quadgram

This is a table of type quadgram and their frequencies. Use it to search & browse the list to learn more about your study carrel.

quadgram frequency
severe acute respiratory syndrome212
porcine epidemic diarrhea virus144
acute respiratory syndrome coronavirus113
in the presence of91
in vero e cells88
cells were infected with80
of severe acute respiratory66
of porcine epidemic diarrhea58
infected vero e cells47
as shown in fig43
for the treatment of42
vero cells were infected40
in vitro and in38
in the present study38
at an moi of38
in the absence of38
the antiviral activity of37
cells were treated with37
vitro and in vivo36
african green monkey kidney35
on vero e cells35
coronavirus infectious bronchitis virus35
of the s protein34
the severe acute respiratory32
washed three times with32
herpes simplex virus type31
of vero e cells30
the cells were fixed30
the intracellular extracts of29
cells were fixed with29
cells were incubated with29
gds and gds strains28
with severe acute respiratory28
with fetal bovine serum27
a and icpc a27
icpc a and icpc27
cells were washed twice27
rna was extracted from27
middle east respiratory syndrome27
vero cells infected with26
in the united states25
on the other hand25
were washed twice with25
the cells were washed25
was used as a25
as well as the24
the vero cell line24
has been shown to24
the gds and gds23
for the production of23
at c for h23
in cells infected with23
after h of incubation23
porcine reproductive and respiratory22
as a negative control22
in the case of22
determined by plaque assay22
supplemented with fetal bovine22
epidemic diarrhea virus in22
reproductive and respiratory syndrome22
the vero cells and21
was added to the21
effect on vero e21
used in this study21
the recombinant ibvs and21
of the viral genome20
and respiratory syndrome virus20
s s cleavage site20
washed twice with pbs20
at a moi of20
total rna was extracted19
an important role in19
incubated for h at19
pcr and western blotting19
vero e cells were19
cells were inoculated with19
east respiratory syndrome coronavirus19
presence or absence of19
at the plasma membrane19
and vero cells were19
at a multiplicity of19
a multiplicity of infection19
intracellular extracts of ln18
in vero cells and18
added to each well18
were washed three times18
cells were washed with18
cells were seeded in18
cells were fixed and18
the presence or absence18
h at room temperature18
of blfp crude extract18
recombinant ibvs and beaudette18
three times with pbs18
vero e cells exposed17
for the detection of17
the coronavirus infectious bronchitis17
avian infectious bronchitis virus17
vero cells were seeded17
isolation and characterization of17
in the vero cells17
cell fusion activity of17
e cells exposed to17
of a novel coronavirus17
at different time points17
in the presence or17
were washed with pbs17
the s s cleavage16
propagated in vero cells16
the cells were incubated16
vero cells and ipec16
pcd and vero cells16
for h at room16
infectivity of icpc a16
for the development of16
the pedv s protein16
the vero e cells16
cells were transfected with16
cells infected with the16
pedv in vero cells16
african swine fever virus16
was added to each15
plates were infected with15
the s protein of15
these results indicated that15
min at room temperature15
than that of the15
egfr pi k akt15
at a concentration of15
the inoculum was removed15
the porcine epidemic diarrhea15
these results suggest that15
vero e and ma15
in the s protein15
cells in the presence15
was used as the15
vero and a cells15
it is important to15
the spike protein of15
the sam binding site15
the expression levels of15
in pbs for min15
vero e cells in14
at room temperature for14
and the cells were14
infected with wild type14
vero e cells and14
used as a negative14
a member of the14
the antiviral effect of14
was performed as described14
with different concentrations of14
was removed and the14
were fixed and stained14
incubated at c for14
in the treatment of14
acute respiratory syndrome in14
vero cells treated with14
the results showed that14
treated with or without14
in cells transfected with14
there was no significant13
in the sam binding13
one of the most13
the infectivity of icpc13
in the vero cell13
cytopathic effect on vero13
of herpes simplex virus13
and characterization of a13
the cells were collected13
for min at room13
patients with severe acute13
is one of the13
the invasion rates of13
at hpi and hpi13
at the same time13
of the mutant virus13
vero cells were treated13
were incubated for h13
c in a co13
viral rna was extracted13
were infected with pedv13
inoculum was removed and13
infection of vero cells13
green monkey kidney cells12
infection in vero cells12
with pedv strains at12
cells were grown in12
with the recombinant ibvs12
porcine epidemic diarrhoea virus12
cells were incubated for12
is a member of12
in vero cells infected12
in vero e and12
the infectivity of the12
of the gds and12
vero cells were inoculated12
were infected with hsv12
at rt for min12
had no effect on12
regulation of cell death12
in the number of12
associated with severe acute12
been shown to be12
characterization of a novel12
monolayers of vero cells12
well plates were infected12
with wild type and12
the in vitro prophylactic12
the expression of the12
the authors declare that12
with the intracellular extracts12
these results suggested that12
were determined by plaque12
cells transfected with the11
avian coronavirus infectious bronchitis11
the presence of increasing11
this work was supported11
the vero e and11
of the coronavirus infectious11
of the rescued virus11
d d d d11
a fixed concentration of11
cells were cultured in11
for min at rt11
a novel coronavirus associated11
infected vero cells were11
compared to those of11
on the surface of11
of infectious bronchitis virus11
as compared to the11
fixed concentration of sars11
cells were maintained in11
the treatment of sars11
the development of a11
the production of viral11
coronavirus associated with severe11
cells were pretreated with11
to those of the11
to a fixed concentration11
fusion activity of s11
was observed in the11
treated with different concentrations11
of vero cells with11
compared to the parental11
was determined using the11
porcine epidemic diarrhea in11
monkey kidney cell line11
cells were collected at11
against pedv in vero11
the invasion efficiency of11
novel coronavirus associated with11
infected with pedv strains11
were infected with the11
length cdna clone of11
were detected in the11
cells infected with wild11
pi k akt pathway11
and incubated for h11
the vero and ipec11
fusion activity of the11
propagation in vero cells11
in vero cells in11
at a density of11
our results suggest that11
as a result of11
were collected at hpi11
cells exposed to a11
exposed to a fixed11
the vero cells were11
lower than that of11
were fixed with paraformaldehyde11
the presence of ribavirin10
presence of increasing concentrations10
carrying mutations in the10
the vero cell lineage10
a concentration ranging from10
centers for disease control10
the end of the10
at a concentration ranging10
the plasma membrane and10
rates of the gds10
pseudovirions with uncleaved s10
it is possible that10
washed with pbs and10
results showed that the10
m f and c10
used at a concentration10
american type culture collection10
of the recombinant ibvs10
against herpes simplex virus10
mutations in the sam10
and then incubated with10
an equal volume of10
of peptide h on10
the vero e cell10
in vitro prophylactic effects10
the study of the10
of increasing concentrations of10
the early stages of10
were observed in the10
replication in vero e10
was carried out by10
