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1 ixteenth serovar-designated serovar 16-of A. pleuropneumoniae.
2 ferase (TAAT) from pathogenic Actinobacillus 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 gy for TAAs to boost the pathogenicity of A. pleuropneumoniae.
7 for the identification of pigs exposed to A. pleuropneumoniae.
8 ar to that seen in pigs not infected with A. pleuropneumoniae.
9 ith Salmonella typhimurium or Actinobacillus 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 ndicates that M. haemolytica, Actinobacillus pleuropneumoniae, and Haemophilus ducreyi form a lineage
22 the lungs and support the hypothesis that A. pleuropneumoniae, and potentially other pulmonary pathog
27 asuis, Pasteurella multocida, Actinobacillus pleuropneumoniae, Bordetella bronchiseptica, and Strepto
28 is common to all 12 capsular serotypes of A. pleuropneumoniae but is not present in the outer membran
29 plicated in the adhesion and virulence of A. pleuropneumoniae, but their role in biofilm formation is
30 first demonstration of the attenuation of A. pleuropneumoniae by introduction of a defined mutation i
31 eloped an assay that uses highly purified A. pleuropneumoniae capsular polysaccharide (CP) conjugated
37 yotic consensus promoters showed that the A. pleuropneumoniae consensus promoter is similar to that f
40 howed that strains of all 12 serotypes of A. pleuropneumoniae contain DNA homologous to this gene, as
42 or 5a CP produced by isogenic strains of A. pleuropneumoniae correlated with the virulence of the ba
44 The delta-proteobacterium Actinobacillus pleuropneumoniae encodes an unusual pathway for N-linked
45 hlyX gene of the pig pathogen Actinobacillus pleuropneumoniae encodes HlyX, a homologue of FNR, the a
47 hat induces the expression of a subset of A. pleuropneumoniae genes identified as specifically induce
50 port the crystal structure of Actinobacillus pleuropneumoniae HMW1C (ApHMW1C), a functional homolog o
51 CDM and attenuated compared to wild-type A. pleuropneumoniae in competitive index experiments in a p
52 stress, and the fitness and virulence of A. pleuropneumoniae in pigs and begin to elucidate the role
53 bute to cross-protective immunity against A. pleuropneumoniae infection remains to be determined.
58 psular polysaccharide (CP) of Actinobacillus pleuropneumoniae is required for virulence of the bacter
62 Adh from Actinobacillus pleuropneumoniae (A. pleuropneumoniae) is required for full bacterial pathoge
66 trations in pulmonary secretions and that A. pleuropneumoniae mutants unable to synthesize BCAA would
67 ify glycopeptide formation by Actinobacillus pleuropneumoniae NGT and determine its substrate specifi
69 allenge with bacterial species other than A. pleuropneumoniae, or after challenge with A. pleuropneum
70 n pigs were intratracheally infected with A. pleuropneumoniae, pigs pretreated with Ad-5/IL-10 showed
72 demonstrated that optimal spacing for an A. pleuropneumoniae promoter is shorter than the spacing id
73 pneumoniae His6-Lrp binds in vitro to the A. pleuropneumoniae promoter regions for ilvI, antisense cp
75 multiplex PCR assay enabled us to detect A. pleuropneumoniae rapidly and to distinguish serotype 5 s
76 assays of Ohr activity demonstrated that A. pleuropneumoniae serotype 1 cultures, but not serotype 5
79 conserved genes required for CP export in A. pleuropneumoniae serotype 1 was cloned and sequenced.
85 ter membrane protein has been cloned from A. pleuropneumoniae serotype 5 and and has been designated
86 pared from outer membranes of Actinobacillus pleuropneumoniae serotype 5 can elicit protective immuni
91 ibacter actinomycetemcomitans, but not by A. pleuropneumoniae serotype 5 itself, in a 96-well microti
92 immunogenic in swine infected with either A. pleuropneumoniae serotype 5 or 1A, as well as in swine v
94 , an ohr gene from serotype 1 cloned into A. pleuropneumoniae serotype 5 was not induced by cumene hy
95 lated from colony biofilms of Actinobacillus pleuropneumoniae serotype 5 were found to inhibit biofil
96 regions of the capsular polysaccharide of A. pleuropneumoniae serotype 5 were used as primers to ampl
100 ride, and outer membrane proteins between A. pleuropneumoniae serotypes and other bacterial species.
102 probe hybridized to genomic DNA from all A. pleuropneumoniae serotypes tested, indicating that this
103 ific to the biosynthesis regions of other A. pleuropneumoniae serotypes would expand the diagnostic a
105 ragment was amplified from all strains of A. pleuropneumoniae tested with the exception of serotype 4
108 e of the O antigen reduces the ability of A. pleuropneumoniae to form a biofilm, and this is associat
109 fluenzae (and the homologous enzymes from A. pleuropneumoniae) to produce a unique set of defined glu
117 hermore, polystyrene surfaces coated with A. pleuropneumoniae wild-type extracts, but not with capsul
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