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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.
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
23 burnetii, Leptospira spp., Rickettsia spp., Salmonella enterica and Salmonella enterica serovar Typh
25 -propanediol utilization microcompartment of Salmonella enterica and use it to analyze the function o
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
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
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
44 vation of MAPK and AKT pathways, mediated by Salmonella enterica effectors secreted during infection,
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
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
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
71 ted microorganisms such as Escherichia coli, Salmonella enterica, Listeria innocua, Mycobacterium par
73 re formed upon recombinant expression of the Salmonella enterica LT2 ethanolamine utilization bacteri
76 ersinia pestis T3S needle protein, YscF, the Salmonella enterica needle proteins PrgI and SsaG, and t
78 uencing (Grad-seq) in the bacterial pathogen Salmonella enterica, partitioning its coding and noncodi
80 into nonphagocytic host cells is central to Salmonella enterica pathogenicity and dependent on multi
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
92 mportant for colonization and persistence of Salmonella enterica serotype Typhimurium in chickens.
94 detects typhoid-causing infectious bacteria Salmonella enterica serovar (Salmonella typhi) in 10 muL
96 4 protected mice against the group D serovar Salmonella enterica serovar Dublin (85% vaccine efficacy
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
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
104 number of human cases of ceftiofur-resistant Salmonella enterica serovar Heidelberg in Quebec and Ont
106 accine (RASV) strains with RDAS derived from Salmonella enterica serovar Paratyphi A and Salmonella e
110 r with Salmonella enterica serovar Typhi and Salmonella enterica serovar Sendai, causes enteric fever
112 1 protected mice against the group B serovar Salmonella enterica serovar Stanleyville (91% vaccine ef
114 ting protein, to influence susceptibility to Salmonella enterica serovar Typhi (S Typhi) infection.
117 Here whole-genome sequence analysis of 1,832 Salmonella enterica serovar Typhi (S. Typhi) identifies
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
123 ent in the Indian subcontinent, with chronic Salmonella enterica serovar Typhi infection reported as
128 lly and results from systemic infection with Salmonella enterica serovar Typhi or Paratyphi pathovars
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
138 the serotyped salmonellae, 14% (21/152) were Salmonella enterica serovar Typhi, whereas 86% (131/152)
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).
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)
152 udies have shown that the enteric bacterium, Salmonella enterica serovar Typhimurium (S. Typhimurium)
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
158 flexneri and other pathogens that use T3SS, Salmonella enterica serovar Typhimurium and Yersinia pse
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
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
168 l compartments and a reduced ability to kill Salmonella enterica serovar Typhimurium compared to that
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
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
181 n simultaneously in pathogen and host during Salmonella enterica serovar Typhimurium infection and re
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
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
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
212 Here we show that the intestinal pathogen Salmonella enterica serovar Typhimurium uses specialized
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
218 n of conserved genes in the PhoPQ regulon of Salmonella enterica serovar Typhimurium with that of Pho
221 Of the 102 typed NTS isolates, 40% (41) were Salmonella enterica serovar Typhimurium, 10% (10) were S
225 ic bacteria, either Klebsiella pneumoniae or Salmonella enterica serovar Typhimurium, enhanced transl
227 R, a highly hydrophobic peptide expressed in Salmonella enterica serovar Typhimurium, inhibits growth
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
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
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).
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
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
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
272 0 of 620 (74.2%) NTS isolates serotyped were Salmonella enterica subspecies enterica serovar Typhimur
274 serovar 9,12:l,v:- belongs to the B clade of Salmonella enterica subspecies enterica, and we show its
276 high-abundance chemoreceptors of E. coli and Salmonella enterica suggests that it may be important fo
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
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
287 hat infection of macrophages and mice with a Salmonella enterica Typhimurium strain containing an ina
290 leic acid, a major lipid in E. coli Last, in Salmonella enterica, ubiK was required for proliferation
292 the beta- and gamma-proteobacteria, such as Salmonella enterica, Vibrio spp., and both Sphingomonas
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
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
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