ライフサイエンスコーパス: Proteus mirabilis

1 roteus-like (MR/P) fimbriae of uropathogenic Proteus mirabilis.

2 philus influenzae, Bacteroides fragilis, and Proteus mirabilis.

3 een of the isolates were E. coli and one was Proteus mirabilis.

4 ion, is a virulence factor for uropathogenic Proteus mirabilis.

5 acid decarboxylase that inhibits swarming in Proteus mirabilis.

6 d for swarming in the urinary tract pathogen Proteus mirabilis.

7 ity to a putrescine-deficient speA mutant of Proteus mirabilis.

8 es in Klebsiella spp., Escherichia coli, and Proteus mirabilis.

9 important virulence factor of uropathogenic Proteus mirabilis.

10 toxin to prevent urinary tract infection by Proteus mirabilis.

11 ifferentiation of Klebsiella pneumoniae from Proteus mirabilis 16S rRNA target sequences differing by

12 (4.4%), Stenotrophomonas maltophilia (4.3%), Proteus mirabilis (4.0%), Klebsiella oxytoca (2.7%), and

13 Here we characterize PmDsbA from Proteus mirabilis, a bacterial pathogen increasingly ass

14 Proteus mirabilis, a cause of complicated urinary tract

15 Proteus mirabilis, a cause of complicated urinary tract

16 Recently, we identified a genomic island of Proteus mirabilis, a common agent of catheter-associated

17 Proteus mirabilis, a common cause of nosocomial and cath

18 Proteus mirabilis, a common cause of urinary tract infec

19 Proteus mirabilis, a gram-negative bacterium associated

20 Proteus mirabilis, a gram-negative bacterium, is a frequ

21 Proteus mirabilis, a Gram-negative bacterium, represents

22 Proteus mirabilis, a leading cause of catheter-associate

23 Proteus mirabilis alternates between motile and adherent

24 Proteus mirabilis, an etiologic agent of complicated uri

25 have shown previously using hyperflagellated Proteus mirabilis and a motile but non-swarming flgN tra

26 significant, especially against the bacteria Proteus mirabilis and Antibiotic resistant Escherichia c

27 of Gram-negative bacterial cells, including Proteus mirabilis and Caulobacter crescentus, initiates

28 We focused on Lrp from Proteus mirabilis and E. coli, orthologs with 98% identi

29 The closely related Proteus mirabilis and Enterobacterlaceae plasmid-encoded

30 of a urease-negative mutant of uropathogenic Proteus mirabilis and its wild-type parent strain was as

31 during UTI caused by the major uropathogens Proteus mirabilis and Klebsiella pneumoniae, in addition

32 operon as a major assimilatory checkpoint in Proteus mirabilis and other Gram-negative bacteria and e

33 The Proteus mirabilis and plasmid-encoded urease loci contai

34 The urease-positive species Proteus mirabilis and Providencia stuartii are two of th

35 zation by urease-positive organisms, such as Proteus mirabilis and Providencia stuartii, commonly occ

36 s II promoter sequences of Escherichia coli, Proteus mirabilis and Salmonella typhimurium allowed det

37 cherichia coli, Pseudomonas aeruginosa PAO1, Proteus mirabilis and Serratia marcescens, possibly by i

38 segregate from other human pathogens such as Proteus mirabilis and Staphylococcus aureus that outcomp

39 ier studies, lrp genes from Vibrio cholerae, Proteus mirabilis, and E. coli were introduced into the

40 ct on the numbers of Salmonella typhimurium, Proteus mirabilis, and Escherichia coli internalized by

41 ization of wild-type Salmonella typhimurium, Proteus mirabilis, and Escherichia coli.

42 i, Salmonella muenchen, Serratia marcescens, Proteus mirabilis, and Proteus vulgaris).

