ライフサイエンスコーパス: Salmonella typhimurium

1 serovar causing this disease is Typhimurium (Salmonella Typhimurium).

2 enterica serovar Typhimurium (also known as Salmonella typhimurium).

3 hia coli O157:H7, Pseudomonas aeruginosa and Salmonella typhimurium.

4 ptional regulation through sensing Mn(2+) in Salmonella typhimurium.

5 tion with herpes simplex virus-1 (HSV-1) and Salmonella typhimurium.

6 to increased susceptibility to infection by Salmonella typhimurium.

7 eome of the Gram-negative bacterial pathogen Salmonella Typhimurium.

8 wnregulated following infection of mice with Salmonella typhimurium.

9 istance to infection by the enteric pathogen Salmonella typhimurium.

10 s O-antigens from Salmonella Choleraesuis in Salmonella Typhimurium.

11 ate that 30 proteins are exported via Tat in Salmonella Typhimurium.

12 Salmonella genus: Salmonella enteritidis and Salmonella typhimurium.

13 n acquisition by the intracellular bacterium Salmonella typhimurium.

14 es their susceptibility to pathogens such as Salmonella typhimurium.

15 olog and ncRNA also associate with PNPase in Salmonella Typhimurium.

16 e housed in SPF conditions by infection with Salmonella typhimurium.

17 mensals and the invasive intestinal pathogen Salmonella Typhimurium.

18 ory ligand, rRL-6-CH2OH, previously found in Salmonella typhimurium.

19 d growth rate in the Gram-negative bacterium Salmonella typhimurium.

20 l specificity of Zur, ZntR, RcnR and FrmR in Salmonella Typhimurium.

21 ation of AI-2-based QS in Vibrio harveyi and Salmonella typhimurium.

22 nternalization of the Gram-negative pathogen Salmonella typhimurium.

23 hout orthologs in either Escherichia coli or Salmonella typhimurium.

24 macrophages with the intracellular pathogen Salmonella typhimurium.

25 se activity of AvrA, the YopJ homologue from Salmonella typhimurium.

26 SipC and accumulate at sites of invasion by Salmonella typhimurium.

27 e detection of type III protein secretion in Salmonella typhimurium.

28 NLRC4 both activate caspase-1 in response to Salmonella typhimurium.

29 for DNA condensation in Escherichia coli and Salmonella typhimurium.

30 nteric bacteria and had no known function in Salmonella Typhimurium.

31 n polymyxin-resistant strains of E. coli and Salmonella typhimurium.

32 n death after intraperitoneal inoculation of Salmonella typhimurium.

33 TD-(SH)(2)] and oxidized (NTD-S(2)) NTD from Salmonella typhimurium.

34 tivates transcription of the SlyA regulon in Salmonella typhimurium.

35 lla pneumophila, Pseudomonas aeruginosa, and Salmonella typhimurium.

36 been identified in both Escherichia coli and Salmonella typhimurium.

37 of the homologues from Escherichia coli and Salmonella typhimurium.

38 Here, we extend this concept to Salmonella typhimurium.

39 timicrobial peptides in Escherichia coli and Salmonella typhimurium.

40 xpression, including in the enteric pathogen Salmonella typhimurium.

41 pecially against the drug-resistant bacteria Salmonella typhimurium.

42 s biplex immunoassay of Escherichia coli and Salmonella typhimurium.

43 mmunomagnetic separation (IMS) for detecting Salmonella typhimurium.

44 osensor to know the concentration of serovar Salmonella typhimurium.

45 actamase-producing Klebsiella pneumoniae and Salmonella typhimurium.

46 acterial pathogens, Francisella novicida and Salmonella typhimurium.

47 Salmonella Enteritidis and 152 (43.3%) were Salmonella Typhimurium.

48 also shifted from Salmonella Enteritidis to Salmonella Typhimurium.

49 related AB5 toxin encoded by the broad-host Salmonella Typhimurium (15) .

50 tivity for other foodborne pathogens such as Salmonella Typhimurium, (7%) Listeria monocytogenes (3%)

51 er) were isolated at higher frequencies than Salmonella Typhimurium, a common cause of human illness.

