Journal List > J Korean Med Sci > v.36(50) > 1148745

Lee, Choe, Jeong, Kim, Kim, Yoo, Park, Kim, Choi, Sim, Park, Huh, Hong, Kim, Song, Lee, Kim, Rhee, Kim, Gwack, Kim, Jeon, Lee, Jeong, Kim, Bae, Kim, Kim, Lee, Lee, Kim, Park, Yu, Choi, Kim, Lee, Jang, Lim, Lee, and Park: Importation and Transmission of SARS-CoV-2 B.1.1.529 (Omicron) Variant of Concern in Korea, November 2021

Abstract

In November 2021, 14 international travel-related severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) B.1.1.529 (omicron) variant of concern (VOC) patients were detected in South Korea. Epidemiologic investigation revealed community transmission of the omicron VOC. A total of 80 SARS-CoV-2 omicron VOC-positive patients were identified until December 10, 2021 and 66 of them reported no relation to the international travel. There may be more transmissions with this VOC in Korea than reported.

Graphical Abstract

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Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) B.1.1.529 omicron variant of concern (VOC) was first reported on November 24, 2021 in South Africa, and has quickly spread globally.1 The first two patients infected with omicron VOC in South Korea was identified on November 25, 2021, during the screening of inbound international travelers at the airport. Herein, we describe the omicron VOC prevalence over time and epidemiological and clinical characteristics of the confirmed patients.
Details of the surveillance system have been described earlier.2 Public health officers interviewed patients about demographics, vaccination history, and symptoms. In all cases and contacts, nasopharyngeal swab specimen was collected for reverse transcriptase polymerase chain reaction (RT-PCR) tests. Incubation period was calculated from time of exposure, and the serial interval was estimated based on the time from symptom onset in index cases to symptom onset in corresponding contacts.
During November 24 - December 10, 2021, a total of 80 SARS-CoV-2 omicron VOC-positive patients were identified in Korea (Table 1). In total, 14 (17.5%) patients had history of international travels within 14 days of symptom onset, or if asymptomatic, SARS-CoV-2 test results (Nigeria, n = 10; South Africa, n = 2; Mozambique, n = 1; Ethiopia, n = 1, Iran, n = 1; Fig. 1A). Among community transmission cases, 26 were from households, and 12 were from church-related clusters (Fig. 1B). Among 78 patients with documented history of vaccination, 48 (60.0%) were unvaccinated, and 25 (31.3%) were vaccinated. The vaccinated persons have received BNT162b (n = 13), mRNA-1273 (n = 5), Ad26.COV2.S (n = 4), and ChAdOx1 (n = 3) vaccines (Table 1).
Most of the first 80 SARS-CoV-2 omicron VOC-positive patients were with mild symptoms, and 27.5% were asymptomatic, and no cases were with severe diseases nor death during 6.1 mean observed days (range, 2–16 days). Estimated incubation period was 4.2 days (range, 2–8 days) and serial interval was 2.8 days (range, 1–7 days).
We describe the first 80 patients of SARS-CoV-2 omicron VOC-positive patients identified in South Korea, which have rapidly transmitted to the community in the households and the church. Epidemiologic features of the omicron VOC have not been fully characterized in other places.3 Our finding of short serial interval of 2.8 days is in line with findings from South Africa, with growing reproductive number compared to the delta VOC.4 Meanwhile, none of the first 80 patients underwent severe disease or death as in the US, which was reassuring, yet, should be monitored further.5 The hypothesis of trade-off between virulence and transmissibility has been proposed decades ago, which may be supportive to the evolution of SARS-CoV-2 in the long term.6
Note that 60% of omicron VOC-positive patients were unvaccinated, which emphasizes the need for vaccination to limit the transmission. Yet, given the high rates of mutation that omicron VOC carries, vaccine effectiveness should be investigated further.7 Earlier findings from South Africa suggest the efficacy of coronavirus disease 2019 vaccine may be significantly reduced against omicron VOC.8
Because information about these early cases of SARS-CoV-2 omicron VOC are selected from import-related incidents, our interpretation should be made cautiously. Moreover, given the relatively short observation time, further follow-up is needed to ascertain the disease severity of this specific VOC as more data are reported globally.
In summary, importation of SARS-COV-2 omicron VOC has caused a substantial community transmission in Korea, especially among unvaccinated persons. Although the initial findings on clinical features are reassuring, continuous monitoring of the disease epidemiology and vaccine effectiveness should be in place.

Ethics statement

The present study used the quarantine data which were constructed as a legally mandated public health investigation under the authority of the Korean Infectious Diseases Control and Prevention Act (No. 12444 and No. 13392). The study protocol was reviewed and approved by Institutional Review Board of the Korea Disease Control and Prevention Agency (2021-12-05-PE-A).

Notes

Disclosure: The authors have no potential conflicts of interest to disclose.

Author Contributions:

  • Conceptualization: Lee JJ, Lee HY, Lim D, Bae BS.

  • Data curation: Lee JJ, Lim D, Kim M, Kim EJ.

  • Formal analysis: Park K, Kim M, Song JS, Lee S.

