Two Gram-stain-negative, aerobic, motile by means of flagella, short rod-shaped bacterial strains, designated IMCC43200(T) and IMCC45268(T), were isolated from coastal seawater samples collected from the South Sea of Korea. Strains IMCC43200(T) and IMCC45268(T) shared 98.6% 16S rRNA gene sequence similarity and were closely related to Congregibacter litoralis KT71(T) (98.8% and 98.7%, respectively). Complete whole-genome sequences of IMCC43200(T) and IMCC45268(T) were 3.93 and 3.86 Mb in size with DNA G + C contents of 54.8% and 54.2%, respectively. Average nucleotide identity (ANI) and digital DNA-DNA hybridization (dDDH) values between the two strains were 74.5% and 23.4%, respectively, revealing that they are independent species. The two strains showed ANI values of ≤ 75.8% and dDDH values of ≤ 23.0% to the type and only species of the genus Congregibacter (C. litoralis), indicating that each strain represents a novel species. Both strains contained summed feature 3 (comprising C(16:1) ω6c and/or C(16:1) ω7c) and summed feature 8 (comprising C(18:1) ω6c and/or C(18:1) ω7c) as major fatty acid constituents. The predominant isoprenoid quinone detected in both strains was ubiquinone-8 (Q-8). The major polar lipids of the two strains were phosphatidylethanolamine, phosphatidylglycerol, phospholipids, and aminolipids. Based on the phylogenetic, genomic, and phenotypic characterization, strains IMCC43200(T) and IMCC45268(T) were considered to represent two novel species within the genus Congregibacter, for which the names Congregibacter variabilis sp. nov. and Congregibacter brevis sp. nov. are proposed with IMCC43200(T) (= KCTC 8133(T) = NBRC 116295(T) = CCTCC AB 2023139(T)) and IMCC45268(T) (= KCTC 92921(T) = NBRC 116135(T)) as the type strains, respectively.
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potential targets for coronaviruses. This study aimed to identify SARS-CoV-2 inhibitors using drug repurposing. In silico
studies and network pharmacology were conducted to validate targets and coronavirus-associated diseases to select potential
candidates, and in vitro assays were performed to evaluate the antiviral effects of the candidate drugs to elucidate the
mechanisms of the viruses at the molecular level and determine the effective antiviral drugs for them. Plaque and cytopathic
effect reduction were evaluated, and real-time quantitative reverse transcription was used to evaluate the antiviral activity
of the candidate drugs against SARS-CoV-2 variants in vitro. Finally, a comparison was made between the molecular docking
binding affinities of fenofibrate and remdesivir (positive control) to conventional and identified targets validated from
protein–protein interaction (PPI). Seven candidate drugs were obtained based on the biological targets of the coronavirus,
and potential targets were identified by constructing complex disease targets and PPI networks. Among the candidates,
fenofibrate exhibited the strongest inhibition effect 1 h after Vero E6 cell infection with SARS-CoV-2 variants. This study
identified potential targets for coronavirus disease (COVID-19) and SARS-CoV-2 and suggested fenofibrate as a potential
therapy for COVID-19.
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investigated the diatom community on the hull samples collected from two Korean research vessels Isabu (IRV) and Onnuri
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communities that are associated with ship hull-fouling at an early stage of biofilm formation. Moreover, ships arriving
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boninense aggressiveness, we employed the DSI and vegetative growth measurement of infected oil palm seedlings. Disease
confirmation was performed through scanning electron microscopy and molecular identification of fungal DNA from both
infected tissue and fungi isolated from Ganoderma selective medium. Two-month-old oil palm seedlings were artificially
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The progression and exacerbation of liver fibrosis are closely related to the gut microbiome. It is hypothesized that some
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data, preventive and therapeutic effect of probiotics Lactobacillus lactis and L. rhamnosus was evaluated by using four
mice fibrosis models. L. lactis and L. rhamnosus were supplied to 3,5-diethoxycarbonyl-1,4-dihydrocollidine or carbon
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expression in the liver were evaluated. The microbiome was analyzed in mouse cecal contents. In the mouse model, the
effects of Lactobacillus in preventing and treating liver fibrosis were different for each microbe species. In case of L. lactis,
all models showed preventive and therapeutic effects against liver fibrosis. In microbiome analysis in mouse models administered
Lactobacillus, migration and changes in the ratio and composition of the gut microbial community were confirmed.
