dc.contributor.author | Gravningen, Kirsten Midttun | |
dc.contributor.author | Henriksen, Stian | |
dc.contributor.author | Hungnes, Olav | |
dc.contributor.author | Svendsen, Kristian | |
dc.contributor.author | Macdonald, Emily Ann | |
dc.contributor.author | Schirmer, Henrik | |
dc.contributor.author | Stene-Johansen, Kathrine | |
dc.contributor.author | Simonsen, Gunnar Skov | |
dc.contributor.author | Kacelnik, Oliver | |
dc.contributor.author | Elstrøm, Petter | |
dc.contributor.author | Bragstad, Karoline | |
dc.contributor.author | Rinaldo, Christine Hanssen | |
dc.date.accessioned | 2022-05-13T10:30:04Z | |
dc.date.available | 2022-05-13T10:30:04Z | |
dc.date.issued | 2022-02-18 | |
dc.description.abstract | Objective: To improve understanding of SARS-CoV-2-transmission and prevention measures on cruise
ships, we investigated a Norwegian cruise ship outbreak from July to August 2020 using a multidisciplinary approach after a rapid outbreak response launched by local and national health authorities.
Methods: We conducted a cross-sectional study among crew members using epidemiologic data and
results from SARS-CoV-2 polymerase chain reaction (PCR) of nasopharynx-oropharynx samples, antibody
analyses of blood samples, and whole-genome sequencing.
Results: We included 114 multinational crew members (71% participation), median age 36 years, and 69%
male. The attack rate was 33%; 32 of 37 outbreak cases were seropositive 5-10 days after PCR. One PCRnegative participant was seropositive, suggesting a previous infection. Network-analysis showed clusters
based on common exposures, including embarkation date, nationality, sharing a cabin with an infected
cabin-mate (adjusted odds ratio [AOR] 3.27; 95% confidence interval [CI] 0.97-11.07, p = 0.057), and specific workplaces (mechanical operations: 9.17 [1.82-45.78], catering: 6.11 [1.83-20.38]). Breaches in testing,
quarantine, and isolation practices before/during expeditions were reported. Whole-genome sequencing
revealed lineage B.1.36, previously identified in Asia. Despite extensive sequencing, the continued transmission of B.1.36 in Norway was not detected.
Conclusions: Our findings confirm the high risk of SARS-CoV-2-transmission on cruise ships related to
workplace and cabin type and show that continued community transmission after the outbreak could be
stopped by implementing immediate infection control measures at the final destination. | en_US |
dc.identifier.citation | Gravningen, Henriksen, Hungnes, Svendsen, Macdonald, Schirmer, Stene-Johansen, Simonsen, Kacelnik, Elstrøm, Bragstad, Rinaldo. Risk factors, immune response and whole‐genome sequencing of SARS‐CoV‐2 in a cruise ship outbreak in Norway. International Journal of Infectious Diseases. 2022;118:10-20 | en_US |
dc.identifier.cristinID | FRIDAID 2018940 | |
dc.identifier.doi | 10.1016/j.ijid.2022.02.025 | |
dc.identifier.issn | 1201-9712 | |
dc.identifier.issn | 1878-3511 | |
dc.identifier.uri | https://hdl.handle.net/10037/25119 | |
dc.language.iso | eng | en_US |
dc.publisher | Elsevier | en_US |
dc.relation.journal | International Journal of Infectious Diseases | |
dc.rights.accessRights | openAccess | en_US |
dc.rights.holder | Copyright 2022 The Author(s) | en_US |
dc.title | Risk factors, immune response and whole‐genome sequencing of SARS‐CoV‐2 in a cruise ship outbreak in Norway | en_US |
dc.type.version | publishedVersion | en_US |
dc.type | Journal article | en_US |
dc.type | Tidsskriftartikkel | en_US |
dc.type | Peer reviewed | en_US |