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 reproductive and respiratory2492
reproductive and respiratory syndrome2483
and respiratory syndrome virus2129
of porcine reproductive and918
the porcine reproductive and152
respiratory syndrome virus infection137
respiratory syndrome virus in137
to porcine reproductive and132
with porcine reproductive and125
in the presence of109
as shown in fig108
pathogenic porcine reproductive and83
highly pathogenic porcine reproductive82
in porcine reproductive and81
of the porcine reproductive77
in the present study67
cells were infected with66
and respiratory syndrome viruses66
were infected with prrsv66
infertility and respiratory syndrome65
swine infertility and respiratory65
infected with porcine reproductive63
in the absence of63
respiratory syndrome virus and61
in the united states60
has been shown to60
at an moi of58
strains of porcine reproductive57
porcine epidemic diarrhea virus57
an important role in57
severe acute respiratory syndrome55
the end of the55
against porcine reproductive and55
used in this study54
in the lungs of54
respiratory syndrome virus by53
of swine infertility and53
the replication of prrsv52
cells were transfected with52
a member of the50
replication of porcine reproductive50
for porcine reproductive and49
by porcine reproductive and49
syndrome virus infection in48
on the other hand47
in pigs infected with46
at a concentration of44
for the detection of43
one of the most42
type porcine reproductive and41
respiratory syndrome virus replication40
protein of porcine reproductive40
strain of porcine reproductive40
incubated for h at40
simian hemorrhagic fever virus39
rna was extracted from39
respiratory syndrome virus isolates38
total rna was extracted38
the economic impact of37
in the current study37
the antiviral activity of37
isolates of porcine reproductive36
pigs infected with prrsv35
the results showed that35
is one of the35
acute respiratory syndrome coronavirus35
cells were treated with35
virus porcine reproductive and35
been shown to be35
respiratory syndrome virus nucleocapsid35
syndrome virus nucleocapsid protein35
assessment of the economic34
play an important role34
impact of porcine reproductive34
innate and adaptive immune34
of the economic impact34
of equine arteritis virus33
and simian hemorrhagic fever33
detection of porcine reproductive33
respiratory syndrome virus gp33
economic impact of porcine33
porcine epidemic abortion and32
and porcine reproductive and32
abortion and respiratory syndrome32
in the case of32
epidemic abortion and respiratory32
respiratory syndrome virus the32
proteins of porcine reproductive31
washed three times with31
studies have shown that31
as shown in figure31
was used as a31
peripheral blood mononuclear cells31
gp and m proteins31
at the time of30
pcd and vero cells30
european porcine reproductive and30
porcine respiratory disease complex30
in vitro and in30
the cells were washed29
respiratory syndrome virus vaccine29
of the immune response29
the causative agent of29
presence or absence of29
the lungs of pigs29
the pi k akt29
north american and european29
for the presence of28
the cells were then28
the presence of prrsv28
infected with prrsv at28
the host immune response28
orf a and orf28
have been shown to28
swine disease in the27
in the development of27
vitro and in vivo27
disease in the netherlands27
live porcine reproductive and27
mystery swine disease in27
respiratory syndrome virus nonstructural27
and vero cells were27
syndrome virus nonstructural protein26
as well as the26
the swine industry worldwide26
isolation of lelystad virus26
a and orf b26
the innate immune response26
of porcine circovirus type26
characterization of swine infertility26
the isolation of lelystad26
pi k akt pathway26
of pigs infected with26
type i ifn signaling26
for the development of26
pigs infected with porcine26
the presence or absence26
play a role in25
of the viral genome25
with fetal bovine serum25
in porcine alveolar macrophages25
at the end of25
important role in the25
is a member of25
min at room temperature25
production of proinflammatory cytokines25
was found to be25
were found to be25
pigs exposed to prrsv25
respiratory syndrome virus porcine24
was observed in the24
van reeth et al24
den boon et al24
h n influenza virus24
response to porcine reproductive24
for min at room24
classical swine fever virus23
replication of prrsv in23
of prrsv and pedv23
plays an important role23
immune response to prrsv23
responses to porcine reproductive23
porcine respiratory and reproductive23
respiratory syndrome virus on23
the unfolded protein response23
pathogenesis of porcine reproductive22
of the north american22
infection of pigs with22
in the infected pigs22
in the respiratory tract22
it is possible that22
in the context of22
cells were maintained in22
isolate of porcine reproductive22
syndrome virus porcine reproductive22
gp of porcine reproductive22
the cells were infected22
the adaptive immune response22
of severe acute respiratory22
enhanced replication of porcine22
the immune response to22
in the presence or22
to that of the22
it has been shown22
us porcine reproductive and22
at the same time22
van dinten et al22
outbreaks of atypical prrs21
unparalleled outbreaks of atypical21
on swine production in21
and incubated for h21
with that of the21
and respiratory syndrome on21
and respiratory syndrome in21
swine production in the21
syndrome on swine production21
of highly pathogenic porcine21
innate and adaptive immunity21
respiratory syndrome virus strain21
was used as the21
of porcine epidemic abortion21
production in the united21
were washed three times21
respiratory syndrome virus comparison21
respiratory and reproductive syndrome21
respiratory syndrome on swine21
the molecular biology of21
and adaptive immune responses21
a homogeneous subpopulation of20
the formation of autophagosomes20
virus in a homogeneous20
of the family arteriviridae20
homogeneous subpopulation of ma20
respiratory syndrome virus nsp20
cells were incubated with20
proteins encoded by orfs20
a key role in20
infection with porcine reproductive20
of atypical prrs in20
similar to that of20
the humoral immune response20
has been shown that20
molecular dissection of the20
in a homogeneous subpopulation20
respiratory syndrome virus strains20
of fatal prrsv variants20
and the cells were20
emergence of fatal prrsv20
dissection of the unique20
atypical prrs in china20
pigs persistently infected with20
be due to the20
of the unique hallmark20
results showed that the20
the prrsv n protein20
to the family arteriviridae19
china and molecular dissection19
prrs in china and19
the expression of il19
and experimental reproduction of19
a nested set of19
as a negative control19
by the use of19
experimental reproduction of the19
of the disease in19
in china and molecular19
of type i ifn19
a multiplicity of infection19
causative agent of porcine19
were incubated for h19
reproduction of the disease19
for h at room19
in the lungs and19
the cells were incubated19
genomic rna and sg19
and molecular dissection of19
the authors declare that19
in the serum of18
the replication of porcine18
new order comprising coronaviridae18
was added to the18
h at room temperature18
as a result of18
order comprising coronaviridae and18
of swine to porcine18
prrsv infection in pigs18
in the number of18
in cells infected with18
respiratory syndrome virus vaccines18
for h at c18
of the most important18
cells were washed with18
of porcine alveolar macrophages18
was detected in the18
in pigs exposed to18
cells were washed twice18
a new order comprising18
the dub activity of18
in north america and18
reproductive failure in sows18
immunity to porcine reproductive18
swine to porcine reproductive18
for h and then18
in this study were18
respiratory syndrome virus date18
the presence of the18
pigs porcine reproductive and18
supplemented with fetal bovine17
shown in figure a17
the disease in gnotobiotic17
were expressed as the17
evolution on two continents17
well tissue culture plates17
a critical role in17
the prrsv e protein17
america and experimental reproduction17
cells were inoculated with17
and porcine circovirus type17
divergent evolution on two17
at a multiplicity of17
prrsv at an moi17
