ライフサイエンスコーパス: trout

1 es (lake whitefish, coho salmon, and rainbow trout).

2 gards to estrogenicity in humans and rainbow trout.

3 pting potential exerted by HF-FPW in rainbow trout.

4 in spontaneous maleness of XX-female rainbow trout.

5 es in gonadotropins and estradiol in rainbow trout.

6 icantly lower rates in comparison to rainbow trout.

7 ish were significantly lower than in rainbow trout.

8 vo exposure experiment with juvenile rainbow trout.

9 M substantially higher than those of rainbow trout.

10 the stress and feeding responses in rainbow trout.

11 CD diastereomers during biotransformation in trout.

12 ction involves abnormal monoamine content in trout.

13 nsporter type 2 in distinct brain regions of trout.

14 reduced fitness (mean reduction of 12 g) to trout.

15 were present, with either native or stocked trout.

16 e modes, respectively, in Lake Michigan lake trout.

17 oup was: catfish, 157 mg kg(-1) (UI 9-2751); trout, 103 mg kg(-1) (UI 5-1951); tilapia, 59 mg kg(-1)

18 Steelhead trout (52 individual fishes) have MeHg of predominantly

19 gh its stimulation of Tnfalpha production in trout, a primitive teleost fish.

20 Simulations show that trout abundance could be greatly reduced under constant

21 The data were a 15-year record of brook trout abundance from 72 sites distributed across a 170-k

22 t contaminant trends due to significant lake trout age structure changes.

23 to mitigate the effect of a fluctuating lake trout age structure to directly improve the log-linear r

24 and visual pigment absorbance in the rainbow trout alevin but only visual pigment absorbance in the s

25 n the single cones of small juvenile rainbow trout (alevin), opsin expression in large juvenile rainb

26 nce, biomass, growth rate, and production of trout all increased with stream temperature.

27 analysis to trace the geographical origin of trout, also according to the type of feed.

28 tibiotic in 82% of pacu, 57% of shad, 57% of trout and 50% of salmon samples.

29 g(-)(1)ww in barbel, 9.2-97.0 ng g(-1)ww in trout and 9.0-239.5 ng g(-1)ww in eel.

30 nvestigated the presence of NDL PCBs in eel, trout and barbel from the River Roya.

31 e expression of all six subgroups in rainbow trout and brown trout Salmo trutta.

32 AEs and 869 BMFs from 19 species (primarily trout and carp) was developed from the literature.

33 cs of hybridization between native cutthroat trout and invasive rainbow trout, the world's most widel

34 organisms, including Daphnia magna, rainbow trout and juvenile crayfish, and is able to capture the

35 rook trout and salmon, suggesting that brook trout and mottled sculpin either use salmon tissue to di

36 ive hybridization between introduced rainbow trout and native cutthroat trout in western North Americ

37 blished in vivo and in vitro data in rainbow trout and new data on the synthesis of gonadotropins in

38 important conservation implications for bull trout and other imperiled species.

39 ic analysis of stock trends found that coral trout and red throat emperor, the two largest species by

40 mottled sculpin differed from those of brook trout and salmon, suggesting that brook trout and mottle

41 e three inland, freshwater datasets are ELA, TROUT and SWAT.

42 We find that NALT is present in rainbow trout and that it resembles other teleost mucosa-associa

43 entrations and age-corrected trends for lake trout and walleye in the Great Lakes over the 2004-2014

44 of TEQ associated with all Great Lakes lake trout and walleye samples is due to the nonortho CP-PCBs

45 elines for wildlife protection based on lake trout and walleye total TEQ were uniformly exceeded in a

46 centration trends in top predator fish (lake trout and walleye) of the Great Lakes (GL) from 2004 to

47 Component B (Dec604 CB), was present in lake trout and whitefish at concentrations of 10-60 ng/g lipi

48 h, gummy shark, oyster (four species), ocean trout and yellowtail kingfish.

49 the absorbance of visual pigments in rainbow trout and zebrafish.

50 h (predominantly largemouth bass and rainbow trout), and 505 prey fish (14 species) at 25 lakes throu

51 on popular cold-water fishes (e.g., salmon, trout, and char) with relatively large body sizes and mo

52 mortality was highest for intermediate-sized trout, and outweighed background mortality for most of t

53 d caloric turnover rates for Lake Huron lake trout, and reveal how these processes are regulated by b

54 Odorous molecules in earthen-ponds rainbow trout aquaculture farming in Germany were investigated w

55 e first time in German earthen-ponds rainbow trout aquaculture water including, amongst others, 4-hyd

56 Alaskan lakes that vary in whether predatory trout are absent, native, or have been stocked within th

57 Brown trout are at the northern limit of their geographic dist

58 ost jumps and increased virulence in rainbow trout are unknown for any fish rhabdovirus.

