ライフサイエンスコーパス: broth

1 Haemophilus influenzae ATCC 49247 (disk and broth).

2 denced by the optical density of the culture broth.

3 method for BLIS from a complex fermentation broth.

4 ties of nanoemulsions and LAE in tryptic soy broth.

5 ion of Scenedesmus dimorphus from the medium broth.

6 2 by yeast in dough and aqueous fermentation broth.

7 tion could be detected in fermented dough or broth.

8 ty was found on 6th day, with 33.08 U on PDA broth.

9 time to sputum-culture conversion in liquid broth.

10 to directly inoculate culture medium and LIM broth.

11 ns in the recovery of BLIS from fermentation broth.

12 separation of butanol from ABE fermentation broth.

13 qually well on aerobic and anaerobic culture broth.

14 m acetone-butanol-ethanol (ABE) fermentation broth.

15 tion of selenite by bacteria incubated in LB broth.

16 ation of S. aureus from Bactec blood culture broth.

17 glycolate broth, and Robertson's cooked meat broth.

18 not produce toxoflavin in Luria-Bertani (LB) broth.

19 ompared to that of F. tularensis cultured in broth.

20 heal stool samples enriched in Gram-negative broth.

21 cific PLC activity after bacterial growth in broth.

22 n agar and 107 cultures grown in Bactec MGIT broth.

23 imal growth medium (M9) than in richer Luria broth.

24 extraction of daunorubicin from fermentation broth.

25 gar (MHA) and cation-adjusted Mueller-Hinton broth.

26 mined by the observation of turbidity of the broth.

27 ces the absorption of NOx in the cultivation broth.

28 ity of 104 Wm(-3) was obtained with nutrient broth.

29 pecific detection of B. anthracis in culture broth.

30 A, vanA, and vanB) in positive blood culture broths.

31 tance determinants in positive blood culture broths.

32 eening enzyme activities from fungal culture broths.

33 tified all organisms present in 54.5% of the broths.

34 mmersed in Streptococcus sanguinis bacterial broth (1 x 10(8) colony forming units/mL) for 48 hours.

35 ed when the anolyte was half-strength marine broth (1/2 MB) (0.28 muW/cm(2)) compared to Luria-Bertan

36 le (0.12 to 1 mug/ml) and Eggerthella lenta (broth, 1 to 4 mug/ml; agar, 1 to 8 mug/ml) were approved

37 to detect 10(3)CFU/mL of Escherichia coli in broth after 7h, and by adding a filter concentration ste

38 enzymes, enzyme mixtures, and crude culture broths against single substrates, substrate mixtures, an

39 MMP7(-/-) C57BL/6 mice were challenged with broth alone as an uninfected control or the H. pylori st

40 ot for bedaquiline MICs determined using 7H9 broth and 7H10 agar or 7H9 broth and 7H11 agar.

41 ermined using 7H9 broth and 7H10 agar or 7H9 broth and 7H11 agar.

42 1,000 generations of growth in rich nutrient broth and analyzed the genetic changes that evolved by w

43 ted better than L. plantarum to fermentative broth and BS counts increased 4.0 logCFU/g up to 48 h of

44 ens was improved by diluting the specimen in broth and by Vero cell coculture.

45 rocompartments in cells cultivated in liquid broth and hyper-flagellated swarmer cells from solid med

46 a in vivo in mice primed with thioglycollate broth and lipopolysaccharide.

47 ing techniques by using brain heart infusion broth and MacConkey agar containing 1 mug/ml or 10 mug/m

48 All five rLm30 vaccines secreted r30 in broth and macrophages; while rLm30 expressing r30 via a

49 increases bacterial resistance to stress in broth and mice.

50 By exposing bacteria to nutrient broth and penicillin or ciprofloxacin, the authors were

51 release of around 80% of total lipids in the broth and production of a hydrolysate suitable as yeast

52 d synergistically with exogenous lysozyme in broth and serum media.

53 aphy (IC) using spiked samples of dilute BBL broth and slightly outperformed the IC in accuracy while

54 PTS components in both defined medium and LB broth and that E. coli Mlc is able to rescue the biofilm

55 to distinct and broad speed distributions in broth and viscous gastric mucin media.

56 s, rectal swabs are screened using selective broth and/or solid medium.