by the addition of17
in the order nidovirales17
syndrome virus and porcine17
animal care and use17
isolation of swine infertility17
comprising coronaviridae and arteriviridae17
the expression of ifn17
disease in gnotobiotic pigs17
we found that the17
differential production of proinflammatory17
rna and sg mrna17
proteolytic processing of the17
were transfected with the17
the expression levels of17
of proteins encoded by17
vivo and in vitro17
north america and experimental17
to the swine industry17
in the porcine reproductive17
previous studies have shown16
in cells treated with16
an infectious cdna clone16
of virus replication in16
inhibits porcine reproductive and16
of pigs persistently infected16
susceptibility to porcine reproductive16
respiratory syndrome virus encoded16
the crystal structure of16
a better understanding of16
with prrsv at an16
african green monkey kidney16
or infected with prrsv16
the expression of the16
respiratory disease in pigs16
humoral immune response to16
tissue culture infectious dose16
infected with prrsv alone16
host innate immune response16
similar to those of16
and reproductive syndrome virus16
in vivo and in16
respiratory syndrome virus characterization15
was added to each15
of the lelystad virus15
the detection of porcine15
syndrome virus characterization of15
the structural proteins of15
authors declare that they15
immune responses to porcine15
these results indicate that15
to ldv and eav15
member of the family15
modified live porcine reproductive15
of the most economically15
is related to ldv15
declare that they have15
prrsv nsp and nsp15
these results indicated that15
added to each well15
that they have no15
the north american and15
were considered statistically significant15
porcine respiratory coronavirus in15
compared to pigs infected15
infected or infected with15
were detected in the15
infected with prrsv and15
molecular biology of arteriviruses15
a large number of15
human immunodeficiency virus type15
these results suggest that15
of the prrsv genome15
were washed twice with15
the development of a15
plates were infected with15
a highly pathogenic porcine15
inhibition of porcine reproductive15
are summarized in table15
of influenza a virus15
encoded by orfs to15
by orfs to of15
pigs experimentally infected with15
the viral life cycle15
van marle et al15
care and use committee15
agent of porcine epidemic15
gp and gp proteins15
respiratory syndrome virus is15
related to ldv and15
and then infected with15
of neutralizing antibodies in15
pigs with porcine reproductive15
lower than that of15
syndrome virus in pigs15
to pigs infected with15
evolution of porcine reproductive15
syndrome virus encoded by15
of the virus in15
the development of the15
analysis of porcine reproductive14
the cysteine protease domain14
cells were harvested and14
syndrome virus in the14
syndrome virus isolates with14
prrsv replication in marc14
host innate immune responses14
at the indicated times14
in the cytoplasm of14
is not required for14
of the virus to14
economic losses to the14
of viral rna in14
syndrome virus replication in14
cells were grown in14
response to swine arterivirus14
antiviral activity against prrsv14
pp a and pp14
is essential for virus14
virus isolates with that14
that of the lelystad14
for the expression of14
was used to detect14
of the infected pigs14
on the surface of14
genotype of porcine reproductive14
belongs to the family14
of the nucleocapsid protein14
respiratory syndrome virus induces14
in accordance with the14
the atpase activity of14
in the lipid rafts14
the host response to14
in the swine industry14
medium was replaced with14
isolates with that of14
immune responses in pigs14
a significant increase in14
the mrna level of14
of the adaptive immune14
was performed as described14
of proinflammatory cytokines in14
in the induction of14
atpase activity of prrsv14
with the porcine reproductive14
of type i ifns14
with the immune system14
structural proteins of the14
in the frequency of13
the severity of the13
data are presented as13
cells were cultured in13
immune response in pigs13
challenge of prrs immunology13
the ability of the13
pigs infected with vr13
the inhibitory effect of13
was not detected in13
of the efficacy of13
of the immune system13
little is known about13
cells were washed three13
a modified live porcine13
during the course of13
the culture medium was13
on the cell surface13
infection and proportion of13
it has been reported13
this is the first13
the pathogenicity of two13
the most economically important13
north american strains of13
of prrsv in marc13
g for min at13
proinflammatory cytokines in the13
the largest rna virus13
better understanding of the13
thai medicinal plant extracts13
the genetic diversity of13
three times with pbs13
of differentiation and activation13
may be due to13
was performed according to13
by interfering with the13
the total number of13
of the arterivirus group13
natural science foundation of13
it has been demonstrated13
with bovine serum albumin13
in a humidified co13
duration of infection and13
failure in sows and13
epidemiology of porcine reproductive13
innate immune response by13
a wide range of13
the challenge of prrs13
the cell lysates were13
has been reported that13
a and pp ab13
cells were fixed with13
have been identified in13
are involved in the13
activity of prrsv helicase13
well plates were infected13
and proportion of pigs13
the role of the13
of the arterivirus replicase13
and the number of13
to the development of13
and activation of monocytes13
there was no significant13
has been reported to13
of infection and proportion13
persistently infected with porcine13
the early stage of13
van gorp et al13
work was supported by13
current knowledge on the13
of the orf gene13
this work was supported13
genes of porcine reproductive13
were significantly lower in13
the innate and adaptive13
proportion of pigs persistently13
lymphoid tissues of pigs12
cells were seeded in12
respiratory syndrome virus emerging12
p r o o12
the cells were lysed12
assay was performed as12
humoral and cellular immune12
and interaction with the12
was supported by the12
pathogenesis and interaction with12
virus on united states12
pig lung during different12
concentration of mg ml12
detection and differentiation of12
arterivirus molecular biology and12
of p and p12
activation of monocytes macrophages12
l p r e12
the present study was12
interaction with the immune12
performed as described previously12
on their susceptibility to12
during different respiratory virus12
identification of porcine reproductive12
the nucleocapsid protein of12
blood samples were collected12
in the pathogenesis of12
from porcine reproductive and12
to porcine respiratory coronavirus12
nsp and nsp are12
r o o f12
comparison of the pathogenicity12
a humidified co incubator12
the presence of sqe12
respiratory syndrome virus rna12
at different time points12
american and european isolates12
the pig lung during12
o u r n12
our results showed that12
european and north american12
and approved the final12
we found that prrsv12
u r n a12
this study was to12
syndrome virus gp ectodomain12
n a l p12
is located in the12
molecular biology and pathogenesis12
antibody repertoire development in12
in contrast to the12
the formation of the12
the innate immune system12
innate immunity and porcine12
of the gdd motif12
cytokines in the pig12
r n a l12
the immune response of12
of a highly pathogenic12
the severe acute respiratory12
virus infection in neonatal12
american porcine reproductive and12
be involved in the12
of the pathogenicity of12
the equine arteritis virus12
mutational analysis of the12
alpha response to swine12
at each time point12
virus belonging to the12
characterization of porcine reproductive12
syndrome virus on united12
was performed using the12
in the late s12
virus emerging in china12
after incubation for h12
immunity and porcine reproductive12
be related to the12
of the present study12
of this study was12
european genotype of porcine12
authors read and approved12
united states pork producers12
followed by cycles of12
type i interferon production12
h prior to infection12
differentiation and activation of12
largest rna virus genome12
different respiratory virus infections12
essential for virus infectivity12
