trigram

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

trigram	frequency
porcine epidemic diarrhea	2712
epidemic diarrhea virus	2217
of porcine epidemic	1231
in this study	447
porcine epidemic diarrhoea	385
the presence of	342
the united states	327
diarrhea virus in	324
transmissible gastroenteritis virus	319
the s protein	300
epidemic diarrhoea virus	279
of the s	267
the cells were	265
in the united	259
based on the	259
of the virus	235
of the pedv	232
in vero cells	230
according to the	217
as well as	210
of pedv in	195
for min at	190
vero cells were	188
the s gene	188
analysis of the	186
infected with pedv	180
in the s	178
as shown in	166
the detection of	166
of the porcine	165
for h at	162
the porcine epidemic	160
acute respiratory syndrome	158
severe acute respiratory	157
respiratory syndrome coronavirus	150
in the presence	149
for the detection	147
the expression of	146
was used to	145
diarrhea virus infection	141
due to the	140
pedv n protein	140
vero e cells	139
the number of	138
the present study	137
to determine the	136
porcine reproductive and	135
reproductive and respiratory	134
jung et al	134
and respiratory syndrome	133
pedv s protein	129
as described previously	129
diarrhea virus strains	126
respiratory syndrome virus	124
genome sequence of	124
in cell culture	121
at room temperature	121
epidemic diarrhea viruses	120
the role of	119
the small intestine	119
virus in the	118
phylogenetic analysis of	117
epidemic diarrhea in	116
showed that the	114
cells in the	114
complete genome sequence	113
data not shown	112
results showed that	111
observed in the	111
in suckling piglets	110
was used as	109
one of the	108
in order to	106
a total of	104
the pedv s	104
a and b	104
in the us	104
diarrhea virus strain	104
of pedv infection	103
was added to	103
detected in the	103
in the present	102
and characterization of	101
were used to	101
detection of porcine	100
the development of	99
compared to the	99
shown in fig	98
was detected in	98
sequence analysis of	96
sequences of the	95
of transmissible gastroenteritis	94
detection of pedv	94
the n protein	94
samples were collected	93
were infected with	91
were collected from	89
pedv and tgev	89
chen et al	88
the end of	88
associated with the	88
type i interferon	87
the results of	87
indicated that the	87
of pedv strains	87
the spike protein	87
as previously described	87
diarrhea virus and	86
compared with the	85
the spike gene	85
were incubated with	84
used as a	84
with diarrhea in	83
as described above	83
and phylogenetic analysis	83
emergence of porcine	83
it has been	83
virus and porcine	83
in the small	82
porcine respiratory coronavirus	81
of pedv and	81
of the spike	81
characterization of porcine	80
wang et al	80
diarrhea in swine	80
type i ifn	80
we found that	80
was performed using	79
the effect of	79
s and s	79
were observed in	79
pedv in the	79
strain of porcine	78
cells were washed	78
pedv infection in	77
protein of pedv	76
were inoculated with	76
the n gene	76
to that of	75
with porcine epidemic	75
associated with diarrhea	74
this study was	74
for h and	74
the orf gene	74
and porcine epidemic	74
three times with	74
porcine aminopeptidase n	73
was observed in	73
rna was extracted	73
in the spike	73
were treated with	72
intestinal epithelial cells	72
in the same	72
shown in figure	72
c for h	71
of the viral	71
than that of	71
of molecular epidemiology	71
in the field	70
in the usa	70
an important role	70
characterization of the	70
cells were infected	70
a new coronavirus	69
amino acid sequences	69
the results showed	68
cells were fixed	68
strains in the	68
li et al	68
analysis of porcine	68
us porcine epidemic	68
the absence of	68
tgev and pedv	68
s protein of	67
end of the	67
of this study	67
positive for pedv	67
related to the	67
cells were incubated	66
gastroenteritis virus and	66
has been reported	66
of a novel	66
to investigate the	66
isolation and characterization	66
washed three times	66
was used for	65
the authors declare	65
in our study	65
mouse hepatitis virus	65
sequence of a	65
in neonatal piglets	65
in the pedv	65
the replication of	64
were detected in	64
used in this	64
the use of	64
for porcine epidemic	64
particle associated with	63
important role in	63
infected vero cells	63
review of molecular	63
were subjected to	63
sequence of the	63
of type i	63
innate immune response	63
strain pc a	63
of pedv was	63
vero cells and	63
infected cells were	63
expression of the	62
hek t cells	62
cells infected with	62
and stored at	62
in south korea	62
the swine industry	62
g and g	62
a comprehensive review	62
comprehensive review of	62
there was no	62
at h post	62
deletion in the	62
and viral genomic	61
of the small	61
gene of porcine	61
involved in the	61
viral genomic sequences	61
found to be	61
that of the	61
the addition of	61
of the disease	61
song et al	61
prrsv and pedv	60
the amino acid	60
like particle associated	60
to evaluate the	60
in the infected	60
were positive for	60
clinical signs of	59
amino acid sequence	59
were obtained from	59
fetal bovine serum	59
against porcine epidemic	58
thermo fisher scientific	58
of pedv rna	58
the activation of	58
of viral rna	58
in the intestinal	58
were transfected with	58
for min and	57
the nucleocapsid protein	57
results indicated that	57
the complete genome	57
the amount of	57
the percentage of	57
none of the	57
mesenteric lymph nodes	56
experimental infection of	56
the family coronaviridae	56
demonstrated that the	56
new variants of	56
of icpc a	56
closely related to	56
found in the	56
in addition to	56
aminopeptidase n is	56
were used as	56
virus in china	55
variants of porcine	55
strain of pedv	55
significantly higher than	55
genes of porcine	55
strains of pedv	55
cells were transfected	55
by porcine epidemic	55
were collected at	55
a member of	55
the production of	55
domain of the	55
incubated for h	55
on the other	55
of vero cells	55
transmissible gastroenteritis coronavirus	54
development of a	54
used for the	54
of pedv n	54
of the n	54
the s and	54
of the study	54
and in the	54
the effects of	54
the levels of	54
revealed that the	53
s gene of	53
g for min	53
added to the	53
with pedv at	53
has been shown	53
the other hand	53
cells were then	53
characterization of a	53
in the cytoplasm	52
was carried out	52
in response to	52
s protein is	52
to pedv infection	52
been shown to	52
were purchased from	52
were stained with	52
present in the	52
virus spike protein	52
