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

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

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

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

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

5 ain strains of commensal and extraintestinal pathogenic Escherichia coli.

6 simultaneously identify specific alleles in pathogenic Escherichia coli.

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

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

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

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

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

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

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

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

15 Avian pathogenic Escherichia coli (APEC) causes respiratory an

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

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

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

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

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

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

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

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

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

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

26 Pathogenic Escherichia coli associated with urinary trac

27 Pathogenic Escherichia coli, but not nonpathogenic E. co

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

29 Extraintestinal pathogenic Escherichia coli can successfully colonize th

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

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

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

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

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

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

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

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

38 Extraintestinal pathogenic Escherichia coli (ExPEC) strains are typicall

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

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

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

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

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

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

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

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

47 Pathogenic Escherichia coli, including enteropathogenic

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

66 Many pathogenic Escherichia coli produce the toxin alpha-hemo

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

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

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

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

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

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

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

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

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

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

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

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

79 However, pathogenic Escherichia coli strains (enteroinvasive and

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

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

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

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

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

85 Adherence of pathogenic Escherichia coli strains to intestinal epithe

86 The adherence of pathogenic Escherichia coli strains to intestinal epithe

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

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

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

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

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

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

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

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

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

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

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