ライフサイエンスコーパス: Salmonella enterica

1 eractions of B. mallei, Yersinia pestis, and Salmonella enterica.

2 for virulence in Yersinia enterocolitica and Salmonella enterica.

3 sponsible for eptA regulation in E. coli and Salmonella enterica.

4 ilament among B. subtilis, P. aeruginosa and Salmonella enterica.

5 s transfer of pSLT, the virulence plasmid of Salmonella enterica.

6 edate the split between Escherichia coli and Salmonella enterica.

7 r Gram-negative species Escherichia coli and Salmonella enterica.

8 egion of the Mg(2+) transporter gene mgtA in Salmonella enterica.

9 ram-negatives including Escherichia coli and Salmonella enterica.

10 orming pathogens: Pseudomonas aeruginosa and Salmonella enterica.

11 Listeria monocytogenes, Escherichia coli and Salmonella enterica.

12 xal 5'-phosphate (PLP)-containing enzymes in Salmonella enterica.

13 of the essential endoribonuclease RNase E in Salmonella enterica.

14 m impacted by the metabolic stress of 2AA in Salmonella enterica.

15 nt-invasive E. coli and the related pathogen Salmonella enterica.

16 ltry to infections with distinct serovars of Salmonella enterica.

17 ntibiotic resistance-conferring mutations in Salmonella enterica and E. coli.

18 Here, we reveal the crystal structures of Salmonella enterica and Escherichia coli LpoB.

19 s of Vibrio cholerae, Citrobacter rodentium, Salmonella enterica and ETEC were capable of complementi

20 The purified BcsE proteins from E. coli, Salmonella enterica and Klebsiella pneumoniae bind c-di-

21 Several intracellular pathogens, including Salmonella enterica and Mycobacterium tuberculosis, requ

22 acteria expressing isocitrate lyase, such as Salmonella enterica and Mycobacterium tuberculosis.

23 burnetii, Leptospira spp., Rickettsia spp., Salmonella enterica and Salmonella enterica serovar Typh

24 Exposure of DCs to influenza, Salmonella enterica and Staphylococcus aureus allows us

25 -propanediol utilization microcompartment of Salmonella enterica and use it to analyze the function o

26 eases caused by pathogenic Escherichia coli, Salmonella enterica, and Clostridium difficile.

27 s, Campylobacter fetus, Helicobacter pylori, Salmonella enterica, and Giardia lamblia were detected i

28 foodborne bacteria such as Escherichia coli, Salmonella enterica, and Listeria innocua, on stainless

29 Strains of Salmonella enterica, and other organisms lacking RidA, h

30 eria, including Corynebacterium diphtheriae, Salmonella enterica, and Vibrio cholerae, are infected w

31 ying host range distribution in a lineage of Salmonella enterica, and we discuss many other potential

32 Salmonella enterica are invasive intracellular pathogens

33 Escherichia coli and Salmonella enterica are models for many experiments in m

34 s have been studied in a few bacteria (e.g., Salmonella enterica, Bacillus subtilis, Escherichia coli

35 at viable Francisella tularensis, as well as Salmonella enterica bacteria transferred from infected c

36 ine/imine intermediates from accumulating in Salmonella enterica by catalyzing their hydrolysis to st

37 -propanediol utilization microcompartment of Salmonella enterica can be controlled using two strategi

38 Collectively, our findings indicate that Salmonella enterica can promote transformation of geneti

39 Salmonella enterica catabolizes ethanolamine inside a co

40 Serovars of Salmonella enterica cause both gastrointestinal and syst

41 Salmonella enterica causes systemic diseases (typhoid an

42 In Escherichia coli and Salmonella enterica, Crl positively regulates the sigma(

43 SpvD is a Salmonella enterica effector protein that we previously

44 vation of MAPK and AKT pathways, mediated by Salmonella enterica effectors secreted during infection,

