ライフサイエンスコーパス: gnotobiotic

1 e regionally profiled enteric neurons across gnotobiotic, allergic, and parasite-infected mice.

2 e detected in diverse biological fluids from gnotobiotic and conventionally colonized mice and traced

3 ora in immunocompetent animals, we generated gnotobiotic and conventionally reared Ig allotype chimer

4 Applying this pipeline to gnotobiotic and human microbiota-colonized mice, we demo

5 t and a model of Giardia mono-association in gnotobiotic and immunodeficient mice to propose an alter

6 ow in multiple specific pathogen-free (SPF), gnotobiotic, and germ-free murine models of GI GVHD that

7 iew summarizes the results of developmental, gnotobiotic, and in vitro studies that showed alteration

8 Advances in immunology, gnotobiotics, and culture-independent molecular techniqu

9 ficantly less cariogenic than JH1140 in both gnotobiotic- and conventional-rodent models.

10 roughput anaerobic culturing techniques with gnotobiotic animal husbandry and metagenomics to show th

11 responses are experimentally delineated via gnotobiotic animal models or alternatively by antibiotic

12 ment microbiota from trial participants into gnotobiotic animals and re-enacting trial conditions all

13 alpha/beta and gamma interferon responses in gnotobiotic animals.

14 and the latest progress in using axenic and gnotobiotic approaches to study insect-microbe interacti

15 and survival of congenitally immunodeficient gnotobiotic beige-athymic (bg/bg-nu/nu) and beige-euthym

16 Earlier results showed that conventional and gnotobiotic but not axenic larvae exhibit midgut hypoxia

17 ibody- and cell-mediated immune responses in gnotobiotic C.B-17 and BALB/c mice.

18 postinfection, all H. saguini-monoassociated gnotobiotic C57BL/129 IL-10(-/-) mice were colonized and

19 undred seventy-nine mice including C57BL/6J, gnotobiotic C57BL/6J, and knockout strains for GPR41, GP

20 n orally inoculated into a BCoV-seronegative gnotobiotic calf, GiCoV-OH3 caused severe diarrhea and v

21 nomes from both the cell culture-adapted and gnotobiotic-calf-passaged strains were also sequenced an

22 gainst the virulent enteric BCoV DB2 strain, gnotobiotic calves (n = 4) were orally inoculated with H

23 e some differences of degree, all inoculated gnotobiotic calves (n = 6) showed abnormal feces between

24 To determine whether HECV-4408 infects gnotobiotic calves and induces cross-protective immunity

25 ervations described previously in studies of gnotobiotic calves and pigs experimentally infected with

26 syncytial virus (RSV) protected the lungs of gnotobiotic calves from RSV infection.

27 Gnotobiotic calves inoculated with fecal filtrates of ea

28 An additional two gnotobiotic calves were inoculated with HECV-4408 and eu

29 In gnotobiotic calves, however, NB virus elicited only diar

30 uated (NCDV/A) bovine group A rotaviruses in gnotobiotic calves.

31 -free male and female MCAD(-/-) mice enabled gnotobiotic colonization combined with untargeted metabo

32 Gnotobiotic colonization of microbiome-depleted dams wit

33 sequencing, in vitro functional assays, and gnotobiotic colonizations to define the microbial compos

34 ifestations under specific-pathogen-free and gnotobiotic conditions, notably increasing plasmacytoid

35 common-garden experiments outside and under gnotobiotic conditions.

36 these trials or in Cxcr2(-/-) mice grown in gnotobiotic conditions.

37 en fixed by BNF to maize and wheat under non-gnotobiotic conditions.

38 t actively suppress Pseudomonas growth under gnotobiotic conditions.

39 Here, we found that colonization of gnotobiotic Drosophila melanogaster with F. nucleatum or

40 mice housed in conventional, germ-free, and gnotobiotic environments.

41 Antibiotic-mediated depletion or gnotobiotic exclusion of fungi enhances responsiveness t

42 Gnotobiotic experiments in Il10(-/-) mice demonstrate th

43 In inbred mice housed in gnotobiotic facilities, the top of the haematopoietic hi

44 Pigs were maintained in gnotobiotic facility and evaluated for human norovirus (

45 we colonize mice that are maintained in the gnotobiotic facility with O. formigenes, using either a

46 Furthermore, gnotobiotic flies bearing an EAA-producing symbiotic mic

47 By contrast, gnotobiotic flies with a mutant microbiome that did not

48 these interactions involved colonization of gnotobiotic Fut2(+) and Fut2(-) mice with Bacteroides th

49 In normal adult gnotobiotic FVB/N animals, network density is on average

50 such colonization by using antimicrobials or gnotobiotic germ-free mice overrides these protective be

51 d IL-2(-/-) mice reared and maintained under gnotobiotic (germfree) conditions.