59 Using rainbow trout as a model we characterized responses to two natur

60 dictions to investigate the success of brown trout as top predators across a stream temperature gradi

61 regulation of B cell populations in rainbow trout, as well as an essential role for sphingolipids in

62 Consumption by bull trout at other settings were lower and more variable, bu

63 both young-of-the-year (YOY) and adult brown trout attained 100% at the end of summer, while seasonal

64 rulent European VHSV strain (DK-3592B) and a trout-avirulent North American VHSV strain (MI03).

65 n a partial gain of function in the chimeric trout-avirulent strain (22% mortality) and complete loss

66 tructure of the systemic and mucosal rainbow trout B cell repertoire.

67 sms that contributed to these responses: (1) trout became more selective in their diet as stream temp

68 ocky Mountains for two native salmonids-bull trout (BT) and cutthroat trout (CT).

69 f head kidney leukocytes from Ag-experienced trout but not naive controls, yet it does not confer pro

70 M concentrations similar to those of rainbow trout but not with sea lamprey.

71 rements of heavier PAHs (>/=5 rings) in lake trout, but lighter PAHs (</=4 rings) were overpredicted,

72 ioconcentration of PFASs in juvenile rainbow trout by exposing the fish in separate tanks under flow-

73 Trout by-product hydrolysates, generated using trout pep

74 Recombinant His-tagged trout CK12a (rCK12a) is not chemotactic in vitro but it

75 Additionally, trout classified as parr generally migrated earlier to t

76 In vitro, tSC present in mucus coats trout commensal isolates such as Microbacterium sp., Sta

77 Studies in rats and rainbow trout confirmed that DHA biosynthesis proceeds through t

78 We also simulated bull trout consumption and growth during salmon smolt outmigr

79 tive salmonids-bull trout (BT) and cutthroat trout (CT).

80 Once validated, Lake Michigan trout data files were analyzed for polyfluoroalkyl acids

81 and temperature had strong effects on brook trout demography.

82 e papillae to some chemicals and showed that trout-derived chemicals, amino acids, and a bile acid pr

83 ncreases in littoral-benthic food resources, trout did not utilize littoral habitat or zoobenthic res

84 One-day consumption by laboratory-held bull trout during the first day of feeding experiments after

85 roperties of lecithins isolated from rainbow trout egg (RL) and trout processing discard (WL) were co

86 d small changes in site occupancy, with bull trout experiencing a 9.2% (95% CI = 8.3%-10.1%) reductio

87 rmer stream reaches, and westslope cutthroat trout experiencing a nonsignificant 1% increase.

88 ranscriptional response of mature male brown trout exposed for 4 days to 1.7, 15.3, and 225.9 mug/L l

89 Furthermore, GST and SOD activities of trout exposed to both Se-Met and parasites were generall

90 ulated mRNAs and lncRNAs in juvenile rainbow trout exposed to E2.

91 lgorithm was applied to a Lake Michigan lake trout extract analyzed by atmospheric pressure gas chrom

92 single-cell CLEM to magnetic cells from the trout failed to identify any intracellular structures co

93 ponent from rainbow trout.IMPORTANCE Rainbow trout farming is a major food source industry worldwide

94 ve stress and oxidative stability of rainbow trout fillets.

95 alysis of MG in different types of water and trout fish samples.

96 the first time in German aquaculture rainbow trout fish, including, amongst others, (E,Z,Z)-2,4,7-tri

97 efficient habitats culminating in decreased trout fitness.

98 e efficient than the synthetic feed to color trout flesh (up to twofold increase in the retention of

99 variation in prey abundance influenced lake trout foraging tactics (i.e., the balance of the number

100 rded the phenotypic sex of 20,210 XX-rainbow trout from a French farm population at 10 and 15 months

101 wed over time 238 individually tagged marble trout from six populations to estimate the trophic chang

102 ntain fish as the apex predator; a cutthroat trout from the experiment, the only fish species in the

103 were much lower than those reported for lake trout from the more urbanized and industrialized Laurent

104 y trends in Walleye, Northern Pike, and Lake Trout from the Province of Ontario, Canada, which contai

105 ] fish cell line) and in vivo (using rainbow trout fry) in a dose-dependent and time-dependent manner

