ライフサイエンスコーパス: inoculation

1 perinfection compared to the control (single inoculation).

2 ation of RSV infection or 6 days after virus inoculation.

3 1,762 downregulated genes in RF under fungus inoculation.

4 mice die soon after systemic or intravaginal inoculation.

5 FN-gamma) knockout mice following intracolon inoculation.

6 rus and Vibrio infection compared to peroral inoculation.

7 decreased in cerberus roots after rhizobial inoculation.

8 etized rats when moribund or 18 h after MRSA inoculation.

9 at received PG-CAT as a treatment post-viral inoculation.

10 sis factor (TNF) within 24 hours of pathogen inoculation.

11 nd carried the vector for over 60 days after inoculation.

12 was used to measure plant disease after TCV inoculation.

13 to the upper genital tract via transcervical inoculation.

14 ected RSV-inoculated AB mDC to secondary IAV inoculation.

15 cervical secretions immediately after HSV-2 inoculation.

16 ming inoculation and post-vaccination A/H1N1 inoculation.

17 induced by intratracheal lipopolysaccharide inoculation.

18 nd susceptible lines in response to pathogen inoculation.

19 ons following infection by various routes of inoculation.

20 swabs for the first 7 to 14 days after each inoculation.

21 al flora at baseline and at 0.05% 4 wk after inoculation.

22 weeks, followed by P. aeruginosa intranasal inoculation.

23 replication and pathogenesis following oral inoculation.

24 formation by medication prior to cancer cell inoculation.

25 ring virus infection, replication, and plant inoculation.

26 ue colonization upon oral or intraperitoneal inoculation.

27 e topically applied on plants prior to virus inoculation.

28 amydia sp. in rectal swabs following an oral inoculation.

29 tory role in stomatal closure after pathogen inoculation.

30 as pancreas and liver just 20 min after oral inoculation.

31 r in immunocompetent mice with 100 cells per inoculation.

32 fy differences between early and delayed BCG inoculation.

33 pathogenicity level was recorded 4-days-post-inoculation.

34 ilation, and soil nutrient dynamics via seed-inoculation.

35 from implants at weekly intervals following inoculation.

36 ntly confirmed QS upregulation within 1 h of inoculation.

37 n among controls by days 2 and 3 after virus inoculation.

38 tion and spread occurs within 1 day of virus inoculation.

39 ein catheter before, 6 h and 12 h after MRSA inoculation.

40 ns' against less effective strains during co-inoculations.

41 determined in rice leaves by spray and punch inoculations.

42 ion of spontaneous HSV-2 shedding post-acute inoculation (10(2) to 10(3) DNA copies/swab) in 80% of R

43 nza A/Wisconsin/67/2005 (H3N2) by intranasal inoculation; 35 healthy control subjects were not subjec

44 Following experimental inoculation, 9 (90%) group I dogs were variably seroreac

45 the leaves of plants 3h after the E. cloacae inoculation, according to a mechanism involving endogeno

46 The correlation between inoculation age and complications were evaluated.

47 Buffy coat inoculation and a shorter interval between sample collec

48 idarum can infect mice both by transcervical inoculation and by natural ascension if introduced into

49 tis into mouse endometrium via transcervical inoculation and compared the infectious yields in mice w

50 from a rhesus macaque fetus that died after inoculation and identified a single intrahost substituti

51 enged at mid-gestation with B. melitensis IT inoculation and monitored for fever and abortions.

52 IV with or without adjuvant), A/H3N2 priming inoculation and post-vaccination A/H1N1 inoculation.

53 cation, and their adults mainly for pathogen inoculation and spread.

54 are expressed as early as a few hours after inoculation and that their mRNAs are also detectable in

55 tranasal (i.n.) or per-oral (p.o.) Chlamydia inoculation and that unlike the female reproductive trac

56 ns might occur more than two years after BCG inoculation and the policy of delayed BCG inoculation wa

57 (PfSPZ) of PfSPZ Challenge by direct venous inoculation and were followed for 35 days for parasitemi

58 00 PfSPZ of PfSPZ Challenge by direct venous inoculation and were followed for 35 days for parasitemi

59 Tracer was injected 15 min after hPBMC inoculation, and a 60-min dynamic PET scan was acquired,

60 Using an oral route of inoculation, and fecal shedding as a marker for GI colon

61 (n = 5) or 39 days (n = 1) after the initial inoculation, and maternal/fetal tissues were collected.

