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Kihyun Lee 3 Articles
Cytoplasmic molecular chaperones in Pseudomonas species
Hyunhee Kim , Seongjoon Moon , Soojeong Ham , Kihyun Lee , Ute Römling , Changhan Lee
J. Microbiol. 2022;60(11):1049-1060.   Published online November 1, 2022
DOI: https://doi.org/10.1007/s12275-022-2425-0
  • 1,111 View
  • 6 Download
  • 5 Web of Science
  • 5 Crossref
AbstractAbstract PDF
Pseudomonas is widespread in various environmental and host niches. To promote rejuvenation, cellular protein homeostasis must be finely tuned in response to diverse stresses, such as extremely high and low temperatures, oxidative stress, and desiccation, which can result in protein homeostasis imbalance. Molecular chaperones function as key components that aid protein folding and prevent protein denaturation. Pseudomonas, an ecologically important bacterial genus, includes human and plant pathogens as well as growth-promoting symbionts and species useful for bioremediation. In this review, we focus on protein quality control systems, particularly molecular chaperones, in ecologically diverse species of Pseudomonas, including the opportunistic human pathogen Pseudomonas aeruginosa, the plant pathogen Pseudomonas syringae, the soil species Pseudomonas putida, and the psychrophilic Pseudomonas antarctica.

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Citations to this article as recorded by  
  • Dietary supplementation of Phaffia rhodozyma enhances growth performance, immune response, and modulates gut microbiota in Apostichopus japonicus
    Xiaofei Tan, Ailin Tang, Zifan Zhou, Haoyu Guo, Siyu Zhang, Yujia Liu, Jian Che, Bingnan Liu
    Aquaculture International.2026;[Epub]     CrossRef
  • Culture-enriched sequencing reveals river confluence sediments as high-risk reservoirs of viable multidrug-resistant pathogens
    Yi Li, Huijuan Huang, Bi Luo, Rong Wang, Zhiwei Zhu
    Journal of Hazardous Materials.2026; 514: 142756.     CrossRef
  • An innovative utilization approach for by-products of biogas desulfurization:Co-hydrothermal treatment of sulfur with biogas slurry to prepare sulfur-enriched liquid fertilizer
    Zhijie Xie, Fang Deng, Yuqin Wan, Yiping Luo, Qin Cao, Yichao Chen, Dong Li
    Process Biochemistry.2024; 147: 522.     CrossRef
  • Isolation of Pseudomonas oleovorans Carrying Multidrug Resistance Proteins MdtA and MdtB from Wastewater
    Haifeng Wang, Chenyang Sun, Xing Chen, Kai Yan, Hongxuan He
    Molecules.2023; 28(14): 5403.     CrossRef
  • Development of heat-shock resistance in Legionella pneumophila modeled by experimental evolution
    Jeffrey Liang, Gillian Cameron, Sébastien P. Faucher, Christopher A. Elkins
    Applied and Environmental Microbiology.2023;[Epub]     CrossRef
Overview of bioinformatic methods for analysis of antibiotic resistome from genome and metagenome data
Kihyun Lee , Dae-Wi Kim , Chang-Jun Cha
J. Microbiol. 2021;59(3):270-280.   Published online February 23, 2021
DOI: https://doi.org/10.1007/s12275-021-0652-4
  • 1,214 View
  • 13 Download
  • 27 Web of Science
  • 23 Crossref
AbstractAbstract PDF
Whole genome and metagenome sequencing are powerful approaches that enable comprehensive cataloging and profiling of antibiotic resistance genes at scales ranging from a single clinical isolate to ecosystems. Recent studies deal with genomic and metagenomic data sets at larger scales; therefore, designing computational workflows that provide high efficiency and accuracy is becoming more important. In this review, we summarize the computational workflows used in the research field of antibiotic resistome based on genome or metagenome sequencing. We introduce workflows, software tools, and data resources that have been successfully employed in this rapidly developing field. The workflow described in this review can be used to list the known antibiotic resistance genes from genomes and metagenomes, quantitatively profile them, and investigate the epidemiological and evolutionary contexts behind their emergence and transmission. We also discuss how novel antibiotic resistance genes can be discovered and how the association between the resistome and mobilome can be explored.

