ライフサイエンスコーパス: bacterial strain

1 tely half of the worms are dominated by each bacterial strain.

2 elium was monitored using a copper biosensor bacterial strain.

3 illin-resistant Staphylococcus aureus (MRSA) bacterial strain.

4 e glucose tolerant than those fed the parent bacterial strain.

5 erved for HD5(ox) against this Gram-positive bacterial strain.

6 saccharides from leaves inoculated with each bacterial strain.

7 pace and mode of evolution of a new invading bacterial strain.

8 potential probiotics or reliable pathogenic bacterial strains.

9 ificant activity against medically important bacterial strains.

10 romised cells after 24 h of exposure of both bacterial strains.

11 n up in both gram-positive and gram-negative bacterial strains.

12 pplying a MASTERMIND approach using purified bacterial strains.

13 ltrated with different immunity inducers and bacterial strains.

14 fferentiate between commensal and pathogenic bacterial strains.

15 icant nephrotoxicity and polymyxin-resistant bacterial strains.

16 ties against various sensitive and resistant bacterial strains.

17 mosGCTLs facilitate colonization by multiple bacterial strains.

18 sure to radiation had selected for resistant bacterial strains.

19 or clonal expansion of preexisting resistant bacterial strains.

20 exhibit potent inhibition of the enzyme and bacterial strains.

21 control of further resistance development of bacterial strains.

22 inst two Gram-positive and two Gram-negative bacterial strains.

23 ases expressed by other clinically prevalent bacterial strains.

24 vers granzymes into bacteria to kill diverse bacterial strains.

25 ficient platelets do not aggregate to 4 of 5 bacterial strains.

26 y and deposition-transport behavior of these bacterial strains.

27 ives that are equally potent against several bacterial strains.

28 ial physiology and for the classification of bacterial strains.

29 ched live bacteria for three different model bacterial strains.

30 Escherichia coli and Salmonella typhimurium) bacterial strains.

31 tinguish between F'-positive and F'-negative bacterial strains.

32 lined because of the appearance of resistant bacterial strains.

33 ombination with 7 other commensal intestinal bacterial strains.

34 f aqueous green tea leaf extract on selected bacterial strains.

35 ity for Mtb over a panel of other pathogenic bacterial strains.

36 interaction network of coexisting phages and bacterial strains.

37 xonomically related and/or distantly related bacterial strains.

38 antimicrobial-resistant versus -susceptible bacterial strains.

39 al activity, in particular for gram-positive bacterial strains.

40 found to be present in at least 70 different bacterial strains.

41 ferring resistance to previously susceptible bacterial strains.

42 mize the development of antibiotic-resistant bacterial strains.

43 e effective against a number of UTI-relevant bacterial strains.

44 gainst the spread of antimicrobial resistant bacterial strains.

45 g multilocus sequence typing to characterize bacterial strains.

46 chnologies and tested against drug-resistant bacterial strains.

47 potential for application to all culturable bacterial strains.

48 ilamentous phage using different vectors and bacterial strains.

49 eased antibiotics were potent against tested bacterial strains.

50 The recently isolated bacterial strain 80/3 represents one of the most abundan

51 f a cell-based biosensor (CBB) panel of pure bacterial strains, a fluorescent dye, and partial least

52 ifferent experimental conditions, models and bacterial strains according to their metabolic response

53 So we isolate a novel marine bacterial strain Achromobacter xylosoxidans from the shr

54 20-400 nm) on the lipids and proteins of two bacterial strains ( Acinetobacter sp. strain PT5I1.2G an

55 A taxonomically unique bacterial strain, Acinetobacter sp. A47, has been recove

56 nverting CO2 into biosuccinic acid using the bacterial strain Actinobacillus succinogenes 130 Z, and

57 TICR) MS to discriminate clinically relevant bacterial strains after species identification performed

58 nimum inhibitory concentrations of reference bacterial strains against common antibiotics and categor

59 Newly isolated Enterococci faecalis bacterial strains AIM06 (DSM100702) and SR14 (DSM100701)

60 The isolated bacterial strains all showed far better growth on buffer

61 atabolic operon in Acinetobacter and related bacterial strains, allowing utilization of hydroxycinnam

