Publications by authors named "Je Hee Lee"

Introduction: Coronavirus disease 2019 (COVID-19) alters the gut microbiome. This study aimed to assess the association between the disease severity of COVID-19 and changes in stool microbes through a seven-month follow-up of stool collection.

Methods: We conducted a multicentre, prospective longitudinal study of 58 COVID-19 patients and 116 uninfected controls.

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Purpose: Extranodal NK/T-cell lymphoma (ENKTL) predominantly manifests in East Asia and Latin America. Despite shared intrinsic factors, such as ethnic and genetic backgrounds, the progression of ENKTL can be influenced by extrinsic factors related to changing lifestyle patterns.

Materials And Methods: This study collected stool samples from newly diagnosed (ND)-ENKTL patients (n=40) and conducted whole genome shotgun sequencing.

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A Gram-stain-positive, anaerobic, motile, and short rod-shaped bacterium, designated KGMB12511, was isolated from the feces of healthy Koreansubjects. Phylogenetic analysis based on the 16S rRNA gene sequence showed that strain KGMB12511 was closely related to Gordonibacter pamelaeae 7-10-1-b (95.2%).

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Article Synopsis
  • * It thrives in specific conditions (optimum temperature of 37°C, pH 7) and produces acetic acid and isobutyric acid as major fermentation products, while also encoding genes related to complex polysaccharide utilization.
  • * The strain has a genome size of about 3.2 million base pairs with a G+C content of 41.4%, and its phylogenetic similarity to related species indicates its novel classification status. *
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The human gut microbiome mediates bidirectional interaction within the gut-liver axis, while liver diseases, including liver cirrhosis, are very closely related to the state of the gut environment. Thus, improving the health of the gut-liver axis by targeting the intestinal microbiota is a potential therapeutic approach in hepatic diseases. This study examines changes in metabolomics and microbiome composition by treating bacteria derived from the human gut in mice with liver cirrhosis.

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Background: The prevalence of Parkinson's disease (PD) has increased steadily with the increase of the elderly population. PD may influence dietary intake and quality, and the gut microbiome composition. The present study examined differences in dietary intake and quality between PD patients and controls according to sex.

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  • - The study explored how the gut microbiome might affect cancer development, specifically looking at newly diagnosed patients with diffuse large B-cell lymphoma (DLBCL), finding significant differences in microbial composition compared to healthy individuals.
  • - Patients with DLBCL showed lower microbial diversity and higher levels of the Enterobacteriaceae family, which were linked to worse treatment outcomes, including shorter progression-free survival.
  • - The presence of Enterobacteriaceae was associated with complications like febrile neutropenia and had connections to specific cytokine levels, highlighting the need for further research on gut dysbiosis in lymphoma patients.
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  • Several studies have shown that people with Parkinson's disease (PD) have a unique gut microbiome, but there's limited research on the oral microbiome's role in PD.
  • By using advanced shotgun metagenomic sequencing, researchers found significant differences in the oral and gut microbiome between PD patients and healthy individuals.
  • Notably, PD patients had higher levels of Lactobacillus in their mouths, which correlated with harmful gut bacteria, and their microbiome showed reduced gene markers for certain amino acid production but increased markers for antimicrobial resistance.
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Two obligately anaerobic, Gram-stain-negative, non-motile, non-spore-forming and short rod shaped bacteria, designated KGMB07931 and KGMB10229, were isolated from faeces of two Korean persons. Phylogenetic analysis based on 16S rRNA gene sequences revealed that strains KGMB07931 and KGMB10229 were very similar to each other (99.9%) and grouped within the genus Bacteroides, displaying the highest similarity with Bacteroides uniformis ATCC 8492 (97.

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Background: Although microbioa-based therapies have shown putative effects on the treatment of non-alcoholic fatty liver disease (NAFLD), it is not clear how microbiota-derived metabolites contribute to the prevention of NAFLD. We explored the metabolomic signature of Lactobacillus lactis and Pediococcus pentosaceus in NAFLD mice and its association in NAFLD patients.

Methods: We used Western diet-induced NAFLD mice, and L.

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A novel actinobacterial strain, Gram-positive, anaerobic, non-motile, and rod-shaped, designated KGMB02528, was isolated from healthy human feces. Cells of strain KGMB02528 grew optimally at pH 7.0 and 37 °C and in the presence of 0% (w/v) NaCl.