was extracted from the10
of the murine coronavirus10
g a and rmv10
of the spike protein10
g for min at10
the presence of trypsin10
fixed and stained with10
in patients with severe10
with ck ch ldl10
have been shown to10
of prrsv and pedv10
supernatants were collected at10
and in the ipec10
propagation of the virus10
and in the vero10
at h post infection10
were inoculated with kpedv10
mechanism of action of10
cells were washed three10
work was supported by10
vero cells were cultured10
at the end of10
these data suggest that10
containing the empty vector10
identification of a novel10
were inoculated with the10
in the footpad with10
bile and bile acids10
of the porcine epidemic10
culture supernatants were collected10
proteolytic cleavage of the10
room temperature for h10
vero cells were grown10
of the in vitro10
in the culture medium10
at h after the10
the inhibitory effect of10
infectious cdna clone of10
studies have shown that10
be due to the9
in vitro antiviral activity9
and then infected with9
apoptosis in vero e9
p mapk signaling pathway9
the cells were then9
the overexpression of the9
at the time of9
was amplified by rt9
cells containing the empty9
after washing three times9
of vero cells were9
of sabin poliovirus type9
production of viral vaccines9
of the viral rna9
of the virus of9
was observed in cells9
epidemic diarrhea in cell9
strains at h after9
when compared to the9
from patients recovered from9
to that of the9
rna was isolated from9
for disease control and9
it was found that9
the p mapk signaling9
by plaque assay and9
of the helicase protein9
and gds strains were9
the regulation of cell9
fusion of the viral9
of pedv icpc a9
ns a and ns9
antiviral activity of ribavirin9
of mouse hepatitis virus9
invasion efficiency of pedv9
error bars represent standard9
e protein mab g9
without blfp crude extract9
the results of the9
al kassaa et al9
cells were overlaid with9
sialic acid binding activity9
pedv icpc a and9
epidemic diarrhea virus strains9
of the sars coronavirus9
the virus of porcine9
may be due to9
of icpc a and9
crude extract against pedv9
by the addition of9
was found to be9
of cell death during9
suggesting that myricetin may9
activation of p mapk9
the growth properties of9
as described above and9
diarrhea in cell culture9
blfp crude extract against9
the ns a protein9
the focus forming assay9
and vero e cells9
well tissue culture plates9
vero e cell line9
virus of porcine epidemic9
we determined that the9
the results indicated that9
added to the cells9
the cells were infected9
infection in vero e9
incubated at room temperature9
flavivirus e protein mab9
the infected cells were9
mers pseudovirions with uncleaved9
vero e cells are9
at the indicated times9
associated with diarrhea in8
disease control and prevention8
green monkey kidney cell8
by the severe acute8
infected with an moi8
vero cells and and8
and r l mutant8
of african green monkey8
cells and and in8
epidemic diarrhea virus infection8
was significantly lower than8
fixed with paraformaldehyde in8
the total number of8
it was shown that8
in cell cultures and8
blood samples were collected8
type i and type8
washing three times with8
feline infectious peritonitis virus8
were observed in cells8
of the viral envelope8
the two cell lines8
results showed that pedv8
an african green monkey8
absence of growth factors8
syndrome coronavirus spike protein8
myricetin may interact with8
s protein of pedv8
in these cell lines8
and hpi for qrt8
a novel coronavirus from8
cells were stained with8
for h at c8
cells were incubated at8
the african green monkey8
results indicated that the8
and all of them8
aminopeptidase n is a8
e and huh cells8
the absence of growth8
passages in cell culture8
was no significant difference8
a and ns b8
line of african green8
similar to that of8
induction of apoptosis by8
is thought to be8
pedv strains at h8
medium was removed and8
collected at hpi and8
the induction of apoptosis8
of three independent experiments8
for the inhibition of8
were considered statistically significant8
abortus and chlamydia pecorum8
syndrome in hong kong8
institutional animal care and8
experimental infection of pigs8
were infected with an8
vero cells grown in8
protein of severe acute8
was determined relative to8
in each group were8
in vero and ipec8
acute respiratory distress syndrome8
care and use committee8
respiratory syndrome in hong8
were infected with a8
on the infection of8
respiratory syndrome coronavirus spike8
the viral titers in8
the world health organization8
r l mutant viruses8
authors declare that they8
the plates were incubated8
and and in the8
intracellular extracts of ypk8
animal care and use8
culture supernatants were harvested8
a functional receptor for8
viral rna synthesis and8
the medium was removed8
at various time points8
glycoprotein of murine coronavirus8
and infected with pedv8
was determined by plaque8
the international committee on8
variants of porcine epidemic8
fold serial dilutions of8
were determined using the8
e cells in the8
with an moi of8
chlamydia abortus and chlamydia8
twice with pbs and8
phosphorylation of p mapk8
acquisition of the cell8
i and type iii8
in vero cells at8
infected vero cells treated8
the detection limit of8
no significant difference between8
vero e and huh8
cells and incubated at8
functional receptor for the8
invasion rates of the8
with vero e cells8
is not essential for8
as described in the8
with or without myricetin8
the s gene of8
genes in vero cells8
for h and then8
in vero cells were8
h of incubation at8
hpi and hpi for8
in cell culture and8
isolated from kefir grains8
is a functional receptor8
virus entry and syncytia8
entry and syncytia formation8
an infectious cdna clone8
spike protein of sars8
that they have no8
are shown in fig8
for the first time8
for h at rt8
genome sequence of the8
pbs for min at8
of porcine epidemic diarrhoea8
infected cells were treated8
the virus life cycle8
significantly lower than that8
incubated with pedv at8
declare that they have8
there is an urgent8
at the s s8
was propagated in vero7
the growth kinetics of7
these results demonstrate that7
and western blotting at7
ic value of this7
no effect on the7
treatment of zikv infection7
infected cells were detected7
the virus inoculum was7
at least three independent7
genomic rna and sg7
pretreated with the intracellular7
in lung epithelial cells7
in cells expressing s7
of no and peroxynitrite7
cell infection by pedv7
to each well and7
that of the parental7
j cells were transfected7
infected cells were fixed7
of the virus in7
cell lines were infected7
on taxonomy of viruses7
were significantly higher than7
infected with chikv ls7
the viral spike protein7
vero cells with the7
in a variety of7
vero e cells infected7
an urgent need to7
a single amino acid7
of vero cells on7
proteolytic processing of the7
of the virus to7
they have no competing7
on the expression of7
cell cycle progression at7
is consistent with the7
as shown in figure7
were incubated with pedv7
have no competing interests7
tcid ml at hpi7
was used for the7
with virus gd protein7
test the invasion efficiency7
the cell monolayers were7
within the helicase protein7
novel coronavirus in patients7
with gds or gds7
is an urgent need7
the replication of the7
of the icpc a7
observed in cells expressing7
is known to be7
and western blotting assay7
rna was extracted using7
in a co atmosphere7
days two and four7
international committee on taxonomy7
well plates until confluence7
functional characterization of the7
to the wt sequence7
as well as to7
was performed using the7
stage of zikv infection7
in the s region7
mutations in the s7
epidemic diarrhea virus strain7
of vesicular stomatitis virus7