106 We then determined whether bull trout genetic diversity was related to climate vulnerabi

107 e to an additional round of WGD, the rainbow trout genome offers a unique opportunity to investigate

108 in vitro screening method using the rainbow trout gill cell line, RTgill-W1, to investigate pH-depen

109 cterize copper and silver binding to rainbow trout gill cells, either as cultured reconstructed epith

110 construct and culture the freshwater rainbow trout gill epithelium on flat permeable membrane support

111 gly inhibits the growth of different rainbow trout Gram-positive and Gram-negative bacteria, namely L

112 Lake trout greatly reduced their use of littoral habitat and

113 560 fish entries ( n: pike > perch >> brown trout > roach ~ Arctic charr) from 3132 lakes across Swe

114 young growing fish, slow growing, older lake trout (>5 yr) recycled an average of 482 Tonnes.yr(-1) o

115 ith shorter springs and longer summers, lake trout had reduced access to littoral habitat and assimil

116 The methodology was validated in trout, hake and Atlantic horse mackerel and was used to

117 ns tumors were induced in zebrafish, rainbow trout, hamsters, and mice by carcinogenic agents (methyl

118 Rainbow trout has a male heterogametic (XY) sex determination sy

119 lso, the low estrogenicity of alternariol in trout has been characterized here for the first time.

120 Recent studies of wolves and trout have employed thousands of markers to reveal previ

121 ed a lymphoid cell line derived from rainbow trout head kidney cells.

122 s study suggest an impact of azamethiphos on trout health through intravascular haemolysis and conseq

123 alcium ion on the ability of PLA2 to inhibit trout hemoglobin-mediated lipid oxidation were investiga

124 sic clearance determined using cryopreserved trout hepatocytes can be extrapolated to the whole anima

125 of this study demonstrate that cryopreserved trout hepatocytes can be used to reliably obtain in vitr

126 ate depletion experiments with cryopreserved trout hepatocytes from a single source.

127 , a significant decreasing trend in the lake trout Hg concentrations was found between 2004 and 2015

128 he proportion of IgT(+) to IgM(+) B cells in trout HK.

129 Furthermore, we identified trout homologs for CD141 and CD103 and demonstrated that

130 ted an innate immune response in the rainbow trout host, making LJ001 potentially useful for future v

131 ale mathematical model of the female rainbow trout hypothalamus-pituitary-ovary-liver axis to use as

132 ased MHC-II surface expression that point to trout IL-6 as a differentiation factor for IgM antibody-

133 e present study was to establish the role of trout IL-6 on B cells, comparing its effects to those in

134 Our results reveal that, in trout, IL-6 is a differentiation factor for B cells, sti

135 teraction with a host component from rainbow trout.IMPORTANCE Rainbow trout farming is a major food s

136 apture-mark-recapture study of eastern brook trout in four streams in Western Massachusetts, USA to p

137 one-year-old (1+) Atlantic salmon and brown trout in response to flow change during summer.

138 ed that salmon are a source of POPs to brook trout in stream reaches receiving salmon spawners from L

139 The degree of binge-feeding by bull trout in the field was slightly reduced but largely in a

140 , 2019 See also the editorial by Dillman and Trout in this issue.

141 ntroduced rainbow trout and native cutthroat trout in western North America will lead to genomic exti

142 nalyses, we show that the myomaker gene from trout includes 14 minisatellites, indicating that it has

143 hat pre-exposure to metals in metal-tolerant trout influences these interactions.

144 NAs (lncRNAs), in skeletal muscle of rainbow trout injected with E2.

145 Spring migrating sea trout juveniles can be classified as parr, pre-smolt or

146 grees C) were evaluated using farmed rainbow trout killed by asphyxia in air or percussion.

147 ks were largely maintained throughout marble trout lifetime in both populations.

148 emicals, mostly fragrance ingredients, using trout liver S9 fractions (RT-S9) and incorporated into i

149 ne fragrance ingredients were measured using trout liver S9 fractions and used as inputs to a recentl

150 o biotransformation experiments with rat and trout liver S9 fractions for different incubation times

151 rthern Pike (NP), and 70% to 76-92% for Lake Trout (LT).

152 utively expressed at high levels in all four trout MALT.

153 irmed that trout MRAP interacts with the two trout MC1R variants and MC2R, but failed to detect regul

154 xperiments in mammalian cells confirmed that trout MRAP interacts with the two trout MC1R variants an

155 ll as an essential role for sphingolipids in trout mucosal homeostasis.

