Myocardial infarction (MI) is a type of cardiovascular disease that influences millions of human beings worldwide and has a great rate of mortality and morbidity. Spironolactone has been used as a critical drug for the treatment of cardiac failure and it ameliorates cardiac dysfunction post-MI. Despite these findings, whether there is a relationship between the therapeutic effects of spironolactone and the gut microorganism after MI has not been determined. In our research, we used male C57BL/6 J mice to explore whether the gut microbiota mediates the beneficial function of spironolactone after myocardial infarction.
We demonstrated that deletion of the gut microbiota eliminated the beneficial function of spironolactone in MI mice, displaying exacerbated cardiac dysfunction, cardiac infarct size. In addition, the gut microbiota was altered by spironolactone after sham or MI operation in mice. We also used male C57BL/6 J mice to investigate the function of a probiotic in the myocardial infarction. In summary, our findings reveal a precious role of the gut flora in the therapeutic function of spironolactone on MI.
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To elucidate the function of proteorhodopsin in Candidatus Puniceispirillum marinum strain IMCC1322, a cultivated representative of SAR116, we produced RNA-seq data under laboratory conditions. We examined the transcriptomes of six different cultures, including sets of expression changes under constant dark (DD), constant light (LL), and diel-cycled (LD; 14 h light: 10 h dark) conditions at the exponential and stationary/death phases. Prepared mRNA extracted from the six samples was analyzed on the Solexa Genome Analyzer with 36 cycles.
Differentially expressed genes on the IMCC1322 genome were distinguished as four clusters by K-mean clustering and each CDS (n = 2546) was annotated based on the KEGG BRITE hierarchy. Cluster 0 (n = 1573) covered most constitutive genes including proteorhodopsin, retinoids, and glycolysis/TCA cycle. Cluster 1 genes (n = 754) were upregulated in stationary/death phase under constant dark conditions and included genes associated with bacterial defense, membrane transporters, nitrogen metabolism, and senescence signaling. Cluster 2 genes (n = 197) demonstrated upregulation in exponential phase cultures and included genes involved in genes for oxidative phosphorylation, translation factors, and transcription machinery. Cluster 3 (n = 22) contained light-stimulated upregulated genes expressed under stationary/phases. Stringent response genes belonged to cluster 2, but affected genes spanned various cellular processes such as amino acids, nucleotides, translation, transcription, glycolysis, fatty acids, and cell wall components. The coordinated expression of antagonistic stringent genes, including mazG, ppx/gppA, and spoT/relA may provide insight into the controlled cultural response observed between constant light and constant dark conditions in IMCC1322 cultures, regardless of cell numbers and biomass.
Acinetobacter baumannii (A. baumannii) causes autophagy flux disorder by degrading STX17, resulting in a serious inflammatory response. It remains unclear whether STX17 can alter the inflammatory response process by controlling autolysosome function. This study aimed to explore the role of STX17 in the regulation of pyroptosis induced by A. baumannii. Our findings indicate that overexpression of STX17 enhances autophagosome degradation, increases LAMP1 expression, reduces Cathepsin B release, and improves lysosomal function.
Conversely, knockdown of STX17 suppresses autophagosome degradation, reduces LAMP1 expression, augments Cathepsin B release, and accelerates lysosomal dysfunction. In instances of A. baumannii infection, overexpression of STX17 was found to improve lysosomal function and reduce the expression of mature of GSDMD and IL-1β, along with the release of LDH, thus inhibiting pyroptosis caused by A.
baumannii. Conversely, knockdown of STX17 led to increased lysosomal dysfunction and further enhanced the expression of mature of GSDMD and IL-1β, and increased the release of LDH, exacerbating pyroptosis induced by A. baumannii. These findings suggest that STX17 regulates pyroptosis induced by A. baumannii by modulating lysosomal function.
