ライフサイエンスコーパス: enterica

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

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

3 redox conduit in both E. coli and Salmonella enterica.

4 ntial endoribonuclease RNase E in Salmonella enterica.

5 challenged C. jejuni and natural Salmonella enterica.

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

7 E. coli and the related pathogen Salmonella enterica.

8 ections with distinct serovars of Salmonella enterica.

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

10 usly uncharacterized branch that contains S. enterica adapted to multiple mammalian species.

11 Despite the high genetic diversity of S. enterica, all ancient bacterial genomes clustered in a s

12 innocua, Pseudomonas fluorescens, Salmonella enterica and Bacillus cereus has not been previously rep

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

14 show related protein domains from Salmonella enterica and Escherichia coli possess similar reactivity

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

16 action using purified DndCDE from Salmonella enterica and IscS from Escherichia coli.

17 uitous serovars of the bacterial pathogen S. enterica and recently has been emerging in many countrie

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

19 hia coli, Listeria monocytogenes, Salmonella enterica and Staphylococcus aureus.

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

21 f the important enteric pathogens Salmonella enterica and Vibrio cholerae by repressing AraC-type tra

22 bacteria strains (B. cereus, E. coli, and S. enterica) and a yeast cell (S. cerevisiae), ranging in s

23 e median C(T) values for M. tuberculosis, S. enterica, and EBV cfDNA were significantly lower in bloo

24 yzing 720 Listeria monocytogenes, Salmonella enterica, and Escherichia coli short-read datasets, we d

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

26 In Escherichia coli, Salmonella enterica, and many other gamma-proteobacteria, the trans

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

28 niae, Mycobacterium tuberculosis, Salmonella enterica, and Staphylococcus aureus, we report that it i

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

30 Salmonella enterica are invasive intracellular pathogens that repli

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

32 from Mycobacterium tuberculosis, Salmonella enterica, Aspergillus fumigatus, and Epstein-Barr virus

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

34 to be RNase E, the major endoribonuclease in enterica bacteria.

35 Salmonella enterica bloodstream infections are an important cause o

36 B-12, [13C]-cyanocobalamin, using Salmonella enterica by providing [13C2]-ethanolamine as a sole carb

37 chia coli, Shigella flexneri, and Salmonella enterica can all fold to form self-complemented monomers

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

39 causative agent of salmonellosis, Salmonella enterica, can occur as a result of eco-evolutionary forc

40 Salmonella enterica catabolizes ethanolamine inside a compartment k

41 Serovars of Salmonella enterica cause both gastrointestinal and systemic diseas

42 Salmonella enterica causes systemic diseases (typhoid and paratypho

43 , phosphorothioate epigenetics in Salmonella enterica Cerro 87, and oxidation-induced abasic sites in

44 like those from Vibrio cholerae, Salmonella enterica, Clostridioides difficile, or Streptococcus pyo

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

46 The pathogenesis of S. enterica depends on flagella, which are appendages that

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

48 The Salmonella enterica effector SteD depletes mature MHC class II (mMH

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

50 um parvum, Entamoeba histolytica, Salmonella enterica, enterotoxigenic Escherichia coli, Vibrio chole

51 illnesses caused by Salmonella enterica (S. enterica) every year.

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

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

54 e recovered eight Salmonella enterica subsp. enterica genomes from human skeletons of transitional fo

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

56 RA domains from Escherichia coli, Salmonella enterica, Haemophilus ducreyi and Neisseria gonorrhoeae,

57 eningitidis, Vibrio cholerae, and Salmonella enterica harbor these prophages.

58 Multidrug-resistant (MDR) Salmonella enterica has been deemed a high-priority pathogen by the

59 The intracellular pathogen Salmonella enterica has evolved an array of traits for propagation

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

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

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

63 to decrease colonization of C. jejuni and S. enterica in poultry gut along with other beneficial attr

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

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

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

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

68 Salmonella enterica including Salmonella Typhi and nontyphoidal Sal

69 ClpS substrates in the bacterium Salmonella enterica, including SpoT, the essential synthase/hydrola

70 We report that Salmonella enterica increases the specificity of the broadly conser

71 rveillance for nontyphoidal and typhoidal S. enterica infections among inpatients and outpatients at

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

73 Salmonella enterica is among the most burdensome of foodborne disea

74 ncept that the emergence of human-adapted S. enterica is linked to human cultural transformations.

