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1 S. enterica cleanly converted all of the acid to acetyl-
2 S. enterica serotype Agona was isolated concurrently fro
3 S. enterica serovar Typhi carrying pTETlpp induced Frag
4 S. enterica serovar Typhimurium and S. flexneri cell ent
5 S. enterica serovar Typhimurium entry requires a functio
6 S. enterica serovar Typhimurium oligonucleotide microarr
7 S. enterica serovar Typhimurium strain 14028 produces tw
8 S. enterica subsp. salamae encodes the Salmonella pathog
10 oquinolone resistance in a collection of 136 S. enterica isolates, including 111 with intermediate or
11 sylvania and nearby states during July 2004: S. enterica serotypes Javiana, Anatum, Thompson, Typhimu
13 ta on 291 Salmonella isolates, including 250 S. enterica subspecies I strains from 32 serovars (52 ge
14 he cecum and large intestine with 10x LD(50) S. enterica serovar Typhimurium challenge at 7 days post
16 owth on 10 mM acetate, acs(+) induction in a S. enterica strain that cannot acetylate (i.e. inactivat
17 Our data suggest that the 12-2 antigen is a S. enterica subspecies I-specific LPS modification that
18 mented the flagella-deficient phenotype of a S. enterica acnB mutant, and the isolated AcnB5-4 polype
19 e corrected the pantothenate auxotrophy of a S. enterica yhhK strain, supporting in vitro evidence ob
22 f phenotypic similarity and diversity across S. enterica subspecies I and shown how the core genome o
23 differentiate the two invasive avian-adapted S. enterica serovar Gallinarum biotypes Gallinarum and P
27 CD8 T cells contribute to protection against S. enterica serovar Typhimurium in mice, but little is k
33 utant retained intact LPS, we constructed an S. enterica serovar Typhimurium triple-knockout (TKO) mu
35 as necessary and sufficient for growth of an S. enterica cobA eutT strain on ethanolamine as a carbon
39 romoter and was used to support growth of an S. enterica strain under conditions that demanded CobC-l
40 positive S. enterica serovar Paratyphi C and S. enterica serovar Dublin isolates revealed the presenc
45 on the concentrations, inhibits E. coli and S. enterica serovar Typhimurium in an additive or antago
48 ties for S. enterica serovar Enteritidis and S. enterica serovar Typhimurium strains when a minimum o
49 PFGE for S. enterica serovar Enteritidis and S. enterica serovar Typhimurium strains, respectively.
51 f S. enterica serovar Typhi CVD 908-htrA and S. enterica serovar Typhimurium SL3261 carrying plasmid
52 on the roles of their aligned Y. pestis and S. enterica partners and showed that up to 73% of the pr
53 S. bongori, S. enterica subsp. salamae, and S. enterica subsp. arizonae share features of the infect
54 Salmonella enterica serotype Typhi (ST) and S. enterica serotype Paratyphi A (SPA) isolates were inc
57 h nontyphoidal Salmonella serotypes, such as S. enterica serotype Typhimurium, are characterized by a
58 In contrast, a highly modified attenuated S. enterica serovar Typhimurium strain was not present i
59 udy used transcriptional differences between S. enterica wild-type and ridA strains to explore the br
60 s that could be used to discriminate between S. enterica serovar Typhimurium isolates from the same g
63 we identified EspJ homologues in S. bongori, S. enterica subsp. salamae, and Salmonella enterica subs
68 almonella enterica infections represented by S. enterica serovar Newport has increased markedly among
69 In summary, MddA is the mechanism used by S. enterica to respond to oxidized forms of methionine,
71 that the MLST scheme employed here clustered S. enterica serovar Newport isolates in distinct molecul
72 gy searches to determine how far the E. coli/S. enterica paradigm can be generalised to other flagell
75 2 proteins restored growth of SIR2-deficient S. enterica on acetate and propionate, suggesting that e
76 of SpvD is highly conserved across different S. enterica serovars, but residue 161, located close to
77 multiple methods is needed to differentiate S. enterica serovar Typhimurium isolates that geneticall
78 ings indicate that c-Abl is activated during S. enterica serovar Typhimurium infection and that its p
80 ndings indicate that the sensor PhoQ enables S. enterica to respond to both host- and bacterial-deriv
81 population structure of commonly encountered S. enterica serotype Enteritidis outbreak isolates in th
82 om Vibrio cholerae, Yersinia enterocolitica, S. enterica serovar Typhimurium, and Klebsiella pneumoni
84 uorescein, biotin and digoxigenin coding for S. enterica, L. monocytogenes and E. coli, respectively.
