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1 onal pathogen that has recently emerged from Yersinia pseudotuberculosis.
2 tal structure of residues 1-129 of YopH from Yersinia pseudotuberculosis.
3 ogenic relatives Yersinia enterocolitica and Yersinia pseudotuberculosis.
4  translocation into HeLa cells infected with Yersinia pseudotuberculosis.
5 lows efficient entry into mammalian cells by Yersinia pseudotuberculosis.
6 ogenic yersiniae Yersinia enterocolitica and Yersinia pseudotuberculosis.
7 inv gene product (invasin) on the surface of Yersinia pseudotuberculosis.
8 osely related pathogens, Yersinia pestis and Yersinia pseudotuberculosis.
9 uring primary infection of C57BL/6 mice with Yersinia pseudotuberculosis.
10 of the T3SS in the gastrointestinal pathogen Yersinia pseudotuberculosis.
11 haracterize modified peptide-cytidylate from Yersinia pseudotuberculosis.
12 , evolved from the gastrointestinal pathogen Yersinia pseudotuberculosis.
13 L-10) in sera of C57BL/6J mice infected with Yersinia pseudotuberculosis.
14 y pathogenic Escherichia coli strains and by Yersinia pseudotuberculosis.
15 ired for the virulence of the enteropathogen Yersinia pseudotuberculosis.
16 nt of plague, has only recently evolved from Yersinia pseudotuberculosis.
17 , regulates virulence in Yersinia pestis and Yersinia pseudotuberculosis.
18  Salmonella enterica serovar Typhimurium and Yersinia pseudotuberculosis.
19 2, inhibit beta1 integrin-promoted uptake of Yersinia pseudotuberculosis.
20 is genomes and the corresponding features in Yersinia pseudotuberculosis.
21 ffected in T cells exposed to low numbers of Yersinia pseudotuberculosis.
22 in the biosynthesis of 3,6-dideoxyhexoses in Yersinia pseudotuberculosis.
23  diverged recently from the enteric pathogen Yersinia pseudotuberculosis.
24 vasion factor in Yersinia enterocolitica and Yersinia pseudotuberculosis.
25 elated food- and waterborne enteric pathogen Yersinia pseudotuberculosis A combination of population
26            Y. pestis and the closely related Yersinia pseudotuberculosis also make biofilms on the cu
27 acterial pathogen that evolved recently from Yersinia pseudotuberculosis, an enteric pathogen transmi
28 the causative agent of plague, diverged from Yersinia pseudotuberculosis, an enteric pathogen, an est
29 secreted in a type III-dependent manner from Yersinia pseudotuberculosis and also secreted from C. tr
30  similarity with YopJ of the animal pathogen Yersinia pseudotuberculosis and AvrRxv of the plant path
31                    Enteric pathogens such as Yersinia pseudotuberculosis and enteropathogenic Escheri
32                                 Nonpigmented Yersinia pseudotuberculosis and Escherichia coli strains
33 s the products of the psaEFABC genes in both Yersinia pseudotuberculosis and Escherichia coli.
34 etermine if YopE is a protective antigen for Yersinia pseudotuberculosis and if primary infection wit
35  the activity of Cif from the human pathogen Yersinia pseudotuberculosis and selected variants, and t
36  other bacterial pathogens, the dam genes of Yersinia pseudotuberculosis and Vibrio cholerae were dis
37 different receptors and for phages infecting Yersinia pseudotuberculosis and Vibrio cholerae.
38  a role in recognition of the enteropathogen Yersinia pseudotuberculosis and whether this results in
39                            Previous study in Yersinia pseudotuberculosis and Yersinia enterocolitica
40                           The binding of the Yersinia pseudotuberculosis and Yersinia enterocolitica
41                The enteropathogenic bacteria Yersinia pseudotuberculosis and Yersinia enterocolitica
42                                              Yersinia pseudotuberculosis and Yersinia enterocolitica
43  Yersinia pestis and pYV in enteropathogenic Yersinia pseudotuberculosis and Yersinia enterocolitica)
44                                           In Yersinia pseudotuberculosis and Yersinia enterocolitica,
45 nia pestis and two enteropathogenic species, Yersinia pseudotuberculosis and Yersinia enterocolitica.
