ライフサイエンスコーパス: Pasteurella

1 cing following biochemical identification as Pasteurella.

2 glycosyltransferase proteins found in Type D Pasteurella.

3 ne-associated isolates (P. dagmatis [n = 2], Pasteurella canis [n = 2], and N. canis [n = 1]) are dis

4 Pasteurella canis was the most common isolate of dog bit

5 ourse of inflammation following experimental Pasteurella challenge was altered in C2D recipients.

6 uld help clinicians to make the diagnosis of Pasteurella conjunctivitis in every day practice.

7 Pasteurella dagmatis and Neisseria canis were repeatedly

8 differences in the active sites of these two Pasteurella enzymes.

9 other members of Haemophilus-Actinobacillus-Pasteurella family, where genetic manipulation is limite

10 lycosyltransferases, EXT1 and 2, or to other Pasteurella glycosaminoglycan synthases that produce hya

11 The Pasteurella HA synthase enzyme, pmHAS, catalyzes the syn

12 A Pasteurella haemolytica A1 gene was identified from a re

13 eningococci (GBMs), Escherichia coli K1, and Pasteurella haemolytica A2.

14 nd expression vectors that replicate both in Pasteurella haemolytica and in Escherichia coli were con

15 Twenty-four matched pairs of isolates of Pasteurella haemolytica and three matched pairs of isola

16 A Pasteurella haemolytica cosmid clone that activates leuk

17 nd generation of chromosomal gene fusions in Pasteurella haemolytica has been devised and used to cre

18 Pasteurella haemolytica is an important respiratory path

19 Pasteurella haemolytica is the principal bacterial patho

20 Recent reports have shown that the Pasteurella haemolytica leukotoxin (LKT) and other RTX t

21 ernatant (CCS) preparations of the RTX toxin Pasteurella haemolytica leukotoxin (LKT) contained LKT a

22 The effects of Pasteurella haemolytica leukotoxin (LKT) on the activity

23 Exposure of bovine neutrophils to Pasteurella haemolytica leukotoxin (LKT) stimulates the

24 ciation of two other RTX toxin proteins, the Pasteurella haemolytica leukotoxin (LktA) and the entero

25 The related RTX toxin, the Pasteurella haemolytica leukotoxin structural protein (L

26 Infection of the bovine lung with Pasteurella haemolytica results in an acute respiratory

27 Leukotoxin and endotoxin derived from Pasteurella haemolytica serotype 1 are the primary virul

28 Pasteurella haemolytica serotype 1 is the bacterial agen

29 Pasteurella haemolytica serotype 1 is the bacterium most

30 Pasteurella haemolytica serotype A1 (bovine strain OK) w

31 ine pulmonary surfactant is bactericidal for Pasteurella haemolytica when surfactant and bacteria mix

32 ication (R-M) system of the bovine pathogen, Pasteurella haemolytica, have been identified immediatel

33 Pasteurella haemolytica, the causative agent of shipping

34 e protein of the bovine respiratory pathogen Pasteurella haemolytica, was cloned, and its nucleotide

35 nary tissue after respiratory infection with Pasteurella haemolytica.

36 , Haemophilus somnus, Neisseria species, and Pasteurella haemolytica.

37 had rising antibody titers against RBCV and Pasteurella haemolytica.

38 nchial epithelium after acute infection with Pasteurella haemolytica.

39 0 and 35,000 [32K and 35K, respectively]) of Pasteurella haemolytica.

40 E from Neisseria meningitidis, and LpsA from Pasteurella haemolytica.

41 Mannheimia (Pasteurella) haemolytica A1 produces several virulence f

42 Leukotoxin secreted by Mannheimia (Pasteurella) haemolytica binds to the intact signal pept

43 Leukotoxin (Lkt) secreted by Mannheimia (Pasteurella) haemolytica is an RTX toxin which is specif

44 bility of ruminant leukocytes to Mannheimia (Pasteurella) haemolytica leukotoxin (Lkt).

45 otoxin structural gene (lktA) of Mannheimia (Pasteurella) haemolytica was investigated by nucleotide

46 of OmpA were investigated in 31 Mannheimia (Pasteurella) haemolytica, 6 Mannheimia glucosida, and 4

47 lktC, lktB, and lktD genes in 23 Mannheimia (Pasteurella) haemolytica, 6 Mannheimia glucosida, and 4

48 eptor for leukotoxin secreted by Mannheimia (Pasteurella) haemolytica.

49 onsisting of various portions of both of the Pasteurella heparosan synthases in a single polypeptide

50 sma isolates or from the Acholeplasma or the Pasteurella isolates, demonstrating a high degree of spe

51 PASTEURELLA: Of the more than 17 species of Pasteurella known, Pasteurella multocida subsp. multocid

52 that the 39-kDa cross-protective protein was Pasteurella lipoprotein B, or PlpB.

