ライフサイエンスコーパス: Bacteroides fragilis

1 ivity associated with the choA orthologue in Bacteroides fragilis.

2 ivated lamina propria lymphocytes (LPLs), or Bacteroides fragilis.

3 Sp1 and our previously determined PS A2 from Bacteroides fragilis.

4 pared cell extracts of the obligate anaerobe Bacteroides fragilis.

5 semination of antibiotic resistance genes in Bacteroides fragilis.

6 alkyl hydroperoxide reductase (ahp) gene in Bacteroides fragilis.

7 ivalis but not that from Escherichia coli or Bacteroides fragilis.

8 identical residues) to the RecA protein from Bacteroides fragilis.

9 ulture of which grew E. coli, Prevotella and Bacteroides fragilis.

10 I from the anaerobic Gram-negative bacterium Bacteroides fragilis.

11 icobacter pylori, Clostridium difficile, and Bacteroides fragilis.

12 nsal bacteria including Escherichia coli and Bacteroides fragilis.

13 homologue of RprY, a response regulator from Bacteroides fragilis.

14 n of dizinc metallo-beta-lactamase CcrA from Bacteroides fragilis.

15 ts containing Escherichia coli (150 CFU) and Bacteroides fragilis (10(4) CFU) into the abdominal cavi

16 polysaccharide biosynthesis locus, PS B2, of Bacteroides fragilis 638R are described, and the sequenc

17 ysaccharide, PS A2, from the clinical strain Bacteroides fragilis 638R.

18 e (FKP), a bifunctional enzyme isolated from Bacteroides fragilis 9343, which converts l-fucose into

19 nimals with the ubiquitous gut microorganism Bacteroides fragilis, a bacterial polysaccharide (PSA) d

20 label various commensal anaerobes, including Bacteroides fragilis, a common and immunologically impor

21 Bacteroides fragilis, a component of the normal intestin

22 tic mechanism of metallo-beta-lactamase from Bacteroides fragilis, a dinuclear Zn(II)-containing enzy

23 Bacteroides fragilis, a Gram-negative colonic bacterium,

24 lates of several bacterial strains including Bacteroides fragilis, a pathogen commonly found in suppu

25 Although Bacteroides fragilis accounts for only 0.5% of the norma

26 demonstrate that the prominent gut commensal Bacteroides fragilis activates the TLR pathway to establ

27 hich is produced by the intestinal commensal Bacteroides fragilis, activates CD4+ T cells, resulting

28 efficient capsule biogenesis in E. coli and Bacteroides fragilis also depends on processive antiterm

29 The obligately anaerobic bacterium Bacteroides fragilis, an opportunistic pathogen and inha

30 plex between the metallo-beta-lactamase from Bacteroides fragilis and 4-morpholinoethanesulfonic acid

31 C57B/6 mice were untreated or treated with Bacteroides fragilis and antibiotic-mediated depletion o

32 : C57B/6 mice were untreated or treated with Bacteroides fragilis and antibiotic-mediated depletion o

33 The combination of Bacteroides fragilis and Bacillus subtilis consistently

34 tative oriT region necessary for transfer in Bacteroides fragilis and Escherichia coli.

35 t dinuclear zinc metallo-beta-lactamase from Bacteroides fragilis and its complex with a biphenyl tet

36 cificity of the metallo-beta-lactamases from Bacteroides fragilis and other similar organisms is the

37 ave protein O-glycosylation systems, that of Bacteroides fragilis and related species is unique in th

38 g LPS structures of various bacteria such as Bacteroides fragilis and Salmonella abortus are observed

39 gainst abscesses induced by bacteria such as Bacteroides fragilis and Staphylococcus aureus.

40 olysaccharide C (PS C) biosynthesis locus of Bacteroides fragilis and to determine whether distinct l

41 n new work with and vaccine development with Bacteroides fragilis and Yersinia, Shigella, and Salmone

42 pathogens, including Staphylococcus aureus, Bacteroides fragilis, and a combination of Enterococcus

43 ntibiofilm effects on Staphylococcus aureus, Bacteroides fragilis, and Candida albicans are investiga

44 mixed cultures containing Escherichia coli, Bacteroides fragilis, and Clostridium perfringens.

45 ing Fusobacterium nucleatum, enterotoxigenic Bacteroides fragilis, and colibactin-producing Escherich

46 uding those found in Haemophilus influenzae, Bacteroides fragilis, and Proteus mirabilis.

47 ed to Stenotrophomonas maltophilia, to a few Bacteroides fragilis, and to rare pathogens.