62 ic condition were very different because the bacterial strain alone degraded phenanthrene with sigmoi

63 utant of this regulatory gene in the nonfood bacterial strain altered its secondary metabolite profil

64 method for discrimination of highly adaptive bacterial strains among the populations present in a giv

65 iotics to establish growth profiles for each bacterial strain and monitor the influence of the antibi

66 ing capable of differentiating Gram-negative bacterial strain and species, for many important applica

67 ne the genome and methylome of an individual bacterial strain and use this information to define the

68 al Collection (miBC), a public repository of bacterial strains and associated genomes from the mouse

69 highly conserved in phylogenetically diverse bacterial strains and contains an unusual hybrid polyket

70 mation and failure behavior for two separate bacterial strains and develop a simplified but nonlinear

71 framework for studies of the inheritance of bacterial strains and discuss the advantages and disadva

72 th a defined consortium of human-gut-derived bacterial strains and fed different combinations of 34 f

73 el simulates the growth of a large number of bacterial strains and incorporates variation in microbio

74 ane integrity, and ultrastructure of various bacterial strains and Leishmania species.

75 Lead fragments were also cocultured with the bacterial strains and RAW M.

76 F, and has been shown to accurately identify bacterial strains and species.

77 e increasing numbers of antibiotic-resistant bacterial strains and the limited success of currently a

78 Communication between different bacterial strains and with the environment is achieved v

79 ed with diverse microbes, including numerous bacterial strains and yeasts, but not viral pathogens.

80 ociated with the emergence of new pathogenic bacterial strains and/or serotypes, there is a dearth of

81 CDI toxin delivery and activity to the same bacterial strain, and that CDI system proteins can media

82 udied their bacteriostatic effect on several bacterial strains, and examined their conformational cha

83 onfirmed using lipid extracts from reference bacterial strains, and sample preparation was optimized

84 amental studies of microorganisms, screening bacterial strains, and toxicity detection in water.

85 s due to clonal expansion of highly virulent bacterial strains are clear and present threats to human

86 Clonally arrayed sequenced collections of bacterial strains are constructed from representative do

87 Worldwide, multiresistant bacterial strains are emerging at unprecedented rates.

88 sively drug-resistant, and pandrug-resistant bacterial strains are now frequently encountered.

89 es in the battle against multidrug-resistant bacterial strains are urgently needed, and one obvious a

90 We screened a panel of 41 bacterial strains as a platform to determine how differe

91 rowth that is induced by a wide diversity of bacterial strains as well as by the entire 185-member co

92 es selective detection of LPS from different bacterial strains as well as LPS on the membrane of livi

93 cability for the discrimination of different bacterial strains, as achieved with typing based on gene

94 ling to isolate and maintain the majority of bacterial strains, as mimicking their native environment

95 all known antibiotics is isolated from these bacterial strains, as well as a variety of other drugs s

96 ycan immunogenicity and the pathogenicity of bacterial strains, as well as investigate glycan-mediate

97 sure of live cells from mesophilic yeast and bacterial strains, as well as the piezophilic archaeon A

98 n screens for C. elegans responses to single bacterial strains associated with nematodes in fruit, we

99 hat allow simultaneous detection of multiple bacterial strains at multiple spatial scales.

100 Four model bacterial strains bearing various classes of beta-lactam

101 However, two native seed-associated bacterial strains belonging to Stenotrophomonas rhizophi

102 B-Glc-Ent probe is sensitive not only to the bacterial strain but also to the iron condition in the e

103 bacterial sensors (inducible or constitutive bacterial strains) but with a different conservation mod

104 unbiased view of structural variation of gut bacterial strains by measuring them in their natural hab

105 We and others have shown that bacterial strains can also express HDC and secrete hista

106 A) showed that three different Gram-negative bacterial strains can be clearly differentiated.

107 udy shows how competition between coevolving bacterial strains can generate antibiotic resistance and

108 effective as a number of standard laboratory bacterial strains can serve as sources for SLiCE extract

109 minobacter sp. MSH1 and ASI1, the only known bacterial strains capable of mineralizing BAM-was large,

