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
porcine epidemic diarrhea virus253
of transmissible gastroenteritis virus157
in the presence of102
porcine reproductive and respiratory97
reproductive and respiratory syndrome96
of transmissible gastroenteritis coronavirus95
of porcine epidemic diarrhea89
porcine transmissible gastroenteritis virus87
and respiratory syndrome virus83
of the s protein70
severe acute respiratory syndrome67
cells were transfected with58
for the detection of58
of porcine transmissible gastroenteritis55
transmissible gastroenteritis virus and54
as shown in fig53
in the absence of52
an important role in51
cells were infected with51
feline infectious peritonitis virus51
of mouse hepatitis virus48
the results showed that48
were infected with tgev47
in the present study46
and porcine respiratory coronavirus45
washed three times with43
on the surface of41
to transmissible gastroenteritis virus40
the transmissible gastroenteritis virus40
acute respiratory syndrome coronavirus38
gastroenteritis virus and porcine37
in the united states37
the s protein of37
cells were incubated with36
cells were treated with36
was used as a36
used in this study34
for min at room34
min at room temperature34
a member of the34
were washed three times33
s and g m33
porcine epidemic diarrhoea virus33
has been shown to32
coronavirus transmissible gastroenteritis virus32
transmissible gastroenteritis virus in32
play an important role32
of porcine respiratory coronavirus32
epidemic diarrhea virus in32
cells infected with tgev31
transmissible gastroenteritis virus infection31
of the s gene31
detection of transmissible gastroenteritis31
infected with tgev at29
the presence of the29
hek t cells were28
it has been shown28
the end of the28
in the small intestine28
as a receptor for28
play a role in28
related to transmissible gastroenteritis27
in the case of27
with transmissible gastroenteritis virus27
aminopeptidase n is a27
and transmissible gastroenteritis virus27
epidemic diarrhea virus and26
in the regulation of26
the coronavirus transmissible gastroenteritis26
with fetal bovine serum26
total rna was extracted25
epidermal growth factor receptor25
results showed that the25
of porcine reproductive and25
at room temperature for25
loss of enteric tropism24
studies have shown that24
work was supported by24
cells were fixed with24
transmissible gastroenteritis of swine24
the molecular biology of24
avian infectious bronchitis virus24
on the basis of24
the tgev s protein24
from transmissible gastroenteritis virus24
coronavirus infectious bronchitis virus24
of feline infectious peritonitis24
these results suggest that24
has been shown that23
for min at rt23
coronavirus mouse hepatitis virus23
of antibody binding to23
the loss of enteric23
the expression levels of23
was significantly higher than23
molecular biology of coronaviruses23
three times with pbs23
as well as the23
this work was supported23
in the s protein22
of severe acute respiratory22
in the s gene22
sialic acid binding activity22
and porcine epidemic diarrhea22
incubated for h at22
porcine transmissible gastroenteritis coronavirus22
in transmissible gastroenteritis virus22
under the control of21
plays an important role21
sequence analysis of the21
these results indicate that21
gene of transmissible gastroenteritis21
is a member of20
antibody binding to the20
complete genome sequence of20
we found that tgev20
of tgev and prcv20
transmissible gastroenteritis in pigs20
of the leader rna20
at an moi of20
a multiplicity of infection20
of the coronavirus transmissible20
of the m protein20
and g m phases20
virus and porcine respiratory20
in vitro and in20
at a multiplicity of20
important role in the19
at the same time19
the cells were washed19
of three independent experiments19
of tgev and pedv19
supplemented with fetal bovine19
on the cell surface19
cell cycle arrest and19
protein of transmissible gastroenteritis19
the control of the19
coronavirus related to transmissible19
between tgev and prcv19
transmissible gastroenteritis virus by19
and then incubated with19
there was no significant18
have been shown to18
found that tgev infection18
we found that the18
in the tgev group18
the degree of antibody18
antigenic sites of the18
virus and porcine epidemic18
degree of antibody binding18
the sequence of the18
related porcine respiratory coronavirus18
nucleotide sequence of the18
at different time points18
end of the genome18
gastroenteritis virus infection induces17
that tgev infection induced17
fixed with paraformaldehyde for17
was no significant difference17
the porcine transmissible gastroenteritis17
were fixed with paraformaldehyde17
n protein of tgev17
of the tgev s17
was found to be17
than that in the17
vitro and in vivo17
of the genomic rna17
rna was extracted from17
are shown in table17
ingezim corona diferencial elisa17
a and orf b17
of a porcine respiratory17
cycle arrest and apoptosis17
for the expression of17
similar to those of17
of the cell cycle16
the sialic acid binding16
at the end of16
the tgev m protein16
expressed in transgenic plants16
absence of e protein16
mouse hepatitis virus strain16
against transmissible gastroenteritis virus16
cells were washed with16
significantly higher than that16
a major receptor for16
four major antigenic sites16
with paraformaldehyde for min16
of the transmissible gastroenteritis16
cells were pretreated with16
of the small intestine16
orf a and orf16
been shown to be16
the s protein is16
were washed twice with16
the structure of the16
detection of porcine epidemic16
structure of transmissible gastroenteritis16
in this study were16
ileum and colon epithelial16
higher than that of16
from three independent experiments16
of p and jnk15
are shown in fig15
induced by tgev infection15
the authors declare that15
in the loss of15
transcription of tgev gene15
pathogenesis of transmissible gastroenteritis15
the detection limit of15
of the spike protein15
in addition to the15
has been reported to15
hepatitis virus strain a15
is a receptor for15
the presence of a15
was added to each15
it is possible that15
of the porcine transmissible15
in cells infected with15
and incubated for h15
n is a major15
porcine intestinal epithelial cells15
that tgev n protein15
is a major receptor15
cells were cotransfected with15
with the exception of15
the development of a15
of porcine epidemic diarrhoea15
cells treated with lp15
and colon epithelial cells15
major receptor for the15
dna and rna viruses14
j cells treated with14
with tgev for h14
purdue strain of tgev14
showed that tgev infection14
the expression of the14
than that of the14
as shown in figure14
cells were grown in14
added to each well14
h at room temperature14
in a co incubator14
a transmissible gastroenteritis in14
swine transmissible gastroenteritis virus14
on the other hand14
cells were washed three14
with porcine respiratory coronavirus14
was added to the14
the s gene of14
for mouse hepatitis virus14
of the virus in14
the porcine epidemic diarrhea14
were detected in the14
a functional receptor for14
activation of p signaling14
middle east respiratory syndrome14
higher than that in14
our results showed that14
porcine epidemic diarrhea in14
the spike gene of14
the epidermal growth factor14
infected cells per well14
infected with tgev for14
the sensitivity of the14
for h at room14
the leader rna sequence14
for porcine epidemic diarrhea14
the level of p14
were washed with pbs14
have shown that the14
the detection of tgev13
was observed in the13
of apn positive cells13
play important roles in13
these results suggested that13
declare that they have13
that they have no13
of the n gene13
is a functional receptor13
and systemic immune responses13
to that of the13
the ingezim corona diferencial13
cells were cultured in13
the tips of the13
to those of the13
for the development of13
were found to be13
is involved in the13
tgev and prcv strains13
authors declare that they13
be involved in the13
binding of tgev to13
the nature of the13
was supported by the13
is not required for13
amino acid changes at13
with tgev at moi13
were performed as described13
induces cell cycle arrest13
