When Salmonella enterica is not in a planktonic state, it persists
in organised communities encased in extracellular polymeric
substances (EPS), defined as biofilms. Environmental
conditions ultimately dictate the key properties of the biofilms
such as porosity, density, water content, charge, sorption
and ion exchange properties, hydrophobicity and mechanical
stability. S. enterica has been extensively studied
due to its ability to infect the gastrointestinal environment.
However, only during the last decades studies on its persistence
and replication in soil, plant and abiotic surfaces have
been proposed. S. enterica is an environmental bacterium
able to effectively persist outside the human host. It does so
by using EPS as tools to cope with environmental fluctuations.
We therefore address this mini-review to classify those
EPS that are produced by Salmonella with focus on the environment
(plant, soil, and abiotic surfaces) by using a classification
of EPS proposed by Flemming and collaborators
in 2007. The EPS are therefore classified as structural, sorptive,
surface-active, active, and informative.
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Inhibition of
Salmonella
Typhimurium biofilm and polysaccharide production via eugenol-glucosyltransferase interactions
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typhi biofilm formation
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adrA
expression in
Salmonella
Enteritidis under anaerobic conditions
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Comparative study on inhibitory effects of ferulic acid and p-coumaric acid on Salmonella Enteritidis biofilm formation Jing-Guo Xu, Hui-Xue Hu, Jing-Yu Chen, Yan-Song Xue, Bekhzod Kodirkhonov, Bei-Zhong Han World Journal of Microbiology and Biotechnology.2022;[Epub] CrossRef
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Secretion of poly-γ-glutamic acid by Bacillus atrophaeus NX-12 enhanced its root colonization and biocontrol activity Jian Xue, Tong Tong, Rui Wang, Yibin Qiu, Yian Gu, Liang Sun, Hong Xu, Peng Lei Frontiers in Microbiology.2022;[Epub] CrossRef
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Synthetic lethality is an extreme form of negative genetic
epistasis that arises when a combination of functional deficiency
in two or more genes results in cell death, whereas none
of the single genetic perturbations are lethal by themselves.
This unconventional genetic interaction is a modification
of the concept of essentiality that can be exploited for the
purpose of targeted cancer therapy. The yeast Saccharomyces
cerevisiae has been pivotally used for early large-scale synthetic
lethal screens due to its experimental advantages, but
recent advances in gene silencing technology have now made
direct high-throughput analysis possible in higher organisms.
Identification of tumor-specific alterations and characterization
of the mechanistic principles underlying synthetic lethal
interaction are the key to applying synthetic lethality to clinical
cancer treatment by enabling genome-driven oncological
research. Here, we provide emerging ideas on the synthetic
lethal interactions in budding yeast, particularly between cellular
processes responsible for oxidative stress response and
DNA damage repair, and discuss how they can be appropriately
utilized for context-dependent cancer therapeutics.
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A Gram-stain-negative, aerobic, non-motile, rod-shaped, and
yellow-pigmented bacterium, designated strain ID1709T, was
isolated from an automotive air conditioning system collected
in Korea. Analysis of 16S rRNA gene sequence similarity
showed that strain ID1709T had 92.2–94.3% similarities with
the type strains of members of the genus Flavisolibacter. The
major cellular fatty acids were iso-C15:0, iso-C15:1 G, iso-C17:0
3-OH, and summed feature 3 (C16:1 ω7c and/or C16:1 ω6c). The
predominant respiratory quinone was MK-7. The polar lipids
comprised phosphatidylethanolamine, aminoglycophospholipid,
two unidentified aminolipids, and three unidentified
lipids. The DNA G + C content of the strain was 35.6 mol%.
Based on phenotypic, chemotaxonomic, and genotypic data,
strain ID1709T represents a novel species in the genus Flavisolibacter,
for which the name Flavisolibacter aluminii sp.
nov. (= KACC 19451T = KCTC 52778T = NBRC 112870T), is
proposed.