in both vero and7
a high level of7
of the expression of7
at days two and7
results suggest that the7
in contrast to the7
with pfu of rzikv7
more than of the7
can be used for7
and porcine epidemic diarrhea7
a novel coronavirus in7
expression of the viral7
in addition to the7
the identity of the7
compared to the control7
the replication of sars7
similar to those of7
cells in the absence7
titer was determined by7
a wide range of7
was carried out using7
in both cell types7
identification and characterization of7
as severe acute respiratory7
used to infect vero7
the neutralization capacity of7
coronavirus in patients with7
with acute respiratory distress7
wild type and ribv7
for min and then7
confluent monolayers of vero7
at nm was measured7
mode of action of7
the absence of trypsin7
higher than that in7
cell death during infection7
as well as in7
entry into host cells7
significant difference between the7
of these cell lines7
data are shown as7
during its propagation in7
monolayers of vero e7
was detected in the7
play an important role7
the antiviral efficacy of7
in severe acute respiratory7
in vero cells as7
were compared to those7
which is consistent with7
in both cell lines7
the percentage of infected7
viral titers in the7
to vero e cells7
in vero cells was7
moi of pfu cell7
associated with acute respiratory7
the g c mutation7
vero cells were pretreated7
new variants of porcine7
the effects of the7
with paraformaldehyde in pbs7
cell fusion activities of7
to test the invasion7
h before virus infection7
cells were then washed7
observed in vero cells7
analysis of the growth7
human airway epithelial cells7
committee on taxonomy of7
complete genome sequence of7
lines were infected with7
the presence of the7
reverse genetics system for7
of the intracellular extracts7
the absence of virus7
cells were resuspended in7
early stages of infection7
cells were seeded at7
in the spike protein7
then infected with pedv7
the early stage of7
in different cell lines7
alone or in combination7
pi k akt signaling7
plates were incubated at7
for vero e cells7
we found that the7
well plates at a7
titers were determined by7
ns a a v7
on the plasma membrane7
the s and s7
test was used to7
in vitro prophylactic and7
entry into vero cells7
the genome of the7
were used at a7
the viability of the7
vero e cell culture7
between the gds and7
vitro prophylactic and therapeutic7
in the cytoplasm of7
with uncleaved s protein7
no conflict of interest7
vitro prophylactic effects of7
the culture supernatants were7
the replication cycle of7
in this study were7
in the vero e7
of viral rna in7
supplemented with fbs and6
the nucleotide sequence of6
were infected with chikv6
the arg residue to6
experiment with two replicates6
incubated with gds or6
studies have suggested that6
sequence of the sars6
herpes simplex virus glycoprotein6
the etiological agent of6
of the virus was6
the authors declare no6
s and s subunits6
in vero cells with6
various time points post6
water was used as6
activity of the s6
in the coinfection group6
was used in the6
species severe acute respiratory6
total rna extracted from6
the species severe acute6
respiratory syndrome coronavirus infection6
tissue culture infectious dose6
at h after transfection6
the addition of trypsin6
antiviral activity against sars6
this is the first6
epidermal growth factor receptor6
the institutional animal care6
cov infection in vero6
infectious bronchitis virus a6
plays an important role6
sirna and infected with6
fit to a variable6
virus is also shown6
lungs and spinal cord6
approximately and in the6
performed as described previously6
both in vitro and6
activities of these s6
were removed by washing6
of these s constructs6
in the beaudette strain6
van dinten et al6
with an equal volume6
caused by a novel6
each well and incubated6
in an atmosphere of6
in vero cells but6
of the international committee6
in the viral genome6
samples were collected from6
entry into vero e6
western blot analysis of6
absence of virus is6
virus entry at the6
the viral life cycle6
three times with pbst6
virus titers in supernatants6
the genome sequence of6
were fixed at hpi6
cells were detected by6
binding and entry process6
were purchased from the6
involved in pedv entry6
of mx and isg6
the footpad with pfu6
a reverse genetics system6
times with pbs and6
of viral rna synthesis6
a new porcine enteric6
vero cells were transfected6
protein has been shown6
in vero cells is6
the results of this6
was also observed in6
j cells were pre6
inhibit the replication of6
that the vero e6
distilled water was used6
by the institutional animal6
to increasing concentrations of6
with paraformaldehyde for min6
of the virus and6
were performed in triplicate6
of the ns a6
vero e cells at6
reverse transcription was performed6
the mutant virus was6
of the severe acute6
in group were inoculated6
were mapped to the6
the treatment of zikv6
new porcine enteric coronavirus6
a potent inhibitor of6
hu carrying mutations in6
inhibition was determined relative6
p p p p6
respiratory syndrome coronavirus in6
cells exposed to increasing6
were carried out in6
of the virus life6
of virus is also6
fusion activities of these6
of the sars vaccine6
bars represent standard deviations6
to test this hypothesis6
experiments were performed in6
with the exception of6
at later time points6
footpad with pfu of6
two replicates is shown6
variable response curve from6
cell viability was measured6
of intracellular viral rna6
and cells were washed6
we did not observe6
cut fragment of p6
was significantly higher than6
stained with crystal violet6
in one of the6
transducer and activator of6
virus inoculum was removed6
with diarrhea in swine6
of the vero cells6
food and drug administration6
nucleotide sequence of the6
hepatitis c virus infection6
of the antiviral activity6
viability of vero cells6
passaged in vero cells6
analysis was performed using6
confirmed by western blotting6
from one representative experiment6
drugs in the absence6
did not affect the6
birds in each group6
of vero cells was6
levels of zikv rna6
percentage of infected cells6
a variable response curve6
were similar to those6
be involved in the6
our data indicated that6
rna and sg mrna6
human immunodeficiency virus type6
and incubated with gds6
cytotoxic effect on vero6
also been shown to6
for the presence of6
then incubated for h6
of at least three6
e cells infected with6
of avian infectious bronchitis6
isolation of a novel6
and infected with junv6
c for h then6
the three cell lines6
single amino acid substitution6
has been reported that6
of the two viruses6
were then incubated with6
like particle associated with6
after h of adsorption6
least three independent experiments6
against porcine epidemic diarrhea6
approved by the institutional6
infected cells treated with6
possessed an in vitro6
inhibition of viral rna6
by severe acute respiratory6
were orally inoculated with6
of hepatitis c virus6
replication of sabin poliovirus6
cells were maintained at6
of the parental virus6
of the cell lines6
cleavage of the s6
induces apoptosis in vero6
female balb c mice6
were approved by the6
immunostaining using the pan6
vero cell monolayers in6
total rna was isolated6
in the icpc a6
particle associated with diarrhea6
prrsv and pedv were6
the cell lysates were6
but there was no6
titrated by plaque assay6
the a v mutation6
all cell lines were6
exposed to increasing concentrations6
containing trypsin for h6
it has been reported6
to be able to6
virus in porcine cell6
titers in the supernatant6
in a volume of6
were infected with sars6
cdna clone of mv6
cells as well as6
for prrsv and pedv6
followed by cycles of6
cells were then incubated6