156 that the majority of tSC is in free form in trout mucus and free tSC is able to directly bind bacter

157 According to gene expression analyses, trout myomaker expression is consistently associated wit

158 We found that the trout myomaker gene encodes a 434-amino acid (aa) protei

159 Our work reveals that trout myomaker has fusogenic function despite containing

160 ng cell-mixing experiments, we observed that trout myomaker has retained the ability to drive the fus

161 The first half of the trout myomaker protein (1-220 aa) is similar to the 221-

162 thod was applied to Nile tilapia and rainbow trout (n=29) and 14% of them contained enrofloxacin at l

163 The predominant B-cell subset found in trout NALT are IgT(+) B cells, similar to skin and gut.

164 Trout NALT consists of diffuse lymphoid cells and lacks

165 Trout NALT is capable of mounting strong anti-viral immu

166 of CK12 (but not CK10 or CK13) expression in trout nasopharynx-associated lymphoid tissue.

167 uleatus), 41 +/- 38 (char), and 9.9 +/- 5.9 (trout) ng g(-1) wet weight.

168 coho salmon (Oncorhynchus kisutch), rainbow trout (O. mykiss), Chinook salmon (O. tshawytscha), Atla

169 etallothionein (MetA and MetB) isolated from trout occupying a polluted and a control river are exami

170 The trout olfactory organ is colonized by abundant symbiotic

171 rax); turbot (Scophthalmus maximus); rainbow trout (Onchorynchus mykiss); and salmon (Salmo salar), i

172 further subgroups (IFN-e and -f) in rainbow trout Oncorhynchus mykiss and analyzed the expression of

173 and Champsocephalus gunnari, and the rainbow trout Oncorhynchus mykiss as a reference.

174 population of threatened Lahontan cutthroat trout (Oncorhynchus clarkii henshawi).

175 omosome-anchored genome assembly for rainbow trout (Oncorhynchus mykiss) and characterize a 55-Mb dou

176 f-odour development in earthen-ponds rainbow trout (Oncorhynchus mykiss) aquaculture farming in Germa

177 CK11 is a rainbow trout (Oncorhynchus mykiss) CC chemokine phylogeneticall

178 n and functional characterization of rainbow trout (Oncorhynchus mykiss) CD4-1(+) T cells and the est

179 the muscle and edible skin parts of rainbow trout (Oncorhynchus mykiss) fillets, sampled at two grow

180 ife of vacuum packaged low processed rainbow trout (Oncorhynchus mykiss) gravad during storage at 7 +

181 he growth of the young of the year steelhead trout (Oncorhynchus mykiss) in the recipient tributary o

182 pithelial barrier model built on the rainbow trout (Oncorhynchus mykiss) intestinal cell line, RTgutG

183 presence of CD8alpha(+) cells in the rainbow trout (Oncorhynchus mykiss) nasal epithelium.

184 wild and first-generation hatchery steelhead trout (Oncorhynchus mykiss) reared in a common environme

185 e, but not benzocaine or MS-222; and rainbow trout (Oncorhynchus mykiss) showed no avoidance to the t

186 ular mass<30kDa (PF30) isolated from rainbow trout (Oncorhynchus mykiss) skin gelatin hydrolysates wa

187 Rainbow trout (Oncorhynchus mykiss) were exposed to waterborne v

188 In rainbow trout (Oncorhynchus mykiss), a nasopharynx-associated ly

189 e that BPA deposition in the eggs of rainbow trout (Oncorhynchus mykiss), an ecologically and economi

190 in benthic invertebrates, juvenile steelhead trout (Oncorhynchus mykiss), and water striders (Gerris

191 negatively affects muscle growth in rainbow trout (Oncorhynchus mykiss), but the mechanisms directin

192 sturgeon (Acipenser fulvescens), and rainbow trout (Oncorhynchus mykiss), were selected to evaluate T

193 ave added to the controversy is that rainbow trout (Oncorhynchus mykiss), which have served as the pr

194 turn to the surface, was examined in rainbow trout (Oncorhynchus mykiss).

195 n high- (HR) and low-responsive (LR) rainbow trout (Oncorhynchus mykiss).

196 of liver S9 fractions isolated from rainbow trout (Oncorhynchus mykiss).

197 he gill and skin mucosal surfaces of rainbow trout (Oncorhynchus mykiss).

198 bioaccumulation of selenium (Se) in rainbow trout (Oncorhynchus mykiss).

199 cently reported a homolog to CCR7 in rainbow trout (Oncorhynchus mykiss).

