ライフサイエンスコーパス: enterica

1 E. coli and the related pathogen Salmonella enterica.

2 ections with distinct serovars of Salmonella enterica.

3 f B. mallei, Yersinia pestis, and Salmonella enterica.

4 ce in Yersinia enterocolitica and Salmonella enterica.

5 or eptA regulation in E. coli and Salmonella enterica.

6 ng B. subtilis, P. aeruginosa and Salmonella enterica.

7 of pSLT, the virulence plasmid of Salmonella enterica.

8 plit between Escherichia coli and Salmonella enterica.

9 tive species Escherichia coli and Salmonella enterica.

10 e Mg(2+) transporter gene mgtA in Salmonella enterica.

11 ntial endoribonuclease RNase E in Salmonella enterica.

12 by the metabolic stress of 2AA in Salmonella enterica.

13 d by low Mg(2+) and C18G as in pathogenic S. enterica.

14 In S. enterica, 2AA inactivates a number of pyridoxal 5'-phose

15 Within Salmonella enterica subspecies enterica, a single lineage exists that includes human an

16 esistance-conferring mutations in Salmonella enterica and E. coli.

17 cholerae, Citrobacter rodentium, Salmonella enterica and ETEC were capable of complementing Aar acti

18 e is rarely found outside subspecies I of S. enterica and often present in nonfunctional allelic form

19 treatment against established biofilms of S. enterica and P. aeruginosa, respectively.

20 Leptospira spp., Rickettsia spp., Salmonella enterica and Salmonella enterica serovar Typhi, and Yers

21 l utilization microcompartment of Salmonella enterica and use it to analyze the function of the micro

22 d by pathogenic Escherichia coli, Salmonella enterica, and Clostridium difficile.

23 acter fetus, Helicobacter pylori, Salmonella enterica, and Giardia lamblia were detected in sewage, a

24 g of the effects Dap has on metabolism in S. enterica, and likely other organisms, and highlight the

25 acteria such as Escherichia coli, Salmonella enterica, and Listeria innocua, on stainless steel surfa

26 Strains of Salmonella enterica, and other organisms lacking RidA, have diverse

27 ding Corynebacterium diphtheriae, Salmonella enterica, and Vibrio cholerae, are infected with lysogen

28 ange distribution in a lineage of Salmonella enterica, and we discuss many other potential applicatio

29 Salmonella enterica are invasive intracellular pathogens that repli

30 Escherichia coli and Salmonella enterica are models for many experiments in molecular bi

31 The same residues in S. enterica ArnT are also needed for function.

32 rancisella tularensis, as well as Salmonella enterica bacteria transferred from infected cells to uni

33 a-lyase (DpaL) alleviated Dap toxicity in S. enterica by catalyzing the degradation of Dap to pyruvat

34 l utilization microcompartment of Salmonella enterica can be controlled using two strategies: by modu

35 ively, our findings indicate that Salmonella enterica can promote transformation of genetically predi

36 Salmonella enterica catabolizes ethanolamine inside a compartment k

37 Serovars of Salmonella enterica cause both gastrointestinal and systemic diseas

38 Salmonella enterica causes systemic diseases (typhoid and paratypho

39 We also show that a S. enterica cobT strain that synthesizes GkCblS ectopically

40 MSX and MSO inhibited the growth of an S. enterica DeltamddA strain unless glutamine or methionine

41 SpvD is a Salmonella enterica effector protein that we previously demonstrate

42 APK and AKT pathways, mediated by Salmonella enterica effectors secreted during infection, is critica

43 , we demonstrate that Dap accumulation in S. enterica elicits a proline requirement for growth and sp

44 Recent papers have shown that the Salmonella enterica FinO-domain protein ProQ binds a large suite of

45 In the Gram-negative bacterium Salmonella enterica, FlgM inhibits late-class flagellar gene expres

46 Insertions in the Salmonella enterica fra locus, which encodes the fructose-asparagin

47 l DNA and glucuronide binding affinity to S. enterica GusR.

