ライフサイエンスコーパス: Burkholderia cepacia

1 and in the use of a prolonged incubation for Burkholderia cepacia.

2 is and other species, including (cultivable) Burkholderia cepacia.

3 bors, such as Burkholderia thailandensis and Burkholderia cepacia.

4 oteobacteria including a clinical isolate of Burkholderia cepacia.

5 ise bacteria previously identified merely as Burkholderia cepacia.

6 and an internal fragment of an NRAMP gene in Burkholderia cepacia.

7 Clearance of Burkholderia cepacia, a major pathogen in CGD, was reduc

8 Burkholderia cepacia AC1100 completely degrades 2,4,5-tr

9 Burkholderia cepacia AC1100 metabolizes 2,4,5-trichlorop

10 Burkholderia cepacia AC1100 uses 2,4,5-trichlorophenoxya

11 ptional activation by insertion sequences in Burkholderia cepacia AC1100 were investigated.

12 ont Rhizobium NGR234 and the root-colonizing Burkholderia cepacia AMMD, conferred to Escherichia coli

13 cretion genes in the gram-negative bacterium Burkholderia cepacia, an important pulmonary pathogen in

14 MN(+) mice survived after being administered Burkholderia cepacia, an opportunistic pathogen in CGD p

15 ese reactive species in host defense against Burkholderia cepacia and Chromobacterium violaceum, orga

16 Protocatechuate dioxygenase from Burkholderia cepacia and the substrate, protocatechuate,

17 gative pathogens, including Yersinia pestis, Burkholderia cepacia, and Acinetobacter haemolyticus, sy

18 Youth, Burkholderia cepacia, and cystic fibrosis-related arthro

19 s of IS285 from Yersinia pestis, IS1356 from Burkholderia cepacia, and ISRm3 from Rhizobium meliloti.

20 late isolates of Pseudomonas aeruginosa and Burkholderia cepacia are associated with differences in

21 monas aeruginosa, Staphylococcus aureus, and Burkholderia cepacia, are known contributors.

22 ipase B) and Amano Lipase PS-C1 (lipase from Burkholderia cepacia) as biocatalysts.

23 ase for phthalate transport, was cloned from Burkholderia cepacia ATCC 17616.

24 ueous Pb(II) sorbed at the interface between Burkholderia cepacia biofilms and hematite (alpha-Fe(2)O

25 during apoptosis induced by phagocytosis of Burkholderia cepacia, Borrelia hermsii, Listeria monocyt

26 spp., Ralstonia spp., Burkholderia gladioli, Burkholderia cepacia, Burkholderia thailandensis, and Ps

27 In HAECs, PAO1, PAK, and Burkholderia cepacia, but not flagellin-deficient strain

28 rbaspirillum species can be misidentified as Burkholderia cepacia by commercially available microbial

29 n the pathogenesis of respiratory disease in Burkholderia cepacia-colonized cystic fibrosis (CF) pati

30 ost described the use of selective media for Burkholderia cepacia complex (99%), Staphylococcus aureu

31 Burkholderia cepacia complex (Bcc) are a group of multid

32 Strains of the Burkholderia cepacia complex (Bcc) are Gram-negative opp

33 Gram-negative bacteria of the Burkholderia cepacia complex (Bcc) are opportunistic pat

34 The localization of Burkholderia cepacia complex (Bcc) bacteria in cystic fi

35 Among them, the Burkholderia cepacia complex (Bcc) bacteria, consisting

36 Members of the Burkholderia cepacia complex (Bcc) cause considerable mo

37 The Burkholderia cepacia complex (Bcc) consists of several s

38 Several species within the Burkholderia cepacia complex (BCC) have emerged as signi

39 Biofilm cultures of Burkholderia cepacia complex (BCC) infection have been f

40 oacae, Stenotrophomonas maltophilia, and the Burkholderia cepacia complex (BCC) may be able to produc

41 undred thirty-eight clinical isolates of the Burkholderia cepacia complex (Bcc) were identified using

42 terization of the opportunistic pathogens of Burkholderia cepacia complex (BCC), a group composed of

43 Burkholderia cepacia complex and Burkholderia pseudomall

44 Organisms from the Burkholderia cepacia complex are important pathogens in

45 However, patients with Burkholderia cepacia complex are often excluded from tra

46 Chronic infection with Burkholderia cepacia complex bacteria in cystic fibrosis

47 initive identification of the species in the Burkholderia cepacia complex by routine clinical microbi

48 Species of the Burkholderia cepacia complex cause chronic and life-thre

49 Bacteria of the Burkholderia cepacia complex consist of five discrete ge

50 fe threatening infection with species of the Burkholderia cepacia complex frequently occurs as a resu

51 or the rapid detection and identification of Burkholderia cepacia complex genomovars directly from sp

52 Burkholderia cepacia complex infections contribute signi

53 t pathogens that account for the majority of Burkholderia cepacia complex infections in cystic fibros

54 Misidentification of A. xylosoxidans as Burkholderia cepacia complex is especially problematic a

55 We analyzed Burkholderia cepacia complex isolates recovered from 1,2

56 r relative levels of accuracy in identifying Burkholderia cepacia complex isolates recovered from cys

57 Our understanding of the virulence of Burkholderia cepacia complex lung infections in cystic f

58 PCR primers targeting loci in the current Burkholderia cepacia complex multilocus sequence typing

59 Pseudomonas aeruginosa and members of the Burkholderia cepacia complex often coexist in both the s

60 y related to, and commonly misidentified as, Burkholderia cepacia complex or Ralstonia species.