passages in tissue culture13
acid changes at the13
induced cell cycle arrest13
swinecheck tgev prcv recombinant13
virus and transmissible gastroenteritis13
similar to that of13
cells infected with rtgev13
the coronavirus infectious bronchitis13
coe and rlppg f13
incubated for min at13
enteric tropism and virulence13
of the porcine epidemic13
the course of the13
the spike protein of13
activation of p mapk12
cv vero adapted strain12
that in the tgev12
tgev at an moi12
monoclonal antibodies to the12
the absence of e12
transmissible gastroenteritis virus of12
pigs inoculated with tgev12
washed with pbs and12
the detection of porcine12
at the time of12
the m protein is12
cells with bound tgev12
was lower than that12
is a determinant of12
the leader rna and12
coronaviruses as the gene12
amino acid sequences of12
cd cd t cells12
as the gene source12
pellet was resuspended in12
the surface of the12
was performed as described12
in agreement with the12
were incubated with tgev12
against transmissible gastroenteritis coronavirus12
the svanovir tgev prcv12
the villous enterocytes of12
the gene source of12
transmissible gastroenteritis coronavirus is12
of tgev n protein12
is responsible for the12
the m protein of12
in contrast to the12
s protein of tgev12
were incubated for h12
as a negative control12
critical epitopes in transmissible12
performed as described previously12
epitopes in transmissible gastroenteritis12
of the viral genome12
transmissible gastroenteritis virus spike12
was used to detect12
room temperature for h12
lower than that of12
isolation of a porcine12
the ability of the12
with tgev at an12
spike gene of transmissible12
epidemic diarrhea virus strain12
in any of the12
may be involved in12
cell cycle arrest at12
is a highly contagious12
it is difficult to12
were cloned into the12
associated with diarrhea in12
in the cytoplasm of12
are located within the12
had no effect on12
the presence of tgev12
at a dilution of12
gastroenteritis coronavirus is a11
were added to the11
assay for the detection11
the percentage of apn11
science foundation of china11
that the spike gene11
after h of incubation11
strain of transmissible gastroenteritis11
it is likely that11
determinant of its enteric11
and cloned into the11
coronavirus is a determinant11
the porcine reproductive and11
the tgev nucleoprotein gene11
early in tgev infection11
nuclei were stained with11
its enteric tropism and11
demonstrates that the spike11
and evolution of the11
by transmissible gastroenteritis virus11
detection limit of the11
cells infected with the11
epithelial cells of the11
the replication of tgev11
mesenteric lymph node cells11
in accordance with the11
these data indicate that11
sites of the coronavirus11
antigenic sites a and11
are located on the11
no conflict of interest11
mutations in the s11
epidemic diarrhea virus infection11
result in the loss11
porcine hemagglutinating encephalomyelitis virus11
of the virus to11
transmissible gastroenteritis virus on11
end of the leader11
enteric coronavirus related to11
changes at the n11
these results indicated that11
two amino acid changes11
a determinant of its11
the results of the11
national natural science foundation11
of the murine coronavirus11
in the formation of11
transmissible gastroenteritis virus neutralization11
by transmissible gastroenteritis coronavirus11
at g for min11
in the induction of11
the enteric tropism of11
was similar to that11
tgev prcv recombinant elisa11
mice orally immunized with11
a porcine respiratory coronavirus11
of its enteric tropism11
for rapid detection of11
a cellular receptor for11
tips of the villi11
of tgev infection on11
with tgev at a11
major antigenic sites of11
group than in the11
and characterization of a11
t cells were transfected11
cell cycle arrest in11
east respiratory syndrome coronavirus11
antibodies for h at11
the role of apn11
of the e glycoprotein11
at s and g11
group was significantly higher11
cells were washed twice11
natural science foundation of11
functional receptor for the11
used as a control11
was expressed as the10
virus are located on10
protein result in the10
for h prior to10
the small intestine and10
recombination demonstrates that the10
interpretation of suspect results10
the cells were fixed10
of apn negative cells10
in a co atmosphere10
the transmissible gastroenteritis coronavirus10
may play a role10
cells which were fixed10
in the lamina propria10
isolation and identification of10
to the cell surface10
j cells infected with10
in porcine intestinal epithelial10
the cells released from10
in the spike protein10
is not essential for10
tgev n protein was10
the small intestine of10
economic losses in the10
paraformaldehyde for min and10
at the cell surface10
in the di rna10
pedv and tgev infection10
are listed in table10
located on the amino10
in the pbs group10
it is important to10
the copy number of10
by the addition of10
the beginning of the10
were stained with hoechst10
the cell culture adapted10
diarrhea virus in the10
the s and g10
the binding of the10
was inserted into the10
targeted recombination demonstrates that10
was carried out using10
were isolated from the10
analyzed by western blotting10
in the cells released10
and porcine epidemic diarrhoea10
the swinecheck tgev prcv10
gastroenteritis coronavirus spike protein10
the piglets in the10
is consistent with the10
international committee on taxonomy10
was used as the10
villous enterocytes of newborn10
gastroenteritis virus spike protein10
transmissible gastroenteritis virus from10
the tropism of the10
m and e proteins10
tgev was detected by10
de groot et al10
in the control of10
internal entry of ribosomes10
for pedv and tgev10
were analyzed by western10
largest rna virus genome10
transmissible gastroenteritis coronavirus genome10
mucosal and systemic immune10
the viral genomic rna10
inoculated with tgev strain10
gastroenteritis virus on the10
in the serum of10
pigs of all ages10
followed by goat anti10
for the first time10
spike protein result in10
in a variety of10
results suggest that tgev10
hepatitis b surface antigen10
the coronavirus mouse hepatitis10
coronavirus spike protein result10
was detected in the10
from porcine transmissible gastroenteritis10
antigenic structure of transmissible10
performed according to the10
the largest rna virus10
in this study was10
a role in the10
were observed in the10
was significantly lower than10
transmissible gastroenteritis coronavirus spike10
under a fluorescence microscope10
and st cells were10
probably due to the10
evolution of the purdue9
recombinant lactic acid bacteria9
intestinal epithelial cell line9
results were interpreted as9
to porcine reproductive and9
studies on transmissible gastroenteritis9
de haan et al9
of swine transmissible gastroenteritis9
suspect results were interpreted9
losses in the swine9
hoechst for min at9
genome sequence of transmissible9
transmissible gastroenteritis virus are9
cells were inoculated with9
to infection with tgev9
could be detected in9
plays a role in9
our results indicate that9
were found in the9
in the culture medium9
terminal half of spike9
from porcine respiratory coronavirus9
sequence of transmissible gastroenteritis9
from mpi to mpi9
the deduced amino acid9
in comparison with the9
the causative agent of9
it has been reported9
transmissible gastroenteritis virus entry9
from the tips of9
of a against tgev9
these results show that9
room temperature for min9
the presence or absence9
have no competing interests9
epidemic diarrhea virus strains9
immunity against transmissible gastroenteritis9
of lactic acid bacteria9
by the use of9
were randomly divided into9
the cells were then9
diagnosis of transmissible gastroenteritis9
arrest at s and9
the amino acid sequence9
the size of the9
on taxonomy of viruses9
it is worth noting9
the authors declare no9
receptor for mouse hepatitis9
on the day of9
with the tgev m9
demonstrated that tgev infection9
was measured at nm9
infected cells which were9
gastroenteritis virus are located9
orally immunized with rlppg9
of avian infectious bronchitis9
presence or absence of9
way analysis of variance9
is worth noting that9
of the purdue virus9
they have no competing9