45 Recent papers have shown that the Salmonella enterica FinO-domain protein ProQ binds a lar

46 In the Gram-negative bacterium Salmonella enterica, FlgM inhibits late-class flagellar

47 Insertions in the Salmonella enterica fra locus, which encodes the fructos

48 Detection of fluoroquinolone resistance in Salmonella enterica has become increasingly difficult du

49 enetic and biochemical studies, primarily in Salmonella enterica, have defined a role for RidA in res

50 , we present crystal structures of wild type Salmonella enterica HisA (SeHisA) in its apo-state and o

51 infection with Burkholderia pseudomallei and Salmonella enterica HMBA treatment was also associated w

52 tructures of GusRs from Escherichia coli and Salmonella enterica in complexes with a glucuronide liga

53 luorescence in situ hybridization identified Salmonella enterica in the liver, subsequently confirmed

54 d in the EnvZ-OmpR two-component system from Salmonella enterica in vitro and in vivo, which directly

55 ps in the epidemiology of diseases caused by Salmonella enterica in West Africa.

56 aMN):DMB phosphoribosyltransferases (CobT in Salmonella enterica), in a reaction that is considered t

57 the foodborne pathogens E. coli O157:H7 and Salmonella enterica, in detail a nucleic acid lateral fl

58 and Salmonella Typhi infection, we show that Salmonella enterica induces malignant transformation in

59 ematical model to culture-confirmed cases of Salmonella enterica infections at Queen Elizabeth Centra

60 he most common manifestation of nontyphoidal Salmonella enterica infections, but little is known abou

61 ity and mortality for invasive non-typhoidal Salmonella enterica infections, we excluded cases attrib

62 Salmonella enterica is a leading cause of community-acqu

63 EutT from Salmonella enterica is a member of a class of enzymes te

64 Salmonella enterica is a ubiquitous Gram-negative intrac

65 Salmonella enterica is among the most burdensome of food

66 Salmonella enterica is one such pathogen, exploiting mul

67 Salmonella enterica is the leading etiologic agent of ba

68 their ability to detect low-level-resistant Salmonella enterica isolates that are not serotype Typhi

69 ccus pneumoniae, Mycobacterium tuberculosis, Salmonella enterica, Klebsiella pneumoniae, and Escheric

70 s are conserved in a distantly related SspH2 Salmonella enterica ligase.

71 ted microorganisms such as Escherichia coli, Salmonella enterica, Listeria innocua, Mycobacterium par

72 Simultaneous detection of Salmonella enterica, Listeria monocytogenes and Escheric

73 re formed upon recombinant expression of the Salmonella enterica LT2 ethanolamine utilization bacteri

74 Serovars of Salmonella enterica, namely Typhi and Typhimurium, repor

75 Salmonella enterica natively possesses both the Pdu and

76 ersinia pestis T3S needle protein, YscF, the Salmonella enterica needle proteins PrgI and SsaG, and t

77 Phase variation of the Salmonella enterica opvAB operon generates a bacterial l

78 uencing (Grad-seq) in the bacterial pathogen Salmonella enterica, partitioning its coding and noncodi

79 d Theiler's virus persistence, and decreased Salmonella enterica pathogenesis.

80 into nonphagocytic host cells is central to Salmonella enterica pathogenicity and dependent on multi

81 We hypothesized that the Salmonella enterica phage SPN3US could be a useful model

82 In Salmonella enterica, PocR is a transcription factor that

83 In Salmonella enterica, PT modification is mediated by four

84 It is known that deleting Salmonella enterica ridA causes Ser sensitivity and that

85 Because Salmonella enterica ser. Typhimurium can overcome metal

86 sed investigation of a recurrent blood-borne Salmonella enterica serotype Enteritidis (S.

