ライフサイエンスコーパス: pathogenic Escherichia coli

1 ed in clinical isolates of Shigella spp. and pathogenic Escherichia coli.

2 e and robust colonization resistance against pathogenic Escherichia coli.

3 olibactin toxin involved in the virulence of pathogenic Escherichia coli.

4 ain strains of commensal and extraintestinal pathogenic Escherichia coli.

5 ctin" has been identified in mutualistic and pathogenic Escherichia coli.

6 th Rhodospirillum rubrum and Extraintestinal Pathogenic Escherichia coli.

7 ric bacterium that models human infection by pathogenic Escherichia coli.

8 the homology to the EspG virulence factor of pathogenic Escherichia coli.

9 t of an important iron acquisition system in pathogenic Escherichia coli.

10 simultaneously identify specific alleles in pathogenic Escherichia coli.

11 vates hemolysin, a toxic protein produced by pathogenic Escherichia coli.

12 e the population dynamics of extraintestinal pathogenic Escherichia coli, a common cause of bacteremi

13 or 1 (CNF1), a virulence factor expressed by pathogenic Escherichia coli, acts on Rho-GTPases and spe

14 pathogen used to model infections with human pathogenic Escherichia coli and inflammatory bowel disea

15 the incidence of mutators among isolates of pathogenic Escherichia coli and Salmonella enterica is h

16 nscription factors and their target genes in pathogenic Escherichia coli and Salmonella revealed usin

17 posure routes by measuring enteric bacteria (pathogenic Escherichia coli) and viruses (rotavirus, ent

18 Similar to phytobacteria, Salmonella, pathogenic Escherichia coli, and cross-domain pathogens

19 cterial pathogens (eg, Salmonella, Shigella, pathogenic Escherichia coli, and Yersinia) and the mecha

20 Avian pathogenic Escherichia coli (APEC) causes one of the mos

21 Avian pathogenic Escherichia coli (APEC) causes respiratory an

22 Although avian pathogenic Escherichia coli (APEC) isolates have been in

23 located in the pathogenicity island of avian pathogenic Escherichia coli (APEC) O1's virulence plasmi

24 We have found an avian pathogenic Escherichia coli (APEC) plasmid, pAPEC-O2-Col

25 Infections of avian pathogenic Escherichia coli (APEC) result in annual mult

26 f proteins and was first identified in avian-pathogenic Escherichia coli (APEC) strain chi7122.

27 Avian pathogenic Escherichia coli (APEC) strains cause one of

28 To identify traits that predict avian pathogenic Escherichia coli (APEC) virulence, 124 avian

29 e gene, tsh, isolated from a strain of avian pathogenic Escherichia coli (APEC) was sufficient to con

30 Avian pathogenic Escherichia coli (APEC), an extraintestinal p

31 combat because the etiological agent, avian pathogenic Escherichia coli (APEC), emerges from ubiquit

32 determinant of P fimbriae of extraintestinal pathogenic Escherichia coli, are of considerable epidemi

33 e related biosynthesis of SPM in response to pathogenic Escherichia coli, assessed by targeted liquid

34 Pathogenic Escherichia coli associated with urinary trac

35 Pathogenic Escherichia coli, but not nonpathogenic E. co

36 We previously showed that pathogenic Escherichia coli, but not normal commensal or

37 CFTR is required for uptake and clearance of pathogenic Escherichia coli by CSF-1-derived primary hum

38 Extraintestinal pathogenic Escherichia coli can successfully colonize th

39 thylcytosine restriction endonuclease) CT of pathogenic Escherichia coli, CT596, by injecting several

40 A (ClyA) is an alpha-pore forming toxin from pathogenic Escherichia coli (E. coli) and Salmonella ent

41 pism and ease of genetic manipulation of non-pathogenic Escherichia coli (E. coli) to deliver key imm

42 In pathogenic Escherichia coli E69, a protein, Wza, forms a

43 mphostatin can be regarded as a multitool of pathogenic Escherichia coli, enabling complex interactio

44 nce of biotic factors on the survival of non-pathogenic Escherichia coli, Enterococcus faecalis, and

