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 idis than with another nontyphoidal serovar, Salmonella Typhimurium.

4 NOX2 collapses the DeltapH of intracellular Salmonella Typhimurium.

5 s biplex immunoassay of Escherichia coli and Salmonella typhimurium.

6 osensor to know the concentration of serovar Salmonella typhimurium.

7 actamase-producing Klebsiella pneumoniae and Salmonella typhimurium.

8 acterial pathogens, Francisella novicida and Salmonella typhimurium.

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

10 also shifted from Salmonella Enteritidis to Salmonella Typhimurium.

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

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

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

14 to increased susceptibility to infection by Salmonella typhimurium.

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

16 wnregulated following infection of mice with Salmonella typhimurium.

17 istance to infection by the enteric pathogen Salmonella typhimurium.

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

19 Salmonella genus: Salmonella enteritidis and Salmonella typhimurium.

20 n acquisition by the intracellular bacterium Salmonella typhimurium.

21 es their susceptibility to pathogens such as Salmonella typhimurium.

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

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

24 mensals and the invasive intestinal pathogen Salmonella Typhimurium.

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

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

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

28 nternalization of the Gram-negative pathogen Salmonella typhimurium.

29 hout orthologs in either Escherichia coli or Salmonella typhimurium.

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

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

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

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

34 for DNA condensation in Escherichia coli and Salmonella typhimurium.

35 eome of human HEK293 cells and the bacterium Salmonella Typhimurium.

36 contain the Na(+)/H(+) antiporter NhaA from Salmonella Typhimurium.

37 infections of mice with influenza virus and Salmonella typhimurium.

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

39 mmunomagnetic separation (IMS) for detecting Salmonella typhimurium.

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

41 macrophages with the intracellular pathogen Salmonella typhimurium.

42 lla pneumophila, Pseudomonas aeruginosa, and Salmonella typhimurium.

43 xpression, including in the enteric pathogen Salmonella typhimurium.

44 pecially against the drug-resistant bacteria Salmonella typhimurium.

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

46 These consisted of 85 Salmonella Typhimurium, 58 Salmonella Enteritidis, 32 ot

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

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

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

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

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

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

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

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

55 139 times (6.1%), of which 8017 (79.1%) were Salmonella Typhimurium and 1608 (15.8%) were Salmonella

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

57 ing with the treatment of mice infected with Salmonella typhimurium and affording preliminary promisi

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

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

60 In Salmonella typhimurium and Escherichia coli, the virulen

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

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

63 Salmonella Typhimurium and its monophasic variant S.

64 cluding multidrug resistant (MDR) strains of Salmonella Typhimurium and Klebsiella pneumoniae.

65 Although Salmonella typhimurium and Legionella pneumophila normal

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

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

68 ass II effector TMD-chaperone complexes from Salmonella Typhimurium and Pseudomonas aeruginosa, respe

69 Salmonella Typhimurium and Salmonella Enteritidis repres

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

71 ies and their antimicrobial activity against Salmonella Typhimurium and Staphylococcus aureus.

72 nosensor were investigated with detection of Salmonella Typhimurium and Staphylococcus aureus.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

89 Salmonella Enteritidis and Salmonella Typhimurium are major causes of bloodstream i

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

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

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

93 ntal work with Serratia marcescens in water, Salmonella Typhimurium ATCC 14028 was inoculated in wate

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

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

96 digmatic organisms such as Escherichia coli, Salmonella typhimurium, Bacillus subtilis and Saccharomy

97 serum from pediatric patients with invasive Salmonella Typhimurium bacteremia (n = 7) and those with

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

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

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

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

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

103 Salmonella Typhimurium can invade and survive within mac

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

105 Salmonella Typhimurium causes a self-limiting gastroente

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

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

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

109 Salmonella Typhimurium combats phagocytic superoxide by

110 ion was correlated with the logarithm of the Salmonella typhimurium concentration in the sample.

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

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

113 a label-free potentiometric immunosensor for Salmonella typhimurium detection based on the blocking s

114 Salmonella Typhimurium diarrhea serves as a paradigm, an

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

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

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

118 The Salmonella typhimurium effector protein SifA regulates t

119 Salmonella Typhimurium, Escherichia coli and Pseudomonas

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

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

122 Salmonella Enteritidis cases have risen and Salmonella Typhimurium fallen.

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

124 We find that a Salmonella typhimurium flagellin fragment comprising the

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

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

127 Salmonella Typhimurium gene STM2215 (rtn) is conserved a

128 rential fluorescence induction to screen the Salmonella Typhimurium genome for loci that respond, at

129 ibe how aspartate/malate can trigger initial Salmonella Typhimurium gut-lumen colonization in mice, p

130 78, B. subtilis, Legionella pneumophila, and Salmonella Typhimurium has demonstrated the capability o

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

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

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

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

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

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

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

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

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

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

141 Salmonella Typhimurium induces inflammatory diarrhea and

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

143 Salmonella typhimurium infection is reported to activate

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

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

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

147 of inflammation-driven thrombosis induced by Salmonella Typhimurium infection of mice.

