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Dive into the research topics where Je Hee Lee is active.

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Featured researches published by Je Hee Lee.


Nature | 2011

Evidence for several waves of global transmission in the seventh cholera pandemic

Ankur Mutreja; Dong Wook Kim; Nicholas R. Thomson; Thomas Richard Connor; Je Hee Lee; Samuel Kariuki; Nicholas J. Croucher; Seon Young Choi; Simon R. Harris; Michael Lebens; Swapan Kumar Niyogi; Eun Jin Kim; Thandavarayan Ramamurthy; Jongsik Chun; J. L. N. Wood; John D. Clemens; Cecil Czerkinsky; G. Balakrish Nair; Jan Holmgren; Julian Parkhill; Gordon Dougan

Vibrio cholerae is a globally important pathogen that is endemic in many areas of the world and causes 3–5 million reported cases of cholera every year. Historically, there have been seven acknowledged cholera pandemics; recent outbreaks in Zimbabwe and Haiti are included in the seventh and ongoing pandemic. Only isolates in serogroup O1 (consisting of two biotypes known as ‘classical’ and ‘El Tor’) and the derivative O139 (refs 2, 3) can cause epidemic cholera. It is believed that the first six cholera pandemics were caused by the classical biotype, but El Tor has subsequently spread globally and replaced the classical biotype in the current pandemic. Detailed molecular epidemiological mapping of cholera has been compromised by a reliance on sub-genomic regions such as mobile elements to infer relationships, making El Tor isolates associated with the seventh pandemic seem superficially diverse. To understand the underlying phylogeny of the lineage responsible for the current pandemic, we identified high-resolution markers (single nucleotide polymorphisms; SNPs) in 154 whole-genome sequences of globally and temporally representative V. cholerae isolates. Using this phylogeny, we show here that the seventh pandemic has spread from the Bay of Bengal in at least three independent but overlapping waves with a common ancestor in the 1950s, and identify several transcontinental transmission events. Additionally, we show how the acquisition of the SXT family of antibiotic resistance elements has shaped pandemic spread, and show that this family was first acquired at least ten years before its discovery in V. cholerae.


Proceedings of the National Academy of Sciences of the United States of America | 2009

Comparative genomics reveals mechanism for short-term and long-term clonal transitions in pandemic Vibrio cholerae

Jongsik Chun; Christopher J. Grim; Nur A. Hasan; Je Hee Lee; Seon Young Choi; Bradd J. Haley; Elisa Taviani; Yoon-Seong Jeon; Dong-Wook Kim; Jae-Hak Lee; Thomas Brettin; David Bruce; Jean F. Challacombe; J. Chris Detter; Cliff Han; A. Christine Munk; Olga Chertkov; Linda Meincke; Elizabeth Saunders; Ronald A. Walters; Anwar Huq; G. Balakrish Nair; Rita R. Colwell

Vibrio cholerae, the causative agent of cholera, is a bacterium autochthonous to the aquatic environment, and a serious public health threat. V. cholerae serogroup O1 is responsible for the previous two cholera pandemics, in which classical and El Tor biotypes were dominant in the sixth and the current seventh pandemics, respectively. Cholera researchers continually face newly emerging and reemerging pathogenic clones carrying diverse combinations of phenotypic and genotypic properties, which significantly hampered control of the disease. To elucidate evolutionary mechanisms governing genetic diversity of pandemic V. cholerae, we compared the genome sequences of 23 V. cholerae strains isolated from a variety of sources over the past 98 years. The genome-based phylogeny revealed 12 distinct V. cholerae lineages, of which one comprises both O1 classical and El Tor biotypes. All seventh pandemic clones share nearly identical gene content. Using analogy to influenza virology, we define the transition from sixth to seventh pandemic strains as a “shift” between pathogenic clones belonging to the same O1 serogroup, but from significantly different phyletic lineages. In contrast, transition among clones during the present pandemic period is characterized as a “drift” between clones, differentiated mainly by varying composition of laterally transferred genomic islands, resulting in emergence of variants, exemplified by V. cholerae O139 and V. cholerae O1 El Tor hybrid clones. Based on the comparative genomics it is concluded that V. cholerae undergoes extensive genetic recombination via lateral gene transfer, and, therefore, genome assortment, not serogroup, should be used to define pathogenic V. cholerae clones.