for an additional h12
in the lung of12
lung during different respiratory12
a l p r12
and the expression of12
north american porcine reproductive12
with a potent adjuvant12
for h prior to12
pigs of all ages12
and european isolates of12
polyclonal b cell activation12
an infectious clone of12
of two us porcine12
infection in neonatal pigs12
two us porcine reproductive12
high morbidity and mortality12
on the replication of12
respiratory coronavirus in pigs12
the infected cells were12
j o u r12
are listed in table12
syndrome virus emerging in12
infectious cdna clone of12
inactivated porcine reproductive and12
respiratory syndrome virus through12
inhibit the replication of12
in the regulation of12
on united states pork12
in the pig lung12
approved the final manuscript12
interaction between prrsv and12
early stage of infection11
the fact that the11
immune response to the11
nonneutralizing epitopes in the11
monocytes macrophages on their11
as a positive control11
and european porcine reproductive11
as an internal control11
during infection of pigs11
that the expression of11
domain of porcine reproductive11
a crucial role in11
c in a humidified11
replaced with fresh dmem11
the multifunctionality of an11
adaptive immune response to11
structural proteins of porcine11
institutional animal care and11
highly pathogenic strain of11
diversity of porcine reproductive11
deubiquitinating and interferon antagonism11
have shown that prrsv11
until the end of11
set of nonstructural proteins11
the porcine respiratory disease11
virulent porcine reproductive and11
of type porcine reproductive11
read and approved the11
the results indicated that11
of the genome of11
pathogenicity of two us11
cells infected with prrsv11
the interaction between prrsv11
the presence of virus11
a concentration of mg11
cells were stained with11
immunity against porcine reproductive11
was shown to be11
of monocytes macrophages on11
cells transfected with the11
had no effect on11
vaccines against porcine reproductive11
neutralizing and nonneutralizing epitopes11
of an intriguing set11
antigen was detected in11
was carried out using11
comparative pathogenicity of nine11
inhibition of prrsv replication11
these data indicate that11
to those of the11
exploring the multifunctionality of11
has been demonstrated that11
the stability of the11
to a lesser extent11
in sows and respiratory11
compared with the control11
of neutralizing and nonneutralizing11
end of the study11
of porcine epidemic diarrhea11
of the humoral immune11
the inflammatory response to11
epitopes in the porcine11
multifunctionality of an intriguing11
the cells were fixed11
that the presence of11
in an attempt to11
development of adaptive immunity11
was performed using a11
common mucosal immune system11
responses of swine to11
by the end of11
of the infected cells11
statistical analyses were performed11
and cellular immune responses11
was no significant difference11
intriguing set of nonstructural11
were inoculated with prrsv11
phosphorylation and nuclear translocation11
and nonneutralizing epitopes in11
genes involved in the11
the presence of a11
cells were incubated for11
science foundation of china11
in addition to the11
of prrsv in the11
a porcine reproductive and11
with prrsv for h11
cells and pam cultures11
to be involved in11
with the exception of11
porcine alveolar macrophages and11
results are expressed as11
the number of cells11
in the expression of11
supernatants were collected and11
an intriguing set of11
from three independent experiments11
they have no competing11
passages in tissue culture11
or swine influenza virus11
response of swine to11
american and european porcine11
the n protein of11
of gp and m11
of cd t cells11
infected with prrsv strain11
the prrsv gp protein11
plays a key role11
for their ability to11
macrophages on their susceptibility11
persistence of porcine reproductive11
at room temperature for11
challenge with mn c11
and infected with prrsv11
studies are needed to11
at the p position11
member of the arterivirus11
and cd t cells11
infected with nc b11
the mrna levels of11
and lymphoid tissues of11
well plates were co11
respiratory syndrome virus entry11
identification of neutralizing and11
with regard to jurisdictional10
c for s and10
prrsv infection of marc10
syndrome virus in swine10
were washed with pbs10
the endoribonuclease activity of10
these data suggest that10
dub activity of nsp10
in published maps and10
genetic diversity of european10
may play a role10
there was a significant10
molecular characterization of porcine10
were observed in the10
coronavirus infectious bronchitis virus10
protein in porcine reproductive10
syndrome virus isolates in10
have been identified as10
state of differentiation and10
and nuclear translocation of10
than that of the10
of prrsv nsp and10
infection by porcine reproductive10
protective immune response in10
virus infection in pigs10
van reeth and nauwynck10
effects of origin and10
type i ifn production10
culture supernatants were collected10
the orf gene of10
status and future direction10
of immune responses to10
respiratory syndrome virus inhibits10
north american type prrsv10
the middle of the10
jurisdictional claims in published10
of the innate immune10
of viral rna synthesis10
the reciprocal of the10
springer nature remains neutral10
than those in the10
immune responses in the10
inflammatory response to porcine10
commercial porcine reproductive and10
atf and xbp s10
pigs infected with nc10
depletion of cellular cholesterol10
with the presence of10
and the percentage of10
novel structural protein in10
response to porcine respiratory10
claims in published maps10
with porcine circovirus type10
postweaning multisystemic wasting syndrome10
performed to determine the10
was used for the10
nonstructural protein of porcine10
the presence of m10
present in all arteriviruses10
analyses were performed using10
did not have an10
of classical swine fever10
repertoire development in fetal10
virus replication in the10
the plp dub activity10
to jurisdictional claims in10
version of this article10
origin and state of10
and state of differentiation10
virus and porcine circovirus10
in fetal and neonatal10
type and type prrsv10
current status and future10
in the endoplasmic reticulum10
between porcine reproductive and10
immune response against prrsv10
effect of porcine reproductive10
n protein of prrsv10
cysteine protease domain of10
culture medium was replaced10
protease domain of porcine10
american strains of porcine10
in dmem supplemented with10
can be used to10
is known about the10
t cells in the10
derived from the er10
the number of cd10
genotype porcine reproductive and10
as a consequence of10
in pigs vaccinated with10
of type i interferon10
reproductive and respiratory virus10
the immune response against10
response to prrsv infection10
to the end of10
were analyzed using the10
the d kv adj10
and porcine respiratory coronavirus10
infection with prrsv and10
immunological responses of swine10
the cells were harvested10
the use of a10
exacerbates the inflammatory response10
published maps and institutional10
and the role of10
data indicate that the10
structural protein in porcine10
mock infected or infected10
were randomly assigned to10
prrsv is an enveloped10
well plates were transfected10
the presence of ribavirin10
national natural science foundation10
in order to investigate10
development in fetal and10
is consistent with the10
nature remains neutral with10
of pigs at different10
replication of prrsv and10
nine us porcine reproductive10
porcine alveolar macrophages in10
in the middle of10
as well as in10
results suggest that the10
was performed to determine10
remains neutral with regard10
a virulent strain of10
did not affect the10
maps and institutional affiliations10
restriction fragment length polymorphism10
immune response to porcine10
our data indicate that10
have shown that the10
neutral with regard to10
the nucleus and the10
cells in the thymus10
of nine us porcine10
the type i ifn10
that the e protein10
regard to jurisdictional claims10
there is a need10
pathogenicity of nine us10
significant increase in the10
european isolates of porcine10
role of porcine reproductive10
north american type porcine10
compared to those in10
