ライフサイエンスコーパス: bacterial culture

1 0.49; p = 0.021, p = 0.011 for the two test bacterial cultures).

2 f CO2 and O2 in situ in the headspace of the bacterial culture.

3 C. trachomatis detection, and nonchlamydial bacterial culture.

4 resence of Mycobacterium tuberculosis in the bacterial culture.

5 the results with those obtained by classical bacterial culture.

6 mastitis, and are traditionally diagnosed by bacterial culture.

7 hat had more than one specimen submitted for bacterial culture.

8 ts properties can limit the growth rate of a bacterial culture.

9 in with a yield of approximately 10 mg/liter bacterial culture.

10 les were subjected to HbA(1c) estimation and bacterial culture.

11 sensitivity and specificity and outperformed bacterial culture.

12 cted by the cryptococcal antigen test and/or bacterial culture.

13 of 15 bacterial targets compared to routine bacterial culture.

14 the results of the accepted "gold standard," bacterial culture.

15 85.6 and 98.6%, respectively, compared with bacterial culture.

16 re compared to the "gold standard" method of bacterial culture.

17 to study the proliferation of mutators in a bacterial culture.

18 between a fungal blood culture and a routine bacterial culture.

19 erial keratitis and confirmation by negative bacterial culture.

20 Strep A molecular assay compared to that of bacterial culture.

21 odel biocatalyst without any optimization of bacterial culture.

22 ogen Panel, an in-house five-virus panel and bacterial culture.

23 cally, and bacterial killing was assessed by bacterial culture.

24 t probe amplification assay and conventional bacterial culture.

25 nchoalveolar lavage (p = 0.011) quantitative bacterial culture.

26 een aptamer)) were readily obtained from 1 l bacterial culture.

27 ed reporter proteins and easily expressed in bacterial cultures.

28 ilic predominance (average 64%) and negative bacterial cultures.

29 in the mature toxin, MccE492m, isolated from bacterial cultures.

30 ish between chromogenic growth for screening bacterial cultures.

31 e biological processing of these analytes in bacterial cultures.

32 shown by light microscopy, and "clumping" of bacterial cultures.

33 e first report of CH(3)SeSSCH(3) produced by bacterial cultures.

34 ed fungi, 10 from fungal cultures and 8 from bacterial cultures.

35 The lungs were homogenized for quantitative bacterial cultures.

36 ecystostomy tube placed (n = 4) had negative bacterial cultures.

37 in proteins expressed in methionine-depleted bacterial cultures.

38 measurements of GFP fluorescence in growing bacterial cultures.

39 ient phenotypic conversion of drug-resistant bacterial cultures.

40 for accelerated and improved measurement of bacterial cultures.

41 usly collected, had correspondingly positive bacterial cultures.

42 latile carboxylic acids (FVCA) in cheese and bacterial cultures.

43 analyses of cDNA prepared from mid-log phase bacterial cultures.

44 ity of the Ni(II)-dependent enzyme urease in bacterial cultures.

45 biochemical assays have been applied to bulk bacterial cultures.

46 from studies of nitrifying and denitrifying bacterial cultures.

47 were treated with cell-free supernatant from bacterial cultures.

48 S, similar to previous experiments with pure bacterial cultures.

49 change of ~80% is achieved after ~200 min of bacterial culturing.

50 patients, and 43 specimens were obtained for bacterial culture; 20 of the specimens (47 percent) were

51 tly positive in bronchoalveolar lavage (BAL) bacterial cultures (46-89%) which leads to a donor-to-re

52 method for screening of CDAD was as follows: bacterial culture, 95%; culture with cytotoxin assay of

53 Nine additional samples were prepared for bacterial culture, after initial irradiation with ultrav

54 cterial culture followed by cytotoxin assay, bacterial culture alone, latex agglutination assay, and

55 , resulting in an underdetection of fungi by bacterial culture alone.