200 bgroup have gained high virulence in rainbow trout (Oncorhynchus mykiss).

201 s of Chinook salmon or in tissues of rainbow trout (Oncorhynchus mykiss).

202 gated whether a relevant model fish (rainbow trout, Oncorhynchus mykiss) could detect OSPW using its

203 ial activity against a wide range of rainbow trout pathogens.

204 out by-product hydrolysates, generated using trout pepsin, were characterized and studied in terms of

205 However, the behaviour and survival of these trout phenotypes upon entering the sea is not well known

206 Rainbow trout pIgR is known to transport IgT and IgM across epit

207 However, other biological functions for trout pIgR or trout secretory component (tSC) remain unk

208 Indo-west Pacific, the large predatory coral trout Plectropomus leopardus (Serranidae), can behaviour

209 Here, we show that a fish--the coral trout Plectropomus leopardus--has partner-choice abiliti

210 The visual stimulus of a top predator (coral trout, Plectropomus leopardus) restricted the foraging a

211 cenarios, refugia with high probabilities of trout population occupancy (>0.9) were predicted to exis

212 We reared offspring of a brown trout population that naturally demonstrates facultative

213 strong gradient in genetic diversity in bull trout populations across the Columbia River Basin, where

214 Furthermore, the majority of brook trout populations are projected to persist if high winte

215 inear mixed models, allelic richness in bull trout populations was positively related to habitat patc

216 egion, had the strongest negative effects on trout populations.

217 and GHR2b, the two type 2 GHRs isolated from trout previously.

218 ins isolated from rainbow trout egg (RL) and trout processing discard (WL) were compared with the soy

219 ical stocking locations with greater rainbow trout propagule pressure, warmer water temperatures, and

220 and defatted (protein) fillet of 130 rainbow trout, reared with feed incorporating a high or low fish

221 ologically relevant to trout, we showed that trout recruit a moray collaborator more often when the s

222 tellite genotypes, we document in situ brook trout reproduction, which is the initial phase in the re

223 l endocrine components of the female rainbow trout reproductive axis.

224 ormation (t0.5 = 6.4 and 38.1 min in rat and trout, respectively), alpha-HBCD appears the most resist

225 and 0.419 after 60 min incubation in rat and trout, respectively).

226 TCDD raw concentrations in Lake Ontario lake trout revealed decreases of 94% and 96%, respectively.

227 In rainbow trout RTG-2 and RTS-11 cells, polyinosinic-polycytidylic

228 terestingly, delta-HBCD was detected only in trout S9 fraction assays indicating metabolic interconve

229 ethod, we consider two populations of marble trout Salmo marmoratus living in Slovenian streams, wher

230 used as a model system the endangered marble trout Salmo marmoratus, a freshwater fish living in a re

231 studies of oxidative stress using the brown trout Salmo trutta as model.

232 all six subgroups in rainbow trout and brown trout Salmo trutta.

233 tally affected by metal pollution, but brown trout (Salmo trutta L.) populations are known to reside

234 ies of mark-recapture-recovery data on brown trout (Salmo trutta) in Norway.

235 n Arctic char (Salvelinus alpinus) and brown trout (Salmo trutta) when the benthic link was included

236 quences for somatic growth in juvenile brown trout (Salmo trutta).

237 or stream fishes and cold-water species like trout, salmon, and char that are already constrained to

238 %, 5.1%, 2.6% and 8.0% for tilapia, catfish, trout, salmon, hybrid striped bass and yellow perch, res

239 c variation and habitat features in 130 bull trout (Salvelinus confluentus) populations from 24 water

240 rvations with laboratory experiments of bull trout (Salvelinus confluentus), a large freshwater pisci

241 ity decline and loss of an established brook trout (Salvelinus fontinalis [Mitchill]) population in B

242 h (Lepomis macrochirus Rafinesque) and brook trout (Salvelinus fontinalis Mitchill), swimming in the

243 spring) on survival and recruitment of brook trout (Salvelinus fontinalis) at a broad spatial scale u

244 agged, sampled seasonally) data set of brook trout (Salvelinus fontinalis) from four sites in a strea

245 ion size and mean body size in eastern brook trout (Salvelinus fontinalis).

246 itat use, resource use, and fitness of Brook Trout (Salvelinus fontinalis).

