Two Gram-stain negative, yellow-pigmented, and mesophilic
bacteria, designated strains R7T and R19T, were isolated from
sandy and forest soil, South Korea, respectively. Both strains
were non-motile rods showing catalase- and oxidase-positive
activities. Both strains were shown to grow at 10–37°C
and pH 6.0–9.0, and in the presence of 0–1.5% (w/v) NaCl.
Strain R7T contained iso-C14:0, iso-C15:0, iso-C16:0, and summed
feature 9 (comprising C16:0 10-methyl and/or iso-C17:1
ω9c), whereas strain R19T contained iso-C11:0 3-OH, C16:1 ω7c
alcohol, iso-C11:0, iso-C15:0, iso-C16:0, and summed feature 9
(comprising C16:0 10-methyl and/or iso-C17:1 ω9c) as major
cellular fatty acids (> 5%). Both strains contained ubiquinone-
8 as the sole isoprenoid quinone and phosphatidylglycerol,
phosphatidylethanolamine, and an unidentified phospholipid
as the major polar lipids. The DNA G + C contents
of strains R7T and R19T calculated from their genomes were
66.9 mol% and 68.9 mol%, respectively. Strains R7T and R19T
were most closely related to Lysobacter panacisoli C8-1T and
Lysobacter niabensis GH34-4T with 98.7% and 97.8% 16S
rRNA sequence similarities, respectively. Phylogenetic analyses
based on 16S rRNA gene sequences showed that strains
R7T and R19T formed distinct phylogenetic lineages within
the genus Lysobacter. Based on phenotypic, chemotaxonomic,
and molecular features, strains R7T and R19T represent novel
species of the genus Lysobacter, for which the names Lysobacter
arenosi sp. nov. and Lysobacter solisilvae sp. nov. are
proposed. The type strains of L. arenosi and L. solisilvae are
R7T (= KACC 21663T = JCM 34257T) and R19T (= KACC
21767T = JCM 34258T), respectively.
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gansuensis, A. inebrians produces an abundance of alkaloids
that enhance plant survival but are toxic to animals. Here
we used in vitro fermentation to study the impact of endophyte-
infected A. inebrians (E+) addition on rumen fermentation
characteristics and on microbial community and diversity
as assessed with amplicon sequencing technology.
We examined E+ addition at five levels, E0, E25, E50, E75,
and E100, corresponding to 0%, 25%, 50%, 75%, and 100%
of the fermentation substrate, respectively. Both the fermentation
characteristics and rumen microbial community structure
differed significantly among treatments. E100 resulted
in the highest values for pH, the Shannon index, Kiritimatiellaeota,
and Lentisphaerae levels relative to the other treatments.
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ammonia nitrogen, total volatile fatty acid, propionate, butyrate,
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Firmicutes, and of the genus Prevotella_1, Succiniclasticum,
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with other treatments. E50 resulted in the greatest values
for the abundance-based coverage estimator (ACE) and the
Chao1 index as compared with other treatments. E0 resulted
in the greatest values for digestibility of dry matter, gas production,
acetate, and Ruminobacter as compared with other
treatments. This approach avoided animal toxicity experiments
and confirmed that rumen fermentation characteristics and
rumen microbiota were affected by E+ toxin. Therefore, E25
showed higher abundance in Prevotella_1, Prevotellaceae_
UCG-001, and Lachnospiraceae_XPB1014_group that implied
they should play significant roles in E+ alkaloids degradation.
And then, we can infer that rumen microorganisms should
function as an antidote with respect to this poisoning reaction
at moderate dietary percentages of E+.
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rhizobacterium that associates with a wide range of host
plants, including agronomically important ones. Inoculation
of wheat seedlings with P. polymyxa strains CCM 1465 and
92 was found to increase the mitotic index of the root cells
1.2- and 1.6-fold, respectively. Treatment of seedlings with
the exopolysaccharides (EPSs) of these strains increased the
mitotic index 1.9-fold (P. polymyxa CCM 1465) and 2.8-fold
(P. polymyxa 92). These increases indicate activation of cell
division in the root meristems. Analysis of the morphometric
variables of the seedlings showed that P. polymyxa CCM
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increasing root and shoot length up to 22% and root and
shoot dry weight up to 28%, as compared with the control.
