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Je Hee Lee 3 Articles
Sutterella faecalis sp. nov., isolated from human faeces
Byeong Seob Oh , Ji-Sun Kim , Seung Yeob Yu , Seoung Woo Ryu , Seung-Hwan Park , Se Won Kang , Jam-Eon Park , Seung-Hyeon Choi , Kook-Il Han , Keun Chul Lee , Mi Kyung Eom , Min Kuk Suh , Han Sol Kim , Dong Ho Lee , Hyuk Yoon , Byung-Yong Kim , Je Hee Lee , Jung-Sook Lee , Ju Huck Lee
J. Microbiol. 2020;58(2):99-104.   Published online January 29, 2020
DOI: https://doi.org/10.1007/s12275-020-9396-9
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  • 7 Web of Science
  • 7 Crossref
AbstractAbstract PDF
An obligately anaerobic, Gram-stain-negative, non-motile, non-spore-forming, and coccobacilli-shaped bacterial strain, designated KGMB03119T, was isolated from human faeces from a Korean. Phylogenetic analysis based on the 16S rRNA gene sequence revealed that the isolate was a member of the genus Sutterella and most closely related to Sutterlla wadsworthensis KCTC 15691T (96.8% 16S rRNA gene sequence similarity). The DNA G + C content of strain KGMB03119T was 58.3 mol% as determined from its whole genome sequence. Strain KGMB03119T was asaccharolytic, catalase-positive, oxidase- and urease-negative. Furthermore, the isolate was positive for alkaline phosphatase, leucine arylamidase, acid phosphatase, arginine arylamidase, alanine arylamidase, and glycine arylamidase. The major cellular fatty acids (> 10%) of the isolate were C18:1ω9c and C16:0. Methylmenaquinone-5 (MMK-5, 100%) was the predominant isoprenoid quinone in the isolate. Based on the phylogenetic, physiological, and chemotaxonomic characteristics, strain KGMB03119T represents a novel species, for which the name Sutterella faecalis sp. nov. is proposed. The type strain is KGMB03119T (= KCTC 15823T = NBRC 114254T).

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    International Journal of Molecular Sciences.2024; 25(23): 12600.     CrossRef
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  • Validation List no. 212. Valid publication of new names and new combinations effectively published outside the IJSEM
    Aharon Oren, Markus Göker
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    mSystems.2023;[Epub]     CrossRef
Anaerotignum faecicola sp. nov., isolated from human faeces
Seung-Hyeon Choi , Ji-Sun Kim , Jam-Eon Park , Keun Chul Lee , Mi Kyung Eom , Byeong Seob Oh , Seung Yeob Yu , Se Won Kang , Kook-Il Han , Min Kuk Suh , Dong Ho Lee , Hyuk Yoon , Byung-Yong Kim , Je Hee Lee , Ju Huck Lee , Jung-Sook Lee , Seung-Hwan Park
J. Microbiol. 2019;57(12):1073-1078.   Published online November 4, 2019
DOI: https://doi.org/10.1007/s12275-019-9268-3
  • 1,436 View
  • 9 Download
  • 16 Web of Science
  • 16 Crossref
AbstractAbstract PDF
A strictly anaerobic bacterium, designated as strain KGMB- 03357T, was isolated from the faeces of a healthy Korean selected by Bundang Seoul National University based on health status. Cells of strain KGMB03357T are Gram-stain-positive, non-motile, non-spore-forming, and observed as straight or curved rods. The isolate grew at 10–45°C (optimum temperature of 40°C) and a pH range of 5.1–10.5 (optimum pH of 6.8). Analysis of phylogenetic trees based on the 16S rRNA gene sequences revealed that strain KGMB03357T forms a lineage within the genus Anaerotignum, and is most closely related to Anaerotignum lactatifermentans G17T (= KCTC 15066T, 96.1%), Anaerotignum propionicum DSM 1682T (= KCTC 5582T, 94.9%), Anaerotignum neopropionicum DSM 03847T (= KCTC 15564T, 94.9%), and Anaerotignum aminivorans SH021T (= KCTC 15705T, 94.8%). The ANI values between strain KGMB 03357T and members of the genus Anaerotignum were 73.3–71.0%, which are below the ANI criterion for interspecies identity. The DNA G + C content based on the whole-genome sequence is 47.3 mol%. The major cellular fatty acids of strain KGMB03357T are C16:0, C18:0, C18:1 cis 9, and anteiso-C15:0. Strain KGMB03357T contains meso-diaminopimelic acid as the diagnostic amino acid in the cell wall peptidoglycan. Based on the phenotypic, phylogenetic, and genomic properties, strain KGMB 03357T represents a novel species of the genus Anaerotignum, for which the name Anaerotignum faecicola sp. nov. is proposed. The type strain is KGMB03357T (= KCTC 15736T = DSM 107953T).

