bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2024,
Номер
unknown
Опубликована: Окт. 25, 2024
Abstract
Background
The
metabolome
of
COVID-19
patients
has
been
studied
sparsely,
with
most
research
focusing
on
a
limited
number
plasma
metabolites
or
small
cohorts.
This
is
the
first
study
to
test
saliva
in
comprehensive
way,
revealing
significant
changes
linked
disease
severity
and
highlighting
potential
as
non-invasive
diagnostic
tool.
Methods
We
included
30
asymptomatic
subjects
no
prior
infection
vaccination,
102
mild
SARS-CoV-2
infection,
61
hospitalized
confirmed
status.
Saliva
samples
were
analyzed
using
hydrophilic
interaction
liquid
chromatography-mass
spectrometry
(HILIC-MS/MS)
positive
negative
ionization
modes.
Results
Significant
identified
patients,
distinct
patterns
based
severity.
Healthy
individuals
exhibited
well-regulated
bacterial
network,
while
severe
cases
showed
disordered
microbial
networks.
Elevated
dipeptides
such
Val-Glu
Met-Gln
moderate
suggest
specific
protease
activity
related
SARS-CoV-2.
Increased
acetylated
amino
acids
like
N-Acetylserine
N-Acetylhistidine
indicate
biomarkers
for
stress
Bacterial
metabolites,
including
muramic
acid
indole-3-carboxaldehyde,
higher
mild-moderate
cases,
indicating
oral
microbiota
changes.
In
polyamines
organ
damage-related
N-acetylspermine
3-methylcytidine,
significantly
increased.
Interestingly,
reduced
elevated
cases.
Conclusions
metabolomics
offers
insight
into
progression
COVID-19.
Nature Communications,
Год журнала:
2024,
Номер
15(1)
Опубликована: Апрель 13, 2024
Knockout
of
the
ORF8
protein
has
repeatedly
spread
through
global
viral
population
during
SARS-CoV-2
evolution.
Here
we
use
both
regional
and
pathogen
sequencing
to
explore
selection
pressures
underlying
its
loss.
In
Washington
State,
identified
transmission
clusters
with
knockout
throughout
evolution,
not
just
on
novel,
high
fitness
backbones.
Indeed,
is
truncated
more
frequently
knockouts
circulate
for
longer
than
any
other
gene.
Using
a
phylogeny,
find
evidence
positive
explain
this
phenomenon:
nonsense
mutations
resulting
in
shortened
products
occur
are
associated
faster
clade
growth
rates
synonymous
ORF8.
Loss
also
reduced
clinical
severity,
highlighting
diverse
impacts
npj Genomic Medicine,
Год журнала:
2025,
Номер
10(1)
Опубликована: Янв. 17, 2025
Immunocompromised
patients
struggle
to
adequately
clear
viral
infections,
offering
the
virus
opportunity
adapt
immune
system
in
host.
Here
we
present
a
case
study
of
patient
undergoing
allogeneic
hematopoietic
stem
cell
transplantation
with
521-day
follow-up
SARS-CoV-2
infection
BF.7.21
variant.
Virus
samples
from
five
time
points
were
submitted
whole
genome
sequencing.
Between
first
detection
and
its
clearance,
patient's
population
acquired
34
amino
acid
substitutions
8
deletions
coding
regions.
With
11
receptor
binding
domain
virus'
spike
protein,
15
times
more
abundant
than
expected
for
random
distribution
this
highly
functional
region.
Amongst
them
S:K417T,
S:N440S,
S:K444R,
S:V445A,
S:G446N,
S:L452Q,
S:N460K,
S:E484V
at
positions
that
are
notorious
their
resistance-mediating
effects.
The
substitution
patterns
found
indicate
ongoing
adaptive
evolution.
medRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2023,
Номер
unknown
Опубликована: Авг. 24, 2023
ABSTRACT
Background
Prolonged
SARS-CoV-2
infections
in
immunocompromised
hosts
may
predict
or
source
the
emergence
of
highly
mutated
variants.
The
types
immunosuppression
placing
patients
at
highest
risk
for
prolonged
infection
and
associated
intrahost
viral
evolution
remain
unclear.
