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1 ferase (TAAT) from pathogenic Actinobacillus pleuropneumoniae.
2 ixteenth serovar-designated serovar 16-of A. pleuropneumoniae.
3  porcine respiratory pathogen Actinobacillus pleuropneumoniae.
4 ologous dispersin B enzyme is produced by A. pleuropneumoniae.
5 of Haemophilus influenzae and Actinobacillus pleuropneumoniae.
6 for the identification of pigs exposed to A. pleuropneumoniae.
7 ar to that seen in pigs not infected with A. pleuropneumoniae.
8 ith Salmonella typhimurium or Actinobacillus pleuropneumoniae.
9 gy for TAAs to boost the pathogenicity of A. pleuropneumoniae.
10  in the serum resistance and virulence of A. pleuropneumoniae.
11 perature-sensitive mutants of Actinobacillus pleuropneumoniae 4074, serotype 1, were isolated after t
12 alveolar macrophages (PAMs) and wild-type A. pleuropneumoniae (5b WT) or an Adh-deletion strain (5b D
13 es demonstrated that Adh from Actinobacillus pleuropneumoniae (A. pleuropneumoniae) is required for f
14 ructure of the Cu,Zn SOD from Actinobacillus pleuropneumoniae, a major porcine pathogen, by molecular
15  the role of this in vivo-induced gene in A. pleuropneumoniae, an hfq mutant strain was constructed.
16 e detail, we studied the glycosylation in A. pleuropneumoniae and functionally transferred the glycos
17 to confer NAD independence on Actinobacillus pleuropneumoniae and H. influenzae, has been determined.
18 tidious veterinary pathogens, Actinobacillus pleuropneumoniae and Haemophilus somnus, were developed
19  PCR assay was developed for detection of A. pleuropneumoniae and identification of serotype 5 isolat
20 ally co-infected (n = 7) with Actinobacillus pleuropneumoniae and Pasteurella multocida.
21 ndicates that M. haemolytica, Actinobacillus pleuropneumoniae, and Haemophilus ducreyi form a lineage
22 ceae, Haemophilus influenzae, Actinobacillus pleuropneumoniae, and M. catarrhalis.
23 the lungs and support the hypothesis that A. pleuropneumoniae, and potentially other pulmonary pathog
24  constructed by modifying the Actinobacillus pleuropneumoniae (Ap) plasmid pYG53.
25                               Actinobacillus pleuropneumoniae (App) is the etiological agent of acute
26                   The UT from Actinobacillus pleuropneumoniae, ApUT, the pathogen that causes porcine
27          The recommended QC organisms are A. pleuropneumoniae ATCC 27090 and H. somnus ATCC 700025.
28 dispersal in A. actinomycetemcomitans and A. pleuropneumoniae biofilms.
29 asuis, Pasteurella multocida, Actinobacillus pleuropneumoniae, Bordetella bronchiseptica, and Strepto
30 is common to all 12 capsular serotypes of A. pleuropneumoniae but is not present in the outer membran
31 plicated in the adhesion and virulence of A. pleuropneumoniae, but their role in biofilm formation is
32 first demonstration of the attenuation of A. pleuropneumoniae by introduction of a defined mutation i
33 eloped an assay that uses highly purified A. pleuropneumoniae capsular polysaccharide (CP) conjugated
34        To begin understanding the role of A. pleuropneumoniae capsule in virulence, we sought to iden
35      Respiratory infection by Actinobacillus pleuropneumoniae causes a highly pathogenic necrotizing
36                               Actinobacillus pleuropneumoniae causes pleuropneumonia, an economically
37 n the serum of goats with contagious caprine pleuropneumoniae (CCPP).
38 %) than that of cps5D and the rest of the A. pleuropneumoniae chromosome (42%).