75 to study 90 antimicrobial resistant (AMR) S. enterica isolates from bovine and human hosts in New Yor

76 AP by analyzing the genomes of 26 Salmonella enterica isolates from Shanghai, China.

77 Two hundred and sixty-four Salmonella enterica isolates recovered over a 16-year period (2000

78 f the pathogens Escherichia coli, Salmonella enterica, Klebsiella pneumoniae and Acinetobacter bauman

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

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

81 chanisms underlying the switch in Salmonella enterica lifestyles from the infectious form to a dorman

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

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

84 eriments, WbaP(Mx) complemented a Salmonella enterica mutant lacking the endogenous WbaP that primes

85 llelic diversity (panallelome) of Salmonella enterica, Mycobacterium tuberculosis, Pseudomonas aerugi

86 Of pathogens, 171 (44.6%) were Salmonella enterica of which 129 (75.4%) were Salmonella Typhi, and

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

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

89 nch that also includes the human-specific S. enterica Paratyphi C, illustrating the evolution of a hu

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

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

92 The most common Salmonella enterica pathovariant associated with invasive nontyphoi

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

94 pulation transmission appear to shape AMR S. enterica population structure in different hosts and geo

95 al pathogens Escherichia coli and Salmonella enterica produce a biofilm matrix composed primarily of

96 With hosts such as Salmonella enterica, Pseudomonas aeruginosa, and Erwinia amylovora,

97 mplemented the growth defect of a Salmonella enterica ridA mutant, an in vivo model of 2AA stress.

98 lop foodborne illnesses caused by Salmonella enterica (S. enterica) every year.

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

100 a large multi-country outbreak of Salmonella enterica serotype Enteritidis in the EU and European Eco

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

102 We reviewed Salmonella enterica serotype Typhi infections reported to the Cente

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

104 Salmonella enterica serotype Typhimurium (S. Typhimurium) boasts a

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

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

107 , a bacterial infection caused by Salmonella enterica serotypes Typhi and Paratyphi A, frequently pre

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

109 me and plasmid of Salmonella enterica subsp. enterica serovar Bareilly and Escherichia coli O157:H7.

110 Analysis of the distribution of Salmonella enterica serovar Derby (S.

111 Salmonella enterica serovar Enteritidis is a common cause of foodbo

112 Salmonella enterica serovar Enteritidis is a major cause of foodbor

113 neonatal chick colonization with Salmonella enterica serovar Enteritidis requires a virulence-factor

114 Overall this work shows that S. enterica serovar Enteritidis strains circulating in Urug

115 epidemiological paradox surrounds Salmonella enterica serovar Enteritidis.

116 Salmonella enterica serovar Infantis (S.

117 We also show that CBA120 infects Salmonella enterica serovar Minnesota, and this host range expansio

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

119 e present a focused minireview on Salmonella enterica serovar Panama, a serovar responsible for invas

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

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

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

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

124 is caused by Salmonella enterica subspecies enterica serovar Typhi (S. Typhi) and can lead to system

125 Salmonella enterica serovar Typhi (S. Typhi) causes substantial mor

126 estion and subsequent invasion of Salmonella enterica serovar Typhi (S. Typhi), a human-restricted pa

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

128 resistance (AMR) in the bacterium Salmonella enterica serovar Typhi (S. Typhi).

129 Salmonella enterica subspecies enterica serovar Typhi (Salmonella Typhi) is the cause o

130 Salmonella enterica serovar Typhi causes the systemic disease typho

131 Salmonella enterica serovar Typhi causes typhoid fever only in huma

132 ions, with the causative pathogen Salmonella enterica serovar Typhi implicated in many outbreaks thro

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

134 Salmonella enterica serovar Typhi is the etiological agent of typho

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

136 Salmonella enterica serovar Typhi isolates from the 2 hospitals wit

137 the secretion of Typhoid toxin in Salmonella enterica serovar Typhi relies on a muramidase.