was found to	52
tbk and irf	52
linked immunosorbent assay	52
polymerase chain reaction	52
coronavirus spike protein	52
ma et al	51
activation of the	51
attenuated porcine epidemic	51
presence of pedv	51
diarrhea virus spike	51
role in the	51
the cell surface	51
of the orf	51
the samples were	50
in vitro and	50
pedv pl pro	50
cells were seeded	50
the vero cells	50
the positive control	50
western blot analysis	50
cells were treated	50
have been reported	50
o u r	49
a l p	49
lin et al	49
genbank accession no	49
region of the	49
outbreak of porcine	49
n a l	49
j o u	49
were analyzed by	49
located in the	49
member of the	49
u r n	49
used in the	49
of n protein	49
antiviral activity of	49
r n a	49
was confirmed by	49
inoculated with the	49
were fixed with	48
and incubated with	48
p r e	48
mutations in the	48
to those of	48
for the pedv	48
cells treated with	48
gene of pedv	48
were determined by	48
in gnotobiotic pigs	48
the infectivity of	48
l p r	48
o o f	48
r o o	48
was determined by	48
p r o	48
the surface of	47
with the pedv	47
was supported by	47
in vero e	47
the sensitivity of	47
in the absence	47
was extracted from	47
losses to the	47
the current study	47
s indel pedv	47
of a porcine	47
obtained from the	47
porcine circovirus type	47
with ml of	47
for detection of	47
in suckling pigs	47
similar to those	47
have been identified	46
in the n	46
the level of	46
care and use	46
pedv infection and	46
similar to that	46
the virulence of	46
were incubated for	46
the new ica	46
s protein was	46
evolution of pedv	46
pigs of all	46
kim et al	46
of neutralizing antibodies	46
all of the	46
during pedv infection	46
were carried out	46
with pbs and	46
jejunum and ileum	46
total rna was	45
added to each	45
of the genome	45
viruses isolated in	45
the pathogenesis of	45
shown in table	45
were cultured in	45
molecular characterization and	45
stevenson et al	45
the virus was	45
a role in	45
the negative control	45
of clinical signs	45
against pedv infection	45
three independent experiments	45
an outbreak of	45
similar to the	44
of all ages	44
negative for pedv	44
the pedv n	44
a variety of	44
of the two	44
of severe acute	44
spike gene of	44
to assess the	44
pedv rna in	44
is characterized by	44
virus strains in	44
clinical signs and	44
diarrhea virus from	44
by western blot	43
and vero cells	43
belongs to the	43
showed that pedv	43
times with pbs	43
human coronavirus e	43
that the pedv	43
n is a	43
blfp crude extract	43
pedv strains were	43
saif et al	43
were performed using	43
on porcine epidemic	43
is the first	43
sensitivity and specificity	43
and incubated at	43
and transmissible gastroenteritis	43
on the surface	43
results suggest that	43
classical attenuated vaccine	43
identified in the	43
well as the	42
multiplicity of infection	42
there were no	42
results of the	42
in the orf	42
the supernatant was	42
of pedv s	42
propagation of the	42
antibodies against pedv	42
expression levels of	42
authors declare that	42
between the two	42
c for min	42
variant porcine epidemic	42
the interaction between	42
receptor for the	42
the lack of	42
and incubated for	41
j cells were	41
pc a in	41
colostrum and milk	41
the fact that	41
is essential for	41
diarrhea in suckling	41
high mortality in	41
neutralizing antibodies against	41
and genotyping of	41
type i and	41
were washed with	41
protein is a	41
at the end	41
orally inoculated with	41
with or without	41
induced by ifn	41
a number of	41
viruses associated with	41
of a new	41
most of the	41
hofmann and wyler	41
collected from the	41
t cells were	41
the s domain	41
the pedv strains	41
results indicate that	41
african green monkey	41
the pedv genome	40
were found to	40
identification of the	40
those of the	40
genotyping of emergent	40
a porcine epidemic	40
open reading frame	40
emergent porcine epidemic	40
consistent with the	40
of pedv antigen	40
serum samples were	40
to determine whether	40
host innate immune	40
antibodies against the	40
of emergent porcine	40
huang et al	40
that pedv infection	40
can be used	40
pathogenesis and immunoprophylaxis	40
porcine transmissible gastroenteritis	40
have shown that	40
for the first	40
analysis was performed	40
green monkey kidney	40
infectious bronchitis virus	40
in contrast to	40
antibodies against porcine	39
the duration of	39
nucleocapsid protein of	39
with a large	39
conjugated goat anti	39
east respiratory syndrome	39
used as the	39
to porcine epidemic	39
n protein was	39
characterization and phylogenetic	39
infection of pigs	39
been reported in	39
the antiviral activity	39
cells were grown	39
at the same	39
found that the	39
igg and iga	39
were washed three	39
attenuated vaccine strains	39
was obtained from	39
in accordance with	39
diarrhea viruses associated	39
responsible for the	39
of antibodies against	39
for pedv and	39
were added to	39
pedv spike protein	39
suggest that the	39
of pedv is	38
differences in the	38
of porcine reproductive	38
epidemic diarrhea coronavirus	38
is associated with	38
specificity of the	38
shown to be	38
icpc a and	38
pedv strain cv	38
pcr products were	38
were incubated at	38
economic losses to	38
animal care and	38
sensitivity of the	38
on the cell	38
zhang et al	38
used to detect	38
the plates were	37
swine enteric coronavirus	37
of s protein	37
with fetal bovine	37
morbidity and mortality	37
be due to	37
the genus alphacoronavirus	37
park et al	37
min at room	37
piglets born to	37
strains of porcine	37
dried porcine plasma	37
with the disease	37
virus strain pc	37
virus of porcine	37
the emergence of	37
by centrifugation at	37
by western blotting	37
of us porcine	37
vero and ipec	37
to each well	37
a previous study	37
this work was	37
genome sequences of	37
the m protein	37
the virus of	37
of tgev and	37
complex evolution of	37
and complex evolution	37
and western blotting	37
a new porcine	37
isolated in korea	37
but not in	37
molecular epidemiology of	37
the disease outbreak	37
were significantly higher	37
distinct characteristics and	36
cov n proteins	36
middle east respiratory	36
the gene source	36
as the gene	36
the concentration of	36
were negative for	36
gene of the	36
protein of the	36
indicating that the	36
the first time	36
emerging and re	36
cd cd t	36
cloned into the	36
song and park	36
of porcine deltacoronavirus	36
feline infectious peritonitis	36
has not been	36
positive ec cells	36
cells were cultured	36
a functional receptor	36
