ライフサイエンスコーパス: Salmonella enterica serovar Typhimurium

1 Gram negative bacteria (Escherichia coli and Salmonella enterica serovar Typhimurium).

2 d by enteric bacteria Citrobacter koseri and Salmonella enterica serovar typhimurium.

3 activate a periplasmic Cu,Zn-SOD (SodCII) in Salmonella enterica serovar Typhimurium.

4 -like cells are required for defense against Salmonella enterica serovar Typhimurium.

5 fy mechanisms of persistence in the pathogen Salmonella enterica serovar Typhimurium.

6 +) homeostasis in the Gram-negative pathogen Salmonella enterica serovar Typhimurium.

7 proportion of these infections are caused by Salmonella enterica serovar Typhimurium.

8 QseC activates virulence gene expression in Salmonella enterica serovar Typhimurium.

9 physiological analyses of a 2-h lag phase in Salmonella enterica serovar Typhimurium.

10 CDGA activity was first tested with Salmonella enterica serovar Typhimurium.

11 t bacterial surface antigens associated with Salmonella enterica Serovar Typhimurium.

12 r (P(class2)) gene expression to assembly in Salmonella enterica serovar Typhimurium.

13 ation as inhibitors of type III secretion in Salmonella enterica serovar Typhimurium.

14 t intracellular states of the model pathogen Salmonella enterica serovar Typhimurium.

15 t doses that did not affect the viability of Salmonella enterica serovar Typhimurium.

16 he primary source of intracellular Mg(2+) in Salmonella enterica serovar Typhimurium.

17 CorA is the primary Mg(2+) channel in Salmonella enterica serovar Typhimurium.

18 thologs OmpT in Escherichia coli and PgtE in Salmonella enterica serovar Typhimurium.

19 ine on the transcriptome of the gut pathogen Salmonella enterica serovar Typhimurium.

20 helial oxygenation, and aerobic expansion of Salmonella enterica serovar Typhimurium.

21 ng activity of macrophages against wild-type Salmonella enterica serovar Typhimurium.

22 injection of the viral genome into the host Salmonella enterica serovar Typhimurium.

23 atory properties of this signaling system in Salmonella enterica serovar Typhimurium.

24 nt decrease in survival when challenged with Salmonella enterica serovar Typhimurium.

25 and related enteric bacteria but differs in Salmonella enterica serovar Typhimurium.

26 ts its 43 kbp genome across the cell wall of Salmonella enterica serovar Typhimurium.

27 e a large set of genes affecting motility in Salmonella enterica serovar Typhimurium.

28 taxis, is essential for swarming motility in Salmonella enterica serovar Typhimurium.

29 me responsible for aerobic NO. metabolism by Salmonella enterica serovar typhimurium.

30 identifying mutations in the MEP pathway of Salmonella enterica serovar Typhimurium.

31 odes the major component of the flagellum in Salmonella enterica serovar Typhimurium.

32 diating resistance to Fe(III) and Al(III) in Salmonella enterica serovar Typhimurium.

33 oQ in the facultative intracellular pathogen Salmonella enterica serovar Typhimurium.

34 charide stimulation or upon coinfection with Salmonella enterica serovar Typhimurium.

35 en Vibrio cholerae and the invasive pathogen Salmonella enterica serovar Typhimurium.

36 of physiological and virulence functions in Salmonella enterica serovar Typhimurium.

37 anced susceptibility to hydrogen peroxide in Salmonella enterica serovar Typhimurium.

38 stinal inflammation during colitis caused by Salmonella enterica serovar Typhimurium.