87 or comparing molecular subtyping methods for Salmonella enterica serotype Enteritidis and survey the

88 association between nalidixic acid-resistant Salmonella enterica serotype Enteritidis infections in t

89 Between March 1, 2010, and Jan 31, 2014, 135 Salmonella enterica serotype Typhi (S Typhi) and 94 iNTS

90 cal failure (ie, blood cultures positive for Salmonella enterica serotype Typhi, or Paratyphi A, B, o

91 Cattle are naturally infected with Salmonella enterica serotype Typhimurium and exhibit pat

92 mportant for colonization and persistence of Salmonella enterica serotype Typhimurium in chickens.

93 Salmonella enterica serotype Typhimurium is a food-borne

94 detects typhoid-causing infectious bacteria Salmonella enterica serovar (Salmonella typhi) in 10 muL

95 nterica serovar Enteritidis, and 3% (3) were Salmonella enterica serovar Arizonae.

96 4 protected mice against the group D serovar Salmonella enterica serovar Dublin (85% vaccine efficacy

97 Salmonella enterica serovar Enteritidis (S. Enteritidis)

98 aluated the capacities of S. Typhimurium and Salmonella enterica serovar Enteritidis DeltaguaBA Delta

99 used for the epidemiological surveillance of Salmonella enterica serovar Enteritidis for over 2 decad

100 Salmonella enterica serovar Enteritidis is a significant

101 We recently detected a large outbreak of Salmonella enterica serovar Enteritidis phage type 14b a

102 enterica serovar Typhimurium, 10% (10) were Salmonella enterica serovar Enteritidis, and 3% (3) were

103 An epidemiological paradox surrounds Salmonella enterica serovar Enteritidis.

104 number of human cases of ceftiofur-resistant Salmonella enterica serovar Heidelberg in Quebec and Ont

105 from the pathogenic, Gram-negative bacteria Salmonella enterica serovar Montevideo.

106 accine (RASV) strains with RDAS derived from Salmonella enterica serovar Paratyphi A and Salmonella e

107 o develop the first human challenge model of Salmonella enterica serovar Paratyphi A infection.

108 Salmonella enterica serovar Paratyphi A is a human-speci

109 Salmonella enterica serovar Paratyphi A is a major cause

110 r with Salmonella enterica serovar Typhi and Salmonella enterica serovar Sendai, causes enteric fever

111 Salmonella enterica serovar Senftenberg is a common nont

112 1 protected mice against the group B serovar Salmonella enterica serovar Stanleyville (91% vaccine ef

113 In areas of Asia, multidrug-resistant Salmonella enterica serovar Typhi (S Typhi) has been the

114 ting protein, to influence susceptibility to Salmonella enterica serovar Typhi (S Typhi) infection.

115 Salmonella enterica serovar Typhi (S Typhi) is responsib

116 Salmonella enterica serovar Typhi (S. Typhi) differs fro

117 Here whole-genome sequence analysis of 1,832 Salmonella enterica serovar Typhi (S. Typhi) identifies

118 The population of Salmonella enterica serovar Typhi (S. Typhi), the causat

119 a human-specific serovar that, together with Salmonella enterica serovar Typhi and Salmonella enteric

120 e used a protein microarray containing 2,724 Salmonella enterica serovar Typhi antigens (>63% of prot

121 Salmonella enterica serovar Typhi causes the systemic di

122 Multiyear epidemics of Salmonella enterica serovar Typhi have been reported fro

123 ent in the Indian subcontinent, with chronic Salmonella enterica serovar Typhi infection reported as

124 Salmonella enterica serovar Typhi is a human-restricted

125 Salmonella enterica serovar Typhi is associated with a d

126 Salmonella enterica serovar Typhi is the etiological age

127 We report a typhoid fever case with a Salmonella enterica serovar Typhi isolate showing extend

128 lly and results from systemic infection with Salmonella enterica serovar Typhi or Paratyphi pathovars

129 Here we used a live attenuated Salmonella enterica serovar Typhi strain to create a biv

130 Salmonella enterica serovar Paratyphi A and Salmonella enterica serovar Typhi to induce protective i

131 ded-spectrum-beta-lactamase (ESBL)-producing Salmonella enterica serovar Typhi was identified, whole-