52 After infection with Salmonella typhimurium, a Gram-negative bacterium that e

53 NMR structure of the PrgI needle protein of Salmonella typhimurium, a human pathogen associated with

54 e have discovered additional SgrS targets in Salmonella Typhimurium, a pathogen related to E. coli th

55 e rapidly succumb to systemic infection with Salmonella Typhimurium, a pathogenic bacterium that mult

56 Here we show that Salmonella Typhimurium activates the plant immune system

57 ncing in goblet cells increased or decreased Salmonella typhimurium adherence, respectively.

58 Salmonella typhimurium AhpC is a founding member of the

59 Here, we present such studies focusing on Salmonella typhimurium alkyl hydroperoxide reductase C c

60 tion system effector protein from broad-host Salmonella Typhimurium allowed Salmonella Typhi to survi

61 tive bacterial cancer therapy by engineering Salmonella typhimurium amino acid auxotrophs which grow

62 139 times (6.1%), of which 8017 (79.1%) were Salmonella Typhimurium and 1608 (15.8%) were Salmonella

63 A majority (88/114 [77%]) of Salmonella Typhimurium and 30% (24/79) of Salmonella Ent

64 icrocystin LR and 10(0) and 10(1) cfu/mL for Salmonella typhimurium and Cronobacter sakazakii respect

65 as induced using 2 established mouse models (Salmonella typhimurium and dextran sodium sulfate) in PH

66 hesion, the type 1 fimbrial FimH adhesins of Salmonella Typhimurium and Escherichia coli share only 1

67 rs resistance to the antibiotic polymyxin in Salmonella typhimurium and Escherichia coli through the

68 In Salmonella typhimurium and Escherichia coli, the virulen

69 bacterial pathogens Listeria monocytogenes, Salmonella typhimurium and Escherichia coli.

70 ta and IL-18 in response to NLRC4 activators Salmonella Typhimurium and flagellin, canonical or non-c

71 Although Salmonella typhimurium and Legionella pneumophila normal

72 nd TLR5 ligands and the intestinal pathogens Salmonella typhimurium and Listeria monocytogenes to ind

73 in-resistant Staphylococcus aureus (MRSA) or Salmonella typhimurium and perish shortly after epicutan

74 Salmonella Typhimurium and Salmonella Enteritidis repres

75 ducted by testing Shigella, Salmonella spp., Salmonella typhimurium and Staphylococcus aureus on E. c

76 c4 phosphorylation by cytosolic flagellin of Salmonella Typhimurium and Yersinia enterocolitica.

77 genetically modified nonhalotolerant cells (Salmonella typhimurium) and dead vs. live differentiatio

78 ed in bottled water extracts using bacteria (Salmonella typhimurium) and human cell lines (HepG2 and

79 the flagellum acts as a 'wetness' sensor in Salmonella typhimurium, and as a mechanosensor in other

80 ative in vitro bioassays for mutagenicity in Salmonella typhimurium, and chronic cytotoxicity and acu

81 for the discrimination of Escherichia coli, Salmonella typhimurium, and Clostridium difficile genome

82 Roseburia intestinalis, Ruminococcus obeum, Salmonella typhimurium, and Clostridium difficile) to qu

83 pathogenic Escherichia coli (EHEC and UPEC), Salmonella typhimurium, and Francisella tularensis.

84 am-negative food-borne pathogens, especially Salmonella typhimurium, and it was, therefore, selected

85 eloped for the detection of E. coli O157:H7, Salmonella Typhimurium, and L. monocytogenes in food sam

86 tested pathogens (Escherichia coli O157:H7, Salmonella typhimurium, and Listeria monocytogenes) in b

87 Three bacterial pathogens (Escherichia coli, Salmonella typhimurium, and methicillin-resistant Staphy

88 ts, including latex beads, Escherichia coli, Salmonella typhimurium, and Mycobacterium tuberculosis i

89 ing Escherichia coli, Citrobacter rodentium, Salmonella typhimurium, and Shigella flexneri are sensed

90 eously detect viable Legionella pneumophila, Salmonella typhimurium, and Staphylococcus aureus in one