Yongchao Guan , Meng Zhang , Yingda Wang , Zhongzhuo Liu , Zelin Zhao , Hong Wang , Dingjie An , Aidong Qian , Yuanhuan Kang , Wuwen Sun , Xiaofeng Shan
J. Microbiol. 2022;60(12):1153-1161. Published online November 10, 2022
Aeromonas veronii is a pathogen which can induce diseases in
humans, animals and aquatic organisms, but its pathogenic
mechanism and virulence factors are still elusive. In this study,
we successfully constructed a mutant strain (ΔascP) by homologous
recombination. The results showed that the deletion
of the ascP gene significantly down-regulated the expression
of associated effector proteins in A. veronii compared
to its wild type. The adhesive and invasive abilities of ΔascP to
EPC cells were 0.82-fold lower in contrast to the wild strain.
The toxicity of ΔascP to cells was decreased by about 2.91-fold
(1 h) and 1.74-fold (2 h). Furthermore, the LD50 of the mutant
strain of crucian carp was reduced by 19.94-fold, and
the virulence was considerably attenuated. In contrast to the
wild strain, the ΔascP content in the liver and spleen was considerably
lower. The titers of serum cytokines (IL-8, TNF-α,
and IL-1β) in crucian carp after the infection of the ΔascP strain
were considerably lower in contrast to the wild strain. Hence,
the ascP gene is essential for the etiopathogenesis of A. veronii
TH0426.
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hemorrhagic fever, and dengue shock syndrome. DENV is
transmitted by mosquitoes, Aedes aegypti and A. albopictus,
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The number of dengue cases reported by the World Health
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5.2 million in 2019. Although vaccine is the most effective method against DENV, only one commercialized vaccine exists,
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age. Currently, many researchers are working to resolve the
various problems hindering the development of effective dengue
vaccines; understanding of the viral antigen configuration
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The global spread of coronavirus disease 2019 caused by severe
acute respiratory syndrome coronavirus 2 (SARS-CoV-2)
infection has provoked an urgent need for prophylactic measures.
Several innovative vaccine platforms have been introduced
and billions of vaccine doses have been administered
worldwide. To enable the creation of safer and more effective
vaccines, additional platforms are under development. These
include the use of nanoparticle (NP) and virus-like particle
(VLP) technology. NP vaccines utilize self-assembling scaffold
structures designed to load the entire spike protein or
receptor-binding domain of SARS-CoV-2 in a trimeric configuration.
In contrast, VLP vaccines are genetically modified
recombinant viruses that are considered safe, as they are
generally replication-defective. Furthermore, VLPs have indigenous
immunogenic potential due to their microbial origin.
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with greater protection by mimicking the physicochemical
characteristics of SARS-CoV-2. The study of NPand
VLP-based coronavirus vaccines will help ensure the development
of rapid-response technology against SARS-CoV-2
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in the East Sea of Korea. This actinomycete harbors a large
number of genes encoding carbohydrate-degrading enzymes,
and its activity to degrade carboxymethyl cellulose into glucose
was experimentally evaluated. Since the genus Isoptericola was
proposed after reclassification based on phylogenetic analysis,
strains of Isoptericola have been continuously isolated from
diverse environments and the importance of this genus in the
ecosystem has been suggested by recent culturomic or metagenomic
studies. The phylogenic relationships of the genus
tended to be closer among strains that had been isolated from
similar habitats. By analyzing the properties of published genome
sequences of seven defined species in the genus, a large
number of genes for carbohydrate hydrolysis and utilization,
as well as several biosynthetic gene clusters for secondary
metabolites, were identified. Genomic information of I. dokdonensis
DS-3 together with comparative analysis of the genomes
of Isoptericola provides insights into understanding
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Terminators and introns are vital regulators of gene expression
in many eukaryotes; however, the functional importance
of these elements for controlling gene expression in Agaricomycetes
remains unclear. In this study, the effects of Ceriporiopsis
subvermispora terminators and introns on the expression
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gene (hph) were characterized. Using a transient transformation
system, we proved that a highly active terminator (e.g.,
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the hph gene. Mutational analyses of the C. subvermispora
gpd terminator revealed that hph expression was dictated by
an A-rich region, which included a putative positioning element,
and polyadenylation sites. In contrast, our results indicated
that introns are not required for the expression of
hph directed by the Csβ1-tub and Csgpd promoters in C.