46 how that PNPase also enhances the ability of Yersinia pseudotuberculosis and Yersinia pestis to withs
47 was required for optimal T3SS functioning in Yersinia pseudotuberculosis and Yersinia pestis.
48 um and to binding of the biofilm produced by Yersinia pseudotuberculosis and Yersinia pestis.
49 nteric pathogens, Salmonella typhimurium and Yersinia pseudotuberculosis, and the second vector teste
50 ch as Escherichia coli, Salmonella enterica, Yersinia pseudotuberculosis, and Vibrio cholerae, among
51 in Escherichia coli, Salmonella typhimurium, Yersinia pseudotuberculosis, and Vibrio cholerae, each o
52 e and are fully conserved between Y. pestis, Yersinia pseudotuberculosis, and Yersinia enterocolitica
53                          Yersinia pestis and Yersinia pseudotuberculosis are closely related facultat
54 nse to pathogenic Listeria monocytogenes and Yersinia pseudotuberculosis as well as commensal bacteri
55 structures, we mapped the RNA structurome of Yersinia pseudotuberculosis at three different temperatu
56 s modest catalase activity, and is shared by Yersinia pseudotuberculosis, but not Yersinia enterocoli
57  and core metabolism in the enteric pathogen Yersinia pseudotuberculosis by integrated transcriptome
58 ary for efficient invasin-promoted uptake of Yersinia pseudotuberculosis by nonphagocytic cells.
59 e, has arisen from a less virulent pathogen, Yersinia pseudotuberculosis, by a rapid evolutionary pro
60                         The enteric pathogen Yersinia pseudotuberculosis causes the disease yersinios
61 tifying a potential association site for the Yersinia pseudotuberculosis chaperone-effector pair SycE
62 virulence genes found in Yersinia pestis and Yersinia pseudotuberculosis compared to other Yersinia s
63  Yersinia pestis, unlike the closely related Yersinia pseudotuberculosis, constitutively produces iso
64 nfected with a different bacterial pathogen, Yersinia pseudotuberculosis, contain damaged DNA.
65                                 In cell-free Yersinia pseudotuberculosis culture supernatants, we hav
66                                              Yersinia pseudotuberculosis delivers several Yop effecto
67                           The virulence of a Yersinia pseudotuberculosis Delta yopM mutant in mice vi
68           The gram-negative enteric pathogen Yersinia pseudotuberculosis employs a type III secretion
69 -borne and water-borne transmission route of Yersinia pseudotuberculosis, from which Y. pestis diverg
70                          The closely related Yersinia pseudotuberculosis, from which Y. pestis recent
71                           The enteropathogen Yersinia pseudotuberculosis, from which Y. pestis recent
72 ucture of CDP-D-glucose 4,6-dehydratase from Yersinia pseudotuberculosis in the resting state.
73                          M-cell targeting by Yersinia pseudotuberculosis in vivo may, therefore, be m
74              The oral LD50 for a yopJ mutant Yersinia pseudotuberculosis increases 64-fold compared w
75                           Cell extracts from Yersinia pseudotuberculosis induced multinucleation in H
76                          Using this tool for Yersinia pseudotuberculosis-infected lymphatic tissues,
77  lymph nodes and associated lymphatics after Yersinia pseudotuberculosis infection and clearance.
78                     Quantitative analysis of Yersinia pseudotuberculosis infection of murine gut loop
79 esponses within SLOs during gastrointestinal Yersinia pseudotuberculosis infection to limit pathogen
80 vated with lipopolysaccharide (LPS) prior to Yersinia pseudotuberculosis infection, caspase-1 is acti
81                          In a mouse model of Yersinia pseudotuberculosis infection, we show that at l
82 ensal microbiota or animal susceptibility to Yersinia pseudotuberculosis infection.