57 tified at least one organism in 95.4% of the broths and correctly identified all organisms present in

58 he purification of ethanol from fermentation broths and the hydroisomerization of alkanes with 18-30

59 treptococcus pneumoniae ATCC 49619 (disk and broth), and Haemophilus influenzae ATCC 49247 (disk and

60 r, Gram stain, Sabouraud agar, thioglycolate broth, and brain heart infusion broth in all cases.

61 ded in test tubes containing sterile culture broth, and followed for 5 days.

62 rsibly abolished growth of L. pneumophila in broth, and growth inhibition was relieved by overproduct

63 se agar, brain heart infusion, thioglycolate broth, and Robertson's cooked meat broth.

64 itivity and specificity comparable to carrot broth- and LIM broth-enhanced real-time PCRs.

65 onclude that additional inputs present in LB broth are required for activation of vps gene transcript

66 Carboxylate-rich broths are electrolyzed in a cathodic chamber from which

67 ene, encoding alpha-hemolysin, when grown in broth, as well as on RNAIII, a posttranscriptional regul

68 of the LVS FTL_0325 mutant in Mueller-Hinton broth at 37 degrees C resulted in the appearance of memb

69 ons for isoniazid and rifampin in commercial broth-based systems.

70 olerae Mlc activates biofilm formation in LB broth but not in defined medium supplemented with either

71 nd fluids, cell culture media, and bacterial broth by the Griess assay, a chemiluminescence analyzer,

72 and Difco) of cation-adjusted Mueller-Hinton broth (CA-MHB), and using three different drug powders:

73 mmended media (cation-adjusted Muller-Hinton broth [CA-MHB]).

74 um concentration of 0.60 g/L in fermentation broth can be detected.

75 Analysis of TTD of positive MTBC cultures in broth can predict the probability of culture negativity

76 erobic and anaerobic agars and thioglycolate broth) compared to inoculation into blood culture bottle

77 ab was used for reference culture (MacConkey broth containing 1 mg/liter of meropenem and subcultured

78 rnight enrichment of the sample in MacConkey broth containing 1 mug/ml of meropenem.

79 or 24 hours in 1/10(th) strength tryptic soy broth containing 9 g/L total NaCl.

80 minants directly from positive blood culture broths containing Gram-positive bacteria.

81 nce in prospectively collected blood culture broths containing Gram-positive cocci.

82 e than INH at inhibiting bacterial growth in broth culture and in macrophages, and also reduced bacte

83 morphology, and was attenuated for growth in broth culture and in macrophages.

84 rA exhibit near-normal patterns of growth in broth culture but are severely attenuated in vivo We hyp

85 that is dispensable for bacterial growth in broth culture but essential for L. monocytogenes virulen

86 ons reduced the pathogenic bacterial load in broth culture by 2 to over 6 logs depending on the strai

87 A shortened period of broth culture enrichment resulted in 1 false-negative re

88 mes defined for Pf-5 grown on seed versus in broth culture overlapped, but most genes were regulated

89 Capsular genogroups detected by broth culture were genogroups W (21 isolates), B (12 iso

90 /a30) expressed the largest amount of r30 in broth culture, all five rLm30 vaccines expressed equival

91 microscopic-observation drug susceptibility broth culture, and in culture-positive samples (n = 252)

92 s 7, 40 and 100 CFU/mL for S. aureus in pure broth culture, and inoculated in food produces and envir

93 th, the mutant shows no defect for growth in broth culture, even under severe iron-limiting condition

94 ine to enhance growth rate and cell yield in broth culture.

95 inhibit bacterial growth at 37 degrees C in broth culture.

96 PCR of broth cultures grown overnight doubled the yield of N. m

97 ble of positive identification from plate or broth cultures in less than 90 minutes.

98 By testing broth cultures of characterized isolates representing al

99 In addition, broth cultures of Deltalvh and DeltavirD4 mutants, which

100 ulence defects can be reversed by incubating broth cultures of dot/icm mutants in water, termed water

101 Broth cultures of PCR-positive samples were tested for S

102 First, in broth cultures that mimicked thymidine limitation or sta

103 es from characterized agar cultures and MGIT broth cultures to the species level, respectively.

104 in both monospecies as well as multispecies broth cultures was inhibited in a dose-dependent manner

105 ed positive samples were detected when fecal broth cultures were tested.