deletion in the nsp10
by the presence of10
of porcine respiratory and10
were performed in triplicate10
role of neutralizing antibodies10
of origin and state10
when the cells were9
of vesicular stomatitis virus9
a clinical and virological9
is important for virus9
play important roles in9
of dendritic cell populations9
immune response of pigs9
essential for virus replication9
prrsv infection in marc9
the united states in9
in the clearance of9
the nuclear localization signal9
and proteolytic processing in9
chinese highly pathogenic strain9
of the pi k9
and porcine epidemic diarrhea9
infected at an moi9
the course of infection9
with prrsv at a9
by porcine respiratory coronavirus9
interferon activation and susceptibility9
not be detected in9
infected with prrsv for9
remains to be determined9
infections of feeder pigs9
immunosuppression exacerbates the inflammatory9
between innate and adaptive9
induced immunosuppression exacerbates the9
characterization of proteins encoded9
infection porcine reproductive and9
the lungs and lymphoid9
it is important to9
arterivirus replicase orf a9
hek t cells were9
the context of prrsv9
highly virulent porcine reproductive9
our results suggest that9
a chinese highly pathogenic9
was replaced with fresh9
respiratory syndrome virus a9
the remainder of the9
the case of prrsv9
and systemic immune responses9
in the early stage9
virus in the lungs9
treatment of cells with9
alternative orf present in9
their susceptibility to porcine9
adaptive immune responses to9
encoded proteinases and proteolytic9
have no competing interests9
neutralizing antibodies in prrsv9
of the n protein9
at the site of9
that the prrsv e9
to the proteins of9
dendritic cells infected with9
structural biology of prrsv9
vr or mn c9
our results indicated that9
virus followed by porcine9
supernatants were collected at9
challenges for porcine reproductive9
virus encoded by an9
proteinases and proteolytic processing9
activation and susceptibility of9
after challenge with mn9
was carried out with9
structural protein of porcine9
respiratory coronavirus or swine9
the ability of prrsv9
the mutant t g9
was used as an9
the open reading frame9
inhibitory effect on the9
nucleus and the cytoplasm9
response to prrsv is9
compared to the vector9
of feeder pigs with9
encoded by an alternative9
african swine fever virus9
the chinese highly pathogenic9
fetal and neonatal piglets9
type i interferon signaling9
pcv a and pcv9
followed by porcine respiratory9
the acute phase of9
the formation and nuclear9
have been reported to9
the structural biology of9
syndrome virus in a9
antiviral activity of ribavirin9
vaccine with a potent9
type i interferon activation9
the antiviral effect of9
cell populations to porcine9
comparison of the north9
a and pcv b9
studies with the porcine9
susceptibility of dendritic cell9
would like to thank9
dendritic cell populations to9
processing in the nidovirales9
orf present in all9
and susceptibility of dendritic9
prrsv and pedv were9
on the development of9
cells were maintained at9
respiratory tract of pigs9
with a chinese highly9
load in the lungs9
sites of virus replication9
an equal volume of9
of antigen presenting cells9
and in vitro interferon9
levels of neutralizing antibodies9
of the equine arteritis9
infected with prrsv or9
the expression of prrsv9
attenuation of porcine reproductive9
was performed as previously9
a broad range of9
committee on taxonomy of9
antibody response to prrsv9
by plasmacytoid dendritic cells9
syndrome virus strain vr9
can be used as9
equine arteritis virus replicase9
the expression of small9
kindly provided by dr9
an increase in the9
feeder pigs with porcine9
virus in swine sera9
were obtained from the9
infection in gnotobiotic pigs9
respiratory syndrome virus identification9
and the presence of9
the e protein is9
molecular epidemiology of prrsv9
prrsv gp and m9
innate immune response to9
the culture supernatants were9
performed as previously described9
of prrsv have been9
in the lung and9
the second lps administration9
to induce neutralizing antibodies9
an alternative orf present9
cells were fixed and9
dual infections of feeder9
with porcine respiratory coronavirus9
expressed as the mean9
coronavirus or swine influenza9
on the structural proteins9
in subgenomic mrna synthesis9
on taxonomy of viruses9
for h at rt9
by intranasal delivery of9
i interferon activation and9
emergence of a virus9
increase in the frequency9
terminal region of the9
replication in cell culture9
then washed three times9
respiratory syndrome virus followed9
the immune system and9
failure of unknown etiology9
a final concentration of9
for min at rt9
was extracted from the9
for the first time9
the authors declare no9
by western blot analysis9
of hepatitis c virus9
the common mucosal immune9
reproductive failure of unknown9
play a key role9
their ability to induce9
were cloned into the9
can be divided into9
was performed in a9
of type i interferons9
immunization of pigs with9
a protective immune response9
likely due to the9
washed twice with pbs9
for the generation of9
in response to prrsv9
could not be detected9
test for the detection9
infection in pigs is9
nsp and nsp were9
pathogenic strain of porcine9
north american isolates of9
in a co atmosphere9
cell lysates were prepared9
syndrome virus followed by9
protective immune response against9
the induction of ifn9
and is important for9
as the reciprocal of9
nucleocapsid protein of porcine9
isolates in a five9
the absence of e9
encoded by orf b9
most economically important diseases9
by an alternative orf9
may be related to9
international committee on taxonomy9
a new group of9
was approved by the9
cells were then washed9
in this study was9
in any of the9
the nature of the9
the replication of both9
the viral genome and9
knowledge on the structural9
viral load in the9
cholesterol is required for9
five times in pbs9
the respiratory tract of9
test was used to9
porcine respiratory coronavirus or9
activation of b cells9
vaccine against porcine reproductive9
populations to porcine arterivirus9
has been observed in9
proteolytic processing in the9
the first line of9
between prrsv and the9
were found in the9
differential type i interferon9
nine open reading frames9
h and then infected9
were washed five times9
were washed once with9
it is difficult to9
on the basis of9
the nsp nsp junction9
was due to the9
has the potential to9
compared to that of9
was found in the9
analysis was performed using9
clinical and virological study9
are shown in table9
the arterivirus replicase orf9
infectious cdna clones of9
monoclonal antibodies to the9
the method of reed9
losses to the swine9
losses in the swine9
of the presence of9
against homologous and heterologous9
of north american type9
the proteins of porcine9
rna was isolated from8
respiratory syndrome virus during8
containing fetal bovine serum8
the pcr products were8
the inhibition of prrsv8
the presence of maternal8
and future vaccine development8
cells were stimulated with8
induction of t helper8
assessment of the efficacy8
a second lps administration8
the prrsv genome is8
to of lelystad virus8
based on measurement of8
at various time points8
induce the expression of8
orfs to of lelystad8
protein possesses deubiquitinating and8
these data show that8
the online version of8
macrophage recruitment in porcine8
acid deletion in the8
were performed using the8
were collected by centrifugation8
to of porcine reproductive8
the arterivirus nsp protease8
involves both glycoprotein as8
immune responses to the8
in our previous study8
were negative for prrsv8
live virus vaccine with8
cells were pretreated with8
but not in the8
pigs infected with the8
after three washes with8
prrsv strain jxwn plp8
respiratory syndrome virus reveals8
equine arteritis virus is8
protein to the nucleolus8
tissues of pigs at8
there were no significant8
in serum and semen8
syndrome virus through glycan8
by dendritic cells infected8
cell and macrophage recruitment8
both glycoprotein as well8
tissue culture infective dose8
serum immune responses to8
in pigs is independent8
that overlaps the gp8
nuclear translocation of isgf8
evolution of prrsv in8
results indicate that the8
respiratory syndrome viruses differ8
significant economic losses to8
to prrsv infection in8
qiaamp viral rna mini8