91 multiplex detection of model food pathogens, Salmonella typhimurium, and Staphylococcus aureus, in wh

92 d with anti-Escherichia coli O157:H7 or anti-Salmonella typhimurium antibodies that can specifically

93 s, and transcripts from Dickeya dadantii and Salmonella typhimurium are cleaved by RNase III when exp

94 Outer membrane vesicles (OMVs) isolated from Salmonella Typhimurium are potentially useful for develo

95 eneration in ethanolamine ammonia-lyase from Salmonella typhimurium at 234-248 K in a dimethylsulfoxi

96 tive also against the Gram negative bacteria Salmonella typhimurium ATCC 13311.

97 da KT2440, Enterococcus faecalis ATCC 29212, Salmonella Typhimurium ATCC 14028, and Escherichia coli

98 acterial species, Pseudomonas putida KT2440, Salmonella Typhimurium ATCC 14028, Staphylococcus epider

99 and two Gram negative (Escherichia coli and Salmonella typhimurium) bacterial strains.

100 -functional viral nanocontainer based on the Salmonella typhimurium bacteriophage P22 capsid, genetic

101 tremely susceptible to systemic infection by Salmonella Typhimurium because of loss-of-function mutat

102 and structural characterization of NirC from Salmonella typhimurium by lipid bilayer electrophysiolog

103 phils during infection with the gut pathogen Salmonella Typhimurium, calprotectin-mediated metal sequ

104 Nonvirulent, tumor-tropic bacteria, such as Salmonella typhimurium, can unmask a tumor by transformi

105 Cobyric acid synthetase (CbiP) from Salmonella typhimurium catalyzes the glutamine and ATP-d

106 Salmonella typhimurium causes a localized enteric infect

107 Salmonella Typhimurium causes a self-limiting gastroente

108 lmonella enterica serovar Typhimurium 12023 (Salmonella typhimurium) causes acute, fatal bacteremia w

109 and Salmonella enterica serovar Typhimurium (Salmonella typhimurium), cell lines expressing S100A8 in

110 The water samples were spiked with standard Salmonella typhimurium cells, and detection was done by

111 The library was expressed in Salmonella typhimurium, clones with increased resistance

112 Salmonella Typhimurium combats phagocytic superoxide by

113 ible to the intracellular bacterial pathogen Salmonella typhimurium, consistent with reduced innate i

114 V. cholerae acfA-phoA reporter strain and a Salmonella typhimurium ctxAp-lacZ reporter strain.

115 luster was introduced into three constructed Salmonella Typhimurium Deltaasd mutants: SLT11 (Deltarfb

116 Ps against the multidrug-resistant bacterium Salmonella typhimurium DT 104.

117 The global epidemic of multidrug-resistant Salmonella Typhimurium DT104 provides an important examp

118 ometry, and inoculated Enterococcus spp. and Salmonella typhimurium during the drying of struvite und

119 The Salmonella typhimurium effector protein SifA regulates t

120 Salmonella typhimurium engineered to deliver cancer/test

121 Expression of BpeGReg in Salmonella typhimurium enhances biofilm formation, while

122 cerevisiae OPRTase is similar to that of the Salmonella typhimurium enzyme, as judged by comparison o

123 t, base pairing-deficient SgrS homologs from Salmonella typhimurium, Erwinia carotovora and Klebsiell

124 domonas fluorescens, Salmonella Enteritidis, Salmonella Typhimurium, Escherichia coli).

125 st a mixture of related pathogens, including Salmonella typhimurium, Escherichia coli, Staphylococcus

126 Salmonella Enteritidis cases have risen and Salmonella Typhimurium fallen.

127 We propose that unlike the Salmonella Typhimurium flagella-TLR5 driven pro-inflamma

128 We find that a Salmonella typhimurium flagellin fragment comprising the

129 The chemoreceptors of Escherichia coli and Salmonella typhimurium form stable oligomers that associ

130 e; Salmonella Enteritidis from 1999 to 2002, Salmonella Typhimurium from 2002 to 2008, and Salmonella

131 re- and posttherapy MDR clinical isolates of Salmonella Typhimurium from a patient that failed antiba

