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