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  • Reshaping of the fecal proteome and metaproteome in obese patients 2 years after bariatric surgery
    Alessandro Tanca, Laura De Diego, Maria Antonietta Deledda, Flavio De Maio, Cristian Boru, Mario Musella, Marco Raffaelli, Gianfranco Silecchia, Giovanni Delogu, Sergio Uzzau, Naseer Sangwan
    mSystems.2026;[Epub]     CrossRef
  • D- and L-lactate consumers are taxonomically, biochemically, and energetically different
    Maximilienne T Allaart, Alexander V Tyakht, Ruth E Ley, Martin Pabst, Gerben R Stouten, Largus T Angenent
    ISME Communications.2026;[Epub]     CrossRef
  • Fecal microbiota fermenting simple organic carbon substrates in vitro as microbial factories capable of distinguishing Crohn’s disease from healthy states
    Anna Detman-Ignatowska, Gabriele Schiro, Rafał Filip, Emilia Samborowska, Jakub Karczmarski, Sara Jarmakiewicz-Czaja, Kinga Jakubowska, Anna Williams, Nabahi Ramos Hickman, Daniel Laubitz, Anna Sikora
    Microbial Cell Factories.2026;[Epub]     CrossRef
  • Comparison of Gut Microbiome Profile of Chickens Infected with Three Eimeria Species Reveals New Insights on Pathogenicity of Avian Coccidia
    Nianyu Xue, Dandan Liu, Qianqian Feng, Yu Zhu, Cheng Cheng, Feiyan Wang, Shijie Su, Jinjun Xu, Jianping Tao
    Microorganisms.2025; 13(12): 2752.     CrossRef
  • Dietary supplementation of solubles from shredded, steam-exploded pine particles modulates cecal microbiome composition in broiler chickens
    Chris Major Ncho, Akshat Goel, Vaishali Gupta, Chae-Mi Jeong, Ji-Young Jung, Si-Young Ha, Jae-Kyung Yang, Yang-Ho Choi
    Journal of Animal Science and Technology.2023; 65(5): 971.     CrossRef
  • Cordyceps militaris polysaccharides modulate gut microbiota and improve metabolic disorders in mice with diet‐induced obesity
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  • Anaeropeptidivorans aminofermentans gen. nov., sp. nov., a mesophilic proteolytic salt-tolerant bacterium isolated from a laboratory-scale biogas fermenter, and emended description of Clostridium colinum
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    Bikiran Pardesi, Anthony M. Roberton, Emily M. Wollmuth, Esther R. Angert, Douglas I. Rosendale, William Lindsey White, Kendall D. Clements
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    Microorganisms.2023; 11(3): 685.     CrossRef
  • Update on Accepted Novel Bacterial Isolates Derived from Human Clinical Specimens and Taxonomic Revisions Published in 2020 and 2021
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  • Genome-scale metabolic modelling enables deciphering ethanol metabolism via the acrylate pathway in the propionate-producer Anaerotignum neopropionicum
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  • Diarrhea with deficiency kidney-yang syndrome caused by adenine combined with Folium senna was associated with gut mucosal microbiota
    Jiayuan Zhu, Xiaoya Li, Na Deng, Xinxin Peng, Zhoujin Tan
    Frontiers in Microbiology.2022;[Epub]     CrossRef
  • The novel oligopeptide utilizing species Anaeropeptidivorans aminofermentans M3/9T, its role in anaerobic digestion and occurrence as deduced from large-scale fragment recruitment analyses
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  • The Gut Bacterial Community Potentiates Clostridioides difficile Infection Severity
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    mBio.2022;[Epub]     CrossRef
  • List of new names and new combinations previously effectively, but not validly, published
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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 , Nurul A. Bhuiyan , S.K. Niyogi , B.L. Sarkar , G. Balakrish Nair , Dae Shick Kim , Anna Lena Lopez , Cecil Czerkinsky , John D. Clemens , Jongsik Chun , Dong Wook Kim
J. Microbiol. 2009;47(6):783-788.   Published online February 4, 2010
DOI: https://doi.org/10.1007/s12275-009-0292-6
  • 822 View
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  • 24 Crossref
AbstractAbstract PDF
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 El Tor type rstR and classical ctxB on the large chromosome.