53 The leukotoxin of Pasteurella (Mannheimia) haemolytica is believed to play

54 Pasteurella (Mannheimia) haemolytica leukotoxin (Lkt) ca

55 The intracellularly acting protein toxin of Pasteurella multocida (PMT) causes numerous effects in c

56 Neuraminidases produced by 16 strains of Pasteurella multocida (serotypes 1 to 16) were character

57 c nonfastidious species were as follows: for Pasteurella multocida and staphylococci tested on Muelle

58 ents were conducted with a zoonotic pathogen Pasteurella multocida and the fluoroquinolone enrofloxac

59 zae, Proteus mirabilis, Vibrio fischeri, and Pasteurella multocida are all cleaved by RNase III as pr

60 Bordetella bronchiseptica and toxigenic Pasteurella multocida are the etiologic agents of swine

61 ly potent against the Gram-negative pathogen Pasteurella multocida both in vitro and in a mouse infec

62 eir potencies against the bacterial pathogen Pasteurella multocida both in vitro and in mouse infecti

63 The fowl cholera pathogen Pasteurella multocida Carter Type A also produces HA in

64 The pnhA gene of Pasteurella multocida encodes PnhA, which is a member of

65 oop sequences from Enterococcus faecalis and Pasteurella multocida gamma-GCS-GS, isoforms that are in

66 To identify Pasteurella multocida genes that are differentially expr

67 The Pasteurella multocida HA synthase, pmHAS, a polymerizing

68 gmented genomic DNA from the animal pathogen Pasteurella multocida has identified a gene encoding a p

69 P]UDP products made by the purified class II Pasteurella multocida HAS were not released by adding un

70 Outer membrane proteins (OMPs) of Pasteurella multocida have various functions related to

71 The Pasteurella multocida heparosan synthases, PmHS1 and PmH

72 The Pasteurella multocida hyaluronan synthase (PmHAS) cataly

73 the literature, of ocular infections due to Pasteurella multocida include: endophtalmitis, keratitis

74 Pasteurella multocida is a bacterial pathogen that cause

75 Pasteurella multocida is a mucosal pathogen that coloniz

76 Pasteurella multocida is a rare cause of neonatal bacter

77 Pasteurella multocida is a small nonmotile gram-negative

78 Pasteurella multocida is a zoonotic Gram-negative cocco-

79 As infection with Pasteurella multocida is common in rabbits, an enzyme im

80 Pasteurella multocida is composed of three subspecies th

81 e rapid, accurate method to detect toxigenic Pasteurella multocida is needed for improved clinical di

82 The dermatonecrotic toxin produced by Pasteurella multocida is one of the most potent mitogeni

83 Pasteurella multocida is the causative agent of a wide r

84 Pasteurella multocida isolates with enrofloxacin MIC of

85 enes encoding Haemophilus influenzae D15 and Pasteurella multocida Oma87 protective outer membrane an

86 hase, PmCS, from the Gram-negative bacterium Pasteurella multocida polymerize the glycosaminoglycan (

87 Toxigenic strains of Pasteurella multocida produce a 146 kDa toxin (PMT) that

88 isolates and 4 attenuated vaccine strains of Pasteurella multocida recovered from multiple avian spec

89 We present a case of fulminant Pasteurella multocida sepsis in a 66-year-old man who ha

90 Fowl cholera is caused by Pasteurella multocida serovars A:1, A:3, and A:4.

91 -ray crystal structures of a multifunctional Pasteurella multocida sialyltransferase (Delta24PmST1) w

92 he structures of a truncated multifunctional Pasteurella multocida sialyltransferase (Delta24PmST1),

93 Pasteurella multocida strains isolated from 15 pigs with

94 ntical for P. multocida subsp. multocida and Pasteurella multocida subsp. gallicida but differs from

95 e more than 17 species of Pasteurella known, Pasteurella multocida subsp. multocida and Pasteurella m

96 Pasteurella multocida subsp. multocida is a commensal an

97 , Pasteurella multocida subsp. multocida and Pasteurella multocida subsp. septica are among the most

98 mediates adhesion of serogroup A strains of Pasteurella multocida to elicited turkey air sac macroph

99 as assessed by exposing broth suspensions of Pasteurella multocida to perflubron for various times.

100 agonists and phospholipase C is activated by Pasteurella multocida toxin (a G(q) alpha-subunit agonis

101 We have shown that Pasteurella multocida toxin (PMT) directly causes transi

102 Pasteurella multocida toxin (PMT) has been hypothesized

103 Pasteurella multocida toxin (PMT) is a potent mitogen fo

104 Pasteurella multocida toxin (PMT) is a potent mitogen kn

105 The Pasteurella multocida toxin (PMT) is a potent mitogen wh

106 atalytic and receptor-binding domains of the Pasteurella multocida toxin (PMT) were investigated.

107 not obvious and is explored with recombinant Pasteurella multocida toxin (rPMT, a Galpha(q) agonist).