56 nd 42 immunological potential predictors for bacterial culture among women with uncomplicated UTI sym

57 results were compared to those with standard bacterial culture and biochemical identification with nu

58 Diagnosis relies on bacterial culture and confirmation of toxin production,

59 cells were assessed by means of quantitative bacterial culture and expressed as colony-forming units

60 Comparison of Q-PCR results with bacterial culture and histopathological results from an

61 Serial quantitative bacterial culture and noninvasive magnetic resonance ima

62 overed in yields of 5-7 mg x L-1 of starting bacterial culture and pure HemT at 10 mg x L-1 x HemA ha

63 n ages 6 to 36 months and included viral and bacterial culture and quantitative PCR for respiratory s

64 treatment of streptococcal pharyngitis since bacterial culture and rapid diagnostic tests are not fea

65 By combining bacterial culture and upper respiratory viral PCR testin

66 The addition of PCT levels to bacterial culture and viral detection results can assist

67 hil and neutrophil percentages, and positive bacterial culture and virus detection rates were similar

68 N, and V144N) interactions were expressed in bacterial culture and were studied with spectroscopy and

69 resistance from gDNA directly extracted from bacterial culture and without PCR amplification.

70 Detection of C. difficile by anaerobic bacterial culture and/or cytotoxicity assays has been la

71 ontaining compounds that were present in the bacterial cultures and absent (or present at only low ab

72 in vanishingly small quantities (mug/L) from bacterial cultures and are believed to be unstable.

73 d levels of reactive oxygen species (ROS) in bacterial cultures and fecal microbiota using 2',7'-dich

74 Different bacterial cultures and groundwater were shown to have co

75 properties of poly-L-lysine were measured in bacterial cultures and in whole CF sputum.

76 Examples include bioprocess monitoring of bacterial cultures and measurement of minute amounts of

77 e assay be used in conjunction with standard bacterial cultures and results interpreted within the co

78 itis grow well in media utilized for routine bacterial cultures and that cryptococcal antigen tests a

79 the low frequencies of persisters in growing bacterial cultures and the complex underlying molecular

80 l-wash specimens were obtained for viral and bacterial cultures and the detection of viral antigens.

81 of ethanol also induced the acidification of bacterial cultures and the production of indole-3-acetic

82 lutenin protein to relatively high levels in bacterial cultures and the protein exhibited the known a

83 of OMPs into serum was highest for immature bacterial cultures and was increased by antibiotics in v

84 Blood was drawn for bacterial culturing and identification at 6 time points

85 solated in high yield (25-33 mg per liter of bacterial culture) and were shown to impart a high degre

86 oach of deep microbiome sequencing, targeted bacterial culture, and in vitro assays.

87 sites using gross and microscopic pathology, bacterial culture, and molecular methods.

88 often reach concentrations of 0.1-30 muM in bacterial cultures, and generally, LuxR-type receptors r

89 ctiveness was assessed by 3 criteria: death, bacterial cultures, and presumptive clinical cure score.

90 hirteen compounds were identified from these bacterial cultures, and the combination of these VOCs cr

91 lume of respiratory secretions; b) effect on bacterial cultures; and c) changes in the inflammatory c

92 ating kairomones, and using a combination of bacterial culturing approaches, bioassay-guided fraction

93 detection, nucleic acid probe detection, and bacterial culture are commonly used to confirm group A s

94 When both cryptococcal antigen tests and bacterial cultures are ordered routinely, eliminating fu

95 Traditional assays available for monitoring bacterial cultures are time-consuming and labor-intensiv

96 All results were compared to routine bacterial culture as the gold standard.

97 on assay (CCCNA), and to anaerobic toxigenic bacterial culture, as the "gold standard," for 285 clini

98 g with WLI was demonstrated as a novel rapid bacterial culture assay with several advantageous capabi

99 High vaginal swabs were obtained for bacterial culture before and after microbicide applicati

100 Also, illumination of bacterial cultures before inoculation of pea roots incre

101 Bacterial cultures (blood, cerebrospinal fluid, lung tis

102 Bacterial culture broth extracts have been the starting

103 d in solution, membrane environments, and in bacterial culture by a combination of chiroptical and so

104 ction was monitored by clinical examination, bacterial culture, C. jejuni-specific PCR, gross patholo

105 Bacterial cultures can harbor subpopulations that are ge

106 Quantitative bacterial cultures, cell counts, chemokine, cytokine, pr

107 ple-to-result molecular test, to a toxigenic bacterial culture/cell cytotoxin neutralization assay (T

108 Conjunctival swab samples were collected for bacterial culture, Chlamydia trachomatis PCR, and RNA is

109 a bacterial culture or were recovered from a bacterial culture collected within 48 h.