106 L mutant strain during exponential growth in broth cultures with or without nitrate defined an approx

107 entry and phagosome acidification defects in broth cultures.

108 tained and cultured using standard plate and broth cultures.

109 c results obtained in duplicate by automated broth dilution (BD Phoenix) and disc diffusion.

110 tested blindly against 15 antimicrobials by broth dilution and the disc diffusion method.

111 r baumannii through in vitro disk diffusion, broth dilution and time-kill studies.

112 luated against 5 foodborne pathogens using a broth dilution assay.

113 conventionally performed by either a serial broth dilution method or with the commercially available

114 l susceptibility testing automatically via a broth dilution method to accurately determine the minimu

115 isc diffusion, disc volatilisation and micro broth dilution method.

116 boratory Standards Institute) recommends the broth dilution method.

117 -AST) was consistent with the results of the broth dilution method.

118 ility testing (dAST) and by the conventional broth dilution testing (BDT).

119 Pseudomonas aeruginosa using disc diffusion, broth dilution, E strip, chequerboard titration and grow

120 tration (MIC) of GEO was determined by micro-broth dilution.

121 robial activity of extracts was evaluated by broth-dilution and agar diffusion assay.

122 culture-based methods and two methods using broth-enhanced real-time PCR.

123 cificity comparable to carrot broth- and LIM broth-enhanced real-time PCRs.

124 Carrot broth-enhanced subculture to GBS Detect (Hardy Diagnosti

125 Antimicrobial susceptibility testing, broth enriched culture, and DNA sequencing were performe

126 Diagnostic performance was assayed in simple broth-enriched blood samples and standard aerobic cultur

127 e molecular tests were compared to those for broth-enriched culture as the gold standard.

128 The sensitivities of the two broth-enriched molecular methods were superior to those

129 nterval [CI] = 94.5% to 96.2%) compared to a broth-enriched reference standard.

130 mpared to the results of combined direct and broth-enriched toxigenic culture methods in a large, mul

131 stic test for the identification of GBS from broth-enriched vaginal/rectal specimens obtained during

132 In our evaluation, we compared broth enrichment and direct plating techniques by using

133 , 93.0%, and 100%, respectively, compared to broth enrichment culture and sequencing of target genes.

134 n/purification platforms without the need of broth enrichment is developed for the first time.

135 Broth enrichment methods performed poorly compared to di

136 Results were compared to those using Lim broth enrichment PCR and culture.

137 to the results of culture with and without a broth enrichment step on 328 rectal, perirectal, and sto

138 oculation methods, negating the need for the broth enrichment step.

139 th ciprofloxacin-resistant E. coli; however, broth enrichment using 1 mug/ml ciprofloxacin was the mo

140 Following 18 to 24 h of broth enrichment, each specimen was tested using the Xpe

141 d period) and 4 to 8 h (shortened period) of broth enrichment.

142 to 96.9% and 90.6%, respectively, following broth enrichment.

143 nt compared to testing of colonies following broth enrichment.

144 with the NAATs, following 18 to 24 h of Lim broth enrichment; 15% of specimens were culture positive

145 S. emergency departments were cultured using broth enrichment; wound specimens were cultured from abs

146 The broth-enrichment method was comparable to CHROMagar for

147 ral product discovery by random screening of broth extracts derived from cultured bacteria often suff

148 Bacterial culture broth extracts have been the starting point for the deve

149 min exposures per 24-h period in tryptic soy broth followed by immersion in a remineralizing solution

150 y product from the cell culture fermentation broth, followed by rapid, multiattribute LC-MS analysis.

151 thawed M. tuberculosis complex cells in 7H9 broth for 20 h before culture on solid Middlebrook 7H10

152 The alcoholic medium was then used as a seed broth for acetic fermentation using Acetobacter aceti as

153 method for processing positive-blood-culture broth for immediate identification of microorganisms by

154 sumption of faba beans together with cooking broth for the maximum potential health benefits.

155 This metabolite was also found in culture broth from the commensal bacterium Bacteroides vulgatus,

156 asal-associated lymphoid tissue in mice than broth-grown bacteria, and were not virulent during septi

157 ectivity of desiccated streptococci has used broth-grown, planktonic populations.

