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1 vealed at least 13 well segregated variants (serovars).
2 thods lack resolution for this highly clonal serovar.
3 solates were distributed among 188 different serovars.
4 the principal reservoirs of many pathogenic serovars.
5 y both nontyphoidal and typhoidal Salmonella serovars.
6 intestinal infections, compared to other NTS serovars.
7 gainst homologous and heterologous Chlamydia serovars.
8 uld likely protect against only one or a few serovars.
9 ped a new multiplex PCR for the detection of serovars 1 to 3, 5 to 8, 10, and 12 along with apxIV, th
11 and a PCR was formulated that differentiated serovar 16 isolates from all 15 known serovars and other
12 used whole-genome sequencing of the proposed serovar 16 reference strain A-85/14 to confirm the prese
15 PCR, using redesigned primers targeting the serovar 3 capsule locus, which differentiates serovars 3
17 erovar 3 capsule locus, which differentiates serovars 3, 6, and 8 Actinobacillus pleuropneumoniae iso
18 erence strain with the exception of those in serovars 5 and 12, which are identical in terms of gene
21 that the previously unsequenced S. enterica serovar 9,12:l,v:- belongs to the B clade of Salmonella
23 cally within both typhoidal and nontyphoidal serovars, although the SrgE protein sequences found with
25 ined from 667 children; 667 yielded a single serovar and 20 grew 2 Salmonella serovars, 1 being NTS.
26 ghly lethal challenge dose of the homologous serovar and determined protection against other group B
28 Multidrug resistance has emerged in all 3 serovars and is seen in the overwhelming majority of iso
29 tiated serovar 16 isolates from all 15 known serovars and other common respiratory pathogenic/commens
30 s is found sporadically throughout different serovars, and several inhibit activation of the innate i
32 ulator TviA, which is absent from Salmonella serovars associated with human gastroenteritis, represse
33 ighly conserved across different S. enterica serovars, but residue 161, located close to the catalyti
35 Human infection with typhoidal Salmonella serovars causes a febrile systemic disease, termed enter
37 tradermal (i.d.) challenge by L. interrogans serovar Copenhageni strain Fiocruz L1-130 in Golden Syri
39 of C3H/HeJ mice with Leptospira interrogans serovar Copenhageni using an enzootic mode of transmissi
41 be applied to humans, we used C. trachomatis serovar D (strain UW-3/Cx) to induce infertility in mice
42 oculations of rhesus macaques with wild-type serovar D strain D/UW-3/Cx or a plasmid-deficient deriva
43 nant MOMP (rMOMP) from Chlamydia trachomatis serovars D (UW-3/Cx), E (Bour), or F (IC-Cal-3) or Chlam
44 ecovered from mice immunized with rMOMP from serovars D, E, and F were 0.38 x 10(6), 7.56 x 10(6), an
47 gical data show the existence of a sixteenth serovar-designated serovar 16-of A. pleuropneumoniae.
49 were decidualised in-vitro, infected with Ct serovar E, and changes in expression of genes of interes
50 omparative genomic analysis reveals that all serovars encode a subset of "core" effectors, suggesting
51 on in different hosts, including S. enterica serovar Enteritidis (multiple hosts), S. Gallinarum (bir
54 es of S. Typhimurium and Salmonella enterica serovar Enteritidis DeltaguaBA DeltaclpX live oral vacci
57 c of Salmonella enterica subspecies enterica serovar Enteritidis phage type (PT) 4, which peaked in 1
58 cted a large outbreak of Salmonella enterica serovar Enteritidis phage type 14b affecting more than 3
59 phimurium, 10% (10) were Salmonella enterica serovar Enteritidis, and 3% (3) were Salmonella enterica
63 stinguished between all previously described serovars except 5 and 12, which were detected by the sam
64 ng (MLST) was able to accurately predict the serovars for 42/46 isolates and showed the best ability
65 isolation of Salmonella of a wide variety of serovars, from an array of animal feeds, food animals, a
66 e the two invasive avian-adapted S. enterica serovar Gallinarum biotypes Gallinarum and Pullorum, and
67 s of ceftiofur-resistant Salmonella enterica serovar Heidelberg in Quebec and Ontario attributable to
68 sults of 2 patients, each infected only with serovar Ia strains, revealed multiple same-serovar infec
69 o investigate the distribution of Salmonella serovars in MCL and their products, a total of 1287 pre-
72 characterization of this locus among the 15 serovars is the first step in understanding the genetic,
73 oenteritis-producing nontyphoidal Salmonella serovars, is a potent inhibitor of T-cell activation.