vero cells in the6
statistical analysis was performed6
increasing concentrations of drugs6
institute of infectious diseases6
fixed with paraformaldehyde for6
with a moi of6
has also been reported6
for h prior to6
a a v mutation6
a moi of for6
sequence analysis of the6
were treated with different6
clarified by centrifugation at6
at a dosage of6
isolation of porcine epidemic6
coronavirus spike protein by6
inhibits the replication of6
to be involved in6
and titrated by plaque6
with two replicates is6
from vero cells infected6
cells as described previously6
been shown to induce6
to a variable response6
the expression of a6
and the supernatants were6
body weight loss and6
introduced into vero cells6
the spike glycoprotein of6
terminal domain of the6
can be used to6
gds or gds strains6
our results showed that6
in cells treated with6
pcr was performed using6
the s domain of6
removed and the cells6
in the context of6
with or without blfp6
of drugs in the6
in the form of6
log s gene copies6
by western blot analysis6
response curve from one6
antiviral activity of the6
cells were fixed at6
has the potential to6
virus gd protein to6
s region of the6
of egfr pi k6
fragment of p tl6
from three independent experiments6
antiviral activity of potential6
of the mock group6
concentrations of peptide h6
were obtained from the6
were infected with zikv6
results confirmed that the6
signal transducer and activator6
expression levels of the6
dephosphorylation of stat in6
group were inoculated with6
is shown in figure6
moi of for h6
infected or infected with6
the presence of mm6
and activator of transcription6
for porcine epidemic diarrhea6
of a variety of6
cells infected with ribv6
for the generation of6
s rrna and rpoa6
the presence of a6
added to vero cells6
the blfp crude extract6
using graphpad prism software6
concentrations of drugs in6
isolates of sars coronavirus6
of the arg residue6
in vero cell culture6
in this study are6
was similar to that6
in dmem supplemented with6
p in vero cells6
s gene copies ml6
infected vero cells with6
the cells three times6
from cells transfected with6
cells were fixed in6
dmem supplemented with fbs6
mutation of the arg6
supernatants were harvested at6
that myricetin may interact6
there were no significant6
activity of peptide h6
conjugated to alexa fluor6
significant difference between groups6
the murine coronavirus spike6
did not show any6
be explained by the6
as early as hpi5
the fusion activity of5
different concentrations of each5
entry at the plasma5
the centers for disease5
followed by staining with5
mechanisms of action of5
effectively inhibit the recently5
which was significantly lower5
and chloroquine effectively inhibit5
as a receptor for5
peripheral blood mononuclear cells5
bands were visualized using5
after the second transfection5
is known about the5
the fact that the5
expression in vero cells5
of pfu per cell5
and clarified by centrifugation5
respiratory syndrome coronavirus replication5
cell lines were maintained5
plaque assay in vero5
by a novel coronavirus5
by plaque assay in5
in order to determine5
depends on ace and5
virus titers were determined5
signal transduction in sars5
entry depends on ace5
belongs to the genus5
diarrhea virus spike protein5
of mm ammonium chloride5
effects against pedv in5
the american type culture5
in vero and huh5
it was reported that5
it will be interesting5
the cells were treated5
to inoculate a cm5
nucleotides to of the5
pcr products were purified5
treatment of vero cells5
fig a and b5
epidemic diarrhea virus spike5
dmso was used as5
cell fusion activity by5
coronavirus induces apoptosis in5
the plaque reduction assay5
to the parental pedvpt5
we also found that5
of pigs with a5
were detected by immunocytochemistry5
cells pretreated with the5
of harringtonine for h5
were added to the5
viral rna mini kit5
in porcine cell cultures5
is lethal to the5
cells infected with sars5
a line of african5
to the cell surface5
viral titers were determined5
extracted from the infected5
data were analyzed by5
blotting at hpi and5
mutant virus from p5
of the mutant rzikv5
the lab isolates were5
at days after challenge5
to further confirm the5
infection of vero e5
the specificity of the5
were significantly more attenuated5
turkey with confirmed covid5
is blocked by a5
drugs were used at5
significance was analyzed from5
of action of ribavirin5
to the research community5
the viral envelope with5
the recombinant ibvs were5
cells treated with the5
and stained with anti5
in dmem containing fbs5
swine pedv positive serum5
sars coronavirus infection in5
as a loading control5
were fixed with formaldehyde5
analyzed by western blotting5
to cells and incubated5
strains were and in5
plaque assays were performed5
patient in turkey with5
signaling pathways are activated5
facilitate the development of5
for replication in cell5
and is blocked by5
or gds strains for5
natural science foundation of5
the s s region5
the data presented as5
on cell infection by5
after days of incubation5
chloroquine effectively inhibit the5
were introduced into vero5
previous studies have shown5
cell entry depends on5
blocks cell cycle progression5
of each viral stock5
by interfering with the5
a or icpc a5
used to determine the5
national institute of infectious5
read and approved the5
to the results of5
may be involved in5
were removed and the5
at each time point5
functions within the helicase5
treated and untreated cells5
via the cyclin d5
vero cells were co5
extracted from vero cells5
mem containing trypsin for5
pedv s protein was5
used to inoculate a5
cell substrates for the5
a better understanding of5
vero cells transfected with5
the mode of action5
a variety of viruses5
an moi of pfu5
followed by incubation with5
the most commonly used5
and approved the final5
cells treated with or5
on the left indicate5
in vitro assembly of5
the e glycoprotein of5
the number of cells5
and virus titers were5
phosphorylation and activation of5
expression of s protein5
the s rrna and5
piglets in group were5
were collected from the5
was analyzed from t5
data presented as mean5
was used to compare5
from the ministry of5
the infection of pedv5
as well as other5
of this ns a5
the wt sequence during5
during the course of5
plates were incubated for5
an atmosphere of co5
pcr was carried out5
wt sequence during its5
and the presence of5
of the subgenomic mrna5
of infected vero e5
of s gene mutants5
end of the genome5
up to days post5
the effect of trypsin5
cov in vero e5
cleavage of the e5
in vitro prophylactic effect5
the groups treated with5
that pedv entry followed5
binding site in the5
groups of five female5
dna and rna viruses5
and western blotting analysis5
vero e cells by5
were propagated in vero5
virus in cultured cells5
fixed at hpi and5
clinically proven protease inhibitor5
was allowed to proceed5
then washed three times5
of the s gene5
tissue culture supernatants were5
a patient in turkey5
the s subunit of5
infection of pigs with5
factors that influence ebola5
tmprss and is blocked5
to of the viral5
no significant differences in5
blfp crude extract were5
of transmissible gastroenteritis coronavirus5
viral titer in the5
and immunostaining using the5
treated with proteinase k5
allowed to proceed for5
the amount of virus5
than those of the5
vero e cells to5
supernatants were determined by5
we found that pedv5
cellulose in mem containing5
have been used to5
of the ibv genome5
in vitro transcribed rna5
diarrhea virus in porcine5
the culture of vero5
was considered to be5
serial dilutions of the5
particular ic value of5
were monitored daily for5
adapted ibv beaudette strain5
the recovery of infectious5
that influence ebola antiviral5