characteristics and complex	36
and ch jx	36
diarrhea in cell	36
inoculated orally with	36
is involved in	36
s gene sequences	36
for the presence	36
conflict of interest	36
molecular characterization of	36
swine in the	36
of the new	36
gene source of	36
approved by the	36
the pedv spike	36
a negative control	36
and subjected to	35
disease outbreak among	35
and icpc a	35
in newborn piglets	35
kindly provided by	35
listed in table	35
rapid detection of	35
changes in the	35
outbreak among swine	35
infected with porcine	35
based on a	35
to identify the	35
pigs in the	35
belong to the	35
such as the	35
to be a	35
stage of infection	35
as a result	35
play a role	35
viral rna was	35
the cell culture	35
type i ifns	35
among swine in	35
pigs inoculated with	35
in the gut	35
the ability of	35
that they have	34
is an enveloped	34
the pedv strain	34
when compared to	34
cell lysates were	34
the recombinant s	34
the inhibition of	34
partial s gene	34
well tissue culture	34
functional receptor for	34
than in the	34
study was to	34
virus infection in	34
are shown in	34
of the piglets	34
coronaviruses as the	34
protein genes of	34
of pigs with	34
inoculated with pedv	34
recombinant s protein	34
is required for	34
deletions in the	34
data indicate that	34
the order nidovirales	34
were used for	34
innate immune responses	34
the innate immune	34
and n genes	34
and use committee	34
the phylogenetic tree	34
the viral genome	34
the s region	34
they have no	34
spike protein of	34
cells were harvested	34
intracellular extracts of	34
pedv rna was	34
were seeded in	34
e cells were	34
understanding of the	34
and avian coronaviruses	34
the formation of	34
suggesting that the	33
were expressed as	33
the intracellular extracts	33
and de bouck	33
infected suckling pigs	33
were similar to	33
isolation of porcine	33
to detect the	33
were grown in	33
indicate that the	33
the pig industry	33
adapted porcine epidemic	33
for the development	33
previous studies have	33
were found in	33
complete genome sequences	33
infected weaned pigs	33
in the study	33
first reported in	33
pigs infected with	33
the small intestines	33
cells were collected	33
in our laboratory	33
and sequence analysis	33
the spread of	33
porcine intestinal epithelial	33
economic losses in	33
diarrhea viruses isolated	33
pensaert and de	33
of the coronavirus	32
fecal samples were	32
sialic acid binding	32
small intestine of	32
was purchased from	32
days of age	32
inducing neutralizing antibodies	32
then infected with	32
depending on the	32
were collected and	32
the majority of	32
the efficacy of	32
piglets infected with	32
declare that they	32
plays an important	32
was significantly higher	32
pcd and vero	32
pedv field isolates	32
are expressed as	32
infection in the	32
balb c mice	32
be divided into	32
of a variant	32
pcr for the	32
losses in the	32
porcine enteric coronavirus	32
with a new	32
contribute to the	32
the detection limit	32
higher than that	32
on the s	32
well plates were	32
feed as a	32
plates were incubated	32
variant of porcine	32
supplemented with fetal	32
in a dose	32
causative agent of	32
with the s	32
these results indicated	32
cells were inoculated	32
different from the	32
institutional animal care	32
a large deletion	32
new variant of	32
is the most	31
to test the	31
to detect pedv	31
there is no	31
nucleotide sequences of	31
is critical for	31
vero cells in	31
described in the	31
s proteins of	31
occurred in the	31
vero cells with	31
lee et al	31
of the nucleocapsid	31
studies have shown	31
high levels of	31
detection of antibodies	31
capable of inducing	31
no significant differences	31
and the united	31
severe diarrhea and	31
piglets in the	31
the orf a	31
a in gnotobiotic	31
an emerging and	31
the host cell	31
resulted in a	31
bovine serum albumin	31
for pedv infection	31
at hpi and	31
fixed with paraformaldehyde	31
in the netherlands	31
be used to	31
the nucleotide sequence	31
expressed as the	31
that the virus	31
new porcine enteric	31
as a negative	31
the causative agent	31
after pedv infection	31
it is possible	31
and quantification of	31
this is the	31
epizootic swine virus	31
washed with pbs	31
a concentration of	31
in cell cultures	30
receptor for pedv	30
the result of	30
orf a and	30
and amino acid	30
large deletion in	30
the g b	30
caused by pedv	30
the s proteins	30
and high mortality	30
deduced amino acid	30
the virus in	30
viral rna in	30
swine enteric coronaviruses	30
differences between the	30
the function of	30
woo et al	30
negative control group	30
to confirm the	30
pathology of us	30
like strain of	30
pig farms in	30
the time of	30
at different time	30
the basis of	30
is a highly	30
the induction of	30
in pigs of	30
to the swine	30
gallien et al	30
in the vero	30
these results indicate	30
in the pig	30
been reported to	30
replication of pedv	30
were maintained in	30
and mortality in	30
on the basis	30
in the intestine	30
of pedv were	30
pigs with a	30
final concentration of	30
h and then	30
n protein is	30
the prevalence of	30
levels in the	30
with the same	29
work was supported	29
of the pigs	29
is responsible for	29
pedv belgorod dom	29
of the complete	29
jung and saif	29
samples collected from	29
presence of trypsin	29
the severe acute	29
detection and quantification	29
any of the	29
a variant porcine	29
the partial s	29
resulting in the	29
acid sequences of	29
in the current	29
min at rt	29
suggested that the	29
was first reported	29
this study were	29
samples were tested	29
pedv is a	29
liu et al	29
infection with the	29
significant economic losses	29
protein of porcine	29
and weaned pigs	29
need to be	29
different concentrations of	29
of the first	29
then incubated with	29
belonging to the	29
performed using the	29
pedv has been	29
pedv strains in	29
in agreement with	29
s t protein	29
needs to be	29
in the feces	29
a multiplicity of	29
a result of	29
in the swine	29
propagated in vero	29
were tested for	29
and pedv s	29
analysis based on	29
and the cells	29
cells were maintained	29
the severity of	29
weeks of age	29
in central china	29
orf a b	29
no competing interests	29
was removed and	29
cell cultures and	29
open reading frames	29
of the intestinal	29
with pedv and	28
amino acid changes	28
in which the	28
at an moi	28
sun et al	28
of the cell	28
n protein of	28
the infection of	28
cell culture medium	28
log copies ml	28
the onset of	28
the highly virulent	28
an moi of	28
for up to	28
the introduction of	28