Journal of Clinical Microbiology | 2009

Cholera Outbreaks Caused by an Altered Vibrio cholerae O1 El Tor Biotype Strain Producing Classical Cholera Toxin B in Vietnam in 2007 to 2008

Binh Minh Nguyen; Je Hee Lee; Ngo Tuan Cuong; Seon Young Choi; Nguyen Tran Hien; Dang Duc Anh; Hye Ri Lee; M. Ansaruzzaman; Hubert P. Endtz; Jongsik Chun; Anna Lena Lopez; Cecil Czerkinsky; John D. Clemens; Dong-Wook Kim

ABSTRACT Vibrio cholerae O1 isolates collected during cholera outbreaks occurring from late 2007 to early 2008 in northern Vietnam were revealed to represent an altered strain containing the RS1 element followed by a CTX prophage harboring El Tor type rstR and classical ctxB on the large chromosome.


Journal of Medical Microbiology | 2010

Multilocus variable-number tandem repeat analysis of Vibrio cholerae O1 El Tor strains harbouring classical toxin B

Seon Young Choi; Je Hee Lee; Yoon-Seong Jeon; Hye Ri Lee; Eun Jin Kim; M. Ansaruzzaman; N. A. Bhuiyan; Hubert P. Endtz; Swapan Kumar Niyogi; B.L. Sarkar; G. Balakrish Nair; Binh Minh Nguyen; Nguyen Tran Hien; Cecil Czerkinsky; John D. Clemens; Jongsik Chun; Dong Wook Kim

Atypical Vibrio cholerae O1 strains - hybrid strains (strains that cannot be classified either as El Tor or classical biotype) and altered strains (El Tor biotype strains that produce classical cholera toxin) - are currently prevalent in Asia and Africa. A total of 74 hybrid and altered strains that harboured classical cholera toxin were investigated by multilocus variable-number tandem repeat analysis (MLVA). The results showed that the hybrid/altered strains could be categorized into three groups and that they were distant from the El Tor strain responsible for the seventh cholera pandemic. Hybrid/altered strains with a tandem repeat of the classical CTX prophage on the small chromosome were divided into two MLVA groups (group I: Mozambique/Bangladesh group; group III: Vietnam group), and altered strains with the RS1-CTX prophage containing the El Tor type rstR and classical ctxB on the large chromosome were placed in two MLVA groups (group II: India/Bangladesh group; group III: India/Vietnam group).


Journal of Bacteriology | 2012

Genome Sequence of Lactobacillus mucosae LM1, Isolated from Piglet Feces

Je Hee Lee; Valerie Diane V. Valeriano; Yu-Ri Shin; Jong Pyo Chae; Geun-Bae Kim; Jun-Sang Ham; Jongsik Chun; Dae-Kyung Kang

Lactobacillus mucosae LM1, isolated from stool samples of a healthy piglet, displays good in vitro mucin adhesion and antimicrobial activity against pathogenic bacteria. To elucidate its antimicrobial effects and to find its epithelial cell and mucin adhesion genes, the genomic sequence of L. mucosae LM1 was investigated.


Journal of Microbiology | 2009

Classification of hybrid and altered Vibrio cholerae strains by CTX prophage and RS1 element structure

Je Hee Lee; Seon Young Choi; Yoon-Seong Jeon; Hye Ri Lee; Eun Jin Kim; Binh Minh Nguyen; Nguyen Tran Hien; M. Ansaruzzaman; M. Sirajul Islam; N. A. Bhuiyan; Swapan Kumar Niyogi; B.L. Sarkar; G. Balakrish Nair; Dae Shick Kim; Anna Lena Lopez; Cecil Czerkinsky; John D. Clemens; Jongsik Chun; Dong Wook Kim

Analysis of the CTX prophage and RS1 element in hybrid and altered Vibrio cholera O1 strains showed two classifiable groups. Group I strains contain a tandem repeat of classical CTX prophage on the small chromosome. Strains in this group either contain no element(s) or an additional CTX prophage or RS1 element(s) on the large chromosome. Group II strains harbor RS1 and CTX prophage, which has an E1 Tor type rstR and classical ctxB on the large chromosome.


Journal of Medical Microbiology | 2008

Characteristics of a pandemic clone of O3 : K6 and O4 : K68 Vibrio parahaemolyticus isolated in Beira, Mozambique.