39 Of the 102 typed NTS isolates, 40% (41) were Salmonella enterica serovar Typhimurium, 10% (10) were S

40 e with Plasmodium yoelii 17XNL (Py17XNL) and Salmonella enterica serovar Typhimurium 12023 (Salmonell

41 Wild-type Salmonella enterica serovar Typhimurium 14028s caused a

42 FrmR from Salmonella enterica serovar typhimurium (a CsoR/RcnR-lik

43 Salmonella enterica serovar Typhimurium, a common enteri

44 udy describes maturation processes in living Salmonella enterica serovar Typhimurium, a prevalent cau

45 ucidate the host transcriptional response to Salmonella enterica serovar Typhimurium, Affymetrix porc

46 scherichia coli, Yersinia enterocolitica and Salmonella enterica serovar Typhimurium (all gram-negati

47 533, following infection of macrophages with Salmonella enterica serovar Typhimurium (also known as S

48 Salmonella enterica serovar Typhimurium, an intracellula

49 Salmonella enterica serovar Typhimurium, an intracellula

50 o control infection by the enteric pathogens Salmonella enterica serovar Typhimurium and Citrobacter

51 ial amyloids using curli fibers, produced by Salmonella enterica serovar Typhimurium and Escherichia

52 ive infection with Pseudomonas aeruginosa or Salmonella enterica serovar Typhimurium and had no or a

53 Bacteriophage P22 infects Salmonella enterica serovar Typhimurium and is a model f

54 charide (LPS) is a major virulence factor of Salmonella enterica serovar Typhimurium and is composed

55 ed IFN-gamma response following infection by Salmonella enterica serovar Typhimurium and Listeria mon

56 n important role in the host defense against Salmonella enterica serovar Typhimurium and perhaps othe

57 We have constructed attenuated Salmonella enterica serovar Typhimurium and Salmonella e

58 were found to be susceptible to invasion by Salmonella enterica serovar Typhimurium and Shigella fle

59 for autophagy of the intracellular pathogen Salmonella enterica serovar Typhimurium and show that th

60 t here that Fur is required for virulence in Salmonella enterica serovar Typhimurium and that Fur is

61 n in the Mg(2+)-sensing mgtA riboswitch from Salmonella enterica serovar Typhimurium and the flavin m

62 flexneri and other pathogens that use T3SS, Salmonella enterica serovar Typhimurium and Yersinia pse

63 Nontyphoidal Salmonella (NTS), particularly Salmonella enterica serovars Typhimurium and Enteritidis

64 sa, Staphylococcus aureus, Escherichia coli, Salmonella enterica serovar Typhimurium, and Salmonella

65 We report that cobC strains of Salmonella enterica serovar Typhimurium are impaired in

66 Type I fimbriae in Salmonella enterica serovar Typhimurium are surface appe

67 Nontyphoidal salmonellae, particularly Salmonella enterica serovar Typhimurium, are a major cau

68 opological configuration is proposed for the Salmonella enterica serovar Typhimurium ArnT.

69 on with the intracellular bacterial pathogen Salmonella enterica serovar Typhimurium as shown by thei

70 Shigella flexneri and the vT3SS and fT3SS of Salmonella enterica serovar Typhimurium at ~5 and ~4 nm

71 Salmonella enterica serovar Typhimurium avoids clearance

72 The pattern of global gene expression in Salmonella enterica serovar Typhimurium bacteria harvest

73 Moreover, purified flagellin from Salmonella enterica serovar Typhimurium behaved like sam

74 The food-borne pathogen Salmonella enterica serovar Typhimurium benefits from ac

75 For the human and animal pathogen Salmonella enterica serovar Typhimurium, biofilm formati

76 tein (ycfR) were specifically upregulated in Salmonella enterica serovar Typhimurium biofilms grown o

77 In Escherichia coli and Salmonella enterica serovar Typhimurium, BipA has been i

78 sette transporters from several rhizobia and Salmonella enterica serovar Typhimurium, but not seconda

79 Here, we report that pyroptosis induced by Salmonella enterica serovar Typhimurium can be positivel

80 Salmonella enterica serovar Typhimurium can inject effec

81 ion system from the bacterial enteropathogen Salmonella enterica serovar Typhimurium can sort its sub

82 Salmonella enterica serovar Typhimurium can utilize mole

83 Escherichia coli and Salmonella enterica serovar Typhimurium cannot synthesiz

84 he 50% lethal dose (LD(50)) or 10x LD(50) of Salmonella enterica serovar Typhimurium caused changes i