t cells were cotransfected9
cd ssc low cells9
sites c and b9
the difference in the9
times with pbs and9
the case of the9
sites a and d9
the pellet was resuspended9
it has been demonstrated9
transmissible gastroenteritis coronavirus pur9
of the pfcrn gene9
with diarrhea in swine9
the cells were incubated9
and phylogenetic analysis of9
that the levels of9
at h post transfection9
in cells transfected with9
results suggest that the9
compared with that of9
the early stage of9
the nucleotide sequence of9
the international committee on9
cd ssc high cells9
residues involved in the9
stained with hoechst for9
copy number of the9
of the e protein9
the activation of p9
and infected with tgev9
was found in the9
emergence of porcine epidemic9
t g e v9
and c antigen sites9
clone and evolution of9
classical swine fever virus9
by sodium dodecyl sulfate9
were used in this9
of the tgev spike9
has been demonstrated that9
the s protein was9
bca protein assay reagent9
the porcine respiratory coronavirus9
the specificity of the9
when suspect results were9
de diego et al9
immunized with tgev antigen9
of the tgev genome9
virulent and attenuated strains9
the effects of tgev9
the mucosal immune response9
conventional duplex pcr rt9
to the s protein9
the purdue virus cluster9
an increase in the9
committee on taxonomy of9
are involved in the9
piglets in the tgev9
the animals immunized with9
and g m phase9
region of the s9
transmissible gastroenteritis and porcine9
mad clone and evolution9
of the assay was9
which were fixed with9
were incubated with the9
in the golgi complex9
the results indicated that9
the formation of the9
a receptor for pdcov9
involved in the regulation9
for the presence of9
the number of cd9
the amount of viral9
member of the coronaviridae9
incubated with tgev at9
these findings suggest that9
as shown in table9
with hoechst for min9
the cell membrane and9
cells were stained with9
i i f test9
protective lactogenic immunity against9
b and c antigen9
virus in the united9
the feline infectious peritonitis9
at a concentration of9
in the respiratory tract9
pedv cv vero adapted9
both ileum and colon9
determinants are located within9
was used to confirm9
half of spike glycoprotein8
avian coronavirus infectious bronchitis8
on transmissible gastroenteritis of8
three major structural proteins8
these data indicated that8
of the family coronaviridae8
the rapid detection of8
within the same domain8
the viral spike protein8
in the feces of8
structural components from porcine8
ra plus tgev s8
terminal domain of the8
by agarose gel electrophoresis8
antigenic homology among coronaviruses8
binding to the m8
common mucosal immune system8
promotes transmissible gastroenteritis virus8
our understanding of the8
the interpretation of suspect8
membrane of infected cells8
to determine whether the8
in the viral envelope8
analysis of the porcine8
was calculated using the8
in the presence or8
the invasion of tgev8
as a result of8
for the formation of8
with different concentrations of8
der most et al8
and the cells were8
cellular receptor for pedv8
with mouse monoclonal anti8
are summarized in table8
the purdue strain of8
in relation to the8
in an attempt to8
serves as a receptor8
reactivity between tgev and8
with a mixture of8
amino acid sequence of8
t cells were co8
has been reported that8
in complex with the8
in a dose dependent8
the enteropathogenic coronavirus tgev8
a dose dependent manner8
located within the same8
to jurisdictional claims in8
the molecular basis of8
antigenic relationship of the8
strains of transmissible gastroenteritis8
and feline infectious peritonitis8
of the s glycoprotein8
nature remains neutral with8
the tgev n protein8
can be used for8
molecular features and virus8
did not neutralize the8
recombinant swinepox virus expressing8
and the expression of8
in the swine industry8
washed twice with pbs8
sites a and b8
regard to jurisdictional claims8
the leader rna sequences8
of structural components from8
aminopeptidase n and its8
the m gene of8
and its inhibition by8
virus in cell culture8
a novel swine enteric8
at moi for h8
the enteric and respiratory8
the culture medium was8
of murine hepatitis virus8
antibody was purchased from8
with bound tgev purdue8
was performed using the8
epidemic diarrhoea virus and8
cells were fixed in8
of the spike glycoprotein8
maps and institutional affiliations8
other cov n proteins8
porcine respiratory coronavirus in8
were significantly higher than8
the pathogenesis of transmissible8
oral corn vaccine on8
of coronavirus mouse hepatitis8
in ml of pbs8
mediated by the viral8
in dmem supplemented with8
structure and genome expression8
receptor for the enteropathogenic8
the n terminus of8
as a source of8
have been reported to8
rna was isolated from8
rapid detection of transmissible8
for the enteropathogenic coronavirus8
as a selective marker8
jurisdictional claims in published8
the basis of the8
expression of tgev n8
cells were purchased from8
for the rapid detection8
than in the tgev8
domain of the transmissible8
inhibition by neutralizing antibodies8
containing fetal calf serum8
clarified by centrifugation at8
of alpha interferon by8
cells in the presence8
binding and neutralization determinants8
of the feline infectious8
the same domain of8
version of this article8
infected cells compared to8
min at rt and8
neutralization determinants are located8
neutral with regard to8
remains neutral with regard8
internalized into the cytoplasm8
tgev at moi for8
to the cell membrane8
were approved by the8
and mucosal immune responses8
tgev at a multiplicity8
the i i f8
on the plasma membrane8
virus genome as an8
antigenicity of structural components8
in this study we8
attenuated and virulent tgev8
with bound tgev miller8
of the structural proteins8
and neutralization determinants are8
of the papn ectodomain8
as the secondary antibody8
its inhibition by neutralizing8
is one of the8
corn vaccine on days8
particle associated with diarrhea8
the inhibitory activity of8
common to five isolates8
with regard to jurisdictional8
terminus of transmissible gastroenteritis8
of the nucleoprotein gene8
for the study of8
virus common to five8
springer nature remains neutral8
in phosphate buffered saline8
glycoprotein of transmissible gastroenteritis8
j cells were pretreated8
this is the first8
that the leader rna8
the expression of small8
may be required for8
goat serum for h8
porcine aminopeptidase n is8
cycle arrest at s8
point mutations in the8
of spike glycoprotein s8
selected characteristics of a8
high morbidity and mortality8
of a murine coronavirus8
grown in the presence8
was higher than that8
claims in published maps8
the interaction between the8
the national natural science8
induction of alpha interferon8
is required for efficient8
published maps and institutional8
for min and the8
same domain of the8
at the indicated time8
for tgev and pcv8
the inhibitory effect of8
with respect to the8
the antigenic sites of8
activity of a against8
we are grateful to8
in published maps and8
for pcv and tgev8
was not affected by8
investigated the effects of8
gastroenteritis virus by rt8
in the control group8
inhibitory activity of a8
previous study showed that8
were inoculated with tgev8
mrna expression levels of8
serum for h at8
between and copies ml8
van der most et8
samples were collected from8
and sequence analysis of7
in the enteric tract7
in the cell membrane7
significantly higher in the7
pi k akt pathway7
entry mediated by the7
with fetal calf serum7
that tgev infection could7
for the design of7
third of the genome7
were shown to be7
the membrane was blocked7
acid changes in the7
in st cells and7
cells were used as7
the s proteins of7
enteric tropism of tgev7
the interaction between tgev7
characteristics of a cytopathogenic7
with bovine serum albumin7
it is not clear7
a major cause of7
were between and copies7
us porcine epidemic diarrhea7
the result showed that7
were compared with those7
a epitope of the7
determine the effect of7
st cells infected with7
online version of this7
has also been shown7
and viral genomic sequences7
no significant difference in7
binding activity with the7
a g magnetic beads7