132 Salmonella Typhimurium gene STM2215 (rtn) is conserved a

133 endent ethanolamine ammonia-lyase (EAL) from Salmonella typhimurium has been studied by using time-re

134 , by exploiting the host cellular machinery, Salmonella Typhimurium has evolved the capacity to broad

135 rmore, systemic administration of attenuated Salmonella typhimurium has little or no significant side

136 ate in ethanolamine ammonia-lyase (EAL) from Salmonella typhimurium have been measured by using time-

137 ermediate in ethanolamine ammonia-lyase from Salmonella typhimurium have been measured on timescales

138 endent ethanolamine ammonia-lyase (EAL) from Salmonella typhimurium have been studied by using pulsed

139 endent ethanolamine ammonia-lyase (EAL) from Salmonella typhimurium have been studied on the 10(-7)-1

140 tructures of a small heat shock protein from Salmonella typhimurium in a dimeric form and two higher

141 l matrix of immunoassay for the detection of Salmonella typhimurium in a sandwich ELISA format.

142 of the LysP-related transporter STM2200 from Salmonella typhimurium in Escherichia coli, its purifica

143 autophagy-mediated intracellular survival of Salmonella typhimurium in mammalian cells.

144 tal structure of the PhoQ sensor domain from Salmonella typhimurium in the Ca2+-bound state, which re

145 cterial autophagy induction and clearance of Salmonella typhimurium in the intestinal epithelial cell

146 l immunoassay device was developed to detect Salmonella typhimurium in the naturally occurring liquid

147 Here, we show that the intestinal pathogen Salmonella typhimurium increases its antibiotic toleranc

148 contrast, TLR4 and TRIF were dispensable for Salmonella typhimurium-induced caspase-1 activation.

149 an animal model of sepsis, we observed that Salmonella typhimurium-infected mice exhibited simultane

150 Macrophages respond to Salmonella typhimurium infection by activating caspase 1

151 Salmonella typhimurium infection is reported to activate

152 that severity of disease induced by enteric Salmonella Typhimurium infection is strongly modulated b

153 r genome-wide association study (GWAS) using Salmonella typhimurium infection of human lymphoblastoid

154 de synthase 2 (NOS2) in macrophages and upon Salmonella typhimurium infection of mice was investigate

155 Similarly, Salmonella typhimurium infection of TLR-deficient mice i

156 Here, we show that Salmonella Typhimurium infection was accompanied by dysb

157 During Salmonella Typhimurium infection, intestinal CX3CR1(+) c

158 Here, using a mouse model of systemic Salmonella Typhimurium infection, we determined that inf

159 emporally correlated with the restriction of Salmonella Typhimurium infection.

160 , anthrax lethal toxin, DNA transfection and Salmonella typhimurium infection.

161 on Salmonella enterica Serovar Typhimurium (Salmonella typhimurium) infection in 2 model organisms,

162 Here, we report that an intestinal pathogen, Salmonella Typhimurium, inhibits anorexia by manipulatin

163 e have inserted the D3 domain of FliCi (from Salmonella typhimurium) into the outer domain of EspA an

164 sub-ng/muL standard DNA and 10(1) copies of Salmonella typhimurium InvA gene sequences (cloned in E.

165 Salmonella typhimurium is a major cause of diarrhea and

166 of host cells, in which growth of cytosolic Salmonella Typhimurium is inhibited independently or pri

167 Although infection with wild-type Salmonella typhimurium is lethal to mice, we show here t

168 he tryptophan synthase bienzyme complex from Salmonella typhimurium is regulated by allosteric intera

169 Salmonella typhimurium is responsible for about a third

170 Salmonella Typhimurium isolate D23580 represents a recen

171 on structure of sub-Saharan African invasive Salmonella Typhimurium isolates and compared these to gl

172 y, the vast majority of sub-Saharan invasive Salmonella Typhimurium isolates fell within two closely

173 79.7% of Salmonella Enteritidis and 90.2% of Salmonella Typhimurium isolates) showed multidrug resist

174 Of Salmonella Typhimurium isolates, 42 of 43 were pathovar

175 zithromycin resistance was noted in 12.7% of Salmonella Typhimurium isolates, appearing in Bas-Congo

176 tryptophan synthase alpha2beta2 complex from Salmonella typhimurium led to the determination of the t

177 py by targeting viable tumor tissue by using Salmonella typhimurium leu-arg auxotrophs.