62 Parasitemia was detected 7 days after inoculation, and parasite concentrations increased until

63 eal injection (IP) 24 hours after the fungal inoculation, and the same amount of SAHA injection or DM

64 ment' into nodule size during single- and co-inoculations, and 'host sanctions' against less effectiv

65 A stem base inoculation approach was used to explore the ability of

66 ent, tadpoles are as resistant to M. marinum inoculation as adult frogs.

67 of bacterial lipopolysaccharide and poxvirus inoculation as tradeoffs for enhanced immunity.

68 rticularly enriched in (15) N, but endophyte inoculation at the individual leaf level did not alter (

69 s goal, we examined WFT oviposition and TSWV inoculation behavior on tomato lines bred to exude varyi

70 Inoculations between distantly related hosts tended to r

71 ession immediately after their intra-femoral inoculation blocks tumor development and preserves a nor

72 Following a single intranasal inoculation, both animal species shed the vaccine viruse

73 g allergic asthmatics early after rhinovirus inoculation but increased late in the infection during s

74 A were compromised for infectivity by needle inoculation, but injected mice seroconverted, indicating

75 inoculated AB mDC responded to secondary IAV inoculation by efficiently upregulating activation marke

76 Inoculation by LJM17 from L. longipalpis-elicited DSG1-c

77 of the initial targets for rickettsiae after inoculation by ticks.

78 Compared to control host plants, R-AEF inoculation caused, on one hand, a decrease in reflectan

79 that resembles human disease, using vaginal inoculation combined with mild cervical injury induced b

80 remdesivir treatment initiated 24 h prior to inoculation completely prevented MERS-CoV-induced clinic

81 Soil inoculation consistently induced resistance against the

82 rming a diagnosis of BMD but that SCID mouse inoculation could be a useful complement to PCR.

83 tages, before symptom appearance, 16 h after inoculation (Ct values = 28.29 +/- 1.1).

84 Beginning 4 or 5 days post inoculation, cynomolgus macaques were treated once daily

85 able of inhibiting yeast development after 4 inoculation days.

86 After Pst inoculation, Deltawak1 plants developed disease symptoms

87 from human carriers were developed, as were inoculations designed to confer immunity against typhoid

88 S system using synthetic pheromones prior to inoculation did not significantly increase the percentag

89 amples collected at 0, 1, 3, and 8 days post inoculation (DPI).

90 Direct venous inoculation (DVI) with PfSPZ Vaccine has been safe, tole

91 Direct venous inoculation (DVI) with PfSPZ vaccine has been safe, tole

92 We compared CLas inoculation efficiency of D. citri nymphs and adults int

93 rinfection by 4 days after initial right lip inoculation elicited failed superinfecting-virus gene ex

94 found that HSV-2 can infect RM after vaginal inoculation, establish latency in the nervous system, an

95 a year-long evolution experiment and a cross-inoculation experiment designed to explore how nitrogen-

96 In a greenhouse inoculation experiment using the black cottonwood (Popul

97 Plant inoculation experiments with deletion mutants in the ind

98 Co-inoculation experiments with Wt and Deltaexlx-gh5 rescue

99 es of host investment in both single- and co-inoculation experiments.

100 Cervical exposure to Nonoxynol-9, 24 h pre-inoculation, facilitates intrauterine UP infection, upre

101 ine (males greater than females), after LAIV inoculation (females greater than males), and after WSP

102 Results in co-inoculation fermentations revealed that the majority com

103 treatment was initiated 25 and 21 days after inoculation for subjects 1 and 2 respectively (peak para

104 an accuracy of >70% after only 14 days after inoculation for TYLCSV and >85% only after 8 days for TS

105 Effect of yeast inoculation format (F), temperature (T), and "on lees" a

106 a infections to be unrelated due to parasite inoculations from different mosquitoes.