porcine respiratory coronavirus differs7
through activation of p7
cd t cells in7
vivo virus replication and7
diarrhea in suckling piglets7
of pedv and tgev7
strain was isolated from7
of the present study7
igg fitc labeled antibodies7
g for min at7
was performed with the7
apoptosis via activation of7
all experiments were performed7
and differentiation from porcine7
tgev prcv blocking elisas7
is an enveloped virus7
and sequence of the7
in the correct orientation7
gastroenteritis virus entry into7
differs from transmissible gastroenteritis7
the severe acute respiratory7
s protein connect the7
the tgev spike protein7
compared with those of7
and identification of porcine7
end of the genomic7
western blot analysis showed7
days after infection and7
be used as a7
from the viral membrane7
bases of coronavirus attachment7
based and duplex mmps7
the presence of maternal7
entry into intestinal epithelial7
gastroenteritis virus by a7
sodium dodecyl sulfate polyacrylamide7
of a cytopathogenic virus7
data indicate that the7
african green monkey kidney7
in intestinal epithelial cells7
from the jejunum of7
the mrna start sites7
and the supernatant was7
incubated with mouse monoclonal7
with tgev antigen alone7
a cytopathogenic virus common7
for the loss of7
of transmissible gastroenteritis in7
a previous study showed7
human immunodeficiency virus type7
it is interesting to7
results showed that tgev7
in pbs for min7
genes a and b7
in the early stage7
propagated in st cells7
and the sensitivity of7
diarrhea virus in china7
gene is not essential7
and van der zeijst7
immune responses induced by7
mechanisms of coronavirus cell7
infection or vaccination with7
responsible for the loss7
targeting the m gene7
tissue culture infective dose7
acid binding activity of7
between the leader rna7
at days of age7
the titers of tgev7
structural bases of coronavirus7
at a density of7
of coronavirus cell entry7
gastroenteritis virus infection in7
at room temperature and7
a wide range of7
virus by a few7
of the coronavirus mouse7
binding domain complexed with7
via activation of p7
protein a g magnetic7
coronavirus attachment to host7
virus and porcine deltacoronavirus7
were used to infect7
acid binding activity with7
that there is a7
enteropathogenicity of transmissible gastroenteritis7
and washed three times7
was derived from the7
to the family coronaviridae7
fixed cells which were7
higher in the lp7
differentiation from porcine respiratory7
a log reduction factor7
challenge with a virulent7
the data indicate that7
and expression of the7
the indirect fluorescent antibody7
components from porcine transmissible7
cells released from g7
the absence of rna7
to determine the effect7
a key role in7
replication of tgev in7
for the production of7
and tropism of transmissible7
the virus in the7
the total number of7
the s protein connect7
n and its inhibition7
transmissible gastroenteritis coronavirus gene7
at the beginning of7
activity with the enteropathogenicity7
signal transducer and activator7
was not significantly different7
into hek t cells7
and hemagglutinating encephalomyelitis virus7
the cells were infected7
and cultured for h7
virus infection induces cell7
porcine intestinal columnar epithelial7
that tgev infection induces7
three times with pbst7
of the tgev n7
with the enteropathogenicity of7
pcr and differentiation from7
in the pathogenesis of7
m and s determinants7
evolution and tropism of7
data are presented as7
as well as in7
compared to that in7
the enteropathogenicity of transmissible7
and immunogenicity of recombinant7
oral lactobacillus casei vaccine7
have been detected in7
divided into three groups7
the common mucosal immune7
have been demonstrated to7
the binding of tgev7
of sows with a7
the difference between the7
followed by incubation with7
classification and nomenclature of7
the tgev and prcv7
for transmissible gastroenteritis virus7
the viral life cycle7
of the human coronavirus7
terminal half of the7
terminal region of the7
attachment to host aminopeptidase7
at the indicated times7
after infection or vaccination7
the e glycoprotein of7
might be involved in7
of cd cd t7
by the viral spike7
respiratory coronavirus differs from7
binding to the n7
the detection of the7
of the tgev and7
coronavirus differs from transmissible7
of coronavirus attachment to7
cells compared with the7
the innate immune response7
as a cellular receptor7
relationship of the feline7
percentage of apn positive7
transducer and activator of7
role of apn in7
in the supernatants of7
of tgev has been7
apn and egfr synergistically7
diarrhea virus and porcine7
infected or infected with7
followed by cycles of7
dodecyl sulfate polyacrylamide gel7
method of estimating fifty7
virus replication and virulence7
when the cells were7
for the synthesis of7
cytopathogenic virus common to7
that the amount of7
well tissue culture plates7
transcription recombinase polymerase amplification7
of tgev in the7
supplemented with fetal calf7
and nomenclature of viruses7
a receptor for tgev7
in vivo and in7
which was consistent with7
in vivo virus replication7
a simple method of7
one of the most7
genetic evolution and tropism7
immunized with rlppg f7
compared with the control7
in the production of7
the results suggest that7
did not affect the7
tgev miller and purdue7
a large number of7
pi k akt and7
of the coronaviridae family7
both tgev and prcv7
the s protein and7
the mouse hepatitis virus7
were carried out in7
of intestinal epithelial cells7
infectious bursal disease virus7
enterocytes of newborn pigs7
is distinct from the7
for the pathogenesis of7
gastroenteritis virus in swine7
after an incubation period7
were used as a7
of the virus of7
infected tissue culture fluid7
could be due to7
into intestinal epithelial cells7
can be used to7
presence of maternal antibodies7
for h and then7
and the absorbance was7
protein connect the sialic7
not essential for viral7
that the m protein7
in the viral genome7
to host aminopeptidase n7
coronavirus cell entry mediated7
membrane was blocked with7
is required for the7
the online version of7
american type culture collection7
the bottom of the7
amino acid changes in7
were considered statistically significant7
cell entry mediated by7
for simultaneous detection of7
of differentially expressed lncrnas7
the separated proteins were7
was based on the7
infection with the porcine7
swine after infection or7
an incubation period of7
tgev is an enveloped7
the extracellular region of7
entry into host cells7
as a function of7
in the tgev genome7
compared to that of7
of the af mab7
the mrna levels of7
was removed and the7
p and jnk phosphorylation7
simple method of estimating7
host aminopeptidase n and7
porcine epidemic diarrhea coronavirus7
with the results of7
is closely related to7
animals immunized with tgev7
under the same conditions7
the absorbance was measured7
gastroenteritis virus of swine7
against porcine epidemic diarrhea7
the intestinal epithelial cells7
the s protein in7
the pedv s protein7
in significant economic losses7
may be related to7
cells were seeded in7
were transfected with the7
connect the sialic acid7
with porcine epidemic diarrhoea7
extracellular region of tfr7
that is responsible for7
with the porcine respiratory7
the epithelial cells of7
the region of the7
the tgev s gene7
were transferred to a6
results indicated that the6
in pigs inoculated with6
mammalian and avian coronaviruses6
coronavirus gene is not6
that the s protein6
protein is essential for6
results demonstrated that the6
and fecal shedding of6
the infectious bronchitis virus6
the mechanism of rna6
rna and dna genomes6
tissue culture infectious dose6
value obtained with tgev6
primary ileum epithelial cells6
tgev n protein expressed6
the n gene of6
st cells were infected6
for systematic assembly of6
significantly increased at h6
of gammacoronavirus and deltacoronavirus6
in tgev n protein6
of kda expressed by6
with tcid animal of6
betacoronavirus and avian coronaviruses6
ileum epithelial cells were6
absorbance was measured at6
and avian coronaviruses in6
in the genus deltacoronavirus6
receptor for the entero6
the activation of the6
then washed three times6
be used for the6