178 sub-Saharan Africa caused by highly related Salmonella Typhimurium lineages that may have occupied n

179 res of the RhamDs from both E. coli K-12 and Salmonella typhimurium LT2 (95% sequence identity) were

180 aracterization on the protein encoded by the Salmonella typhimurium LT2 genome (GI:16766982; STM3697)

181 We recode 200 kb of the Salmonella typhimurium LT2 genome through a process we t

182 urli subunit homologs from Escherichia coli, Salmonella typhimurium LT2, and Citrobacter koseri were

183 show that IIA(Glc) directly binds to MelB of Salmonella typhimurium (MelB(St)) and Escherichia coli M

184 The melibiose permease of Salmonella typhimurium (MelB(St)) catalyzes symport of m

185 The MelB permease of Salmonella typhimurium (MelB-ST) catalyzes the coupled s

186 the three-dimensional crystal structures of Salmonella typhimurium MelBSt in two conformations, repr

187 increasingly constrained solution spaces of Salmonella Typhimurium metabolism during growth in both

188 ng Salmonella Enteritidis (n = 244 [35.5%]), Salmonella Typhimurium (n = 221 [32.2%]), I:4,[5],12:i:-

189 esized to investigate the impact of coupling Salmonella typhimurium O-antigen to different amino acid

190 firmed infection with the outbreak strain of Salmonella Typhimurium occurring between September 1, 20

191 Autophagic capture of Salmonella Typhimurium occurs predominantly via generati

192 ng an E2 phage-coated ME biosensor to detect Salmonella typhimurium on tomato surfaces.

193 The determination of Salmonella typhimurium, on screen-printed carbon electro

194 ptpn6 knockdown embryos were challenged with Salmonella typhimurium or Mycobacterium marinum at earli

195 uring intestinal infection with the pathogen Salmonella Typhimurium or pneumonic infection with Burkh

196 lly bound by IgY from chickens infected with Salmonella Typhimurium or S.

197 Salmonella typhimurium or Toxoplasma gondii were adminis

198 ates with NLRC4 in macrophages infected with Salmonella typhimurium or transfected with flagellin.

199 ens Mycobacterium tuberculosis, M bovis BCG, Salmonella typhimurium, or Toxoplasma gondii release fro

200 ophage P22, a podovirus infecting strains of Salmonella typhimurium, packages a 42-kbp genome using a

201 o be multidrug resistant, whereas a dominant Salmonella Typhimurium pathotype, ST313, was primarily a

202 n (MVC) site of the tryptophan synthase from Salmonella typhimurium plays essential roles in catalysi

203 In culture, Salmonella Typhimurium populations are bistable for the

204 murium isolates and compared these to global Salmonella Typhimurium populations.

205 In this study, we demonstrate that MVs from Salmonella typhimurium potently stimulated professional

206 minths induce IgG1, whereas Th1 Ags, such as Salmonella Typhimurium, predominantly induce IgG2a.

207 merging from the surface of bacteria such as Salmonella typhimurium propel the cells toward nutrient

208 To assess the roles of these residues in the Salmonella typhimurium QAPRTase reaction, they were indi

209 months (OR, 4.8; 95% CI, 1.1-21.1; P = .039).Salmonella Typhimurium represented 106 of 238 (44.5%) se

210 deletion mutants to identify novel genes of Salmonella Typhimurium required for survival during ente

211 d 28cfumL(-1) for Staphylococcus aureus, and Salmonella typhimurium, respectively.

212 The gastrointestinal pathogen, Salmonella Typhimurium, responds to acidic pH and CAMP t

213 infection of draining lymph nodes (DLNs) by Salmonella typhimurium results in the specific downregul

214 by independent exposures to flagellins from Salmonella typhimurium (S. typhimurium) and Bacillus sub

215 The Gram-negative bacterium, Salmonella Typhimurium (S. Typhimurium) is a food borne

216 ing Escherichia coli, Klebsiella pneumoniae, Salmonella typhimurium, S. aureus, and Enterococcus faec

217 rmine the three-dimensional structure of the Salmonella typhimurium Saf pilus.

