Hye Kwon Kim

Prof. Hye Kwon Kim

Department of Microbiology, College of Natural Science, Chungbuk National University, Cheongju 28644, South Korea

Research Focus & Metrics

Academic Career Length

11Years (2016-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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20 February 2017 in Archives of Virology
Verified
Journal Article
Closed access
PDF file
JNJi Yeong Noh
Ji Yeong Noh
SYSun-Woo Yoon
Sun-Woo Yoon
DKDoo-Jin Kim
Doo-Jin Kim
MLMoo-Seung Lee
Moo-Seung Lee
JKJi-Hyung Kim
Ji-Hyung Kim
HKHye Kwon Kim
Hye Kwon Kim

22 August 2018 in Scientific Reports
Verified
Journal Article
Open access
PDF file
JNJi Yeong Noh
Ji Yeong Noh
DJDae Gwin Jeong
Dae Gwin Jeong
SYSun-Woo Yoon
Sun-Woo Yoon
JKJi Hyung Kim
Ji Hyung Kim
YCYong Gun Choi
Yong Gun Choi
HKHye Kwon Kim
Hye Kwon Kim
The bat paramyxovirus B16-40 was first isolated in Korea in this study. Using the isolated virus, we could obtain not only genomic information, but also several biological characteristics of the virus. In the phylogenetic analysis, the virus was found to belong to the recently proposed genus Shaanvirus. Through sequence analyses and in vitro testing, the isolated virus was also found to have haemagglutinin-neuraminidase (HN) protein as one of the structural proteins. When mouse antiserum was generated against the isolated virus and tested, it was cross-reactive to human parainfluenza virus 1 in an indirect immunofluorescence assay but could not cross-neutralize human parainfluenza virus 1. In addition, the bat paramyxovirus B16-40 was not infectious in the mouse model. Collectively, this study provided basic information on further classification of the bat paramyxovirus B16-40 and related viruses in the proposed genus Shaanvirus.

5 March 2018 in Transboundary and Emerging Diseases
Verified
Journal Article
Closed access
PDF file
JKJi Hyung Kim
Ji Hyung Kim
JJJ.-H. Jang
J.-H. Jang
SYS.-W. Yoon
S.-W. Yoon
JNJ. Y. Noh
J. Y. Noh
MAM.-J. Ahn
M.-J. Ahn
HKHye Kwon Kim
Hye Kwon Kim

21 April 2022 in Computational and Structural Biotechnology Journal
Verified
Journal Article
Open access
HCHoyin Chung
Hoyin Chung
JNJi Yeong Noh
Ji Yeong Noh
BKBon-Sang Koo
Bon-Sang Koo
JHJUNG JOO HONG
JUNG JOO HONG
HKHye Kwon Kim
Hye Kwon Kim
Since the outbreak of coronavirus disease (COVID-19) in 2019, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has evolved into diverse variants. Here, an early isolate of SARS-CoV-2 was serially passaged in multiple cell lines of human origin in triplicate, and selected mutations were compared to those found in natural SARS-CoV-2 variants. In the spike protein, Q493R and Q498R substitutions from passaged viruses were consistent with those in the B.1.1.529 (Omicron) variant. Y144del and H655Y substitutions from passaged viruses were also reported in B.1.1.7 (Alpha), P.1 (Gamma), and B.1.1.529 (Omicron) variants. Several single nucleotide polymorphisms (SNPs) found in first-passaged viruses have also been identified as selected mutation sites in serially passaged viruses. Considering the consistent mutations found between serially passaged SARS-CoV-2 and natural variants, there may be host-specific selective mutation patterns of viral evolution in humans. Additional studies on the selective mutations in SARS-CoV-2 experiencing diverse host environments will help elucidate the direction of SARS-CoV-2 evolution. SARS-CoV-2 isolate (SARS-CoV-2/human/KOR/KCDC03-NCCP43326/2020) was serially passaged in A549, CaCO2, and HRT-18 cells in triplicate. After 12 times of serial passages in each cell lines, several consistent selected mutations were found on spike protein between the serially passaged SARS-CoV-2 in human cell lines and recent natural variants of SARS-CoV-2 like omicron. On the non-spike protein genes, selected mutations were more frequent in viruses passaged in Caco-2 and HRT-18 cells (Colon epithelial-like) than in those passaged in A549 cells (Lung epithelial-like). In addition, several SNPs identified after one round of passaging were consistently identified as the selected mutation sites in serially passaged viruses. Thus, mutation patterns of SARS-CoV-2 in certain host environments may provide researchers information to understand and predict future SARS-CoV-2 variants.

15 June 2020 in Transboundary and Emerging Diseases
Verified
Journal Article
Closed access
PDF file
VLVan Thi Lo
Van Thi Lo
SYSun-Woo Yoon
Sun-Woo Yoon
JNJi Yeong Noh
Ji Yeong Noh
YKYoungji Kim
Youngji Kim
YCYong Gun Choi
Yong Gun Choi
HKHye Kwon Kim
Hye Kwon Kim

7 May 2021 in Frontiers in Veterinary Science
Verified
Journal Article
Open access
YKYoung Ji Kim
Young Ji Kim
SYSun-Woo Yoon
Sun-Woo Yoon
JJJin Ho Jang
Jin Ho Jang
DJDae Gwin Jeong
Dae Gwin Jeong
BLBeom-Jun Lee
Beom-Jun Lee
HKHye Kwon Kim
Hye Kwon Kim
Feline parvovirus (FPV) is a small, non-enveloped, single-stranded DNA virus that infects cats. We recently isolated a feline parvovirus Fe–P2 strain from a dead stray cat in Iksan, 2017. Its partial genomic sequence (4,643 bases) was obtained, and phylogenetic analysis based on the VP2 nucleotide sequence showed that the FPV Fe-P2 strain was closely related to the FPV isolate Gigucheon in cat, 2017 (MN400978). In addition, we performed a serum neutralization (SN) test with the FPV isolates in various mammalian sera. These were from raccoon dog, water deer, Eurasian otter, Korean hare, leopard cat, and Asian badger, which were kindly provided by Chungnam Wild Animal Rescue Center. Notably, serological evidence of its infection was found in Asian badger, Meles leucurus (2/2) and leopard cat, Prionailurus bengalensis (5/8) through SN tests, whereas there was no evidence in raccoon dog, water deer, Eurasian otter, and Korean hare based on the collected sera in this study. These findings might provide partial evidence for the possible circulation of FPV or its related viruses among wild leopard cat and Asian badger in Korea. There should be additional study to confirm this through direct detection of FPVs in the related animal samples.