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A novel bacterium designated RR4-40T was isolated from a
biofilter of seawater recirculating aquaculture system in Busan,
South Korea. Cells are strictly aerobic, Gram-negative, irregular
short rod, non-motile, and oxidase- and catalase-negative.
Growth was observed at 15–30°C, 0.5–6% NaCl (w/v),
and pH 5.0–9.5. The strain grew optimally at 28°C, 3% salinity
(w/v), and pH 8.5. The phylogenetic analysis based on
16S rRNA gene sequences showed that strain RR4-40T was
most closely related to Marinirhabdus gelatinilytica NH83T
(94.16% of 16S rRNA gene similarity) and formed a cluster
with genera within the family Flavobacteriaceae. The values
of the average nucleotide identity (ANI), digital DNA-DNA
hybridization (dDDH), and average amino acid identity (AAI)
between genomes of strain RR4-40T and M. gelatinilytica
NH83T were 72.91, 18.2, and 76.84%, respectively, and the
values against the strains in the other genera were lower than
those. The major fatty acids were iso-C15:0 (31.34%), iso-C17:0
3-OH (13.65%), iso-C16:0 3-OH (10.61%), and iso-C15:1 G
(10.38%). The polar lipids comprised phosphatidylglycerol,
diphosphatidylglycerol, aminophospholipid, aminolipid, glycolipid,
and sphingolipid. The major respiratory quinone was
menaquinone-6 (MK-6) and the DNA G + C content of strain
RR4-40T was 37.4 mol%. According to the polyphasic analysis,
strain RR4-40T is considered to represent a novel genus within
the family Flavobacteriaceae, for which the name Rasiella
rasia gen. nov, sp. nov. is proposed. The type strain is RR4-40T
(= KCTC 52650T = MCCC 1K04210T).
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As of February 2022, SARS-CoV-2 is still one of the most
serious public health threats due to its high mortality rate and
rapid spread of novel variants. Since the first outbreak in 2019,
general understanding of SARS-CoV-2 has been improved
through basic and clinical studies; however, knowledge gaps
still exist in our understanding of the emerging novel SARSCoV-
2 variants, which impacts the corresponding development
of vaccines and therapeutics. Especially, accumulation of
mutations in SARS-CoV-2 and rapid spread in populations
with previous immunity has resulted in selection of variants
that evade the host immune response. This phenomenon threatens
to render current SARS-CoV-2 vaccines ineffective for
controlling the pandemic. Proper animal models are essential
for detailed investigations into the viral etiology, transmission
and pathogenesis mechanisms, as well as evaluation of the
efficacy of vaccine candidates against recent SARS-CoV-2
variants. Further, the choice of animal model for each research
topic is important for researchers to gain better knowledge
of recent SARS-CoV-2 variants. Here, we review the advantages
and limitations of each animal model, including mice,
hamsters, ferrets, and non-human primates, to elucidate variant
SARS-CoV-2 etiology and transmission and to evaluate
therapeutic and vaccine efficacy.
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High-risk genotypes of human papillomaviruses (HPVs) are
directly implicated in various abnormalities associated with
cellular hyperproliferation, including cervical cancer. E6 is one
of two oncoproteins encoded in the HPV genome, which recruits
diverse PSD-95/Dlg/ZO-1 (PDZ) domain-containing
human proteins through its C-terminal PDZ-binding motif
(PBM) to be degraded by means of the proteasome pathway.
Among the three PDZ domain-containing protein tyrosine
phosphatases, protein tyrosine phosphatase non-receptor type
3 (PTPN3) and PTPN13 were identified to be recognized by
HPV E6 in a PBM-dependent manner. However, whether
HPV E6 associates with PTPN4, which also has a PDZ domain
and functions as an apoptosis regulator, remains undetermined.
Herein, we present structural and biochemical evidence
demonstrating the direct interaction between the PBM
of HPV16 E6 and the PDZ domain of human PTPN4 for the
first time. X-ray crystallographic structure determination and
binding measurements using isothermal titration calorimetry
demonstrated that hydrophobic interactions in which Leu158
of HPV16 E6 plays a key role and a network of intermolecular
hydrogen bonds sustain the complex formation between
PTPN4 PDZ and the PBM of HPV16 E6. In addition, it was
verified that the corresponding motifs from several other highrisk
HPV genotypes, including HPV18, HPV31, HPV33, and
HPV45, bind to PTPN4 PDZ with comparable affinities, suggesting
that PTPN4 is a common target of various pathogenic
HPV genotypes.