fold serial dilution of5
at day after infection5
together with the n5
h and incubated with5
the feasibility of generating5
was used to detect5
spike protein is a5
expressed as the mean5
possessed in vitro prophylactic5
the vero jcrb cell5
coronavirus associated with human5
time course analysis of5
a duplicated subgenomic promoter5
these results indicate that5
jejunum and ileum of5
c bl j mice5
the entire genome of5
in hek t cells5
linear fit to a5
ebola antiviral activities in5
of viral protein expression5
twice with sterile pbs5
on the cell surface5
member of the genus5
control cells containing the5
institute of biomedical sciences5
cell lines such as5
cotton rats in groups5
virus in vero cells5
did not observe a5
cycle progression at g5
the qiaamp viral rna5
it should be noted5
from a patient with5
with the n transcripts5
identity of the rescued5
of the parental pedvpt5
harvested at h post5
carried out in the5
stages of viral infection5
the recently emerged novel5
we were able to5
with respect to the5
of african swine fever5
as a positive control5
that the inhibition of5
apoptosis induced by sars5
compared with the zikv5
us porcine epidemic diarrhea5
with methylcellulose in dmem5
pfu ml at hpi5
to the method described5
the drug was added5
of the e glycoprotein5
confluent vero cells in5
science foundation of china5
these data indicate that5
its propagation in vero5
the membrane was incubated5
detection limit of the5
cdna clone of the5
supernatants were collected and5
the virus titer in5
the heptad repeat region5
significantly higher than that5
acidophilus cmul and l5
removed and the monolayers5
be attributed to the5
a wide variety of5
in turkey with confirmed5
treated with lm snap5
by grants from the5
vero cells were prepared5
the cyclin d prb5
treated with the recombinant5
conformational changes in the5
were found to be5
was determined by a5
cells but not in5
the treatment of covid5
qiaamp viral rna mini5
with increasing concentrations of5
into vero e cells5
order genetic assembly system5
to determine whether the5
provided in supplementary file5
the seven recombinant ibvs5
assay was performed to5
was used at a5
with a new porcine5
we are grateful to5
mutation in a domain5
to further investigate the5
a clinically proven protease5
standard deviations of the5
in a line of5
of the bacterial intracellular5
was measured using a5
growth properties of the5
supported by grants from5
plates at a density5
were incubated for min5
and tmprss and is5
for h followed by5
hsv binding and entry5
numbers on the left5
drugs for treatment of5
icpc a or icpc5
cellular egfr pi k5
of an antisense oligonucleotide5
infectious bronchitis virus in5
the infectious bronchitis virus5
the infected vero cells5
e glycoprotein of murine5
h prior to infection5
progression at g g5
vero cells pretreated with5
vero e and llcmk5
our understanding of the5
the particular ic value5
results were confirmed by5
were used to infect5
of an avian coronavirus5
of human coronavirus e5
cyclin d prb pathway5
at room temperature with5
pigs with a new5
antiviral activities in cell5
from the american type5
protein to interfere with5
are listed in table5
of icpc a was5
the viral rna was5
could be due to5
at rt for h5
the bacterial intracellular extracts5
patients recovered from covid5
the bac cdna clone5
at room temperature and5
the generation of a5
and u cell lines5
inhibit the recently emerged5
and naming it sars5
genomic characterization of a5
of the infected cells5
when the drug was5
concentrations of each compound5
significant difference in the5
the activation of egfr5
was approved by the5
all animal experiments were5
little is known about5
of the viral life5
further characterization of the5
at this time point5
transcripts containing the g5
antiviral activity in vitro5
antiviral drug candidates against5
were then overlaid with5
the viability of vero5
the mechanism of action5
and then shifted to5
nucleotide sequences of the5
stocks were prepared by5
a broad range of5
of west nile virus5
the detection of icpc5
resuspended in ml of5
results were expressed as5
the detection of the5
higher than those of5
with porcine epidemic diarrhea5
was added at the5
of the vero cell5
in a similar manner5
was carried out with5
with the zikv group5
weight loss and survival5
cells infected with chikv5
human respiratory disease in5
recently emerged novel coronavirus5
ace and tmprss and5
the entry mechanism of5
in vitro inhibition of5
well and incubated at5
western blotting at hpi5
demonstrate the feasibility of5
added to cells and5
infected with pedv at5
the egfp reporter gene5
in the pathogenesis of5
in accordance with the5
and foetal calf serum5
and hepatitis c virus5
invasion rates of pedv5
gd protein to interfere5
allowed to incubate for5
in mem containing trypsin5
removed and cells were5
was not observed in5
of a number of5
swine acute diarrhea syndrome5
into the host cell5
inoculated with ml of5
these results confirm that5
h after the first5
of the cell monolayer5
the vero cell monolayers5
remdesivir and chloroquine effectively5
the consensus sequence of5
adsorption and membrane fusion5
were incubated at room5
methyl cellulose in mem5
treatment of cells with5
assay was performed as5
a high degree of5
an essential role in5
approved for clinical use5
plaque assay and immunostaining5
in cells electroporated with5
in a domain with5
the plasma membrane of5
the pcr products were5
of virus to the5
stock was determined by5
will be interesting to5
and incubated for min5
groups treated with the5
drug candidates against sars5
tcid ml of the5
new coronavirus associated with5
log rna copies ml5
at different stages of5
the oxygen atom of5
after the first transfection5
the pedv blfp group5
gds strains for h5
those of the parental5
rrna and rpoa gene5
were treated with or5
myricetin may block hsv5
the sialic acid binding5
be used for the5
were fixed with acetone5
the parental vaccine strain5
these results demonstrate the5
pedv entry into vero5
substrates for the production5
were analyzed using the5
error bars represent the5
and mechanism of action5
were added to each5
effect of trypsin on5
rna was detected in5
of middle east respiratory5
were and in the5
with human respiratory disease5
authors declare no conflict5
were added to cells5
in the perinuclear region5
between the two cell5
vero cells as described5
influence ebola antiviral activities5
of the pedv s5
statistical significance was analyzed5
paraformaldehyde in pbs for5
cell lines for the5
in vitro models of5
the difference in the5
virus infection in vitro5
was kindly provided by5
the induction of cell5
wild type and mutant5
the cell monolayer was5
morbidity and mortality rates5
declare no conflict of5
the molecular biology of5
sam binding site in5
in the pedv blfp5
for h and incubated5
at g g phase5
with various concentrations of5
blocked by a clinically5
the number of foci5
study of the antiviral5
results of this study5
the icpc a and5
and the virus titer5
was washed three times5
in a co incubator5
the virus titer was5
g c mutant transcripts5
on ace and tmprss5
assay and immunostaining using5
commercially available antiviral agents5
the ministry of health5
in different cell types5
significantly higher than those5
infected with the recombinant5
was removed and cells5
test compared with the5
it is known that5
as the primary antibody5
in order to evaluate5
was carried out in5
and rpoa gene sequence5
sequence during its propagation5
were found in the5
peptide h and pedv5
would like to thank5
is a receptor for5
or absence of ribavirin5
detection of icpc a5
added into each well5
on the basis of5
were no significant differences5