83 s also been demonstrated in a mouse model of Yersinia pseudotuberculosis infection.
84                                              Yersinia pseudotuberculosis infects many mammals and bir
85   We demonstrate that, in addition to MyD88, Yersinia pseudotuberculosis inhibits TRIF signaling thro
86                                              Yersinia pseudotuberculosis initiates systemic disease a
87 sequences of wild-type and mutant strains of Yersinia pseudotuberculosis interactions with the macrop
88                          Efficient uptake of Yersinia pseudotuberculosis into cultured mammalian cell
89                                 The entry of Yersinia pseudotuberculosis into cultured mammalian cell
90             Efficient entry of the bacterium Yersinia pseudotuberculosis into mammalian cells require
91 ency entry of the enteropathogenic bacterium Yersinia pseudotuberculosis into nonphagocytic cells is
92                                              Yersinia pseudotuberculosis inv mutant strains cured of
93 munoglobulin-like (Big) domains, such as the Yersinia pseudotuberculosis invasin and Escherichia coli
94  localization to an amino terminal-truncated Yersinia pseudotuberculosis invasin derivative.
95                              Transfer of the Yersinia pseudotuberculosis invasin gene into E.coli DH1
96           To determine if recognition of the Yersinia pseudotuberculosis invasin protein and natural
97                                          The Yersinia pseudotuberculosis invasin protein promotes bac
98                                          The Yersinia pseudotuberculosis invasin protein promotes bac
99  fused EHEC intimin to a homologous protein, Yersinia pseudotuberculosis invasin, or to maltose-bindi
100                       Quorum sensing (QS) in Yersinia pseudotuberculosis involves two pairs of LuxRI
101    Mating pair formation proteins (Trb) from Yersinia pseudotuberculosis IP31758 are the mostly close
102                                              Yersinia pseudotuberculosis is a foodborne pathogenic ba
103                                              Yersinia pseudotuberculosis is a Gram-negative bacterial
104 e dimeric [2Fe-2S] protein, E 1, cloned from Yersinia pseudotuberculosis, is the only known enzyme wh
105 fied IS100 sequences in a specific subset of Yersinia pseudotuberculosis isolates that were also sens
106 osum and periarthritis due to infection with Yersinia pseudotuberculosis IV was followed 13 months la
107                                              Yersinia pseudotuberculosis lcrF-null mutants showed att
108                                              Yersinia pseudotuberculosis LcrQ is a transcriptional re
109                                              Yersinia pseudotuberculosis localizes to the distal ileu
110       To test these models, we constructed a Yersinia pseudotuberculosis mutant expressing YopD devoi
111                       Here, we constructed a Yersinia pseudotuberculosis mutant strain with arabinose
112                                              Yersinia pseudotuberculosis mutants deficient for the ad
113                                              Yersinia pseudotuberculosis mutants that overproduce the
114                                              Yersinia pseudotuberculosis mutants that overproduce the
115 e found that only a small fraction of either Yersinia pseudotuberculosis or Yersinia pestis bacteria
116  cytotoxicity induced by Yersinia pestis and Yersinia pseudotuberculosis paradoxically leads to decre
117                                          The Yersinia pseudotuberculosis pH6 antigen mediates haemagg
118 itating biofilm on Caenorhabditis elegans by Yersinia pseudotuberculosis represents a tractable model
119 have suggested that rfaH may be required for Yersinia pseudotuberculosis resistance to antimicrobial
120 fection during C. trachomatis infections, in Yersinia pseudotuberculosis resulted in its secretion vi
121           We report that oral infection with Yersinia pseudotuberculosis results in the development o
122         The gram-negative bacterial pathogen Yersinia pseudotuberculosis secretes into macrophages a