48 of fluoroquinolone resistance in Salmonella enterica has become increasingly difficult due to evolvi

49 biochemical studies, primarily in Salmonella enterica, have defined a role for RidA in responding to

50 t crystal structures of wild type Salmonella enterica HisA (SeHisA) in its apo-state and of mutants D

51 ith Burkholderia pseudomallei and Salmonella enterica HMBA treatment was also associated with better

52 f GusRs from Escherichia coli and Salmonella enterica in complexes with a glucuronide ligand.

53 emporal dynamics of Salmonella enterica spp. enterica in feedlot cattle.

54 in situ hybridization identified Salmonella enterica in the liver, subsequently confirmed as S. ente

55 vZ-OmpR two-component system from Salmonella enterica in vitro and in vivo, which directly contribute

56 of the selective pressures encountered by S. enterica in vivo.

57 pidemiology of diseases caused by Salmonella enterica in West Africa.

58 osphoribosyltransferases (CobT in Salmonella enterica), in a reaction that is considered to be the ca

59 rne pathogens E. coli O157:H7 and Salmonella enterica, in detail a nucleic acid lateral flow and an e

60 lla Typhi infection, we show that Salmonella enterica induces malignant transformation in predisposed

61 del to culture-confirmed cases of Salmonella enterica infections at Queen Elizabeth Central Hospital,

62 invasive infections due to non-typhoidal S. enterica infections resulted in the highest burden, caus

63 mon manifestation of nontyphoidal Salmonella enterica infections, but little is known about the patho

64 tality for invasive non-typhoidal Salmonella enterica infections, we excluded cases attributed to HIV

65 Salmonella enterica is a leading cause of community-acquired bloods

66 EutT from Salmonella enterica is a member of a class of enzymes termed ATP:Co

67 Salmonella enterica is a ubiquitous Gram-negative intracellular bac

68 Salmonella enterica is among the most burdensome of foodborne disea

69 Salmonella enterica is one such pathogen, exploiting multiple aspec

70 Salmonella enterica is the leading etiologic agent of bacterial foo

71 ity to detect low-level-resistant Salmonella enterica isolates that are not serotype Typhi.

72 inolone resistance in a collection of 136 S. enterica isolates, including 111 with intermediate or re

73 niae, Mycobacterium tuberculosis, Salmonella enterica, Klebsiella pneumoniae, and Escherichia coli We

74 escein, biotin and digoxigenin coding for S. enterica, L. monocytogenes and E. coli, respectively.

75 lS proteins restore alpha-RP synthesis in S. enterica lacking the CobT enzyme.

76 ganisms such as Escherichia coli, Salmonella enterica, Listeria innocua, Mycobacterium parafortuitum,

77 Simultaneous detection of Salmonella enterica, Listeria monocytogenes and Escherichia coli ba

78 pon recombinant expression of the Salmonella enterica LT2 ethanolamine utilization bacterial microcom

79 We further demonstrate that S. enterica LT2 retained the ability to grow on 1,2-propane

80 Serovars of Salmonella enterica, namely Typhi and Typhimurium, reportedly, are

81 Salmonella enterica natively possesses both the Pdu and Eut operons

82 EutQ is required during anoxic growth of S. enterica on ethanolamine and tetrathionate.

83 erotypes impact the ecology of pathogenic S. enterica on-farm.

84 Phase variation of the Salmonella enterica opvAB operon generates a bacterial lineage with

85 ad-seq) in the bacterial pathogen Salmonella enterica, partitioning its coding and noncoding transcri

86 the roles of their aligned Y. pestis and S. enterica partners and showed that up to 73% of the predi

87 agocytic host cells is central to Salmonella enterica pathogenicity and dependent on multiple genes w

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

89 rica ridA causes Ser sensitivity and that S. enterica RidA and its homologs from other organisms hydr

90 It is known that deleting Salmonella enterica ridA causes Ser sensitivity and that S. enteric

91 g complemented the Ser sensitivity of the S. enterica ridA mutant.

