To study the role of intestinal flora in the development of bloodstream infections (BSIs). 42 patients and 19 healthy controls (HCs) were screened into the study and their intestinal flora was measured by 16S rRNA gene sequencing.
The bacterial diversity was significantly lower in the BSI group compared with that in the HCs (P < 0.001), and beta diversity was significantly differentiated between the two groups (PERMANOVA, P = 0.001). The four keystone species [Roseburia, Faecalibacterium, Prevotella, and Enterococcus (LDA > 4)] differed significantly between the two groups. Dysbiosis of fecal microbial ecology is a common condition present in patients with BSI. The proliferation of certain pathogens or reduction of SCFA-producing bacteria would cause susceptibility to BSI.
Two novel bacterial strains CJ74T
and CJ75T
belonging to the genus Flavobacterium were isolated from freshwater of Han
River and ginseng soil, South Korea, respectively. Strain CJ74T
was Gram-stain-negative, aerobic, rod-shaped, non-motile,
and non-flagellated, and did not produce flexirubin-type pigments. Strain CJ75T
was Gram-stain-negative, aerobic, rodshaped,
motile by gliding, and non-flagellated, and produced flexirubin-type pigments. Both strains were shown to grow
optimally at 30 °C in the absence of NaCl on R2A medium. Phylogenetic analysis based on 16S rRNA gene sequences showed
that strains CJ74T
and CJ75T
belonged to the genus Flavobacterium and were most closely related to Flavobacterium niveum
TAPW14T
and Flavobacterium foetidum CJ42T
with 96.17% and 97.29% 16S rRNA sequence similarities, respectively.
Genomic analyses including the reconstruction of phylogenomic tree, average nucleotide identity, and digital DNA-DNA
hybridization suggested that they were novel species of the genus Flavobacterium. Both strains contained menaquinone 6
(MK-6) as the primary respiratory quinone and phosphatidylethanolamine as a major polar lipid. The predominant fatty acids
of both strains were iso-C15:0 and summed feature 3 (
C16:1 ω7c and/or C16:
1 ω6c). Based on the polyphasic taxonomic study,
strains CJ74T
and CJ75T
represent novel species of the genus Flavobacterium, for which names Flavobacterium psychrotrophum
sp. nov. and Flavobacterium panacagri sp. nov. are proposed, respectively. The type strains are CJ74T
(=KACC
19819T
=JCM 32889T)
and CJ75T
(=KACC 23149T
=JCM 36132T).
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Congregibacter variabilis sp. nov. and Congregibacter brevis sp. nov. Within the OM60/NOR5 Clade, Isolated from Seawater, and Emended Description of the Genus Congregibacter Hyeonsu Tak, Miri S. Park, Hyerim Cho, Yeonjung Lim, Jang-Cheon Cho Journal of Microbiology.2024; 62(9): 739. CrossRef
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Bacteria employ a diverse array of cellular regulatory
mechanisms to successfully adapt and thrive in ever-changing
environments, including but not limited to temperature
changes, fluctuations in nutrient availability, the presence
or absence of electron acceptors such as oxygen, the availability
of metal ions crucial for enzyme activity, and the
existence of antibiotics. Bacteria can virtually modulate
any step of gene expression from transcr!ptional initiation
to posttranslational modification of a protein for the control
of cellular processes. Furthermore, one gene regulator
often controls another in a complex gene regulatory network.
Thus, it is not easy to fully understand the intricacies of
bacterial regulatory mechanisms in various environments. In
this special issue, while acknowledging the challenge of covering
all aspects of bacterial regulatory mechanisms across
diverse environments, seven review articles are included to
provide insight into the recent progress in understanding
such mechanisms from different perspectives: positive regulatory
mechanisms by secondary messenger (cAMP receptor
protein), two-component signal transduction mechanisms
(Rcs and Cpx), diverse regulatory mechanisms by a specific
environmental factor in specific bacteria (oxygen availability
in Mycobacterium and manganese ion availability in Salmonella),
diverse regulatory mechanisms by a specific environmental
factor (temperature and antibiotics), and regulatory
mechanisms by antibiotics in cell wall synthesis.