158 rotease expression when strains are grown in broth, hla regulation is highly responsive to factors as

159 eloped in the mid-1800s-growth on agar or in broth-identification and susceptibility profiling for bo

160 hioglycolate broth, and brain heart infusion broth in all cases.

161 growth environments: S. flexneri growing in broth (in vitro), S. flexneri growing within epithelial

162 Turbidity of the broth indicated bacterial leakage.

163 olution is 50 ng/mL, whereas that in chicken broth is only 500 ng/mL.

164 Sap secreted by the B. anthracis in culture broth just after 1h of growth.

165 ), brain-heart infusion (BHI), Luria-Bertani broth (LB), and glucose (G) medium) made from components

166 in histidine (HDB) and lysine decarboxylase broth (LDB).

167 h microdilution with polysorbate 80 (BMD-T), broth macrodilution (TDS), and the Etest.

168 Yeast-form fungi can be tested using broth macrodilution and microdilution assays.

169 fusion was better than the agreement between broth macrodilution and the agar-based methods.

170 tin resistance determination as performed by broth macrodilution was compared to results from clinica

171 lates of Rhodococcus equi were determined by broth macrodilution, disk diffusion, and Etest.

172 charide derivative was evaluated in nutrient broth media against three bacteria strains that are comm

173 nts with sputum-culture conversion in liquid broth medium at 2 months.

174 We developed a low-cost selective broth medium containing thioglycolic acid and l-cystine,

175 m tuberculosis H37Rv (M. tb) grown either in broth medium or inside macrophages.

176 as measurable bacterial growth inhibition in broth medium required >10-fold higher concentrations.

177 Lysogeny Broth medium samples reconstituted in MeOH/H2O ratios ra

178 mycobacterial isolates grown on solid and/or broth medium were included in the study.

179 ature, and addition of serum and albumin for broth methods.

180 lymyxin resistance determination compared to broth microdilution (16 to 20 h), our study indicates th

181 vancomycin and daptomycin MICs, measured by broth microdilution (BMD) and Etest, was prospectively a

182 Illumina MiSeq WGS and broth microdilution (BMD) assays were performed on 90 bl

183 icroScan panel compared to that of reference broth microdilution (BMD) during the testing of 64 strai

184 and AST-XN06 cards to those obtained by CLSI broth microdilution (BMD) for 255 isolates of Enterobact

185 oratory Standards Institute (CLSI) reference broth microdilution (BMD) for 99 isolates of Pseudomonas

186 oratory Standards Institute (CLSI) reference broth microdilution (BMD) method by testing 2 quality co

187 the Etest compared to determinations by the broth microdilution (BMD) method.

188 ntimicrobial Susceptibility Testing (EUCAST) broth microdilution (BMD) methods.

189 al and Laboratory Standards Institute (CLSI) broth microdilution (BMD) methods.

190 al and Laboratory Standards Institute (CLSI) broth microdilution (BMD) reference method for 134 staph

191 Clinical and Laboratory Standards Institute broth microdilution (BMD) reference methods.

192 phylococcus aureus isolates using (i and ii) broth microdilution (BMD) with 50-mg/liter calcium mediu

193 Broth microdilution (BMD), macrodilution (MD), and agar

194 All isolates underwent testing by the broth microdilution (in duplicate) and agar dilution (in

195 es, 25 were determined to be PB resistant by broth microdilution (MIC > 2 mug/ml), including all 7 JM

196 rospective testing (Etest and CLSI reference broth microdilution [BMD] method) of stored isolates fro

197 arious antibiotic classes were determined by broth microdilution according to the guidelines of the C

198 All isolates were MIC tested by broth microdilution against ciprofloxacin, levofloxacin,

199 erived day 1 and 2 thresholds for AUC/MIC by broth microdilution and AUC/MIC by Etest.

200 or amikacin and methicillin resistance using broth microdilution and disk diffusion testing.

201 Broth microdilution and drug disk diffusion assays demon

202 ane MIC50/MIC9(0)s to </= 0.25/0.5 mug/ml by broth microdilution and Etest.

203 d for vancomycin susceptibility phenotype by broth microdilution and modified population analysis.

204 lin, doxycycline, lincomycin, and tylosin by broth microdilution and that to carbadox by agar dilutio

205 al agreement by all four dilution tests (two broth microdilution and two agar dilution) was achieved

206 man MRSA from the same geographic area using broth microdilution antimicrobial susceptibility testing

207 foxitin disk diffusion test and an oxacillin broth microdilution assay were examined.