agents associated with respiratory8
identification and characterization of8
cells in the lungs8
to the lack of8
for the assembly of8
and interferon antagonism functions8
in agreement with previous8
glycoprotein as well as8
the structure of the8
should be noted that8
american type porcine reproductive8
american isolates of porcine8
of a virus subpopulation8
gene that overlaps the8
immune responses against prrsv8
in the thymus of8
was significantly reduced in8
increase in the number8
performed according to the8
a significant reduction in8
of nap on prrsv8
play a critical role8
of commercial porcine reproductive8
virus nucleocapsid protein to8
of the order nidovirales8
caused by porcine reproductive8
by inhibition of the8
region of the arterivirus8
those in the vector8
as well as glycoprotein8
producing cells and virological8
discovery of a small8
could be used to8
virological parameters of protection8
important for virus production8
a virus subpopulation during8
belonging to the family8
expression levels of the8
online version of this8
and macrophage recruitment in8
regulatory cells by dendritic8
orfs to of porcine8
to the absence of8
syndrome virus strains of8
the north american type8
with paraformaldehyde for min8
and then incubated with8
ability of prrsv to8
of a modified live8
are presented as the8
and transport of proteins8
antibodies in prrsv protective8
the interaction between trim8
in this study we8
normalized to that of8
different time intervals after8
with a mixture of8
was carried out in8
intervals after inoculation with8
cells as described previously8
detected in the serum8
pigs is independent of8
glycan shielding involves both8
of protection upon challenge8
virulent strain of porcine8
polyclonal activation of b8
t cell responses to8
was determined to be8
of the number of8
sequence and is important8
of a porcine reproductive8
used to detect the8
as compared to the8
modulates host innate immune8
pigs at different time8
mucosal and systemic immune8
vaccines based on measurement8
it should be noted8
family arteriviridae in the8
virus nonstructural protein possesses8
cells infected with porcine8
from the endoplasmic reticulum8
severe reproductive failure in8
virus infection or vaccination8
for prrsv and pedv8
of t helper regulatory8
the global swine industry8
during entry of the8
through glycan shielding involves8
is in agreement with8
study was supported by8
of mouse hepatitis virus8
de lima et al8
to the site of8
at rpm for min8
were harvested and the8
targets in the lungs8
and virological parameters of8
by inhibiting irf activation8
by antagonizing irf activation8
each of the two8
of a small arterivirus8
monkey kidney cell line8
the plates were incubated8
protein is essential for8
on measurement of serologic8
efficacy of commercial porcine8
the virus from the8
for the production of8
the entry of prrsv8
over the course of8
to western blot analysis8
of plp dub activity8
plates were incubated for8
morbidity and mortality in8
statistical analysis was performed8
a pivotal role in8
a live virus vaccine8
small arterivirus gene that8
time intervals after inoculation8
measurement of serologic response8
to better understand the8
den born et al8
t helper regulatory cells8
were performed according to8
infected cells were maintained8
induce the formation of8
evasion of porcine reproductive8
in immortalized porcine alveolar8
end of the first8
sodium azide in pbs8
in the lung homogenate8
that the n protein8
parameters of protection upon8
the specificity of the8
may be involved in8
nonstructural protein possesses deubiquitinating8
possesses deubiquitinating and interferon8
not induce treg cells8
in prrsv protective immunity8
dmem supplemented with fbs8
immortalized porcine alveolar macrophages8
all authors read and8
reproductive failure induced by8
is responsible for the8
interaction between trim and8
van gucht et al8
of prrsv infection on8
immune evasion of porcine8
the level of virus8
of the prrs virus8
new group of positive8
the autophagosomes induced by8
is independent of virus8
end of the genome8
demonstrated that prrsv nsp8
used as a negative8
the expression of cd8
nested set of six8
key role in the8
syndrome virus identification of8
potentiation of porcine reproductive8
in pigs inoculated with8
two genotypes of prrsv8
the efficacy of commercial8
a small arterivirus gene8
prrsv and mycoplasma hyopneumoniae8
respiratory syndrome virus at8
the viral loads in8
experimentally infected with porcine8
are fully resistant to8
on prrsv replication was8
virus infection in gnotobiotic8
group was injected with8
the p and p8
arteriviridae in the order8
tl co hb kg8
the relative levels of8
samples were collected from8
the results of this8
nucleocapsid protein to the8
of european porcine reproductive8
derived dendritic cells and8
cells and virological parameters8
inoculation with porcine reproductive8
overlaps the gp coding8
virus by monoclonal antibodies8
to the arteriviridae family8
both mucosal and systemic8
economic losses in the8
significantly higher levels of8
responses to the proteins8
nuclei were stained with8
protection against reproductive failure8
the family arteriviridae in8
after inoculation with porcine8
with prrsv and pedv8
k fitsrcrl and f8
was supported by a8
recruitment in porcine reproductive8
in infected pigs and8
van den born et8
implications for current vaccine8
pigs were randomly assigned8
cellular targets in the8
gp coding sequence and8
virus isolates in the8
virus through glycan shielding8
and emergence of a8
our understanding of the8
replicase orf a protein8
experiments were performed in8
transport of proteins encoded8
tonsil and lymph nodes8
the gp coding sequence8
the replication cycle of8
independent of virus load8
randomly assigned to one8
of cellular targets in8
at different time intervals8
under the control of8
fitsrcrl and f gymtfvhf8
assigned to one of8
was significantly higher than8
arterivirus gene that overlaps8
irf phosphorylation and nuclear8
as a model for8
helper regulatory cells by8
were no significant differences8
coding sequence and is8
a chimeric virus with8
cells by dendritic cells8
and c kv adj8
syndrome viruses differ in8
at the indicated time8
shielding involves both glycoprotein8
transmission of porcine reproductive8
rule out the possibility7
delivery of a live7
nuclear accumulation of isgf7
the immune response in7
respiratory syndrome virus contains7
of prrsv infection in7
play a crucial role7
sufficient to increase susceptibility7
replicase is mediated by7
probably due to the7
detection of viral rna7
gp protein encoded by7
extracted from lysates of7
in pigs experimentally infected7
pigs upon experimental infection7
rna was reverse transcribed7
susceptibility of piglets to7
used to evaluate the7
vaccine efficacy and future7
response in porcine reproductive7
viral rna in serum7
protein is the most7
following infection with prrsv7
was used to evaluate7
endoribonuclease activity of nsp7
the ectodomain of gp7
against a heterologous prrsv7
is sufficient to increase7
the early stages of7
of lelystad virus and7
replication and sg mrna7
derived dendritic cells but7
to increase susceptibility of7
reproductive syndrome virus strain7
genomic rna replication and7
no significant differences in7
blocked the dub activity7
response by antagonizing irf7
rna virus belonging to7
it is likely that7
hyopneumoniae potentiation of porcine7
protease and is essential7
identification of cellular targets7
macrophages and dendritic cells7
virus vaccine with a7
shown to interact with7
cd and cd t7
the first week of7
the supernatants were collected7
serum and semen of7
north american prrsv strains7
absence of e protein7
was used for all7
porcine high fever syndrome7
viral loads in the7
dendritic cells and compromises7
of genomic rna and7
three washes with pbs7
entry of porcine reproductive7
were considered to be7
with d kv adj7
the absence of a7
the concentration of the7
syndrome virus contains a7
for simultaneous detection and7
fold lower than that7
infection remains to be7
essential for porcine reproductive7
comparison of the structural7
was used to calculate7
cdna clone of a7
not related to its7
of lipid rafts in7
the majority of the7
and sg mrna transcription7
virus is sufficient to7
syndrome virus infection or7
