Article

Letter to the Editor

Ann Lab Med 2022; 42(3): 363-366

Published online May 1, 2022 https://doi.org/10.3343/alm.2022.42.3.363

Copyright © Korean Society for Laboratory Medicine.

Incidence Evaluation of SARS-CoV-2 Variants in the Ulsan Area, Korea, Using PowerChek SARS-CoV-2 S-gene Mutation Detection Kit: A Pilot Study

Sang Hyuk Park, M.D., Ph.D.1 , Hyun-Ki Kim, M.D.1 , Hang Kang, Ph.D.2 , Jung Heon Kim, Ph.D.2 , Jaeseung Lee, M.S.2 , Ji-Hun Lim, M.D., Ph.D.1 , Seon-Ho Lee, M.D., Ph.D.1 , and Joseph Jeong, M.D., Ph.D.1

1Department of Laboratory Medicine, University of Ulsan College of Medicine, Ulsan University Hospital, Ulsan, Korea; 2Kogene Biotech, Seoul, Korea

Correspondence to: Joseph Jeong, M.D., Ph.D.
Department of Laboratory Medicine, University of Ulsan College of Medicine, Ulsan University Hospital, 877 Bangujin-sunhwando-ro, Dong-gu, Ulsan 44033, Korea
Tel: +82-52-250-7273, Fax: +82-52-250-8270
E-mail: joseph@uuh.ulsan.kr

Received: May 23, 2021; Revised: June 2, 2021; Accepted: November 25, 2021

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Dear Editor,

In Korea, more than 130,000 cases of coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2), were recorded from January 1, 2020 to May 14, 2021, with approximately 600 cases diagnosed per day following published guidelines for the laboratory diagnosis of COVID-19 in Korea [1]. The number of SARS-CoV-2 variants has been increasing, posing a significant threat in terms of increased infectivity and clinical severity accompanied by reduced immunity upon vaccination [2-4].

Most SARS-CoV-2 variants arise due to changes in the N-terminal domain (NTD) and receptor-binding domain (RBD) [4, 5]. Among NTD variants, the spike deletion H69/V70 (del69-70), which exerts a marginal effect on 50% neutralization values in plaque reduction neutralization tests of post-vaccination serum samples, is present in the B.1.1.7 variant that was initially dominant in the United Kingdom (UK) before spreading worldwide [6]. N501Y is the most prominent RBD variant, which improves SARS-CoV-2 binding affinity, and is present in the UK (B.1.1.7), the Republic of South Africa (RSA) (B.1.351), and Brazil/Japan (P.1.) variants [4, 6]. In addition, K417N, which can improve the receptor binding of SARS-CoV-2, is present in the RSA variant B.1.351, and E484K, associated with immune escape from monoclonal antibodies, has been detected in both the RSA and Brazilian variants [4, 7, 8].

PowerChek SARS-CoV-2 S-gene Mutation Detection Kit (Kogene Biotech, Seoul, Korea) based on multiplex real-time reverse transcription (rRT)-PCR was developed for detecting COVID-19 variants, especially the UK (B.1.1.7), RSA (B.1.351), Brazil/Japan (P.1), and UK (B.1.525)/Brazil (P.2) variants. Using this kit, we evaluated the incidence of SARS-CoV-2 variants in the Ulsan area of Korea; to our knowledge, this is the first study to evaluate the incidence of SARS-CoV-2 variants in a specific area of Korea. This study was approved by the Institutional Review Board of Ulsan University Hospital, Ulsan, Korea (approval number: 2021-05-025).

Data from 36 SARS-CoV-2–positive respiratory samples, tested using PowerChek SARS-CoV-2 Real-time PCR Kit (Kogene Biotech) at our institution between April 1 and April 30, 2021, were assessed retrospectively. RNA samples were subjected to SARS-CoV-2 variant screening using PowerChek SARS-CoV-2 S-gene Mutation Detection Kit following the manufacturer’s instructions. Three mutation sites (N501Y, E484K, and K417N) were screened, and the results were classified as (1) UK (B.1.1.7) variant if only N501Y was detected, (2) Brazil/Japan (P.1) variant if both N501Y and E484K were detected, (3) RSA (B1.351) variant if all three variants were detected, and (4) UK (B1.525)/Brazil (P.2) variant if only E484K was detected. Direct sequencing of both the NTD (for the 69/70 deletion) and RBD was subsequently performed to confirm the detected variants, using primers designed in-house (for del69-70: forward 5´-CAC ACG TGG TGT TTA CCC T-3´, reverse 5´-GTT AGA CTT CTC AGT GGA AGC A-3´; for RBD: forward 5´-GAG GTG ATG AAG TCA GAC AAA TCG-3´, reverse 5´-CTC TGT ATG GTT GGT AAC CAA CA-3´). Examples of rRT-PCR and direct sequencing results of SARS-CoV-2 variants are presented in Fig. 1, and the results of all 36 samples are summarized in Table 1.