Citations

Citations to this article as recorded by  
  • The Application of artificial intelligence in periprosthetic joint infection
    Pengcheng Li, Yan Wang, Runkai Zhao, Lin Hao, Wei Chai, Chen Jiying, Zeyu Feng, Quanbo Ji, Guoqiang Zhang
    Journal of Advanced Research.2026; 79: 633.     CrossRef
  • Computational Genomics for Resistome Characterization: Current Advancements and Future Challenges Under a One Health Perspective
    Lenin García Gutiérrez, Alfonso Méndez-Tenorio, Mario Ángel López-Luis, Sandra Alejandra Ávila-Huerta, Gloria León-Ávila, Santiago R. Castaño-Valencia, Gabriela Ibáñez-Cervantes
    Antibiotics.2026; 15(8): 804.     CrossRef
  • Interpreting antimicrobial resistance from bacterial whole-genome sequencing: prediction tools, database fragmentation, analytical trade-offs, and harmonized reporting
    Abdullateef Abdullah Alshehri
    Frontiers in Microbiology.2026;[Epub]     CrossRef
  • Evolution of pathogenic Escherichia coli harboring the transmissible locus of stress tolerance: from food sources to clinical environments
    Maxsueli Machado, Pedro Panzenhagen, Flávia Figueira Aburjaile, Bertram Brenig, Mateus Matiuzzi da Costa, Vasco Ariston de Carvalho Azevedo, Eduardo Eustáquio de Souza Figueiredo, Carlos Adam Conte-Junior
    Scientific Reports.2025;[Epub]     CrossRef
  • Integrating whole-genome sequencing into antimicrobial resistance surveillance: methodologies, challenges, and perspectives
    Yasufumi Matsumura, Masaki Yamamoto, Ryota Gomi, Yasuhiro Tsuchido, Koh Shinohara, Taro Noguchi, Miki Nagao, Jose M. Munita, Alexander Sundermann
    Clinical Microbiology Reviews.2025;[Epub]     CrossRef
  • Unraveling resistance mechanisms in combination therapy: A comprehensive review of recent advances and future directions
    Nami Morales-Durán, Angel León-Buitimea, José R. Morones-Ramírez
    Heliyon.2024; 10(6): e27984.     CrossRef
  • Resistome Mapping in Foodborne Pathogens: Understanding Role in the Transmission Dynamics of Resistance Genes
    Muneer Oladipupo Yaqub, Chinedu Eucharia Joseph, Aashika Jain, Lekshmi K. Edison
    Applied Microbiology.2024; 4(4): 1476.     CrossRef
  • Metagenomic assemblies tend to break around antibiotic resistance genes
    Anna Abramova, Antti Karkman, Johan Bengtsson-Palme
    BMC Genomics.2024;[Epub]     CrossRef
  • Comprehensive genomic landscape of antibiotic resistance in Staphylococcus epidermidis
    Do-Hoon Lee, Kihyun Lee, Yong-Seok Kim, Chang-Jun Cha, Jack A. Gilbert
    mSystems.2024;[Epub]     CrossRef
  • Web-Based Tools Validation for Antimicrobial Resistance Prediction: An Empirical Comparative Analysis
    Sweta Padma Routray, Swayamprabha Sahoo, Debasish Swapnesh Kumar Nayak, Sejal Shah, Tripti Swarnkar
    SN Computer Science.2024;[Epub]     CrossRef
  • Genome-centric analyses of 165 metagenomes show that mobile genetic elements are crucial for the transmission of antimicrobial resistance genes to pathogens in activated sludge and wastewater
    Nafi’u Abdulkadir, Joao Pedro Saraiva, Junya Zhang, Stefan Stolte, Osnat Gillor, Hauke Harms, Ulisses Rocha, Adriana E. Rosato
    Microbiology Spectrum.2024;[Epub]     CrossRef
  • Identification of Antibiotic Resistance in ESKAPE Pathogens through Plasmonic Nanosensors and Machine Learning
    Ting Yu, Ying Fu, Jintao He, Jun Zhang, Yunlei Xianyu
    ACS Nano.2023; 17(5): 4551.     CrossRef
  • The challenges of defining the human nasopharyngeal resistome
    Lucy O’Connor, Robert Heyderman
    Trends in Microbiology.2023; 31(8): 816.     CrossRef
  • Resistome profiling reveals transmission dynamics of antimicrobial resistance genes from poultry litter to soil and plant
    Animesh Tripathi, Dinesh Kumar, Priyank Chavda, Dalip Singh Rathore, Ramesh Pandit, Damer Blake, Fiona Tomley, Madhvi Joshi, Chaitanya G. Joshi, Suresh Kumar Dubey
    Environmental Pollution.2023; 327: 121517.     CrossRef
  • Prioritization of Critical Factors for Surveillance of the Dissemination of Antibiotic Resistance in Pseudomonas aeruginosa: A Systematic Review
    Jung Hun Lee, Nam-Hoon Kim, Kyung-Min Jang, Hyeonku Jin, Kyoungmin Shin, Byeong Chul Jeong, Dae-Wi Kim, Sang Hee Lee