mg kg body weight7
may contribute to the7
respiratory syndrome virus into7
identification of a novel7
incubated for min at7
are expressed as the7
expressing gp and m7
were mock infected or7
effect of prrsv on7
associated with respiratory diseases7
coding sequences of the7
and its role in7
treatment and prevention of7
structural protein coding regions7
remains to be elucidated7
syndrome virus by monoclonal7
the severity of clinical7
of an infectious clone7
comparison of lelystad virus7
entry of the porcine7
irf activation in immortalized7
by nsp serine protease7
in the activation of7
and ability to induce7
t cells were transfected7
in the writing of7
these findings suggest that7
virus in pigs during7
virus in infected pigs7
were collected at different7
directed mutagenesis of the7
epidemic diarrhea virus infection7
the infected pigs at7
was measured at nm7
as the negative control7
of the parental virus7
the host immune system7
the activation of the7
and respiratory disease in7
has not yet been7
membrane was incubated with7
not a togavirus but7
the transcript abundance of7
n protein between the7
efficacy and future vaccine7
inhibit type i interferon7
togavirus but belongs to7
of arterivirus replicase is7
ii porcine reproductive and7
van breedam et al7
glycosylation of porcine reproductive7
vero cells were treated7
lungs and lymphoid tissues7
a result of the7
and respiratory distress in7
been shown to inhibit7
on the presence of7
were significantly higher in7
at c for min7
were used as the7
of infection under farm7
treated with ng ml7
swine influenza h n7
and transferred to a7
challenge by streptococcus suis7
cd expression confers susceptibility7
type i ifn response7
infected cells at hpi7
the infected cells at7
during the critical window7
and identification of cellular7
infected cells were then7
of prrsv genomic rna7
serine protease and is7
detection of antibody to7
viral rna was extracted7
the purpose of this7
and mycoplasma hyopneumoniae co7
virus by intranasal delivery7
a secondary antibody staining7
the relative abundance of7
quantification and identification of7
at h after the7
to the fact that7
the highly pathogenic prrsv7
inhibited the replication of7
to challenge by streptococcus7
but belongs to the7
the etiological agent of7
prrsv infectious cdna clone7
virus nucleocapsid protein modulates7
the titers of prrsv7
increase susceptibility of piglets7
subpopulation during infection of7
i interferon signaling by7
virus mystery swine disease7
at h post infection7
the evolution of porcine7
well cell culture plates7
and cloned into the7
heart and lymphoid system7
subtype porcine reproductive and7
between the nucleus and7
mediated by nsp serine7
is mediated by nsp7
open reading frame b7
crystal structure of the7
the presence of viral7
reciprocal of the highest7
and lymphoid system of7
cells infected with isolate7
a togavirus but belongs7
viruses differ in non7
data were analyzed using7
amplified by pcr and7
syndrome virus in serum7
of the first week7
sows and respiratory distress7
response in the lungs7
sequence analysis of the7
syndrome virus variant associated7
to determine whether the7
set of subgenomic mrnas7
with porcine high fever7
syndrome virus infection of7
at all time points7
infected with porcine respiratory7
green monkey kidney cell7
confers susceptibility to porcine7
related to its virulence7
after challenge with vr7
were positive for prrsv7
that prrsv strain jxwn7
virus and swine infertility7
of mystery swine disease7
this study was supported7
incubated for an additional7
and swine influenza virus7
in the production of7
of an inactivated vaccine7
previous studies demonstrated that7
nb activation by prrsv7
and swine infertility and7
care and use of7
semen of adult boars7
a highly pathogenic prrsv7
van nieuwstadt et al7
for the purpose of7
and gp of porcine7
and the north american7
virus subpopulation during infection7
was detected with a7
were purchased from sigma7
individual pigs upon experimental7
virus in serum and7
cd join forces during7
variation of porcine reproductive7
syndrome virus productively infects7
we focused on the7
number of infected cells7
no significant difference in7
characterization of the humoral7
syndrome virus gp on7
virus gp on virus7
china is not related7
porcine high fever disease7
it is clear that7
but does not induce7
expressed as the reciprocal7
experimental porcine reproductive and7
in the heart and7
inhibits the replication of7
the time of infection7
classical north american type7
are shown in fig7
virus variant associated with7
were performed for each7
were shown to be7
respiratory syndrome virus type7
in the nsp of7
the hepatitis c virus7
emerging in china is7
development of the interferon7
was used in this7
early stages of infection7
recovery of virus replication7
we would like to7
of the severe acute7
respiratory syndrome virus isolate7
of piglets to challenge7
was significantly higher in7
associated with porcine high7
did not affect viral7
in china is not7
reverse genetics system for7
is not a togavirus7
recombination between north american7
nsp of highly pathogenic7
current vaccine efficacy and7
blocked with bovine serum7
ability to induce neutralizing7
detection of antibodies to7
the heart and lymphoid7
by in situ hybridization7
the s specificity pocket7
in individual pigs upon7
forces during entry of7
note springer nature remains7
simultaneous detection and differentiation7
lelystad virus and swine7
were determined using the7
the data presented in7
chinese highly pathogenic porcine7
of clinical signs and7
phenotype and genotype diversity7
clone of a highly7
of the sdd motif7
the duration of the7
in the sdd motif7
quasispecies and emergence of7
significant difference between the7
of the structural protein7
the level of atpase7
respiratory syndrome virus molecular7
virus and establishes sterilizing7
between north american strains7
is also possible that7
immune response by antagonizing7
cells were then incubated7
of a canadian porcine7
antigenic comparison of lelystad7
at c for h7
located in the middle7
on ice for min7
porcine circovirus type and7
processing of the open7
treated with dnase i7
the north american genotype7
the membrane was incubated7
host response to prrsv7
is involved in the7
was used to determine7
properties of tulathromycin in7
the mechanism of prrsv7
mediated innate immunity and7
of prrsv in a7
washed once with pbs7
failure induced by a7
syndrome virus and establishes7
the intensity of the7
the major structural proteins7
it was demonstrated that7
syndrome virus in china7
with type porcine circovirus7
of pigs with a7
level of atpase activity7
be attributed to the7
the development of an7
intranasal delivery of a7
at a ratio of7
aliquoted and stored at7
respiratory syndrome virus variant7
virus quantification and identification7
virus is not a7
of transmissible gastroenteritis virus7
against reproductive failure induced7
and cd join forces7
a canadian porcine reproductive7
at a density of7
closely related to the7
with respiratory diseases in7
the absence of any7
syndrome virus in semen7
into porcine alveolar macrophages7
molecular evolution of prrsv7
evaluation of immune responses7
formation and nuclear translocation7
the international committee on7
the existence of two7
heterogeneity of porcine reproductive7
collected by centrifugation at7
cells were subjected to7
the virus inoculum was7
type i interferon induction7
viral titers were measured7
viral rna mini kit7
gp on virus infectivity7
activation in immortalized porcine7
dna and rna viruses7
standard error of the7
expression of prrsv nsp7
encoded part of arterivirus7
cells were incubated at7
lower than those in7
the national natural science7
virus and related viruses7
the writing of the7
to induce protection against7
of a live virus7
under the same conditions7
dendritic cells but does7
part of arterivirus replicase7
transcription polymerase chain reaction7
piglets to challenge by7
for nsp to inhibit7
due to the absence7
virus productively infects monocyte7
of plasma membrane cholesterol7
the production of ifn7
statistical significance was determined7
by a virulent strain7
in pigs of all7
of the virus from7
and establishes sterilizing immunity7
does not induce treg7
as a template for7