110 Furthermore, identification of the bacterial strains capable of suppressing sensory neuron

111 Bacterial strains carrying nonsense suppressor tRNA gene

112 More and more multi-drug-resistant bacterial strains cause life-threatening infections and

113 labeling of marker proteins derived from two bacterial strains cocultured in media supplemented with

114 cultured isolates, was used to characterize bacterial strain composition in the fecal microbiota of

115 We here demonstrate for eight bacterial strains comprising four species, that bacteria

116 e were able to study the behavior of LacI in bacterial strains containing the natural copy numbers (

117 Moreover, we found that lead exposed bacterial strains could be successfully discriminated fr

118 Hundreds of diverse bacterial strains cultured from such rotting fruit allow

119 n fed a Bangladeshi diet were colonized with bacterial strains cultured from the duodenal aspirates.

120 ed young germ-free mice with a consortium of bacterial strains cultured from the fecal microbiota of

121 g samples of human liver with metastases and bacterial strains, cultured on solid medium, belonging t

122 d with 54 phylogenetically diverse human gut bacterial strains, defined sugar-rich diets containing w

123 We find that evolution of focal bacterial strains depends on properties both of the foca

124 mutated 5S rRNA with 23S rRNA we generated a bacterial strain devoid of free 5S rRNA.

125 tial, and tracked them over time to evaluate bacterial strain dispersal among infants.

126 This bacterial strain displays potent antimicrobial activitie

127 Studying how bacterial strains diverge over space and time and how di

128 Metagenomic inferences of bacterial strain diversity and infectious disease transm

129 bendazole (TBZ) at 100 mug L(-1)) and two AR bacterial strains (E. coli and E. faecalis, at 10(5) CFU

130 on strategy that relies on co-culture of two bacterial strains, each expressing a half-antibody.

131 Pathogenic bacterial strains emerge largely due to transfer of viru

132 established in recent years, with particular bacterial strains emerging as potential therapeutics rat

133 Administration of bacterial strains engineered to express the TMP epitope

134 e door to develop an array of methanotrophic bacterial strain-engineering strategies currently employ

135 to assay cellobiohydrolase activity on model bacterial strains (Escherichia coli and Bacillus subtili

136 In experiments on the same bacterial strain exposed to ampicillin, frequency noise

137 uce 12,13-diHOME, and treatment of mice with bacterial strains expressing 3EH caused a decrease in th

138 Dehalococcoides mccartyi (Dhc) bacterial strains expressing active reductive dehalogena

139 cy against resistant clinical and laboratory bacterial strains expressing carbapenemases while showin

140 growing threat posed by antibiotic-resistant bacterial strains, extensive research is currently focus

141 Methods to select bacterial strains for drug discovery have historically b

142 on efficiency, and it is not uncommon that a bacterial strain forms functional (Fix(+)) nodules on on

143 We isolated a novel bacterial strain from a prokaryotic consortium associate

144 roducts, current changes are specific to the bacterial strain from which the PCR fragment is produced

145 germ-free mice were colonized with cultured bacterial strains from a 6-mo-old stunted infant and fed

146 characterization and genome sequencing of 79 bacterial strains from all major taxonomic clades of the

147 In this work we isolated 201 bacterial strains from fifteen samples belonging to seve

148 using LC-MS/MS and identified TTX-producing bacterial strains from four genera, including Aeromonas,

149 Here we isolate a consortium of 11 bacterial strains from healthy human donor faeces that i

150 led to increased isolation of drug resistant bacterial strains from respiratory samples.

