Increased transmissibility of the alpha SARS-CoV-2 variant: evidence from contact tracing data in Oslo, January to February 2021.

SARS-CoV-2 alpha variant contact tracing data household transmission secondary attack rate transmissibility

Journal

Infectious diseases (London, England)
ISSN: 2374-4243
Titre abrégé: Infect Dis (Lond)
Pays: England
ID NLM: 101650235

Informations de publication

Date de publication:
Jan 2022
Historique:
pubmed: 8 10 2021
medline: 25 12 2021
entrez: 7 10 2021
Statut: ppublish

Résumé

Information about the contagiousness of new SARS-CoV-2 variants, including the alpha lineage, and how they spread in various locations is essential. Country-specific estimates are needed because local interventions influence transmissibility. We analysed contact tracing data from Oslo municipality, reported from January through February 2021, when the alpha lineage became predominant in Norway and estimated the relative transmissibility of the alpha lineage with the use of Poisson regression. Within households, we found an increase in the secondary attack rate by 60% (95% CI 20-114%) among cases infected with the alpha lineage compared to other variants; including all close contacts, the relative increase in the secondary attack rate was 24% (95% CI -6%-43%). There was a significantly higher risk of infecting household members in index cases aged 40-59 years who were infected with the alpha lineage; we found no association between transmission and household size. Overall, including all close contacts, we found that the reproduction number among cases with the alpha lineage was increased by 24% (95% CI 0%-52%), corresponding to an absolute increase of 0.19, compared to the group of index cases infected with other variants. Our study suggests that households are the primary locations for rapid transmission of the new lineage alpha.

Sections du résumé

BACKGROUND BACKGROUND
Information about the contagiousness of new SARS-CoV-2 variants, including the alpha lineage, and how they spread in various locations is essential. Country-specific estimates are needed because local interventions influence transmissibility.
METHODS METHODS
We analysed contact tracing data from Oslo municipality, reported from January through February 2021, when the alpha lineage became predominant in Norway and estimated the relative transmissibility of the alpha lineage with the use of Poisson regression.
RESULTS RESULTS
Within households, we found an increase in the secondary attack rate by 60% (95% CI 20-114%) among cases infected with the alpha lineage compared to other variants; including all close contacts, the relative increase in the secondary attack rate was 24% (95% CI -6%-43%). There was a significantly higher risk of infecting household members in index cases aged 40-59 years who were infected with the alpha lineage; we found no association between transmission and household size. Overall, including all close contacts, we found that the reproduction number among cases with the alpha lineage was increased by 24% (95% CI 0%-52%), corresponding to an absolute increase of 0.19, compared to the group of index cases infected with other variants.
CONCLUSION CONCLUSIONS
Our study suggests that households are the primary locations for rapid transmission of the new lineage alpha.

Identifiants

pubmed: 34618665
doi: 10.1080/23744235.2021.1977382
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

72-77

Auteurs

Jonas Christoffer Lindstrøm (JC)

Division of Infection Control and Environmental Health, Norwegian Institute of Public Health, Oslo, Norway.

Solveig Engebretsen (S)

SAMBA, Norwegian Computing Center, Oslo, Norway.

Anja Bråthen Kristoffersen (AB)

Division of Infection Control and Environmental Health, Norwegian Institute of Public Health, Oslo, Norway.

Gunnar Øyvind Isaksson Rø (GØI)

Division of Infection Control and Environmental Health, Norwegian Institute of Public Health, Oslo, Norway.

Alfonso Diz-Lois Palomares (AD)

Division of Infection Control and Environmental Health, Norwegian Institute of Public Health, Oslo, Norway.

Kenth Engø-Monsen (K)

Telenor Research, Oslo, Norway.

Elisabeth Henie Madslien (EH)

Division of Infection Control and Environmental Health, Norwegian Institute of Public Health, Oslo, Norway.

Frode Forland (F)

Division of Infection Control and Environmental Health, Norwegian Institute of Public Health, Oslo, Norway.

Karin Maria Nygård (KM)

Division of Infection Control and Environmental Health, Norwegian Institute of Public Health, Oslo, Norway.

Frode Hagen (F)

Oslo Municipality Health Service, Oslo, Norway.

Gunnar Gantzel (G)

Oslo Municipality Health Service, Oslo, Norway.

Ottar Wiklund (O)

Oslo Municipality Health Service, Oslo, Norway.

Arnoldo Frigessi (A)

Oslo Centre for Biostatistics and Epidemiology, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Oslo Centre for Biostatistics and Epidemiology, Oslo University Hospital, Oslo, Norway.

Birgitte Freiesleben de Blasio (BF)

Division of Infection Control and Environmental Health, Norwegian Institute of Public Health, Oslo, Norway.
Oslo Centre for Biostatistics and Epidemiology, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.

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