in the serum	28
pedv was first	28
and gds strains	28
detection of the	28
outbreaks of porcine	28
diarrhoea virus in	28
gds and gds	28
is a functional	28
structure of the	28
is a major	28
lower than that	28
were detected by	28
vaccinated with the	28
the same time	28
has also been	28
at h after	28
a vero cell	28
small and large	28
of the three	28
with regard to	28
room temperature for	28
at the time	28
other pedv strains	28
there is a	28
pedv s gene	28
was detected by	28
a receptor for	28
united states porcine	28
are needed to	28
and evolution of	27
in serum and	27
in the early	27
highly virulent pedv	27
in figure a	27
virus porcine epidemic	27
is one of	27
plates were washed	27
was performed as	27
of the most	27
to investigate whether	27
of ped in	27
cells of the	27
and pedv were	27
and pathogenicity of	27
has been used	27
in the control	27
were analyzed using	27
infected with the	27
of the genus	27
villous epithelial cells	27
was found in	27
spike protein is	27
four structural proteins	27
old weaned pigs	27
the s glycoprotein	27
significant differences in	27
were able to	27
to analyze the	27
the natural host	27
virus and transmissible	27
cells transfected with	27
been identified in	27
in england in	27
identification of a	27
diarrhea and vomiting	27
difference in the	27
supernatants were collected	27
pigs at pid	27
the expression levels	27
vitro and in	27
and then incubated	27
of tbk and	27
is an important	27
was identified in	27
the proportion of	27
and the s	27
be associated with	27
i ifn production	27
than those of	27
at c for	27
cells were co	27
a and icpc	27
inhibition of pedv	27
to transmissible gastroenteritis	27
in the natural	27
were pretreated with	27
interferon production by	27
washed twice with	27
in recent years	27
orf gene of	27
those in the	27
rna was detected	27
detection limit of	27
and in vivo	27
antibody responses in	27
considered statistically significant	27
was performed to	27
diarrhea and dehydration	27
between pedv and	27
cv and lnct	27
the control group	26
results demonstrated that	26
at days post	26
hu et al	26
each group were	26
and porcine deltacoronavirus	26
the jejunum and	26
is possible that	26
cell culture isolation	26
of pedv to	26
epithelial cells of	26
spike protein genes	26
tissue culture plates	26
did not show	26
infectious peritonitis virus	26
log ge ml	26
of the four	26
transmission of pedv	26
like particles in	26
some of the	26
play an important	26
a pedv strain	26
g a and	26
these results suggest	26
levels of pedv	26
be involved in	26
protein in the	26
fragment length polymorphism	26
pedv infection of	26
accordance with the	26
s indirect elisa	26
comparison of the	26
strain with a	26
the epitope region	26
induced by pedv	26
activity of the	26
the course of	26
type iii interferon	26
positive control group	26
determination of the	26
disease in pigs	26
in the healthy	26
extracted from the	26
susceptible to pedv	26
paraformaldehyde for min	26
a review of	26
influenza a virus	26
of the samples	26
supported by the	26
has been demonstrated	26
no conflict of	26
s protein and	26
was able to	26
the pedv outbreak	26
virus in porcine	26
pedv infection was	26
and then infected	26
diarrhea in piglets	26
isolated from the	26
have no competing	26
coronavirus nucleocapsid protein	26
have been used	26
pcr was performed	26
cd t cell	26
carried out in	26
of diarrhea in	26
molecular evolutionary genetics	25
g a pedv	25
the specificity of	25
group a rotavirus	25
korean pedv field	25
pcr assay for	25
the in vitro	25
phylogenetic analysis based	25
pedv strains and	25
in southern china	25
determined to be	25
the immune response	25
the endoplasmic reticulum	25
and the results	25
characteristics of the	25
kweon et al	25
of the us	25
on vero cells	25
assays were performed	25
infection with pedv	25
part of the	25
apoptotic cell death	25
included in the	25
spread of the	25
could be detected	25
of each virus	25
by pedv infection	25
cells per well	25
genetic diversity of	25
of the partial	25
at a concentration	25
the possibility of	25
s gene and	25
in europe and	25
the m gene	25
were stored at	25
serial dilutions of	25
considered to be	25
amino acid mutations	25
region capable of	25
the pcr products	25
against the pedv	25
heat and rnase	25
positive and negative	25
been used to	25
for min to	25
molecular epidemiology and	25
severe watery diarrhea	25
hepatitis c virus	25
fcov type and	25
the aim of	25
against the porcine	25
summarized in table	25
to the s	25
different time points	25
acute pedv infection	25
mortality in piglets	25
restriction fragment length	25
porcine nidovirus infection	25
in china and	25
in a humidified	25
of the full	25
nsp and nsp	25
at rt and	25
indicated that pedv	25
of inducing neutralizing	25
evolutionary genetics analysis	25
korean pedv strains	25
of the infected	25
of pedv has	25
demonstrated that pedv	25
a recent study	25
calculated using the	24
of the viruses	24
as described in	24
proof of concept	24
presence of the	24
the lamina propria	24
mouth disease virus	24
strain isolated in	24
in pedv infection	24
presence or absence	24
different types of	24
in weaned pigs	24
the porcine apn	24
were performed in	24
crude extract containing	24
type iii ifn	24
virus in cell	24
at a multiplicity	24
prior to the	24
watery diarrhea and	24
of the host	24
all samples were	24
from each group	24
of the sars	24
oh et al	24
was assessed by	24
united states and	24
of pedv replication	24
pcr and western	24
by using the	24
study showed that	24
assay for the	24
porcine group a	24
the gastrointestinal tract	24
completion of the	24
culture supernatants were	24
virulence of pedv	24
after the first	24
differential detection of	24
the identification of	24
against pedv in	24
as a vehicle	24
of the recombinant	24
the supernatants were	24
like particles associated	24
sequencing of the	24
of the ifn	24
was defined as	24
neutralizing antibodies in	24
particles associated with	24
crystal structure of	24
of a recombinant	24
were blocked with	24
chang et al	24
cleavage of the	24
with paraformaldehyde for	24
korean field strains	24
the infected cells	24
the study of	24
pedv s proteins	24
porcine apn transgenic	24
us pedv strains	24
outbreaks of ped	24
was determined using	24
and approved the	24
at rt for	24
experiments were performed	24
for the simultaneous	24
or absence of	24
vero cell monolayers	24
assay was performed	24
pedv replication in	24
mortality in suckling	24