48 hpCF, dps, and katB in the obligate anaerobe Bacteroides fragilis are controlled by the redox-sensiti

49 Strains of Bacteroides fragilis associated with diarrhea in childre

50 Strains of Bacteroides fragilis associated with diarrheal disease (

51 (Omp200, composed of Omp121 and Omp71) from Bacteroides fragilis ATCC 25285 was purified and tryptic

52 The proteinase was recovered from Bacteroides fragilis ATCC 25285(pFD340-prtP) cells by 3-

53 d to T-cell stimulating immunogen PS A1 from Bacteroides fragilis ATCC 25285/NCTC 9343 via a physiolo

54 etobacter baumannii, Neisseria meningitidis, Bacteroides fragilis, Bacillus anthracis, Yersinia pesti

55 g glycoantigen (GlyAg) polysaccharide A from Bacteroides fragilis but not conventional peptides.

56 el is inconsistent with the observation that Bacteroides fragilis can colonize the colon in the absen

57 Bacteroides fragilis can replicate in atmospheres contai

58 rom the Gram-negative opportunistic pathogen Bacteroides fragilis, can rescue the ultraviolet sensiti

59 The Bacteroides fragilis capsular polysaccharide complex is

60 gulatory mechanism is similar to that of the Bacteroides fragilis capsular polysaccharides and establ

61 s directed to a preferred target site in the Bacteroides fragilis chromosome by a transposon-encoded

62 7, a new 52-kb transfer factor isolated from Bacteroides fragilis clinical isolate LV23.

63 nd was isolated from an antibiotic resistant Bacteroides fragilis clinical isolate.

64 developed to detect the bft gene subtypes in Bacteroides fragilis clinical isolates.

65 lent bacterial gastrointestinal inhabitants: Bacteroides fragilis, Clostridium perfringens, Escherich

66 The Bacteroides fragilis conjugal plasmid pBFTM10 contains t

67 The symbiont Bacteroides fragilis constitutes a relatively small prop

68 Bacteroides fragilis constitutes about 1% of the bacteri

69 nt of MIA offspring with the human commensal Bacteroides fragilis corrects gut permeability, alters m

70 The human commensal Bacteroides fragilis delivers immunomodulatory molecules

71 Bacteroides fragilis-derived LPS, however, can effective

72 s of two Uxs-type UDP-GlcA decarboxylases of Bacteroides fragilis, designated BfUxs1 and BfUxs2.

73 de, PSA, produced by the commensal bacterium Bacteroides fragilis directs development of the immune s

74 ort herein that a prominent human commensal, Bacteroides fragilis, directs the development of Foxp3(+

75 enzyme from Bacillus cereus differs from the Bacteroides fragilis enzyme in sequence, zinc stoichiome

76 inally in two Bacteroides clinical isolates, Bacteroides fragilis ERL and B. thetaiotaomicron DOT.

77 taphylococci (CNS), Peptostreptococcus spp., Bacteroides fragilis, Escherichia coli, Enterococcus spp

78 Enterotoxigenic Bacteroides fragilis (ETBF) causes diarrhea and is impli

79 Enterotoxigenic Bacteroides fragilis (ETBF) cells produce a 20-kDa heat-

80 Enterotoxigenic Bacteroides fragilis (ETBF) has been implicated in infla

81 tinal disease, the bacterium enterotoxigenic Bacteroides fragilis (ETBF) is a significant source of c

82 The human commensal enterotoxigenic Bacteroides fragilis (ETBF) is linked to both inflammato

83 Enterotoxigenic Bacteroides fragilis (ETBF) produces the Bacteroides fra

84 Enterotoxigenic Bacteroides fragilis (ETBF) secretes a 20-kDa metallopro

85 Enterotoxigenic Bacteroides fragilis (ETBF) strains produce a 20-kDa zin

86 Enterotoxigenic Bacteroides fragilis (ETBF) strains, which produce a 20-

87 gens, Arcobacter species and enterotoxigenic Bacteroides fragilis (ETBF), in 201 U.S. and European tr

88 ith the human gut bacterium, enterotoxigenic Bacteroides fragilis (ETBF), to investigate the link bet

89 The burden of enterotoxigenic Bacteroides fragilis (ETBF)-related diarrhea was determi

90 y a human colonic bacterium, enterotoxigenic Bacteroides fragilis (ETBF).

91 at may promote such competition, we screened Bacteroides fragilis for the production of antimicrobial

92 Bacteroides fragilis, for example, synthesizes eight cap

93 Bacteroides fragilis GA3 is known to mediate potent inte

94 A Bacteroides fragilis gene (argF'(bf)), the disruption of

95 .6%), Porphyromonas species (11.3%), and the Bacteroides fragilis group (10.2%).

96 The predominant anaerobes were as follows: Bacteroides fragilis group (85 isolates), Peptostreptoco

97 (n = 43), Sphingobacterium spp. (n = 3), and Bacteroides fragilis group (n = 15).