the care and use7
and evolution of porcine7
prrsv n protein was7
then inoculated with prrsv7
the synthesis of prrsv7
length sequence of a7
the control pigs at7
persistence in individual pigs7
mycoplasma hyopneumoniae potentiation of7
that the pi k7
the expression of trim7
with the expression of7
for the study of7
of the arterivirus replication7
and compromises their antigen7
could be due to7
of pigs with vr7
sialoadhesin and cd join7
were monitored daily for7
in the lymph nodes7
in pigs during early7
pigs were negative for7
the inhibition of ifn7
acid sequence of nsp7
sequence of a canadian7
the gp and gp7
antigen in the heart7
the detection of antibody7
prevention and control of7
respiratory syndrome virus productively7
with prrsv or pedv7
be found in the7
and semen of adult7
for current vaccine efficacy7
cells and compromises their7
in agreement with the7
prrsv infection and the7
dendritic cells to porcine7
ability of the virus7
presence of maternal antibodies7
standard curve was generated7
in porcine nidovirus infection7
no conflict of interest7
of the prrsv n7
plates were transfected with7
by streptococcus suis type7
were measured using a7
the role of porcine7
nonstructural and structural proteins7
expression confers susceptibility to7
of the gp ectodomain7
of genes involved in7
pigs did not show7
or a combination of7
of the chimeric vlps7
an inhibitory effect on7
canadian porcine reproductive and7
nsp serine protease and7
were introduced into the7
states porcine reproductive and7
inhibiting irf activation in7
were inoculated with acaprrs7
to the major structural7
used for detection of7
was also observed in7
highly pathogenic prrsv strain7
approximately kb in length7
for the swine industry7
cd cd t cells7
during early stage of7
to investigate whether the7
modulating properties of tulathromycin7
no effect on the7
gradual development of the7
join forces during entry7
prrsv infection in the7
of green fluorescent protein7
emergence of highly pathogenic7
description of persistence in7
pigs during early stage7
stage of infection under7
evolving the largest rna7
the number of infected7
syndrome virus is sufficient7
nucleic acid sequence of7
after vaccination with a7
amino acid sequences of7
prrsv antigen was detected7
sasa quelpaertensis nakai extract7
after removal of the7
have been used as7
were stained with dapi7
how to make sense7
the clearance of prrsv7
response against prrsv is7
cells but does not7
the active site loop7
cells of the monocyte7
of the open reading7
and reproductive failure in7
of interferon regulatory factor7
washed five times in7
it is also possible7
syndrome virus by intranasal7
the indicated time points7
in their ability to7
the swine industry in7
following infection with porcine7
the host innate immune7
variant associated with porcine7
streptococcus suis type ii7
replication of prrsv was7
of the host response7
is not related to7
induced by a virulent7
used as a control7
of persistence in individual7
arterivirus replicase is mediated7
infection under farm conditions7
elevating virus and related7
it is known that7
and is essential for7
sequences of the vr7
the nsp of highly7
variation in porcine reproductive6
prevention of porcine reproductive6
cells supporting virus replication6
essential for nsp to6
viral respiratory disease in6
an essential role in6
with highly pathogenic porcine6
adaptive immunity against porcine6
is required for the6
in the modulation of6
neutralizing antibody response to6
new insights into the6
immune response to infection6
the data indicated that6
cellular rna was extracted6
the pigs infected with6
between trim and rig6
homologous and heterologous challenges6
of balb c mice6
endoribonuclease nendou exerts pleiotropic6
of the unfolded protein6
detected in the lungs6
interaction between nsp and6
infected pigs compared with6
were washed with cold6
infected with type porcine6
the viral genome is6
due to porcine reproductive6
bovine viral diarrhea virus6
immune dysregulation is caused6
an inactivated vaccine against6
of the nidovirus replicative6
vaccine investigated by parallel6
on porcine alveolar macrophages6
due to lack of6
swine with a chinese6
shuffling of the gp6
resulting in immune dysregulation6
contains a cluster of6
which was associated with6
virus comparative pathogenicity of6
ribosomes to synthesize an6
respiratory syndrome virus immune6
complete nucleotide sequence of6
production by interfering with6
as early as days6
the mechanisms by which6
lymphoid system of three6
the nsp main proteinase6
is caused by porcine6
on prrsv replication in6
to be associated with6
protected from porcine reproductive6
at c in a6
of new genetic subtypes6
for detection of porcine6
virus strains of exceptional6
was to characterize the6
their ability to cause6
nap on prrsv replication6
specificity of the immune6
we also found that6
transducer and activator of6
for foreign gene expression6
coding regions for nonstructural6
nucleocapsid protein modulates interferon6
whole cell lysate of6
the critical window of6
ability against a heterologous6
to control prrsv infection6
to the parental virus6
levels of pedv n6
has been used to6
with an improved cross6
in eastern europe support6
macrophages porcine reproductive and6
a novel structural protein6
were divided into three6
products were purified using6
respiratory diseases in pigs6
a significant role in6
the arterivirus life cycle6
at dpi and the6
infection in porcine lung6
activity did not affect6
at the concentration of6
strains of the prrs6
gnotobiotic pigs porcine reproductive6
were added to the6
was propagated in marc6
maintained in fresh medium6
was extracted from lysates6
crystal structure of prrsv6
of north american and6
middle east respiratory syndrome6
envelope protein requirements for6
for h and were6
of prrsv or pedv6
hepatitis c virus ns6
syndrome virus in infected6
of pigs following vaccination6
to investigate the effect6
the predicted helicase of6
virus strains of the6
was calculated using the6
of two genotypes of6
with the indicated antibodies6
solutions for treatment and6
between the presence of6
were fixed with paraformaldehyde6
were treated with m6
kda structural protein of6
least open reading frames6
combination of p and6
into the porcine macrophage6
and prevention of porcine6
localization signal of the6
mucosal and systemic sites6
be detected in the6
and found that the6
pigs coinfected with a6
novel structural protein of6
performed in accordance with6
reduced ability to induce6
from an infectious clone6
respiratory syndrome virus using6
existence of two genotypes6
at a dilution of6
method of estimating fifty6
of positive strand rna6
of african swine fever6
has been found to6
to test the stability6
prrsv infection in porcine6
observed in the infected6
be responsible for the6
to be able to6
after infection with prrsv6
were approved by the6
hek cells were transfected6
support the definition of6
lower in iln than6
and evasion strategies for6
a high mutation rate6
immune responses of pigs6
infected pigs at dpi6
in their susceptibility to6
these results demonstrate that6
the midwestern united states6
american strains of prrsv6
european strains of porcine6
respiratory syndrome virus emerged6
hypotheses in porcine reproductive6
characterization of a new6
ifa as described above6
the development of new6
we demonstrated that the6
united states swine with6
the plates were washed6
no inhibitory effect on6
serum samples were collected6
with different isolates of6
there was no evidence6
lymphoid hyperplasia resulting in6
nsp was essential for6
was measured using a6
of the highly pathogenic6
collected at different time6
growth of porcine reproductive6
and differentiation of hp6
were used in this6
and replication of porcine6
chimeric construction with vaccine6
link between innate and6
of prrsv nsp in6
of the gp genes6
tomography of porcine reproductive6
syndrome virus in porcine6
time pcr was performed6
as a source of6
epitope of porcine respiratory6
protective immunity to porcine6
responses and evasion strategies6
paraformaldehyde for min at6
major histocompatibility complex class6
vitro prrsv and mycoplasma6
of prrsv helicase was6
exceptional diversity in eastern6
perspective from the united6
were challenged with prrsv6
united states porcine reproductive6
