Staphylococcus aureus is a leading cause of hospital- and community-
acquired infections. Despite current advances in antimicrobial
chemotherapy, the infections caused by S. aureus
remain challenging due to their ability to readily develop resistance.
Indeed, antibiotic resistance, exemplified by methicillin-
resistant S. aureus (MRSA) is a top threat to global health
security. Furthermore, the current rate of antibiotic discovery
is much slower than the rate of antibiotic-resistance development.
It seems evident that the conventional in vitro bacterial
growth-based screening strategies can no longer effectively
supply new antibiotics at the rate needed to combat bacterial
antibiotic-resistance. To overcome this antibiotic resistance
crisis, screening assays based on host–pathogen interactions
have been developed. In particular, the free-living nematode
Caenorhabditis elegans has been used for drug screening
against MRSA. In this review, we will discuss the general
principles of the C. elegans-based screening platform and
will highlight its unique strengths by comparing it with conventional
antibiotic screening platforms. We will outline major
hits from high-throughput screens of more than 100,000
small molecules using the C. elegans–MRSA infection assay
and will review the mode-of-action of the identified hit compounds.
Lastly, we will discuss the potential of a C. elegansbased
screening strategy as a paradigm shift screening platform.
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The Lactobacillus genus is widely used for fermentation of
plant materials and dairy products. These species are typically
found in highly specialized environments, with the bee gut
serving as one of the niche locations in which Lactobacillus
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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A Gram-negative aerobic bacterium, designated RR4-38T,
was isolated from a biofilter in a seawater recirculating aquaculture
system (RAS) in Busan, South Korea. The bacteria
were irregular, short, rod-shaped, non-motile, oxidase-positive,
and catalase-negative. Growth of the strain RR4-38T
was observed at 15–35°C (optimum, 25–30°C), pH 5.5–9.5
(optimum, pH 8.0), and in the presence of 0–5% (w/v) NaCl
(optimum, 3%). Phylogenetic analysis based on the 16S rRNA
gene sequences showed that the strain RR4-38T formed a distinct
lineage with close genera Ulvibacter (≤ 95.01% 16S rRNA
gene sequence similarity), Aureitalea (94.74%), Aureisphaera
(≤ 93.27%), and Jejudonia (93.07%) that all belong to the
family Flavobacteriaceae. Whole-genome sequence comparison
revealed that the ANI (average nucleotide identity) and
digital DDH (DNA-DNA hybridization) values between strain
RR4-38T and the two closest strains, Ulvibacter antarcticus
DSM 23424T and Aureitalea marina S1-66T, were 68.96–
69.88% and 17.4–19%, respectively. The genome analysis
revealed that the strain might be involved in biodegradation
of organic debris produced by farmed fish in aquaculture
systems. The predominant respiratory quinone was menaquinone
MK-6 and the major cellular fatty acids were iso-
C15:0 (26.5%), iso-C17:0 3-OH (16.4%), iso-C15:1 G (15%), and
iso-C16:0 3-OH (9.6%). The major cellular polar lipids were
diphosphatidylglycerol, phosphatidylethanolamine, unidentified
aminolipids, and glycolipids. Based on phenotypic, chemotaxonomic,
and phylogenetic features, strain RR4-38T represents
a novel genus and species in the family Flavobacteriaceae,
for which the name Pukyongia salina gen. nov., sp.
nov. is proposed. The type strain is RR4-38T (= KCTC 52651T
= DSM 108068T).
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this strain belonged to the family Halieaceae which shared
the highest sequence similarities with Luminiphilus syltensis
NOR5-1BT (94.5%) and Halioglobus pacificus S1-72T (94.5%),
followed by 92.3–94.3% sequence similarities with other species
within the aforementioned family. Phylogenetic analyses
demonstrated that strain IMCC3088T was robustly clustered
with Luminiphilus syltensis NOR5-1BT within the family
Halieaceae. However, average amino acid identity (AAI), percentages
of conserved proteins (POCP), average nucleotide
identity (ANI), and alignment fraction (AF) between strain
IMCC3088T and Luminiphilus syltensis NOR5-1BT were 54.5%,
47.7%, 68.0%, and 16.5%, respectively, suggesting that they
belonged to different genera. Whole-genome sequencing of
strain IMCC3088T revealed a 3.1 Mbp genome size with a
DNA G + C content of 51.7 mol%. The genome encoded diverse
metabolic pathways including sulfur oxidation, phenol
degradation, and proteorhodopsin phototrophy. Mono-unsaturated
fatty acids were found to be the predominant cellular
fatty acid components in the strain. Phosphatidylethanolamine,
phosphatidylglycerol, and diphosphatidylglycerol
were the primarily identified polar lipids, and ubiquinone-8
was identified as a major respiratory quinone. The taxonomic
data collected herein suggested that strain IMCC3088T represented
a novel genus and species of the family Halieaceae,
for which the name Aequoribacter fuscus gen. nov., sp. nov.
is proposed with the type strain (= KACC 15529T = NBRC
108213T).
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intact plasmid and plasmids with deleted cryptic prophages
into Escherichia coli DH5α. The E. coli transconjugants carrying
the plasmid with intact cryptic prophages showed increased
survival during treatment with a high concentration
of NaCl, high and low temperatures, an oxidative stressor
(H2O2), and an immunological stressor (human serum). By
contrast, the transconjugants carrying the plasmid with a
single-cryptic prophage knockout did not show any change
in survival rates. mRNA expression analyses revealed that the
genes encoding sigma factor proteins were highly upregulated
by the tested stressors and affected the expression of
various proteins (antioxidant, cell osmosis-related, heat shock,
cold shock, and universal stress proteins) associated with the
specific defense against each stress. These findings indicate
that a bacterial strain carrying a plasmid with intact carbapenemase
gene and cryptic prophage regions exhibited an increased
resistance against simulated environmental stresses,
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enhanced stress resistance. Our study indicated that the coselection
of antibiotic resistance and resistance to other stresses
may help bacteria to increase survival rates against adverse
environments and disseminate.