39 yotic consensus promoters showed that the A. pleuropneumoniae consensus promoter is similar to that f
40                              However, the A. pleuropneumoniae consensus promoter is unique in the spa
41                       A comparison of the A. pleuropneumoniae consensus with other prokaryotic consen
42 howed that strains of all 12 serotypes of A. pleuropneumoniae contain DNA homologous to this gene, as
43                      We hypothesized that A. pleuropneumoniae contains a regulator similar to Lrp and
44  or 5a CP produced by isogenic strains of A. pleuropneumoniae correlated with the virulence of the ba
45                                      This A. pleuropneumoniae DNA fragment encoded four open reading
46     The delta-proteobacterium Actinobacillus pleuropneumoniae encodes an unusual pathway for N-linked
47 hlyX gene of the pig pathogen Actinobacillus pleuropneumoniae encodes HlyX, a homologue of FNR, the a
48                           The hfq gene in A. pleuropneumoniae, encoding the RNA chaperone and posttra
49 hat induces the expression of a subset of A. pleuropneumoniae genes identified as specifically induce
50                                 Wild-type A. pleuropneumoniae grew in CDM+BCAA but not in CDM-BCAA in
51             We further show that purified A. pleuropneumoniae His6-Lrp binds in vitro to the A. pleur
52 port the crystal structure of Actinobacillus pleuropneumoniae HMW1C (ApHMW1C), a functional homolog o
53  CDM and attenuated compared to wild-type A. pleuropneumoniae in competitive index experiments in a p
54  stress, and the fitness and virulence of A. pleuropneumoniae in pigs and begin to elucidate the role
55 bute to cross-protective immunity against A. pleuropneumoniae infection remains to be determined.
56        Serologic detection of Actinobacillus pleuropneumoniae infections in swine have been problemat
57 roduced the P5PAB operon from Actinobacillus pleuropneumoniae into an Escherichia coli K-12 strain th
58                               Actinobacillus pleuropneumoniae is a gram-negative bacterial pathogen t
59                               Actinobacillus pleuropneumoniae is a Gram-negative bacterium belonging
60                 Serotyping of Actinobacillus pleuropneumoniae is based on detection of the serotype-s
61 psular polysaccharide (CP) of Actinobacillus pleuropneumoniae is required for virulence of the bacter
62                               Actinobacillus pleuropneumoniae is the causative agent of porcine pleur
63                               Actinobacillus pleuropneumoniae is the etiological agent of a highly co
64                               Actinobacillus pleuropneumoniae is the etiological agent of porcine ple
65 Adh from Actinobacillus pleuropneumoniae (A. pleuropneumoniae) is required for full bacterial pathoge
66 entiates serovars 3, 6, and 8 Actinobacillus pleuropneumoniae isolates, is described.
67  and that it is similar to an Actinobacillus pleuropneumoniae lipoprotein, OmlA.
68                     A genetically defined A. pleuropneumoniae lrp mutant was constructed using an all
69 trations in pulmonary secretions and that A. pleuropneumoniae mutants unable to synthesize BCAA would
70 ized for glycosylation by the Actinobacillus pleuropneumoniae N-glycosyltransferase (NGT) at every po
71 ify glycopeptide formation by Actinobacillus pleuropneumoniae NGT and determine its substrate specifi
72                 Among the 12 serotypes of A. pleuropneumoniae, ohr was found in only serotypes 1, 9,
73 allenge with bacterial species other than A. pleuropneumoniae, or after challenge with A. pleuropneum
74 n pigs were intratracheally infected with A. pleuropneumoniae, pigs pretreated with Ad-5/IL-10 showed
75                   These data suggest that A. pleuropneumoniae produces a group II family capsule simi
76  demonstrated that optimal spacing for an A. pleuropneumoniae promoter is shorter than the spacing id
77 pneumoniae His6-Lrp binds in vitro to the A. pleuropneumoniae promoter regions for ilvI, antisense cp
78                               Actinobacillus pleuropneumoniae promoter-containing clones were isolate
79  multiplex PCR assay enabled us to detect A. pleuropneumoniae rapidly and to distinguish serotype 5 s
80  assays of Ohr activity demonstrated that A. pleuropneumoniae serotype 1 cultures, but not serotype 5
81        We report the identification of an A. pleuropneumoniae serotype 1 gene encoding a protein with
82           Electroporation of cps5ABC into A. pleuropneumoniae serotype 1 strain 4074 generated strain
83 conserved genes required for CP export in A. pleuropneumoniae serotype 1 was cloned and sequenced.