74 175) and compared with strains from the same serovars isolated from human clinical cases, livestock,
76 d caspase-inducing, wild-type C. trachomatis serovar L2 led to infertility, but the noninflammation-i
77 ranuloma venereum isolate of C. trachomatis, serovar L2, with either the original shuttle vector (pGF
81 ) in attenuating infectivity across multiple serovars of C. trachomatis without host cell toxicity.
82 variation within the capsule loci of the 15 serovars of H. parasuis, for rapid molecular serotyping.
89 spira-nonresponsive cells, bound to multiple serovars of two Leptospira species, L. borgpetersenii, a
90 is a relatively new species name for certain serovars of Ureaplasma urealyticum, and PCR is useful fo
92 ca serovar Typhi, whereas 86% (131/152) were serovars other than Typhi (nontyphoidal Salmonella).
95 s with RDAS derived from Salmonella enterica serovar Paratyphi A and Salmonella enterica serovar Typh
99 i or Salmonella enterica subspecies enterica serovar Paratyphi A or C were only isolated in 14 (0.03%
101 and the expression of SPI-1 in the typhoidal serovarS Paratyphi A compared to that of the nontyphoida
102 e chronic shedding of Leptospira interrogans serovar Pomona in California sea lions (Zalophus califor
104 uter membrane protein (MOMP) to elicit cross-serovar protection, groups of mice were immunized by the
105 abolically with most, if not all, Salmonella serovars, representing a novel approach to control of th
107 nce of any association between load and age, serovar, risk of transmission, hormone levels, and concu
108 CVD 1944 protected mice against the group D serovar Salmonella enterica serovar Dublin (85% vaccine
109 CVD 1931 protected mice against the group B serovar Salmonella enterica serovar Stanleyville (91% va
111 sing infectious bacteria Salmonella enterica serovar (Salmonella typhi) in 10 muL of sample volume.
113 with Salmonella enterica subspecies enterica serovar Senftenberg are often associated with exposure t
117 -translational modifications (PTM), identify serovar specific markers, and validate genomic predicted
119 the first time we show that reproducible and serovar specific systemic biomarkers can be detected dur
120 onstruct promoted strong immune responses to serovar-specific epitopes, the conserved LNPTIAG epitope
121 genetic, molecular, and structural bases of serovar specificity in this poorly studied but important
122 inst the group B serovar Salmonella enterica serovar Stanleyville (91% vaccine efficacy), and S. Ente
124 rgE protein sequences found within typhoidal serovars tend to cluster separately from those found in
125 rica serovar Paratyphi A is a human-specific serovar that, together with Salmonella enterica serovar
129 ubiquitous species contains more than 2,600 serovars that may differ in their host specificity, clin
130 this new niche support a bloom of Salmonella serovars, thereby ensuring transmission of the pathogen
131 ion of typhoidal and nontyphoidal Salmonella serovars to invasive disease varies considerably in plac
132 sia, multidrug-resistant Salmonella enterica serovar Typhi (S Typhi) has been the main cause of enter
136 quence analysis of 1,832 Salmonella enterica serovar Typhi (S. Typhi) identifies a single dominant MD
138 ovar that, together with Salmonella enterica serovar Typhi and Salmonella enterica serovar Sendai, ca
139 roarray containing 2,724 Salmonella enterica serovar Typhi antigens (>63% of proteome) and identified
141 Multiyear epidemics of Salmonella enterica serovar Typhi have been reported from countries across e
142 bcontinent, with chronic Salmonella enterica serovar Typhi infection reported as a significant risk f
146 yphoid fever case with a Salmonella enterica serovar Typhi isolate showing extended spectrum beta-lac
148 Salmonella enterica subspecies enterica serovar Typhi or Salmonella enterica subspecies enterica
149 e used a live attenuated Salmonella enterica serovar Typhi strain to create a bivalent mucosal plague
150 ed a Salmonella enterica subspecies enterica serovar Typhi strain with resistance against beta-lactam
151 serovar Paratyphi A and Salmonella enterica serovar Typhi to induce protective immunity against bact
152 ctamase (ESBL)-producing Salmonella enterica serovar Typhi was identified, whole-genome sequence type
153 binding sites were identified in S. enterica serovar Typhi, 22 of which were associated with OmpR-reg
154 Salmonella enterica and Salmonella enterica serovar Typhi, and Yersinia pestis), and 3 protozoa (Lei
155 Mycobacterium leprae and Salmonella enterica serovar Typhi, but the function of parkin in immunity ha
156 agent of typhoid fever, Salmonella enterica serovar Typhi, can partially subvert this critical innat
157 Enteric fever, caused by Salmonella enterica serovar Typhi, is an important public health problem in