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A novel Gram-stain-negative, aerobic, motile by means of
gliding, and short rod-shaped bacterium, designated strain
SH35T, was isolated from the dry surface of a tidal flat in
Hwasung-si, South Korea. Growth occurred at 10–40°C
(optimum 30°C), at pH 6.0–8.0 (optimum pH 7.0), in 1–12%
NaCl (optimum 2%), and was inhibited in the absence of
NaCl and Ca2+ ions. Phylogenetic analysis based on the 16S
rRNA gene sequences showed that strain SH35T belonged
to the genus Gramella and was a member of the family Flavobacteriaceae
with highest sequence similarity to Gramella
flava JLT2011T (96.1%), followed by Gramella oceani CCAMSZ-
TT (95.6%), and 93.0–94.9% to other recognized Gramella
species. The major cellular fatty acids (> 5% of the total)
of strain SH35T were iso-C15:0, Iso-C16:0, anteiso-C15:0, iso-C17:0
3-OH and summed feature 9 (C16:0 10-methyl and/or C17:1
iso ω9с). The major polar lipids were phosphatidylethanolamine,
two unidentified aminolipids and nine unidentified
polar lipids. The major respiratory quinone and the predominant
polyamine were menaquinone-6 (MK-6) and symhomospermidine,
respectively. The DNA G + C content was
40.5 mol% (39.7% based on total genome calculations). Based
on phylogenetic analysis and physiological and biochemical
characterization, strain SH35T represents a novel species of
the genus Gramella, for which the name Gramella fulva sp.
nov. is proposed. The type strain is SH35T (= KACC 19447T
= JCM 32369T).
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White colony-forming yeasts (WCFYs) often appear in fermented
foods, depending on the storage method. Despite
the ongoing research on fermented foods, the community
and genome features of WCFYs have not been well studied.
In this study, the community structures of WCFYs on fermented
vegetables (kimchi) prepared with various raw materials
were investigated using deep sequencing. Only eight
operational taxonomic units (OTUs) were detected, indicating
that the community structure of WCFYs on kimchi is very
simple. The five most abundant OTUs represented Pichia
kluyveri, Yarrowia lipolytica, Candida sake, Hanseniaspora
uvarum, and Kazachstania servazzii. Using a culture-dependent method , 41 strains representing the five major OTUs
were isolated from the surface of the food samples. Whole
genomes of the five major yeast strains were sequenced and
annotated. The total genome length for the strains ranged
from 8.97 Mbp to 21.32 Mbp. This is the first study to report
genome sequences of the two yeasts Pichia kluyveri and Candida
sake. Genome analysis indicated that each yeast strain
had core metabolic pathways such as oxidative phosphorylation;
purine metabolism; glycolysis/gluconeogenesis; aminoacyl-
tRNA biosynthesis; citrate cycle; but strain specific
pathways were also found. In addition, no toxin or antimicrobial
resistance genes were identified. Our study provides
genome information for five WCFY strains that may highlight
their potential beneficial or harmful metabolic effects
in fermented vegetables.
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A Gram-stain-positive, obligately anaerobic, non-motile, nonspore-
forming, and rod-shaped bacterial strain, designated
KGMB01110T, was isolated from a faecal sample of a healthy
male in South Korea. Phylogenetic analysis based on 16S rRNA
gene showed that strain KGMB01110T belonged to Clostridium
cluster XIVa and was most closely related to Mediterraneibacter
glycyrrhizinilyticus KCTC 5760T (95.9% 16S rRNA
gene sequence similarity). The DNA G + C content of strain
KGMB01110T based on its whole genome sequence was 44.1
mol%. The major cellular fatty acids (> 10%) of the isolate
were C14:0 and C16:0. The strain KGMB01110T was positive for
arginine dihydrolase, β-galactosidase-6-phosphatase, and
alkaline phosphatase. The strain KGMB01110T also produced
acid from D-glucose and D-rhamnose, and hydrolyzed gelatin
and aesculin. Furthermore, HPLC analysis and UV-tests
of culture supernatant revealed that the strain KGMB01110T
produced butyrate as the major end product of glucose fermentation.
Based on the phylogenetic and phenotypic characteristics,
strain KGMB01110T represent a novel species of
the genus Mediterraneibacter in the family Lachnospiraceae.
The type strain is KGMB01110T (= KCTC 15684T = CCUG
72830T).