Methods
Adults
aged
≥18
years
were
enrolled
5
hospitals
followed
from
4/11/2022
–
2/1/2023.
Eligible
SARS-CoV-2-positive
previous
14
days
had
a
moderate
severely
immunocompromising
condition
treatment.
Nasal
specimens
tested
by
rRT-PCR
every
2–4
weeks
until
negative
consecutive
specimens.
Positive
underwent
culture
whole
genome
sequencing.
A
Cox
proportional
hazards
model
was
used
to
assess
factors
with
duration
infection.
Results
We
150
with:
B
cell
malignancy
anti-B
therapy
(n=18),
solid
organ
hematopoietic
stem
transplant
(SOT/HSCT)
(n=59),
AIDS
(n=5),
non-B
(n=23),
autoimmune/autoinflammatory
conditions
(n=45).
Thirty-eight
(25%)
rRT-PCR-positive
12
(8%)
culture-positive
≥21
after
initial
detection
illness
onset.
Patients
dysfunction
longer
rRT-PCR-
positivity
compared
those
(aHR
0.32,
95%
CI
0.15-0.64).
Consensus
(>50%
frequency)
spike
mutations
identified
individuals
who
>56
days;
61%
receptor-binding
domain
(RBD).
Mutations
shared
multiple
rare
(<5%)
global
circulation.
Conclusions
In
this
cohort,
replication-competent
Omicron
uncommon.
Within-host
evolutionary
rates
similar
across
patients,
but
lasting
accumulated
mutations,
which
distinct
seen
globally.
Advanced Science,
Год журнала:
2024,
Номер
unknown
Опубликована: Окт. 14, 2024
Abstract
The
severe
acute
respiratory
syndrome
coronavirus
2
(SARS‐CoV‐2)
has
evolved
many
high‐risk
variants,
resulting
in
repeated
COVID‐19
waves
over
the
past
years.
Therefore,
accurate
early
warning
of
variants
is
vital
for
epidemic
prevention
and
control.
However,
detecting
through
experimental
epidemiological
research
time‐consuming
often
lags
behind
emergence
spread
these
variants.
In
this
study,
HiRisk‐Detector
a
machine
learning
algorithm
based
on
haplotype
network,
developed
computationally
SARS‐CoV‐2
Leveraging
7.6
million
high‐quality
complete
genomes
metadata,
effectiveness,
robustness,
generalizability
are
validated.
First,
evaluated
actual
empirical
data,
successfully
all
13
preceding
World
Health
Organization
announcements
by
27
days
average.
Second,
its
robustness
tested
reducing
sequencing
intensity
to
one‐fourth,
noting
only
minimal
delay
3.8
days,
demonstrating
effectiveness.
Third,
applied
detect
risks
among
Omicron
variant
sub‐lineages,
confirming
broad
applicability
high
ROC‐AUC
PR‐AUC
performance.
Overall,
features
powerful
capacity
detection
bearing
great
utility
any
public
emergency
caused
infectious
diseases
or
viruses.
Abstract
Viral
mutations
within
patients
nurture
the
adaptive
potential
of
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
during
chronic
infections,
which
are
a
source
variants
concern.
However,
there
is
no
integrated
framework
for
evolutionary
analysis
intra-patient
SARS-CoV-2
serial
samples.
Herein,
we
describe
Intra-Patient
Evolution
Reporting
and
Analysis
(VIPERA),
new
software
that
integrates
evaluation
ancestry
sequences
with
trajectories
from
same
viral
infection.
We
have
validated
it
using
positive
negative
control
datasets
successfully
applied
to
case,
revealed
population
dynamics
evidence
evolution.
VIPERA
available
under
free
license
at
https://github.com/PathoGenOmics-Lab/VIPERA.
This
case
report
highlights
the
prolonged
SARS-CoV-2
reverse
transcriptase
polymerase
chain
reaction
positivity
in
a
32-year-old
immunocompromised
male
with
history
of
kidney
transplants
and
chronic
disease.