85 BlnI, SfiI, and PacI as most concordant for S. enterica serovar Enteritidis, while XbaI, BlnI, and S
87 9% and 96% for five-enzyme combined PFGE for S. enterica serovar Enteritidis and S. enterica serovar
89 scriminatory PFGE-based subtyping scheme for S. enterica serovar Enteritidis that relies on a single
90 100% correlation among Dice similarities for S. enterica serovar Enteritidis and S. enterica serovar
91 port here that CD8 T-cell lines derived from S. enterica serovar Typhimurium-infected BALB/c mice lys
93 parameters of K(m) and k(cat) for FlgJ from S. enterica were determined to be 0.64 +/- 0.18 mg ml(-1
94 . enterica serovar Typhimurium and four from S. enterica serovar Typhi were used to create an assay c
96 var Typhimurium or pulsed with proteins from S. enterica serovar Typhimurium culture supernatants.
97 he His6-tagged PduS cobalamin reductase from S. enterica was produced at high levels in Escherichia c
100 to Escherichia coli phages lambda and HK97, S. enterica phage ST64T, or a Shigella flexneri prophage
110 ere, we demonstrate that Dap accumulation in S. enterica elicits a proline requirement for growth and
113 esponse to osmotic challenge is conserved in S. enterica, dependence on these two sRNA regulators is
116 gg albumen, while disruption of this gene in S. enterica serovar Enteritidis rendered the organism mo
118 tative OmpR binding sites were identified in S. enterica serovar Typhi, 22 of which were associated w
121 on, we screened a transposon library made in S. enterica serovar Typhimurium for the ability to persi
122 ding of the effects Dap has on metabolism in S. enterica, and likely other organisms, and highlight t
124 ng with ratA, sivI, and sivH were present in S. enterica subsp. II and S. bongori in addition to S. e
125 bial drug resistance is a growing problem in S. enterica that threatens to further compromise patient
131 is of the determinants of thermotolerance in S. enterica serovar Typhimurium, we isolated the chr-1 m
132 onia-lyase (DpaL) alleviated Dap toxicity in S. enterica by catalyzing the degradation of Dap to pyru
133 und that SP control of rpoS transcription in S. enterica involves repression of the major rpoS promot
136 ause infection in different hosts, including S. enterica serovar Enteritidis (multiple hosts), S. Gal
138 biosynthetic gene, wcaM, was introduced into S. enterica serovar Typhimurium strain BJ2710 and was fo
140 n of inflammatory responses by intracellular S. enterica serovar Typhimurium, and perhaps Shigella fl
141 ductase) reduces the growth of intracellular S. enterica serovar Typhimurium and has no effect on ext
142 ane permeability) upon infection by invasive S. enterica serovar Typhimurium than do infected control
143 context suggest that the evolution of known S. enterica sublineages is mediated mostly by two mechan
144 to identify both novel and previously known S. enterica virulence factors (HilA, HilD, InvH, SptP, R
145 e types and other S. enterica serovars, like S. enterica serovar Infantis, possessing SGI1, while DT1
151 nd phenotypically characterized nontyphoidal S. enterica strains to 11 previously sequenced S. enteri
152 G, or sthABCDE did not reduce the ability of S. enterica serotype Typhimurium to colonize the spleen
154 c phenotype caused by the rpoD1181 allele of S. enterica allows past in vitro results to be incorpora
158 ave been isolated from the culture broths of S. enterica and uropathogenic E. coli, but MGE and TGE h
159 ntribute to long-term intestinal carriage of S. enterica serotype Typhimurium in genetically resistan
160 e genes important for intestinal carriage of S. enterica serotype Typhimurium in vertebrate animals.