218 ity, Choi et al. (2013) demonstrate that the Salmonella Typhimurium-secreted protein tyrosine phospha

219 mpD surface antigen extraction was done from Salmonella typhimurium serovars, under the optimized gro

220 mic structure of the flagellar filament from Salmonella typhimurium serves as a model for all bacteri

221 egative bacteria including Escherichia coli, Salmonella typhimurium, Shigella flexneri, and Burkholde

222 Flagellin isolated from the Salmonella Typhimurium SJW1660 strain, which differs by

223 In Salmonella typhimurium, some of these genes are controll

224 ive and sensitive immunosensor for detecting Salmonella typhimurium species.

225 Salmonella Typhimurium specifically targets antigen-samp

226 exemplified by a ubiquitin-binding domain in Salmonella Typhimurium SseL.

227 tegy incorporating delivery of the bacterium Salmonella typhimurium (ST), naturally tropic for the hy

228 nates (irrespective of HIV status), and with Salmonella Typhimurium ST313.

229 The B cell response to Salmonella typhimurium (STm) occurs massively at extrafo

230 Salmonella Typhimurium (STm) remain a prominent cause of

231 The first component is Salmonella typhimurium strain chi8937, with deletions of

232 in the Salmonella mutagenicity assay, using Salmonella typhimurium strain TA98 (with and without met

233 Salmonella typhimurium strain TA98 was used with and wit

234 able co-culture of metabolically competitive Salmonella typhimurium strains in microfluidic devices.

235 against sodium azide induced mutagenicity of Salmonella typhimurium strains TA 98 and TA 1531.

236 tivity of flavonoids, by the Ames test, with Salmonella typhimurium strains TA98, TA100 and TA102.

237 logical containment system using recombinant Salmonella Typhimurium strains that are attenuated yet c

238 nism that co-ordinates the expression of the Salmonella Typhimurium T3SS chaperone SicP and its cogna

239 ere, we show that human NAIP also senses the Salmonella Typhimurium T3SS inner rod protein PrgJ and t

240 revertants per nanomole of amine, log m, in Salmonella typhimurium TA 98 and TA 100 correlates with

241 ine-N-oxide (4-NQO), a direct mutagen toward Salmonella typhimurium TA 98 and TA 100.

242 ine-N-oxide (4-NQO), a direct mutagen toward Salmonella typhimurium TA 98 and TA 100.

243 benzo[a]pyrene, an indirect mutagen, toward Salmonella typhimurium TA 98 and TA 100.

244 ine-N-oxide (4-NQO), a direct mutagen toward Salmonella typhimurium TA 98 and TA 100.

245 exhibited maximum anti-mutagenicity against Salmonella typhimurium TA 98 and TA 1538, respectively a

246 monstrated both DNA adducts in target cells (Salmonella typhimurium TA100 and Chinese hamster V79) of

247 ed oxidant-induced mutagenicity (26%) in the Salmonella typhimurium TA102 strain, as determined by th

248 spectively, 69% and 64.8% in the presence of Salmonella typhimurium TA104, and 79.7% and 68.9% in the

249 showed mutagenic effect by Ames test against Salmonella typhimurium TA98 and TA100 strains.

250 Artocarpus heterophyllus Lam) extract, using Salmonella typhimurium tester strains TA98 and TA100 wit

251 luorescently labeled Escherichia coli HS and Salmonella typhimurium that passed through from the muco

252 bacterial cells (up to approximately 45% for Salmonella typhimurium) that is comparable to the widely

253 bacter aerogenes, Pseudomonas aeruginosa and Salmonella Typhimurium The geranylated residues are loca

254 In Salmonella typhimurium, the external needle is assembled

255 ely studied flagella of Escherichia coli and Salmonella typhimurium, the flagella of Campylobacter je

256 la While we tested for efficacy only against Salmonella Typhimurium, the modified Salmonella strain m