gastroenteritis coronavirus gene is6
norwalk virus capsid protein6
been shown that the6
coronavirus defective interfering rna6
of primary porcine enterocytes6
the a epitope of6
roswell park memorial institute6
cells were synchronized at6
by the oral route6
coe of kda expressed6
analyzed by flow cytometry6
cells at h p6
the loss of the6
of neutralizing antibodies in6
vaccination with transmissible gastroenteritis6
activity and promotes transmissible6
in the development of6
these data suggest that6
of spleen lymphocytes from6
milk of swine after6
were then incubated with6
the cellular receptor for6
like particle associated with6
and attenuated strains of6
suggest that tgev infection6
swine transmissible gastroenteritis coronavirus6
enjuanes and van der6
and avian coronaviruses as6
not essential but influences6
but not in the6
strand cdna synthesis kit6
tgev infection and replication6
it was found that6
a final concentration of6
of bovine coronavirus is6
as a positive control6
better understanding of the6
homology among coronaviruses related6
rapid and efficient detection6
cholesterol depletion from the6
positive cells with bound6
the phosphorylation of cofilin6
protein of tgev and6
the reciprocal of the6
the s protein has6
studies have found that6
diarrhea virus spike protein6
apn is a receptor6
the economic impact of6
serial dilutions of the6
of tgev n gene6
the expression of cd6
of tgev spike protein6
an infectious bacterial artificial6
the d antigenic site6
produced in transgenic plants6
cells were maintained in6
born to vaccinated sows6
was carried out as6
was shown to be6
of the economic impact6
and milk of swine6
distinct from the enzymatic6
the leader and ig6
the cells were lysed6
discussed in section v6
and replication of tgev6
of swine after infection6
the detection limits of6
our results suggest that6
in a swine herd6
wild type and mutant6
supports bat coronaviruses as6
antigens on the surface6
genome as an infectious6
has not been determined6
source of alphacoronavirus and6
infection induces apoptosis through6
strains of porcine epidemic6
interacting with n protein6
porcine respiratory coronavirus from6
single amino acid changes6
in colostrum and milk6
was amplified by pcr6
it was shown that6
susceptible cells did not6
by the finding that6
an equal volume of6
was significantly higher in6
localization of apn and6
and differential diagnosis of6
have been used to6
to be involved in6
of the same age6
compatible ends into the6
bel rv g p6
translocation to the nucleus6
times with lysis buffer6
leader complex binding site6
transmissible gastroenteritis coronavirus neutralization6
we investigated the effects6
pcr assay for tgev6
similar to transmissible gastroenteritis6
from the enzymatic site6
virus infection induces apoptosis6
a virulent strain of6
encodes four structural proteins6
apoptosis through activation of6
than those in the6
compared with the mock6
end and a poly6
a putative second receptor6
growth factor receptor regulates6
role of transmembrane glycoprotein6
reproduced with permission from6
density value obtained with6
by low speed centrifugation6
proteins of interest by6
m protein of tgev6
cells compared to that6
prepared in our laboratory6
the effect of tgev6
the nucleocapsid protein of6
statistical analysis was performed6
polypeptide structure of transmissible6
by western blotting using6
activation of the ifn6
deltacoronavirus supports bat coronaviruses6
the activities of caspase6
the respiratory tract and6
respiratory syndrome virus infection6
academy of agricultural sciences6
by any of the6
levels of neutralizing antibodies6
major structural proteins of6
as an infectious bacterial6
antigenic site of the6
the tgev strain purdue6
the polypeptide structure of6
were also observed in6
the gene encoding the6
characterization and pathogenesis of6
j cells were infected6
cells were collected and6
that is distinct from6
as the optical density6
interesting to note that6
the effects of mir6
protein was used as6
animals infected with the6
and activator of transcription6
to the leader rna6
of the three commercial6
spleen lymphocytes from mice6
rna was extracted using6
resuspended in ml of6
the virulent and attenuated6
not included in the6
genome sequence of a6
lower than that in6
avian coronaviruses as the6
receptor interaction reside within6
interaction reside within a6
less than weeks old6
virus was detected in6
of the partial s6
are presented as the6
with the m protein6
apn negative cells were6
used as the secondary6
is not essential but6
cells were fixed and6
analysis was performed using6
the induction of ifn6
against swine transmissible gastroenteritis6
resulting in significant economic6
that the expression of6
using purified tgev as6
time pcr was performed6
were incubated for min6
caused by transmissible gastroenteritis6
essential but influences in6
assess the role of6
response specific for pedv6
t cells in the6
added to the cells6
the plates were washed6
multiplicity of infection of6
j cells were transfected6
transcripts of porf a6
and apoptosis through activation6
data indicate that rtgev6
vomiting and wasting disease6
the finding that the6
were collected at different6
of the peplomer protein6
factor receptor regulates cofilin6
based on the s6
in order to determine6
balb c mice were6
cofilin activity and promotes6
the infectivity of tgev6
studies have demonstrated that6
of the tgev nucleoprotein6
of the international committee6
f i p v6
n terminus of the6
the complete genome sequence6
intestinal columnar epithelial cells6
characterization of a novel6
sequence of the peplomer6
the m and e6
both pedv and tgev6
vaccines for porcine epidemic6
mock infected or infected6
was obtained from the6
st cells stably expressing6
has been previously described6
are present in the6
a virulent us pedv6
protein was expressed in6
cell lysates were prepared6
expressed as the optical6
negative cells with bound6
kindly provided by dr6
receptor for the pedv6
each of the two6
and pathogenesis of transmissible6
essential for the transmissible6
apoptosis induced by tgev6
against pedv and tgev6
avian coronaviruses in the6
phase of the cell6
of cell cycle arrest6
generating recombinant plasmid ppg6
used as a source6
among coronaviruses related to6
important role in tgev6
and promotes transmissible gastroenteritis6
identification of a new6
around the cell membrane6
investigate the effect of6
of the genome encodes6
for the transmissible gastroenteritis6
n that is distinct6
containing normal goat serum6
d antigenic site of6
used to confirm the6
proteins were transferred to6
coe at saci and6
deduced amino acid sequences6
shown in fig a6
dmem supplemented with fbs6
cells were permeabilized with6
j cells were incubated6
of enteric tropism in6
by porcine epidemic diarrhea6
molecular characterization and pathogenesis6
the nuclear translocation of6
samples were between and6
of the coronavirus infectious6
effect of cholesterol depletion6
protein concentrations were measured6
is possible that the6
the formation of virus6
systematic assembly of large6
vivo and in vitro6
five isolates from transmissible6
the m and s6
influences in vivo virus6
centrifugation at g for6
lactogenic immunity against tgev6
or vaccination with transmissible6
in the intestinal tract6
by the presence of6
the differentially expressed proteins6
mechanisms of transmissible gastroenteritis6
for the pedv coronavirus6
relative to the optical6
been reported to be6
large rna and dna6
of tgev and the6
group was comprised of6
tropism of transmissible gastroenteritis6
sd from three independent6
in the colostrum and6
regulates cofilin activity and6
the cells transfected with6
in the gut of6
but influences in vivo6
within a domain of6
supported by the national6
that the n protein6
porcine intestinal epithelial cell6
has been detected in6
of the tgev rbd6
discovery of seven novel6
is interesting to note6
divided into four groups6
of the bovine coronavirus6
the mucosal immune system6
immunity to transmissible gastroenteritis6
cells derived from the6
the upper respiratory tract6
the plasma membrane of6
the genus deltacoronavirus supports6
encoding gene of transmissible6
c in a co6