161 munization of newborn mice with 10(9) CFU of S. enterica serovar Typhi CVD 908-htrA and S. enterica s
162 A unique epidemiological characteristic of S. enterica serovar Enteritidis is its association with
163 e addition of propionaldehyde to cultures of S. enterica caused growth arrest from 8 to 20 mM, but no
164 ntitative, spatial, and temporal dynamics of S. enterica interactions are key to understanding how im
165 SfiI, PacI, and NotI) for 74 strains each of S. enterica serovar Enteritidis and S. enterica serovar
166 exchange, and loss play in the evolution of S. enterica sublineages, which to a certain extent are r
167 of an rpoE null mutant and the psp genes of S. enterica and Shigella flexneri are highly induced dur
168 alamae strain 3588/07 against the genomes of S. enterica subsp. enterica serovar Typhimurium strain L
171 gene is rarely found outside subspecies I of S. enterica and often present in nonfunctional allelic f
172 terica, and the dose-dependent inhibition of S. enterica by a soluble carbohydrate antiadhesive.
174 ay complementary roles in the interaction of S. enterica serovar Typhimurium with the host intestinal
175 ci were useful in distinguishing isolates of S. enterica serovars Typhimurium and Newport that had di
179 nonoxidative early intracellular killing of S. enterica serovar Typhimurium by human macrophages and
181 select the fliC transcript from a library of S. enterica transcripts; thus, the effect of AcnB on Fli
183 the previously uncharacterized aer locus of S. enterica serovar Typhimurium revealed them to be cont
185 A library of 960 signature-tagged mutants of S. enterica serovar Choleraesuis was constructed and scr
187 re that transcription of the vapBC operon of S. enterica is controlled by a recently discovered regul
190 was used to understand the pathogenicity of S. enterica serovar Choleraesuis in its natural host and
191 xamined the distribution of PFGE patterns of S. enterica serotype Typhi isolates from patients with a
192 aecal shedding and intestinal persistence of S. enterica serotype Typhimurium ATCC14028 in Salmonella
193 l in assessing the evolutionary potential of S. enterica sublineages and aid in the prediction and pr
195 wo organisms showed this to be a property of S. enterica rather than of the FadR proteins per se.
198 r infection, suggesting that the recovery of S. enterica serotype Typhimurium from fecal samples clos
199 ACDEFG did not result in reduced recovery of S. enterica serotype Typhimurium from fecal samples coll
203 h five strains each of the target species of S. enterica and L. monocytogenes, along with five strain
204 complicate efforts to control the spread of S. enterica serovar Heidelberg in food animal and human
205 ype protein, supported growth of a strain of S. enterica devoid of Acs (acetyl-CoA synthetase; AMP-fo
208 of the growth behavior of mutant strains of S. enterica lacking specific functions encoded by the 17
210 (by single and double mutations) strains of S. enterica serovars Typhimurium and Typhi were recovere
212 cherichia coli is similar overall to that of S. enterica but is seen in the absence of glucose and, u
216 ibitor, Co(III) hexaammine, had no effect on S. enterica serovar Typhimurium invasion of Caco-2 epith
217 pecies in all samples, with detection of one S. enterica and two Listeria TRFs in all cases, and dete
219 eement with results obtained in the original S. enterica serovar Typhimurium STM screen, illustrating
220 ca serovar Typhimurium phage types and other S. enterica serovars, like S. enterica serovar Infantis,
221 ved in other Salmonella strains, i.e., other S. enterica serovar Typhimurium phage types and other S.
222 y following eradication of the fowl pathogen S. enterica serovar Gallinarum in the mid-20th century.