85 The Gram-negative bacterium Salmonella enterica serovar Typhimurium causes a natural

86 The enteric pathogen Salmonella enterica serovar Typhimurium causes food pois

87 Conversely, Salmonella enterica serovar Typhimurium causes gastroent

88 lness in humans, termed typhoid fever, while Salmonella enterica serovar Typhimurium causes localized

89 The Gram-negative intracellular bacterium Salmonella enterica serovar Typhimurium causes persisten

90 Salmonella enterica serovar Typhimurium causes typhoid-l

91 Mice were infected with Salmonella enterica serovar typhimurium; cecum and small

92 Each Salmonella enterica serovar Typhimurium cell produces a

93 We observed enhanced Salmonella enterica serovar Typhimurium colonization in

94 l compartments and a reduced ability to kill Salmonella enterica serovar Typhimurium compared to that

95 The ST313 pathovar of Salmonella enterica serovar Typhimurium contributes to a

96 ighly conserved loop, (281)EFMPELKWS(289) in Salmonella enterica serovar Typhimurium CorA, is the onl

97 We also demonstrate that the Salmonella enterica serovar Typhimurium core promoter is

98 inserts, we determined that infection with a Salmonella enterica serovar Typhimurium csgBA mutant, wh

99 Mutants of Salmonella enterica serovar Typhimurium deficient in DNA

100 Salmonella enterica serovar Typhimurium definitive phage

101 gions of IpaB from S. flexneri and SipB from Salmonella enterica serovar Typhimurium determined at 2.

102 d ProU transporter from Escherichia coli and Salmonella enterica serovar Typhimurium did not function

103 toxified outer membrane vesicles (OMVs) from Salmonella enterica serovar Typhimurium displaying the v

104 dentified the dissemination of two prevalent Salmonella enterica serovar Typhimurium DT104 clones in

105 provide an important colonization niche for Salmonella enterica serovar Typhimurium during gastroint

106 merozoite antigen EAMZ250 were fused to the Salmonella enterica serovar Typhimurium effector protein

107 Salmonella enterica serovar Typhimurium encodes two type

108 ic bacteria, either Klebsiella pneumoniae or Salmonella enterica serovar Typhimurium, enhanced transl

109 A recent study showed that Salmonella enterica serovar Typhimurium exhibits sliding

110 The Gram-negative pathogen Salmonella enterica serovar Typhimurium experiences a nu

111 Salmonella enterica serovar Typhimurium exploits actin d

112 Salmonella enterica serovar Typhimurium exploits the hos

113 ranasal immunization of mice with attenuated Salmonella enterica serovar Typhimurium expressing the O

114 In Salmonella enterica serovar Typhimurium, flagella-mediat

115 , we tested the immunoadjuvant properties of Salmonella enterica serovar Typhimurium flagellin (FliC)

116 fic monoclonal IgA, is a potent inhibitor of Salmonella enterica serovar Typhimurium flagellum-based

117 Flagellin from Salmonella enterica serovar Typhimurium (FliC) can impac

118 on significantly attenuates the virulence of Salmonella enterica serovar Typhimurium following intrap

119 ite sequencing (TraDIS) to screen mutants of Salmonella enterica serovar Typhimurium for their abilit

120 enotyping methods to distinguish isolates of Salmonella enterica serovar Typhimurium from different f

121 ance of the Gram-negative bacterial pathogen Salmonella enterica serovar Typhimurium from macrophages

122 tracellular gram-negative bacterial pathogen Salmonella enterica serovar Typhimurium gains entry into

123 ur genome-wide analysis of core genes within Salmonella enterica serovar Typhimurium genomes reveals

124 Salmonella enterica serovar Typhimurium harbors five pat

125 ugars on the virulence and immunogenicity of Salmonella enterica serovar Typhimurium has not been sys

126 e human chitotriosidase and a chitinase from Salmonella enterica serovar Typhimurium hydrolyze LacNAc

127 is the major regulator of LPS alterations in Salmonella enterica serovar Typhimurium, impaired growth

128 ed and surface-associated cell components of Salmonella enterica serovar Typhimurium, including O ant

129 and RcsC/YojN/RcsB two-component systems of Salmonella enterica serovar Typhimurium independently pr