208 ecutive clinical isolates of the MAC using a broth microdilution assay.

209 The cefoxitin disk diffusion and oxacillin broth microdilution assays categorized 100% and 61.3% of

210 ositive bacterium, Staphylococcus hyicus, in broth microdilution assays.

211 A commercial broth microdilution device (Sensititre; Thermo Fisher Sc

212 e performance of the HP D300 inkjet-assisted broth microdilution digital dispensing method (DDM), whi

213 ility testing (AST) methods were compared to broth microdilution for testing of Staphylococcus aureus

214 We compared Etest and disk diffusion to broth microdilution for the detection of fluoroquinolone

215 The standard broth microdilution method (BMD) is demanding and requir

216 esistance currently relies on a conventional broth microdilution method that requires a 16- to 20-h i

217 ptibility rates determined with the standard broth microdilution method using cation-adjusted Mueller

218 Using a reference broth microdilution method, we found that the serial iso

219 Candida species by both the CLSI and EUCAST broth microdilution methodologies.

220 CLSI reference broth microdilution methods and species-specific interpr

221 Agar dilution and broth microdilution methods were evaluated.

222 ories (Etest, disk diffusion, and Sensititre broth microdilution methods) for testing of minocycline,

223 ngin, and micafungin were determined by CLSI broth microdilution methods.

224 erived MIC (MICFAST) correspond closely with broth microdilution MIC (MICBMD, Matthew's correlation c

225 ntituberculosis drugs, with a convenient 7H9 broth microdilution MIC method suitable for use in resou

226 multidrug-resistant tuberculosis using a 7H9 broth microdilution MIC method.

227 Antimicrobial susceptibility results from broth microdilution MIC testing of 993 Staphylococcus lu

228 For the 7H9 broth microdilution MIC, a 3-dilution QC range (0.015 to

229 on MICs and 0.015 to 0.06 mug/ml for the 7H9 broth microdilution MIC.

230 t tested positive for amikacin resistance by broth microdilution or disk diffusion testing were inves

231 mpared the performance of a new colorimetric broth microdilution panel (SensiQuattro Candida EU) for

232 em's MIC test strip and the EUCAST reference broth microdilution protocol.

233 in comparison to the results obtained with a broth microdilution reference standard.

234 In comparison with the standard broth microdilution results, very major rates were low (

235 Isolates tested by the broth microdilution showed high levels of resistance; su

236 were each inoculated onto specially prepared broth microdilution susceptibility panels containing van

237 The telavancin broth microdilution susceptibility testing method was re

238 Standardized broth microdilution techniques can be used to distinguis

239 By broth microdilution techniques, we determined the MIC va

240 submitted to a central reference monitor for broth microdilution testing by Clinical and Laboratory S

241 microbiology laboratories to perform at-will broth microdilution testing of antimicrobials and to add

242 lts showed unsatisfactory reproducibility of broth microdilution testing of ceftriaxone with N. cyria

243 e 2-fold serial dilution series required for broth microdilution testing.

244 er desorption ionization-time of flight, and broth microdilution tests were repeated to confirm the C

245 of the SensiQuattro panel with the reference broth microdilution was slightly higher for C. albicans

246 isolates determined to be PB susceptible by broth microdilution were NP test negative.

247 sistant (MDR) Gram-negative bacilli (GNB) by broth microdilution with polysorbate 80 (BMD-T), broth m

248 in parallel using BMD-T, TDS, agar dilution, broth microdilution without polysorbate 80 (BMD), and th

249 ffusion, Microscan broth microdilution, CLSI broth microdilution, and Etest).

250 ing which included disk diffusion, Microscan broth microdilution, Clinical and Laboratory Standards I

251 c testing methods (disk diffusion, Microscan broth microdilution, CLSI broth microdilution, and Etest

252 oratory Standards Institute (CLSI) reference broth microdilution, gradient diffusion (Etest), 23S rRN

253 dards Institute (CLSI)-recommended method of broth microdilution, susceptibility testing of 170 isola

254 use, we explored a novel, automated, at-will broth microdilution-based susceptibility testing platfor

255 ical scavenging activity, disc-diffusion and broth microdilution.