Bacteria, as ubiquitous organisms that can be found in
almost every environment, carry out complex cellular processes
that allow them to survive and thrive in a variety of
different conditions despite their small size and relative simplicity.
One of the key factors that allows bacteria to carry
out these complex processes is their ability to regulate gene
expression through various mechanisms. Gene expression
is a fundamental biological process by which the genetic
information encoded in a gene is transcribed into an RNA
molecule and subsequently translated into a functional gene
product, often a protein. Furthermore, the activity levels of
proteins may further be altered by posttranslational modification.
Regulation of gene expression refers to the control
of the amount and timing of gene expression, and thus it
can be divided into transcr!ptional, translational, and posttranslational
levels.
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The PhoBR two-component system upregulates virulence in Aeromonas dhakensis C4–1 Wei Feng, Xuesong Li, Nuo Yang, Lixia Fan, Guiying Guo, Jun Xie, Xiuqing Cai, Yuqi Meng, Jifeng Zeng, Yu Han, Jiping Zheng Aquaculture.2025; 595: 741665. CrossRef
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Escherichia coli
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With the growing threat of antibiotic resistance, researchers around the globe are seeking alternatives to stem bacterial
pathogenesis. One such alternative is bacteriocins, proteins produced by bacterial species to inhibit the growth and viability
of related bacterial species. With their diverse mechanisms, which include pore formation and nuclease activities, and
narrow spectrum of activities, which limit their impact to only certain bacterial species, unlike many chemical antibiotics,
bacteriocins offer intriguing possibilities to selectively control individual bacterial populations. Within this review, therefore,
we highlight current research exploring the application of colicins and microcins, a subset of bacteriocins, with an emphasis
on their activities against drug-resistant pathogens, both in in vitro and in vivo settings.
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Transposon mutant libraries are an important resource to
study bacterial metabolism and pathogenesis. The fitness
analysis of mutants in the libraries under various growth conditions
provides important clues to study the physiology and
biogenesis of structural components of a bacterial cell. A transposon
library in conjunction with next-generation sequencing
techniques, collectively named transposon sequencing (Tnseq),
enables high-throughput genome profiling and synthetic
lethality analysis. Tn-seq has also been used to identify essential
genes and to study the mode of action of antibacterials.
To construct a high-density transposon mutant library, an efficient
delivery system for transposition in a model bacterium
is essential. Here, I describe a detailed protocol for generating
a high-density phage-based transposon mutant library in a
Staphylococcus aureus strain, and this protocol is readily applicable
to other S. aureus strains including USA300 and MW2.
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Recent rapid air temperature increases across the northernlatitude
tundra have prolonged permafrost thawing and snow
melting periods, resulting in increased soil temperature (Ts)
and volumetric soil water content (SWC). Under prolonged
soil warming at 8°C, Alaskan tundra soils were incubated in
a microcosm system and examined for the SWC differential
influence on the microbial decomposition activity of large
molecular weight (MW) humic substances (HS). When one
microcosm soil (AKC1-1) was incubated at a constant SWC
of 41% for 90 days (T = 90) and then SWC was gradually
decreased from 41% to 29% for another T = 90, the initial
HS was partly depolymerized. In contrast, in AKC1-2 incubated
at a gradually decreasing SWC from the initial 32% to
10% for T = 90 and then increasing to 27% for another T =
90, HS depolymerization was undetected. Overall, the microbial
communities in AKC1-1 could maintain metabolic
activity at sufficient and constant SWC during the initial T =
90 incubation. In contrast, AKC1-2 microbes may have been
damaged by drought stress during the drying SWC regimen,
possibly resulting in the loss of HS decomposition activity,
which did not recover even after re-wetting to an optimal
SWC range (20–40%). After T = 90, the CO2 production in
both treatments was attributed to the increased decomposition
of small-MW organic compounds (including aerobic
HS-degradative products) within an optimal SWC range. We
expect this study to provide new insights into the early effects
of warming- and topography-induced SWC variations on
the microbial contribution to CO2 emissions via HS decomposition
in northern-latitude tundra soil.
