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1 aused in mammals by Bordetella pertussis and Bordetella bronchiseptica.
2 ol), crucial for early nasal colonization of Bordetella bronchiseptica.
3 d A modification in F. tularensis as well as Bordetella bronchiseptica.
4 , Mycoplasma felis, Chlamydophila felis, and Bordetella bronchiseptica.
5 ent in some strains of Bordetella hinzii and Bordetella bronchiseptica.
6 ontrol system regulates biofilm formation in Bordetella bronchiseptica.
7 lated pathogens Bordetella parapertussis and Bordetella bronchiseptica.
8 pertussis, as shown in a previous study with Bordetella bronchiseptica.
9 transport genes in Bordetella pertussis and Bordetella bronchiseptica.
10 to have a branchial cleft cyst infected with Bordetella bronchiseptica.
11 spiratory pathogens Bordetella pertussis and Bordetella bronchiseptica Although B. pertussis represen
13 fusions to gfp fusions in Escherichia coli, Bordetella bronchiseptica and Agrobacterium tumefaciens.
15 We have also identified equivalent loci in Bordetella bronchiseptica and Bordetella parapertussis a
16 produce pertussis toxin (PT); however, both Bordetella bronchiseptica and Bordetella parapertussis c
18 hern blot analysis indicates that strains of Bordetella bronchiseptica and Bordetella parapertussis h
21 agL gene encoding lipid A 3-O-deacylase from Bordetella bronchiseptica and by inactivation of the lgt
22 on of motility and coregulated phenotypes in Bordetella bronchiseptica and by the expression of vrg l
23 the Bvg-phase, characterized by motility in Bordetella bronchiseptica and by the expression of vrg l
24 nnotated genomes of Bordetella pertussis and Bordetella bronchiseptica and controls their infectious
25 anno-heptose 1beta-ADP pathways operative in Bordetella bronchiseptica and Mesorhizobium loti and by
26 e Bvg- phase is characterized by motility in Bordetella bronchiseptica and the expression of vrg loci
27 co-infections with the respiratory bacterium Bordetella bronchiseptica and the gastrointestinal helmi
28 assembly of O antigen on the animal pathogen Bordetella bronchiseptica and the human pathogen B. para
34 ella pertussis, Bordetella parapertussis and Bordetella bronchiseptica are closely related Gram-negat
35 lla pertussis, Bordetella parapertussis, and Bordetella bronchiseptica are closely related subspecies
37 y structure of a ZIP-family transporter from Bordetella bronchiseptica at 3.05 angstrom resolution in
38 ta-1,6-GlcNAc by various Bordetella species (Bordetella bronchiseptica, B. pertussis, and B. parapert
39 rally occurring analog to phage display, the Bordetella bronchiseptica bacteriophage (BP) employs a h
40 we present a study on a prokaryotic ZIP from Bordetella bronchiseptica (BbZIP) by combining structura
41 ensive research on the prototypical ZIP from Bordetella bronchiseptica (BbZIP) have suggested an elev
43 rt-like protein (ZIP) metal transporter from Bordetella bronchiseptica (BbZIP) revealed an unpreceden
44 but failed to grow on any tested strains of Bordetella bronchiseptica, Bordetella hinzii, Bordetella
46 B. pertussis, Bordetella parapertussis, and Bordetella bronchiseptica by allelic exchange generated
47 erentiated from Bordetella parapertussis and Bordetella bronchiseptica by hybridization with organism
50 orter protein produced by all members of the Bordetella bronchiseptica cluster, which includes B. per
51 onella enterica, Pseudomonas aeruginosa, and Bordetella bronchiseptica contain an outer membrane 3-O-
53 reparing a conjugate vaccine composed of the Bordetella bronchiseptica core oligosaccharide with one
54 by constructing an in-frame deletion in the Bordetella bronchiseptica cyaA structural gene and compa
56 oli, the fauA genes of both B. pertussis and Bordetella bronchiseptica directed the production of a 7
57 spiratory pathogens Bordetella pertussis and Bordetella bronchiseptica employ a type III secretion sy