culture isolation and	24
tbk or irf	24
virus nucleocapsid protein	24
the nucleotide sequences	24
have not been	24
clinical signs were	24
the host innate	24
be used as	24
in north america	24
higher than those	24
performed as described	24
caused by porcine	24
the sars coronavirus	24
were tested in	24
the culture medium	23
using graphpad prism	23
higher than the	23
data indicated that	23
of the cells	23
the simultaneous detection	23
we investigated the	23
used to determine	23
a source of	23
ml of pedv	23
at a moi	23
intact s gene	23
neutralizing antibody titers	23
was performed in	23
the random forest	23
a final concentration	23
can be divided	23
was performed by	23
this study are	23
in terms of	23
an ion channel	23
was isolated from	23
and stained with	23
the genome of	23
china complete genome	23
with pedv strains	23
in infected cells	23
the coronaviridae family	23
i interferon production	23
of the outbreak	23
the loss of	23
was analyzed by	23
particles in japan	23
were then washed	23
entry into cells	23
with transmissible gastroenteritis	23
diagnosis of pedv	23
in the nucleus	23
the gds and	23
genetic characterization of	23
within the same	23
minimum essential medium	23
are listed in	23
a series of	23
and porcine respiratory	23
epidemiology of porcine	23
the proliferation of	23
of prrsv and	23
novel porcine epidemic	23
of the isolate	23
well plates and	23
insertions and deletions	23
reported in the	23
us pedv strain	23
a novel strain	23
culture medium was	23
the cellular receptor	23
emerging epizootic swine	23
the s subunit	23
compared to those	23
porcine enteric coronaviruses	23
of the assay	23
a and g	23
as determined by	23
of peptide h	23
relationship between the	23
the ica kit	23
is a member	23
function of the	23
have been developed	23
insights into the	23
was performed with	23
epitope region capable	23
on pedv replication	23
the release of	23
significantly lower than	23
no effect on	23
positive cells in	23
the vero cell	23
of the same	23
and orf b	23
n gene of	23
outbreak of swine	23
ranging from to	23
that the s	23
immune response in	23
antibodies were detected	23
sequence of porcine	23
is important for	23
the day of	23
could not be	23
in china in	23
obtained from a	23
by indirect elisa	23
and immunogenicity of	23
of the epitope	23
be related to	22
and analysis of	22
of the trial	22
to explore the	22
at the indicated	22
statistical analysis was	22
of aminopeptidase n	22
could be used	22
in the p	22
acid binding activity	22
the importance of	22
to be the	22
prior to farrowing	22
the entire genome	22
huge economic losses	22
approved the final	22
mucosal and systemic	22
as seen in	22
similar to us	22
the us strains	22
was propagated in	22
the cytoplasm of	22
authors declare no	22
of infected cells	22
an intact s	22
the survival of	22
can be found	22
cellular receptor for	22
and attenuation of	22
to amplify the	22
pedv specific siga	22
new syndrome of	22
for clinical signs	22
states porcine epidemic	22
infection of pedv	22
antibodies in serum	22
m and n	22
of suckling piglets	22
first time in	22
removed and the	22
a moi of	22
the heat and	22
divided into two	22
and rnase treated	22
with a high	22
into vero cells	22
suckling and weaned	22
more than of	22
of a vero	22
spread of porcine	22
in the dark	22
and western blot	22
nk cell activity	22
to examine the	22
the plasma membrane	22
of vero cell	22
diarrhea in china	22
swine farms in	22
prior to inoculation	22
was applied to	22
diarrhea virus date	22
was calculated using	22
duration of the	22
the risk of	22
s or s	22
the in vivo	22
mortality in neonatal	22
syndrome of porcine	22
the reemerging korean	22
multiple sequence alignment	22
analysis showed that	22
because of the	22
all pigs were	22
differentially expressed genes	22
pedv at a	22
than that in	22
fecal viral rna	22
in the jejunum	22
united states in	22
were euthanized at	22
gerber et al	22
adaptation in vitro	22
circulating in the	22
nk cell frequencies	22
or s t	22
associated with coronavirus	22
the pathogenicity of	22
evaluation of a	22
reported to be	22
genbank accession number	22
to study the	22
is shown in	22
used as an	21
b and c	21
the pedv coronavirus	21
in fecal samples	21
s domain of	21
was reported in	21
an evaluation of	21
ohio state university	21
were harvested and	21
cells were pre	21
of the protein	21
analysis of orf	21
from three independent	21
to us strains	21
were located in	21
found that pedv	21
were isolated from	21
in the family	21
of swine diarrhea	21
g b strains	21
rectal swabs were	21
no significant difference	21
the interaction of	21
study demonstrated that	21
ec cells in	21
type iii ifns	21
virus shedding in	21
outbreak of diarrhea	21
pedv n and	21
clarified by centrifugation	21
focused on the	21
was shown to	21
proteins in the	21
apn transgenic mice	21
and large intestines	21
serial propagation of	21
the ohio state	21
source of the	21
a and orf	21
growth adaptation in	21
gilts and sows	21
of porcine circovirus	21
virulence in vivo	21
pedv in vero	21
blood samples were	21
we demonstrated that	21
was based on	21
virus strains similar	21
strains similar to	21
signs of diarrhea	21
could be a	21
on pedv infection	21
in serum samples	21
the first report	21
tissue culture infectious	21
suggests that the	21
in situ hybridization	21
of cell culture	21
our results showed	21
pigs at pids	21
are presented as	21
of s proteins	21
pedv s or	21
of the different	21
were visualized using	21
the viral envelope	21
of porcine enteric	21
is consistent with	21
to the pedv	21
were used in	21
may not be	21
of the authors	21
and orf genes	21
herpes simplex virus	21
primers and probes	21
be detected in	21
antibodies in the	21
discovery of a	21
portion of the	21
of pedv on	21
immune responses to	21
into three groups	21
that in the	21
between the pedv	21
of q r	21
in vitro prophylactic	21
of pedv strain	21
ml of the	21
fcov type s	21
in ml of	21
virus and its	21
on the pedv	20
related porcine epidemic	20
in the host	20
the suppression of	20
analysis of genetically	20
in the cells	20
crypt epithelial cells	20
and fecal samples	20
are summarized in	20
type associated with	20
genetically diverse us	20
analysis indicated that	20
tgev and prcv	20
the pedv infection	20
cells were pretreated	20
in each group	20
were washed twice	20
characterized by vomiting	20
in the cell	20
piglets in group	20
the final manuscript	20
mortality rates in	20
activity of pedv	20
the vaccine strain	20