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Backfat thickness (BF) is an important indicator of fat deposition
capacity and lean meat rate in pigs and is very important
in porcine genetics and breeding. Intestinal microbiota
plays a key role in nutrient digestion and utilization with a
profound impact on fat deposition of livestock animals. To
investigate the relationship between the pig gut microbiome
and BF, 20 low-BF (L-BF) and 20 high-BF (H-BF) pigs were
selected as two groups from Yunong Black pigs in the present
study. Fecal samples from pigs were analyzed for microbial
diversity, composition, and predicted functionality using 16S
rRNA gene sequencing. The results showed that there were
significant differences in microbial β diversity between the
two groups. LEfSe analysis revealed a number of bacterial features
being differentially enriched in either L-BF or H-BF pigs.
Spearman correlation analysis identified the abundance of
Oscillospira, Peptococcus, and Bulleidia were significantly
positive correlations with BF (P < 0.05), while Sutterella and
Bifidobacterium were significantly negatively correlated with
BF (P < 0.05). Importantly, the bacteria significantly positively
correlated with BF mainly belong to Clostridium, which can
ferment host-indigestible plant polysaccharides into shortchain
fatty acid (SCFA) and promote fat synthesis and deposition.
Predictive functional analysis indicated that the pathway
abundance of cell motility and glycan biosynthesis were
significantly widespread in the microbiota of the H-BF group.
The results of this study will be useful for the development of
microbial biomarkers for predicting and improving porcine
BF, as well as for the investigation of targets for dietary strategies.
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Systemic candidiasis, which is mainly caused by Candida albicans,
is a serious acute fungal infection in the clinical setting.
In a previous study, we reported that compound 22h (designated
as AB-22 in this study), a vinyl sulfate compound, is a
fast-acting fungicidal agent against a broad spectrum of fungal
pathogens. In this study, we aimed to further analyze the
in vitro and in vivo efficacy of AB-22 against filamentation,
biofilm formation, and virulence of C. albicans. Under in vitro
hyphal growth-inducing condition, AB-22 effectively inhibited
germ tube formation and hyphal growth, which are required
for the initiation of biofilm formation. Indeed, AB-22
significantly suppressed C. albicans biofilm formation in a
dose-dependent manner. Moreover, AB-22 treatment inhibited
the normal induction of ALS3, HWP1, and ECE1, which
are all required for hyphal transition in C. albicans. Furthermore,
AB-22 treatment increased the survival of mice systemically
infected with C. albicans. In conclusion, in addition
to its fungicidal activity, AB-22 inhibits filamentation and
biofilm formation in C. albicans, which could collectively contribute
to its potent in vivo efficacy against systemic candidiasis.
Acinetobacter baumannii causes multidrug resistance, leading
to fatal infections in humans. In this study, we showed that
Lys AB2 P3-His–a hexahistidine-tagged form of an antimicrobial
peptide (AMP) loaded onto DNA aptamer-functionalized
gold nanoparticles (AuNP-Apt)–can effectively inhibit
A. baumannii infection in mice. When A. baumannii-infected
mice were intraperitoneally injected with AuNP-Apt loaded
with Lys AB2 P3-His, a marked reduction in A. baumannii
colonization was observed in the mouse organs, leading to
prominently increased survival time and rate of the mice compared
to those of the control mice treated with AuNP-Apt or
Lys AB2 P3-His only. This study shows that AMPs loaded
onto AuNP-Apt could be an effective therapeutic tool against
infections caused by multidrug-resistant pathogenic bacteria
in humans.
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species in starters and the early fermentation stage
of Chinese liquor (Baijiu). However, the genetic diversity of
the species remains largely unknown. Here we sequenced
the genomes of 97 S. fibuligera strains from different Chinese
Baijiu companies. The genetic diversity and population structure
of the strains were analyzed based on 1,133 orthologous
genes and the whole genome single nucleotide polymorphisms
(SNPs). Four main lineages were recognized. One lineage
contains 60 Chinese strains which are exclusively homozygous
with relatively small genome sizes (18.55–18.72 Mb) and low
sequence diversity. The strains clustered in the other three
lineages are heterozygous with larger genomes (21.85–23.72
Mb) and higher sequence diversity. The genomes of the homozygous
strains showed nearly 100% coverage with the genome
of the reference strain KPH12 and the sub-genome A
of the hybrid strain KJJ81 at the above 98% sequence identity
level. The genomes of the heterozygous strains showed
nearly 80% coverage with both the sub-genome A and the
whole genome of KJJ81, suggesting that the Chinese heterozygous
strains are also hybrids with nearly 20% genomes
from an unidentified source. Eighty-three genes were found
to show significant copy number variation between different
lineages. However, remarkable lineage specific variations in
glucoamylase and α-amylase activities and growth profiles in
different carbon sources and under different environmental
conditions were not observed, though strains exhibiting relatively
high glucoamylase activity were mainly found from
the homozygous lineage.