160 ellae, 14% (21/152) were Salmonella enterica serovar Typhi, whereas 86% (131/152) were serovars other
163 enteric fever caused by Salmonella enterica serovars Typhi and Paratyphi is substantial and has high
164 degrees C-42 degrees C) Salmonella enterica serovars Typhi, Paratyphi A, and Sendai significantly at
165 were Salmonella enterica subspecies enterica serovar Typhimurium (45% [116/258] of which were multilo
167 sinia enterocolitica and Salmonella enterica serovar Typhimurium (all gram-negative bacteria) and Sta
168 ed melibiose permease of Salmonella enterica serovar Typhimurium (MelBSt) demonstrates that MelB is a
169 araginase II produced by Salmonella enterica serovar Typhimurium (S Typhimurium) inhibits T cell resp
175 rtant foodborne pathogen Salmonella enterica serovar Typhimurium (S. Typhimurium) simultaneously acti
176 ere that Salmonella enterica subsp. enterica serovar Typhimurium (S. Typhimurium) uses d-glucosaminat
177 t the enteric bacterium, Salmonella enterica serovar Typhimurium (S. Typhimurium), is a vacuolar path
183 acteriophage P22 infects Salmonella enterica serovar Typhimurium and is a model for icosahedral viral
184 pathogens that use T3SS, Salmonella enterica serovar Typhimurium and Yersinia pseudotuberculosis.
186 lular bacterial pathogen Salmonella enterica serovar Typhimurium as shown by their superior containme
187 d the vT3SS and fT3SS of Salmonella enterica serovar Typhimurium at ~5 and ~4 nm resolution using ele
188 The food-borne pathogen Salmonella enterica serovar Typhimurium benefits from acute inflammation in
191 med typhoid fever, while Salmonella enterica serovar Typhimurium causes localized gastroenteritis in
192 intracellular bacterium Salmonella enterica serovar Typhimurium causes persistent systemic inflammat
193 We observed enhanced Salmonella enterica serovar Typhimurium colonization in the intestinal epith
194 reduced ability to kill Salmonella enterica serovar Typhimurium compared to that of macrophages isol
195 The ST313 pathovar of Salmonella enterica serovar Typhimurium contributes to a high burden of inva
196 lso demonstrate that the Salmonella enterica serovar Typhimurium core promoter is more active than pr
197 inflammatory response induced by Salmonella serovar Typhimurium creates a favorable niche for this g
198 ane vesicles (OMVs) from Salmonella enterica serovar Typhimurium displaying the variable N terminus o
199 ination of two prevalent Salmonella enterica serovar Typhimurium DT104 clones in Israel, which are ge
200 t colonization niche for Salmonella enterica serovar Typhimurium during gastrointestinal infections.
201 that Salmonella enterica subspecies enterica serovar Typhimurium employs a dedicated mechanism, drive
202 ng in this locus in FQ-resistant S. enterica serovar Typhimurium epidemic clones resulted in the same
203 recent study showed that Salmonella enterica serovar Typhimurium exhibits sliding motility under magn
205 IS) to screen mutants of Salmonella enterica serovar Typhimurium for their ability to infect and grow
207 sis of core genes within Salmonella enterica serovar Typhimurium genomes reveals a high degree of all
208 ase and a chitinase from Salmonella enterica serovar Typhimurium hydrolyze LacNAc from Galbeta1-4GlcN
209 entrations, inhibits E. coli and S. enterica serovar Typhimurium in an additive or antagonistic manne
212 found that intracellular Salmonella enterica serovar Typhimurium induced the binucleation of a large
213 pathogen and host during Salmonella enterica serovar Typhimurium infection and reveal the molecular i
215 RD9 is suppressed during Salmonella enterica serovar Typhimurium infection, facilitating increased IL
221 ate immune resistance of Salmonella enterica serovar Typhimurium is attributed to the high-molecular-
222 n efflux transporters in Salmonella enterica serovar Typhimurium is discussed in the context of cellu
223 c mechanism of FrmR from Salmonella enterica serovar Typhimurium is triggered by metals in vitro, and
226 re absent in the closely related S. enterica serovar Typhimurium LT2 and from a mutant of S Montevide
228 U microcompartments from Salmonella enterica serovar Typhimurium LT2 that were imaged previously.
229 li K12, E. coli O157:H7, Salmonella enterica serovar Typhimurium LT2, Staphylococcus aureus, and Stre
230 s initially found on the Salmonella enetrica serovar Typhimurium multi-resistance plasmid pMG101 from
231 ompetent, but avirulent, Salmonella enterica serovar Typhimurium mutant for its ability to compete wi
232 ture of the prototypical Salmonella enterica serovar Typhimurium pathogenicity island 1 basal body, d
233 entify most of the 3,838 Salmonella enterica serovar Typhimurium promoters in just two RNA-seq runs.