247 In lake trout (Salvelinus namaycush) from northern Canada (e.g.,

248 To address this concern, lake trout (Salvelinus namaycush) were collected in 2005/2006

249 ture dataset to test if a population of lake trout (Salvelinus namaycush), a cold-water stenotherm, a

250 lculated by surveying wounding rates on lake trout (Salvelinus namaycush), and trap surveys are used

251 es Basin), and species identity (i.e., brook trout [Salvelinus fontinalis] or mottled sculpin [Cottus

252 other biological functions for trout pIgR or trout secretory component (tSC) remain unknown.

253 dant symbiotic bacteria, which are coated by trout secretory immunoglobulin.

254 as low relative to its host, and parasitized trout showed slowed Se accumulation in the muscle as com

255 ntraperitoneal injection in juvenile rainbow trout showed that exchanges of the viral P or M genes ha

256 hts into mRNA and lncRNA networks in rainbow trout skeletal muscle and their regulation by E2 while u

257 Our results show that the majority of trout skin and gut bacteria are coated in vivo by tSC.

258 , opsin expression in large juvenile rainbow trout (smolt), zebrafish, or killifish remained unchange

259 round mortality decreased with body size for trout spawning above the dam and increased for those spa

260 Two larger-bodied trout species exhibited small changes in site occupancy,

261 n lakes with pH > 6.5 that were stocked with trout species.

262 llowed by evolution of dramatic increases in trout-specific virulence.

263 may result in inaccurate assessments of sea trout stocks in rivers.

264 are regularly observed in all-female farmed trout stocks.

265 The selected trout strain fed the plant protein mixture with amino ac

266 A rainbow trout strain selected for high performance on a plant pr

267 In rainbow trout such lines have existed for decades and has become

268 comparable among the different phenotypes of trout, suggesting that the higher proportion of returnin

269 The analysis of Ig repertoire in control trout suggests different structures of IgM and IgT splee

270 el memIgD(+)memIgM(-) B lymphocyte subset in trout that expresses memCCR7 and responds to viral infec

271 native cutthroat trout and invasive rainbow trout, the world's most widely introduced invasive fish,

272 or CD141 and CD103 and demonstrated that, in trout, this skin CD8(+) DC-like subpopulation expresses

273 health status of aquaculture reared rainbow trout through the investigation of clinical chemistry, h

274 Recombinant trout Tnfalpha (rTnfalpha) and PGF2alpha recapitulate th

275 fferences in body shape and kinematics allow trout to produce more thrust than bluegill, suggesting t

276 mechanisms employed by the River Hayle brown trout to tolerate high metal concentrations.

277 . major sphingolipids modulate the growth of trout total skin and gill symbiotic bacteria.

278 sequenced, assembled and annotated the brown trout transcriptome using a de novo approach.

279 X1 is enriched in the fetal ovary in rainbow trout, turtle, mouse, goat, and human.

280 trategies for seaward-migrating juvenile sea trout, ultimately affecting their return rate to the nat

281 enrichment of (-)-alpha-HBCD in rat than in trout underlines the species-specific differences in HBC

282 s of Ichthyophthirius multifiliis in rainbow trout using a simple macroparasite model by including ho

283 empts to identify the viral genes containing trout virulence determinants of viral hemorrhagic septic

284 her contain the determinants responsible for trout virulence in VHSV.

285 the viral P or M genes had no effect on the trout virulence phenotype of either parental strain.

286 N gene contains an essential determinant of trout virulence that is strongly enhanced by the viral P

287 the N and P genes, were exchanged between a trout-virulent European VHSV strain (DK-3592B) and a tro

288 h complete loss of virulence in the chimeric trout-virulent strain (0% mortality).

289 complete loss of virulence for the chimeric trout-virulent strain (2% mortality).

290 The biotransformation rate in trout was slower than in rat.

291 nderlying spontaneous maleness in XX-rainbow trout, we recorded the phenotypic sex of 20,210 XX-rainb

292 but modified to be ecologically relevant to trout, we showed that trout recruit a moray collaborator

293 efine the genetic basis of high virulence in trout, we used reverse genetics to create chimeric VHSVs

294 Finally, when trout were bath challenged with viral hemorrhagic septic

295 Candidate species identified in lake trout were qualified using theoretical isotopic profile

296 Growing rainbow trout with diets where FO was replaced by either 50% or

297 Infection of brown trout with hemorrhagic septicemia virus resulted in earl

298 ld play a more important role in the diet of trout with increasing stream temperature.

299 us primarily on farmed salmonids (salmon and trout) within a comparative context and will give an ove

300 le-cone opsin expression in juvenile rainbow trout, zebrafish, and killifish and on the absorbance of