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seedling root surface. Thus, P. polymyxa EPSs are active metabolites
that, along with whole cells, are responsible for the
contact interactions of the bacteria with wheat roots and are
implicated in the induction of plant responses to these interactions.
The strains used in this work are of interest for
further study to broaden the existing understanding of the
mechanisms of plant–bacterial interactions and to develop
effective biofertilizers for agricultural purposes.
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fungi and has great potential for the biological control of nematode
diseases. Lectin is a protein that binds to carbohydrates
and their complexes with high specificity, which mediates recognition
events in various physiological and pathological
processes. This study aimed to investigate the role of the
Jacalin-related lectin (JRL) gene, AOL_s00083g511, in A. oligospora
development. Through a homology recombination
approach, we obtained the AOL_s00083g511 knockout mutant
strain (Δg511). Next, the biological characteristics of the
Δg511 mutant strain, including growth rate, conidia germination
rate, adaptation to environmental stresses, and nematocidal
activity, were compared with those of the wild-type
(WT) strain. The results showed that the JRL gene AOL_
s00083g511 did not affect fungal growth, conidia germination,
3D-trap formation, and the ability of A. oligospora to
prey on nematodes significantly. We speculate that this phenomenon
may be caused by a loss of the key β1–β2 loops in
the AOL_ s00083g511-encoded JRL domain and an intrinsic
genetic compensation of AOL_s00083g511 in this fungus.
The growth rates of both strains on high salt or surfactant media
were similar; however, in the strong oxidation medium,
the growth rate of the Δg511 mutant was significantly lower
than that of the WT strain, indicating that AOL_s00083g511
might play a role in oxidative stress resistance. These findings
provide a basis for further analysis of the related functions
of the JRL gene in A. oligospora and their potential roles
in the biological control of nematodes in the future.
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of one of the VosA-VelB-activated developmental genes vadJ
in development and production of the mycotoxin sterigmatocystin
in the model fungus Aspergillus nidulans. The vadJ
gene is predicted to encode a 957-amino acid length protein
containing a highly conserved sensor histidine kinase domain.
The deletion of vosA or velB resulted in decreased mRNA
levels of vadJ throughout the life cycle, suggesting that VosA
and VelB are necessary for proper expression of vadJ. Nullifying
vadJ led to highly restricted colony growth, lowered formation
of asexual spores, and about two-fold reduction in
conidial viability. Conversely, the deletion of vadJ resulted in
elevated production of sexual fruiting bodies and sterigmatocystin.
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of asexual and sexual development, and sterigmatocystin
production. In accordance with this idea, the deletion
of vadJ led to elevated mRNA levels of the two key sexual
developmental activators esdC and nsdD. In summary, the
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of the strains were analyzed based on 1,133 orthologous
genes and the whole genome single nucleotide polymorphisms
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sequence diversity. The strains clustered in the other three
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level. The genomes of the heterozygous strains showed
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whole genome of KJJ81, suggesting that the Chinese heterozygous
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from an unidentified source. Eighty-three genes were found
to show significant copy number variation between different
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glucoamylase and α-amylase activities and growth profiles in
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triggers host cell signaling pathway. It has been reported that
CagL polymorphisms may influence the severity of disease
development. To explore the contribution of CagL polymorphisms
between East Asian and Western H. pylori in pathogenesis,
cagL gene in G27 H. pylori was swapped by K74 cagL
which is identical to East Asian CagL consensus sequence and
by Western 26695 H. pylori, resulting in G27ΔcagL/cagLK74
and G27ΔcagL/cagL26695, respectively. Intriguingly, G27ΔcagL/
cagLK74 showed significantly less ability of IL-8 induction