the titer of prrsv6
fixed in neutral buffered6
effects on the arterivirus6
from lysates of the6
with various strains of6
these data suggested that6
been found to be6
arteritis virus is not6
eastern europe support the6
porcine circovirus type in6
that the ability of6
study was to characterize6
was detected in all6
pigs were monitored daily6
response and persistence of6
genome of lelystad virus6
are representative of the6
to inhibit prrsv replication6
epithelial cells of the6
respiratory syndrome virus non6
r d systems inc6
simple method of estimating6
control of prrsv infection6
in immune dysregulation is6
total cellular rna was6
complete genome analysis of6
representative of the mean6
in type i ifn6
stat stat nuclear translocation6
of the two major6
protein of equine arteritis6
gilts and multiparous sows6
a major cause of6
of virus replication with6
the gp genes of6
in cells transfected with6
and the development of6
associated with prrsv infection6
combination of both organisms6
the transcription factor complex6
the use of peptide6
like porcine reproductive and6
under a fluorescence microscope6
were inserted into the6
pbs for min at6
compared to the control6
were obtained from a6
may play an important6
were removed from the6
isolates in the midwestern6
syndrome virus gp protein6
against a heterologous challenge6
was used in the6
a heterologous prrsv strain6
modulation of host cell6
critical role in the6
generation of an infectious6
was associated with a6
protein has been shown6
be used as an6
pleiotropic effects on the6
it was reported that6
as indicated by the6
at a dose of6
porcine epidemic diarrhoea virus6
pams were transfected with6
infectious virions of porcine6
to prrsv in utero6
more severe clinical signs6
of human immunodeficiency virus6
of phenotype and genotype6
fixed with paraformaldehyde for6
with an antigenically distinct6
as well as a6
the detection of antibodies6
belonging to the arteriviridae6
protection against prrsv infection6
room temperature for min6
to the use of6
type isolate of porcine6
proinflammatory cytokines and viral6
and h n influenza6
there was no effect6
beta modulates host innate6
spread of the virus6
i interferon production by6
regions for nonstructural and6
mrna levels of pedv6
samples were positive for6
and respiratory syndrome to6
in the lung parenchyma6
to protect gilts against6
confers protection against reproductive6
it is reasonable to6
have been observed in6
the complete nucleotide sequence6
evasion strategies for porcine6
antibodies directed against the6
for the care and6
in the immune system6
the efficacy of a6
in the viral envelope6
the type i interferon6
expression of both tnf6
frameshifting by mammalian ribosomes6
cells were washed once6
page and transferred to6
not included in the6
geographical dissection of north6
in most of the6
genetic variation in porcine6
for the analysis of6
the c kv adj6
be explained by the6
of coding regions for6
the viral copy numbers6
essential genes a and6
when compared to those6
to be the major6
of six or seven6
and geographical dissection of6
and control of the6
characterization of antigenic regions6
a continuous cell line6
south dakota state university6
primer pairs sf sr6
antigenic regions in the6
the cells were treated6
pigs vaccinated with prrs6
the site of infection6
a simple method of6
proteins of the virion6
a perspective from the6
the possibility that the6
a vital role in6
used as the negative6
most of the virus6
tropism in cell culture6
syndrome virus entry into6
have an effect on6
in the innate immune6
used to determine the6
the virus life cycle6
of cd and cd6
failure of an inactivated6
as shown by the6
immune correlates of protection6
clearance of the virus6
binding motif of sla6
in the first experiment6
three times with cold6
for min on ice6
genetic diversity of the6
the number of prrsv6
production by inhibiting irf6
lysates of the infected6
domains i and ii6
effect of tomatidine on6
influenza a virus in6
and evolution of the6
protein requirements for the6
to the coronaviruslike superfamily6
inhibitory effect of nap6
and viral respiratory disease6
pigs naturally infected with6
set of six or6
various strains of porcine6
persistence of the porcine6
with the n protein6
may be important for6
activity of nsp was6
virus and mycoplasma hyopneumoniae6
is the causative agent6
in a continuous cell6
syndrome virus strain mn6
cd t cells in6
in balb c mice6
expression of type i6
response of pigs following6
were separated by sds6
and hypotheses in porcine6
onset of humoral immunity6
were used for the6
porcine circovirus type infection6
are derived from the6
for the existence of6
acute phase of infection6
is the most abundant6
the assembly of infectious6
and then treated with6
of the putative m6
were incubated for an6
following vaccination with various6
prrsv infection has been6
produces a chimeric virus6
respiratory syndrome virus immunobiology6
nested set of subgenomic6
then infected with prrsv6
the us prrsv vr6
required for prrsv replication6
carried out with the6
dysregulation is caused by6
as the secondary antibody6
protein coding sequences of6
from pigs infected with6
results suggested that the6
role in the clearance6
investigated by parallel mutations6
on the arterivirus life6
nendou exerts pleiotropic effects6
in the level of6
inactivated vaccine against porcine6
of humoral immune response6
the nidovirus replicative endoribonuclease6
respiratory syndrome to protect6
synergism between porcine reproductive6
jxwn at an moi6
the activation of autophagy6
virus encoded by orf6
the clearance of the6
of the porcine respiratory6
electron tomography of porcine6
of host cell responses6
european subtype porcine reproductive6
regions in the porcine6
a combination of both6
innate immune response and6
the antiviral function of6
europe and north america6
at h post transfection6
separation of coding regions6
was significantly lower in6
de vries et al6
by nsp and nsp6
internalized viruses were titrated6
was significantly increased in6
includes equine arteritis virus6
in a previous study6
this article can be6
were used to detect6
the protection conferred by6
followed by incubation with6
expression and replication of6
of infectious cdna clones6
replicative endoribonuclease nendou exerts6
cd in the lipid6
nucleocapsid protein attenuate virus6
nsp to inhibit ifn6
by mammalian ribosomes to6
virus vaccine investigated by6
the later stages of6
rna virus with a6
interfering with the rig6
transferred to a nitrocellulose6
did not result in6
studies have indicated that6
positive strand rna virus6
heterologous challenge with prrsv6
their susceptibility to prrsv6
expanding diversity of porcine6
these results are consistent6
is required for porcine6
functional properties of the6
the african green monkey6
were infected at an6
the rjxwn challenge and6
the absence of prrsv6
respiratory syndrome viruses in6
for replication in cell6
results of this study6
origin and evolution of6
method of reed and6
of a novel structural6
cells were harvested at6
at g for min6
to evaluate the efficacy6
efficacy of porcine reproductive6
after the second lps6
of infectious virions of6
supported by the national6
vaccinated pigs had significantly6
field isolates of prrsv6
the proteolytic activity of6
current state of play6
in the control group6
virus with an improved6
proteins of lactate dehydrogenase6
the lungs of prrsv6
a standard curve was6
lelystad virus strains of6
foot and mouth disease6
primary pams treated with6
significant differences between the6
will be required to6
diagnosis of porcine reproductive6
prrsv replication in vitro6
europe support the definition6
virions of porcine reproductive6
then incubated for h6
doubts and hypotheses in6
with different concentrations of6
syndrome virus vaccine investigated6
partial protection against prrsv6
the structural protein coding6
been shown that the6
was no effect of6
membrane cholesterol is required6
the data suggest that6
experimental infection of united6
reproductive failure in pregnant6
of cholesterol in the6
are protected from porcine6
construction with vaccine sequence6
monitored for clinical signs6
in the sera of6
the nucleocapsid protein n6
was essential for nsp6
cytokines and viral respiratory6
specific cd t cells6