52 he phylogenetically unassigned NB strain, in gnotobiotic (Gn) calves.

53 We evaluated the gnotobiotic (Gn) pig as a model to study the pathogenesi

54 human rotavirus (HRV) vaccine efficacy in a gnotobiotic (Gn) piglet model of HRV diarrhea.

55 idney cell line, and the WT PEC, passaged in gnotobiotic (Gn) pigs, were used to orally inoculate 13

56 oV-HS66) infects and causes mild diarrhea in gnotobiotic (Gn) pigs.

57 contents of PDCoV OH-FD22 strain-inoculated gnotobiotic (Gn) pigs.

58 pression in buccal and intestinal tissues of gnotobiotic (Gn) pigs; (ii) to determine if virus-like p

59 Both conventionally-raised and gnotobiotic Gpr41-/- mice colonized with the model ferme

60 Gnotobiotic growth systems and controlled environments e

61 e degree of gastrointestinal inflammation in gnotobiotic HLA-B27 transgenic rats monoassociated with

62 Utilizing gnotobiotic hosts, we showed that the ID2-dependent earl

63 togenes and orally acquired listeriosis in a gnotobiotic humanized mouse model.

64 study, we demonstrate that immunosuppressed gnotobiotic (IGB) piglets orally inoculated with wild-ty

65 we observed with E. faecalis-induced IBD in gnotobiotic IL-10 KO mice.

66 erichia coli (NC101, which causes colitis in gnotobiotic IL-10(-/-) mice).

67 els of colitis: naive T-cell transfer and in gnotobiotic IL-10(-/-) mice.

68 icantly decreased the DNA damage response in gnotobiotic Il10(-/-) mice.

69 cal microbiota elicited lung inflammation in gnotobiotic Il10-deficient mice.

70 velop GIN and if H pylori accelerates GIN in gnotobiotic INS-GAS mice.

71 onic acid, colitis induced by microflora (in gnotobiotic interleukin-10(-/-)), and colitis induced by

72 sufficient for the organism to colonize the gnotobiotic intestine competitively.

73 Studies of gnotobiotic knockout mice that lack fasting-induced adip

74 howed that bacteria in nonsterile larvae and gnotobiotic larvae inoculated with wild-type E. coli red

75 In our study, we developed axenic and gnotobiotic methods for fall armyworm (Spodoptera frugip

76 s the growth of only E. coli-to bi-colonized gnotobiotic mice abolished the colonization-resistance c

77 the underlying mechanisms, we introduce into gnotobiotic mice an artificial community composed of hum

78 d metabolites that circulate in the blood of gnotobiotic mice and are also detected in plasma from he

79 Finally, using a combination of gnotobiotic mice and ex vivo mucus analysis, we demonstr

80 study UTI89 recovered from the distal gut of gnotobiotic mice and from IBCs harvested by laser captur

81 SAM and MAM microbiota were characterized in gnotobiotic mice and gnotobiotic piglets colonized with

82 tryptophanase, we can modulate IS levels in gnotobiotic mice and in the background of a conventional

83 Herein, gnotobiotic mice and mass spectrometry-based metabolomic

84 nta, critical for enterolignan production in gnotobiotic mice and unique to Coriobacteriia.

85 bicans depleted simple sugars in the ceca of gnotobiotic mice but required oxygen to grow on these re

86 position of a diverse synthetic community in gnotobiotic mice can be quantitatively predicted from ba

87 Moreover, gnotobiotic mice can be used to shape these personalized

88 lico, and using sequencing data derived from gnotobiotic mice colonized with a synthetic fecal microb

89 ng to microbial stimuli, which we confirm in gnotobiotic mice colonized with C. innocuum.