than G27ΔcagL/cagL26695 while displayed similar abilities of
CagA phosphorylation, and cell elongation. Taken together,
this study suggests that the CagL polymorphism may influence
IL-8 induction, and K74 CagL has less ability to induce
IL-8 secretion than G27 or 26695 CagL. Further research
should address how the different capabilities of IL-8 induction
between intraspecies-CagL are associated with the large
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individuals. Microglia are the main target cells
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the precise mechanisms by which they trigger neuroinflammatory
processes remain unknown. The BV2 microglial
cell line and a murine model of L. monocytogenes infection
were used for experiments in this study. Listeria monocytogenes
induced pyroptosis and nucleotide binding and oligomerization,
leucine-rich repeat, pyrin domain-containing
3 (NLRP3) inflammasome activation in BV2. Pharmacological
inhibition of the NLRP3 inflammasome attenuated L. monocytogenes-
induced pyroptosis. Moreover, inhibition of nuclear
factor kappa-B (NF-κB) and extracellular regulated protein
kinases (ERK) pathways induced a decrease in caspase1
activation and mature IL-1β-17 secretion. Our collective findings
support critical involvement of the NLRP3 inflammasome
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to an extent, ROS production. In addition, ERK and NF-κB
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Autophagy is an important cellular homeostatic mechanism
for recycling of degradative proteins and damaged organelles.
Autophagy has been shown to play an important role in cellular
responses to bacteria and bacterial replication. However,
the role of autophagy in Mycoplasma hyopneumoniae infection
and the pathogenic mechanism is not well characterized.
In this study, we showed that M. hyopneumoniae infection
significantly increases the number of autophagic vacuoles in
host cells. Further, we found significantly enhanced expressions
of autophagy marker proteins (LC3-II, ATG5, and
Beclin 1) in M. hyopneumoniae-infected cells. Moreover, immunofluorescence
analysis showed colocalization of P97 protein
with LC3 during M. hyopneumoniae infection. Interestingly,
autophagic flux marker, p62, accumulated with the induction
of infection. Conversely, the levels of p62 and LC3-II
were decreased after treatment with 3-MA, inhibiting the
formation of autophagosomes, during infection. In addition,
accumulation of autophagosomes promoted the expression
of P97 protein and the survival of M. hyopneumoniae in PK-
15 cells, as the replication of M. hyopneumoniae was downregulated
by adding 3-MA. Collectively, these findings provide
strong evidence that M. hyopneumoniae induces incomplete
autophagy, which in turn enhances its reproduction in
host cells. These findings provide novel insights into the interaction
of M. hyopneumoniae and host.
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Viridans group streptococci are a serious health concern because
most of these bacteria cause life-threatening infections,
especially in immunocompromised and hospitalized individuals.
We focused on two alpha-hemolytic Streptococcus
strains (I-G2 and I-P16) newly isolated from an ileostomy
effluent of a colorectal cancer patient. We examined their pathogenic
potential by investigating their prevalence in human
and assessing their pathogenicity in a mouse model. We also
predicted their virulence factors and pathogenic features by
using comparative genomic analysis and in vitro tests. Using
polyphasic and systematic approaches, we identified the isolates
as belonging to a novel Streptococcus species and designated
it as Streptococcus ilei. Metagenomic survey based on
taxonomic assignment of datasets from the Human Microbiome
Project revealed that S. ilei is present in most human
population and at various body sites but is especially abundant
in the oral cavity. Intraperitoneal injection of S. ilei was
lethal to otherwise healthy C57BL/6J mice. Pathogenomics
and in vitro assays revealed that S. ilei possesses a unique set
of virulence factors. In agreement with the in vivo and in vitro
data, which indicated that S. ilei strain I-G2 is more pathogenic
than strain I-P16, only the former displayed the streptococcal
group A antigen. We here newly identified S. ilei sp.
nov., and described its prevalence in human, virulence factors,
and pathogenicity. This will help to prevent S. ilei strain
misidentification in the future, and improve the understanding
and management of streptococcal infections.
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