92 Because Salmonella enterica ser. Typhimurium can overcome metal ion starvat

93 gation of a recurrent blood-borne Salmonella enterica serotype Enteritidis (S.

94 g molecular subtyping methods for Salmonella enterica serotype Enteritidis and survey the population

95 between nalidixic acid-resistant Salmonella enterica serotype Enteritidis infections in the United S

96 A total of 52 S. enterica serotype Enteritidis isolates representing 16 m

97 ulation structure of commonly encountered S. enterica serotype Enteritidis outbreak isolates in the U

98 major lineages and ecological origins of S. enterica serotype Enteritidis.

99 a in the liver, subsequently confirmed as S. enterica serotype I 4,5,12:-:1,2.

100 ch 1, 2010, and Jan 31, 2014, 135 Salmonella enterica serotype Typhi (S Typhi) and 94 iNTS isolates w

101 (ie, blood cultures positive for Salmonella enterica serotype Typhi, or Paratyphi A, B, or C) on day

102 r colonization and persistence of Salmonella enterica serotype Typhimurium in chickens.

103 Salmonella enterica serotype Typhimurium is a food-borne pathogen t

104 d colonization resistance of mice against S. enterica serotype Typhimurium.

105 phoid-causing infectious bacteria Salmonella enterica serovar (Salmonella typhi) in 10 muL of sample

106 ovar Enteritidis, and 3% (3) were Salmonella enterica serovar Arizonae.

107 mice against the group D serovar Salmonella enterica serovar Dublin (85% vaccine efficacy).

108 e infection in different hosts, including S. enterica serovar Enteritidis (multiple hosts), S. Gallin

109 capacities of S. Typhimurium and Salmonella enterica serovar Enteritidis DeltaguaBA DeltaclpX live o

110 e epidemiological surveillance of Salmonella enterica serovar Enteritidis for over 2 decades.

111 Salmonella enterica serovar Enteritidis is a significant cause of g

112 ntly detected a large outbreak of Salmonella enterica serovar Enteritidis phage type 14b affecting mo

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

114 epidemiological paradox surrounds Salmonella enterica serovar Enteritidis.

115 ferentiate the two invasive avian-adapted S. enterica serovar Gallinarum biotypes Gallinarum and Pull

116 uman cases of ceftiofur-resistant Salmonella enterica serovar Heidelberg in Quebec and Ontario attrib

117 athogenic, Gram-negative bacteria Salmonella enterica serovar Montevideo.

118 he first human challenge model of Salmonella enterica serovar Paratyphi A infection.

119 Salmonella enterica serovar Paratyphi A is a human-specific serovar

120 ovar Typhi or Salmonella enterica subspecies enterica serovar Paratyphi A or C were only isolated in

121 isplaced by infections with drug-resistant S enterica serovar Paratyphi A.

122 onella enterica serovar Typhi and Salmonella enterica serovar Sendai, causes enteric fever.

123 fections with Salmonella enterica subspecies enterica serovar Senftenberg are often associated with e

124 Salmonella enterica serovar Senftenberg is a common nontyphoidal Sa

125 mice against the group B serovar Salmonella enterica serovar Stanleyville (91% vaccine efficacy), an

126 reas of Asia, multidrug-resistant Salmonella enterica serovar Typhi (S Typhi) has been the main cause

127 n, to influence susceptibility to Salmonella enterica serovar Typhi (S Typhi) infection.

128 Salmonella enterica serovar Typhi (S Typhi) is responsible for an e

129 genome sequence analysis of 1,832 Salmonella enterica serovar Typhi (S. Typhi) identifies a single do

130 The population of Salmonella enterica serovar Typhi (S. Typhi), the causative agent o

131 cific serovar that, together with Salmonella enterica serovar Typhi and Salmonella enterica serovar S

132 Salmonella enterica serovar Typhi causes the systemic disease typho

133 Multiyear epidemics of Salmonella enterica serovar Typhi have been reported from countries

134 Indian subcontinent, with chronic Salmonella enterica serovar Typhi infection reported as a significa

135 Salmonella enterica serovar Typhi is a human-restricted Gram-negati

136 Salmonella enterica serovar Typhi is the etiological agent of typho

137 eport a typhoid fever case with a Salmonella enterica serovar Typhi isolate showing extended spectrum

