Severe Acute Respiratory Syndrome Coronavirus 2 Delta Vaccine Breakthrough Transmissibility in Alachua County, Florida.


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
29 10 2022
Historique:
received: 30 11 2021
pubmed: 11 3 2022
medline: 2 11 2022
entrez: 10 3 2022
Statut: ppublish

Résumé

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Delta variant has caused a dramatic resurgence in infections in the United Sates, raising questions regarding potential transmissibility among vaccinated individuals. Between October 2020 and July 2021, we sequenced 4439 SARS-CoV-2 full genomes, 23% of all known infections in Alachua County, Florida, including 109 vaccine breakthrough cases. Univariate and multivariate regression analyses were conducted to evaluate associations between viral RNA burden and patient characteristics. Contact tracing and phylogenetic analysis were used to investigate direct transmissions involving vaccinated individuals. The majority of breakthrough sequences with lineage assignment were classified as Delta variants (74.6%) and occurred, on average, about 3 months (104 ± 57.5 days) after full vaccination, at the same time (June-July 2021) of Delta variant exponential spread within the county. Six Delta variant transmission pairs between fully vaccinated individuals were identified through contact tracing, 3 of which were confirmed by phylogenetic analysis. Delta breakthroughs exhibited broad viral RNA copy number values during acute infection (interquartile range, 1.2-8.64 Log copies/mL), on average 38% lower than matched unvaccinated patients (3.29-10.81 Log copies/mL, P < .00001). Nevertheless, 49% to 50% of all breakthroughs, and 56% to 60% of Delta-infected breakthroughs exhibited viral RNA levels above the transmissibility threshold (4 Log copies/mL) irrespective of time after vaccination. Delta infection transmissibility and general viral RNA quantification patterns in vaccinated individuals suggest limited levels of sterilizing immunity that need to be considered by public health policies. In particular, ongoing evaluation of vaccine boosters should specifically address whether extra vaccine doses curb breakthrough contribution to epidemic spread.

Sections du résumé

BACKGROUND
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Delta variant has caused a dramatic resurgence in infections in the United Sates, raising questions regarding potential transmissibility among vaccinated individuals.
METHODS
Between October 2020 and July 2021, we sequenced 4439 SARS-CoV-2 full genomes, 23% of all known infections in Alachua County, Florida, including 109 vaccine breakthrough cases. Univariate and multivariate regression analyses were conducted to evaluate associations between viral RNA burden and patient characteristics. Contact tracing and phylogenetic analysis were used to investigate direct transmissions involving vaccinated individuals.
RESULTS
The majority of breakthrough sequences with lineage assignment were classified as Delta variants (74.6%) and occurred, on average, about 3 months (104 ± 57.5 days) after full vaccination, at the same time (June-July 2021) of Delta variant exponential spread within the county. Six Delta variant transmission pairs between fully vaccinated individuals were identified through contact tracing, 3 of which were confirmed by phylogenetic analysis. Delta breakthroughs exhibited broad viral RNA copy number values during acute infection (interquartile range, 1.2-8.64 Log copies/mL), on average 38% lower than matched unvaccinated patients (3.29-10.81 Log copies/mL, P < .00001). Nevertheless, 49% to 50% of all breakthroughs, and 56% to 60% of Delta-infected breakthroughs exhibited viral RNA levels above the transmissibility threshold (4 Log copies/mL) irrespective of time after vaccination.
CONCLUSIONS
Delta infection transmissibility and general viral RNA quantification patterns in vaccinated individuals suggest limited levels of sterilizing immunity that need to be considered by public health policies. In particular, ongoing evaluation of vaccine boosters should specifically address whether extra vaccine doses curb breakthrough contribution to epidemic spread.

Identifiants

pubmed: 35271704
pii: 6546683
doi: 10.1093/cid/ciac197
pmc: PMC9617581
doi:

Substances chimiques

RNA, Viral 0
Viral Vaccines 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1618-1627

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press for the Infectious Diseases Society of America.

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Auteurs

Brittany Rife Magalis (B)

Emerging Pathogens Institute, University of Florida, Gainesville, Florida, USA.
Department of Pathology, University of Florida, Gainesville, Florida, USA.

Shannan Rich (S)

Department of Epidemiology, University of Florida, Gainesville, Florida, USA.
Florida Department of Health, Alachua County, Gainesville, Florida, USA.

Massimiliano S Tagliamonte (MS)

Emerging Pathogens Institute, University of Florida, Gainesville, Florida, USA.
Department of Pathology, University of Florida, Gainesville, Florida, USA.

Carla Mavian (C)

Emerging Pathogens Institute, University of Florida, Gainesville, Florida, USA.
Department of Pathology, University of Florida, Gainesville, Florida, USA.

Melanie N Cash (MN)

Emerging Pathogens Institute, University of Florida, Gainesville, Florida, USA.
Department of Pathology, University of Florida, Gainesville, Florida, USA.

Alberto Riva (A)

Interdisciplinary Center for Biotechnology Research, University of Florida, Gainesville, Florida, USA.

Simone Marini (S)

Department of Pathology, University of Florida, Gainesville, Florida, USA.
Department of Epidemiology, University of Florida, Gainesville, Florida, USA.

David Moraga Amador (DM)

Interdisciplinary Center for Biotechnology Research, University of Florida, Gainesville, Florida, USA.

Yanping Zhang (Y)

Interdisciplinary Center for Biotechnology Research, University of Florida, Gainesville, Florida, USA.

Jerne Shapiro (J)

Department of Epidemiology, University of Florida, Gainesville, Florida, USA.
Florida Department of Health, Alachua County, Gainesville, Florida, USA.

Amelia Horine (A)

Florida Department of Health, Alachua County, Gainesville, Florida, USA.

Petr Starostik (P)

Department of Pathology, University of Florida, Gainesville, Florida, USA.

Maura Pieretti (M)

BayCare Laboratories LLC, Tampa, Florida, USA.

Samantha Vega (S)

BayCare Laboratories LLC, Tampa, Florida, USA.

Ana Paula Lacombe (A)

University of Miami Miller School of Medicine, Miami, Florida, USA.

Jessica Salinas (J)

University of Miami Miller School of Medicine, Miami, Florida, USA.

Mario Stevenson (M)

University of Miami Miller School of Medicine, Miami, Florida, USA.

Paul Myers (P)

Florida Department of Health, Alachua County, Gainesville, Florida, USA.

J Glenn Morris (J)

Emerging Pathogens Institute, University of Florida, Gainesville, Florida, USA.
Department of Medicine, College of Medicine, University of Florida, Gainesville, Florida.

Michael Lauzardo (M)

Emerging Pathogens Institute, University of Florida, Gainesville, Florida, USA.
Florida Department of Health, Alachua County, Gainesville, Florida, USA.
Department of Medicine, College of Medicine, University of Florida, Gainesville, Florida.

Mattia Prosperi (M)

Department of Epidemiology, University of Florida, Gainesville, Florida, USA.

Marco Salemi (M)

Emerging Pathogens Institute, University of Florida, Gainesville, Florida, USA.
Department of Pathology, University of Florida, Gainesville, Florida, USA.

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