of pedv pl	20
the type i	20
of genetically diverse	20
high mortality rates	20
divided into four	20
spread of pedv	20
human immunodeficiency virus	20
pedv is an	20
field strains by	20
were mixed with	20
and pathogenesis of	20
the icpc a	20
are involved in	20
including a novel	20
terminus of the	20
the most abundant	20
induced by the	20
diarrhea of a	20
which is the	20
to the us	20
the small and	20
with bovine serum	20
apparently new syndrome	20
isolation and sequence	20
the structural proteins	20
were orally inoculated	20
in pbs for	20
diverse us porcine	20
shown that the	20
was first detected	20
was subjected to	20
transfected with the	20
s protein in	20
inhibited pedv infection	20
of the fusion	20
the sequences of	20
culture infectious dose	20
villous atrophy in	20
development of an	20
treated with the	20
swine diarrhea of	20
provided by the	20
an apparently new	20
the vaccine strains	20
to the pig	20
the mechanisms of	20
to those in	20
of this virus	20
and functional characterization	20
due to its	20
replication in the	20
pc a strain	20
serum and colostrum	20
cov pl pro	20
diarrhea in canada	20
and used for	20
the presence or	20
swine fever virus	20
cells were lysed	20
debouck and pensaert	20
cell adapted porcine	20
sequences of pedv	20
analyses were performed	20
novel strain with	20
and infected with	20
analyses of the	20
regions of the	20
serum samples from	20
entry of porcine	20
sequence of pedv	20
complete s gene	20
strains including a	20
suckling pigs had	20
the ability to	20
large number of	20
length polymorphism analysis	20
diarrhea virus by	20
of innate immune	20
virus strains including	20
genomic rna and	20
in nursing piglets	20
new ica was	20
simultaneous detection and	20
with other pedv	20
it is also	20
nucleotide sequence of	20
survival of pedv	19
expression level of	19
with the virus	19
h prior to	19
in us swine	19
alphacoronavirus and betacoronavirus	19
and the other	19
results suggested that	19
by restriction fragment	19
diarrhea virus dr	19
mrna levels of	19
there was a	19
and g b	19
introduction of pedv	19
data were analyzed	19
swine porcine epidemic	19
the sequence of	19
contaminated complete feed	19
to be an	19
antiviral activity against	19
with the virulent	19
ion channel protein	19
was measured by	19
serum samples collected	19
virulent strain of	19
the results were	19
differentiation of a	19
gammacoronavirus and deltacoronavirus	19
leading to the	19
from korean field	19
piglets from the	19
of alphacoronavirus and	19
with virulent pedv	19
in of the	19
of ch jx	19
the dna damage	19
were collected for	19
was identified as	19
to the nucleus	19
spike glycoprotein gene	19
korean field isolates	19
with an intact	19
transferred to a	19
which is a	19
in porcine intestinal	19
with the n	19
review of current	19
modified eagle medium	19
and negative controls	19
viral rna shedding	19
in the genus	19
large numbers of	19
lower than those	19
diseases of swine	19
epithelial cells and	19
original us pedv	19
propagation of porcine	19
of pedv with	19
de arriba et	19
in pregnant sows	19
of attenuated porcine	19
and sg mrna	19
after infection with	19
seen in figure	19
the intestinal mucosa	19
strains by restriction	19
the evolution of	19
of pedv from	19
our previous study	19
to elucidate the	19
been identified as	19
to understand the	19
and cloned into	19
early stage of	19
of current epidemiology	19
infection in pigs	19
the us and	19
carvajal et al	19
and centrifuged at	19
virus from korean	19
diarrhoea virus and	19
of mouse hepatitis	19
terminal region of	19
of pedv nsp	19
incubated with pedv	19
the feces of	19
the genus deltacoronavirus	19
arriba et al	19
of pdcov in	19
to each other	19
nucleotide and amino	19
the korean pedv	19
a cellular receptor	19
a highly contagious	19
to the nucleolus	19
diarrhea virus field	19
of the reemerging	19
and that the	19
the mixture was	19
amino acid residues	19
for an additional	19
as a template	19
vero cell adapted	19
h at c	19
and available vaccines	19
not significantly different	19
epidemiology and available	19
during the first	19
read and approved	19
polymorphism analysis of	19
is a type	19
in the ipec	19
rna in serum	19
acute diarrhea in	19
than those in	19
tcid ml of	19
the virus and	19
pedv and the	19
was first identified	19
swabs were collected	19
was significantly lower	19
vero cells grown	19
funded by the	19
incubated for min	19
of s gene	19
a type i	19
was to determine	19
resulted in the	19
at and dpi	19
pigs porcine epidemic	19
pedv reference strains	19
of sows with	19
in this group	19
the s indel	19
inhibitory effects of	19
of hnrnp a	19
were cloned into	19
current epidemiology and	19
in the future	19
further studies are	19
diarrhea virus porcine	19
is the main	19
epidemic diarrhoea coronavirus	19
based on these	19
the detection and	19
of virulence in	19
prevention and control	19
of other coronaviruses	19
caused by a	18
indicates that the	18
a cause of	18
attenuation of virulence	18
polyacrylamide gel electrophoresis	18
the coronavirus spike	18
role of the	18
claims in published	18
remains neutral with	18
surface s proteins	18
daily for clinical	18
and serial propagation	18
hou et al	18
were measured by	18
each of the	18
to jurisdictional claims	18
in published maps	18
pedv rna shedding	18
had the highest	18
of the sows	18
the mortality rate	18
were inoculated orally	18
was similar to	18
arch virol doi	18
that n protein	18
weaned pigs at	18
s and n	18
of amino acids	18
difference between the	18
of blfp crude	18
would like to	18
replaced with fresh	18
nature remains neutral	18
of sars coronavirus	18
the assay was	18
limit of the	18
diarrhea in pigs	18
maps and institutional	18
substantial economic losses	18
length s gene	18
that can be	18
the regulation of	18
a critical role	18
were considered statistically	18
the difference in	18
in significant economic	18
research and development	18
vero cell attenuated	18
the beginning of	18
with different concentrations	18
in both the	18
n protein and	18
isolation and serial	18
neutral with regard	18
to the cytoplasm	18
vero cells at	18
and treated with	18
each well and	18
h at room	18
functional characterization of	18
were no significant	18
during the early	18
that pedv entry	18
studies showed that	18
vero cells infected	18
than of the	18
of fcov type	18
terminal domain of	18
vlasova et al	18
the virus is	18
infection with a	18
the viral rna	18
c in a	18
the cv strain	18
and g a	18