of tgev was detected6
the rest of the6
immune responses in the6
monoclonal antibodies directed against6
predicted to encode a6
correlated positively with time6
and betacoronavirus and avian6
has been identified as6
seven novel mammalian and6
fold higher than that6
assembly of large rna6
protein induces cell cycle6
between tgev s and6
to assess the role6
to five isolates from6
herpes simplex virus type6
entry of tgev was6
be related to the6
on the villous enterocytes6
a receptor for human6
gene source of gammacoronavirus6
glycoprotein s from tgev6
for each of the6
the site of virus6
respiratory and fecal shedding6
for detection of tgev6
circulating in a swine6
the effect of these6
sense rna genome of6
inhibit the replication of6
indirect fluorescent antibody technique6
previous studies have shown6
of st cells were6
have been described in6
an attenuated variant of6
infectious peritonitis virus to6
h n influenza virus6
epidemic diarrhea virus from6
the surface of infected6
and the percentage of6
rna virus genome as6
is involved in tgev6
the effect of cholesterol6
tc bel rv g6
the optical density value6
of the method was6
transmissible gastroenteritis virus a6
the fixed cells were6
tissue culture fluid was6
the levels of anti6
s protein interacts with6
a consequence of the6
coronaviruses in the genus6
of p mapk pathway6
commercial tgev prcv blocking6
the antigenic relationship of6
leader sequence at the6
were analyzed by a6
be responsible for the6
with the cell culture6
novel mammalian and avian6
followed by the addition6
of porcine enteric coronaviruses6
entry of porcine epidemic6
the synthesis of a6
an integral membrane protein6
n is a receptor6
of large rna and6
determinants essential for the6
tgev and prcv s6
the apn expression to6
by a few genomic6
virus entry into intestinal6
infectious bacterial artificial chromosome6
it has been suggested6
novel swine enteric alphacoronavirus6
in viral rna synthesis6
genetic analysis of porcine6
a few genomic deletions6
may play an important6
effects of tgev infection6
were inserted into the6
n is a functional6
analysis of porcine respiratory6
was defined as the6
transmissible gastroenteritis virus model6
the presence of rna6
strategy for systematic assembly6
infected with tgev or6
stably transformed with the6
the proportion of cells6
tgev infection on the6
in ileum epithelial cells6
in the jejunum of6
used as a negative6
is associated with the6
end of the tgev6
as evidenced by the6
were transfected with nm6
epidemic diarrhea virus spike6
and matrix protein genes6
genus deltacoronavirus supports bat6
alphacoronavirus and betacoronavirus and6
human aminopeptidase n is6
the membranes were blocked6
attenuated transmissible gastroenteritis virus6
not significantly different from6
of transmissible gastroenteritis of6
coronaviruses related to transmissible6
biology of transmissible gastroenteritis6
in the infected cells6
sensitivity of the assay6
of infectious bronchitis virus6
the jejunum and ileum6
recombinant s protein was6
in the cell culture6
or egfp empty vector6
the standard deviation for6
sows that had been6
of seven novel mammalian6
negative cells were infected6
the assembly of the6
type i interferon production6
the three commercial elisas6
the ra plus tgev6
and then infected with6
the n protein of6
identification of porcine transmissible6
results of this study6
british field isolate of6
proportion of cells in6
carried out as described6
bat coronaviruses as the6
directed against virion proteins6
gene of the prcv6
differentially expressed proteins were6
kda expressed by rlppg6
hp dna transfection reagent6
and tgev inactivated vaccine6
as the reciprocal of6
be explained by the6
in the process of6
efficacy and immunogenicity of6
apn positive cells and6
engineering the largest rna6
optical density value obtained6
based on the transmissible6
is located in the6
course of the disease6
molecular biology of transmissible6
the nucleocapsid gene of6
g for min and6
a domain of aminopeptidase6
the ectodomain of the6
and genetic characterization of6
not present in the6
in the s and6
gene source of alphacoronavirus6
reverse transcription recombinase polymerase6
removed by centrifugation at6
the pcr products were6
by the coronavirus infectious6
of the carcinoembryonic antigen6
of alphacoronavirus and betacoronavirus6
reside within a domain6
purified tgev as antigen6
was evaluated by real6
source of gammacoronavirus and6
arrest and apoptosis through6
of the mouse hepatitis6
the age of the6
reverse genetics system for6
and the formation of6
was performed according to6
variant porcine epidemic diarrhea6
intestinal epithelial cells of6
for the generation of6
was used for the6
amino acids of the6
those in the tgev6
sulfate polyacrylamide gel electrophoresis6
the ratio of the6
the construction of a6
on the transmissible gastroenteritis6
of vesicular stomatitis virus6
tgev and pedv were6
receptor regulates cofilin activity6
for a porcine respiratory6
recombinase polymerase amplification assay6
were used as the6
have been developed for6
of glycoprotein s expressed6
in the mesenteric lymph6
to the loss of6
gastroenteritis virus in vitro6
were tested for tgev6
a pair of primers5
normal goat serum for5
for the care and5
is incorporated into virions5
virus strain pc a5
immunity against tgev in5
in the event of5
removal of sa from5
are consistent with the5
amplified by pcr using5
of the prcv isolates5
care and use of5
report of the international5
infected with transmissible gastroenteritis5
maintained in maintenance medium5
can be divided into5
studies have suggested that5
changes in the viral5
to porcine respiratory coronavirus5
a and l b5
tgev m protein and5
important roles in the5
by western blot analysis5
of apn and egfr5
cells transfected with n5
of the expression of5
ddx is involved in5
was obtained from a5
of the wt group5
of a coronavirus from5
declare no conflict of5
crystal structures of the5
glycoprotein m affect induction5
cells were subjected to5
could significantly increase the5
clinical illness and better5
is thought to be5
against the s protein5
were compared with the5
pig kidney cell line5
with that of the5
supernatant was collected and5
the s protein gene5
shown in table i5
and is required for5
a portion of the5
quantitative pcr and the5
diarrhea virus and discovery5
was used as control5
expressing glycoprotein s polypeptides5
during the assembly of5
of a per cent5
attenuated porcine epidemic diarrhea5
verified by dna sequencing5
a leader sequence at5
and better lactogenic immunity5
the s gene that5
used in the present5
humoral and cellular immune5
were treated with the5
of the probiotic bacteria5
an oral lactobacillus casei5
epidemic diarrhea in china5
total rna extracted from5
the glycoprotein s from5
st cell monolayers in5
as well as to5
partial protection against prrsv5
this study was to5
primed as neonates with5
and mouth disease virus5
was used to analyze5
no significant difference between5
both in vitro and5
tgev was evaluated by5
of orf a and5
virus titers were determined5
the percentage of sa5
were euthanized at days5
has been used for5
pedv n in the5
infection induces dramatic changes5
performed to determine the5
relationship between tgev and5
expressed tgev n gene5
of the innate immune5
from santa cruz biotechnology5
pfu ml in ml5
detection and differentiation of5
phosphorylation level of egfr5
of transmissible gastroenteritis on5
gene counteracts host defenses5
diarrhea virus and transmissible5
the highest levels of5
also been shown to5
the development of new5
of apn as a5
enveloped virus with a5
the viral replication cycle5
the viral glycoprotein m5
this article can be5
binding to viral determinants5
evidence for a putative5
were expressed as the5
antibodies directed against virion5
the two parental viruses5
vector based on the5
has been demonstrated to5
was considered statistically significant5
was more sensitive than5
extracted using trizol reagent5
of ibv and mhv5
restriction fragment length polymorphism5
incubated in dmem containing5
respiratory syndrome virus in5
in the antigenic sites5
the levels of p5
the expression level of5
of transmissible gastroenteritis coronaviruses5