138 ults from systemic infection with Salmonella enterica serovar Typhi or Paratyphi pathovars A, B or C(

139 Salmonella enterica subspecies enterica serovar Typhi or Salmonella enterica subspecies

140 Here we used a live attenuated Salmonella enterica serovar Typhi strain to create a bivalent mucos

141 ho acquired a Salmonella enterica subspecies enterica serovar Typhi strain with resistance against be

142 m-beta-lactamase (ESBL)-producing Salmonella enterica serovar Typhi was identified, whole-genome sequ

143 sia spp., Salmonella enterica and Salmonella enterica serovar Typhi, and Yersinia pestis), and 3 prot

144 causative agent of typhoid fever, Salmonella enterica serovar Typhi, can partially subvert this criti

145 Enteric fever, caused by Salmonella enterica serovar Typhi, is an important public health pr

146 Salmonella enterica serovar Typhi, the causative agent of typhoid f

147 ed salmonellae, 14% (21/152) were Salmonella enterica serovar Typhi, whereas 86% (131/152) were serov

148 acteremia, with a predominance of Salmonella enterica serovar Typhi.

149 eable Haemophilus influenzae, and Salmonella enterica serovar Typhi/Typhimurium.

150 erotyped were Salmonella enterica subspecies enterica serovar Typhimurium (45% [116/258] of which wer

151 FrmR from Salmonella enterica serovar typhimurium (a CsoR/RcnR-like transcrip

152 coli, Yersinia enterocolitica and Salmonella enterica serovar Typhimurium (all gram-negative bacteria

153 (+)-coupled melibiose permease of Salmonella enterica serovar Typhimurium (MelBSt) demonstrates that

154 hat l-asparaginase II produced by Salmonella enterica serovar Typhimurium (S Typhimurium) inhibits T

155 more resistant to infection with Salmonella enterica serovar Typhimurium (S Typhimurium).

156 Salmonella enterica serovar Typhimurium (S.

157 lular [Listeria monocytogenes and Salmonella enterica serovar Typhimurium (S.

158 en investigated in the context of Salmonella enterica serovar Typhimurium (ST).

159 s using curli fibers, produced by Salmonella enterica serovar Typhimurium and Escherichia coli.

160 Bacteriophage P22 infects Salmonella enterica serovar Typhimurium and is a model for icosahed

161 nd other pathogens that use T3SS, Salmonella enterica serovar Typhimurium and Yersinia pseudotubercul

162 configuration is proposed for the Salmonella enterica serovar Typhimurium ArnT.

163 intracellular bacterial pathogen Salmonella enterica serovar Typhimurium as shown by their superior

164 exneri and the vT3SS and fT3SS of Salmonella enterica serovar Typhimurium at ~5 and ~4 nm resolution

165 The food-borne pathogen Salmonella enterica serovar Typhimurium benefits from acute inflamm

166 Salmonella enterica serovar Typhimurium can inject effector protein

167 Conversely, Salmonella enterica serovar Typhimurium causes gastroenteritis in h

168 -negative intracellular bacterium Salmonella enterica serovar Typhimurium causes persistent systemic

169 nts and a reduced ability to kill Salmonella enterica serovar Typhimurium compared to that of macroph

170 The ST313 pathovar of Salmonella enterica serovar Typhimurium contributes to a high burde

171 We also demonstrate that the Salmonella enterica serovar Typhimurium core promoter is more activ

172 ter membrane vesicles (OMVs) from Salmonella enterica serovar Typhimurium displaying the variable N t

173 important colonization niche for Salmonella enterica serovar Typhimurium during gastrointestinal inf

174 we show that Salmonella enterica subspecies enterica serovar Typhimurium employs a dedicated mechani

175 A recent study showed that Salmonella enterica serovar Typhimurium exhibits sliding motility u

176 Salmonella enterica serovar Typhimurium exploits the host's type I

177 ing (TraDIS) to screen mutants of Salmonella enterica serovar Typhimurium for their ability to infect

178 ide analysis of core genes within Salmonella enterica serovar Typhimurium genomes reveals a high degr

179 totriosidase and a chitinase from Salmonella enterica serovar Typhimurium hydrolyze LacNAc from Galbe

180 the concentrations, inhibits E. coli and S. enterica serovar Typhimurium in an additive or antagonis

181 ignaling pathway and promote virulence of S. enterica serovar Typhimurium in mice.

