Frontiers research topics,
Journal Year:
2023,
Volume and Issue:
unknown
Published: Jan. 1, 2023
it
is
a
pioneering
approach
to
the
world
of
academia,
radically
improving
way
scholarly
research
managed.The
grand
vision
Frontiers
where
all
people
have
an
equal
opportunity
seek,
share
and
generate
knowledge.Frontiers
provides
immediate
permanent
online
open
access
its
publications,
but
this
alone
not
enough
realize
our
goals.
journal
seriesThe
series
multi-tier
interdisciplinary
set
openaccess,
journals,
promising
paradigm
shift
from
current
review,
selection
dissemination
processes
in
academic
publishing.All
journals
are
driven
by
researchers
for
researchers;
therefore,
they
constitute
service
community.At
same
time,
operates
on
revolutionary
invention,
tiered
publishing
system,
initially
addressing
specific
communities
scholars,
gradually
climbing
up
broader
public
understanding,
thus
serving
interests
lay
society,
too.
Dedication
qualityEach
article
landmark
highest
quality,
thanks
genuinely
collaborative
interactions
between
authors
review
editors,
who
include
some
world's
best
academicians.Research
must
be
certified
peers
before
entering
stream
knowledge
that
may
eventually
reach
-and
shape
society;
only
applies
most
rigorous
unbiased
reviews.Frontiers
revolutionizes
freely
delivering
outstanding
research,
evaluated
with
no
bias
both
social
point
view.By
applying
advanced
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technologies,
catapulting
into
new
generation.
MicrobiologyOpen,
Journal Year:
2024,
Volume and Issue:
13(2)
Published: March 31, 2024
Abstract
Microbial
products
are
essential
for
developing
various
therapeutic
agents,
including
antibiotics,
anticancer
drugs,
vaccines,
and
enzymes.
Genetic
engineering
techniques,
functional
genomics,
synthetic
biology
unlock
previously
uncharacterized
natural
products.
This
review
highlights
major
advances
in
microbial
biotechnology,
focusing
on
gene‐based
technologies
medical
applications.
International Journal of Infectious Diseases,
Journal Year:
2024,
Volume and Issue:
141, P. 106987 - 106987
Published: Feb. 26, 2024
Tuberculosis
(TB)
remains
a
leading
cause
of
death
globally
and
is
estimated
to
have
caused
1.3
million
deaths
worldwide
in
2022.
Approximately
one
quarter
the
world's
population
are
infected
with
Mycobacterium
tuberculosis,
whom
up
10%
will
progress
developing
active
TB
disease.
Achieving
WHO
End
Strategy
targets
95%
reduction
mortality
90%
incidence
worldwide,
by
2035,
daunting
task.
The
continuing
spread
multi-drug
resistant
adds
another
obstacle
achieving
global
control.
Larger
funding
pledges
coupled
technological
advances
recently
enabled
enhancement
vaccine
development
efforts.
These
yielding
pipeline
over
17
products
currently
different
stages
clinical
trials.
Emerging
promising
phase
1
2
trials'
results
advancement
3
trials
necessitated
"vaccine
preparedness"
parallel
so
that
smooth
transition
from
any
positive
4
evaluation
implementation
into
policy
practice
can
follow.
Promotion
human-rights-based
approach
which
recognizes
upholds
fundamental
rights
all
affected
disease,
essential
ensure
universal
access
quality
vaccines
regardless
their
background
or
personal
circumstances.
Frontiers in Microbiology,
Journal Year:
2024,
Volume and Issue:
15
Published: April 25, 2024
The
clinical
challenge
of
differentiating
suspected
tuberculosis
with
positive
T-SPOT.TB
results
persist.
This
study
aims
to
investigate
the
utility
Systemic
Immune-Inflammation
Index
(SII),
Fibrinogen,
and
in
distinguishing
between
active
pulmonary
(PTB)
non-tuberculous
lung
diseases.
Frontiers in Microbiology,
Journal Year:
2024,
Volume and Issue:
15
Published: Oct. 11, 2024
Tuberculosis
remains
a
serious
global
health
threat,
exacerbated
by
the
rise
of
resistant
strains.
This
study
investigates
potential
two
benzofuroxan
(
Bfx
)
derivatives,
5n
and
5b,
as
targeted
treatments
for
MDR-TB
using
in
silico
,
vitro
vivo
methodologies.
In
analyses
showed
that
compounds
have
significant
activity
against
Mtb
H37Rv,
with
standing
out
MIC
90
0.09
±
0.04
μM.
Additionally,
their
efficacy
MDR
pre-XDR
strains
was
superior
compared
to
commercial
drugs.
These
narrow
spectrum
mycobacteria,
which
helps
avoid
dysbiosis
gut
microbiota,
they
also
exhibit
high
selectivity
low
toxicity.
