Most bacteria will use their toxins to interact with the host cell, causing damage to the cell and then escaping from it. When bacteria enter the cell, they will be transported via the endosomal pathway. Rab GTPases are involved in bacterial transport as major components of endosomes that bind to their downstream effector proteins. The bacteria manipulate some Rab GTPases, escape the cell, and get to survive. In this review, we will focus on summarizing the many processes of how bacteria manipulate Rab GTPases to control their escape.
Dark septate endophytes (DSEs) are widely distributed and improve plant growth. DSEs secrete large amounts of enzymes
to mineralize insoluble phosphorus in soil and convert it into soluble phosphorus, promoting plant uptake of phosphorus.
However, the effects of DSEs with phosphate-solubilizing ability on host plants need further study. In this study, phosphorusdissolving
DSEs were screened for growth-promoting effects. We isolated, identified and characterized three DSE species
(Thozetella neonivea, Pezicula ericae and Hyaloscyphaceae sp.) showing phosphate-solubilizing ability. The impact of single,
dual or triple inoculation of DSEs on blueberry plant characteristics was studied. Their effects on colonization intensity,
seedling biomass, nutrients in plants and soil, and activities of plant resistance enzymes and soil enzymes were markedly
upregulated relative to the control (P < 0.05). The available phosphorus and acid phosphatase levels in different combinations
were significantly increased. These findings indicate that the application of the three DSEs may be valuable in facilitating
the cultivation of blueberry with a higher biomass and improved plant quality.
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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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Toxin-antitoxin (TA) systems are growth-controlling genetic
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normal growth conditions, antitoxins tightly counteract the
activity of the toxins. Upon stresses, antitoxins are inactivated,
releasing activated toxins, which induce growth arrest or cell
death. In this study, among nine functional TA modules in
Bosea sp. PAMC 26642 living in Arctic lichen, we investigated
the functionality of BoHigBA2. BohigBA2 is located close to
a genomic island and adjacent to flagellar gene clusters. The
expression of BohigB2 induced the inhibition of E. coli growth
at 37°C, which was more manifest at 18°C, and this growth
defect was reversed when BohigA2 was co-expressed, suggesting
that this BoHigBA2 module might be an active TA
module in Bosea sp. PAMC 26642. Live/dead staining and
viable count analyses revealed that the BoHigB2 toxin had
a bactericidal effect, causing cell death. Furthermore, we demonstrated
that BoHigB2 possessed mRNA-specific ribonuclease
activity on various mRNAs and cleaved only mRNAs
being translated, which might impede overall translation and
consequently lead to cell death. Our study provides the insight
to understand the cold adaptation of Bosea sp. PAMC 26642
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J. Microbiol. 2020;58(12):998-1009. Published online October 23, 2020
Members of the genus Vibrio are ubiquitous in aquatic environments
and can be found either in a culturable or a viable
but nonculturable (VBNC) state. Despite widespread concerns
as to how to define the occurrence and dynamics of
Vibrio populations by culture-independent approaches, further
physiological research and relevant biotechnological
developments will require the isolation and cultivation of the
microbes from various environments. The present work provides
data and perspectives on our understanding of culturable
Vibrio community structure and diversity in the Beibu
Gulf. Finally, we isolated 1,037 strains of Vibrio from 45 samples
and identified 18 different species. Vibrio alginolyticus,
V. cyclitrophicus, V. tasmaniensis, V. brasiliensis, and V. splendidus
were the dominant species that had regional distribution
characteristics. The correlation between the quantitative
distribution and community structure of culturable Vibrio and
environmental factors varied with the Vibrio species and geographical
locations. Among them, salinity, nitrogen, and phosphorus
were the main factors affecting the diversity of culturable
Vibrio. These results help to fill a knowledge gap on
Vibrio diversity and provide data for predicting and controlling
pathogenic Vibrio outbreaks in the Beibu Gulf.