    International Journal of Molecular Sciences.2023; 24(20): 15209.     CrossRef
  • Flavobacterium psychrotrophum sp. nov. and Flavobacterium panacagri sp. nov., Isolated from Freshwater and Soil
    Yong-Seok Kim, Eun-Mi Hwang, Chang-Myeong Jeong, Chang-Jun Cha
    Journal of Microbiology.2023; 61(10): 891.     CrossRef
  • Antimicrobial Resistance Genes (ARGs), the Gut Microbiome, and Infant Nutrition
    Rufus J. Theophilus, Diana Hazard Taft
    Nutrients.2023; 15(14): 3177.     CrossRef
  • Metagenomic Insight into Sulfonamide-Induced Variation in Antibiotic Resistome of Soil Associated with Taxonomy, Mobile Genetic Elements (MGEs), and Function
    Mi Li, Xiaoyu Xiao, Zhangsong Jiang, Haihui Tang, Lingling Rong, Tiao Zhang, Taijia Li, Cui Hu, Ligui Wu, Xiaoming Zou
    ACS Agricultural Science & Technology.2022; 2(1): 123.     CrossRef
  • Gold nanoparticle-DNA aptamer-assisted delivery of antimicrobial peptide effectively inhibits Acinetobacter baumannii infection in mice
    Jaeyeong Park, Eunkyoung Shin, Ji-Hyun Yeom, Younkyung Choi, Minju Joo, Minho Lee, Je Hyeong Kim, Jeehyeon Bae, Kangseok Lee
    Journal of Microbiology.2022; 60(1): 128.     CrossRef
  • Promising Acinetobacter baumannii Vaccine Candidates and Drug Targets in Recent Years
    Yong Chiang Tan, Chandrajit Lahiri
    Frontiers in Immunology.2022;[Epub]     CrossRef
  • Recent Advances in Rapid Antimicrobial Susceptibility Testing
    Rucha Datar, Sylvain Orenga, Romain Pogorelcnik, Olivier Rochas, Patricia J Simner, Alex van Belkum
    Clinical Chemistry.2021; 68(1): 91.     CrossRef
  • Chromosomal integration of Tn5253 occurs downstream of a conserved 11-bp sequence of the rbgA gene in Streptococcus pneumoniae and in all the other known hosts of this integrative conjugative element (ICE)
    Francesco Santoro, Valeria Fox, Alessandra Romeo, Elisa Lazzeri, Gianni Pozzi, Francesco Iannelli
    Mobile DNA.2021;[Epub]     CrossRef
  • Omics-based microbiome analysis in microbial ecology: from sequences to information
    Jang-Cheon Cho
    Journal of Microbiology.2021; 59(3): 229.     CrossRef
Comparative genomic analysis of pyrene-degrading Mycobacterium species: Genomic islands and ring-hydroxylating dioxygenases involved in pyrene degradation
Dae-Wi Kim , Kihyun Lee , Do-Hoon Lee , Chang-Jun Cha
J. Microbiol. 2018;56(11):798-804.   Published online October 24, 2018
DOI: https://doi.org/10.1007/s12275-018-8372-0
  • 983 View
  • 1 Download
  • 24 Crossref
AbstractAbstract PDF
The genome sequences of two pyrene-degrading bacterial strains of Mycobacterium spp. PYR10 and PYR15, isolated from the estuarine wetland of the Han river, South Korea, were determined using the PacBio RS II sequencing platform. The complete genome of strain PYR15 was 6,037,017 bp in length with a GC content of 66.5%, and contained 5,933 protein- coding genes. The genome of strain PYR10 was 5,999,427 bp in length with a GC content of 67.7%, and contained 5,767 protein-coding genes. Based on the average nucleotide identity values, these strains were designated as M. gilvum PYR10 and M. pallens PYR15. A genomic comparison of these pyrene-degrading Mycobacterium strains with pyrene- non-degrading strains revealed that the genomes of pyrene-degrading strains possessed similar repertoires of ringhydroxylating dioxygenases (RHDs), including the pyrenehydroxylating dioxygenases encoded by nidA and nidA3, which could be readily distinguished from those of pyrenenon- degraders. Furthermore, genomic islands, containing catabolic gene clusters, were shared only among the pyrenedegrading Mycobacterium strains and these gene clusters contained RHD genes, including nidAB and nidA3B3. Our genome data should facilitate further studies on the evolution of the polycyclic aromatic hydrocarbon-degradation pathways in the genus Mycobacterium.

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  • Biodegradation of high-molecular-weight PAHs in polluted mangrove sediments using indigenous microflora and exogenous strains Rhodococcus erythropolis T902.1 and Bacillus subtilis
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    Biodegradation.2026;[Epub]     CrossRef
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