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Neisseria gonorrhoeae, an obligatory human pathogen causes
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mucosa of the genitourinary tract, which in women, is colonized
by natural microbiota, dominated by Lactobacillus spp.,
that protect human cells against pathogens. In this study, we
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decreased expression of genes encoding the proinflammatory
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a consequence of N. gonorrhoeae infection, was observed in
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with L. crispatus or preincubated with enolase and
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complex process and that L. crispatus and its proteins enolase
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is detected. Lactobacillus species isolated from the bee gut and
bee-related habitats were phylogenetically classified into three
distinct groups, Lactobacillus kunkeei, Firm-4, and Firm-5.
The L. kunkeei group was clearly differentiated from other
members of the Lactobacillus buchneri group isolated from
non-bee habitats. In comparison with non-bee members of the
L. buchneri group, three bee-symbiotic Lactobacillus groups
had a small-sized genome with low G + C content and showed
a sharp reduction in the number of genes involved in energy
production, carbohydrate transport and metabolism, and
amino acid transport and metabolism. In addition, all three
groups lacked the mutY gene, which encodes A/G-specific
adenine glycosylase. The phylogenetic dendrogram based on
the presence or absence of 1,199 functional genes indicated
that these bee-symbiotic groups experienced convergent evolution.
The occurrence of convergent evolution is thought to
stem from the three bee-symbiotic groups sharing a similar
habitat, i.e., the bee gut. The causative factor underlying genomic
reduction was postulated to be mutY, which was absent
in all three groups. Here, a novel strain, BHWM-4T, isolated
from the gut of Bombus ignites was studied using polyphasic
taxonomy and classified as a new member of the L.
kunkeei group. The strain was Gram-positive, facultative anaerobic,
and rod-shaped. The 16S ribosomal RNA gene sequence
and genome analysis revealed that strain BHWM-4T was
clustered into the L. kunkeei group, forming a compact cluster
with L. kunkeei and Lactobacillus apinorum. Biochemical,
chemotaxonomic, and genotypic data of strain BHWM-4T
supports the proposal of a novel species, Lactobacillus bombintestini
sp. nov., whose type strain is BHWM-4T (= KACC
19317T = NBRC 113067T).
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Apical periodontitis is caused by biofilm-mediated root canal
infection. Early phase oral bacterial biofilms are inhibited by
Lactobacillus plantarum lipoteichoic acid (Lp.LTA). However,
mature biofilms that develop over 3 weeks are more resistant
to traditional endodontic medicaments. Therefore, this study
examined the effectiveness of Lp.LTA on disrupting mature
Enterococcus faecalis biofilms, and on enhancing the effects
of endodontic medicaments. LTA was purified from L. plantarum
through butanol extraction followed by hydrophobic
and ion-exchange chromatography. E. faecalis biofilms were
formed over 3 weeks on glass bottom dishes and in dentin
blocks obtained from human single-rooted premolars. These
mature biofilms were treated with or without Lp.LTA for 1 h,
followed by additional treatment with either chlorhexidine
digluconate (CHX), calcium hydroxide (CH), or triple antibiotics
for 24 h. Biofilms on glass were live/dead stained and
quantified by ZEN through confocal laser microscopy. Biofilms
in dentin were fixed, sputter coated and analyzed by
ImageJ with scanning electron microscopy. Preformed E. faecalis
mature biofilms on the culture dishes were dose-dependently
disrupted by Lp.LTA. Lp.LTA potentiated the effects
of CHX or CH on the disruption of mature biofilm. Interestingly,
CHX-induced disruption of preformed E. faecalis
mature biofilms was synergistically enhanced only when pretreated
with Lp.LTA. Furthermore, in the dentin block model,
Lp.LTA alone reduced E. faecalis mature biofilm and
pre-treatment with Lp.LTA promoted the anti-biofilm activity
of CHX. Lp.LTA could be an anti-biofilm or supplementary
agent that can be effective for E. faecalis-biofilminduced
diseases.