151 harboring a consortium of sequenced cultured bacterial strains from the Bangladeshi donor's microbiot

152 lex medical treatments can deplete commensal bacterial strains from the intestinal microbiota, thereb

153 ignals controlling swarming, we isolated two bacterial strains from the same red seaweed, Vibrio algi

154 (3)) precipitation (MICP) in three ureolytic bacterial strains from the Sporosarcina family, includin

155 ring and whole-genome sequencing of over 800 bacterial strains from these babies identified virulence

156 The emergence of multi-drug-resistant bacterial strains further complicates patient treatment.

157 Wolfe-Simon et al. reported that the bacterial strain GFAJ-1 can grow by using arsenic (As) i

158 Wolfe-Simon et al. reported that bacterial strain GFAJ-1 can substitute arsenic for phosp

159 t study described the isolation of a special bacterial strain, GFAJ-1, that could grow in medium cont

160 tion of neonatal airways with the pathogenic bacterial strains Haemophilus influenzae, Moraxella cata

161 pact on clinical outcomes and variation with bacterial strain has rarely been explored using integrat

162 Unfortunately, the development of resistant bacterial strains has compromised the effectiveness of m

163 complex of multidrug-resistant Gram-positive bacterial strains, has proven especially problematic in

164 Many heavy metal resistant bacterial strains have a high biosorption capacity and t

165 PS identified 363 and 146 bacterial strains in CM and H milk samples respectively,

166 and evaluated in several clinically relevant bacterial strains in cultures and in living mice.

167 Administration of bacterial strains in drinking water was used, respective

168 ethods for predicting resistance profiles of bacterial strains in hospital microbiology and public he

169 e detection and discrimination of the tested bacterial strains in less than 10 h from an initial bact

170 Identifying bacterial strains in metagenome and microbiome samples u

171 The levels of bacterial strains in microbiota recovered from duodenal

172 periments were conducted with selected fecal bacterial strains in pure culture.

173 in this study, with genes common among other bacterial strains in the gut microbiome.

174 eficiency to an enrichment of H2O2-producing bacterial strains in the gut.

175 AIT cells are activated by a wide variety of bacterial strains in vitro, but their role in defense ag

176 clear antimicrobial activity against several bacterial strains in vitro.

177 a variety of gram-positive and gram-negative bacterial strains in vitro.

178 es demonstrating the attenuated virulence of bacterial strains in which modified carbohydrate biosynt

179 zolid-resistant MRSA and other Gram-positive bacterial strains, in vivo efficacy in a mouse model of

180 th a detection limit of 10(2)CFU/mL for four bacterial strains including Escherichia coli (E. coli),

181 at show improved whole cell activity against bacterial strains including methicillin-resistant Staphy

182 olium and imidazole-derived PDA with various bacterial strains including MRSA (methicillin-resistant

183 ctivity observed against clinically relevant bacterial strains including MRSA and VRE.

184 inhibition phenotype, whereas transfer of 11 bacterial strains, including B. rodentium, enriched in R

185 This method was tested on four bacterial strains, including both Gram-negative and Gram

186 ated against Gram-positive and Gram-negative bacterial strains, including drug-resistant pathogens, r

187 effectively killed a panel of representative bacterial strains, including multidrug-resistant hospita

188 Most bacterial strains, including those extracted from cecal

189 Certain bacterial strains increased viral co-infection of mammal

190 hylogenetically diverse, sequenced human gut bacterial strains introduced into adult gnotobiotic mice

191 lism by human gut microbiota and to identify bacterial strains involved.

192 encing of pooled samples of large numbers of bacterial strains is a robust, rapid and cost-efficient

193 ividuality, so identification of conspecific bacterial strains is imperative for improved understandi

194 rr) /J mice albeit the damage caused by both bacterial strains is more severe in these transgenic mic

195 and selection of highly antibiotic-resistant bacterial strains is of major concern, the clinical rele

196 artificial mineralization of a polyresistant bacterial strain isolated from an acidic, oligotrophic l

197 The ability of Bacillus sp. 3B6, a bacterial strain isolated from cloudwaters, to biotransf

198 xtent of mutually positive interaction among bacterial strains isolated from a common aquatic environ

199 A quarter of bacterial strains isolated from saltmarsh sediment produ

200 present a detailed polyphasic analysis of 10 bacterial strains isolated from three coastal lichens Li

201 osystem Therapeutic (MET-1) consisting of 33 bacterial strains, isolated from human stool and previou

202 Transient pauses were previously observed in bacterial strains lacking CheY, and these events could n

203 ype mast cells fail to inhibit the growth of bacterial strains lacking CSP-1.

204 of 30S assembly intermediates purified from bacterial strains lacking particular maturation factors.