61 thods is difficult, and differentiation from Burkholderia cepacia complex organisms may be especially

62 Over a 6-year period, Burkholderia cepacia complex species were isolated from

63 n of only 44% of the genes between LB400 and Burkholderia cepacia complex strain 383.

64 rosis (CF) patients including members of the Burkholderia cepacia complex that cause a high rate of m

65 ted from biofilms produced by species of the Burkholderia cepacia complex were shown to possess clust

66 It is also a member of the Burkholderia cepacia complex, a group of closely related

67 ia cenocepacia is an important member of the Burkholderia cepacia complex, a group of closely related

68 s species and closely related species in the Burkholderia cepacia complex, accurate identification is

69 elective media designed for the isolation of Burkholderia cepacia complex, along with two media desig

70 Within the Burkholderia cepacia complex, B. cenocepacia is the most

71 epacia strain K56-2, a representative of the Burkholderia cepacia complex, is part of the epidemic an

72 Gram-negative bacterium and a member of the Burkholderia cepacia complex, which is frequently associ

73 to identify species (genomovars) within the Burkholderia cepacia complex.

74 ptible to life-threatening infections by the Burkholderia cepacia complex.

75 were initially identified as members of the Burkholderia cepacia complex.

76 cep781, whose hosts are soil isolates of the Burkholderia cepacia complex.

77 ars I, III, and IV) currently constitute the Burkholderia cepacia complex.

78 Burkholderia cepacia DBO1 is able to utilize phthalate a

79 A gene was cloned from Burkholderia cepacia DBO1 that is homologous with Escher

80 enzymes needed for phthalate degradation by Burkholderia cepacia DBO1.

81 We investigated the utility of PCR to detect Burkholderia cepacia directly in sputum samples at two c

82 more active than other tetracyclines against Burkholderia cepacia, Escherichia coli, Serratia marcesc

83 on of the related toluene o-monooxygenase of Burkholderia cepacia G4 and a previously reported T4MO G

84 vity of toluene ortho-monooxygenase (TOM) of Burkholderia cepacia G4 for both chlorinated ethenes and

85 ion and toluene ortho-monooxygenase (TOM) of Burkholderia cepacia G4 hydroxylates at the ortho positi

86 Toluene 2-monooxygenase from Burkholderia cepacia G4 is implicated in trichloroethyle

87 alyzed a collection of 97 well-characterized Burkholderia cepacia genomovar III isolates to evaluate

88 Burkholderia cepacia has emerged as a serious respirator

89 Burkholderia cepacia has emerged as an important pulmona

90 Burkholderia cepacia has recently been recognized as an

91 Burkholderia cepacia infection decreased survival, regar

92 Burkholderia cepacia is an emerging opportunistic pathog

93 Burkholderia cepacia is an important opportunistic human

94 Burkholderia cepacia is an important pathogen in cystic

95 Burkholderia cepacia is an opportunistic pathogen that h

96 More Burkholderia cepacia isolates (P < 0.01), Candida albica

97 phan catabolic pathway is characterized from Burkholderia cepacia J2315.

98 t some other nonfermentative bacilli such as Burkholderia cepacia (MIC(90), >/=128 microg/ml).

99 ), Stenotrophomonas maltophilia (n = 1), and Burkholderia cepacia (n = 1).

100 egorize patients into panresistant (n = 27) (Burkholderia cepacia, n = 6, and Pseudomonas aeruginosa,

101 Recurrence of infection with Burkholderia cepacia or Serratia marcescens was caused b

102 We experienced two Burkholderia cepacia outbreaks over a 1-year period.

103 ied within a 27-kb region of DNA cloned from Burkholderia cepacia R34, a strain that grows using 2,4-

104 oblematic, and analysis of isolates from the Burkholderia cepacia Research Laboratory and Repository

105 ng a panel of 102 isolates obtained from the Burkholderia cepacia Research Laboratory and Repository.

106 ferredoxins (the Thermus Rieske protein, the Burkholderia cepacia Rieske-type biphenyl dioxygenase fe

107 veral clinical and environmental isolates of Burkholderia cepacia secreted ATP-utilizing enzymes to t

108 m of this study was to compare RGM medium to Burkholderia cepacia selective agar (BCSA) and a standar

109 ients with CF by extending incubation of the Burkholderia cepacia selective agar (BCSA) from 5 to 14

110 Extended incubation on Burkholderia cepacia selective agar (BCSA) has been reco

111 subspecies level, from Middlebrook 7H11 and Burkholderia cepacia selective agars.

112 Burkholderia cepacia sepsis/pneumonia was the second mos

113 dation of tryptophan through anthranilate by Burkholderia cepacia, several plasposon mutations were c

114 ung disease including Staphylococcal aureus, Burkholderia cepacia, Stenotrophomonas maltophilia, Achr

115 led tobramycin did not increase isolation of Burkholderia cepacia, Stenotrophomonas maltophilia, or A

116 y reviewing isolates initially identified as Burkholderia cepacia susceptible to all antibiotics test

117 but was less sensitive for the detection of Burkholderia cepacia than the standard method.

118 Burkholderia cepacia was isolated from 3 of [corrected]

119 rgillus fumigatus, Staphylococcus aureus, or Burkholderia cepacia were compared in wild-type, X-CGD m

120 The final case grew Burkholderia cepacia, which was not grown in the sputum.

121 incubated with P. aeruginosa strain PAK and Burkholderia cepacia, while little activation was observ