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Lactobacillus plantarum is a non-gas-producing lactic acid
bacterium that is generally regarded as safe (GRAS) with
Qualified Presumption of Safety (QPS) status. Although traditionally
used for dairy, meat and vegetable fermentation,
L. plantarum is gaining increasing significance as a probiotic.
With the newly acclaimed gut-heart-brain axis, strains of L.
plantarum have proven to be a valuable species for the development
of probiotics, with various beneficial effects on gut
health, metabolic disorders and brain health. In this review,
the classification and taxonomy, and the relation of these
with safety aspects are introduced. Characteristics of L. plantarum
to fulfill the criteria as a probiotic are discussed. Emphasis
are also given to the beneficial functions of L. plantarum
in gut disorders such as inflammatory bowel diseases,
metabolic syndromes, dyslipidemia, hypercholesteromia, obesity,
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Cyclomaltodextrinases (CDases) belong to Glycoside Hydrolases
(GH) family 13, which show versatile hydrolyzing
and/or transglycosylation activity against cyclodextrin (CD),
starch, and pullulan. Especially, some CDases have been reported
to hydrolyze acarbose, a potent α-glucosidase inhibitor,
and transfer the resulting acarviosine-glucose to various
acceptors. In this study, a novel CDase (LPCD) gene was
cloned from Lactobacillus plantarum WCFS1, which encodes
574 amino acids (64.6 kDa) and shares less than 44% of identities
with the known CDase-family enzymes. Recombinant
LPCD with C-terminal six-histidines was produced and purified
from Escherichia coli. It showed the highest activity
on β-CD at 45°C and pH 5.0, respectively. Gel permeation
chromatography analysis revealed that LPCD exists as a dodecameric
form (~826 kDa). Its hydrolyzing activity on β-
CD is almost same as that on starch, whereas it can hardly
attack pullulan. Most interestingly, LPCD catalyzed the unique
modes of action in acarbose hydrolysis to produce maltose
and acarviosine, as well as to glucose and acarviosineglucose.
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Genetic and enzymatic characterization of Amy13E from
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reclassifies it as a cyclodextrinase also capable of α-diglucoside degradation
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The potential use of dietary measures to treat influenza can
be an important alternative for those who lack access to influenza
vaccines or antiviral drugs. Lactobacillus plantarum
(Lp) is one of many lactic acid bacteria that grow in ‘kimchi’,
an essential part of Korean meal, and several strains of Lp
reportedly show protective effects against influenza. Using
heat-killed Lp (nF1) isolated from kimchi, which is known
for its immunomodulatory effects, we investigated whether
regular oral intake of nF1 could influence the outcome of influenza
virus infection in a mouse model. In a lethal challenge
with influenza A (H1N1 and H3N2 subtypes) and influenza
B (Yamagata lineage) viruses, daily oral administration
of nF1 delayed the mean number of days to death of the
infected mice and resulted in increased survival rates compared
with those of the non-treated mice. Consistent with
these observations, nF1 treatment also significantly reduced
viral replication in the lungs of the infected mice. Taken together,
our results might suggest the remedial potential of heatkilled
Lactobacillus probiotics against influenza.
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Lactobacillus strains have been considered good candidates
as biological control agents for prevention or treatment of
plant and animal infections. One L. plantarum strain FB003
and three strains (FB011, FB081, and FB110) which closed
to L. sakei were isolated from fermented and salted shrimp
and their abilities in inhibiting growth of Vibrio parahaemolyticus
were characterized. These strains were selected as
potential probiotics based on their oro-gastro-intestinal resistance,
gut colonization, adhesion to Caco-2 cells, antimicrobial
activities, antibiotic resistance, and safety aspects. Results of this study revealed that these isolates possessed high
aggregation activities against pathogens in host intestines.
Strain FB011 strain showed higher coaggregation and immunomodulatory
activity in the gastro-intestinal tract than
L. plantarum. These difference effects of Lactobacillus strains
provide valuable information about using them to prevent
Vibrio infections in the aquaculture industry.
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