182 We found that intracellular Salmonella enterica serovar Typhimurium induced the binucleation of

183 ously in pathogen and host during Salmonella enterica serovar Typhimurium infection and reveal the mo

184 Salmonella enterica serovar Typhimurium infection of immunocompeten

185 CARD9 is suppressed during Salmonella enterica serovar Typhimurium infection, facilitating inc

186 Salmonella enterica serovar Typhimurium is a bacterial pathogen cau

187 Salmonella enterica serovar Typhimurium is a common cause of food-b

188 Salmonella enterica serovar Typhimurium is a food-borne pathogen th

189 Salmonella enterica serovar Typhimurium is a Gram-negative food-bor

190 vivo innate immune resistance of Salmonella enterica serovar Typhimurium is attributed to the high-m

191 allosteric mechanism of FrmR from Salmonella enterica serovar Typhimurium is triggered by metals in v

192 and multilocus sequence typing on Salmonella enterica serovar Typhimurium isolates was performed.

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

194 ations were absent in the closely related S. enterica serovar Typhimurium LT2 and from a mutant of S

195 richia coli K12, E. coli O157:H7, Salmonella enterica serovar Typhimurium LT2, Staphylococcus aureus,

196 lically competent, but avirulent, Salmonella enterica serovar Typhimurium mutant for its ability to c

197 the structure of the prototypical Salmonella enterica serovar Typhimurium pathogenicity island 1 basa

198 of the tviA gene in nontyphoidal Salmonella enterica serovar Typhimurium reduced flagellin-induced p

199 by the enteropathogenic bacterium Salmonella enterica serovar Typhimurium requires a T6SS encoded wit

200 The intracellular pathogen Salmonella enterica serovar Typhimurium requires the mgtC gene to c

201 07 against the genomes of S. enterica subsp. enterica serovar Typhimurium strain LT2 and Salmonella b

202 We genetically engineered a Salmonella enterica serovar Typhimurium strain of multilocus sequen

203 om Mycobacterium tuberculosis, in Salmonella enterica serovar Typhimurium strain SL3261.

204 s bacteriostatic activity against Salmonella enterica serovar Typhimurium that is not shared by the r

205 ystem coordinates the response of Salmonella enterica serovar Typhimurium to diverse environmental ch

206 study, we examined the ability of Salmonella enterica serovar Typhimurium to infect the central nervo

207 ivo by the CspA family members of Salmonella enterica serovar Typhimurium to link the constitutively

208 ulator (Fur) in the resistance of Salmonella enterica serovar Typhimurium to the reactive nitrogen sp

209 fine YvyG as an orthologue of the Salmonella enterica serovar Typhimurium type III secretion system c

210 Conversely, Salmonella enterica serovar Typhimurium uses a T3SS encoded by Salm

211 show that the intestinal pathogen Salmonella enterica serovar Typhimurium uses specialized metal tran

212 Salmonella enterica serovar Typhimurium utilizes molecular hydrogen

213 action between FlgM and FliS from Salmonella enterica serovar Typhimurium was characterized using gel

214 pigs experimentally infected with Salmonella enterica serovar Typhimurium was investigated.

215 Listeria monocytogenes V7 and Salmonella enterica serovar Typhimurium were used as model pathogen

216 Cs) to explore the interaction of Salmonella enterica serovar Typhimurium with iHOs.

217 ved genes in the PhoPQ regulon of Salmonella enterica serovar Typhimurium with that of PhoPQ-regulate

218 Salmonella (Salmonella enterica serovar Typhimurium) secrete numerous effector

219 ve bacteria (Escherichia coli and Salmonella enterica serovar Typhimurium).

