Jin-Won Song

Prof. Jin-Won Song

Korea University, Seoul, Republic of Korea
orcid

Research Focus & Metrics

Academic Career Length

33Years (1994-Present)

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

Representative Publications

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7 May 2019 in Archives of Virology
Verified
Journal Article
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AAAbulikemu Abudurexiti
Abulikemu Abudurexiti
SAScott Adkins
Scott Adkins
DADaniela Alioto
Daniela Alioto
SASergey Alkhovsky
Sergey Alkhovsky
TATatjana Avsic-Zupanc
Tatjana Avsic-Zupanc
Jens H. KuhnJens H. Kuhn
Jens H. Kuhn

4 September 2020 in Archives of Virology
Verified
Journal Article
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Jens H. KuhnJens H. Kuhn
Jens H. Kuhn
SAScott Adkins
Scott Adkins
DADaniela Alioto
Daniela Alioto
SASergey Alkhovsky
Sergey Alkhovsky
GAGaya Amarasinghe
Gaya Amarasinghe
XZXueping Zhou
Xueping Zhou

1 September 2006 in Applied and Environmental Microbiology
Verified
Journal Article
Closed access
CKChul-Min Kim
Chul-Min Kim
YYYing-Hua Yi
Ying-Hua Yi
DYDo-Hyeon Yu
Do-Hyeon Yu
MLMi-Jin Lee
Mi-Jin Lee
MCMae-Rim Cho
Mae-Rim Cho
JCJoon-Seok Chae
Joon-Seok Chae
In order to investigate the prevalence of tick-borne infectious agents among ticks, ticks comprising five species from two genera (Hemaphysalisspp. andIxodesspp.) were screened using molecular techniques. Ticks (3,135) were collected from small wild-caught mammals or by dragging/flagging in the Republic of Korea (ROK) and were pooled into a total of 1,638 samples (1 to 27 ticks per pool). From the 1,638 tick samples, species-specific fragments ofAnaplasma phagocytophilum(1 sample),Anaplasma platys(52 samples),Ehrlichia chaffeensis(29 samples),Ehrlichia ewingii(2 samples),Ehrlichia canis(18 samples), andRickettsia rickettsii(28 samples) were amplified by PCR assay. Twenty-one pooled and individual tick samples had mixed infections of two (15 samples) or three (6 samples) pathogens. In addition, 424 spleen samples from small captured mammals (389 rodents, 33 insectivores, and 2 weasels) were screened for selected zoonotic pathogens. Species-specific DNA fragments ofA. phagocytophilum(110 samples),A. platys(68 samples),E. chaffeensis(8 samples),E. ewingii(26 samples),E. canis(51 samples), andRickettsiasp. (22 samples) were amplified by PCR assay. One hundred thirty small mammals had single infections, while 4, 14, and 21 striped field mice (Apodemus agrarius) had mixed infections of four, three, and two pathogens, respectively. Phylogenetic analysis based on nucleotide sequence comparison also revealed that Korean strains ofE. chaffeensisclustered closely with those from China and the United States, while theRickettsia(rOmpA) sequences clustered within a clade together with a Chinese strain. These results suggest that these agents should be considered in differential diagnosis while examining cases of acute febrile illnesses in humans as well as animals in the ROK.

15 June 2009 in Journal of Virology
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Journal Article
Closed access
JSJin-Won Song
Jin-Won Song
HKHae Ji Kang
Hae Ji Kang
SGSe Hun Gu
Se Hun Gu
SMSung Sil Moon
Sung Sil Moon
SBShannon N. Bennett
Shannon N. Bennett
RYRichard Yanagihara
Richard Yanagihara
Until recently, the single known exception to the rodent-hantavirus association was Thottapalayam virus (TPMV), a long-unclassified virus isolated from the Asian house shrew ( Suncus murinus ). Robust gene amplification techniques have now uncovered several genetically distinct hantaviruses from shrews in widely separated geographic regions. Here, we report the characterization of a newly identified hantavirus, designated Imjin virus (MJNV), isolated from the lung tissues of Ussuri white-toothed shrews of the species Crocidura lasiura (order Soricomorpha, family Soricidae, subfamily Crocidurinae) captured near the demilitarized zone in the Republic of Korea during 2004 and 2005. Seasonal trapping revealed the highest prevalence of MJNV infection during the autumn, with evidence of infected shrews' clustering in distinct foci. Also, marked male predominance among anti-MJNV immunoglobulin G antibody-positive Ussuri shrews was found, whereas the male-to-female ratio among seronegative Ussuri shrews was near 1. Plaque reduction neutralization tests showed no cross neutralization for MJNV and rodent-borne hantaviruses but one-way cross neutralization for MJNV and TPMV. The nucleotide and deduced amino acid sequences for the different MJNV genomic segments revealed nearly the same calculated distances from hantaviruses harbored by rodents in the subfamilies Murinae, Arvicolinae, Neotominae, and Sigmodontinae. Phylogenetic analyses of full-length S, M, and L segment sequences demonstrated that MJNV shared a common ancestry with TPMV and remained in a distinct out-group, suggesting early evolutionary divergence. Studies are in progress to determine if MJNV is pathogenic for humans.

1 July 2014 in Virus Research
Verified
Journal Article
Closed access
Richard YanagiharaRichard Yanagihara
Richard Yanagihara
SGSe Hun Gu
Se Hun Gu
SASatoru Arai
Satoru Arai
HKHae Ji Kang
Hae Ji Kang
JSJin-Won Song
Jin-Won Song

1 January 2007 in Virology Journal
Verified
Journal Article
Open access
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JSJin-Won Song
Jin-Won Song
SGSe H Gu
Se H Gu
SBShannon N Bennett
Shannon N Bennett
SASatoru Arai
Satoru Arai
MPMaria Puorger
Maria Puorger
RYRichard Yanagihara
Richard Yanagihara
More than 20 years ago, hantaviral antigens were reported in tissues of the Eurasian common shrew (Sorex araneus), Eurasian water shrew (Neomys fodiens) and common mole (Talpa europea), suggesting that insectivores, or soricomorphs, might serve as reservoirs of unique hantaviruses. Using RT-PCR, sequences of a genetically distinct hantavirus, designated Seewis virus (SWSV), were amplified from lung tissue of a Eurasian common shrew, captured in October 2006 in Graubünden, Switzerland. Pair-wise analysis of the full-length S and partial M and L segments of SWSV indicated approximately 55%–72% similarity with hantaviruses harbored by Murinae, Arvicolinae, Neotominae and Sigmodontinae rodents. Phylogenetically, SWSV grouped with other recently identified shrew-borne hantaviruses. Intensified efforts are underway to clarify the genetic diversity of SWSV throughout the geographic range of the Eurasian common shrew, as well as to determine its relevance to human health.