110 peutically relevant bioactive molecules from bacterial culture collections, but the large-scale manip

111 mmunities and with their corresponding fecal bacterial culture collections.

112 uit yogurts were made from goat's milk using bacterial cultures comprising, Lactobacillus acidophilus

113 s and demonstrate that subtle differences in bacterial culture conditions may have important implicat

114 affected by shallow standing versus shaking bacterial culture conditions prior to macrophage infecti

115 ve humidity, aerosol exposure technique, and bacterial culture conditions to optimize the spray facto

116 As a result, a clonal bacterial culture could comprise subpopulations of cells

117 All bacterial cultures demonstrated efficient caproate produ

118 Bacterial cultures detected anaerobes in 83% of lesions

119 Anaerobic bacterial culture determined the occurrence of potential

120 eatment of axenic embryos with feces-derived bacterial cultures did not affect eclosure.

121 The bacterial culture diluted to 33% in water and coated on

122 Fluctuations in the growth rate of a bacterial culture during unbalanced growth are generally

123 amount of SGP increased with the age of the bacterial culture, elevated temperature, or acidic pH.

124 cular techniques against comparator methods (bacterial culture, ELISA, and PCR) using 867 diarrhoeal

125 Spent liquid medium from 27/84 bacterial cultures enhanced iodide oxidation 2-10 fold i

126 After bacterial culture enrichment, we tested for pneumococci

127 ty acids (CFAs) are generally synthesized as bacterial cultures enter stationary phase.

128 Bacterial cultures, especially biofilms, produce a small

129 Anaerobic bacterial culture examination was performed on the poole

130 The experiments consisted of bacterial cultures exposed to a nondisturbed nonaqueous

131 Lysate of bacterial cultures expressing the protein converted the

132 but are culture negative or in regions where bacterial culturing facilities are not available.

133 Here, bacterial culturing, fluorescence-based cell sorting, an

134 xin in stool by tissue culture, C. difficile bacterial culture followed by cytotoxin assay, bacterial

135 e causative Corynebacterium spp., usually by bacterial culture followed by enzymatic and toxin detect

136 employed in routine diagnostics are based on bacterial culture followed by morphological trait differ

137 Compared to bacterial culture followed by PCR identification of resi

138 to all periprosthetic specimens received for bacterial culture from 198 revision arthroplasty procedu

139 cells/ml were obtained using genomic DNA and bacterial culture from M. capricolum subsp. capripneumon

140 detection methods rely almost exclusively on bacterial culture from sputum which limits sampling to o

141 ta included antibiotic resistance results of bacterial cultures from hospitalized patients, alongside

142 tration in the lungs and liver, and positive bacterial cultures from internal organs.

143 ls also underwent necropsy with quantitative bacterial cultures from multiple organ tissue samples.

144 SLIP involves transferring arrayed bacterial cultures from multiwell plates onto large agar

145 At 48 hrs, cardiac function, bacterial cultures from the septic focus, and inflammato

146 BAL to examine viral nucleic acid sequences, bacterial cultures, granulocyte counts, and phlebotomy f

147 Bacterial culture grew aerobic bacteria from three cysts

148 Bacterial cultures grew Capnocytophaga canimorsus.

149 arge filamentous aggregates in the medium of bacterial culture growing at 37 degrees C.

150 By comparing the metabolomes of bacterial cultures grown in halide-replete and deficient

151 platform was built for headspace sampling of bacterial cultures grown in standard culture flasks via

152 achieved biosynthetically through the use of bacterial cultures grown on isotopically enriched media,

153 Out of the 27 sequenced samples, only 20 had bacterial culture growth, while the microbiological and

154 nd suspected VAP, bilateral BAL quantitative bacterial cultures had significant growth on one side on

155 yranopterin monophosphate (1), isolated from bacterial culture, has previously been shown to be effec

156 in sequencing technology, animal models, and bacterial culturing have facilitated the discovery of sp

157 Two novel compounds so far undetected in bacterial culture headspace, CH3Se2SCH3 and CH3SeSeSeCH3

158 roduces volatile organoselenium compounds in bacterial culture headspace.