to the end of5
cultured in the presence5
infection of pedv icpc5
gds strains were and5
the clinical management of5
infected with the mutant5
jnk and pi k5
infectivity of the in5
time points post infection5
according to the method5
porcine transmissible gastroenteritis virus5
replication in cell culture5
virus into vero cells5
associated with human respiratory5
and ck ch ldl5
the rescued virus was5
these s constructs are5
a new coronavirus associated5
and vero cell lines5
crude extract were determined5
or without blfp crude5
performed as described above5
of porcine reproductive and5
after washing twice with5
were cultured overnight in5
and the plaques were5
are thought to be5
ncov and naming it5
were separated by sds5
might be due to5
and the data presented5
was added to vero5
respiratory disease in china5
by a clinically proven5
in the heptad repeat5
and swine pedv positive5
difference between the gds4
the hpi time point4
porcine epidemic diarrhea coronavirus4
treated with various concentrations4
in mammalian cell lines4
is a class i4
for the study of4
avian infectious bronchitis coronavirus4
terminal region of the4
results indicated that pedv4
r k and r4
inoculum was removed followed4
the amount of gd4
for h in the4
fusion and syncytia formation4
a one sample t4
vero cell monolayers were4
cell cultures and mice4
step growth curves of4
respiratory syncytial virus infection4
new coronavirus of probable4
in the release of4
a new coronavirus of4
coronavirus of probable bat4
the expression of s4
icpc a replicated to4
the different cell lines4
of vero cells vol4
detection and quantification of4
and hela cell lines4
that the differences between4
grew to high titer4
at c followed by4
diarrhea virus into vero4
results demonstrate that the4
control by the humoral4
k akt signaling pathway4
amplification of cdna ends4
virions interacted with vero4
from a vero cell4
play important roles in4
mapk and its downstream4
in this report we4
murine coronavirus spike protein4
onset of clinical signs4
for min to remove4
to the s protein4
the percentage inhibition was4
for the clinical management4
lethal to the coronavirus4
transfected with the mutant4
seeded with vero e4
reduction of the viral4
vero cells were incubated4
cell spread of hsv4
the reason for the4
newly discovered coronavirus associated4
an increase in the4
with prrsv or pedv4
porcine aminopeptidase n is4
figure a and b4
or in combination with4
coronavirus of bat origin4
that the intracellular extracts4
inhibitory effects against pedv4
prevention and control of4
efficacy of m f4
percentage inhibition was determined4
outbreak associated with a4
data were analyzed using4
the type i interferon4
viral replication in the4
u ml penicillin and4
based on the sequence4
prepared by freezing thawing4
representative of three separate4
with an excess of4
on ice for min4
human suspension cell lines4
to infection by sars4
at the amino acid4
during the early stages4
a man with pneumonia4
protein was detected by4
characterization of a newly4
replication of prrsv and4
that pedv enters vero4
using the mmessage mmachine4
the central nervous system4
used in the pcr4
coronavirus severe acute respiratory4
activity of toremifene citrate4
as early as h4
analyzed by western blot4
with error bars represent4
in vero cells by4
with pedv at moi4
is due to the4
pedv entry relies on4
and added to the4
moi of pfu per4
the number of viral4
at concentrations ranging from4
when data are compared4
of the small intestine4
vero cells in a4
the time of infection4
with sabin poliovirus type4
by the world health4
viral control by the4
important role in the4
than the gds strain4
the presence of rounded4
to the best of4
p mapk and its4
attenuated in vitro and4
its interaction with the4
associated with porcine epidemic4
species as well as4
identification of antiviral drug4
d the vero cells4
similar results were obtained4
petrus jansen van vuren4
by the humoral immune4
the selection of the4
from a man with4
entire genome of each4
values are representative of4
myricetin may be able4
it is necessary to4
fold dilutions of the4
in the vero and4
the result shown is4
mixture of two viruses4
is a major receptor4
biology and pathogenesis of4
and isg genes in4
were used as a4
were incubated with rabbit4
the large polymerase protein4
to this article can4
emergence of resistant viruses4
time of infection or4
knockdown of the expression4
detected in vero cells4
in human lung cells4
entry mechanism of pedv4
in the s s4
the culture supernatant was4
those of the mock4
do not appear to4
targeting the n gene4
related coronavirus of bat4
the genetic stability of4
did not exhibit any4
sabin poliovirus type in4
to the fact that4
simplex virus type infection4
antigens targeting the s4
replication in vero cells4
are statistically significant when4
represent standard deviations of4
effects of chloroquine on4
this article can be4
that some of the4
electroporated into vero cells4
more insight into the4
both icpc a and4
to investigate the effect4
inoculated with ped virus4
a betacoronavirus in group4
were more susceptible to4
derived vero cell line4
data are expressed as4
to the coronavirus infectious4
pedv enters vero cells4
sequence derived from the4
vero cells were first4
virus titer was determined4
duration of the experiment4
the peak viral titer4
like particles associated with4
type and mutant viruses4
amount of gd protein4
member of the family4
the use of a4
on the consensus sequence4
in vero jcrb cells4
constitutive activation of stat4
effect of ribavirin on4
amount of viral rna4
the phosphorylation of egfr4
duplicated subgenomic promoter and4
located in the c4
crude extract of blfp4
pellet was resuspended in4
a bacterial artificial chromosome4
rna was extracted and4
were conducted based on4
with the seven recombinant4
as a percentage of4
active in vero cells4
cells were lysed with4
apoptosis and necrosis have4
frames encode nonessential functions4
number of asterisks indicate4
on porcine nidovirus replication4
reading frames encode nonessential4
were assessed with a4
for severe acute respiratory4
inhibited at a concentration4
pedv rna was detected4
at and h post4
produced by escherichia coli4
the differentially expressed proteins4
intranasal and ocular routes4
with phosphate buffered saline4
based on the consensus4
to the negative control4
signaling pathways in sars4
assess the antiviral activity4
gene was amplified by4
adsorbed to hela cells4
both apoptosis and necrosis4
blfp as a feed4
the total amount of4
was used in all4
is a potent inhibitor4
the development of new4
the polybasic cleavage motif4
titer in vero cells4
each well and the4
s protein by trypsin4
virus produced in c4
indicate that the differences4
of p mapk and4
compared the effects of4
virus strains in the4
as a feed additive4
of influenza a viruses4
and extracellular supernatants of4
through direct interaction with4
were treated with proteinase4
the small intestine of4
by the duplex rt4
protection against challenge with4
for the sars coronavirus4
are expressed as the4
to evaluate the viral4
receptor for the sars4
vero cells have been4
cme to enter cells4
has also been shown4
the production of vaccines4
conducted based on three4
vero cells could be4
well plates were inoculated4
a major receptor for4
with virus adsorption and4
have been deposited in4
well plates were washed4
higher than that of4
heptad repeat region of4
in the nearby clusters4
asterisks indicate that the4
caused by an hku4
cell death and survival4
not human coronavirus nl4
addition of guanosine to4
for the recombinant ibvs4
bars represent the mean4
on the viability of4
shown to induce apoptosis4
interaction with virus gd4