identified as the	18
assays for the	18
germany and the	18
cells as described	18
the membrane was	18
under field conditions	18
the activity of	18
inoculated gn pigs	18
results revealed that	18
the united kingdom	18
to the genus	18
the university of	18
the intestinal contents	18
and institutional affiliations	18
of the gene	18
gene in the	18
induction of neutralizing	18
and partial characterization	18
targeted rna recombination	18
in spike protein	18
of the animals	18
evaluation of the	18
of global porcine	18
the inoculum was	18
jurisdictional claims in	18
extracts of ln	18
with growth adaptation	18
diarrhea viruses from	18
using monoclonal antibodies	18
s proteins were	18
amount of pedv	18
virus is a	18
glycoprotein gene of	18
for pedv detection	18
in the g	18
from the united	18
in piglets in	18
europe and asia	18
to determine if	18
virulence of the	18
the piglets were	18
by reverse transcription	18
against the s	18
and permeabilized with	18
analysis of a	18
jnk and erk	18
comparison of porcine	18
of the virulent	18
these data indicate	18
tryptose phosphate broth	18
structural and functional	18
piglets less than	18
contributed to the	18
of these viruses	18
in pigs and	18
was present in	18
experimentally infected with	18
to the editor	18
sodium dodecyl sulfate	18
severe clinical signs	18
vero cells as	18
mammalian and avian	18
the possibility that	18
as a cause	18
the impact of	18
in pedv infected	18
infected vero e	18
inhibitory effect of	18
this suggests that	18
severe atrophic enteritis	18
an indirect elisa	18
published maps and	18
onset of clinical	18
were confirmed by	18
in cultured cells	18
replication and pathogenesis	18
as a receptor	18
indel pedv strain	18
for pedv rna	18
supernatants were harvested	18
cell entry of	18
are associated with	18
aminopeptidase n and	18
antigenic relationships among	18
regard to jurisdictional	18
yuan et al	18
pedv at an	18
the cell lysates	18
to verify the	18
the findings of	18
mediated by the	18
cells were detected	18
virus in south	18
springer nature remains	18
at dpi and	18
pedv strains from	18
the disease was	18
endoplasmic reticulum stress	18
a class i	18
global porcine epidemic	18
heterogeneity in spike	18
first identified in	18
a vehicle for	18
partial characterization of	18
pedv replication and	18
cells were stained	18
identified in this	18
of the entire	18
data suggest that	18
serve as a	18
been shown that	18
and the pedv	18
s genes of	18
of diarrhea and	18
could be observed	17
the cleavage of	17
viral replication in	17
are shown as	17
to the family	17
is known to	17
or infected with	17
using vero cells	17
in a previous	17
equal volume of	17
from the same	17
cultures and partial	17
currently circulating in	17
veterinary diagnostic laboratory	17
role of transportation	17
vitro and attenuation	17
detection of transmissible	17
blocked with bovine	17
the porcine aminopeptidase	17
significant difference between	17
in amino acid	17
bat coronaviruses as	17
up to days	17
pan et al	17
with those of	17
interfere with the	17
in comparison with	17
after inoculation with	17
virus shedding and	17
was performed on	17
associated with porcine	17
i and type	17
class i virus	17
and evaluation of	17
to the original	17
china isolation and	17
identity with the	17
were as follows	17
cells and ipec	17
source of alphacoronavirus	17
collected at hpi	17
yc pedv strain	17
infection in vero	17
is a class	17
is not a	17
that there were	17
prevent and control	17
to weaned pigs	17
content of the	17
associated with growth	17
that pedv is	17
and has been	17
large amounts of	17
supports bat coronaviruses	17
limit of detection	17
like to thank	17
in the virus	17
gene and the	17
of pedv by	17
outbreak of pedv	17
cd t cells	17
dmem supplemented with	17
diarrhea virus nucleocapsid	17
and type iii	17
levels of the	17
compared with ifn	17
the two pedv	17
i virus fusion	17
the proteins were	17
immune responses by	17
and molecular epidemiology	17
protective efficacy of	17
orf genes of	17
were then incubated	17
the application of	17
avian coronaviruses in	17
discovery of seven	17
associated lymphoid tissues	17
is necessary to	17
performed in triplicate	17
and analyzed by	17
coronavirus spike proteins	17
of gammacoronavirus and	17
were selected for	17
were centrifuged at	17
with pedv in	17
a fluorescence microscope	17
at least one	17
was mixed with	17
and further sequence	17
of pedv into	17
hematoxylin and eosin	17
was calculated as	17
and s t	17
enteric disease in	17
corresponding to the	17
virus was detected	17
observed between the	17
of seven novel	17
quantification of transmissible	17
determined by a	17
rt for min	17
source of gammacoronavirus	17
avian coronaviruses as	17
relative to the	17
further sequence analysis	17
by the addition	17
with each other	17
novel mammalian and	17
in the nucleolus	17
reported that the	17
were challenged with	17
from germany and	17
virulent pedv strain	17
contribution of the	17
deltacoronavirus supports bat	17
and can be	17
g b pedv	17
of cellular cholesterol	17
and comparison of	17
log tcid ml	17
in asia and	17
real time rt	17
the virus to	17
genome copies ml	17
absence of trypsin	17
level of the	17
higher in the	17
compared to that	17
epithelium of the	17
only a few	17
the invasion rates	17
high morbidity and	17
porcine alveolar macrophages	17
coronaviruses in the	17
cell attenuated porcine	17
protection against pedv	17
pedv infection is	17
rna in the	17
the transmissible gastroenteritis	17
in pigs in	17
supported by a	17
s t proteins	17
natural feeding behavior	17
confirmed that the	17
n protein with	17
virus fusion protein	17
followed by cycles	17
strains from the	17
addition to the	17
of pigs in	17
aim of this	17
for the duration	17
virus in italy	17
insight into the	17
samples stored at	17
for viral replication	17
used to amplify	17
the clinical signs	17
performed using a	17
madson et al	17
encodes an ion	17
inoculated with a	17
at pids and	17
the p group	17
pigs compared to	17
response to pedv	17
h at rt	17
and betacoronavirus and	17
to develop a	17
thought to be	17
epidemiology of pedv	17
to the global	17
in the viral	17
the membranes were	17
cells grown in	17
to the control	17
inoculum was removed	17
fecal samples from	17
was kindly provided	17
infectivity of pedv	17
the cytoplasm and	17
viruses from germany	17
vaccines for porcine	17
the early stage	17
in the pathogenesis	17
western blotting analysis	17
was added and	17