107 ved (CDCD) pigs allocated to the following 5 inoculation groups of 10 pigs each: (i) negative control

108 For monocots, new methods of inoculation have been tried to obtain increased silencin

109 age of pathogen establishment (48 hours post inoculation, hpi) to a late stage of symptom expression

110 esponse to fungus infection in RF (24 h post-inoculation-HPI), being 68-fold and 53-fold more express

111 Further, these data support the retrograde inoculation hypothesis, whereby the infant oral cavity i

112 al detection in approximately one hour after inoculation, i.e. in the lag-phase.

113 table more than 40 days after the last virus inoculation.IMPORTANCE Herpes simplex virus 2 (HSV-2) in

114 s was induced by cultivated autologous feces inoculation in anesthetized, mechanically ventilated, an

115 viral neuropathogenicity after intracerebral inoculation in human subjects, for stable expression of

116 of differential gene expression at 24 h post inoculation in med15b.D mutants, suggesting that transcr

117 WFhb1-1 accumulation, 12 hours post Fusarium inoculation in non-Qfhb1-carrier wheat but not in Qfhb1-

118 r (OO) model, herpes simplex virus 1 (HSV-1) inoculation in one side of the lip propagates virus to i

119 the end of the First World War, the value of inoculation in preventing the spread of typhoid had been

120 orter interval between sample collection and inoculation in the laboratory were associated with a hig

121 strongest transcriptomic response 24 h after inoculation in the resistant genotype.

122 ectrum of attainable data after experimental inoculation in this species, is paramount.

123 and as a source for blood to perform needle inoculations in naive animals for tick feeding studies.

124 alyses of the rhizobial strains in the mixed inoculation indicate that rhizobial genes involved in ch

125 The B19V NS1-induced ApoBod inoculation induced dsDNA autoantibodies in a dose-depen

126 Bacterial inoculation induced the production of phenolic compounds

127 exposure promotes the development of stress inoculation-induced resilience.

128 Pathogen inoculation induces LCBK1 expression, especially in guar

129 nerated abnormal PrP assemblies, which after inoculation into further groups of 117VV Tg30 mice, prod

130 r survival following macrophage infection or inoculation into mice.

131 distribution of oral vaccines may result in inoculation into people and applied a Markov chain to es

132 evelop an animal model utilizing direct ZIKV inoculation into the uterine wall of pregnant, immunocom

133 Experimental inoculation is an important tool for common cold and ast

134 Following an intravaginal inoculation, live chlamydial organisms were detected in

135 Inoculation location was weakly associated with bacteria

136 We observed a striking effect of inoculation method on gametocyte production, suggesting

137 have emerged, partly because of the lack of inoculation methods.

138 fectious status developed after intragastric inoculation might be induced by a combination of gastric

139 This frequency was highest if cell culture inoculation occurred on the same day as blood sample col

140 Direct venous inoculation of 3.2 x 103 aseptic, purified, cryopreserve

141 0 volunteers underwent CHMI by direct venous inoculation of 3200 Pf sporozoites (Sanaria(R) PfSPZ Cha

142 ce were pretreated or not with an intranasal inoculation of 5 x 10(7) CFU M. muris 24 h before coinfe

143 we demonstrate that a single intraperitoneal inoculation of a cDNA clone encoding an attenuated rZIKV

144 Following inoculation of a highly sensitive immunodeficient mouse

145 The inoculation of a human rabbitized (FdltB(r)) strain demo

146 Intraplantar inoculation of a WT strain of MAYV into immunocompetent

147 Lastly, inoculation of alpha-Syn fibrils in aged mice, but not y

148 Here, we show that in TgM83(+/-) mice, inoculation of alpha-Syn preformed fibrils (PFFs) into t

149 Inoculation of an OSCC cell line caused mechanical and t

150 Here, we show that inoculation of Arabidopsis leaves with the bacterial pat

151 can also be detected at 35 DPI, intravaginal inoculation of artificial insemination fluid from these

152 In Taiwan, the inoculation of Bacillus Calmette-Guerin (BCG) Tokyo-172

153 Here, we report that salivary gland inoculation of BALB/cByJ mice with tcMCMV or recombinant

154 -1) boosts the incidence of the disease; and inoculation of both the nonpathogenic ALV-E and SB-1 esc

155 l titers postinfection in vitro Transcranial inoculation of C57Bl/6 mice with RSA59 (PP) or RSA59 (P)

156 Inoculation of cats with this engineered parasite strain

157 hat relatively low-risk activities including inoculation of cell cultures or the early stages of in v

158 changes in the leaf transcriptome after the inoculation of detached rose leaves with each pathogen.