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

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

140 70s, this threat has increased in Salmonella enterica serovar Typhi, driven in part by the emergence

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

142 id toxin is a virulence factor of Salmonella enterica serovar Typhi, the causative agent of typhoid f

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

144 opment of antimicrobial-resistant Salmonella enterica serovar Typhi.

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

146 ty to bacterial pathogens such as Salmonella enterica serovar Typhimurium (7.8%), Listeria monocytoge

147 The human pathogen Salmonella enterica serovar Typhimurium (S Typhimurium) contains a

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

149 Salmonella enterica serovar Typhimurium (S Typhimurium) is a Gram-n

150 Salmonella enterica serovar Typhimurium (S Typhimurium) relies upon

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

152 Salmonella enterica serovar Typhimurium (S.

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

154 al regulatory system PhoP/PhoQ of Salmonella enterica serovar Typhimurium (S. Typhimurium) in mildly

155 fection of human macrophages with Salmonella enterica serovar Typhimurium (S. Typhimurium) leads to i

156 d a mouse model of infection with Salmonella enterica serovar Typhimurium (STM) to identify changes i

157 se against the bacterial pathogen Salmonella enterica serovar Typhimurium (STm).

158 curate detection of low levels of Salmonella enterica serovar typhimurium and enteritidis in blood sa

159 cteria (Escherichia coli O157:H7, Salmonella enterica serovar Typhimurium and S.

160 ection by two bacterial pathogens-Salmonella enterica serovar Typhimurium and Shigella flexneri.

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

162 two species, Escherichia coli and Salmonella enterica serovar Typhimurium as model microbes, a common

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

164 Salmonella enterica serovar Typhimurium can inject effector protein

165 Conversely, Salmonella enterica serovar Typhimurium causes gastroenteritis in h

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

167 Bloodstream infections by Salmonella enterica serovar Typhimurium constitute a major health b

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

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

170 acultative intracellular pathogen Salmonella enterica serovar Typhimurium decreases H-NS amounts 16-f

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

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

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

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

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

176 susceptibilities to infection by Salmonella enterica serovar Typhimurium has just been published in

177 is proposed to restrict growth of Salmonella enterica serovar Typhimurium in host tissues by causing

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

179 3) can disrupt biofilms formed by Salmonella enterica serovar Typhimurium in vitro and in vivo.

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

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

182 renders cells more susceptible to Salmonella enterica serovar Typhimurium infection in a NOD1-depende

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

184 During Salmonella enterica serovar Typhimurium infection, host inflammatio

185 ition, the intracellular pathogen Salmonella enterica serovar Typhimurium initiates an anti-inflammat

186 Salmonella enterica serovar Typhimurium is a facultative intracellu

187 Salmonella enterica serovar Typhimurium is an intracellular bacteri

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

189 mal intervention for inactivating Salmonella enterica serovar Typhimurium LT2 (ST2) in tender coconut

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

191 n bacterial microcompartment from Salmonella enterica serovar Typhimurium LT2, one of the most widely

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

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

194 in IRG1 rescued the virulence defect of a S. enterica serovar Typhimurium mutant specifically defecti

195 fe including turtles, but S. enterica subsp. enterica serovar Typhimurium or lesions associated with

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

197 ing proteins PrgH and PrgK in the Salmonella enterica serovar Typhimurium Salmonella pathogenicity is

198 on TNF-alpha and Salmonella enterica subsp. enterica serovar Typhimurium secretome (STS)-induced out

199 07 against the genomes of S. enterica subsp. enterica serovar Typhimurium strain LT2 and Salmonella b

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

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

202 he persistence of Salmonella enterica subsp. enterica serovar Typhimurium through liver-resident immu

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

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

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

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

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

208 , G, I, K, N, O, and Q); however, Salmonella enterica serovar Typhimurium was the most predominant se

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

210 me PCR detection of low levels of Salmonella enterica serovar Typhimurium without culture enrichment.