234 viA gene in nontyphoidal Salmonella enterica serovar Typhimurium reduced flagellin-induced pyroptosis
235 teropathogenic bacterium Salmonella enterica serovar Typhimurium requires a T6SS encoded within Salmo
236 e intracellular pathogen Salmonella enterica serovar Typhimurium requires the mgtC gene to cause dise
237 se to the catalytic triad, is variable, with serovar Typhimurium SpvD having an arginine and serovar
238 t the genomes of S. enterica subsp. enterica serovar Typhimurium strain LT2 and Salmonella bongori st
239 genetically engineered a Salmonella enterica serovar Typhimurium strain of multilocus sequence type 3
241 ostatic activity against Salmonella enterica serovar Typhimurium that is not shared by the related pu
242 rdinates the response of Salmonella enterica serovar Typhimurium to diverse environmental challenges
243 examined the ability of Salmonella enterica serovar Typhimurium to infect the central nervous system
244 e CspA family members of Salmonella enterica serovar Typhimurium to link the constitutively expressed
245 ur) in the resistance of Salmonella enterica serovar Typhimurium to the reactive nitrogen species pro
246 as an orthologue of the Salmonella enterica serovar Typhimurium type III secretion system chaperone,
248 the intestinal pathogen Salmonella enterica serovar Typhimurium uses specialized metal transporters
250 tween FlgM and FliS from Salmonella enterica serovar Typhimurium was characterized using gel shift, i
252 ria monocytogenes V7 and Salmonella enterica serovar Typhimurium were used as model pathogens to eval
254 in the PhoPQ regulon of Salmonella enterica serovar Typhimurium with that of PhoPQ-regulated horizon
257 isolates, 40% (41) were Salmonella enterica serovar Typhimurium, 10% (10) were Salmonella enterica s
259 almonellae, particularly Salmonella enterica serovar Typhimurium, are a major cause of invasive disea
260 uman and animal pathogen Salmonella enterica serovar Typhimurium, biofilm formation is correlated wit
263 bic peptide expressed in Salmonella enterica serovar Typhimurium, inhibits growth in macrophages thro
265 herichia coli (EHEC) and Salmonella enterica serovar Typhimurium, or the surrogate murine infection m
266 r bacteria, specifically Salmonella enterica serovar Typhimurium, Pectobacterium carotovorum and Legi
267 aps of Escherichia coli, Salmonella enterica serovar Typhimurium, Pseudomonas aeruginosa, Bacillus su
268 in Escherichia coli and Salmonella enterica serovar Typhimurium, suggesting that CyaY and YggX might
269 Unlike the nontyphoidal Salmonella enterica serovar Typhimurium, the genomes of S. Typhi and S. Para
270 al functions, strains of Salmonella enterica serovar Typhimurium, the murine model of S Typhi, in whi
271 III protein secretion in Salmonella enterica serovar Typhimurium, we discovered that several TCMs can
272 reus and Salmonella enterica subsp. enterica serovar Typhimurium, were exposed to 25 kGy gamma radiat
273 2+) channel gene corA in Salmonella enterica serovar Typhimurium, which was previously thought to be
274 an efficiently attenuate Salmonella enterica serovar Typhimurium-induced pyroptosis and proinflammato
284 Mice were infected with Salmonella enterica serovar typhimurium; cecum and small-intestine tissues w
285 ella (NTS), particularly Salmonella enterica serovars Typhimurium and Enteritidis, is responsible for
287 raction was done from Salmonella typhimurium serovars, under the optimized growth conditions for its
288 th the winning metabolic strategy Salmonella serovars use to edge out competing microbes in the infla
289 uation of the ability to identify Salmonella serovars using (i) different molecular subtyping methods
290 nvasive NTS from whom 1 of the 4 predominant serovars was isolated in pure culture, 448 (81.0%) were
291 al for Salmonella spp., which include >2,600 serovars, we performed an initial evaluation of the abil
293 istinct from the previously characterized 15 serovars were described, and a proposal was put forward
296 ons (1.2%) and nontyphoidal Salmonella (NTS) serovars were isolated 10,139 times (6.1%), of which 801
297 ontrolling virulence phenotypes in typhoidal serovars, which is likely to play a role in the distinct
298 association of nontyphoidal Salmonella (NTS) serovars with invasive infections, 48,345 Salmonella cas
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