220 typed NTS isolates, 40% (41) were Salmonella enterica serovar Typhimurium, 10% (10) were Salmonella e

221 phoidal salmonellae, particularly Salmonella enterica serovar Typhimurium, are a major cause of invas

222 For the human and animal pathogen Salmonella enterica serovar Typhimurium, biofilm formation is corre

223 , either Klebsiella pneumoniae or Salmonella enterica serovar Typhimurium, enhanced translocation.

224 In Salmonella enterica serovar Typhimurium, flagella-mediated motility

225 hydrophobic peptide expressed in Salmonella enterica serovar Typhimurium, inhibits growth in macroph

226 In Salmonella enterica serovar Typhimurium, Mg(2+) limitation induces

227 hagic Escherichia coli (EHEC) and Salmonella enterica serovar Typhimurium, or the surrogate murine in

228 -phasor maps of Escherichia coli, Salmonella enterica serovar Typhimurium, Pseudomonas aeruginosa, Ba

229 c changes in Escherichia coli and Salmonella enterica serovar Typhimurium, suggesting that CyaY and Y

230 Unlike the nontyphoidal Salmonella enterica serovar Typhimurium, the genomes of S. Typhi an

231 individual functions, strains of Salmonella enterica serovar Typhimurium, the murine model of S Typh

232 for type III protein secretion in Salmonella enterica serovar Typhimurium, we discovered that several

233 coccus aureus and Salmonella enterica subsp. enterica serovar Typhimurium, were exposed to 25 kGy gam

234 t the Mg(2+) channel gene corA in Salmonella enterica serovar Typhimurium, which was previously thoug

235 protein can efficiently attenuate Salmonella enterica serovar Typhimurium-induced pyroptosis and proi

236 acultative intracellular pathogen Salmonella enterica serovar Typhimurium.

237 holerae and the invasive pathogen Salmonella enterica serovar Typhimurium.

238 mulation or upon coinfection with Salmonella enterica serovar Typhimurium.

239 ogical and virulence functions in Salmonella enterica serovar Typhimurium.

240 ptibility to hydrogen peroxide in Salmonella enterica serovar Typhimurium.

241 ular states of the model pathogen Salmonella enterica serovar Typhimurium.

242 enation, and aerobic expansion of Salmonella enterica serovar Typhimurium.

243 Salmonella enterica serovars Enteritidis and Kentucky differ greatl

244 burden of enteric fever caused by Salmonella enterica serovars Typhi and Paratyphi is substantial and

245 fever (39 degrees C-42 degrees C) Salmonella enterica serovars Typhi, Paratyphi A, and Sendai signifi

246 al Salmonella (NTS), particularly Salmonella enterica serovars Typhimurium and Enteritidis, is respon

247 SpvD is highly conserved across different S. enterica serovars, but residue 161, located close to the

248 apA), Shigella spp. (ipaH), and a Salmonella enterica-specific (SE) DNA sequence at seven Great Lakes

249 F (Pseudomonas aeruginosa), PrgI (Salmonella enterica SPI-1), SsaG (Salmonella enterica SPI-2), or Mx

250 Salmonella enterica SPI-1), SsaG (Salmonella enterica SPI-2), or MxiH (Shigella flexneri).

251 yphi A, and genes conserved among Salmonella enterica spp. and utilized strongly magnetized nanoparti

252 cline on the temporal dynamics of Salmonella enterica spp. enterica in feedlot cattle.

253 d Citrobacter rodentium Moreover, Salmonella enterica strains encode up to three NleB orthologs named

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

255 y of various Escherichia coli and Salmonella enterica strains.