257 inhibitors of QS in both Vibrio harveyi and Salmonella typhimurium, the two organisms with defined A

258 nced cytokine expression during infection by Salmonella typhimurium This occurred in the first 3 d of

259 s citrate and iron from the enteric pathogen Salmonella Typhimurium to arrest growth and ameliorate t

260 n electrophysiological analysis of FocA from Salmonella typhimurium to characterize the channel prope

261 We used Escherichia coli 0157:H7 and Salmonella typhimurium to demonstrate that this design p

262 In order to assess the ability of Salmonella Typhimurium to replicate in human macrophages

263 estigated if the transcriptional response of Salmonella Typhimurium to temperature and acid variation

264 We therefore screened a Salmonella Typhimurium transposon library to identify ba

265 Many intracellular pathogens, including Salmonella typhimurium, trigger autophagy in host cells,

266 nteractions regulate substrate channeling in Salmonella typhimurium tryptophan synthase.

267 onstrate the killing of Escherichia coli and Salmonella typhimurium, two common pathogens, at levels

268 hat the phosphoinositide phosphatase SopB, a Salmonella Typhimurium type III secreted effector protei

269 t a high-resolution in situ structure of the Salmonella Typhimurium type III secretion machine obtain

270 Here we report the engineering of the Salmonella Typhimurium type III secretion system in achr

271 AhpC and AhpF from Salmonella typhimurium undergo a series of electron tran

272 -Dyer lipid extracts of Escherichia coli and Salmonella typhimurium using liquid chromatography/tande

273 The PhoQ sensor kinase is essential for Salmonella typhimurium virulence for animals, and a homo

274 Infection of DR3(-/-) mice with Salmonella typhimurium was associated with defective mic

275 tion from macrophages infected in vitro with Salmonella typhimurium was dependent on caspase 1 and Ip

276 e role of Irgm1 in controlling resistance to Salmonella typhimurium was explored to further define th

277 The bacterial pathogen Salmonella typhimurium was grown aboard Space Shuttle mi

278 Salmonella Typhimurium was infrequent (2.3% pups; 4/175)

279 emonstrated and no significant adsorption of Salmonella typhimurium was observed.

280 In contrast, although Salmonella typhimurium was proposed to induce the presen

281 ediators of PhoPQ-regulated OM remodeling in Salmonella Typhimurium, we identified PbgA, a periplasmi

282 Here, by studying Salmonella Typhimurium, we show that the E3 ligase LUBAC

283 Highly specific DNA aptamers to live Salmonella typhimurium were selected via the cell-system

284 esponses and protection against infection by Salmonella typhimurium were spared.

285 Listeria monocytogenes and Salmonella Typhimurium were used as negative controls.

286 ,6-trinitrobenzene sulfonic acid (TNBS), and Salmonella typhimurium were used to induce colitis in A(

287 intensively studied flagellar filament (from Salmonella typhimurium), which has approximately 5.5 sub

288 Motile Salmonella typhimurium, which are specifically attracted

289 -cell response to the intracellular pathogen Salmonella typhimurium, which can disrupt metabolism by

290 he bistable expression of virulence genes in Salmonella typhimurium, which leads to phenotypically vi

291 primarily been studied Escherichia coli and Salmonella typhimurium, which possess a single CheR invo

292 Comparative genomics of Salmonella Typhimurium will provide insight into factors

293 eement with available experimental data from Salmonella typhimurium with only a single free parameter

294 ies of ethanolamine ammonia-lyase (EAL) from Salmonella typhimurium with site-directed mutations in a

295 ich allowed a direct label-free detection of Salmonella Typhimurium with the limit of detection (LOD)

296 chnique was used to capture a food pathogen, Salmonella typhimurium, with starting concentrations as

297 Two isozymes are found in Salmonella typhimurium, with the A-isozyme expressed und

298 Survival of Salmonella typhimurium within a vacuole in host cells de

299 We show that the PilZ domain proteins of Salmonella Typhimurium, YcgR and BcsA, demonstrate a 43-

300 erived AMT databases (Shewanella oneidensis, Salmonella typhimurium, Yersinia pestis) for training an