90 in vitro during growth in rich medium and in gnotobiotic mice colonized with defined communities of h

91 IgA-seq of FMT recipient samples and gnotobiotic mice colonized with donor microbiota identif

92 and lactulose increased luminal butyrate in gnotobiotic mice colonized with feces from an allergic i

93 in the gut of germ-free mice and restored in gnotobiotic mice colonized with members of the classes B

94 Here, we show that gnotobiotic mice colonized with microbiota from undernou

95 on sialylated substrates, we showed that-in gnotobiotic mice colonized with R. gnavus wild-type (WT)

96 n bacterial membranes, experiments employing gnotobiotic mice colonized with recombinant PG overprodu

97 Gnotobiotic mice colonized with the amino acid fermenter

98 Gnotobiotic mice colonized with the fecal samples of mal

99 n following Plasmodium infection compared to gnotobiotic mice colonized with the fecal samples of mal

100 onally, orally administering glycan beads to gnotobiotic mice confirmed specificity in glycan binding

101 eneChips to characterize their expression in gnotobiotic mice consuming polysaccharide-rich or -defic

102 We then show MDSINE's utility on two new gnotobiotic mice datasets, investigating infection with

103 In gnotobiotic mice engrafted with a community of 17 human

104 In gnotobiotic mice engrafted with a defined community of 1

105 gut bacterial strains introduced into adult gnotobiotic mice fed a polysaccharide-rich diet, and (ii

106 these fungal species on metabolic health in gnotobiotic mice fed standard (SD) or high-fat-high-sucr

107 ad SG preparation was orally administered to gnotobiotic mice harboring a consortium of 56 cultured,

108 matexigens in vitro and in the intestines of gnotobiotic mice harboring a prominent saccharolytic bac

109 We found that gnotobiotic mice harbouring different microbial communit

110 re most obvious in the gut, where studies of gnotobiotic mice have disclosed that the microbiota affe

111 hich human gut communities are replicated in gnotobiotic mice have provided an opportunity to identif

112 Unique signatures of in vivo competition in gnotobiotic mice include an adhesin enriched in poor col

113 Studies in gnotobiotic mice indicate that Methanobrevibacter smithi

114 cation for controlling the gut microbiota of gnotobiotic mice infected with Clostridium difficile and

115 Gnotobiotic mice inoculated with PSC-derived microbiota

116 end of treatment are introduced into female gnotobiotic mice just after delivery of their pups.

117 The humanized gnotobiotic mice mimic humans with a nonsecretor phenoty

118 lethal for adult or neonatal IFN-gamma(-/-) gnotobiotic mice over the 15-week study.

119 ransfer of a hypertensinogenic microbiota to gnotobiotic mice recapitulated the prebiotic-deprived hy

120 Gnotobiotic mice require specific nutritional and enviro

121 thetaiotaomicron population dynamics within gnotobiotic mice reveal that these populations are relat

122 analysis of intestinal epithelial cells from gnotobiotic mice revealed a previously unidentified mech

123 ota samples and purified fecal VLPs from the gnotobiotic mice revealed a reproducible nonsimultaneous

124 Pharmacokinetic studies using gnotobiotic mice revealed that dietary protein reduces t

125 nd reuniting them in various combinations in gnotobiotic mice should facilitate preclinical studies d

126 Competition experiments in gnotobiotic mice showed that bacteria harbouring this pa

127 to experiments in conventionally raised and gnotobiotic mice suggest that variations in gut microbia

128 ly higher in the ceca of H. saguini-infected gnotobiotic mice than in the controls.

129 M. smithii's transcriptome and metabolome in gnotobiotic mice that do or do not harbor Bacteroides th

130 eropathy of the small intestine developed in gnotobiotic mice that had been colonized with cultured d

131 file of C. difficile within the intestine of gnotobiotic mice to identify genes regulated in response

132 y underpinning such treatments, we have used gnotobiotic mice to model microbiota manipulations in th

133 species, were introduced simultaneously into gnotobiotic mice together with 11 other wild-type strain

134 Using gnotobiotic mice we show that microbiota composition det

135 Here, gnotobiotic mice were colonized with a defined consortiu

136 In this study, gnotobiotic mice were colonized with an artificial micro

137 Gnotobiotic mice were colonized with an assemblage of se

138 Gnotobiotic mice were colonized with defined human gut c

139 Gnotobiotic mice were then colonized with DR and FF micr

140 epithelial progenitors (GEPs) in transgenic gnotobiotic mice with a ChAG-like phenotype harbor intra

141 Colonization of gnotobiotic mice with a sialidase-deficient mutant of Ba

142 Mono-association of gnotobiotic mice with Bacteroides, a major succinate pro

143 The use of immunodeficient gnotobiotic mice with combined defects in T cells and na

144 Colonization of gnotobiotic mice with ddbABCDEF mutants reveals that thi

145 les and microbial transplantation studies in gnotobiotic mice with defined synthetic communities show

146 les and microbial transplantation studies in gnotobiotic mice with defined synthetic communities show