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The growing threat of emergent multidrug-resistant enteric
bacterial pathogens, and their adopted virulence properties
are directing to find alternative antimicrobials and/or development
of dietaries that can improve host gut health and/or
defense. Recently, we found that modified Lactobacillus casei
(Lc + CLA) with increased production of conjugated linoleic
acid has antimicrobial and other beneficial properties.
Further, prebiotic alike products such as berry pomace extracts
(BPEs), increase the growth of probiotics and inhibit
the growth of certain bacterial pathogens. In this study, we
evaluated the antibacterial effect of genetically modified Lc +
CLA along with BPEs against major enteric pathogen Salmonella
enterica serovar Typhimurium (ST). In mixed culture
condition, the growth of ST was significantly reduced in the
presence of Lc + CLA and/or BPEs. Bacterial cell-free cultural
supernatant (CFCS) collected from wild-type Lc or modified
Lc + CLA strains also inhibited the growth and survival of ST,
and those inhibitory effects were enhanced in the presence of
BPEs. We also found that the interaction of the pathogen with
cultured host (HD-11 and INT-407) cells were also altered in
the presence of either Lc or Lc + CLA strain or their CFCSs
significantly. Furthermore, the relative expression of genes
related to ST virulence and physicochemical properties of ST
was altered by the effect of CFCSs of either Lc or Lc + CLA.
These findings indicate that a diet containing synbiotic, specifically
linoleic acid, over-produced Lc + CLA and prebiotic
product BPEs, might have the potential to be effective in controlling
ST growth and pathogenesis.
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RaoN is a Salmonella-specific small RNA that is encoded in
the cspH-envE intergenic region on Salmonella pathogenicity
island-11. We previously reported that RaoN is induced under
conditions of acid and oxidative stress combined with nutrient
limitation, contributing to the intramacrophage growth
of Salmonella enterica serovar Typhimurium. However, the
role of RaoN in nitrosative stress response and virulence has
not yet been elucidated. Here we show that the raoN mutant
strain has increased susceptibility to nitrosative stress by
using a nitric oxide generating acidified nitrite. Extending
previous research on the role of RaoN in oxidative stress resistance,
we found that NADPH oxidase inhibition restores
the growth of the raoN mutant in LPS-treated J774A.1 macrophages.
Flow cytometry analysis further revealed that the
inactivation of raoN leads to an increase in the intracellular
level of reactive oxygen species (ROS) in Salmonella-infected
macrophages, suggesting that RaoN is involved in the inhibition
of NADPH oxidase-mediated ROS production by mechanisms
not yet resolved. Moreover, we evaluated the effect
of raoN mutation on the virulence in murine systemic
infection and determined that the raoN mutant is less virulent
than the wild-type strain following oral inoculation. In conclusion , small regulatory RNA RaoN controls nitrosativeoxidative
stress resistance and is required for virulence of
Salmonella in mice.
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resistance and pathogenicity in bacteria. Here, we report
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division) efflux pump, AcrAB, in Acinetobacter nosocomialis.
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AcrAB efflux pump, comprising AcrA and AcrB, are widely
distributed among different bacterial species. Deletion of acrA
and/or acrB genes led to decreased biofilm/pellicle formation
and reduced antimicrobial resistance in A. nosocomialis. RNA
sequencing and mRNA expression analyses showed that expression
of acrA/B was downregulated in a quorum sensing
(QS) regulator (anoR)-deletion mutant, indicating transcriptional
activation of the acrAB operon by AnoR in A. nosocomialis.
Bioassays showed that secretion of N-acyl homoserine
lactones (AHLs) was unaffected in acrA and acrB deletion
mutants; however, AHL secretion was limited in a deletion
mutant of acrR, encoding the acrAB regulator, AcrR.
An in silico analysis indicated the presence of AcrR-binding
motifs in promoter regions of anoI (encoding AHL synthase)
and anoR. Specific binding of AcrR was confirmed by electrophoretic
mobility shift assays, which revealed that AcrR
binds to positions -214 and -217 bp upstream of the translational
start sites of anoI and anoR, respectively, demonstrating
transcriptional regulation of these QS genes by AcrR.
The current study further addresses the possibility that AcrAB
is controlled by the osmotic stress regulator, OmpR, in A.
nosocomialis. Our data demonstrate that the AcrAB efflux
pump plays a crucial role in biofilm/pellicle formation and
antimicrobial resistance in A. nosocomialis, and is under the
transcriptional control of a number of regulators. In addition,
the study emphasizes the interrelationship of QS and AcrAB
efflux systems in A. nosocomialis.
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important for the conversion of choline to the osmoprotectant,
glycine betaine. The betIBA operon is polycistronic
and is under the regulation of the first gene, betI, of the same
operon. A bioinformatics analysis revealed the presence of
a BetI-binding motif upstream of the betIBA operon, and
electrophoretic mobility shift assays confirmed the specific
binding of BetI. An mRNA expression analysis revealed that
expression of betI, betB, and betA genes is elevated in a betIeletion
mutant compared with the wild type, confirming that
the autorepressor BetI represses the betIBA operon in A.
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under the transcriptional control of the quorum-sensing (QS)
regulator, AnoR in, A. nosocomialis. A subsequent analysis
of the impact of BetI on expression of the QS genes, anoR
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stress-response systems are correlated in A. nosocomialis
and that the expression of genes in both systems is
finely tuned by various feedback loops depending on osmolarity
conditions.
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