159 ant pigtail macaques received choriodecidual inoculation of either group B Streptococcus (GBS) or sal

160 Inoculation of Galleria mellonella (wax moth) larvae wit

161 viously characterized response to intranasal inoculation of GAS.

162 and bentonite to botrytized must obtained by inoculation of grapes with B. cinerea strain 213.

163 ly females were positively affected by R-AEF inoculation of host plants.

164 Our data demonstrate that inoculation of HSV-1 in the lip propagates virus to both

165 Mosquito inoculation of humans with arthritogenic alphaviruses re

166 anding of the events that lead to successful inoculation of infectious sporozoites by mosquitoes is c

167 ted species that often arises from traumatic inoculation of inhabited soil and organic debris into sk

168 zation at baseline and after debridement and inoculation of labeled strains.

169 against bone destruction induced by femoral inoculation of Lewis lung cancer cells.

170 Inoculation of MAYV/IRES in BALB/c mice induced strong s

171 Transcervical inoculation of medroxyprogesterone-treated HLA-DR4 trans

172 Neurovirulence following intracerebral inoculation of mice was not affected by the deletion of

173 However, intraperitoneal inoculation of mice with gammaHV68 was associated with i

174 we compared in vivo T cell responses to skin inoculation of mice with infectious or UV-inactivated HS

175 versity across time and space following oral inoculation of mice.

176 Inoculation of NF-kappaB-luciferase and Ifnar1(-/-) mice

177 it was demonstrated that intratracheal (IT) inoculation of nonpregnant guinea pigs would replicate f

178 After inoculation of P. flocculosa, the tripartite interaction

179 Inoculation of plants with full-length clones showed the

180 riodontal disease in 2 animal models through inoculation of Porphyromonas gingivalis and ligature aro

181 Inoculation of primary duck cells with recombinant influ

182 Inoculation of raw vCJD urine caused no disease, confirm

183 We analyzed larvae after inoculation of recombinant zebrafish type I IFN, or infe

184 Intramammarily inoculation of repeated doses of 2.5 x 10(7) allogenic A

185 Moreover, subcutaneous inoculation of RGS12-overexpressed OSCC cells in NOD sci

186 Intranasal inoculation of SARS-CoV-2 in K18-hACE2 mice results in h

187 dent gut microbiota and Salmonella following inoculation of SE in two-week-old layer chicks.

188 Inoculation of severe combined immunodeficient (SCID) mi

189 Here, we demonstrate that intravenous inoculation of SIV-infected macaques, a well-accepted no

190 cells, plasmid challenge or HSV-1DeltaUL41N inoculation of T cell lines provoked an entirely cGAS-de

191 pulmonary microbes demonstrates significant inoculation of the lower airways of immunocompromised ch

192 osis but is free of exogenous ALV infection; inoculation of the nonpathogenic ALV-E or MDV-2 (SB-1) b

193 IKV was also recovered after intraperitoneal inoculation of the rZIKV cDNA in the absence of transfec

194 DCs migrated out of human skin explants upon inoculation of the skin with B. miyamotoi.

195 Inoculation of these mutant-expressing cells in athymic

196 Inoculation of this strain into mice significantly incre

197 We also performed sequential inoculation of tomato plants by adult psyllids following

198 Here we demonstrate that inoculation of transgenic mice with different strains of

199 showed that body weight was decreased after inoculation of tumor cells, but ankle loading restored a

200 ptible mice is similar after an intracranial inoculation of two flaviviruses, but amplification of vi

201 ne responses was evaluated after intravenous inoculation of two Mamu-A*01 (+) RRV-naive rhesus monkey

202 re rarely observable in nature, experimental inoculations of pathogens into novel host species provid

203 ogressions of 514 experimental cross-species inoculations of rabies virus, a widespread zoonosis whic

204 was a significant influence of the timing of inoculation on the volatile composition of the wines jus

205 diate resistance to WFT oviposition and TSWV inoculation on tomato leaves.