147 Furthermore, we show that colonization of gnotobiotic mice with purine-degrading bacteria modulate

148 erm-free, deliberately colonized adult mice (gnotobiotic mice) were used to examine the efficacy of c

149 ing >90,000 isogenic transposon mutants into gnotobiotic mice, along with the other artificial commun

150 When transplanted into gnotobiotic mice, AMER and CRON microbiota responded pre

151 enced human gut bacteria was introduced into gnotobiotic mice, and changes in species abundance and m

152 odulate serum levels of these metabolites in gnotobiotic mice, and show that in turn this affects int

153 immunocompetent and defined immunodeficient gnotobiotic mice, by reverse-transcription polymerase ch

154 rocessed foods affect the microbiota, we fed gnotobiotic mice, colonized with 54 phylogenetically div

155 When transplanted into gnotobiotic mice, complete and cultured communities exhi

156 In gnotobiotic mice, hCom2 exhibited increased stability to

157 ences in beta -defensin expression in gf and gnotobiotic mice, they also suggest a role for these pep

158 ic pathways, some of which were confirmed in gnotobiotic mice, together with observed changes in the

159 By selectively colonizing gnotobiotic mice, we demonstrate that the allergy-protec

160 ges across four human Bacteroides strains in gnotobiotic mice, we observed positive selection on thou

161 ividuals with obesity when transplanted into gnotobiotic mice.

162 on decreases prednisolone bioavailability in gnotobiotic mice.

163 did not affect colonic MHC-II expression in gnotobiotic mice.

164 oduced into injured conventionally raised or gnotobiotic mice.

165 ory bowel disease (IBD)-like inflammation in gnotobiotic mice.

166 confer resistance to toxins in vitro and in gnotobiotic mice.

167 the number of CD4(+)CD8alphaalpha(+) IELs in gnotobiotic mice.

168 disease patient that exacerbates colitis in gnotobiotic mice.

169 xpression in S. copri BgF5_2 in vitro and in gnotobiotic mice.

170 l pathology when isolated and transferred to gnotobiotic mice.

171 l controls or defined microbial consortia in gnotobiotic mice.

172 Entry was unaffected in gnotobiotic mice.

173 discordant pairs were each transplanted into gnotobiotic mice.

174 A newly developed gnotobiotic model of intestinal amebiasis should enable

175 n disease, and mechanistic studies employing gnotobiotic model organisms.

176 The generation of axenic (germ-free) and gnotobiotic model systems has been vital to dissecting t

177 microbiota and immune system, we employed a gnotobiotic model using human fecal transfers into ATG16

178 tudies of host-microorganism interactions in gnotobiotic models and in vitro systems, to molecular me

179 Combining antigenically defined diets with gnotobiotic models, we show that food and microbiota dis

180 allo-HCT and exacerbates disease severity in gnotobiotic models.

181 NMRI mice were colonized at birth from their gnotobiotic mothers, who harbored this anaerobic Gram-ne

182 Using in vitro systems and gnotobiotic mouse colonization models, we find that extr

183 Here, we utilize a gnotobiotic mouse colonized with the Altered Schaedler F

184 demonstrate that initial colonization of the gnotobiotic mouse intestine by B. fragilis requires that

185 the wild-type strain for colonization of the gnotobiotic mouse intestine.

186 and promoted MDCF-dependent weight gain in a gnotobiotic mouse model emulating the clinical trials.

187 act to regulate gut motility, we developed a gnotobiotic mouse model that mimics short-term dietary c

188 Here, we use a gnotobiotic mouse model to examine how gut bacterial fru

189 We have used a gnotobiotic mouse model to show that Bacteroides thetaio

190 Using a gnotobiotic mouse model, in which animals were colonized

191 y significantly alters nucleobase pools in a gnotobiotic mouse model.

192 t of cancer immunotherapy with the humanized gnotobiotic mouse model.

193 itol lipids decreased bacterial fitness in a gnotobiotic mouse model.

194 Functional studies using gnotobiotic mouse models and genetic manipulation of bac

195 rthermore, the use of genetically engineered gnotobiotic mouse models may increase our understanding

196 Recent studies in gnotobiotic mouse models of ChAG have shown that parieta

197 se the efficacy of chemotherapy in humanized gnotobiotic mouse models of PDAC.