123 the mechanism(s) of complement resistance in Yersinia pseudotuberculosis showed that the outer membra
124 ium evolved from an ancestral enteroinvasive Yersinia pseudotuberculosis strain by gene loss and acqu
125          Infection assays carried out with a Yersinia pseudotuberculosis strain producing YopER144A d
126 ersinia enterocolitica strains and 2 (of 10) Yersinia pseudotuberculosis strains at the restrictive t
127                                              Yersinia pseudotuberculosis strains expressing the mutan
128 expressing these proteins were infected with Yersinia pseudotuberculosis strains that secrete functio
129 ith a panel of different Yersinia pestis and Yersinia pseudotuberculosis strains to determine whether
130 lar delivery of IcsA in Escherichia coli and Yersinia pseudotuberculosis, suggesting that the mechani
131                                          The Yersinia pseudotuberculosis surface protein invasin bind
132                       Following clearance of Yersinia pseudotuberculosis, sustained inflammation and
133 ia coli expressing invA, a gene product from Yersinia pseudotuberculosis that mediates cellular invas
134                                              Yersinia pseudotuberculosis, the closely related food-an
135                                              Yersinia pseudotuberculosis, the relatively recent proge
136 ed a systematic deletion analysis of YopM in Yersinia pseudotuberculosis to determine which regions a
137 es and synthesizing the invasin protein from Yersinia pseudotuberculosis to enhance cellular entry we
138                                    YscU is a Yersinia pseudotuberculosis type III secretion system pr
139                                              Yersinia pseudotuberculosis uses a plasmid (pYV)-encoded
140                                              Yersinia pseudotuberculosis uses a type III secretion sy
141                       The bacterial pathogen Yersinia pseudotuberculosis uses type III secretion mach
142 itor identified by in vitro screening, using Yersinia pseudotuberculosis Using a mouse model of P. ae
143                    The lipopolysaccharide of Yersinia pseudotuberculosis V includes a 3,6-dideoxyhexo
144 oxyhexose found in the lipopolysaccharide of Yersinia pseudotuberculosis V, have shown that the C-3 d
145 trasaccharide of the lipopolysaccharide from Yersinia pseudotuberculosis V.
146 he L-colitose biosynthetic gene cluster from Yersinia pseudotuberculosis VI.
147 seudomonas aeruginosa, Erwinia chrysanthemi, Yersinia pseudotuberculosis, Vibrio cholerae (30-70% seq
148 he evolution of Y. pestis from the ancestral Yersinia pseudotuberculosis was a significant reduction
149                        In mice infected with Yersinia pseudotuberculosis, we found that PP barrier dy
150 es of YopB, YopD, and YopE (BDE) secreted by Yersinia pseudotuberculosis were purified by affinity ch
151   During 2001, 89 culture-confirmed cases of Yersinia pseudotuberculosis were reported in Finland; 55
152 stis (the plague bacillus) and its ancestor, Yersinia pseudotuberculosis (which causes self-limited b
153 to colonization by another enteric pathogen, Yersinia pseudotuberculosis, which normally invades the
154 ulated by RovA in both Y. enterocolitica and Yersinia pseudotuberculosis while negatively regulated b
155                             Dissemination of Yersinia pseudotuberculosis within mice after oral inocu
156 ic plague, evolved from the enteric pathogen Yersinia pseudotuberculosis within the past 20,000 years
157 ying degrees of homology to genomic DNA from Yersinia pseudotuberculosis, Yersinia enterocolitica, an
158 as the Yersinia pestis, which causes plague, Yersinia pseudotuberculosis, Yersinia enterocolitica.
159              After oral inoculation of mice, Yersinia pseudotuberculosis yopE and yopH mutants coloni
160  N-terminal domain (residues 1-129) from the Yersinia pseudotuberculosis YopH (YopH-NT) in complex wi
161 iI complexes from Escherichia coli EC869 and Yersinia pseudotuberculosis YPIII to explore the evoluti
162 nal peptide generated by auto-proteolysis of Yersinia pseudotuberculosis YscU, is secreted by the T3S

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