223 for bacterial colonization after pathogenic S. enterica serovar Enteritidis inoculation and for circ
226 alysis of viaB-associated DNA in Vi-positive S. enterica serovar Paratyphi C and S. enterica serovar
228 fications were absent in the closely related S. enterica serovar Typhimurium LT2 and from a mutant of
230 ions occurring in this locus in FQ-resistant S. enterica serovar Typhimurium epidemic clones resulted
231 smid-associated genes in multidrug resistant S. enterica serovar Heidelberg, antimicrobial resistance
232 e transfer; different isolates from the same S. enterica serovar can exhibit significant variation in
234 enterica strains to 11 previously sequenced S. enterica genomes to carry out the most comprehensive
235 es are missing (e.g., avrA, sopB, and sseL), S. enterica subsp. salamae invades HeLa cells and contai
237 These gene panels distinguish all tested S. enterica subspecies I serovars and their known genova
238 nterica ridA causes Ser sensitivity and that S. enterica RidA and its homologs from other organisms h
239 ing 12/15-lipoxygenase (12/15-LOX), and that S. enterica serovar Typhimurium and S. flexneri share ce
241 urther into this pathway, we also found that S. enterica serovar Typhimurium and S. flexneri activate
242 The results of this study indicate that S. enterica serovar Typhimurium can outgrow E. coli in h
244 oreover, the data raise the possibility that S. enterica DeltafrdABCD DeltasdhCDA double mutants and
249 xpressed in C. elegans intestinal cells, the S. enterica TTSS-exported effector protein SptP inhibite
257 es between the two organisms showed that the S. enterica FadE and FadBA enzymes were responsible for
258 trophic CO(2) fixation), suggesting that the S. enterica organelles and carboxysomes have a related m
260 y was not enhanced by Mg(2+) and, unlike the S. enterica CobA enzyme, it was >50% inhibited by Mn(2+)
263 e that YafD provides a survival advantage to S. enterica serovar Enteritidis in eggs by repairing DNA
265 This difference in growth was attributed to S. enterica having higher cytosolic levels of the induci
266 glycerol dehydratase family, in contrast to S. enterica, which relies on a B12-dependent enzyme.
267 A, SopA, SopB, SopD, and SopE2 contribute to S. enterica serotype Typhimurium invasion of epithelial
269 NPs as molecular markers for the response to S. enterica serovar Enteritidis may result in the enhanc
270 inacin genes with the phenotypic response to S. enterica serovar Enteritidis, an F1 population of chi
273 Although excess Fe2+ was slightly toxic to S. enterica serovar Typhimurium, we were unable to elici
275 et al. that oral inoculation with wild-type S. enterica serovar Typhimurium strains lead to bacteria
276 egulator (prpR)) were evaluated in wild-type S. enterica serovar Typhimurium TR6583 and prpB(-) or pr
278 and invasive infections due to non-typhoidal S. enterica infections resulted in the highest burden, c
281 We show that the previously unsequenced S. enterica serovar 9,12:l,v:- belongs to the B clade of
282 ritidis, whose overexpression conferred upon S. enterica serovar Typhimurium enhanced resistance to e
284 In vitro methylation analyses utilizing S. enterica and Thermotoga maritima CheR proteins and MC
287 (CD11b+), and dendritic cells (CD11c+) with S. enterica serovar Typhimurium induced an up-regulation
288 was first formed followed by challenge with S. enterica serovar Typhimurium, there was significant b
289 lysed bone marrow macrophages infected with S. enterica serovar Typhimurium or pulsed with proteins
290 H2-M3-transfected fibroblasts infected with S. enterica serovar Typhimurium SL3261 or treated with S
291 oducing EcN to mice previously infected with S. enterica substantially reduced intestinal colonizatio
292 l vaccine, rabbits were orally infected with S. enterica Typhimurium strain chi3987 harboring phagemi
294 To identify cases of human infection with S. enterica serotype Typhimurium potentially related to
295 tion model, mice were orally inoculated with S. enterica 24 h post-initiation of abrupt withdrawal fr
297 um chloride (DPI), but infection of MDM with S. enterica serovar Typhimurium did not cause an increas
298 These operons are widely distributed within S. enterica but absent from the closely related Escheric
299 reaching the level in cells infected with WT S. enterica serovar Typhimurium, than the level in host
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