159 ral PS-I due to its low expression levels in bacterial cultures, improved chemical synthesis protocol

160 ments (CLIA)-waived setting in comparison to bacterial culture in 481 children and adults.

161 pools performed throughout the growth of the bacterial culture in rich medium revealed a dramatic inc

162 ts is often restricted by the limitations of bacterial culture in terms of time requirements and low

163 ts is often restricted by the limitations of bacterial culture in terms of time requirements and low

164 rmining persistence versus extinction of the bacterial culture in the chemostat.

165 tails of these bacterium in JCP, we enforced bacterial culture in the nose and cytology in the nasal

166 e was evaluated by slit lamp examination and bacterial cultures in both a rabbit intrastromal model a

167 alveolar lavage, as the diagnostic source of bacterial cultures in cases of suspected aspiration pneu

168 vitreous samples by combined analysis using bacterial cultures in pediatric blood culture bottles an

169 Bacterial culturing in combination with whole-genome seq

170 Six hundred bacterial cultures, including M. avium subsp. paratuberc

171 Even in clonal bacterial cultures, individual bacteria can show substan

172 (Ti) plasmid, stabbing the crown region with bacterial cultures induced gall-like structures formed o

173 m single colonies or from less than 1ml of a bacterial culture is possible.

174 Bacterial culture is the gold standard for diagnosis, bu

175 A bacterial culture is vacuum-infiltrated into leaves, and

176 collagen-rich hydrogel successfully treated bacterial cultures isolated from patient samples via an

177 s formed from pyrene by two pyrene-degrading bacterial cultures known to be geographically widespread

178 of bacteria in these samples was assessed by bacterial culture, light microscopy, and 16S rRNA gene s

179 Quantitative bacterial cultures, measurement of C. difficile toxin ti

180 We then screened bacterial culture media for TTX using LC-MS/MS and ident

181 5'- cyclic adenosine monophosphate (cAMP) in bacterial culture media.

182 for the biological route due to the required bacterial culture media.

183 which we demonstrate through the analysis of bacterial culture media.

184 (yeast culture medium) broth, Luria-Bertani (bacterial culture medium) broth, and minimal essential m

185 onse to increased salt concentrations in the bacterial culture medium, and, concordant with the in vi

186 putum samples compared with that detected in bacterial culture medium, resulting in an underdetection

187 .1% of CIF-positive samples were detected in bacterial culture medium, whereas greater rates of detec

188 entrations of sodium chloride present in the bacterial culture medium.

189 ed for secretion of T3SS2 effectors into the bacterial culture medium; however, it is essential for t

190 Standard identification approaches include bacterial culturing method, which takes several days.

191 the molecular panel to routine quantitative bacterial culture methods on remnant BALF.

192 Bacterial culture methods, e.g. Plate Counting Method (P

193 previous studies using conventional in vitro bacterial culture methods.

194 lmost interchangeably, impacting non-growing bacterial cultures more significantly than actively grow

195 cimens that were fungal culture positive but bacterial culture negative.

196 egative in all 1,312 aerobic bottles and 810 bacterial culture-negative anaerobic bottles.

197 In summary, we found that bacterial culture of BAL fluid is largely effective in d

198 Quantitative bacterial culture of bronchoalveolar lavage fluids (BALF

199 SIBO was evaluated by bacterial culture of duodenal aspirate, glucose and lact

200 One week later, a liquid bacterial culture of Escherichia coli was injected into

201 rveyed by enzyme-linked immunosorbent assay; bacterial culture of liver, colon, and cecum; histology;

202 Bacterial culture of mesenteric lymph nodes in these mic

203 Colonization was determined by bacterial culture of nasal wash, and humoral immune resp

204 hat mice colonized for 2 months with a mixed bacterial culture of opportunistic pathogens showed an i

205 We retrospectively studied the quantitative bacterial cultures of 399 BAL sample pairs collected fro

206 Bacterial cultures of bronchoalveolar lavage fluid and l

207 Routine bacterial cultures of corneal scrapings from seven cats

208 ombined use of cryptococcal antigen test and bacterial cultures of CSF could replace routine fungal c

209 ermal colloid antibodies in a mixture of two bacterial cultures of different cell shape and size.