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

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

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

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

152 emporally correlated with the restriction of Salmonella Typhimurium infection.

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

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

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

156 Salmonella typhimurium is a major cause of diarrhea and

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

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

159 Salmonella Typhimurium is metabolically adaptable and ca

160 Salmonella typhimurium is responsible for about a third

161 Salmonella Typhimurium isolate D23580 represents a recen

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

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

164 79.7% of Salmonella Enteritidis and 90.2% of Salmonella Typhimurium isolates) showed multidrug resist

165 Of Salmonella Typhimurium isolates, 42 of 43 were pathovar

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

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

168 ection with Gram-negative pathogens, such as Salmonella Typhimurium, leptin receptor (Lepr) expressio

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

170 sex toward a systemic immune stimulation by Salmonella typhimurium lipopolysaccharide (LPS).

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

172 oidal Salmonella Typhi Ty2, the nontyphoidal Salmonella Typhimurium LT2, and a clinical isolate Typhi

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

174 ties were also promising, especially against Salmonella typhimurium (MBC = 0.44 mg/mL).

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

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

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

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

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

180 A Salmonella Typhimurium mutant deficient in flagellin met

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

182 We also observed that Salmonella Typhimurium needs lipid metabolism genes in p

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

184 A P22-like TSP confers specificity for the Salmonella Typhimurium O-antigen.

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

186 Autophagic capture of Salmonella Typhimurium occurs predominantly via generati

187 he pathogen killing was evaluated by plating Salmonella typhimurium on agar plates and showed that th

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

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

190 n of Lacc1 (Lacc1(Deltamye)) were given oral Salmonella Typhimurium or dextran sodium sulfate.

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

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

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

194 Salmonella typhimurium or Toxoplasma gondii were adminis

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

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

197 In culture, Salmonella Typhimurium populations are bistable for the

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

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

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

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

202 biosensor was able to quantitatively detect Salmonella typhimurium ranging from 1.4 x 10(2) to 1.4 x

203 ative pathogens such as Shigella flexneri or Salmonella Typhimurium remains incompletely understood [

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

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

206 While it is clear that Salmonella Typhimurium requires access to glucose during

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

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

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

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

211 cells, rendered mice susceptible to invasive Salmonella typhimurium (S.t.) infection.

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

213 Salmonella Typhimurium sequence type (ST) 313 causes inv

214 invasive nontyphoidal Salmonella disease is Salmonella Typhimurium sequence type (ST)313.

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

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

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

218 In Salmonella typhimurium, some of these genes are controll

219 ive and sensitive immunosensor for detecting Salmonella typhimurium species.

220 Salmonella Typhimurium specifically targets antigen-samp

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

222 nteritidis ST11, Salmonella Heidelberg ST15, Salmonella Typhimurium ST 19, and Salmonella II 42:r:- S

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

224 itidis ST11 in East Africa, but not of human Salmonella Typhimurium ST313 infection.

225 Salmonella Typhimurium ST313 was isolated exclusively fr

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

227 e Salmonella Enteritidis ST11 and 62 (36.0%) Salmonella Typhimurium ST313.

228 erococcus faecalis, Pseudomonas fluorescens, Salmonella typhimurium, Staphylococcus aureus); and fung

229 race the emergence and evolutionary paths-of Salmonella Typhimurium (STM) from nine years of Australi

230 on and long-term pathogen persistence during Salmonella Typhimurium (STm) infection.

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

232 Salmonella Typhimurium (STm) remain a prominent cause of

233 arance of intracellular infections caused by Salmonella Typhimurium (STm) requires IFN-gamma and the

234 munization with the trimeric porin OmpD from Salmonella Typhimurium (STmOmpD) protects against infect

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

236 Salmonella typhimurium strain TA98 was used with and wit

237 Specifically, we screen Salmonella typhimurium strains expressing and delivering

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

239 We report that Salmonella Typhimurium strains lacking lipid metabolism

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

256 suggest that during systemic infection, the Salmonella Typhimurium that relies upon host lipids to r

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

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

259 In Salmonella typhimurium, the external needle is assembled

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

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

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

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

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

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

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

267 ylation of flagellin facilitates adhesion of Salmonella Typhimurium to hydrophobic host cell surfaces

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

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

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

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

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

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

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

275 residues of the needle filament protein of a Salmonella Typhimurium type III secretion system that ar

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

277 inactivation of a pathogenic species such as Salmonella typhimurium, using a luminometer assay.

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

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

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

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

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

283 's roles in the intracellular human pathogen Salmonella Typhimurium, we analyzed their expression in

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

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

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

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

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

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

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

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

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

293 Comparative genomics of Salmonella Typhimurium will provide insight into factors

294 agnetic beads, could efficiently concentrate Salmonella Typhimurium with a capturing efficiency of 95

295 irs the interactions of the enteric pathogen Salmonella Typhimurium with host cells and its fitness i

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

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

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

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