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Metabolic associated fatty liver disease (MAFLD) is a new concept where the presence of both fatty liver and metabolic abnormality are necessary for diagnosis. Several studies have reported that altered gut microbiome is closely associated with metabolic diseases and non-alcoholic fatty liver disease. However, the studies on MAFLD population are scarce.

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Objectives: The increasing prevalence of multidrug-resistant microorganisms (MDRO) is increasing the frequency of poor clinical outcomes, prolonging hospitalizations, and raising healthcare costs. This study evaluated the eradication efficacy of fecal microbiota transplantation (FMT) and identified microbial and functional biomarkers of MDRO decolonization.

Methods: Fecal solution obtained from healthy unrelated donors was infused in the participants' guts which had been colonized with carbapenemase-producing enterobacteriacea (CPE), vancomycin-resistant enterococci (VRE), or both CPE and VRE.

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The clinical spectra of irritable bowel syndrome (IBS) and inflammatory bowel disease (IBD) intersect to form a scantily defined overlap syndrome, termed pre-IBD. We show that increased Enterobacteriaceae and reduced Clostridia abundance distinguish the fecal microbiota of pre-IBD patients from IBS patients. A history of antibiotics in individuals consuming a high-fat diet was associated with the greatest risk for pre-IBD.

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Article Synopsis
  • A study was conducted on the gut microbiome of healthy young male soldiers in South Korea to understand how lifestyle factors influence its composition.
  • Researchers collected stool samples from 100 soldiers and analyzed the bacterial DNA to identify prevalent types and their abundances.
  • Results showed distinct gut microbiome profiles based on smoking status and lifestyle habits, revealing that current smokers had lower levels of certain beneficial bacteria compared to non-smokers.
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An obligately anaerobic, Gram-stain-negative, non-motile, non-spore-forming, and coccobacilli-shaped bacterial strain, designated KGMB03119, 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 15691 (96.8% 16S rRNA gene sequence similarity).

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A novel actinobacterial strain, designated KGMB04484, was isolated from healthy human faeces sampled in the Republic of Korea. Cells of strain KGMB04484 were strictly anaerobic, Gram-stain-positive, catalase-positive, oxidase-negative, non-motile coccobacilli and formed tiny colonies on Columbia agar with 5 % horse blood. On the basis of 16S rRNA gene sequence similarity, strain KGMB04484 was affiliated with the genus in the family and its closest relative was JC110 (96.

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A strictly anaerobic bacterium, designated as strain KGMB-03357, was isolated from the faeces of a healthy Korean selected by Bundang Seoul National University based on health status. Cells of strain KGMB03357 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.

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The toxigenic classical and El Tor biotype serogroup O1 strains are generated by lysogenization of host-type-specific cholera toxin phages (CTX phages). Experimental evidence of the replication and transmission of an El Tor biotype-specific CTX phage, CTX-1, has explained the evolution of El Tor biotype strains. The generation of classical biotype strains has not been demonstrated in the laboratory, and the classical biotype-specific CTX phage, CTX-cla, is considered to be defective with regard to replication.

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Background And Objectives: Metastatic colon cancer patients are treated with the chemotherapy regimens, FOLFOX and FOLFIRI, in either order. So far, we cannot predict the response of chemotherapeutic agent, so it is necessary to find which regimen is adequate before starting chemotherapy.

Methods: Enrolled patients are randomized into either conventional treatment or planned treatment preceded by pretreatment genetic analysis.

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Objectives: We aimed at evaluating the virulence of atypical Shigella flexneri II:(3)4,7(8) by DNA microarray and invasion assay.

Methods: We used a customized S. flexneri DNA microarray to analyze an atypical S.

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Klebsiella pneumoniae is a Gram-negative, rod-shaped, nonmotile, and opportunistic pathogenic species with clinical importance. It is a part of natural flora of humans and animals. Here we report the draft genome sequence of the type strain of Klebsiella pneumoniae subsp.

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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.

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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.

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Here we report the complete genome sequence of the Mycobacterium intracellulare clinical strain MOTT-36Y, previously grouped into the INT5 genotype among the 5 genotypes of M. intracellulare. This genome sequence will serve as a valuable reference for understanding the disparity in virulence and epidemiologic traits between M.

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