210 Conditioned media from bacterial cultures of NU14 DeltaampG and NU14 DeltawaaL

211 Bacterial cultures of the recovered surgical material an

212 hea (n = 452) were similarly studied, except bacterial cultures of the stool were limited only to cas

213 ogical tests of intraocular samples included bacterial culturing of pediatric blood culture bottles;

214 r bacterial detection require time-consuming bacterial cultures on plates before the pathogens can be

215 was not observed on the surface of a drop of bacterial culture, on bacteria-free culture supernatant,

216 a show that pB15 invades static (nonshaking) bacterial cultures only at intermediate densities.

217 achieved through enhanced correlation of the bacterial culture optical density and the number of CFU.

218 vations and microbiological testing based on bacterial culture or DNA detection in individuals with p

219 tional growth effect was performed either in bacterial culture or in an animal model of infection.

220 wo standard abutments were either exposed to bacterial culture or left sterile to serve as positive a

221 requires microscopy of Gram-stained samples, bacterial culture or nucleic acid amplification tests.

222 density values from the EIA with results of bacterial culture or skin test, the reference test, esta

223 had either been previously recovered from a bacterial culture or were recovered from a bacterial cul

224 se) B incubated with purified enzymes, whole bacterial cultures, or their separated components-cells

225 (92 and 77%, respectively, when adjusted for bacterial culture outcomes).

226 mely the global interpretation of diagnostic bacterial culture plates, including presumptive pathogen

227 discordant cases were one specimen that was bacterial culture positive but fungal culture negative a

228 lerae infection was defined as a V. cholerae bacterial culture positive result during the 1-month sur

229 PCRs were positive in 27/5,594 (0.5%) bacterial culture-positive anaerobic bottles that contai

230 Clusters 5 and 6 are associated with bacterial culture positivity, with the former consistent

231 By using bacterial cultures present in the surroundings or raw ma

232 Production steps involve bacterial culture, protein isolation, denaturation, puri

233 Addition of hREG3A to bacterial cultures reduced levels of ROS and increased s

234 ed biochemically and by E. faecalis-specific bacterial cultures, respectively, in day 3 postburn rats

235 Macrophage crude cell lysates added to bacterial cultures resulted in the death of the SalY mut

236 eatment, but it takes several days to obtain bacterial culture results.

237 .02, and 0.11mgkg(-1), respectively, and for bacterial culture samples were 1.32, 0.09, and 0.54mgkg(

238 tion of the target metabolites in cheese and bacterial culture samples.

239 Quantitative bacterial cultures showed a mean log10 C. difficile coun

240 Bacterial culture significantly underestimates the burde

241 sed to generate 50 different simulated mixed bacterial cultures similar to that done for an initial b

242 in the infected mouse lung, and in vitro in bacterial cultures subjected to gradual oxygen depletion

243 nutrients but also in initially homogeneous bacterial cultures, suggesting that bacteria can generat

244 erase (LesA) that was abundantly secreted in bacterial culture supernatant and was characterized as a

245 by macrophages stimulated with gram-positive bacterial culture supernatants (GPCSs) after their LTA w

246 PIF was purified from bacterial culture supernatants by anion/cation exchange

247 kine responses induced by partially purified bacterial culture supernatants containing a mixture of e

248 We screened bacterial culture supernatants for such activity using r

249 For the microtiter assay, either spent bacterial culture supernatants or extracts are added to

250 HPLC peptide fractionation of bacterial culture supernatants revealed several distinct

251 The Bartonella mitogen was found in bacterial culture supernatants, the soluble cell lysate

252 tudies examined legiobactin contained within bacterial culture supernatants.