crystal structure of the5
of the reproductive tract5
s domain of the5
results indicate that egfr5
has not been established5
to interact with the5
be detected in the5
a membrane protein that5
gastroenteritis virus shxb isolated5
gastroenteritis and porcine respiratory5
were mock infected or5
the inhibition of tgev5
role in tgev infection5
than that observed in5
a significant increase in5
of tgev was evaluated5
tgev in porcine iecs5
and high mortality in5
mouse hepatitis virus is5
gastroenteritis coronavirus nucleocapsid protein5
the s glycoprotein of5
the remainder of the5
piglets were obtained from5
for human coronavirus e5
it has also been5
residues to of the5
tgev infection induces ifn5
and ingezim corona diferencial5
consistent with previous reports5
pedv and tgev have5
in the test sample5
virulent strain of tgev5
reduced clinical illness and5
premix ex taq ii5
a variety of viruses5
to the end of5
labeled antibodies for h5
discovery of a novel5
affect induction of alpha5
the exception of the5
surface of infected cells5
promoter for tgev entry5
virus replication in the5
is the most abundant5
were removed from the5
the supernatant was collected5
recombinant protein expressed in5
s protein of transmissible5
that were primed as5
foot and mouth disease5
gastroenteritis coronavirus genome is5
a common feature of5
antigenically similar to transmissible5
tgev shaanxi strain was5
could not be detected5
impact of transmissible gastroenteritis5
levels of p and5
analysis of relative gene5
of dna and rna5
the pathogenesis of tgev5
the cauliflower mosaic virus5
were primed as neonates5
nasal shedding of prcv5
m gene of tgev5
piglets were inoculated with5
to the mammary gland5
presented as the mean5
depletion from the viral5
in the immunized group5
the expression of ifn5
in each group were5
time quantitative pcr and5
that transmissible gastroenteritis virus5
antibodies containing normal goat5
similar results were also5
commercial pig production in5
for a putative second5
acid sequences of the5
neutralizing antibody titers were5
fecal samples were collected5
nucleotide and amino acid5
porcine small intestine epithelial5
outbreaks of diarrhea in5
to be associated with5
development and evaluation of5
proteolytic cleavage of the5
better lactogenic immunity against5
the expression of il5
growth factor receptor is5
cells expressed tgev n5
dmem containing dispase ii5
nested polymerase chain reaction5
expression data using real5
prevalence of porcine epidemic5
molecular basis of transmissible5
increase the number of5
in gilts that were5
the concentration of the5
were used to evaluate5
both pcv and tgev5
second receptor for porcine5
proteomic analysis reveals that5
the fusion of the5
damage via targeting rb5
virus infection induces dramatic5
limit of the method5
cells of the small5
lactic acid bacteria can5
mouse hepatitis virus and5
was prepared in our5
cellular receptor for tgev5
results indicate that the5
the enteric tropism determinant5
domain of glycoprotein s5
st cells were synchronized5
egfp expression vector or5
of each sample was5
that of the wt5
western blot analysis of5
with tgev strain miller5
m and n genes5
membrane protein that is5
was kindly provided by5
piglets were challenged with5
to the absence of5
salmonella enterica serovar typhimurium5
not appear to be5
kits evaluated in this5
h prior to infection5
for the construction of5
paraformaldehyde for min at5
for the preparation of5
morbidity and mortality in5
this type of di5
than that of conventional5
by the indirect fluorescent5
a highly contagious disease5
induces apoptosis through fasl5
of monoclonal antibodies directed5
shxb isolated in china5
compared with the pbs5
has not been elucidated5
plays a crucial role5
not the related porcine5
the carcinoembryonic antigen family5
gastroenteritis on commercial pig5
the prcv s protein5
morphogenesis and proliferative rule5
of protective lactogenic immunity5
the immune response of5
shedding of prcv tgev5
responsible for receptor binding5
were blocked for h5
in apn negative cells5
the s gene from5
and washed with pbs5
s group was significantly5
prevention and control of5
m and n proteins5
have not yet been5
to a lesser extent5
recent studies have shown5
in the level of5
s b and table5
at seven days cultivation5
terminal domain of spike5
epidemic diarrhea virus into5
with any of the5
the potential role of5
receptor porcine aminopeptidase n5
using monoclonal antibodies to5
for min and then5
the crystal structure of5
reported that tgev infection5
in the natural host5
that observed in the5
characteristics of a coronavirus5
coronavirus gene counteracts host5
piglets born to vaccinated5
the antiviral activity of5
previous studies showed that5
in the form of5
the activation of egfr5
was carried out with5
a high level of5
j cells were seeded5
were identical to those5
were washed five times5
as shown in figures5
sequence comparison of porcine5
pcr was performed on5
stat in the lp5
lactic acid bacteria nc5
before and after nebulization5
isolate of transmissible gastroenteritis5
b cells and cd5
of a reverse transcription5
the binding site of5
modified live virus vaccine5
the intensity of the5
site of the tgev5
moi for h at5
the results of three5
mab to n protein5
the tip of the5
quantitative proteomic analysis reveals5
for the detection and5
the presence of tunicamycin5
encoding the s protein5
supplemented with fbs and5
s gene from the5
from transmissible gastroenteritis coronavirus5
were harvested at the5
see materials and methods5
in the viral glycoprotein5
is not clear whether5
attenuated variant of transmissible5
in the dko group5
cells transfected with the5
mrna and protein levels5
the prevention and control5
the results show that5
the fact that the5
to test this hypothesis5
synergistically promote tgev invasion5
protein of tgev has5
neutralizing antibodies against the5
with porcine epidemic diarrhea5
play a key role5
swine enteric coronavirus from5
and modulates virus virulence5
the results indicate that5
length infectious cdna clone5
simulation of the economic5
of type i interferon5
cells were harvested at5
cells were used for5
and its role in5
mt d in ml5
mitochondrial damage via targeting5
in animals immunized with5
designed to amplify the5
the recombinant lactobacillus strain5
porcine epidemic diarrhoea in5
virulent strain of transmissible5
deficient virus vector based5
a polypeptide of m5
washed five times with5
the tgev group at5
expression levels of zap5
to determine whether tgev5
junctions and microfilaments of5
in dmem containing dispase5
the stability of the5
diarrhoea virus and transmissible5
diarrhoea virus infection induces5
of the sars coronavirus5
the villi to the5
in the splenic lymphocytes5
shedding of porcine respiratory5
by inserting the oligo5
or g m phase5
amount of phosphorylated stat5
the use of the5
of the heterologous gene5
to human rotavirus in5
relative gene expression data5
results showed that nc5
genomic sequence of the5
with tgev strain purdue5
tremegene hp dna transfection5
arranged in the order5
is essential for the5
were used to determine5
the target of mir5
changes in the tight5
tgev entry in a5
in the secretory pathway5
the levels of viral5
as neonates with porcine5
involved in the induction5
of swine enteric coronaviruses5
t g and pbs5
of a novel swine5
in the concentration of5
twice with pbs and5
and entry of tgev5
national center for biotechnology5
of the tgev group5
article can be found5
in the replication of5
the limit of detection5
basis of transmissible gastroenteritis5
the s proteins from5
the epitopes recognized by5
were performed in triplicate5
the importance of cholesterol5
induction of cell cycle5
of sglt and glut5
nucleocapsid protein of transmissible5
cell supernatants were harvested5
of the presence of5
is similar to that5
m affect induction of5
of hepatitis c virus5
was not observed in5
the length of the5
in escherichia coli and5
gene expression data using5
cells were then incubated5
recombinant swine enteric coronavirus5
a and d in5
tgev infection caused the5
domain complexed with its5
as described in the5
s a and table5
differences were considered significant5