45 Extra-intestinal pathogenic Escherichia coli (ExPEC) belonging to sequenc

46 Extra-intestinal pathogenic Escherichia coli (ExPEC) can cause a variety

47 ColV plasmids of extraintestinal pathogenic Escherichia coli (ExPEC) encode a variety of

48 l colonisation potential of extra-intestinal pathogenic Escherichia coli (ExPEC) in comparison with t

49 Extraintestinal pathogenic Escherichia coli (ExPEC) is an important huma

50 Extraintestinal pathogenic Escherichia coli (ExPEC) is the leading cause

51 Extraintestinal pathogenic Escherichia coli (ExPEC) is the leading cause

52 Extraintestinal pathogenic Escherichia coli (ExPEC) is the most common g

53 Extraintestinal pathogenic Escherichia coli (ExPEC) reside in the enteri

54 Extracellular pathogenic Escherichia coli (ExPEC) strains are common c

55 nguishing characteristics of extraintestinal pathogenic Escherichia coli (ExPEC) strains are incomple

56 Extraintestinal pathogenic Escherichia coli (ExPEC) strains are typicall

57 A heterogeneous subset of extraintestinal pathogenic Escherichia coli (ExPEC) strains, referred to

58 been proposed as carriers of extraintestinal pathogenic Escherichia coli (ExPEC) with infectious pote

59 nine reservoir hypothesis of extraintestinal pathogenic Escherichia coli (ExPEC), 63 environmental ca

60 RNA modifying enzyme MiaA in extraintestinal pathogenic Escherichia coli (ExPEC), a major cause of ur

61 Extraintestinal pathogenic Escherichia coli (ExPEC), so named because th

62 ids is a defining feature of extraintestinal pathogenic Escherichia coli (ExPEC), such as avian patho

63 of the pks genomic island of extraintestinal pathogenic Escherichia coli (ExPEC), which encodes the g

64 dins (PAC) interaction with extra-intestinal pathogenic Escherichia coli (ExPEC).

65 Multilocus sequence types of potentially pathogenic Escherichia coli from the CRC patients also e

66 s and secrete multiple bacteriocins from non-pathogenic Escherichia coli host strains.

67 A to histone ratios show that microwebs trap pathogenic Escherichia coli in a manner similar to NETs

68 line and endline antibody production against pathogenic Escherichia coli in Laotian children (aged 6-

69 rous studies have examined the prevalence of pathogenic Escherichia coli in poultry and poultry produ

70 Pathogenic Escherichia coli, including enteropathogenic

71 robacter rodentium as a physiologic model of pathogenic Escherichia coli-induced diarrheal disease, c

72 Hemolysin toxin produced and secreted by pathogenic Escherichia coli is one of a family of cytoly

73 e colonization of the human urinary tract by pathogenic Escherichia coli is the mannose-sensitive bin

74 Hemolysin, a toxic protein secreted by pathogenic Escherichia coli, is converted from nontoxic

75 Hemolysin, a toxic protein produced by pathogenic Escherichia coli, is one of a family of homol

76 es encoding Shiga toxin are found in certain pathogenic Escherichia coli (known as Shiga toxin produc

77 efore, it is possible to easily engineer non-pathogenic Escherichia coli lab strains to produce geOMV

78 P fimbriae of extraintestinal pathogenic Escherichia coli mediate digalactoside-specif

79 lthough many strain typing methods exist for pathogenic Escherichia coli, most have drawbacks in term

80 nkages among 804 proteins, and the resulting pathogenic Escherichia coli network composed of 2,043 li

81 We found no difference in the prevalence of pathogenic Escherichia coli, norovirus, or Giardia genes

82 An atypical, Stx2-producing, pathogenic Escherichia coli O157:H(-) strain has been is

83 e (SHSAW) was used for the detection of food pathogenic Escherichia coli O157:H7 (E.coli O157:H7), a

84 he carbon sources that support the growth of pathogenic Escherichia coli O157:H7 in the mammalian int

85 rometric assay to detect single cells of the pathogenic Escherichia coli O157:H7 serotype.