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Sphingorhabdus sp. YGSMI21, a novel microbial strain with
an enantioselective epoxide hydrolase activity, was isolated
from tidal samples contaminated by accidental oil spills subjected
to enriched culture with polycyclic aromatic hydrocarbon.
This strain was able to optically decompose (R)-styrene
oxide (SO) and showed 100% optical purity. In addition, it
showed a good enantioselectivity for the derivatives of (S)-
SO, (S)-2-chlorostyrene oxide (CSO), (S)-3-CSO and (S)-4-
CSO. For (S)-2-CSO, (S)-3-CSO and (S)-4-CSO, 99.9%ee was
obtained with the yield of 26.2%, 24.8%, and 11.0%, respectively,
when using 10 mg cells of Sphingorhabdus sp. YGSMI21
at pH 8.0 with 4 mM racemic substrates at pH 8.0 and 25°C.
The values obtained in this study for (S)-2-CSO, particularly
the yield of 26.2%, is noteworthy, considering that obtaining
an enantiomerically pure form is difficult. Taken together,
Sphingorhabdus sp. YGSMI21 can be regarded as a wholecell
biocatalyst in the production of various (S)-CSO with the
chlorine group at a different position.
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Description of Polaribacter batillariae sp. nov., Polaribacter cellanae sp. nov., and Polaribacter pectinis sp. nov., novel bacteria isolated from the gut of three types of South Korean shellfish Su-Won Jeong, Jeong Eun Han, June-Young Lee, Ji-Ho Yoo, Do-Yeon Kim, In Chul Jeong, Jee-Won Choi, Yun-Seok Jeong, Jae-Yun Lee, So-Yeon Lee, Euon Jung Tak, Hojun Sung, Hyun Sik Kim, Pil Soo Kim, Dong-Wook Hyun, Jin-Woo Bae Journal of Microbiology.2022; 60(6): 576. CrossRef
Soil contamination with diesel oil is quite common during
processes of transport and storage. Bioremediation is considered
a safe, economical, and environmentally friendly approach
for contaminated soil treatment. In this context, studies
using hydrocarbon bioremediation have focused on total
petroleum hydrocarbon (TPH) analysis to assess process effectiveness,
while ecotoxicity has been neglected. Thus, this
study aimed to select a microbial consortium capable of detoxifying
diesel oil and apply this consortium to the bioremediation
of soil contaminated with this environmental pollutant
through different bioremediation approaches. Gas chromatography
(GC-FID) was used to analyze diesel oil degradation,
while ecotoxicological bioassays with the bioindicators
Artemia sp., Aliivibrio fischeri (Microtox), and Cucumis
sativus were used to assess detoxification. After 90 days of
bioremediation, we found that the biostimulation and biostimulation/
bioaugmentation approaches showed higher rates
of diesel oil degradation in relation to natural attenuation
(41.9 and 26.7%, respectively). Phytotoxicity increased in the
biostimulation and biostimulation/bioaugmentation treatments
during the degradation process, whereas in the Microtox
test, the toxicity was the same in these treatments as that
in the natural attenuation treatment. In both the phytotoxicity
and Microtox tests, bioaugmentation treatment showed lower
toxicity. However, compared with natural attenuation, this
approach did not show satisfactory hydrocarbon degradation.
Based on the microcosm experiments results, we conclude
that a broader analysis of the success of bioremediation requires
the performance of toxicity bioassays.
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production inside host cells. The purpose of this study is to
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induced EV production in human endothelial cells via Rab-
27b upregulation. The suppression of Rab27b expression in
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