  • Investigation: Lee HY, Lee SE, Kim JM, Park H, Yu M, Choi JH, Kim J, Lee HR, Jung JE, Jeong HS, Kim Ms, Kim SG, Yoo HN, Park K, Kim C, Choi S, Sim JW, Park Y, Huh I, Hong G, Lee J, Rhee JE, Kim IH, Gwack J, Kim JY, Jeon JH, Lee WG, Jeong SY, Kim JS, Bae BS, Kim JE, Kim HS, Lee S.

  • Methodology: Lee SE, Kim JM, Park H, Yu M, Choi JH, Kim J, Lee HR, Jung JE, Kim Ms, Yoo HN, Choi S, Sim JW, Park Y, Huh I, Hong G, Song JS, Lee J, Rhee JE, Kim IH, Gwack J, Jeon JH, Kim JS, Kim HS.

  • Project administration: Kim C.

  • Resources: Park H, Jeong HS, Kim EJ, Lee WG.

  • Supervision: Choe YJ, Park YJ.

  • Validation: Lee JJ.

  • Visualization: Lee JJ.

  • Writing - original draft: Lee JJ, Choe YJ, Park YJ.

  • Writing - review & editing: Lee JJ, Choe YJ, Park YJ.

References

1. World Health Organization. Tracking SARS-CoV-2 variants. Updated 2021. Accessed December 13, 2021. https://www.who.int/en/activities/tracking-SARS-CoV-2-variants .
2. Park YJ, Choe YJ, Park O, Park SY, Kim YM, Kim J, et al. Contact tracing during coronavirus disease outbreak, South Korea, 2020. Emerg Infect Dis. 2020; 26(10):2465–2468. PMID: 32673193.
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3. Gu H, Krishnan P, Ng DY, Chang LD, Liu GY, Cheng SS, et al. Probable transmission of SARS-CoV-2 Omicron variant in Quarantine Hotel, Hong Kong, China, November 2021. Emerg Infect Dis. Forthcoming. 2021; DOI: 10.3201/eid2802.212422.
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4. Callaway E, Ledford H. How bad is Omicron? What scientists know so far. Nature. 2021; 600(7888):197–199. PMID: 34857948.
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5. CDC COVID-19 Response Team. SARS-CoV-2 B.1.1.529 (Omicron) Variant – United States, December 1–8, 2021. MMWR Morb Mortal Wkly Rep. 2021; 70(50):1731–1734. PMID: 34914670.
6. Callaway E. Beyond Omicron: what’s next for COVID’s viral evolution. Nature. 2021; 600(7888):204–207. PMID: 34876665.
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7. Chen J, Wang R, Gilby NB, Wei GW. Omicron (B.1.1.529): infectivity, vaccine breakthrough, and antibody resistance. ArXiv. December. 1. 2021; https://arxiv.org/abs/2112.01318 .
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8. Mahase E. Covid-19: do vaccines work against omicron-and other questions answered. BMJ. 2021; 375(3062):n3062. PMID: 34893476.
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Fig. 1

Chronological distribution of SARS-CoV-2 B.1.1.529 (omicron) variant of concern cases. (A) Epidemic curve of reported confirmed cases (n = 80). (B) Patterns of community transmission.

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Table 1

Characteristics of reported confirmed SARS-CoV-2 B.1.1.529 (omicron) variant of concern cases (n = 80), South Korea, November 24 - December 10, 2021

jkms-36-e346-i001
Characteristics No. (%) of patients
Age group, yr
< 20 17 (21.3)
20–39 37 (46.3)
40–59 19 (23.8)
60+ 7 (8.8)
Sex
Male 37 (46.3)
Female 43 (53.8)
International travel historya 14 (17.5)
COVID-19 vaccination status
Unvaccinated 48 (60.0)
Partially vaccinated 5 (6.3)
Vaccinatedb 25 (31.3)
Symptom profile
Asymptomatic 22 (27.5)
Symptomatic 58 (72.5)
Initial signs or symptoms
Fever 19 (23.8)
Chills 14 (17.5)
Cough 26 (32.5)
Sputum 9 (11.3)
Sore throat 28 (35.0)
Headache 19 (23.8)
Myalgia 11 (13.8)
Anosmia/Ageusia 1 (1.3)
Outcomesc
Severe disease 0
Death 0
aInternational travel within 14 days of symptom onset, or if asymptomatic, SARS-CoV-2 test date; (Nigeria, n = 10; South Africa, n = 2; Mozambique, n = 1; Ethiopia, n = 1; Iran, n = 1).
bAn unvaccinated person had received no COVID-19 vaccine. A partially vaccinated person had received a COVID-19 vaccine but not completed the primary series ≥ 14 days before illness onset or receipt of a positive SARS-CoV-2 test result. A vaccinated person had completed the primary series of COVID-19 vaccine ≥ 14 days before illness onset or receipt of a positive SARS-CoV-2 test result. Vaccinated persons have received BNT162b, n = 13; mRNA-1273, n = 5; Ad26.COV2.S, n = 4, ChAdOx1, n = 3.
c6.1 mean observed days (range, 2–16 days).
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