132 p., Rickettsia spp., Salmonella enterica and Salmonella enterica serovar Typhi, and Yersinia pestis),

133 n humans, including Mycobacterium leprae and Salmonella enterica serovar Typhi, but the function of p

134 e that the causative agent of typhoid fever, Salmonella enterica serovar Typhi, can partially subvert

135 Enteric fever, caused by Salmonella enterica serovar Typhi, is an important publi

136 Salmonella enterica serovar Typhi, the causative agent o

137 Salmonella enterica serovar Typhi, the cause of typhoid,

138 the serotyped salmonellae, 14% (21/152) were Salmonella enterica serovar Typhi, whereas 86% (131/152)

139 childhood bacteremia, with a predominance of Salmonella enterica serovar Typhi.

140 osa, nontypeable Haemophilus influenzae, and Salmonella enterica serovar Typhi/Typhimurium.

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

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

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

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

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

146 Salmonella enterica serovar Typhimurium (S.

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

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

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

150 Salmonella enterica serovar Typhimurium (S. Typhimurium)

151 Salmonella enterica serovar Typhimurium (S. typhimurium)

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

153 Salmonella enterica serovar Typhimurium (ST) sense Toll-

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

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

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

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

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

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

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

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

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

163 Salmonella enterica serovar Typhimurium can inject effec

164 Conversely, Salmonella enterica serovar Typhimurium causes gastroent

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

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

167 We observed enhanced Salmonella enterica serovar Typhimurium colonization in

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

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

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

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

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

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

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

175 Salmonella enterica serovar Typhimurium exploits the hos

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

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

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

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

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

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

182 Salmonella enterica serovar Typhimurium infection of imm

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

184 Salmonella enterica serovar Typhimurium is a bacterial p

185 Salmonella enterica serovar Typhimurium is a common caus

186 Salmonella enterica serovar Typhimurium is a food-borne

187 Salmonella enterica serovar Typhimurium is a Gram-negati

188 Salmonella enterica serovar Typhimurium is an enteropath

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

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

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

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

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

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

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

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

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

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

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

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

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

202 The intracellular pathogen Salmonella enterica serovar Typhimurium requires the mgt

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

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

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

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

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

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

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

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

211 Conversely, Salmonella enterica serovar Typhimurium uses a T3SS enco

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

213 Salmonella enterica serovar Typhimurium utilizes molecul

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

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

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

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

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

219 Salmonella (Salmonella enterica serovar Typhimurium) secrete numerou

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

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

222 Salmonella enterica serovar Typhimurium, an intracellula

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

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

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

226 In Salmonella enterica serovar Typhimurium, flagella-mediat

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

247 Salmonella enterica serovars Enteritidis and Kentucky di

248 The burden of enteric fever caused by Salmonella enterica serovars Typhi and Paratyphi is subs

249 ivalent to fever (39 degrees C-42 degrees C) Salmonella enterica serovars Typhi, Paratyphi A, and Sen

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

251 r jejuni (mapA), Shigella spp. (ipaH), and a Salmonella enterica-specific (SE) DNA sequence at seven

252 estis), PscF (Pseudomonas aeruginosa), PrgI (Salmonella enterica SPI-1), SsaG (Salmonella enterica SP

253 sa), PrgI (Salmonella enterica SPI-1), SsaG (Salmonella enterica SPI-2), or MxiH (Shigella flexneri).

254 he 2.1 A resolution crystal structure of the Salmonella enterica SPI-2-encoded ATPase, SsaN.

255 i, S. Paratyphi A, and genes conserved among Salmonella enterica spp. and utilized strongly magnetize

256 hlortetracycline on the temporal dynamics of Salmonella enterica spp. enterica in feedlot cattle.

257 (EPEC), and Citrobacter rodentium Moreover, Salmonella enterica strains encode up to three NleB orth

258 The NGS data set of the Salmonella enterica strains were used as a case study to

259 tic activity of various Escherichia coli and Salmonella enterica strains.

