-Barr A; Molecular & Genomic Pathology Laboratory, Thomas Jefferson University Hospital, Philadelphia, PA.
  • Cressman L; Jefferson Occupational Health Network for Employees and Students (JOHN), Thomas Jefferson University, Philadelphia, PA.
  • Loughrey S; Molecular & Genomic Pathology Laboratory, Thomas Jefferson University Hospital, Philadelphia, PA.
  • Ganguly A; Department of Anatomy, Pathology, and Cell Biology, Thomas Jefferson University Hospital, Philadelphia, PA.
  • Feldman MD; Leonard Davis Institute of Health Economics, University of Pennsylvania, Philadelphia, PA.
  • Collman RG; Department of Family Medicine and Community Health, University of Pennsylvania, Philadelphia, PA.
  • Rodino KG; Leonard Davis Institute of Health Economics, University of Pennsylvania, Philadelphia, PA.
  • Kelly BJ; Department of Family Medicine and Community Health, University of Pennsylvania, Philadelphia, PA.
  • Bushman FD; Division of Infectious Diseases; Department of Medicine & Department of Biostatistics, Epidemiology, and Informatics; Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
medRxiv ; 2021 Nov 17.
Article en En | MEDLINE | ID: mdl-34704098
ABSTRACT
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 three-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 of 1.25-3.18). This study thus provides a detailed picture of viral evolution in the Delaware Valley and a geographically matched analysis of vaccine breakthroughs; it also introduces a rigorous statistical approach to interrogating enrichment of viral variants.
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: MedRxiv Año: 2021 Tipo del documento: Article País de afiliación: Panamá

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: MedRxiv Año: 2021 Tipo del documento: Article País de afiliación: Panamá