43 as Klebsiella pneumoniae, Escherichia coli, Proteus mirabilis, and Salmonella enterica serovar Typhi

44 olates of Escherichia coli, Klebsiella spp., Proteus mirabilis, and Salmonella spp. and are associate

45 ted urinary tract infections (UTI) caused by Proteus mirabilis are associated with severe pathology i

46 Fimbriae of the human uropathogen Proteus mirabilis are the only characterized surface pro

47 Using Proteus mirabilis as a model, we investigate the role of

48 ol for application of the mini-Tn7 system in Proteus mirabilis as an example of a bacterium with a se

49 Proteus mirabilis, associated with complicated urinary t

50 One of the six predicted Proteus mirabilis autotransporters (ATs), ORF c2341, is

51 onstructed from the 50 %-identical TEM-1 and Proteus mirabilis beta-lactamases.

52 become encrusted and blocked by crystalline Proteus mirabilis biofilms.

53 Proteus mirabilis can rapidly utilize choline to enhance

54 Proteus mirabilis causes complicated urinary tract infec

55 fundamental behaviors of motile, rod-shaped Proteus mirabilis cells (3 mum in length) adsorbed to th

56 re also found in cell-free supernatants from Proteus mirabilis, Citrobacter freundii and Enterobacter

57 A total of 63 clinical isolates of Proteus mirabilis collected over a 19-month period were

58 Proteus mirabilis colonies exhibit striking geometric re

59 Proteus mirabilis commonly infects the complicated urina

60 Proteus mirabilis compromises the care of many patients

61 n CFT073, is a functional homolog of MrpJ of Proteus mirabilis; ectopic expression of papX in P. mira

62 ns), Listeria monocytogenes (three strains), Proteus mirabilis, Escherichia coli (three strains), and

63 Proteus mirabilis forms extensive crystalline biofilms o

64 Proteus mirabilis forms extensive crystalline biofilms o

65 In this study, we describe wosA, a Proteus mirabilis gene identified by its ability to incr

66 In a search for Proteus mirabilis genes that were regulated by cell-to-c

67 rming motility by the urinary tract pathogen Proteus mirabilis has been a long-studied but little und

68 -ray crystal structure of a Crl homolog from Proteus mirabilis in conjunction with in vivo and in vit

69 se-resistant Proteus-like (MR/P) fimbriae of Proteus mirabilis, indicate that MrpB functions as the t

70 acteriaceae and in particular the pathobiont Proteus mirabilis, induced robust IL-1beta release that

71 , Seo et al. (2015) show that the pathobiont Proteus mirabilis induces NLRP3 inflammasome-dependent i

72 hat provides a clear visual early warning of Proteus mirabilis infection and subsequent blockage.

73 The enteric bacterium Proteus mirabilis is a common cause of complicated urina

74 Proteus mirabilis is a common cause of urinary tract inf

75 Proteus mirabilis is a common uropathogen in patients wi

76 Proteus mirabilis is a dimorphic motile bacterium well k

77 Proteus mirabilis is a dimorphic, motile bacterium often

78 The gram-negative enteric bacterium Proteus mirabilis is a frequent cause of urinary tract i

79 Proteus mirabilis is a Gram-negative bacterium that exis

80 Proteus mirabilis is a Gram-negative bacterium that unde

81 Proteus mirabilis is a model organism for urease-produci

82 Proteus mirabilis is a urinary tract pathogen and well k

83 Proteus mirabilis is a urinary tract pathogen that diffe

84 Proteus mirabilis is an opportunistic pathogen that is f

85 The enteric bacterium Proteus mirabilis is associated with a significant numbe

86 The bacterium Proteus mirabilis is capable of movement on solid surfac

87 Swarming by Proteus mirabilis is characterized by cycles of rapid an

88 rotease, ZapA, of the urinary tract pathogen Proteus mirabilis is co-ordinately expressed along with

89 loacae isolates, 2 S. marcescens isolates, 1 Proteus mirabilis isolate, and 2 A. baumannii isolates)

90 Swarming colonies of independent Proteus mirabilis isolates recognize each other as forei

91 6 (3%) Klebsiella sp. isolates, and 7 (100%) Proteus mirabilis isolates tested were CTX-M positive, w

92 ebsiella pneumoniae, Klebsiella oxytoca, and Proteus mirabilis isolates, including phenotypically ESB

93 gh level of similarity to sequences encoding Proteus mirabilis mannose-resistant fimbriae.