260 ith Escherichia coli, Neisseria gonorrhoeae, Salmonella enterica, Streptococcus pyogenes and Xenorhab

261 S. bongori, S. enterica subsp. salamae, and Salmonella enterica subsp. arizonae The beta-lactamase T

262 aced this domain with a nuclease domain from Salmonella enterica subsp. arizonae This modified V. cho

263 We report here that Salmonella enterica subsp. enterica serovar Typhimurium

264 , Bacillus cereus, Staphylococcus aureus and Salmonella enterica subsp. enterica serovar Typhimurium,

265 tudy, we compared a draft genome assembly of Salmonella enterica subsp. salamae strain 3588/07 agains

266 by >170%, driven primarily by an epidemic of Salmonella enterica subspecies enterica serovar Enteriti

267 nterica subspecies enterica serovar Typhi or Salmonella enterica subspecies enterica serovar Paratyph

268 Human infections with Salmonella enterica subspecies enterica serovar Senftenb

269 Salmonella enterica subspecies enterica serovar Typhi or

270 We report a traveler who acquired a Salmonella enterica subspecies enterica serovar Typhi st

271 Here we show that Salmonella enterica subspecies enterica serovar Typhimur

272 0 of 620 (74.2%) NTS isolates serotyped were Salmonella enterica subspecies enterica serovar Typhimur

273 Within Salmonella enterica subspecies enterica, a single lineag

274 serovar 9,12:l,v:- belongs to the B clade of Salmonella enterica subspecies enterica, and we show its

275 sis indicated that srgE is found only within Salmonella enterica subspecies.

276 high-abundance chemoreceptors of E. coli and Salmonella enterica suggests that it may be important fo

277 In Salmonella enterica, sulfur is trafficked to both thiami

278 The common human pathogen Salmonella enterica takes up citrate as a nutrient via t

279 thogens or prolonged exposure to heat-killed Salmonella enterica, the Gram-positive bacterium Bacillu

280 III secretion system (T3SS) of intracellular Salmonella enterica translocates effector proteins into

281 Within host cells such as macrophages, Salmonella enterica translocates virulence (effector) pr

282 Two major serovars of Salmonella enterica, Typhi and Typhimurium, have evolved

283 report the intrabacterial redox dynamics of Salmonella enterica Typhimurium (S. Typhimurium) residin

284 onlethal gastric infections of Gram-negative Salmonella enterica Typhimurium (ST), a major source of

285 phoQ(W104C-A128C) Salmonella enterica Typhimurium is virulent in mice, ind

286 An essential feature of Salmonella enterica Typhimurium pathogenesis is its abil

287 hat infection of macrophages and mice with a Salmonella enterica Typhimurium strain containing an ina

288 By training with sRNAs in Salmonella enterica Typhimurium, we were able to success

289 in bacterial cells, particularly E. coli and Salmonella enterica Typhimurium.

290 leic acid, a major lipid in E. coli Last, in Salmonella enterica, ubiK was required for proliferation

291 In the enteric pathogen Salmonella enterica, using chromatin immunoprecipitation

292 the beta- and gamma-proteobacteria, such as Salmonella enterica, Vibrio spp., and both Sphingomonas

293 Dap accumulation in Salmonella enterica was previously shown to inhibit grow

294 es in an investigation of host adaptation in Salmonella enterica We highlight the value of the method

295 res of R-LPS from either Escherichia coli or Salmonella enterica were directly infused into the mass

296 lobacter jejuni, Campylobacter concisus, and Salmonella enterica were recovered.

297 Antibiotic-resistant isolates of Salmonella enterica were selected on plates containing l

298 eal disease agents, especially non-typhoidal Salmonella enterica, were also responsible for the major

299 bserved PPI, including Bacillus subtilis and Salmonella enterica which are predicted to have up to 18

300 rimers specific for E. coli eaeA (151bp) and Salmonella enterica yfiR (375bp) genes.