The
whole
genome
sequencing
nasopharyngeal
samples
for
collected
12
days
apart
showed
presence
BA.1.1
Omicron
variant.
It
revealed
evidence
intra-host
viral
evolution,
showing
development
loss
specific
mutations
over
time.
emphasizes
need
continuous
monitoring
strategies
patients,
as
they
may
serve
reservoirs
evolution
potentially
give
rise
to
immune
escape
variants.
PLoS Pathogens,
Год журнала:
2024,
Номер
20(10), С. e1012624 - e1012624
Опубликована: Окт. 15, 2024
Neutralising
antibodies
against
the
SARS-CoV-2
spike
(S)
protein
are
major
determinants
of
protective
immunity,
though
insufficient
antibody
responses
may
cause
emergence
escape
mutants.
We
studied
humoral
immune
response
causing
intra-host
evolution
in
a
B-cell
depleted,
haemato-oncologic
patient
experiencing
clinically
severe,
prolonged
infection
with
virus
lineage
B.1.177.81.
Following
bamlanivimab
treatment
at
an
early
stage
infection,
developed
bamlanivimab-resistant
mutation,
S:S494P.
After
five
weeks
apparent
genetic
stability,
additional
substitutions
and
deletions
within
N-terminal
domain
(NTD)
receptor
binding
(RBD)
S
was
observed.
Notably,
composition
frequency
mutations
changed
short
period
unprecedented
dynamic.
The
triple
mutant
S:Delta141-4
E484K
S494P
became
dominant
until
elimination.
Routine
serology
revealed
no
evidence
patient.
A
detailed
analysis
variant-specific
by
pseudotyped
neutralisation
test,
surrogate
immunoglobulin-capture
enzyme
immunoassay
showed
that
onset
IgM-dominated
coincided
appearance
mutations.
formation
neutralising
correlated
One
year
later,
experienced
mild
re-infection
Omicron
BA.1.18,
which
treated
sotrovimab
resulted
increase
Omicron-reactive
antibodies.
In
conclusion,
endogenous
immunocompromised
NTD
RBD
virus.
Although
elimination
ultimately
achieved,
this
escaped
detection
routine
diagnosis
created
situation
temporarily
favouring
rapid
various
mutants
known
epidemiological
relevance.
medRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2024,
Номер
unknown
Опубликована: Март 4, 2024
Abstract
Accumulating
evidence
points
to
persistent
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
infections
in
immunocompromised
individuals
as
a
source
of
genetically
divergent,
novel
lineages,
generally
characterised
by
increased
transmissibility
and
immune
escape.
While
intrahost
evolutionary
dynamics
the
virus
chronically
infected
patients
have
been
previously
reported,
existing
knowledge
is
primarily
based
on
samples
obtained
from
nasopharyngeal
compartment.
In
this
study,
we
investigate
evolution
genetic
diversity
that
accumulated
during
prolonged
SARS-CoV-2
infection
with
Omicron
sublineage
BF.7,
estimated
persisted
for
over
one
year
an
immunosuppressed
patient.
Based
sequencing
eight
viral
genomes
collected
patient
at
six
time
points,
identified
86
single-nucleotide
variants
(iSNVs),
two
indels,
362
bp
deletion.
Our
analysis
revealed
distinct
genotypes
(NP),
endotracheal
aspirate
(ETA),
bronchoalveolar
(BAL)
samples.
Notably,
while
significant
divergence
was
observed
between
NP
BAL
samples,
most
iSNVs
found
ETA
were
also
detected
or
This
suggests
may
not
offer
comprehensive
representation
overall
diversity.
Nonsynonymous
mutations
frequent
spike
envelope
genes,
along
loss-of-function
ORF8,
generated
frameshift
mutation
large
deletion
respectively.
Using
long-range
PCR
sequenced
part
routine
surveillance,
validated
similar
deletions
causing
ORF8
loss
function
can
be
carried
infection.
findings
only
demonstrate
BF.7
further
diverge
its
already
exceptionally
mutated
state
but
highlight
develop
specific
populations
across
anatomical
compartments.
provides
insights
into
intricate
nature
infections.