M. Ansaruzzaman; Ashrafuzzaman Chowdhury; N. A. Bhuiyan; Marzia Sultana; Ashrafus Safa; Marcelino Lucas; Lorenz von Seidlein; Avertino Barreto; Claire-Lise Chaignat; David A. Sack; John D. Clemens; G. Balakrish Nair; Seon Young Choi; Yoon Seong Jeon; Je Hee Lee; Hye Ri Lee; Jongsik Chun; Dong Wook Kim

The genetic characteristics of Vibrio parahaemolyticus strains isolated in 2004 and 2005 in Mozambique were assessed in this study to determine whether the pandemic clone of V. parahaemolyticus O3 : K6 and O4 : K68 serotypes has spread to Mozambique. Fifty-eight V. parahaemolyticus strains isolated from hospitalized diarrhoea patients in Beira, Mozambique, were serotyped for O : K antigens and genotyped for toxR, tdh and trh genes. A group-specific PCR, a PCR that detects the presence of ORF8 of the filamentous phage f237, arbitrarily primed PCR, PFGE and multilocus sequence typing were performed to determine the pandemic status of the strains and their ancestry. All strains of serovars O3 : K6 (n=38) and O4 : K68 (n=4) were identified as a pandemic clonal group by these analyses. These strains are closely related to the pandemic reference strains of O3 : K6 and O4 : K68, which emerged in Asia in 1996 and were later found globally. The pandemic serotypes O3 : K6 and O4 : K68 including reference strains grouped into a single cluster indicating emergence from a common ancestor. The O3 : K58 (n=8), O4 : K13 (n=6), O3 : KUT (n=1) and O8 : K41 (n=1) strains showed unique characteristics different from the pandemic clone.


Journal of Medical Microbiology | 2010

Classical RS1 and environmental RS1 elements in Vibrio cholerae O1 El Tor strains harbouring a tandem repeat of CTX prophage: revisiting Mozambique in 2005

Seon Young Choi; Je Hee Lee; Eun Jin Kim; Hye Ri Lee; Yoon-Seong Jeon; Lorenz von Seidlein; Jaqueline L. Deen; M. Ansaruzzaman; G. Marcelino E. S. Lucas; Avertino Barreto; Francisco F. Songane; Catarina Mondlane; G. Balakrish Nair; Cecil Czerkinsky; John D. Clemens; Jongsik Chun; Dong Wook Kim

Currently, Vibrio cholerae O1 serogroup biotype El Tor strains producing classical type cholera toxin (altered strains or El Tor variants) are prevalent in Asia and in Mozambique. Mozambican strains collected in 2004 contained a tandem repeat of CTX prophage on the small chromosome and each CTX prophage harboured the classical rstR and classical ctxB. We found that the majority of the strains collected in 2005 in Mozambique contained extra elements on the large chromosome in addition to the tandem repeat of CTX prophage on the small chromosome. New type RS1 elements RS1(cla) and RS1(env), and a CTX(env) with rstR(env) and the classical ctxB were identified on the large chromosome of the Mozambican isolates collected in 2005.


Journal of Bacteriology | 2011

Genome Sequence of Lactobacillus johnsonii PF01, Isolated from Piglet Feces

Je Hee Lee; Jong Pyo Chae; Ji Yoon Lee; Jong-Sung Lim; Geun-Bae Kim; Jun-Sang Ham; Jongsik Chun; Dae-Kyung Kang

Lactobacillus johnsonii PF01, an autochthonous bacterium of the gastrointestinal tract, was isolated from a fecal sample from a piglet. The strain adhered specifically to the duodenal and jejunal epithelial cells of the piglet and had high bile resistance activity. Here we report the genomic sequence of L. johnsonii PF01.


Journal of Bacteriology | 2012

Draft Genome Sequence of Weissella koreensis KCTC 3621T

Je Hee Lee; Jin-Woo Bae; Jongsik Chun

Weissella koreensis is a Gram-positive, rod-shaped, nonmotile, and facultative anaerobic species belonging to the lactic acid bacteria (LAB). The members of this species have been repeatedly isolated from kimchi (a traditional Korean fermented food) and are known for their beneficial effects on human and animal intestinal microflora through producing various clinically important amino acids such as γ-aminobutyric acid and ornithine. Here we report the genome sequence of the type strain of W. koreensis (KCTC 3621(T)) to provide taxonomic and functional insights into the species.

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Jongsik Chun

University of Maryland Biotechnology Institute

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Seon Young Choi

Seoul National University

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John D. Clemens

International Vaccine Institute

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Hye Ri Lee

International Vaccine Institute

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Yoon-Seong Jeon

Seoul National University

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Cecil Czerkinsky

French Institute of Health and Medical Research

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Dong-Wook Kim

Seoul National University

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