206 on-founder (T/F) virus at 5 x 10(5) TCID(50) inoculation, on day 4, 7 and 14 post-SubQ treatments (PT

207 T plants close stomata within an hour of Pst inoculation or flg22 (a 22 amino acid peptide from bacte

208 e infected with B. miyamotoi by subcutaneous inoculation or tick bite were collected for immunoblotti

209 gnificant aerosol exposures, accidental self-inoculation, or bite-related infections.

210 TORC1), either in all tissues upon poly(I:C) inoculation, or specifically in haemopoietic stem cells,

211 Inoculations originating from bats rather than carnivore

212 emain effective up to three days post lethal inoculation, our approach may successfully treat infecti

213 astrovirus infection via multiple routes of inoculation, our studies aimed to determine whether muri

214 of retention period, acquisition period and inoculation period parameters.

215 ios to model larval abundance, entomological inoculation rate (EIR) and malaria prevalence at each da

216 predictors of vector density, entomological inoculation rate and malaria incidence.

217 The P. vivax entomological inoculation rate was reduced by 12.5-fold (95% confidenc

218 The relationship between the entomological inoculation rate, the malaria prevalence in humans deter

219 days after 13762 Mat B III cell intraductal inoculation, rats were divided into treatment groups and

220 Experimental inoculation reduced social contacts between honey bee co

221 ghout infection sites at 24 h and 48 h after inoculation, respectively.

222 We show that ZIKV-rectal inoculation results in viremia with subclinical infectio

223 -DOTA-E[c(RGDfK)](2) peptide at day 10 after inoculation revealed significantly higher uptake in the

224 The influence of the timing of inoculation (sequential and simultaneous alcoholic ferme

225 of ZIKV-195 administered 5 days after virus inoculation showed marked protection against lethality i

226 onditions between 17-27 weeks of age: Stress inoculation (SI) with continuous access to mother (SI +

227 e 2 MDV, SB-1, in addition to AF227 or AF229 inoculation, significantly enhanced the spontaneous LL-l

228 oss multiple anatomical sites distant to the inoculation site preceded extensive ZIKV persistence aft

229 Deltabbk13 spirochetes to proliferate in the inoculation site was followed by reduced numbers of B. b

230 ators, primary MARV targets, and skin at the inoculation site, where highest viral loads and initial

231 omoting spirochete proliferation in the skin inoculation site.

232 r bacteria are observed at distance from the inoculation site.

233 lture pH, NaNO(2) initial concentrations and inoculation sizes of strain F2 were 8-10, 0.4-0.8 g/L an

234 Four hours after inoculation, strain LH128-GFP showed about 99% reduction

235 A pair of inoculation strategies are proposed which aim at returni

236 sted 14 and 35 days post infection (DPI) for inoculation studies and 14, 35 and 70 DPI for histopatho

237 ells to form lung colonies after intravenous inoculation, suggesting a differential role for DDR1b in

238 o colonize the colon following an intracolon inoculation, suggesting that pGP3-deficient Chlamydia sp

239 model with treatment initiation 5 days post inoculation, supporting further assessment of remdesivir

240 y the finding that following an intrajejunal inoculation that bypasses the gastric barrier, pGP3-defi

241 Following an intrajejunal inoculation that bypasses the gastric barrier, plasmid-d

242 Finally, following an intracolon inoculation, the dependence of chlamydial colonization o

243 Following an intragastric inoculation, the plasmid significantly improved chlamydi

244 virus from aerosols and surfaces hours after inoculation, the real-world studies that detect viral RN

245 However, intracolon inoculation to bypass the gastric barrier rescued the co

246 Inoculation to N. benthamiana showed TYLCV to be capable

247 f intragastric, intrajejunal, and intracolon inoculations to reveal the impact of the plasmid on chla

248 M. marinum inoculation triggered a robust proinflammatory CD8(+) T

249 host and symbiont fitness in single- and co-inoculations under fertilization treatments of zero adde

250 ld-type UMH9 in the kidneys and spleen after inoculation via the tail vein in a bacteremia mouse mode

251 CG inoculation and the policy of delayed BCG inoculation was implemented since 2016, longer observati

252 Inoculation was particularly successful in preventing ty

253 Finally, Th1 differentiation after UV-HSV inoculation was rescued by targeted Ag delivery to CD8al

254 egg-laying (oviposition) decreased and TSWV inoculation was suppressed.