94 lular migration in a non-swarming but motile Proteus mirabilis mutant lacking the FIgN facilitator of

95 ae (n = 4), Pseudomonas aeruginosa (n = 14), Proteus mirabilis (n = 3), Serratia spp. (n = 10), Steno

96 Molecular analyses have revealed that Proteus mirabilis possesses two genes, flaA and flaB, th

97 Uropathogenic Proteus mirabilis produces at least four types of fimbri

98 kb PAI, designated ICEPm1, that is common to Proteus mirabilis, Providencia stuartii, and Morganella

99 scherichia coli 1021, Klebsiella pneumoniae, Proteus mirabilis, Providencia stuartii, and Pseudomonas

100 ibrary included probes for Escherichia coli, Proteus mirabilis, Pseudomonas aeruginosa, Enterocococcu

101 gram negative bacteria are Escherichia coli, Proteus mirabilis, Pseudomonas aeruginosa, Klebsiella pn

102 An isolate of Proteus mirabilis recovered from blood cultures of a dia

103 Escherichia coli, Klebsiella pneumoniae, and Proteus mirabilis remains unknown.

104 structures of CaiT from Escherichia coli and Proteus mirabilis revealed an inverted five-transmembran

105 prevent colonization by common uropathogens Proteus mirabilis, Staphylococcus aureus and Escherichia

106 y used to assess the relatedness of swarming Proteus mirabilis strains, was used to study 15 P. aerug

107 by Escherichia coli, Klebsiella pneumoniae, Proteus mirabilis, Streptococcus pyogenes, Bacillus subt

108 Proteus mirabilis swarming behavior is characterized by

109 een to identify rhomboid-encoding genes from Proteus mirabilis, tatA was identified as a multicopy su

110 Here, we identified a gene from Proteus mirabilis that encodes a 135-amino acid residue

111 In laboratory models of colonization by Proteus mirabilis, the sensor signaled encrustation at a

112 MR/P fimbriae of uropathogenic Proteus mirabilis undergo invertible element-mediated ph

113 Proteus mirabilis urease catalyzes the hydrolysis of ure

114 Expression of Proteus mirabilis urease is governed by UreR, an AraC-li

115 We tested the hypothesis that experimental Proteus mirabilis urinary tract infection in mice would

116 truncated form of hemolysin A (HpmA265) from Proteus mirabilis using a series of functional and struc

117 Patients with Proteus mirabilis UTIs were more likely to have a foreig

118 higher than the averages were observed with Proteus mirabilis versus imipenem and with Klebsiella pn

119 e arfA hairpins from Haemophilus influenzae, Proteus mirabilis, Vibrio fischeri, and Pasteurella mult

120 to virulence in other pathogens, its role in Proteus mirabilis was investigated by constructing a str

121 A TnphoA mutant of Proteus mirabilis was isolated, which had lost the abili

122 genesis of urinary tract infection caused by Proteus mirabilis, we constructed a nonmotile, nonswarmi

123 riminating strains of Myxococcus xanthus and Proteus mirabilis, we found the rates of killing between

124 tract pathogens, Pseudomonas aeruginosa and Proteus mirabilis, were made bioluminescent by stable in

125 ebsiella pneumoniae, Klebsiella oxytoca, and Proteus mirabilis with an ertapenem-susceptible extended

126 plementation studies with hemolysin-negative Proteus mirabilis WPM111 (a HpmA(-) mutant of BA6163) tr