98 The predominant anaerobes were Bacteroides fragilis group (n = 9) and Peptostreptococcu

99 Members of the Bacteroides fragilis group are among the most common ana

100 More Bacteroides fragilis group bacteremias were detected onl

101 which phenotypically resemble members of the Bacteroides fragilis group but phylogenetically display

102 robial susceptibility data of species of the Bacteroides fragilis group for 1989-1990 and 1998-1999 s

103 s bile sensitive and quite distinct from the Bacteroides fragilis group of anaerobes.

104 ntly better for several genera including the Bacteroides fragilis group, Fusobacterium, Clostridium,

105 One member of this family from Bacteroides fragilis had exquisite substrate specificity

106 Here, we demonstrate that Bacteroides fragilis has a general O-glycosylation syste

107 The human gut symbiont Bacteroides fragilis has a general protein O-glycosylati

108 Enterotoxigenic Bacteroides fragilis has been associated with diarrheal

109 nine biosynthesis in the anaerobic bacterium Bacteroides fragilis has been purified and crystallized

110 The chromosome of Bacteroides fragilis has been shown to undergo 13 distin

111 olymerization of polysaccharide A (PSA) from Bacteroides fragilis in the endosome depends on the APC'

112 specificity metallo-beta-lactamase CcrA from Bacteroides fragilis in the presence and absence of a ti

113 Survival of Bacteroides fragilis in the presence of oxygen was depen

114 We report a case of metronidazole-resistant Bacteroides fragilis in the United States and demonstrat

115 ssion of CcrA, a metallo-beta-lactamase from Bacteroides fragilis, in Escherichia coli requires a mut

116 munomodulatory molecule of the gut commensal Bacteroides fragilis, induces regulatory T cells to secr

117 ate early-phase immunologic events following Bacteroides fragilis infection in the peritoneal cavity,

118 g bacteria such as Staphylococcus aureus and Bacteroides fragilis initiate this host response when tr

119 tin capsules containing Escherichia coli and Bacteroides fragilis into the abdomens of rats (n = 9).

120 The opportunistic pathogen Bacteroides fragilis is a commensal organism in the larg

121 Bacteroides fragilis is a constituent of the normal resi

122 The anaerobe Bacteroides fragilis is a gram-negative, opportunistic p

123 The anaerobe Bacteroides fragilis is a highly aerotolerant, opportuni

124 Bacteroides fragilis is a member of the normal colonic m

125 t polysaccharide A (PSA) from the capsule of Bacteroides fragilis is a potent activator of CD4(+) T c

126 Enterotoxigenic anaerobic Bacteroides fragilis is a significant source of inflamma

127 jor clinical manifestation of infection with Bacteroides fragilis is the formation of intra-abdominal

128 Bacteroides fragilis is the leading cause of anaerobic b

129 Bacteroides fragilis is the most common anaerobe isolate

130 The obligate anaerobe, Bacteroides fragilis, is a highly aerotolerant intestina

131 The human intestinal microorganism, Bacteroides fragilis, is able to extensively modulate it

132 strate that the human colonic microorganism, Bacteroides fragilis, is able to modulate its surface an

133 The intestinal anaerobic symbiont, Bacteroides fragilis, is highly aerotolerant and resista

134 d that the anaerobic, opportunistic pathogen Bacteroides fragilis lacks the glutathione/glutaredoxin

135 of Tn5520, a new mobilizable transposon from Bacteroides fragilis LV23.

136 coli R1, Pseudomonas aeruginosa PAC608, and Bacteroides fragilis), mixed together to form a cocktail

137 Here, we report that the intestinal microbe Bacteroides fragilis modifies the homeostasis of host in

138 A Bacteroides fragilis mutant resistant to hydrogen peroxi

139 We previously showed that a Bacteroides fragilis mutant unable to synthesize 4 of th

140 onic capsular polysaccharide of the anaerobe Bacteroides fragilis NCTC 9343, designated polysaccharid

141 ry to identify the sphingolipids produced by Bacteroides fragilis NCTC 9343.

142 ements were found in the genome sequences of Bacteroides fragilis NCTC9343 and Bacteroides thetaiotao

143 The genetic element flanking the Bacteroides fragilis pathogenicity island (BfPAI) in ent

144 yl-(1-3)-beta-glucopyranose (PGG)-glucan and Bacteroides fragilis polysaccharide A (PS A), were evalu

145 icha coli, beta-hemolytic streptococcus, and Bacteroides fragilis predominating.

146 metabolites, but symptoms are relieved by a Bacteroides fragilis probiotic.