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  • Development of Heterologous Expression System and Optimization of the Method of Cholera Toxin β-Subunit Production in E. coli
    Hamesd H. Jamgochian, Mikhail V. Zamakhaev, Nikolai N. Sluchanko, Anna V. Goncharenko, Mikhail S. Shumkov
    Biochemistry (Moscow).2023; 88(9): 1304.     CrossRef
  • Development of a heterologous expression system and optimization of the algorithm for cholera toxin β-subunit production in E. coli
    H. H Jamgochian, M. V Zamakhaev, N. N Sluchanko, A. V Goncharenko, M. S Shumkov
    Биохимия.2023; 88(9): 1581.     CrossRef
  • Atypical and dual biotypes variant of virulent SA-NAG-Vibrio cholerae: an evidence of emerging/evolving patho-significant strain in municipal domestic water sources
    Bright E. Igere, Anthony I. Okoh, Uchechukwu U. Nwodo
    Annals of Microbiology.2022;[Epub]     CrossRef
  • VicPred: A Vibrio cholerae Genotype Prediction Tool
    Imchang Lee, Sung-Min Ha, Min-gyung Baek, Dong Wook Kim, Hana Yi, Jongsik Chun
    Frontiers in Microbiology.2021;[Epub]     CrossRef
  • Alterations in glucose metabolism in Vibrio cholerae serogroup O1 El Tor biotype strains
    Donghyun Lee, Eun Jin Kim, Yeongjun Baek, Jiwon Lee, Youngbae Yoon, G. B. Nair, Sang Sun Yoon, Dong Wook Kim
    Scientific Reports.2020;[Epub]     CrossRef
  • Characterization of Vibrio cholerae O1 isolates responsible for cholera outbreaks in Kenya between 1975 and 2017
    Martin Bundi, Mohammad Monir Shah, Eric Odoyo, Cyrus Kathiiko, Ernest Wandera, Gabriel Miring'u, Sora Guyo, Daniel Langat, Kouichi Morita, Yoshio Ichinose
    Microbiology and Immunology.2019; 63(9): 350.     CrossRef
  • Herd protection of unvaccinated adults by oral cholera vaccines in rural Bangladesh
    Mohammad Ali, Peter Kim, K Zaman, John Clemens
    International Health.2019; 11(3): 229.     CrossRef
  • Comparative genomics of Vibrio cholerae El Tor strains isolated at epidemic complications in Siberia and at the Far East
    Liliya V. Mironova, Anna S. Gladkikh, Anna S. Ponomareva, Sergey I. Feranchuk, Nikita О. Bochalgin, Evgenii A. Basov, Zhanna Yu. Khunkheeva, Sergey V. Balakhonov
    Infection, Genetics and Evolution.2018; 60: 80.     CrossRef
  • Mutation Landscape of Base Substitutions, Duplications, and Deletions in the Representative Current Cholera Pandemic Strain
    Wen Wei, Lifeng Xiong, Yuan-Nong Ye, Meng-Ze Du, Yi-Zhou Gao, Kai-Yue Zhang, Yan-Ting Jin, Zujun Yang, Po-Chun Wong, Susanna K P Lau, Biao Kan, Jun Zhu, Patrick C Y Woo, Feng-Biao Guo, Charles Baer
    Genome Biology and Evolution.2018; 10(8): 2072.     CrossRef
  • Phylogenetic Diversity of Vibrio cholerae Associated with Endemic Cholera in Mexico from 1991 to 2008
    Seon Young Choi, Shah M. Rashed, Nur A. Hasan, Munirul Alam, Tarequl Islam, Abdus Sadique, Fatema-Tuz Johura, Mark Eppinger, Jacques Ravel, Anwar Huq, Alejandro Cravioto, Rita R. Colwell, Patricia A. Rosa
    mBio.2016;[Epub]     CrossRef
  • Emergence of Tetracycline ResistantVibrio choleraeO1 Biotype El Tor Serotype Ogawa with ClassicalctxBGene from a Cholera Outbreak in Odisha, Eastern India
    M. Jain, P. Kumar, A. K. Goel
    Journal of Pathogens.2016; 2016: 1.     CrossRef
  • Whole-genome sequence comparisons reveal the evolution of Vibrio cholerae O1
    Eun Jin Kim, Chan Hee Lee, G. Balakrish Nair, Dong Wook Kim
    Trends in Microbiology.2015; 23(8): 479.     CrossRef
  • Hybrid Vibrio cholerae El Tor Lacking SXT Identified as the Cause of a Cholera Outbreak in the Philippines