256 were 25 and 100%, respectively, compared to broth microdilution.

257 Antimicrobial susceptibility was measured by broth microdilution.

258 results for 128 A. urinae isolates tested by broth microdilution.

259 evofloxacin susceptibility was determined by broth microdilution.

260 were tested for antimicrobial resistance by broth microdilution.

261 d tested for antibiotic susceptibility using broth microdilution.

262 MICs were determined via broth microdilution.

263 elegans clinical isolates were determined by broth microdilution.

264 MTBC) resistance determinants from solid and broth Middlebrook culture media.

265 ibitory substance (BLIS) from a fermentation broth of Pediococcus acidilactici Kp10, and the amount p

266 of curvularides A-E, isolated from a culture broth of the endophytic fungus Curvularia geniculata, is

267 and prepared with 2x prediluted drugs in 7H9 broth-oleic acid albumin dextrose catalase.

268 TCC 25923 (disk only), S. aureus ATCC 29213 (broth only), Enterococcus faecalis ATCC 29212 (broth onl

269 oth only), Enterococcus faecalis ATCC 29212 (broth only), Streptococcus pneumoniae ATCC 49619 (disk a

270 r diet initiation, mice were inoculated with broth or H. bilis and were necropsied at several time po

271 Growth of Ft in Muller-Hinton Broth or on Muller-Hinton-based chocolate agar plates or

272 e samples were digested in the buffer, Luria broth, or mouse plasma (LOD ~ 30 attomol/injection = 5 f

273 in complex matrices including Luria-Bertani broth, orange juice, and skimmed milk.

274 ence was observed between 24 h ESwab and Lim broth PCRs.

275 orresponding sensitivities of Trypticase soy broth plus ertapenem or meropenem were 78% and 47%, resp

276 CHROMagar (BD Diagnostics) was compared to a broth preenrichment followed by plating to Baird-Parker

277 ities of 21 S. delphini strains by reference broth, rapid disc, and rapid slide methods.

278 lower limits of detection of 12CFUmL(-1) in broth samples and 30-300CFUmL(-1) in spiked complex food

279 nstrate that the Lvh T4ASS functions in both broth stationary-phase cultures conventionally used for

280 Broth stationary-phase cultures of most dot/icm mutants

281 a pre-enrichment step in Luria-Bertani (LB) broth supplemented with isopropyl beta-d-thiogalactopyra

282 ) was investigated in tyrosine decarboxylase broth (TDB) using HPLC.

283 s, maintaining stable yield for two weeks in broth that reaches >15% farnesene by volume.

284 by PCR testing; (ii) seeding in Todd-Hewitt broth (THB) and, after culture overnight, testing by PCR

285 purified from the engineered Pichia pastoris broth to homogeneity by anion exchange chromatography, H

286 e-distilled water (ddH2O) versus tryptic soy broth (TSB) to incubate disks, and incubation of plates

287 rmulations of 4 different media (tryptic soy broth (TSB), brain-heart infusion (BHI), Luria-Bertani b

288 a real-time PCR for bla(KPC) from enrichment broth versus direct plating of rectal surveillance swabs

289 An aliquot of positive-blood-culture broth was incubated with lysis buffer for 2 to 4 min at

290 To detect the VRE subpopulation, tryptic soy broth was inoculated from positive blood cultures and a

291 tivation method (mCIM), in which tryptic soy broth was substituted for water during the inactivation

292 od using cation-adjusted Mueller-Hinton (MH) broth were 77.6% for minocycline and 29% for doxycycline

293 nd hydrolyzed carbapenems from an enrichment broth were developed.

294 es that contribute to ExPEC fitness in mucus broth were identified, with genes that are directly or i

295 ve compounds than those of resulting cooking broths, which was the opposite observation when autoclav

296 ent assays using E. coli O157:H7 grown in LB broth with a reporter phage concentration of 1.76 x 10(2

297 st grew wild-type cells in buffered tryptone broth with glucose and monitored acetylation over time b

298 CCFA-HT), and cycloserine-cefoxitin mannitol broth with taurocholate and lysozyme (CCMB-TAL) were com

299 and l-cystine, termed C. difficile brucella broth with thioglycolic acid and l-cystine (CDBB-TC), fo

300 as 10(0) CFU, from 100 or 250 mL of culture broth within similar timeframes as above.