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cyanobacteria present in the samples, and genes coding for
cyanotoxins such as microcystins (mcyE), saxitoxins (sxtA),
and cylindrospermopsins (cyrJ) were investigated. The presence
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amplification of the sxtA gene was related to the presence of
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The Aspergilli and Their Mycotoxins: Metabolic Interactions With Plants and the Soil Biota Walter P. Pfliegler, István Pócsi, Zoltán Győri, Tünde Pusztahelyi Frontiers in Microbiology.2020;[Epub] CrossRef
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Efficacy of volatile compounds from
Streptomyces philanthi
RL‐1‐178 as a biofumigant for controlling growth and aflatoxin production of the two aflatoxin‐producing fungi on stored soybean seeds
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Fungal development and secondary metabolism are closely
associated via the activities of the fungal NK-kB-type velvet
regulators that are highly conserved in filamentous fungi.
Here, we investigated the roles of the velvet genes in the aflatoxigenic
fungus Aspergillus flavus. Distinct from other Aspergillus
species, the A. flavus genome contains five velvet genes,
veA, velB, velC, velD, and vosA. The deletion of velD blocks
the production of aflatoxin B1, but does not affect the formation
of sclerotia. Expression analyses revealed that vosA and
velB mRNAs accumulated at high levels during the late phase
of asexual development and in conidia. The absence of vosA
or velB decreased the content of conidial trehalose and the
tolerance of conidia to the thermal and UV stresses. In addition,
double mutant analyses demonstrated that VosA and
VelB play an inter-dependent role in trehalose biosynthesis
and conidial stress tolerance. Together with the findings of
previous studies, the results of the present study suggest that
the velvet regulators play the conserved and vital role in sporogenesis,
conidial trehalose biogenesis, stress tolerance, and
aflatoxin biosynthesis in A. flavus.
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Corynespora cassiicola is a species of fungus that is a plant
pathogen of many agricultural crop plants, including severe
target spot disease on cucumber. Cassiicolin is an important
effector of pathogenicity of this fungus. In this study, we
collected 141 Corynespora isolates from eighteen hosts, and
the casscolin gene was detected in 82 C. cassiicola strains.
The deduced protein sequences revealed that 72 isolates
contained the Cas2 gene, two strains from Gynura bicolor
harboured the Cas2.2 gene, and 59 isolates without a cassiicolin
gene were classified as Cas0. Phylogenetic analyses was
performed for the 141 isolates using four loci (ITS, ga4, caa5,
and act1) and revealed two genetic clusters. Cluster A is composed
of four subclades: subcluster A1 includes all Cas2
isolates plus 18 Cas0 strains, subcluster A2 includes the eight
Cas5 isolates and one Cas0 isolate, and subclusters A3 and
A4 contain Cas0 strains. Cluster B consists of 21 Cas0 isolates.
Twenty-two C. cassiicola strains from different toxin
classes showed varying degrees of virulence against cucumber.
Cas0 or Cas2 strains induced diverse responses on cucumber,
from no symptoms to symptoms of moderate or severe
infection, but all Cas5 isolates exhibited avirulence on cucumber.
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Important staple foods (peanuts, maize and rice) are susceptible
to contamination by aflatoxin (AF)-producing fungi such
as Aspergillus flavus. The objective of this study was to explore
non-aflatoxin-producing (atoxigenic) A. flavus strains
as biocontrol agents for the control of AFs. In the current
study, a total of 724 A. flavus strains were isolated from different
regions of China. Polyphasic approaches were utilized
for species identification. Non-aflatoxin and non-cyclopiazonic
acid (CPA)-producing strains were further screened
for aflatoxin B1 (AFB1) biosynthesis pathway gene clusters
using a PCR assay. Strains lacking an amplicon for the regulatory
gene aflR were then analyzed for the presence of the
other 28 biosynthetic genes. Only 229 (32%) of the A. flavus
strains were found to be atoxigenic. Smaller (S) sclerotial phenotypes
were dominant (51%) compared to large (L, 34%) and
non-sclerotial (NS, 15%) phenotypes. Among the atoxigenic
strains, 24 strains were PCR-negative for the fas-1 and aflJ
genes. Sixteen (67%) atoxigenic A. flavus strains were PCRnegative
for 10 or more of the biosynthetic genes. Altogether,
18 new PCR product patterns were observed, indicating great
diversity in the AFB1 biosynthesis pathway. The current study
demonstrates that many atoxigenic A. flavus strains can be
isolated from different regions of China. In the future laboratory
as well as field based studies are recommended to test
these atoxigenic strains as biocontrol agents for aflatoxin
contamination.
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