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play pivotal roles in the pathogenesis of SARS-CoV-2.
While optimal IFN and inflammasome responses are essential
for limiting SARS-CoV-2 infection, aberrant activation of
these innate immune responses is associated with COVID-19
pathogenesis. In this review, we focus our discussion on recent
findings on SARS-CoV-2-induced type I and III IFNs
and NLRP3 inflammasome responses and the viral proteins
regulating these mechanisms.
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Helicobacter pylori outer membrane inflammatory protein
A (OipA) was originally named for its role in inducing inflammation
in the host, as evidenced by high mucosal IL-8
levels. Expression of OipA is regulated by phase variation of
a CT dinucleotide-repeat located in the 5region of the gene.
However, little is known about OipA geographic diversity
across isolates. To address this gap, we conducted a large-scale
molecular epidemiologic analysis using H. pylori clinical isolates
obtained from two geographically distinct populations:
Korea and the United States (US). Most Korean isolates (98.7%)
possessed two copies of oipA located at two specific loci (A
and B) while all US isolates contained only one copy of oipA
at locus A. Furthermore, most Korean oipA (94.8%) possessed
three or less CT repeats while most US oipA (96.6%) contained
five or more CT repeats. Among the two copies, all Korean
H. pylori possessed at least one oipA ‘on’ phase variant while
the single copy of oipA in US isolates showed 56.2% ‘on’ and
43.8% ‘off.’ Thus, host differences seem to have driven geographic
diversification of H. pylori across these populations
such that OipA expression in US isolates is still regulated by
phase variation with 5 or more CT repeats, while Korean isolates
always express OipA; duplication of the oipA combined
with a reduction of CT repeats to three or less ensures continued
expression. En masse, these findings suggest that diversity
in the oipA gene copy number, CT repeats, and phase
variation among H. pylori from different populations may
confer a benefit in adaptation to particular host populations.
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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.
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generation of an enormous amount of nitric oxide metabolites
and the growing depletion of oil resources as a result of
AA production from a mixture of cyclohexanol and cyclohexanone,
the microbial methods for synthesizing AA have
attracted significant attention. Of the several AA-producing
pathways, the reverse adipate degradation pathway in
Thermobifida fusca (Tfu RADP) is reported to be the most
efficient, which has been confirmed in Escherichia coli. In this
study, the heterologous Tfu RADP was constructed for producing
AA in S. cerevisiae by co-expressing genes of Tfu_
0875, Tfu_2399, Tfu_0067, Tfu_1647, Tfu_2576, and Tfu_
2576. The AA titer combined with biomass, cofactors and
other by-products was all determined after fermentation.
During batch fermentation in a shake flask, the maximum AA
titer was 3.83 mg/L, while the titer increased to 10.09 mg/L
during fed-batch fermentation in a 5-L bioreactor after fermentation
modification.
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that pose a potential threat to human health worldwide.
Urban wastewater treatment plants (WWTPs) are a main
source of both antibiotic-resistant bacteria and ARGs released
into the environment. Nevertheless, the propagation of ARGs
and their underlying mechanisms and the dynamics of mobile
genetic elements (MGEs) in WWTPs have rarely been
investigated in South Korea. In this study, shotgun metagenomic
analysis was used to identify comprehensive ARGs and
their mechanisms, bacterial communities, and MGEs from
4 configurations with 2 activated sludge (AS) and 2 anaerobic
digestion sludge (ADS) samples. A total of 181 ARG subtypes
belonging to 22 ARG types were broadly detected, and the
ARG abundances in the AS samples were 1.3–2.0 orders of
magnitude higher than in the ADS samples. Multidrug and
bacitracin resistance genes were the predominant ARG types
in AS samples, followed by ARGs against sulfonamide, tetracycline,
and β-lactam. However, the composition of ARG
types in ADS samples was significantly changed. The abundance
of multidrug and β-lactam resistance genes was drastically
reduced in the ADS samples. The resistance genes of
MLS were the predominant, followed by ARGs against sulfonamide
and tetracycline in the ADS samples. In addition,
plasmids were the dominant MGEs in the AS samples, while
integrons (intI1) were the dominant MGEs in the ADS samples.
These results provide valuable information regarding
the prevalence of ARG types and MGEs and the difference
patterns between the AS and ADS systems.
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