130 We found that intracellular Salmonella enterica serovar Typhimurium induced the binu

131 that TcpB protein can efficiently attenuate Salmonella enterica serovar Typhimurium-induced pyroptos

132 Most 6N+ macrophages from Salmonella enterica serovar Typhimurium-infected mice co

133 n simultaneously in pathogen and host during Salmonella enterica serovar Typhimurium infection and re

134 Salmonella enterica serovar Typhimurium infection of imm

135 his study investigates the effect of peroral Salmonella enterica serovar Typhimurium infection on the

136 CARD9 is suppressed during Salmonella enterica serovar Typhimurium infection, facil

137 In contrast to Salmonella enterica serovar Typhimurium infection, which

138 R, a highly hydrophobic peptide expressed in Salmonella enterica serovar Typhimurium, inhibits growth

139 on contact with intestinal epithelial cells, Salmonella enterica serovar Typhimurium injects a set of

140 ty Island (SPI)-2 permitted the expansion of Salmonella enterica serovar Typhimurium into the intrace

141 Salmonella enterica serovar Typhimurium invade non-phago

142 Salmonella enterica serovar Typhimurium is a bacterial p

143 Salmonella enterica serovar Typhimurium is a common caus

144 Salmonella enterica serovar Typhimurium is a food-borne

145 Salmonella enterica serovar Typhimurium is a Gram-negati

146 Salmonella enterica serovar Typhimurium is a Gram-negati

147 Salmonella enterica serovar Typhimurium is a Gram-negati

148 Salmonella enterica serovar Typhimurium is a Gram-negati

149 Salmonella enterica serovar Typhimurium is a leading cau

150 Salmonella enterica serovar Typhimurium is a pathogen th

151 Here, we show that Salmonella enterica serovar Typhimurium is able to adher

152 Salmonella enterica serovar Typhimurium is able to resis

153 Invasion of intestinal epithelial cells by Salmonella enterica serovar Typhimurium is an energetica

154 Salmonella enterica serovar Typhimurium is an enteropath

155 Salmonella enterica serovar Typhimurium is an intracellu

156 h of the in vivo innate immune resistance of Salmonella enterica serovar Typhimurium is attributed to

157 expression of the Mg(2+) transporter MgtA of Salmonella enterica serovar Typhimurium is controlled by

158 The production of type 1 fimbriae in Salmonella enterica serovar Typhimurium is controlled, i

159 very of putative iron efflux transporters in Salmonella enterica serovar Typhimurium is discussed in

160 We now report that RpoS accumulates when Salmonella enterica serovar Typhimurium is growing logar

161 e invasion of intestinal epithelial cells by Salmonella enterica serovar Typhimurium is mediated by a

162 ism for enforcing this temporal hierarchy in Salmonella enterica serovar Typhimurium is the sigma(28)

163 tedly, the allosteric mechanism of FrmR from Salmonella enterica serovar Typhimurium is triggered by

164 Salmonella enterica serovar Typhimurium isolates are res

165 We applied the algorithm to a set of Salmonella enterica serovar Typhimurium isolates collect

166 Sixty-one Salmonella enterica serovar Typhimurium isolates of anim

167 ty testing and multilocus sequence typing on Salmonella enterica serovar Typhimurium isolates was per

168 Macrophage recognition of Salmonella enterica serovar Typhimurium leads to a casca

169 The Salmonella enterica serovar Typhimurium lipopolysacchari

170 We identified a homolog of the Salmonella enterica serovar Typhimurium lipoprotein (lpp

171 inhibits the peptide hydrolysis activity of Salmonella enterica serovar Typhimurium Lon.

172 the rabbit ileal loop model inoculated with Salmonella enterica serovar Typhimurium LPS.