86 tz crystal microbalance for the detection of pathogenic Escherichia coli O157:H7 using TCEP-reduced a

87 405 nm light emitting diodes (LEDs) against pathogenic Escherichia coli O157:H7, Listeria monocytoge

88 viously sequenced evolutionarily instructive pathogenic Escherichia coli O157:H7, O157:H(-), and O55:

89 tein, Shiga toxin type 2 (Stx2), produced by pathogenic Escherichia coli O157:H7.

90 were found in nonremote vs. remote villages [pathogenic Escherichia coli: odds ratio (OR) = 8.4, conf

91 Many pathogenic Escherichia coli produce the toxin alpha-hemo

92 n given orally before enteral infection with pathogenic Escherichia coli reduced bacteremia and morta

93 ultidrug-resistant Klebsiella pneumoniae and pathogenic Escherichia coli, represent potentially novel

94 cer Streptoalloteichus tenebrarius and human pathogenic Escherichia coli, respectively.

95 sing the sensor to various concentrations of pathogenic Escherichia coli revealed detection limits of

96 ed clinical development-ie, extra-intestinal pathogenic Escherichia coli, Salmonella enterica serotyp

97 a and its role in enteric diseases caused by pathogenic Escherichia coli, Salmonella enterica, and Cl

98 of flagella in nonmotile variants of several pathogenic Escherichia coli serotypes.

99 The avian pathogenic Escherichia coli strain (chi)7122 (serotype O

100 was recently identified in the extracellular pathogenic Escherichia coli strain CP9.

101 technique to isolate RNA polymerase from the pathogenic Escherichia coli strain O157:H7 Sakai.

102 f some Gram-negative bacteria, including the pathogenic Escherichia coli strain O157:H7.

103 a 56-kb pathogenicity island (PAI) in avian pathogenic Escherichia coli strain O1:K1 (APEC-O1).

104 Here we engineered a non-pathogenic Escherichia coli strain to specifically lyse

105 ylcytosine (m5C) residues in the genome of a pathogenic Escherichia coli strain.

106 However, pathogenic Escherichia coli strains (enteroinvasive and

107 c necrotizing factors (CNFs) are produced by pathogenic Escherichia coli strains and by Yersinia pseu

108 equence identity to the cdtABC genes of some pathogenic Escherichia coli strains and Haemophilus ducr

109 ondary mutations occurred in extraintestinal pathogenic Escherichia coli strains CP9, CFT073, and RS2

110 normal colonization of the colonic mucosa by pathogenic Escherichia coli strains producing a cyclomod

111 Afa/Dr family of adhesins are produced by pathogenic Escherichia coli strains that are especially

112 an autotransporter protein secreted by avian-pathogenic Escherichia coli strains that colonize the re

113 Adherence of pathogenic Escherichia coli strains to intestinal epithe

114 The adherence of pathogenic Escherichia coli strains to intestinal epithe

115 A library of recombinant non-pathogenic Escherichia coli strains was engineered to ex

116 ed as secondary reservoirs for commensal and pathogenic Escherichia coli strains, but the ecological

117 To elucidate the evolution of pathogenic Escherichia coli strains, here we sequenced s

118 rate the ability to discriminate between two pathogenic Escherichia coli strains, O157:H7 Sakai and u

119 Notably, homologous GRMs are also encoded in pathogenic Escherichia coli strains.

120 nicity islands in all Shigella spp. and some pathogenic Escherichia coli strains.

121 on is enhanced when platelets are exposed to pathogenic Escherichia coli that produce the pore-formin

122 factor type 1 (CNF1) and CNF2 are toxins of pathogenic Escherichia coli that share 85% identity over

123 Microcin PDI inhibits a diversity of pathogenic Escherichia coli through the action of an eff

124 The FimH type-1 fimbrial adhesin allows pathogenic Escherichia coli to adhere to glycoproteins i

125 ic respiration is required for commensal and pathogenic Escherichia coli to colonize mice.

126 Fimbrial adhesins mediate the attachment of pathogenic Escherichia coli to various host tissues lead

127 Extra-intestinal pathogenic Escherichia coli ubiquitously colonize the hu

128 eviously used for studies of extraintestinal pathogenic Escherichia coli were clinically relevant for