arg residue to a4
used as the primary4
of this graph is4
has not yet been4
nonstructural protein ns a4
to block viral entry4
nucleocapsid protein of sars4
s s region of4
differences were considered significant4
analyzed by flow cytometry4
man with pneumonia in4
in virus growth medium4
are shown as m4
in virus entry and4
in or near the4
for the prevention of4
the importance of this4
jev production in huh4
to replicate in these4
hepatitis virus strain a4
and middle east respiratory4
design of the study4
respiratory distress syndrome in4
infection with chlamydia abortus4
at c for min4
binding of gd to4
k and r l4
revealed that pedv entry4
passages in vero cells4
in vitro using the4
a final concentration of4
viral stocks were prepared4
entry step of sars4
and used to infect4
is possible that the4
kit according to the4
with a lethal dose4
of the family coronaviridae4
asterisks indicate significant difference4
we compared the effects4
productivity and susceptibility to4
allergy and infectious diseases4
at the beginning of4
to determine the effect4
the sequence of the4
can enter cells through4
to further assess the4
cells were then overlaid4
representative of the mean4
an increase in virus4
in blocking buffer for4
mmessage mmachine t kit4
not appear to be4
cm tissue culture flask4
against the pedv s4
cell lines can support4
reversion of the mutant4
with the mutant virus4
interacted with vero cells4
mm nh cl or4
after washing with pbs4
and characterization of the4
was performed according to4
mutation at nucleotide position4
the ministry of education4
mixed infections with chlamydia4
assay for detection and4
can be found in4
diarrhea virus strain pc4
that acquisition of the4
performed to determine the4
membrane fusion and reduces4
the causative agent of4
and monitored for cpe4
observed in cells infected4
expression of viral proteins4
was detected by qrt4
and used to inoculate4
statistical significance was determined4
point mutation in the4
we next sought to4
a positively charged amino4
shown is a representative4
of the number of4
targets of p mapk4
of ck ch ldl4
the mean from three4
positively charged amino acid4
vero e cells was4
due to the low4
the potential emergence of4
a of the coronavirus4
to further evaluate the4
and the overexpression of4
landscape of vero cells4
to ensure that the4
human and animal cells4
were aligned using the4
in vivo compared to4
characterization of severe acute4
virus to the cells4
below the detection limit4
by deka et al4
or near the catalytic4
the inhibitory activities of4
g for min to4
and the lack of4
plaques were visualized by4
in the spike glycoprotein4
scrofa and chlorocebus sabaeus4
mice infected with pfu4
detection and titration of4
cells and incubated for4
activity against both hsv4
in cultured cells and4
vero cells via clathrin4
for the duration of4
prior to incubation with4
most commonly used cell4
as a measure of4
in multiple cell types4
determine the effect of4
travel history to iran4
using the unpaired t4
the replication of porcine4
are summarized in table4
the most effective inhibitor4
been tested in humans4
observed in cells transfected4
the expression level of4
these two cell lines4
from the first patient4
cells transfected with z4
coronavirus spike protein for4
for the use of4
spike protein for membrane4
which belongs to the4
was removed followed by4
for membrane fusion and4
on sv in tissue4
the addition of guanosine4
for the ratio of4
absorbance at nm was4
supplemented with fetal calf4
was cloned by three4
a discontinuous transcription mechanism4
length transcripts containing the4
plaque assay on vero4
detected as early as4
infected with a moi4
have shown that the4
the virus passage virus4
activity of s protein4
the unpaired t test4
of cell death in4
strain was more sensitive4
were reported to have4
the limit of detection4
coronavirus replication in cell4
the morbidity and mortality4
at the institute of4
that vero e cells4
coronavirus in vero cells4
the cells were harvested4
were washed with phosphate4
were grown in dmem4
proteins were separated by4
enters vero cells via4
in the groups treated4
related to the sars4
cell lines infected with4
rapid amplification of cdna4
chikv ls and ls4
were used in this4
cells was determined using4
a role in the4
in both lungs and4
necrosis have been observed4
fold diluted virus stock4
for the staining of4
and found that the4
titers in supernatants were4
coronavirus associated with acute4
of the amino acid4
genetic stability of the4
viral rna in the4
calculated and expressed as4
emergent porcine epidemic diarrhea4
domain with undefined functions4
were incubated for days4
assay on vero cells4
enhancement of the cell4
for the induction of4
of infected cells was4
cases of severe acute4
coronavirus mouse hepatitis virus4
of lactic acid bacteria4
that the replication of4
nonessential functions for replication4
a pneumonia outbreak associated4
after the addition of4
and activation of p4
was able to induce4
before washing with pbs4
major receptor for the4
of the m protein4
based on the use4
when it was added4
the other cell lines4
and cells were incubated4
for h and were4
isolation in cell culture4
the correlation between the4
of antiviral activity of4
the ability of the4
infectious bronchitis virus is4
the coronavirus spike protein4
that the recombinant ibvs4
infectious virus from the4
virus strain pc a4
the production of virions4
successful entry into cells4
were washed once with4
a cm tissue culture4
tissue culture infective dose4
genotyping of emergent porcine4
by means of the4
in the s gene4
infection was allowed to4
cells were then infected4
pneumonia in saudi arabia4
replication in cell cultures4
of the novel human4
were intranasally inoculated with4
antiviral activity of ata4
cultured in vero cells4
prophylactic effects of the4
authors read and approved4
mesenteroides ypk against pedv4
vero jcrb cell line4
respiratory syndrome coronavirus entry4
was significantly inhibited by4
was quantified by real4
could be inhibited by4
for human coronavirus e4
e cells were treated4
in balb c mice4
were significantly lower than4
cathepsin l to infect4
the number of infected4
washed for three times4
on the replication of4
strain of porcine epidemic4
the s protein gene4
of infectious viral progeny4
samples was determined by4
the mutant virus from4
compared using the unpaired4
calpain and cathepsin inhibitors4
culture of vero e4
all of them survived4
important insights into the4
an inverted fluorescence microscope4
incubated for min at4
were approximately and in4
the method described by4
the igg and igm4
the species rhinolophus bat4
a percentage of the4
cell culture supernatants were4
of the mean from4
the duration of the4
but not human coronavirus4
late stage of zikv4
their effects on the4
to induce apoptosis in4
the s protein on4
the mmessage mmachine t4
which suggested that the4
incubated for h with4
guanosine to the ribavirin4
obtained from the american4
apoptosis via a caspase4
and iu ml for4
the concentration of the4
was supported by grants4
with pneumonia in saudi4
of the plasma membrane4
the internalization rates of4
protein similar to p4
of the synthetic viruses4
of the negative strand4
of stat in sars4
has been reported to4
strains in the united4
membrane fusion activity of4
for the propagation of4
the phosphorylation and activation4
both levels of zikv4
to the presence of4
between virus and host4
then the amount of4
with the plasma membrane4
of the antisense oligonucleotide4
visualized by staining with4
viral protein expression in4
encode nonessential functions for4
sv in tissue culture4
viruses at a multiplicity4
in agreement with these4