256 bongori, S. enterica subsp. salamae, and S. enterica subsp. arizonae share features of the infection

257 , S. enterica subsp. salamae, and Salmonella enterica subsp. arizonae The beta-lactamase TEM-1 report

258 omain with a nuclease domain from Salmonella enterica subsp. arizonae This modified V. cholerae strai

259 mae strain 3588/07 against the genomes of S. enterica subsp. enterica serovar Typhimurium strain LT2

260 cereus, Staphylococcus aureus and Salmonella enterica subsp. enterica serovar Typhimurium, were expos

261 S. enterica subsp. salamae encodes the Salmonella pathogeni

262 Concurrently, S. enterica subsp. salamae infection of J774.A1 macrophages

263 are missing (e.g., avrA, sopB, and sseL), S. enterica subsp. salamae invades HeLa cells and contains

264 mpared a draft genome assembly of Salmonella enterica subsp. salamae strain 3588/07 against the genom

265 These results show that S. bongori, S. enterica subsp. salamae, and S. enterica subsp. arizonae

266 identified EspJ homologues in S. bongori, S. enterica subsp. salamae, and Salmonella enterica subsp.

267 species enterica serovar Typhi or Salmonella enterica subspecies enterica serovar Paratyphi A or C we

268 Human infections with Salmonella enterica subspecies enterica serovar Senftenberg are oft

269 Salmonella enterica subspecies enterica serovar Typhi or Salmonella

270 report a traveler who acquired a Salmonella enterica subspecies enterica serovar Typhi strain with r

271 4.2%) NTS isolates serotyped were Salmonella enterica subspecies enterica serovar Typhimurium (45% [1

272 Here we show that Salmonella enterica subspecies enterica serovar Typhimurium employs

273 Within Salmonella enterica subspecies enterica, a single lineage exists th

274 Most lineages of the S. enterica subspecies Typhimurium cause gastroenteritis in

275 cing EcN to mice previously infected with S. enterica substantially reduced intestinal colonization b

276 In Salmonella enterica, sulfur is trafficked to both thiamine biosynth

277 Our results indicate that S. enterica synthesizes alpha-R, a metabolite that had not

278 The common human pathogen Salmonella enterica takes up citrate as a nutrient via the sodium s

279 l drug resistance is a growing problem in S. enterica that threatens to further compromise patient ou

280 prolonged exposure to heat-killed Salmonella enterica, the Gram-positive bacterium Bacillus subtilis,

281 ngs indicate that the sensor PhoQ enables S. enterica to respond to both host- and bacterial-derived

282 on system (T3SS) of intracellular Salmonella enterica translocates effector proteins into mammalian c

283 n host cells such as macrophages, Salmonella enterica translocates virulence (effector) proteins acro

284 en-specific depolymerase enzyme missing in S enterica Typhi, and we exploited this enzyme to isolate

285 Two major serovars of Salmonella enterica, Typhi and Typhimurium, have evolved a two-comp

286 intrabacterial redox dynamics of Salmonella enterica Typhimurium (S. Typhimurium) residing inside ma

287 stric infections of Gram-negative Salmonella enterica Typhimurium (ST), a major source of human food

288 phoQ(W104C-A128C) Salmonella enterica Typhimurium is virulent in mice, indicating tha

289 accine, rabbits were orally infected with S. enterica Typhimurium strain chi3987 harboring phagemid N

290 l cells, particularly E. coli and Salmonella enterica Typhimurium.

291 a major lipid in E. coli Last, in Salmonella enterica, ubiK was required for proliferation in macroph

292 Dap accumulation in Salmonella enterica was previously shown to inhibit growth by unkno

293 vestigation of host adaptation in Salmonella enterica We highlight the value of the method in identif

294 S from either Escherichia coli or Salmonella enterica were directly infused into the mass spectromete

295 Antibiotic-resistant isolates of Salmonella enterica were selected on plates containing lethal conce

296 agents, especially non-typhoidal Salmonella enterica, were also responsible for the majority of deat

297 Some hazards, such as non-typhoidal S. enterica, were important causes of FBD in all regions of

298 , including Bacillus subtilis and Salmonella enterica which are predicted to have up to 18,000 and 31

299 used transcriptional differences between S. enterica wild-type and ridA strains to explore the bread

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