198 a on enteric-associated neurons by combining gnotobiotic mouse models with transcriptomics, circuit-t

199 Using gnotobiotic mouse models, we found that CT induction of

200 Gnotobiotic NOD Toll4-negative mice monocolonized with E

201 BSH enzymes in the gastrointestinal tract of gnotobiotic or conventionally raised mice significantly

202 rus vaccination regimens were evaluated in a gnotobiotic pig model of rotavirus infection and disease

203 This study utilized the neonatal gnotobiotic pig model to evaluate the protective efficac

204 l and systemic T cell responses by using the gnotobiotic pig model.

205 of the attaching and effacing lesion in the gnotobiotic pig.

206 ere constructed and subsequently included in gnotobiotic piglet challenge studies, and their pathogen

207 and subsequently evaluated clinically in the gnotobiotic piglet infection model.

208 h toxin separately and in combination in the gnotobiotic piglet model of CDI.

209 In this study, we used a gnotobiotic piglet model to study determinants of pathog

210 that LT enhanced bacterial colonization in a gnotobiotic piglet model.

211 decrease the incidence of septicemia in the gnotobiotic piglet model.

212 iarrhea but resulting in less mortality in a gnotobiotic piglet-infection model.

213 When administered i.p. to gnotobiotic piglets 6 or 12 h after infection with E. co

214 filaments in the tongues of immunosuppressed gnotobiotic piglets and when embedded in agar, demonstra

215 up population dynamics were recapitulated in gnotobiotic piglets as they transitioned from exclusive

216 a were characterized in gnotobiotic mice and gnotobiotic piglets colonized with age- and growth-discr

217 y, we evaluated the efficacy of MMV665917 in gnotobiotic piglets experimentally infected with Cryptos

218 e virulence of these strains was compared in gnotobiotic piglets expressing receptors for F4(+) fimbr

219 Thirty-six gnotobiotic piglets from six litters were given one of f

220 cted mice challenged with Stx2 and protected gnotobiotic piglets infected with STEC from fatal system

221 Gnotobiotic piglets inoculated with Escherichia coli O15

222 cked-cell volume and plasma total protein of gnotobiotic piglets inoculated with the LT-positive stra

223 Using gnotobiotic piglets orally infected with E. coli O157:H7

224 ions or symptoms developed in 18 (90%) of 20 gnotobiotic piglets orally infected with strain 86-24, i

225 These effects were also documented in gnotobiotic piglets using the same consortium and Malawi

226 Gnotobiotic piglets were colonized with EcN, LGG, or EcN

227 cytotoxin in the pathogenesis of gastritis, gnotobiotic piglets were colonized with either toxigenic

228 Gnotobiotic piglets were orally challenged with C homini

229 Gnotobiotic piglets were used to investigate cross-prote

230 Gnotobiotic piglets were used to study the importance of

231 To investigate this, we challenged gnotobiotic piglets with equal number of oocysts of type

232 e orally inoculated five groups of 5-day-old gnotobiotic piglets with the three mutants, icPC22A, or

233 owever, in contrast to previous studies with gnotobiotic piglets, there was no evidence that the expr

234 In gnotobiotic piglets, vaccination suppresses but does not

235 e severity and mortality rates in humans and gnotobiotic piglets.

236 culation of 9-day-old F4ac receptor-positive gnotobiotic piglets.

237 ment after the onset of diarrhea in infected gnotobiotic piglets.

238 s evaluated in sheep, conventional pigs, and gnotobiotic piglets.

239 ariant prv 4S, was found to be pathogenic in gnotobiotic piglets.

240 from macaques with AIDS to immunosuppressed gnotobiotic piglets.

241 ogenicities of the mutants were evaluated in gnotobiotic piglets.

242 irHRV) infection and immunity using neonatal gnotobiotic piglets.

243 Gnotobiotic pigs and calves serve as useful models to ev

244 in serum and intestinal contents of neonatal gnotobiotic pigs and IL-12, IFN-gamma, IL-4, and IL-10 c

245 Neonatal gnotobiotic pigs are the only animal model susceptible t

246 n RV (AttHRV) and virulent human RV (HRV) in gnotobiotic pigs colonized with probiotics (Lactobacillu

247 Of 31 neonatal gnotobiotic pigs inoculated with K88ab+ or K88ac+ ETEC,

248 The 2/6-VLPs were administered to gnotobiotic pigs intranasally (i.n.) with a mutant Esche

249 Neonatal gnotobiotic pigs orally inoculated with virulent (intest

250 inoculated pigs was confirmed by inoculating gnotobiotic pigs orally with pooled HRV-positive serum.