84 pleuropneumoniae, or after challenge with A. pleuropneumoniae serotype 1, 5, or 7.
85          A riboflavin-requiring mutant of A. pleuropneumoniae serotype 1, designated AP233, was const
86                                        In A. pleuropneumoniae serotype 1, expression of ohr was induc
87 e polysaccharides in biofilm formation by A. pleuropneumoniae serotype 1.
88 ype-specific positive regulator of ohr in A. pleuropneumoniae serotype 1.
89 ter membrane protein has been cloned from A. pleuropneumoniae serotype 5 and and has been designated
90 pared from outer membranes of Actinobacillus pleuropneumoniae serotype 5 can elicit protective immuni
91                                       The A. pleuropneumoniae serotype 5 capsular DNA products were r
92      A DNA region involved in Actinobacillus pleuropneumoniae serotype 5 capsular polysaccharide (CP)
93                                           A. pleuropneumoniae serotype 5 capsular polysaccharide is o
94             Our findings suggest that the A. pleuropneumoniae serotype 5 capsule inhibits cell-to-cel
95 ibacter actinomycetemcomitans, but not by A. pleuropneumoniae serotype 5 itself, in a 96-well microti
96 immunogenic in swine infected with either A. pleuropneumoniae serotype 5 or 1A, as well as in swine v
97 r 1A, as well as in swine vaccinated with A. pleuropneumoniae serotype 5 outer membranes.
98 , an ohr gene from serotype 1 cloned into A. pleuropneumoniae serotype 5 was not induced by cumene hy
99 lated from colony biofilms of Actinobacillus pleuropneumoniae serotype 5 were found to inhibit biofil
100 regions of the capsular polysaccharide of A. pleuropneumoniae serotype 5 were used as primers to ampl
101 ar polysaccharide produced by Actinobacillus pleuropneumoniae serotype 5.
102                 A 5.3-kb XbaI fragment of A. pleuropneumoniae serotype 5a J45 genomic DNA that hybrid
103 ys were developed to identify Actinobacillus pleuropneumoniae serotypes 1, 2, and 8.
104 ride, and outer membrane proteins between A. pleuropneumoniae serotypes and other bacterial species.
105          The biotin-CPs of at least three A. pleuropneumoniae serotypes could be combined for use in
106  probe hybridized to genomic DNA from all A. pleuropneumoniae serotypes tested, indicating that this
107 ific to the biosynthesis regions of other A. pleuropneumoniae serotypes would expand the diagnostic a
108                               Actinobacillus pleuropneumoniae synthesizes a serotype-specific capsula
109 ragment was amplified from all strains of A. pleuropneumoniae tested with the exception of serotype 4
110                     Recently, isolates of A. pleuropneumoniae that were serologically distinct from t
111                     When transformed into A. pleuropneumoniae, this cloned gene allowed NAD-independe
112 e of the O antigen reduces the ability of A. pleuropneumoniae to form a biofilm, and this is associat
113 fluenzae (and the homologous enzymes from A. pleuropneumoniae) to produce a unique set of defined glu
114 hether the type or quantity of CP affects A. pleuropneumoniae virulence has not been reported.
115         The role of Hfq in the fitness of A. pleuropneumoniae was assessed in a natural host infectio
116       The consensus promoter sequence for A. pleuropneumoniae was found to be TATAAT and TTG/AAA, cen
117 d, and a consensus promoter structure for A. pleuropneumoniae was identified.
118                          When Actinobacillus pleuropneumoniae was tested, a susceptibility breakpoint
119                            In Actinobacillus pleuropneumoniae, which causes porcine pleuropneumonia,
120                                           A. pleuropneumoniae wild-type extracts did not inhibit S. a
121 hermore, polystyrene surfaces coated with A. pleuropneumoniae wild-type extracts, but not with capsul

 
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