    David C. Klinzing, Seon Young Choi, Nur A. Hasan, Ronald R. Matias, Enrique Tayag, Josefina Geronimo, Evan Skowronski, Shah M. Rashed, Kent Kawashima, C. Nicole Rosenzweig, Henry S. Gibbons, Brian C. Torres, Veni Liles, Alicia C. Alfon, Maria Luisa Juan,
    mBio.2015;[Epub]     CrossRef
  • Vibrio cholerae O1 Ogawa El Tor strains with the ctxB7 allele driving cholera outbreaks in south-western India in 2012
    P. Kumar, D.K. Mishra, D.G. Deshmukh, M. Jain, A.M. Zade, K.V. Ingole, A.K. Goel, P.K. Yadava
    Infection, Genetics and Evolution.2014; 25: 93.     CrossRef
  • Molecular Insights Into the Evolutionary Pathway of Vibrio cholerae O1 Atypical El Tor Variants
    Eun Jin Kim, Dokyung Lee, Se Hoon Moon, Chan Hee Lee, Sang Jun Kim, Jae Hyun Lee, Jae Ouk Kim, Manki Song, Bhabatosh Das, John D. Clemens, Jean William Pape, G. Balakrish Nair, Dong Wook Kim, Matthew K. Waldor
    PLoS Pathogens.2014; 10(9): e1004384.     CrossRef
  • Zebrafish as a Natural Host Model for Vibrio cholerae Colonization and Transmission
    Donna L. Runft, Kristie C. Mitchell, Basel H. Abuaita, Jonathan P. Allen, Sarah Bajer, Kevin Ginsburg, Melody N. Neely, Jeffrey H. Withey
    Applied and Environmental Microbiology.2014; 80(5): 1710.     CrossRef
  • Molecular-genetic analysis of Vibrio cholerae El Tor strains of epidemic risk isolated in Siberian and Far East regions of Russia
    L. V. Mironova, S. V. Balakhonov, L. Ya. Urbanovich, A. S. Kozhevnikova, V. S. Polovinkina, E. S. Kulikalova, M. V. Afanasiev
    Molecular Genetics, Microbiology and Virology.2012; 27(2): 61.     CrossRef
  • Rapid detection by multiplex PCR of Genomic Islands, prophages and Integrative Conjugative Elements in V. cholerae 7th pandemic variants
    Matteo Spagnoletti, Daniela Ceccarelli, Mauro M. Colombo
    Journal of Microbiological Methods.2012; 88(1): 98.     CrossRef
  • Phenotypic and Genetic Analysis of Altered Variants of Vibrio cholerae Biovar El Tor
    S. P. Zadnova, A. V. Shashkova, Ya. M. Krasnov, N. I. Smirnova
    Problems of Particularly Dangerous Infections.2012; (1(111)): 57.     CrossRef
  • Molecular characterization reveals involvement of altered el tor biotype Vibrio cholerae O1 strains in cholera outbreak at Hyderabad, India
    Ajay Kumar Goel, Meenu Jain, Pramod Kumar, Pennagaram Sarguna, Meera Bai, Neha Ghosh, Natrajan Gopalan
    The Journal of Microbiology.2011; 49(2): 280.     CrossRef
  • Evidence for several waves of global transmission in the seventh cholera pandemic
    Ankur Mutreja, Dong Wook Kim, Nicholas R. Thomson, Thomas R. Connor, Je Hee Lee, Samuel Kariuki, Nicholas J. Croucher, Seon Young Choi, Simon R. Harris, Michael Lebens, Swapan Kumar Niyogi, Eun Jin Kim, T. Ramamurthy, Jongsik Chun, James L. N. Wood, John
    Nature.2011; 477(7365): 462.     CrossRef
  • New V. cholerae atypical El Tor variant emerged during the 2006 epidemic outbreak in Angola
    Daniela Ceccarelli, Matteo Spagnoletti, Donatella Bacciu, Piero Cappuccinelli, Mauro M Colombo
    BMC Microbiology.2011; 11(1): 130.     CrossRef
  • 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, Nurul A. Bhuiyan, Hubert P. Endtz, S. K. Niyogi, B. L. Sarkar, G. Balakrish Nair, Binh Minh Nguyen, Nguyen Tran Hien, Cecil Czerkinsky, John D. Clemens, Jongsik Chun,
    Journal of Medical Microbiology.2010; 59(7): 763.     CrossRef
  • The evolution of the Vibrio cholerae genome during the modern period
    N. I. Smirnova, A. A. Goryaev, V. V. Kutyrev
    Molecular Genetics, Microbiology and Virology.2010; 25(4): 148.     CrossRef

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