251 ptibility to human rotavirus (HRV) diarrhea, gnotobiotic pigs provide a useful model for rotaviral di

252 hese results suggest that GE immunodeficient gnotobiotic pigs serve as a novel model for biomedical r

253 evel serum and mucosal antibody responses in gnotobiotic pigs than those induced by the tissue cultur

254 pe 2 (BoG2) Cryptosporidium parvum, neonatal gnotobiotic pigs were given 1-10 HuG1 or BoG2 oocysts.

255 Four gnotobiotic pigs were inoculated orally with HS206 (6 x

256 Newborn gnotobiotic pigs were inoculated twice perorally (p.o.)

257 Neonatal gnotobiotic pigs were orally inoculated once with virule

258 ate that 2/6-VLP vaccines are immunogenic in gnotobiotic pigs when inoculated i.n. and that the adjuv

259 However, i.n. inoculation of gnotobiotic pigs with 2/6-VLPs did not confer protection

260 HuNoV infects B cells in vivo, we colonized gnotobiotic pigs with E. cloacae and inoculated pigs wit

261 in addition to gastrointestinal infection in gnotobiotic pigs, confirming previous reports of rotavir

262 In neonatal gnotobiotic pigs, the icPC22A-S1Delta197 virus caused mi

263 r respiratory tract infections or viremia in gnotobiotic pigs, we inoculated them with attenuated or

264 lls were not a target cell type for HuNoV in gnotobiotic pigs, with or without E. cloacae colonizatio

265 of an intestinal content fluid filtrate from gnotobiotic pigs.

266 ition of intestinal contents from uninfected gnotobiotic pigs.

267 ty to human rotavirus (HRV) were examined in gnotobiotic pigs.

268 to reduce human rotavirus (HRV) diarrhea in gnotobiotic pigs.

269 this strain and human RV (HRV) Wa G1P[8] in gnotobiotic pigs.

270 Comparison of gnotobiotic Rag1-/- mice with and without subcutaneous 2

271 treptococcus mutans increases virulence in a gnotobiotic rat model and also promotes in vivo accumula

272 stinguishable from its wild-type parent in a gnotobiotic rat model of caries but was significantly le

273 In the gnotobiotic rat model, the gbpA mutant strain was hyperc

274 ish make it an attractive model organism for gnotobiotic research.

275 g gut-resident microorganisms and of rearing gnotobiotic rodents have made it possible to assess the

276 re limited to T follicular helper cells in a gnotobiotic setting, without appreciable induction of ot

277 Gnotobiotic studies revealed that germ-free zebrafish ar

278 Gnotobiotic studies revealed that while Fusobacterium nu

279 Importantly, the development of several gnotobiotic systems is allowing causative and mechanisti

280 Using gnotobiotic techniques, we show that strains of Klebsiel

281 We combined gut commensal genetics with gnotobiotics to measure brivudine drug metabolism across

282 produced a fitness defect in the stomachs of gnotobiotic transgenic mice but not in wild-type litterm

283 Gnotobiotic transgenic mice with an engineered ablation

284 e cancer-associated strain was less fit in a gnotobiotic transgenic mouse model of human ChAG and bet

285 tropism of H. pylori clinical isolates in a gnotobiotic transgenic mouse model of human chronic atro

286 Previously, we used a gnotobiotic transgenic mouse model with an engineered ab

287 Gnotobiotic transgenic rats raised in Trexler isolators

288 Conversely, gnotobiotic treatment of axenic embryos with feces-deriv

289 and during 14 months of monocolonization of gnotobiotic wild-type, Rag1-/-, or Myd88-/- mice.

290 Together, these studies establish gnotobiotic zebrafish as a useful model for dissecting t

291 Further, a gnotobiotic zebrafish experiment clarified whether micro

292 rescent fatty acid (FA) analogs delivered to gnotobiotic zebrafish hosts, we reveal that microbiota s

293 These results demonstrate the utility of gnotobiotic zebrafish in defining the behavior and local

294 To test this assumption, we colonized gnotobiotic zebrafish with zebrafish-derived bacterial i

295 Using the gnotobiotic zebrafish, we discovered that the normal exp

296 perimental evolution of Aeromonas veronii in gnotobiotic zebrafish, we identify bacterial traits prom

297 Using gnotobiotic zebrafish, which allow high-resolution exami

298 Using a gnotobiotic zebrafish-Pseudomonas aeruginosa model, we s

299 e to the commensal microbiota in transparent gnotobiotic zebrafish.

300 e commensal microbiota on gene expression in gnotobiotic zebrafish.