62 ogenic bacteria Bordetella parapertussis and Bordetella bronchiseptica express a lipopolysaccharide O
64 rtussis are nonmotile human pathogens, while Bordetella bronchiseptica expresses flagellin and causes
65 from pH 6.0 to 7.6, Bordetella pertussis and Bordetella bronchiseptica FtrABCD system mutants showed
68 determined, in addition to the structure of Bordetella bronchiseptica GmhB bound to Mg(2+) and ortho
72 y by Taylor-Mulneix et al. demonstrates that Bordetella bronchiseptica has two different gene suites
73 nducing a protective immune response against Bordetella bronchiseptica in a mouse model of intranasal
74 e norepinephrine could promote the growth of Bordetella bronchiseptica in iron-restricted medium cont
75 in the shedding of the respiratory bacterium Bordetella bronchiseptica in rabbits with one or two gas
76 er, in the absence of either P. multocida or Bordetella bronchiseptica, induced a mild but statistica
77 the same transplant center developed severe Bordetella bronchiseptica infections within 3 days of ea
79 annel ZIPB from the Gram-negative bacterium, Bordetella bronchiseptica Irradiating ZIPB by microsecon
87 the hurIR bhuRSTUV heme utilization locus in Bordetella bronchiseptica is coordinately controlled by
88 spiratory pathogens Bordetella pertussis and Bordetella bronchiseptica is dependent on the BfeA outer
92 pertussis is thought to have derived from a Bordetella bronchiseptica-like ancestor, we hypothesized
97 We investigated Bordetella pertussis and Bordetella bronchiseptica LPS-derived core oligosacchari
98 A ortholog present in each of the genomes of Bordetella bronchiseptica (lpxA(Br)), Bordetella paraper
102 A mutant, with the heterologous wlb locus of Bordetella bronchiseptica or B. parapertussis restored p
105 scribe the identification of a novel gene in Bordetella bronchiseptica, plrS, the product of which sh
106 e mammal-adapted Bordetella species (such as Bordetella bronchiseptica) produce a capsule of undeterm
109 unlike a closely related zoonotic pathogen, Bordetella bronchiseptica, raising important questions a
110 present in Bordetella pertussis Tohama I and Bordetella bronchiseptica RB50 differ in the number of 9
117 wer generation of vaccines, we constructed a Bordetella bronchiseptica strain (LPaV) that does not ex
118 und that alcaligin siderophore production by Bordetella bronchiseptica strain RB50 is Bvg repressed.
120 lI and PtlF in nonreduced cell extracts of a Bordetella bronchiseptica strain which overexpresses the
121 oral and steady-state manner by constructing Bordetella bronchiseptica strains in which the bvgAS pro
122 ratory infection by Bordetella pertussis and Bordetella bronchiseptica strains whose genomes are curr
124 velop acute pneumonia after inoculation with Bordetella bronchiseptica, suggesting that TLR4 is requi
125 The ability of Bvg(-)-phase and Bvg(+)-phase Bordetella bronchiseptica swine isolates, grown under mo
126 ecently, we identified a phenotypic phase of Bordetella bronchiseptica that displays reduced virulenc
127 tified a gene expressed in the Bvg+ phase of Bordetella bronchiseptica that shows a high degree of se
129 the molecular characterization of ZIPB from Bordetella bronchiseptica, the first ZIP homolog to be p
132 - phase genes are involved in the ability of Bordetella bronchiseptica to grow and disseminate via th
133 ins play an important role in the binding of Bordetella bronchiseptica to mammalian cells, an event t
136 we report an immunomodulation involving the Bordetella bronchiseptica type III secretion system (TTS
141 sms, including the broad host range pathogen Bordetella bronchiseptica We recently discovered an addi
146 hooping cough, is a human-adapted variant of Bordetella bronchiseptica, which displays a broad host r
148 d on the structure of a prokaryotic homolog, Bordetella bronchiseptica ZrT/Irt-like protein (bbZIP),