205 A screen of bacterial strains led to the discovery of a two-componen

206 ion of 16S rRNA analytes of three pathogenic bacterial strains: Legionella pneumophila, Pseudomonas a

207 even a few genes between otherwise identical bacterial strains may result in critical phenotypic diff

208 Genome-scale models (GEMs) of bacterial strains' metabolism have been formulated and u

209 we describe the mechanism by which a single bacterial strain, Methylocella silvestris, can use metha

210 In reference and wild bacterial strains, minimal inhibitory concentrations (MI

211 antibiotic resistance in clinically relevant bacterial strains necessitates the development and refin

212 his study, we exposed the CBB panel of seven bacterial strains (nitrifying and non-nitrifying) to 28

213 s revealed several HCM-like enzymes in other bacterial strains not related to MTBE degradation, indic

214 The pattern of fitness of bacterial strains observed across the different coloniza

215 hat proliferation of a series of recombinant bacterial strains occurred over the past few decades.

216 n-vitro CAP detection is performed using the bacterial strain of Haemophilus influenza.

217 n be adapted for specific detection of other bacterial strains of either the same or different specie

218 better understand capabilities of different bacterial strains on peptide decomposition, four Gammapr

219 ever, current strategies require specialised bacterial strains or laborious protocols.

220 the bacterial test strains from either other bacterial strains or plants (in our laboratory we use ei

221 ombination among 55 metabolisms of different bacterial strains or species, and show that their novel

222 n applied to differentiate amongst different bacterial strains or the same strain under different gro

223 ific biological entities, such as particular bacterial strains or viruses, remains a largely unsolved

224 e than 10000 single-cell Raman spectra of 34 bacterial strains out of 13 different species was built

225 The secreted pyocyanin levels from two bacterial strains, PA11 and PA14, were measured to have

226 ith an increased antibiotic activity against bacterial strains possessing high level vancomycin resis

227 ion, neither patients' CD4(+) cell count nor bacterial strain properties necessarily predicted the cl

228 e to the type III secretion system-deficient bacterial strain Pseudomonas syringae pv tomato (Pst) DC

229 antify DC field effects on the deposition of bacterial strains Pseudomonas putida KT2440 and Pseudomo

230 This study reports the characterization of a bacterial strain, Pseudomonas veronii JW3-6, which was i

231 haracterized gram-positive and gram-negative bacterial strains published by ARLG investigators.

232 The engineered bacterial strain, referred to as SYNB1891, targets STING

233 reen tea have been studied, its role against bacterial strains related to skin infections and mechani

234 components mapping to 906 T6SSs found in 498 bacterial strains representing 240 species, as well as a

235 Most current clinical methods that identify bacterial strains require time-consuming culture of the

236 The increase in the number of bacterial strains resistant to known antibiotics is alar

237 The rapid emergence of bacterial strains resistant to multiple antibiotics is p

238 ble to tackle the continuous outbreak of new bacterial strains resistant to traditional antibiotics.

239 me, direct tracking of a single plasmid in a bacterial strain responsible for an outbreak is possible

240 Mining the microbiota for bacterial strains responsible for shaping the structure

241 Whole genome analysis of this bacterial strain revealed the presence of an N-acyl homo

242 rial genomes, but only one non-Agrobacterium bacterial strain, Rhizobium etli CFN42, harbors a comple

243 Here, we show that the bacterial strain Rhodococcus jostii RHA1 can biotransfor

244 Bacterial strains Rhodococcus rhodochrous EP4 and Rhodoc

245 ere able to inhibit the antibiotic resistant bacterial strains (Salmonell typhii, Staphylococcus areu

246 growth inhibition assay with three different bacterial strains showed significant activity of several

247 We isolated and identified 101 distinct bacterial strains spanning 6 phyla including (1) novel s

248 icate that DOM effects on Hg methylation are bacterial strain specific, depend on the DOM:Hg ratio or

249 eumolysin contributes to cardiac damage in a bacterial strain-specific manner, and pneumolysin kills

250 s enantiomers of alpha-HCH using two aerobic bacterial strains: Sphingobium indicum strain B90A and S

251 his bubble-driven detachment process for the bacterial strain Staphylococcus aureus.