147 Enterotoxigenic strains of Bacteroides fragilis produce an extracellular metallopro

148 Bacteroides fragilis produces a capsular polysaccharide

149 Bacteroides fragilis produces a capsular polysaccharide

150 n CNS demyelination, and we demonstrate that Bacteroides fragilis producing a bacterial capsular poly

151 investigated the cellular mechanism by which Bacteroides fragilis promotes the development of intraab

152 In the gut, Bacteroides fragilis protects against colitis through in

153 eport here that the prominent human symbiont Bacteroides fragilis protects animals from experimental

154 is factor for the human intestinal commensal Bacteroides fragilis, protects against central nervous s

155 In Bacteroides fragilis, PS synthesis is regulated so that

156 unomodulatory effects of the archetypal ZPS, Bacteroides fragilis PSA.

157 ysaccharides in the important human symbiont Bacteroides fragilis raised the critical question of how

158 We reveal that Bacteroides fragilis releases PSA in outer membrane vesi

159 ebsiella oxytoca, Staphylococcus aureus, and Bacteroides fragilis remains largely undefined and test

160 mmensal bacteria, Bifidobacterium longum and Bacteroides fragilis, representative members of the gut

161 F1687 proteins from Bacteroides vulgatus and Bacteroides fragilis respectively are members of the Pfa

162 tion of the ccf genes in the model symbiont, Bacteroides fragilis, results in colonization defects in

163 -terminal sequence of sialidases produced by Bacteroides fragilis SBT3182, another commensal enteric

164 pellets inoculated with Escherichia coli and Bacteroides fragilis (sepsis).

165 ng animals with polysaccharide A (PS A) from Bacteroides fragilis shortly before or after challenge p

166 /-7 motifs (TTTG/TANNTTTG) were identical to Bacteroides fragilis sigma(ABfr) consensus -33/-7 promot

167 atalysis of metallo-beta-lactamase CcrA from Bacteroides fragilis, site-directed mutants of CcrA were

168 function of the metallo-beta-lactamase from Bacteroides fragilis, spectroscopic and metal-binding st

169 capsular polysaccharides of many strains of Bacteroides fragilis, Staphylococcus aureus, and Strepto

170 YT135.2.8, a Tn4400' insertion mutant of Bacteroides fragilis strain TM4000, grows poorly when us

171 Enterotoxigenic Bacteroides fragilis strains associated with childhood d

172 Bacteroides fragilis, Streptococcus pneumoniae, Prevotel

173 cillospira, Rickenellaceae, Parabacteroides, Bacteroides fragilis, Sutterella, Lachnospiraceae, 4-met

174 switching roles between the two species (as Bacteroides fragilis switches roles between humans and m

175 A single strain of Bacteroides fragilis synthesizes eight distinct capsular

176 Bacteroides fragilis synthesizes eight distinct capsular

177 tly nonmotile (Bacteroides thetaiotaomicron, Bacteroides fragilis, Tannerella forsythensis, Porphyrom

178 Strains of Bacteroides fragilis that produce a ca. 20-kDa heat-labi

179 Enterotoxigenic Bacteroides fragilis that secrete a zinc-dependent metal

180 factor contributing to the pathogenicity of Bacteroides fragilis, the most common anaerobic species

181 Bacteroides fragilis, though only a minor component of t

182 valuate the role of the C-terminal region in Bacteroides fragilis toxin (BFT) activity, processing, a

183 The Bacteroides fragilis toxin (BFT) is the only known virul

184 role of the zinc-binding metalloprotease in Bacteroides fragilis toxin (BFT) processing and activity

185 high-level expression of biologically active Bacteroides fragilis toxin (BFT), we studied the express

186 The only known ETBF virulence factor is the Bacteroides fragilis toxin (BFT), which induces E-cadher

187 nic Bacteroides fragilis (ETBF) produces the Bacteroides fragilis toxin, which has been associated wi

188 A modified version of the Bacteroides fragilis transposon Tn4400, designated Tn440

189 P. gingivalis with a modified version of the Bacteroides fragilis transposon Tn4400.

190 ntained on conserved ICE and are confined to Bacteroides fragilis Unlike GA1 and GA2 T6SS loci, most

191 the reaction pathway for binuclear CcrA from Bacteroides fragilis using density functional theory bas

192 tyrosine site-specific recombinase (Tsr) of Bacteroides fragilis was characterized.

193 atB catalase gene in the anaerobic bacterium Bacteroides fragilis was studied.

194 a sixth target, the zinc beta-lactamase from Bacteroides fragilis, was screened against the fragment-

195 lysaccharide biosynthesis locus promoters of Bacteroides fragilis were determined from bacteria grown

196 f the opportunistic human anaerobic pathogen Bacteroides fragilis, which is currently classified as a

197 We characterized the nanLET operon in Bacteroides fragilis, whose products are required for th

198 of Escherichia coli, Neisseria meningitidis, Bacteroides fragilis, Yersinia pestis, Chlamydia trachom

199 MD) simulations of the dinuclear form of the Bacteroides fragilis zinc beta-lactamase.