255 Following inoculation, we observed gastrointestinal deficits and p

256 d as the "nephrocomplex." By an intrabladder inoculation, we showed high susceptibility of this nephr

257 ts principally at the point of initial virus inoculation, where small virus populations encounter wel

258 gular-vein catheter before or 6 h after MRSA inoculation, while an equal volume of saline was adminis

259 rom the lungs of C57BL/6J mice at 24 h after inoculation, while there was no MGAS2221 clearance from

260 Following C. muridarum inoculation, wild-type mice develop robust hydrosalpinx,

261 at different time points after intracerebral inoculation with 263K and sCJDMM1 prions, respectively.

262 Inoculation with a commercial formulation of AM fungi in

263 ug/cm(3)) or filtered air, followed by nasal inoculation with a vaccine dose of live attenuated influ

264 dy provides evidence for the first time that inoculation with AM fungi can increase colonization of r

265 Inoculation with AM fungi had no effect on N and P conce

266 We tested whether inoculation with AM fungi in the two soils changed plant

267 We investigated the effects of inoculation with AM fungi on rice plants in two differen

268 Following inoculation with AM fungi, BdRAM1-overexpressing plants

269 ays 1, 2, 3, and 10, followed by intravenous inoculation with approximately 2800 P. falciparum parasi

270 es in the salivary gland vs. the PGLNs after inoculation with attenuated virus vs. a nominal protein

271 Intravaginal inoculation with C. muridarum readily induces fibrotic b

272 Surprisingly, inoculation with Candida dubliniensis and S. aureus resu

273 in wild-type mice following an intravaginal inoculation with Chlamydia Since T cells in OT1 mice are

274 t human skin infection following intradermal inoculation with community-associated methicillin-resist

275 esistant barley genotype CI9831, followed by inoculation with Fusarium graminearum, led to the down r

276 ic response to both plasmid DNA challenge or inoculation with HSV-1DeltaUL41N.

277 ted general inflammation around day 21 after inoculation with infective eggs that is transcriptionall

278 Using intracerebral inoculation with MuPyV, we found that MuPyV encephalitis

279 nced acid and alcohol production, whereas co-inoculation with non-acid producing Lc. lactis increased

280 ddition to more efficient crop varieties and inoculation with P solubilising microorganisms.

281 Moreover, in a mouse model of subcutaneous inoculation with P. aeruginosa, rTCP96 reduced bacterial

282 el also increasing in participants following inoculation with P. falciparum For both species, the mos

283 Differently, inoculation with P. pannosa leads in addition to the gen

284 F levels increased in participants following inoculation with P. vivax (n = 16) or P. falciparum (n =

285 cripts were transiently upregulated 1 d post-inoculation with Pgt, but not in mock-inoculated plants.

286 ymicrobial biofilm infection model involving inoculation with Pseudomonas aeruginosa PAO1 and Acineto

287 e volunteers were immunized by direct venous inoculation with radiation-attenuated, aseptic, purified

288 In contrast, after inoculation with replication-deficient adenoviruses, lym

289 hese trials, the response to an experimental inoculation with rhinovirus-16 among asthmatics with hig

290 s to compare the response to an experimental inoculation with rhinovirus-16 in allergic asthmatics wi

291 legume plants, T. repens and M. sativa, upon inoculation with strains of their cognate and non-cognat

292 After inoculation with tcMCMV, lymphocytes from the submandibu

293 eriodontal infections were generated by oral inoculation with the encapsulated W50 wild-type strain o

294 Interestingly, inoculation with the RSA59 (P)-carrying MHV significantl

295 plants overexpressing OsPT8 (OsPT8-OX) after inoculation with these pathogens.

296 Initial inoculation with thymidine kinase-deficient HSV-1 (TK(de

297 cted at early time points after experimental inoculation, with an average time of 439 days before cli

298 B16-F10-luc tumors were detected 4 d after inoculation, without differences in volume or blood flow

299 To determine if IT inoculation would induce reproductive disease, guinea pi

300 etects skin PrP(Sc) as early as 2 weeks post inoculation (wpi) in hamsters and 4 wpi in Tg40h mice; R