pedv and pdcov	17
on day post	17
vaccines have been	17
virus strain from	17
seven novel mammalian	17
to compare the	17
the culture supernatants	17
authors read and	17
essential for the	17
characterized by acute	17
cloning and further	17
betacoronavirus and avian	17
immune responses in	17
virus titers were	17
from the us	17
was collected from	17
of pedv hljby	17
in europe in	17
of this article	17
required for the	16
the reciprocal of	16
that there is	16
were present in	16
numbers of pedv	16
the proportions of	16
protein and the	16
number of pigs	16
the fusion core	16
disease characterized by	16
coe and rlppg	16
numbers of serotonin	16
phylogenetic trees were	16
and found that	16
effects of the	16
vet res doi	16
s gene were	16
fusion of the	16
stranded rna virus	16
and cultured in	16
been reported that	16
as the reciprocal	16
in the previous	16
western blot and	16
in group were	16
signs of ped	16
debouck et al	16
evolution of the	16
diarrhoea caused by	16
as a control	16
pedv infection by	16
binding to the	16
medium supplemented with	16
be used for	16
hpi and hpi	16
and genetic characterization	16
of three independent	16
not detected in	16
the mesenteric lymph	16
and specificity of	16
a novel porcine	16
that pedv nsp	16
were separated by	16
in swine porcine	16
a lack of	16
targeting the s	16
within the s	16
nuclei were stained	16
that did not	16
fusion core complex	16
h after transfection	16
the recombinant protein	16
determined by the	16
in conventional pigs	16
of the order	16
pedv strain pc	16
pbs for min	16
amino acid positions	16
all authors read	16
at pid and	16
and cells were	16
as a source	16
h post infection	16
letter to the	16
in the negative	16
coronavirus related to	16
studies are needed	16
murine hepatitis virus	16
rna genome of	16
the sialic acid	16
were measured using	16
suggested that pedv	16
of the data	16
and then the	16
it can be	16
porcine deltacoronavirus in	16
seven open reading	16
an equal volume	16
of the proteins	16
virus replication in	16
infectivity of icpc	16
in the sera	16
groups a and	16
were calculated using	16
a consequence of	16
contaminated feed as	16
apn positive cells	16
prrsv or pedv	16
regulates virus production	16
but not the	16
virus infection and	16
the results indicated	16
pedv g b	16
and pedv infection	16
the analysis of	16
was lower than	16
of the inoculated	16
virus infection of	16
strains isolated in	16
cells with pedv	16
pl pro s	16
were consistent with	16
swine industry in	16
phosphate buffered saline	16
and used as	16
science and technology	16
was approved by	16
the results are	16
the structure of	16
by cycles of	16
was expressed as	16
fecal virus shedding	16
defined as the	16
genbank accession numbers	16
strains have been	16
epithelial cell line	16
watery diarrhea in	16
virus associated with	16
revealed that pedv	16
along with the	16
channel protein and	16
data showed that	16
in south china	16
had no effect	16
diarrhea virus genome	16
across the country	16
increase in the	16
to be more	16
the inhibitory effects	16
high mortality rate	16
such as pedv	16
old piglets were	16
for at least	16
of the experiment	16
epidemic of diarrhoea	16
in viral replication	16
monitored daily for	16
strains in china	16
is based on	16
virus replication and	16
not in the	16
diarrhea virus isolate	16
of spike gene	16
proteolytic cleavage of	16
phylogenetic tree was	16
the nucleus and	16
twice with pbs	16
deposited in genbank	16
were determined using	16
n protein in	16
that pedv n	16
was visualized using	16
rate of the	16
was evaluated by	16
apn negative cells	16
with cell culture	16
and control groups	16
the titer of	16
the binding of	16
variant strain of	16
using trizol reagent	16
protein gene of	16
with some modifications	16
immune response to	16
infected or infected	16
with bound tgev	16
pedv classical attenuated	16
be responsible for	16
was replaced with	16
of two novel	16
until the end	16
and serum samples	16
divided into three	16
positive cells were	16
and vaccine strains	16
and control of	16
attenuated vaccine strain	16
the pigs were	16
length genome sequence	16
to control the	16
infection of vero	16
pedv entry into	16
a cell culture	16
the mechanism of	16
pedv antibodies in	16
was not detected	16
critical role in	16
the duplex rt	16
the occurrence of	16
in the colostrum	16
of diarrhoea caused	16
the piglets in	16
sows with a	16
were exposed to	16
of the other	15
concentrations of the	15
a nitrocellulose membrane	15
been used as	15
antiviral innate immune	15
the source of	15
the crude extract	15
involved in pedv	15
of the villi	15
cv and dr	15
titer in the	15
pedv strains at	15
infected with a	15
the inhibitory effect	15
rna and sg	15
as a viral	15
a final extension	15
of virus shedding	15
to our knowledge	15
of pedv field	15
parts of the	15
a virulent pedv	15
for rapid detection	15
in all groups	15
in the gastrointestinal	15
nucleotide sequence identity	15
the origin of	15
novel swine enteric	15
of transportation in	15
and regulates virus	15
and application of	15
the plate was	15
pedv and other	15
the content of	15
the partial spike	15
vaccine strain cv	15
the host cells	15
after washing with	15
of less than	15
for h prior	15
caused by the	15
in a single	15
derived from the	15
for induction of	15
weaned pigs had	15
has shown that	15
and porcine group	15
proteolytic activation of	15
and virulence of	15
of human coronavirus	15
graphpad prism software	15
tested in the	15
clinical disease and	15
orally immunized with	15
may be a	15
virulent pedv strains	15
epitopes of the	15
proteins have been	15
genome of the	15
specificity and sensitivity	15
values of the	15
times with pbst	15
shown in the	15
immune response against	15
c for s	15
of the method	15
sense rna virus	15
method for the	15
pigs had significantly	15
and protective efficacy	15
the differences between	15
density to porcine	15
used to infect	15
as vaccine candidate	15
the molecular epidemiology	15
gene expression of	15
were observed between	15
indirect elisa was	15
role in pedv	15
in the regulation	15
innate immune system	15
first detected in	15
the us in	15
epidermal growth factor	15
p and p	15
was conducted using	15
in the development	15
from the pedv	15
in the lamina	15
activation of nf	15
in spread of	15
filtered through a	15
region of pedv	15
reciprocal of the	15
together with the	15
pedv isolates and	15
of the negative	15
basis for the	15
new insights into	15
i and iii	15
on ice for	15