Synergism
studies
indicate
derivatives
could
be
combined
rifampicin
enhance
treatment
reduce
its
duration.
Scanning
electron
microscopy
revealed
severe
damage
morphology
following
5n,
showing
distortions
bacillary
structures.
Whole-genome
sequencing
5n-resistant
isolate
suggests
resistance
mechanisms
mediated
Rv1855c
gene,
supported
studies.
compound
reduced
pulmonary
load
3.0
log
10
CFU/mL,
demonstrating
superiority
over
rifampicin,
achieved
reduction
1.23
CFU/mL.
conclusion,
especially
effectively
address
infections
caused
suggesting
solid
foundation
future
therapeutic
developments
MDR-TB.
Cureus,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Jan. 9, 2024
For
decades,
tuberculosis
(TB),
caused
by
Mycobacterium
(MTB),
has
remained
a
global
health
challenge.
Central
to
this
issue
are
the
proline-proline-glutamic
acid
(PPE)
proteins,
which
play
pivotal
role
in
pathogenesis
and
persistence
of
MTB.
This
article
explores
molecular
mechanisms
PPE
proteins
their
roles
facilitating
MTB’s
evasion
host’s
immune
system
while
enhancing
virulence
transmission.
Focusing
on
structural
functional
aspects
review
provides
detailed
analysis
antigenic
variation,
crucial
mechanism
allowing
MTB
elude
detection.
It
also
probes
genetic
diversity
these
complex
interactions
with
host
immunity,
offering
insights
into
challenges
they
pose
for
therapeutic
development.
delves
potential
targeting
novel
strategies,
discussing
prospects
drug
vaccine
The
evidence
reviewed
underscores
pressing
need
innovative
approaches
combat
TB,
especially
face
increasing
resistance.
Ultimately,
highlights
untapped
revolutionizing
TB
treatment,
paving
way
breakthroughs
Cystatin
F
(CstF)
is
a
protease
inhibitor
of
cysteine
cathepsins,
including
those
involved
in
acti-vating
the
perforin/granzyme
cytotoxic
pathways.
It
targeted
to
endolysosomal
pathway
but
can
also
be
secreted
extracellular
milieu
or
endocytosed
by
bystander
cells.
CtsF
was
shown
significantly
increased
tuberculous
pleurisy,
and
during
HIV
coinfection,
pleural
fluids
display
high
viral
loads.
In
human
macrophages,
we
revealed
strong
upregulation
CstF
infection
with
Mycobacterium
tuberculosis
(Mtb).
manipulation
using
RNA
si-lencing
led
proteolytic
activity
lysosomal
improving
Mtb
intracellular
killing.
Here,
investigate
impact
depletion
coinfection
Mtb-infected
mac-rophages
lymphocytes
infected
HIV.
Our
results
indicate
that
decreasing
released
phagocytes
impacts
major
pro-granzyme
convertase
cathepsin
C
immune
Consequently,
an
observed
increase
granzyme
B
apoptotic
effects
leads
significant
re-duction
replication
HIV-infected
lymphocytes.
Overall,
our
mecha-nism
Mtb/HIV
evasion
mediated
pathogen
killing
driven
ax-is
CstF/
catC/granzymes
contributing
this
syndemic
interaction.
Ultimately,
knowledge
crucial
for
developing
new
therapeutic
approaches
control
both
pathogens
based
on
manipulating
CstF.
Vaccines,
Journal Year:
2024,
Volume and Issue:
12(6), P. 622 - 622
Published: June 4, 2024
Tuberculosis
(TB)
is
a
major
global
health
threat
despite
its
virtual
elimination
in
developed
countries.
Issues
such
as
drug
accessibility,
emergence
of
multidrug-resistant
strains,
and
limitations
the
current
BCG
vaccine
highlight
urgent
need
for
more
effective
TB
control
measures.
This
study
constructed
strains
overexpressing
Rv1002c
found
that
rBCG-Rv1002c
strain
secreted
glycosylated
proteins,
significantly
enhancing
macrophage
activation
immune
protection
against
Mycobacterium
tuberculosis
(M.
tb).
These
results
indicate
overexpression
promotes
elevated
levels
O-glycosylation
bacteriophages,
their
phagocytic
antigenic
presentation
functions.
Moreover,
upregulated
regulatory
molecules
on
surface,
activated
NF-κB
pathway,
facilitated
release
large
amounts
NO
H2O2,
thereby
bacterial
control.
In
mice,
immunization
induced
greater
innate
adaptive
responses,
including
increased
production
multifunctional
long-term
memory
T
cells.
Furthermore,
rBCG-Rv1002c-immunized
mice
exhibited
reduced
lung
load
histological
damage
upon
M.
tb
infection.
result
shows
it
has
potential
to
be
an
excellent
candidate
preventive
TB.