173 The genome of Salmonella enterica serovar Typhimurium LT2 encodes 26 G

174 Strains of Salmonella enterica serovar Typhimurium LT2 lacking a fu

175 milar to purified PDU microcompartments from Salmonella enterica serovar Typhimurium LT2 that were im

176 we demonstrate detection of genomic DNA from Salmonella enterica serovar Typhimurium LT2 with a limit

177 alis, Escherichia coli K12, E. coli O157:H7, Salmonella enterica serovar Typhimurium LT2, Staphylococ

178 adenosylcobalamin (coenzyme B12) pathway of Salmonella enterica serovar Typhimurium LT2.

179 te phosphatase (CobC; EC 3.1.3.73) enzyme of Salmonella enterica serovar Typhimurium LT2.

180 The MgtA protein from Salmonella enterica serovar Typhimurium mediates Mg(2+)

181 The melibiose permease of Salmonella enterica serovar Typhimurium (MelB(St)) catal

182 e of the Na(+)-coupled melibiose permease of Salmonella enterica serovar Typhimurium (MelBSt) demonst

183 In Salmonella enterica serovar Typhimurium, Mg(2+) limitati

184 To infect an animal host, Salmonella enterica serovar Typhimurium must penetrate t

185 Salmonella enterica serovar Typhimurium must successfull

186 ed a metabolically competent, but avirulent, Salmonella enterica serovar Typhimurium mutant for its a

187 The growth of Salmonella enterica serovar Typhimurium mutants lacking

188 LPS mutants, which are derived from E. coli, Salmonella enterica serovar Typhimurium, Neisseria gonor

189 srR target is inactivated by mutation at the Salmonella enterica serovar Typhimurium nrf promoter.

190 prising two and three O-antigen repeats from Salmonella enterica serovar Typhimurium: octasaccharide

191 o the secretion and translocation signals of Salmonella enterica serovar Typhimurium of the type III

192 eria monocytogenes but not vacuole-localized Salmonella enterica serovar Typhimurium or extracellular

193 her structure of CMV, adenovirus serotype 2, Salmonella enterica serovar Typhimurium, or of cells use

194 nterohemorrhagic Escherichia coli (EHEC) and Salmonella enterica serovar Typhimurium, or the surrogat

195 A total of 190 isolates from eight Salmonella enterica serovar Typhimurium outbreaks and 15

196 ein translocases SipB, SipC, and SipD of the Salmonella enterica serovar Typhimurium pathogenicity is

197 Here we report that Salmonella enterica serovar Typhimurium pathogenicity is

198 we present the structure of the prototypical Salmonella enterica serovar Typhimurium pathogenicity is

199 cted targets in other bacteria, specifically Salmonella enterica serovar Typhimurium, Pectobacterium

200 The Salmonella enterica serovar Typhimurium PhoP/PhoQ system

201 Here we show that the Salmonella enterica serovar Typhimurium PhoQ sensor kina

202 Salmonella enterica serovar Typhimurium possesses a stim

203 The enteric pathogen Salmonella enterica serovar Typhimurium possesses four f

204 The PhoPQ two-component system of Salmonella enterica serovar Typhimurium produces a remod

205 were combined to identify most of the 3,838 Salmonella enterica serovar Typhimurium promoters in jus

206 create FLIM-phasor maps of Escherichia coli, Salmonella enterica serovar Typhimurium, Pseudomonas aer

207 ntroduction of the tviA gene in nontyphoidal Salmonella enterica serovar Typhimurium reduced flagelli

208 In Salmonella enterica serovar Typhimurium, removal of the

209 Salmonella enterica serovar Typhimurium replicates in ma

210 Salmonella enterica serovar Typhimurium replicates withi

211 in the gut by the enteropathogenic bacterium Salmonella enterica serovar Typhimurium requires a T6SS

212 The intracellular pathogen Salmonella enterica serovar Typhimurium requires the mgt

213 ly showed that l-asparaginase II produced by Salmonella enterica serovar Typhimurium (S Typhimurium)

214 BA would be more resistant to infection with Salmonella enterica serovar Typhimurium (S Typhimurium).

215 Salmonella enterica serovar Typhimurium (S.

216 wo intracellular [Listeria monocytogenes and Salmonella enterica serovar Typhimurium (S.

217 facultative intracellular bacterial pathogen Salmonella enterica serovar Typhimurium (S.