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

212 Salmonella enterica serovar Typhimurium, a Gram-negative bacterium,

213 In Salmonella enterica serovar Typhimurium, DSFs repress the activity

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

215 We show that both flagellins of Salmonella enterica serovar Typhimurium, FliC and FljB, are methyla

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

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

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

219 ection initiation of phage P22 in Salmonella enterica serovar Typhimurium, revealing how a channel fo

220 In Salmonella enterica serovar Typhimurium, siroheme is produced by a

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

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

223 g defect in their ability to kill Salmonella enterica serovar Typhimurium, which was rescuable after

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

225 Testing the methodology on Salmonella enterica serovar Typhimurium-infected murine bone-marrow

226 n with enteric pathogens, such as Salmonella enterica serovar Typhimurium.

227 ch as Clostridium perfringens and Salmonella enterica serovar Typhimurium.

228 duct phenotypic comparison with the model S. enterica serovar Typhimurium.

229 holerae and the invasive pathogen Salmonella enterica serovar Typhimurium.

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

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

232 acultative intracellular pathogen Salmonella enterica serovar Typhimurium.

233 to bacterial infections, such as Salmonella enterica serovar Typhimurium.

234 lines, typically challenged with Salmonella enterica serovar Typhimurium.

235 Although S. enterica serovars Enteritidis and Typhimurium are respon

236 persistence of international lineages of S. enterica serovars in food production chain is supported

237 haracteristics and genomes of 10 atypical S. enterica serovars linked to multistate foodborne outbrea

238 ages belonging to 28 serovars, including, S. enterica serovars S.

239 led multiple independent lineages such as S. enterica serovars S.

240 ure to the dominant NTS serovars, Salmonella enterica serovars Typhimurium and Enteritidis, were asse

241 Salmonella enterica subsp. enterica serovars Typhimurium and its four closest relat

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

243 ility of PCR for the detection of Salmonella enterica shedding and to compare that ability to culture

244 Studies in Escherichia coli and Salmonella enterica showed that such sRNAs are natural products of

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

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

247 um NleB effectors, as well as the Salmonella enterica SseK effectors are glycosyltransferases that mo

248 erococcus spp., Escherichia coli, Salmonella enterica, Staphylococcus aureus and Streptococcus pneumo

249 t that typhoidal and nontyphoidal Salmonella enterica strains activate MAIT cells.

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

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

252 y of various Escherichia coli and Salmonella enterica strains.

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

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

255 Here, we recovered eight Salmonella enterica subsp. enterica genomes from human skeletons of

256 entire chromosome and plasmid of Salmonella enterica subsp. enterica serovar Bareilly and Escherichi

257 y shed by wildlife including turtles, but S. enterica subsp. enterica serovar Typhimurium or lesions

258 secretome (LrS) on TNF-alpha and Salmonella enterica subsp. enterica serovar Typhimurium secretome (

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

260 contribute to the persistence of Salmonella enterica subsp. enterica serovar Typhimurium through liv

261 Salmonella enterica subsp. enterica serovars Typhimurium and its fo

262 S. enterica subsp. salamae encodes the Salmonella pathogeni

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

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

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

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

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

268 Typhoid fever is caused by Salmonella enterica subspecies enterica serovar Typhi (S. Typhi) an

269 Salmonella enterica subspecies enterica serovar Typhi (Salmonella T

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

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

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

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

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

275 e present the genome sequences of Salmonella enterica tailed phages Sasha, Sergei, and Solent.

276 Here, we report that, in Salmonella enterica, the sirtuin deacylase CobB long isoform (CobB(

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

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

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

280 nd 28 HEG out of 130 Phage and 36 HEGs in S. enterica Typhi CT18, which shows that it is more efficie

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

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

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

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

285 Using Toxoplasma gondii and Salmonella enterica Typhimurium we demonstrate HRMAn's capacity to

286 cathepsin inhibitor (stefin B) suppressed S. enterica Typhimurium-induced cell death.

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

288 intracellular bacterial pathogen Salmonella enterica Typhimurium.

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

290 hi5, LpThi5 functioned in vivo in Salmonella enterica under multiple growth conditions.

291 Salmonella enterica variants exhibit diverse host adaptation, outco

292 nation of drinking water by C. jejuni and S. enterica was also observed, suggesting a potential funct

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

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

295 y organisms, Escherichia coli and Salmonella enterica, we show that copper resistance requires both t

296 icrobiological techniques and serovars of S. enterica were determined by PCR and/or agglutination wit

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

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.