Table 1 . Results of rRT-PCR and direct sequencing of 36 SARS-CoV-2 samples

NrRT-PCRDirect sequencing


N501Y (Ct)E484K (Ct)K417N (Ct)SARS-CoV-2 (Ct)Variantdel69-70RBDVariant

N501Y (T/A)E484K (A/G)K417N (T/G)
124.7--22.2B.1.1.7+TGGB.1.1.7
227.6--25.7B.1.1.7+TGGB.1.1.7
328.3--24.6B.1.1.7+TGGB.1.1.7
428.1--25.9B.1.1.7+TGGB.1.1.7
533.3--29.4B.1.1.7+TGGB.1.1.7
630.2--28.2B.1.1.7+TGGB.1.1.7
729.6--27.8B.1.1.7+TGGB.1.1.7
831.7--29.3B.1.1.7+TGGB.1.1.7
921.7--20.6B.1.1.7+TGGB.1.1.7
1035.1--30.2B.1.1.7+TGGB.1.1.7
1135.9--31.0B.1.1.7+TGGB.1.1.7
1229.9--27.6B.1.1.7+TGGB.1.1.7
1321.6--20.8B.1.1.7+TGGB.1.1.7
1420.6--19.8B.1.1.7+TGGB.1.1.7
1531.631.9-29.5P.1-TAGP.1
16---29.4SARS-CoV-2-AGGSARS-CoV-2
1720.0--17.7B.1.1.7+TGGB.1.1.7
1831.4--29.6B.1.1.7+TGGB.1.1.7
1925.4--24.3B.1.1.7+TGGB.1.1.7
2015.6--15.0B.1.1.7+TGGB.1.1.7
2118.6--18.8B.1.1.7+TGGB.1.1.7
2212.5--12.1B.1.1.7+TGGB.1.1.7
2314.9--14.5B.1.1.7+TGGB.1.1.7
2415.0--14.4B.1.1.7+TGGB.1.1.7
2531.1--28.8B.1.1.7+TGGB.1.1.7
2624.7--23.1B.1.1.7+TGGB.1.1.7
2724.5--22.6B.1.1.7+TGGB.1.1.7
28---25.4SARS-CoV-2-AGGSARS-CoV-2
2928.0--26.4B.1.1.7+TGGB.1.1.7
3027.3--26.0B.1.1.7+TGGB.1.1.7
3134.5--32.7B.1.1.7+TGGB.1.1.7
3224.4--23.0B.1.1.7+TGGB.1.1.7
3330.8--29.9B.1.1.7+TGGB.1.1.7
3432.8--30.1B.1.1.7+TGGB.1.1.7
3533.2--29.4B.1.1.7+TGGB.1.1.7
3627.2--25.9B.1.1.7+TGGB.1.1.7

-, not determined.

Abbreviations: rRT-PCR, real-time reverse transcription PCR; RBD, receptor-binding domain; N, asparagine; Y, tyrosine; E, glutamate; K, lysine; T, thymine; G, guanine; A, adenine; del, deletion; Ct, cycle threshold.



Figure 1. Examples of rRT-PCR and direct sequencing results of SARS-CoV-2 variants. (A) rRT-PCR results. Amplification curves for N501Y, E484K, K417N, SARS-CoV-2, and the internal control are shown in red, green, blue, black, and purple, respectively. (B) Direct sequencing results for del69-70, K417N, E484K, and N501Y variants.
Abbreviations: rRT-PCR, real-time reverse transcription PCR; N, asparagine; Y, tyrosine; E, glutamate; K, lysine; IC, internal control; UK, United Kingdom; RSA, Republic of South Africa; T, thymine; G, guanine; A, adenine; C, cytosine; U, uracil.

Using rRT-PCR, N501Y, E484K, and K417N were detected in 34 (94.4%), 1 (2.8%), and 0 (0.0%) samples, respectively, and the incidence rates of the B.1.1.7 (UK) and P.1 (Brazil/Japan) variants were calculated as 33/36 (91.7%) and 1/36 (2.8%), respectively. Using direct sequencing, del69-70, N501Y (A→T), E484K (G→A), and K417N (G→T) were detected in 33 (91.7%), 34 (94.4%), 1 (2.8%), and 0 (0.0%) samples, respectively, and the incidence rates of the B.1.1.7 (UK) and P.1 (Brazil/Japan) variants were calculated as 33/36 (91.7%) and 1/36 (2.8%), respectively. rRT-PCR and direct sequencing results were concordant in all samples (Table 1).

The incidence rate of the UK variant was very high in the Ulsan area. Recent studies have reported that although the UK variant does not hinder vaccine-induced immunity, it may increase fatality by up to 18% compared with that due to non-UK SARS-CoV-2 variants [9, 10]. These results suggest that UK variant-infected patients need to be managed cautiously. The high incidence of the UK variant in the Ulsan area compared with other areas in Korea [11] can be attributed to the frequent entry of foreigners at the Ulsan trading port, increasing the probability of transmission of variants. Although the incidence rates of the RSA and Brazil/Japan variants were low in our study, considering some limitations, including the small sample size, single institutional nature, and use of direct sequencing rather than whole-genome sequencing for validation, a more comprehensive study is needed to confirm these preliminary results.

In conclusion, the incidence of infection due to the UK variant is very high (91.7%), whereas that due to the RSA and Brazil/Japan variants is low in the Ulsan area of Korea. A large-scale study is required to confirm our results. Powerchek SARS-CoV-2 S-gene Mutation Detection Kit is useful for the rapid screening of SARS-CoV-2 variants.


Kang H, Kim JH and Lee J were involved in the implementation of SARS-CoV-2 variant screening. Park SH, Kang H, JH and Lee J analyzed the data. Park SH drafted the first submitted manuscript and Jeong J supervised the manuscript preparation and submission. Kim HK, Lim JH and Lee SH contributed to the conception. All authors reviewed the manuscript and provided critical feedback.


Kang H, Kim JH and Lee J are from the Kogene Biotech and these three authors supported the implementation and analysis of SARS-CoV-2 variant screening performed with the PowerChek SARS-CoV-2 S-gene Mutation Detection Kit (Kogene Biotech).

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