218 udies have shown that the enteric bacterium, Salmonella enterica serovar Typhimurium (S. Typhimurium)

219 ody directed against the O antigen (O-Ag) of Salmonella enterica serovar Typhimurium (S. Typhimurium)

220 pression limits laboratory grown cultures of Salmonella enterica serovar typhimurium (S. typhimurium)

221 ow that two antibiotic-associated pathogens, Salmonella enterica serovar Typhimurium (S. typhimurium)

222 nse during acute infection with the pathogen Salmonella enterica serovar Typhimurium (S. Typhimurium)

223 phenomenon of persister cells and models of Salmonella enterica serovar Typhimurium (S. Typhimurium)

224 pathogens, including the bacterial pathogen Salmonella enterica serovar Typhimurium (S. typhimurium)

225 iology, metabolism, and molecular biology of Salmonella enterica serovar Typhimurium (S. Typhimurium)

226 lamine) confers a marked growth advantage on Salmonella enterica serovar Typhimurium (S. Typhimurium)

227 uantification of the replication dynamics of Salmonella enterica serovar Typhimurium (S. Typhimurium)

228 n significant impairment of the virulence of Salmonella enterica serovar Typhimurium (S. Typhimurium)

229 Salmonella enterica serovar Typhimurium (S. typhimurium)

230 w here that the important foodborne pathogen Salmonella enterica serovar Typhimurium (S. Typhimurium)

231 d persisted in tissues of mice infected with Salmonella enterica serovar Typhimurium (S. Typhimurium)

232 Salmonella enterica serovar Typhimurium (S. Typhimurium)

233 Salmonella enterica serovar Typhimurium (S. typhimurium)

234 thogenesis is based on research conducted on Salmonella enterica serovar Typhimurium, S. Enteritidis

235 he effects of autophagy gene inactivation on Salmonella enterica Serovar Typhimurium (Salmonella typh

236 asion assays with Listeria monocytogenes and Salmonella enterica serovar Typhimurium (Salmonella typh

237 The intracellular pathogenic bacterium Salmonella enterica serovar typhimurium (Salmonella) rel

238 Salmonella (Salmonella enterica serovar Typhimurium) secrete numerou

239 In response to iron deprivation, Salmonella enterica serovar Typhimurium secretes two cat

240 Escherichia coli and Salmonella enterica serovar Typhimurium share high degre

241 ownstream of the translocation domain of the Salmonella enterica serovar Typhimurium sopE gene in the

242 The mgtCBR operon from Salmonella enterica serovar Typhimurium specifies the vi

243 (TCA) cycle operates as a full cycle during Salmonella enterica serovar Typhimurium SR-11 peroral in

244 Previously, we showed that the Salmonella enterica serovar Typhimurium SR-11 tricarboxy

245 Salmonella enterica serovar Typhimurium (ST) sense Toll-

246 We have previously shown that Salmonella enterica serovar Typhimurium (ST), a leading

247 have not been investigated in the context of Salmonella enterica serovar Typhimurium (ST).

248 ptional programme and metabolomic profile of Salmonella enterica serovar Typhimurium ST4/74 were comp

249 To evade host resistance mechanisms, Salmonella enterica serovar Typhimurium (STM), a faculta

250 tenuated Salmonella vaccines (RASVs) such as Salmonella enterica serovar Typhimurium strain chi9447.

251 We genetically engineered a Salmonella enterica serovar Typhimurium strain of multil

252 antigen from Mycobacterium tuberculosis, in Salmonella enterica serovar Typhimurium strain SL3261.