pedv entry followed clathrin4
and analyzed by flow4
and human leukocyte interferon4
gds strain was more4
it was observed that4
in vero cells for4
the second passage of4
vitro prophylactic effect against4
in the blfp crude4
the enzymatic activities of4
carried out using the4
that of the single4
either mm nh cl4
then washed with pbs4
mouse hepatitis virus strain4
genomic and subgenomic rna4
type i interferon in4
prophylactic effect against pedv4
respiratory syndrome coronavirus by4
the genomic and subgenomic4
entry of mers pseudovirions4
by western blot with4
virus binding and entry4
on the use of4
pck and cho cells4
of antiviral drug candidates4
room temperature for min4
bronchitis virus a polyprotein4
may be related to4
plays important roles in4
with fetal calf serum4
was performed using a4
staining with crystal violet4
samples were incubated for4
zika virus infection in4
to hepatitis c virus4
sus scrofa and chlorocebus4
porcine intestinal epithelial cells4
to further analyze the4
all authors read and4
associated with a new4
to the ribavirin treatment4
were then washed with4
of wild type and4
used in the treatment4
in order to test4
mice infected with the4
of guanosine to the4
treatment of vero e4
value of this graph4
of probable bat origin4
the percentage of ebov4
used for the production4
polyclonal antibody to the4
cells were cultured overnight4
pneumonia outbreak associated with4
of the african green4
simplex virus glycoprotein d4
at the same position4
infected with junv at4
were randomly assigned to4
virus infection and the4
was assigned values of4
been shown to have4
acute respiratory syndrome a4
the development of vaccine4
and hamster cell lines4
could be attributed to4
and pi k akt4
the activity of cyclin4
the outer capsid layer4
removed followed by three4
the infectivity of ibv4
in vitro inhibitory activity4
inhibitory activity of peptide4
were performed using the4
no significant difference in4
by staining with crystal4
of the s subunit4
transmission of zika virus4
japanese encephalitis reporter virus4
the cells were stained4
inhibitor of chikv replication4
both lungs and spinal4
plates were inoculated with4
that the compound may4
and then permeabilized with4
no and peroxynitrite on4
monolayer of vero e4
induced cell death than4
the humoral immune response4
pensaert and de bouck4
were inoculated with pfu4
statistically significant when data4
were used to amplify4
was effective against chikv4
and approved by the4
in the cell culture4
viral titer was determined4
observed for other alphaviruses4
cells were compared to4
changes in the viral4
cell culture model of4
cell fusion and syncytia4
containing the g c4
it has been shown4
approved the final manuscript4
the nucleocapsid protein of4
higher cell metabolic activity4
with a new coronavirus4
a part of the4
viral protein expression was4
from cells treated with4
was used to identify4
were fixed with methanol4
and the development of4
that the isolated virus4
error of the mean4
of virus yield inhibition4
of emergent porcine epidemic4
a result of the4
which recognizes residues to4
and infected with the4
with the addition of4
been used to treat4
belong to the species4
the majority of the4
isg genes in vero4
buffer for h at4
probably due to the4
passaged sabin poliovirus type4
the fact that they4
are available upon request4
cells for h at4
was shown to be4
in supernatants were determined4
g g phase via4
of a newly discovered4
death during infection by4
challenge with the parental4
in all groups were4
authors declare that there4
fusion and reduces viral4
virus adsorption and membrane4
swollen head syndrome in4
to vero cell monolayers4
enhanced the infectivity of4
the avian coronavirus infectious4
distress syndrome in humans4
are compared using the4
the plaques were counted4
region of the s4
in the ns a4
a crucial role in4
of prrsv or pedv4
with undefined functions within4
the ck ch ldl4
utilizes cathepsin l to4
bronchitis virus in cultured4
a domain with undefined4
to various types of4
used as a template4
we found that a4
and the number of4
the effects of chloroquine4
genome landscape of vero4
the vero cell culture4
result shown is a4
the mixture of two4
of vero cells is4
later stages of infection4
of the genome of4
based on three replicates4
preliminary step for cancer4
and genotyping of emergent4
and those less than4
the upper and lower4
a region of the4
were incubated at c4
s domain of mers4
indicate significant difference between4
compared to infected cells4
taiwan porcine epidemic diarrhea4
the number of plaques4
pellets were resuspended in4
the n transcripts were4
inoculate a cm tissue4
was reported to be4
downstream targets of p4
have been observed in4
the s protein was4
we set out to4
grown on glass coverslips4
with the mutant transcripts4
lungs were collected for4
antibody conjugated to alexa4
as shown in table4
g a grew to4
were added into each4
swine acute diarrhoea syndrome4
were harvested at h4
in a mouse model4
for h before infection4
inactivated fetal bovine serum4
adsorbed but not internalized4
the novel human betacoronavirus4
vero cells were pre4
calculated based on the4
the genome landscape of4
a newly discovered coronavirus4
virus titers were calculated4
s and s species4
is a representative of4
the nucleotide sequences of4
were prepared by freezing4
of pedv n proteins4
the same results were4
clone was fully stable4
and akt proteins in4
compared to the non4
or infected with prrsv4
the gds strain was4
than of the cells4
the annotations in the4
infection through direct interaction4
carried out using a4
a monolayer of vero4
kda protein similar to4
effects on the infection4
did not differ significantly4
the absence of serum4
suggested that the compound4
levels of intracellular viral4
cell monolayers were washed4
leader sequence derived from4
ypk possessed in vitro4
levels of viral rna4
antiviral effect of ribavirin4
diarrhea virus strains in4
is a determinant of4
that the s protein4
novel coronavirus from a4
and the monolayers were4
and the supernatant was4
antibody to the sars4
of asterisks indicate significant4
were expressed as the4
drug was added at4
of an african green4
activity of blfp crude4
the levels of phosphorylated4
extract were determined by4
studies on sv in4
the replication of prrsv4
and necrosis have been4
the supernatants were harvested4
that myricetin possessed anti4
in the supernatants of4
with the vero cell4
of the nucleocapsid protein4
l to infect ace4
of action of chloroquine4
cell infection by tgev4
near the catalytic centers4
in the design of4
inhibitors of cathepsin l4
were then infected with4
evaluated by western blot4
gene sequences of the4
a limited number of4
were confirmed by western4
recovery of infectious virus4
a dosage of mg4
with pbs and then4
ml per well of4
performed according to the4
produced in vero cells4
infectious virus could be4
the bac plasmid pbelobac4
a porcine epidemic diarrhea4
enzyme is a functional4
during serial passages in4
of pedv in vero4
and the infected cells4
for mouse hepatitis virus4
h prior to incubation4
two and four after4
potential emergence of resistant4
direct interaction with virus4
data are compared using4
hepatitis c virus rna4
infectious virus was recovered4
icpc a and coinfection4
of type i interferons4
rpoa gene sequence analysis4
the a protein of4
intracellular viral rna levels4
were washed twice in4
epidemic diarrhea virus into4
this graph is indicated4
infectious bronchitis virus and4
significant when data are4
into each well and4
blfp crude extract was4
of sars coronavirus infection4
growth kinetics of sars4
positive for both viruses4
apoptosis was observed in4
cell lines that are4