252 One bacterial strain (Streptomyces sp. CLI2509) from the bra

253 ylase LigM from Sphingomonas paucimobilis, a bacterial strain that metabolizes lignin-derived aromati

254 herichia coli and Enterococcus faecalis, two bacterial strains that are commonly encountered in urina

255 poultry microbiota was assembled, including bacterial strains that are not typically retrieved from

256 might someday be able to mine for intestinal bacterial strains that can be used in the diagnosis or t

257 ndation for the selection of seed indigenous bacterial strains that could limit seed transmission of

258 However, the bacterial strains that drive gut IgA production remain l

259 Importantly, bacterial strains that induced viral co-infection facili

260 dwide, is infection with Helicobacter pylori bacterial strains that inject cytotoxin-associated gene

261 Bacterial strains that lacked the O Ag or failed to repl

262 Here, we report stable, engineered bacterial strains that maintain their function for 6 mon

263 Collectively, this screen identifies bacterial strains that may use ZPSs to interact with the

264 lysins were able to lyse only Gram-positive bacterial strains that possess PG with D-Ala(4)-->D-Asx-

265 Of the bacterial strains that were obtained from the children,

266 roperties and charge environment of two live bacterial strains: the Gram-negative Escherichia coli an

267 ut they restrain the virulence of pathogenic bacterial strains, thereby preventing infections caused

268 mice across a range of conditions (mouse and bacterial strain, time post infection) and was validated

269 r of cumulative recoding changes in a single bacterial strain to date.

270 Preadaptation of bacterial strains to fucose alleviated growth hindrance

271 onses can be exploited to construct reporter bacterial strains to probe the temporal and spatial envi

272 WGS (n = 206) revealed diverse bacterial strain type (STs).

273 icrobial engineering applications, including bacterial strain typing, immunization of cultures, autoi

274 alse-negative results were observed among 90 bacterial strains used to evaluate assay specificity.

275 quencing now brings finer resolution to both bacterial strain variation and the host genetic state th

276 Bacterial strains vary in their colonization efficiency

277 ransformation of chloroanilines by these two bacterial strains via dissimilar dehalogenation pathways

278 e pathogen detection, a mixture of all three bacterial strains was isolated and identified within the

279 In contrast, the representative bacterial strains we studied were able to acquire iron f

280 o neutrally competing, fluorescently labeled bacterial strains, we observe stochastically driven bimo

281 Using 24 model compounds and 4 different bacterial strains, we optimized the screening technology

282 neither all humans nor mice harbor the same bacterial strains, we posited that more prevalent factor

283 ontained much higher SCFA levels and related bacterial strains, we selected 4 SCFA-producers (Bifidob

284 Using seven bacterial strains, we show that SMALR yields significant

285 Bacterial strains were isolated from fecal samples.

286 E. coli when present together with competing bacterial strains which are known to have similar shape.

287 to C. burnetii NMII infection and that this bacterial strain, which activates the immune deficiency

288 istical model was validated with independent bacterial strains, which were grown in ascitic fluid.

289 Moreover, a mixture of 20 bacterial strains, which were selected and isolated from

290 The particles were tested with several bacterial strains, while biocompatibility was verified w

291 antibacterial activity against Gram positive bacterial strains, while their evaluation against wild-t

292 fficient microbial inhibition against tested bacterial strains, whilst high local rigidity of peptide

293 of cell-surface interaction forces for seven bacterial strains with a wide range of cell morphology,

294 otein in order to survive, we have generated bacterial strains with enhanced periplasmic folding capa

295 f Pi is crucial in stimulating the growth of bacterial strains with high RNA contents and thus faster

296 Bacterial strains with industrial and therapeutic releva

297 The use of bacterial strains with regulated uppS expression and inh

298 thus identified endogenous anti-tumourigenic bacterial strains with strong diagnostic, therapeutic an

299 o low density mock communities of 11 diverse bacterial strains (with and without human DNA supplement

300 t show any bacterial capture for these other bacterial strains within a 15 min incubation period.