253 In this work, we constructed a Salmonella enterica serovar Typhimurium strain that synt

254 The Salmonella enterica serovar Typhimurium strain UK-1 exhi

255 ewly developed regulated delayed attenuation Salmonella enterica serovar Typhimurium strains chi9088

256 r N2 worms grown on mixed lawns of bacteria, Salmonella enterica serovar Typhimurium substantially ou

257 h phenotypic changes in Escherichia coli and Salmonella enterica serovar Typhimurium, suggesting that

258 ecific MerR family regulator named GolS from Salmonella enterica serovar Typhimurium that controls th

259 sine harbors bacteriostatic activity against Salmonella enterica serovar Typhimurium that is not shar

260 Salmonella enterica serovar Typhimurium that lacks the D

261 popolysaccharide (LPS) modification genes in Salmonella enterica serovar Typhimurium, the etiologic a

262 Unlike the nontyphoidal Salmonella enterica serovar Typhimurium, the genomes of

263 To examine individual functions, strains of Salmonella enterica serovar Typhimurium, the murine mode

264 However, Salmonella enterica serovar Typhimurium thrives in the i

265 egulatory system coordinates the response of Salmonella enterica serovar Typhimurium to diverse envir

266 njugative HGT of the colicin-plasmid p2 from Salmonella enterica serovar Typhimurium to E. coli.

267 he current study, we examined the ability of Salmonella enterica serovar Typhimurium to infect the ce

268 bound in vivo by the CspA family members of Salmonella enterica serovar Typhimurium to link the cons

269 olymerase is essential for the resistance of Salmonella enterica serovar Typhimurium to RNS in a muri

270 uptake regulator (Fur) in the resistance of Salmonella enterica serovar Typhimurium to the reactive

271 urrounding swarming and nonswarming cells of Salmonella enterica serovar Typhimurium to wet a nonpola

272 Salmonella enterica serovar typhimurium translocates a g

273 ed 129X1/SvJ mice provide a natural model of Salmonella enterica serovar Typhimurium transmission.

274 In Salmonella enterica serovar Typhimurium, trxA encodes th

275 t are not permissive for secretion through a Salmonella enterica serovar Typhimurium type III secreti

276 We define YvyG as an orthologue of the Salmonella enterica serovar Typhimurium type III secreti

277 but is present in the highly invasive strain Salmonella enterica serovar Typhimurium UK-1 (stands for

278 otility of the poorly motile yhjH mutants of Salmonella enterica serovar Typhimurium UMR1.

279 y overexpressing the caf operon in wild-type Salmonella enterica serovar Typhimurium under a potent p

280 Conversely, Salmonella enterica serovar Typhimurium uses a T3SS enco

281 Here we show that the intestinal pathogen Salmonella enterica serovar Typhimurium uses specialized

282 Salmonella enterica serovar Typhimurium uses the Salmone

283 Salmonella enterica serovar Typhimurium utilizes molecul

284 efficacy of a sopB deletion mutation on two Salmonella enterica serovar Typhimurium vaccine strains

285 We have validated this system, using Salmonella enterica serovar Typhimurium vaccines for ant

286 reover, the ZupT transporter is required for Salmonella enterica serovar Typhimurium virulence in Nra

287 , the interaction between FlgM and FliS from Salmonella enterica serovar Typhimurium was characterize

288 pontaneous sepsis and on oral infection with Salmonella enterica serovar Typhimurium was examined.

289 instance, pigs experimentally infected with Salmonella enterica serovar Typhimurium was investigated

290 In vitro mutational and genetic screening in Salmonella enterica serovar Typhimurium was performed in

291 the FlgE (flagellar hook subunit) protein in Salmonella enterica serovar Typhimurium was posttranscri

292 l pathogens, Salmonella enterocolitis (using Salmonella enterica serovar Typhimurium) was induced in

293 hput assay for type III protein secretion in Salmonella enterica serovar Typhimurium, we discovered t

294 Listeria monocytogenes V7 and Salmonella enterica serovar Typhimurium were used as mod

295 urported trimeric autotransporter adhesin of Salmonella enterica serovar Typhimurium, were examined.

296 possesses genes related to the lsr operon of Salmonella enterica serovar Typhimurium which function t

297 report that the Mg(2+) channel gene corA in Salmonella enterica serovar Typhimurium, which was previ

298 cells (hIPSCs) to explore the interaction of Salmonella enterica serovar Typhimurium with iHOs.

299 n of conserved genes in the PhoPQ regulon of Salmonella enterica serovar Typhimurium with that of Pho

300 nd O-antigen, is a major virulence factor of Salmonella enterica serovar Typhimurium, with lipid A be