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The severity of cryptococcosis in lupus from varying geneticbackgrounds
might be different due to the heterogeneity of
lupus-pathogenesis. This study explored cryptococcosis in
lupus mouse models of pristane-induction (normal geneticbackground)
and FcGRIIb deficiency (genetic defect). Because
the severity of lupus nephritis, as determined by proteinuria
and serum creatinine, between pristane and FcGRIIb-/- mice
were similar at 6-month-old, Cryptococcus neoformans was
intravenously administered in 6-month-old mice and were
age-matched with wild-type. Indeed, the cryptococcosis disease
severity, as evaluated by mortality rate, internal-organ
fungal burdens and serum cytokines, between pristane and
FcGRIIb-/- mice was not different. However, the severity of
cryptococcosis in wild-type was less severe than the lupus
mice. On the other hand, phagocytosis activity of peritoneal
macrophages from lupus mice (pristane and FcGRIIb-/-)
was more predominant than the wild-type without the difference
in macrophage killing-activity among these groups.
In addition, the number of active T helper cells (Th-cell) in
the spleen, including Th-cells with intracellular IFN-γ, from
lupus mice (pristane and FcGRIIb-/-) was higher than wildtype.
Moreover, these active Th-cells were even higher after
2 weeks of cryptococcal infection. These data support enhanced
macrophage activation through prominent Th-cells
in both lupus models. In conclusion, an increased susceptibility
of cryptococcosis in both lupus models was independent
to genetic background. This might due to Th-cell enhanced
macrophage phagocytosis with the interference of macrophage
killing activity from Cryptococcal immune-evasion
properties.
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Cordyceps militaris is a species of Cordyceps that is classified
in the Cordycipitaceae family and is well known in East Asia
as a traditional medicinal mushroom. Its artificial fruit body
has been widely cultivated for commercial use in cosmetics,
functional food, and medicine. To explore the metabolites
associated with fruit body development, we conducted gas
chromatography mass spectrometry (GC-MS) analyses based
on developmental stage, which was divided into the growth
period (stage 1, stage 2, and stage 3) and aging period (stage
4). We detected 39 biochemical metabolites associated with
nucleotide, carbohydrate, and amino acid metabolism. Cordycepin,
one of the representative bioactive compounds in
C. militaris, was significantly enriched in stage 4 of aging period
and is associated with glucose accumulation. The accumulation
of cordycepin in stage 4 of aging period also seems
to be related to the glutamine and glutamic acid pathway. Our results also showed enrichment of other bioactive compounds
such as mannitol and xylitol in stage 4 of aging period. Our
metabolomic profiling based on the developmental stages of
C. militaris is useful for exploring bioactive compounds (e.g.,
cordycepin, mannitol, GABA, and xylitol) that are enriched
in stage 4 of aging period and understanding the biosynthetic
mechanisms associated with cordycepin production. Through
optimization of fruit body cultivation by selecting stage 4 of
aging period as a harvesting time, our findings can be utilized
in food and medical applications of C. militaris in future.
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Salmonella enterica is a major human pathogen that causes
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significant morbidity and mortality. Although a number of
pre-clinical and clinical studies have reported on the feasibility
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protect against NTS strains. Vaccine formulations of highest
priority for NTS are live attenuated vaccines, which can elicit
effective induction of intestinal mucosal and intracellular
bacteria-specific cell mediated immune responses. Since glucose
is crucial for intracellular survival and replication in
host cells, we constructed strains with mutations in components
of the glucose uptake system, called the phosphotransferase
system (PTS), and compared the relative virulence and
immune responses in mice. In this study, we found that the
strain with mutations in both ptsI and crr (KST0556) was the
most attenuated strain among the tested strains, and proved
to be highly effective in inducing a mucosal immune response
that can protect against NTS infections in mice. Thus, we suggest
here that KST0556 (ΔptsIΔcrr) is a potential live vaccine
candidate for NTS, and may also be a candidate for a live delivery
vector for heterologous antigens. Moreover, since PTS
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and Gram-positive bacteria, the ptsI and crr genes
may be potential targets for creating live bacterial vectors or
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Harringtonine (HT) and homoharringtonine (HHT), alkaloid
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potent antiviral activity. In this study, we investigated
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inactive parental alkaloid cephalotaxine (CET), significantly
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In the article by Kim et al. published in Journal of Microbiology 2015; 53, 805–811, the first sentence of 2nd paragraph in the
section of ‘Rpd31: The repressor of hyphal induction and the activator of hyphal extension interacting with Ssn6’ on page 808
should have read: In C. albicans, there are two proteins as the orthologue of S. cerevisiae Rpd3: Rpd31 (orf19.6801, orf19.14093)
and Rpd32 (orf19.2834, orf19.10352) (Hnisz et al., 2009).
And the figure 1 should be corrected as below.
We apologize for any inconvenience that this may have caused.