is expressed in the5
the increased concentration of5
viral glycoprotein m affect5
involved in the antigenic5
u m a n5
the tgev n gene5
tropism of the virus5
n protein expressed pk5
the he protein of5
the major structural proteins5
fipv type i viruses5
immunoprecipitation of glycoprotein s5
epidemic diarrhoea virus infection5
adapted to grow in5
results were analyzed by5
with neutralizing activity against5
in the coronaviridae family5
translation of orf b5
the majority of the5
deletion in the s5
to days after infection5
increased concentration of il5
an enveloped virus with5
were fixed in absolute5
has been used to5
increased litter survival rates5
be due to the5
of iga b cells5
been identified as a5
and processing of the5
and the results were5
it is known that5
separated proteins were transferred5
virulent british field isolate5
used as templates for5
induces dramatic changes in5
a virulent british field5
pigs of the same5
nucleocapsid protein induces cell5
tight junctions and microfilaments5
and functional characterization of5
the mortality rate of5
predicted amino acid sequences5
in pedv and tgev5
and their ability to5
developed in this study5
and rna viruses in5
protein that is incorporated5
used to determine the5
modified live tgev vaccine5
and macrophage cell lines5
peripheral blood mononuclear cells5
coronavirus nucleocapsid protein gene5
half of the s5
similar results were obtained5
porcine respiratory coronavirus and5
propagation of the virus5
previous studies have found5
authors declare no conflict5
used to analyze the5
was performed in triplicate5
the best of our5
an infectious cdna clone5
expression vector or egfp5
of enteric viral infections5
challenge with transmissible gastroenteritis5
as a template for5
expression levels of the5
derived from the anpep5
weaned pigs and sequence5
virus shxb isolated in5
pbs and lysed in5
host innate immune response5
promoter luciferase report plasmids5
for the differentiation of5
the data shown are5
for cv fecal suspension5
with pbs and fixed5
ability of the virus5
expression levels in the5
on commercial pig production5
chain reaction assay for5
read and approved the5
receptor determinants for coronaviruses5
the age of days5
inoculation of sows with5
between prcv and tgev5
debris was removed by5
the expression of p5
well culture chamber slides5
is believed to be5
fixed in absolute acetone5
h u m a5
receptor for porcine transmissible5
antigenic sites of transmissible5
differentiation between transmissible gastroenteritis5
cells were incubated for5
outbreak of porcine epidemic5
activating p mapk pathway5
a mouse hepatitis virus5
the cell culture medium5
bca protein assay kit5
van gorp et al5
the care and use5
of the virus and5
of swine and a5
were purchased from sigma5
of the sa protein5
cloned into the same5
the related porcine respiratory5
the structural proteins of5
discovery of a recombinant5
related group was comprised5
of the s domain5
the presence of glucose5
coronavirus spike protein is5
infected st cells was5
was resuspended in ml5
the leader rna of5
cellular proteins were identified5
experiment was performed in5
were expressed as means5
of the m gene5
tgev infection in pk5
were interpreted as negative5
differences were found between5
entry in a dose5
due to the absence5
among transmissible gastroenteritis virus5
tgev and prcv is5
transmissible gastroenteritis virus the5
times to remove unbound5
at the nonpermissive temperature5
collected by centrifugation at5
virus vector based on5
in the tight junctions5
the respiratory activity of5
the present study was5
the transcription start site5
tgev infection induced the5
agent of transmissible gastroenteritis5
at the plasma membrane5
was extracted using trizol5
evidence for a porcine5
virulent rv inoculated pigs5
in well culture chamber5
has also been demonstrated5
were stained with antibodies5
against tgev in gilts5
observed in the animals5
transmissible gastroenteritis coronavirus nucleocapsid5
diarrhea virus strain pc5
for both tgev and5
in roswell park memorial5
of freezing and thawing5
a recombinant vaccinia virus5
the murine coronavirus spike5
virus and discovery of5
a large deletion in5
in mice orally immunized5
in vitro inhibition of5
infection of pigs with5
attached to the cells5
cells in the s5
as a loading control5
of the dko pigs5
were orally inoculated with5
were fixed in paraformaldehyde5
like particles associated with5
sequence of the coronavirus5
the g m phase5
economic impact of transmissible5
compared to the control5
which is consistent with5
as the log of5
had been inoculated with5
characterization of a coronavirus5
the late stage of5
antibody responses in serum5
development of a reverse5
was isolated from an5
hydrophobic protein encoded at5
in transmissible gastroenteritis of5
at the level of5
illness and better lactogenic5
receptor for human coronavirus5
to the best of5
comparison of porcine respiratory5
host defenses and modulates5
was not isolated from5
a against tgev replication5
of a recombinant swine5
it is also possible5
the transcription of tgev5
pigs and sequence of5
antigenic differentiation between transmissible5
and mesenteric lymph node5
as receptor determinants for5
used to amplify the5
were obtained from the5
appl microbiol biotechnol doi5
the virulent strain of5
and incubated for min5
the time of farrowing5
transmissible gastroenteritis of pigs5
of viral host range5
higher than those in5
were verified by dna5
properties of monoclonal antibodies5
p infected cell lysates5
in the cells transfected5
the phosphorylation of p5
m and s antigens5
transfected with p sirna5
tgev nucleocapsid protein induces5
the large size of5
of this study was5
determinant was expressed as5
transmissible gastroenteritis virus molecular5
greater than that of5
specified by the coronavirus5
of tgev in porcine5
each of the three5
of relative gene expression5
pedv and rotavirus a5
acids as receptor determinants5
sialic acids as receptor5
for porcine transmissible gastroenteritis5
different from that of5
gastroenteritis virus of pigs5
cells were then washed5
pcr was performed using5
encodes a membrane protein5
fecal shedding of porcine5
were transfected with p5
of the coronavirus genome5
transmissible gastroenteritis virus shxb5
cauliflower mosaic virus s5
fitc labeled antibodies for5
in this paper we5
the villi of the5
the university of minnesota5
in order to test5
is related to the5
end of the s5
in the current study5
large deletion in the5
was provided by dr5
sem of three independent5
the possibility that the5
days after the last5
interaction between tgev s5
orf encodes a membrane5
h and h of5
compared with the tgev5
sentinel weaned pigs and5
antibody binding to viral5
transmissible gastroenteritis on commercial5
of the subgenomic mrnas5
protein is the most5
the porcine aminopeptidase n5
the cd and papn5
the mechanism by which5
tgev in gilts that5
and position of the5
between virulent and attenuated5
study is the first5
was supported by grants5
variant of transmissible gastroenteritis5
no deletions or insertions5
that apn is not5
has a sialic acid5
by grants from the5
la monica et al5
in pbs for h5
by centrifugation at g5
mouse hepatitis virus a5
porcine coronavirus transmissible gastroenteritis5
the role of the5
have been identified in5
is required for tgev5
was determined using a5
were performed using the5
in sentinel weaned pigs5
was performed using a5
that the e protein5
a better understanding of5
it has been proposed5
to the development of5
in the i i5
having specificity for the5
of the gastrointestinal tract5
for an additional h5
is also possible that5
dilution was added to5
neonates with porcine respiratory5
the detection of pedv5
harvested at the indicated5
for the avian coronavirus5
evaluated in this study5
sequence of the partial5
a co atmosphere incubator5
on the detection of5
t cells were cultured5
extracellular receptor binding domain5
and discovery of a5
three times to remove5
a and table s5
and porcine hemagglutinating encephalomyelitis5
were considered significant at5
microfilaments of polarized ipec5
the united states and5
e protein is essential5
normalized to control conditions5