253 A bacterial culture swab taken from the underlying granula

254 uctively dissolve Fe and Mn oxyhydroxides in bacterial culture systems, but the impact of PCA upon Fe

255 In five of these six recipients (83.3%) bacterial cultures taken from the explanted lungs contin

256 Here, using bacterial culture techniques, we show that a subset of l

257 e capture by MR1 of 5-OP-RU and 5-OE-RU from bacterial cultures that activate MAIT cells, but not fro

258 d material was from 10 to 50 mg per liter of bacterial culture, the protein was soluble at concentrat

259 ollowing: conventional anaerobic and aerobic bacterial cultures; the Ibis T5000 universal biosensor (

260 ly optimized for the detection of toxin from bacterial cultures; the limit of detection was approxima

261 owth of S. enteritidis and S. typhimurium in bacterial cultures; this was the result of a decrease in

262 o show applicability to clinical samples and bacterial cultures, through extraction of PCR-amplifiabl

263 tion procedure, significantly shortening the bacterial culture time.

264 For this study, we used bacterial culture to perform analyses not accurate with

265 zed by the ability of a subpopulation within bacterial cultures to survive exposure to antibiotics an

266 and WTC (n = 29) samples were collected for bacterial culturing to illustrate the relationship betwe

267 This was confirmed when the bacterial culture, treated with chloramphenicol before t

268 testing included microscopy, fungal culture, bacterial culture, tuberculosis culture, multiplex FilmA

269 ulture was attempted, five provided positive bacterial culture under both aerobic and anaerobic condi

270 Importantly, compared to bacterial culture under planktonic conditions, the intra

271 shed on the health effects of yogurt and the bacterial cultures used in the production of yogurt.

272 h Corporation (SLRC), compared with standard bacterial culture using 966 clean-catch urine specimens

273 fungal meningitis in patients with negative bacterial culture, viral culture and molecular testing w

274 Of the nine experimental samples where bacterial culture was attempted, five provided positive

275 Bacterial culture was enforced symptomatic patients of J

276 The proportion of cases confirmed by bacterial culture was higher in the 1990s than in the 19

277 A purified enzyme or bacterial culture was mixed with the BODIPY-alpha-casein

278 Toxigenic bacterial culture was performed as follows.

279 2,3-diol, and propane-1,3-diol in cheese and bacterial cultures was developed.

280 s very broad, from 0 to 1000mgkg(-1), and in bacterial cultures was from 0 to 5000mgkg(-1) with R(2)>

281 d on experiments in which the growth rate of bacterial cultures was observed to decrease as the osmol

282 For bacterial cultures we further demonstrate quantification

283 Urine specimens submitted for bacterial culture were plated onto CPSE agar with a 1-mu

284 nization mass spectrometry (MALDI-MS), mixed bacterial cultures were analyzed in a double-blind fashi

285 treated with different supernatants (SNs) of bacterial cultures were detected during real-time analys

286 ctive interleukin 8 (IL-8), and quantitative bacterial cultures were done in BALF from 54 CF (median

287 Bacterial cultures were grown, and protein synthesis was

288 Viral and bacterial cultures were obtained from ill students.

289 Bacterial cultures were performed on the sampling soluti

290 Bacterial cultures were positive in 64% of KPro eyes, 76

291 Bacterial cultures were screened for lactase activity in

292 ed the intracellular concentration of ATP in bacterial cultures, what happens in individual bacterial

293 s and thus should be recommended for enteric bacterial culture when bulk fecal specimens are unavaila

294 mination in pure cultures; analysis of mixed bacterial cultures, where examining one species in the p

295 cles can support the growth of heterotrophic bacterial cultures, which implicates these structures in

296 synthetic target, purified genomic DNA, and bacterial culture with a limit of detection (LoD) of 3.9

297 ll suited to multi-well imaging, analysis of bacterial cultures with high cell density (thousands of

298 Bacterial cultures with positive results were identified

299 ial identification was defined by a positive bacterial culture within 48 hours after intubation in en

300 aped as a compact disc facilitates long-term bacterial culture without external pumps and tubing and