108 ion on its own, it potentiated the effect of Pasteurella multocida toxin by 2-fold and ionomycin by 3

109 quires protein kinase C and MEK activity) by Pasteurella multocida toxin, a Galpha(q) agonist that pr

110 er these conditions, treatment of cells with Pasteurella multocida toxin, a selective inhibitor of Ga

111 channel current inhibition was diminished by Pasteurella multocida toxin, mimicked by constitutively

112 These include Pasteurella multocida toxin, which uniquely acts as a mi

113 otein ChaN, and an uncharacterized domain of Pasteurella multocida toxin.

114 ogous to the membrane targeting C1 domain of Pasteurella multocida toxin.

115 des tryptophanase; as well as a homologue of Pasteurella multocida tsaA, which encodes an alkyl perox

116 in a single polypeptide as was found for the Pasteurella multocida Type A PmHAS, the hyaluronan synth

117 Heparosan synthase 1 (PmHS1) from Pasteurella multocida Type D is a dual action glycosyltr

118 Pasteurella multocida Type D, a causative agent of atrop

119 noculated intranasally with 9 x 10(7) CFU of Pasteurella multocida type D.

120 Pasteurella multocida Type F, the minor fowl cholera pat

121 The extracellular polysaccharide capsules of Pasteurella multocida types A, D, and F are composed of

122 ue of the NeuA C-terminal domain (Pm1710) in Pasteurella multocida was also shown to be an esterase,

123 Pasteurella multocida was grown in iron-free chemically

124 ytica and three matched pairs of isolates of Pasteurella multocida were isolated by using a nasal swa

125 The major outer membrane protein (OmpH) of Pasteurella multocida X-73 was purified by selective ext

126 Type A Pasteurella multocida, a prevalent animal pathogen, empl

127 l pathogens, including Haemophilus parasuis, Pasteurella multocida, Actinobacillus pleuropneumoniae,

128 Synechocystis sp., Deinococcus radiodurans, Pasteurella multocida, and Actinobacillus actinomycetemc

129 ose of Salmonella enterica, Vibrio cholerae, Pasteurella multocida, and Haemophilus influenzae.

130 Fowl cholera, a disease caused by Pasteurella multocida, continues to be a major problem f

131 tein, PfhB2, from the opportunistic pathogen Pasteurella multocida, in our analysis.

132 bacteria, including Haemophilus influenzae, Pasteurella multocida, Neisseria gonorrhoeae, Neisseria

133 se of rapidly evolving conjunctivitis due to Pasteurella multocida, occurring after direct inoculatio

134 e genome sequence of a common avian clone of Pasteurella multocida, Pm70.

135 an synthases from the Gram-negative bacteria Pasteurella multocida, PmHS1 and PmHS2, were efficiently

136 5 from Haemophilus influenzae and Oma87 from Pasteurella multocida.

137 ia meningitidis, Haemophilus influenzae, and Pasteurella multocida.

138 nia pestis and the human and animal pathogen Pasteurella multocida.

139 tion of the pig's upper respiratory tract by Pasteurella multocida.

140 ilus influenzae, Neisseria meningitidis, and Pasteurella multocida.

141 ely related species, Actinobacillus suis and Pasteurella multocida.

142 acteria including Haemophilus influenzae and Pasteurella multocida.

143 Haemophilus spp., Neisseria gonorrhoeae, and Pasteurella multocida.

144 the second most common site of infection for PASTEURELLA: Of the more than 17 species of Pasteurella

145 The 35K and 32K major OMPs, designated Pasteurella outer membrane proteins A and B (PomA and Po

146 induced periodontitis ( n = 6-7/group) where Pasteurella pneumotropica ( Pp)-reactive immune response

147 ally infected by the opportunistic bacterium Pasteurella pneumotropica.

148 plex microbiologic mix that usually includes pasteurella species but may also include many other orga

149 lity testing were performed on 73 strains of Pasteurella species isolated from human infections and o

150 Pasteurella species were the most frequent isolates from

151 ear reliable for testing susceptibilities of Pasteurella species.

152 American Type Culture Collection strains of Pasteurella species.

153 ences of the D15-related proteins from other Pasteurella spp.

154 Two and 17 cattle nasally shed Pasteurella spp. before and after transport, respectivel

155 espiratory tract infections with viruses and Pasteurella spp. were determined sequentially among 26 c

156 ive of the 26 lung samples were positive for Pasteurella spp., and their CFU ranged between 4.0 x 10(

157 longs to the HAP (Haemophilus-Actinobacillus-Pasteurella) theta replicon family.

158 ) haemolytica, 6 Mannheimia glucosida, and 4 Pasteurella trehalosi strains by comparative nucleotide

159 ) haemolytica, 6 Mannheimia glucosida, and 4 Pasteurella trehalosi strains.

160 two related species Mannheimia glucosida and Pasteurella trehalosi, and four contain recombinant segm

161 cal Subject Headings Francisella tularensis, Pasteurella tularensis, biological weapon, biological te