ライフサイエンスコーパス: bacterial adherence

1 g such infection, likely by interfering with bacterial adherence.

2 pifluorescence assay of chloride efflux, and bacterial adherence.

3 ivalis but had no influences on F. nucleatum bacterial adherence.

4 roscopy (scanning EM) was used to quantitate bacterial adherence.

5 (IgA), the main immune mechanism preventing bacterial adherence.

6 g, and secretion of ECM proteins to increase bacterial adherence.

7 exposure of the polysaccharide receptor for bacterial adherence.

8 serum increased significantly ULVWF-mediated bacterial adherence.

9 st evidence of a novel mechanism to regulate bacterial adherence.

10 lC2 is necessary for K. kingae piliation and bacterial adherence.

11 ates and sterilizes the crypt, thus reducing bacterial adherence.

12 abrogate LT's ability to promote subsequent bacterial adherence.

13 s directed against either SpaB or SpaC block bacterial adherence.

14 nd in the cell-attached form participates in bacterial adherence.

15 ree energy of the metal probes, facilitating bacterial adherence.

16 ty of sera from immunized animals to inhibit bacterial adherence.

17 , which acts to bind fibronectin and promote bacterial adherence.

18 binding domains are required for full-level bacterial adherence.

19 en antibody raised to each protein inhibited bacterial adherence.

20 n results in antibody-mediated inhibition of bacterial adherence, a critical early event in the patho

21 R phosphorylation by AG1478 had no effect on bacterial adherence, actin recruitment to sites of attac

22 letion of aggR or aggA significantly reduced bacterial adherence and (independently) translocation of

23 d a collective/cooperative increase in their bacterial adherence and aggregation.

24 ariety of cell surface factors which mediate bacterial adherence and colonization at the intestinal e

25 en implicated as an important determinant of bacterial adherence and colonization of the urinary trac

26 infection and in vitro cell culture model of bacterial adherence and defense gene and signaling pathw

27 rabbit tracheal explant cultures and assayed bacterial adherence and host cell Ca(2+) signaling.

28 the important functions of the CBP family to bacterial adherence and identify a pneumococcal vaccine

29 d immunity, to explore the trade-off between bacterial adherence and immune evasion.

30 l surface virulence factors involved in both bacterial adherence and inflammation.

31 Abnormal bacterial adherence and internalization in enterocytes h

32 The hpIgR-mediated bacterial adherence and invasion were abolished by eithe

33 ggesting a novel mechanism for regulation of bacterial adherence and microcolony formation.

34 to rabbits, produced antibodies that reduced bacterial adherence and neutralized the cell-killing act

35 ding proteins (Gbp) that play major roles in bacterial adherence and pathogenesis.

36 of Escherichia coli K12 (E. coli), promoting bacterial adherence and phagocytosis.

37 ptor for Escherichia coli K-12 that promotes bacterial adherence and phagocytosis.

38 hypothesis that keratinocyte injury promotes bacterial adherence and the development of group A strep

39 ich are produced after skin injury, modulate bacterial adherence and the initiation of group A strept

40 his interaction significantly contributes to bacterial adherence and thus may play a significant role

41 ne designed to generate antibodies to reduce bacterial adherence and to neutralize the cytotoxic acti

42 viral surface-exposed proteins that enhance bacterial adherence and/or invasion.

43 cterium have been suggested to play roles in bacterial adherence, and also in inflammation, by trigge

44 anslocation, that intestinal mucus modulates bacterial adherence, and that increased levels of mucosa

45 Bacterial virulence gene expression, bacterial adherence, and transepithelial electrical resi

46 Bacterial adherence assay was performed on in vivo corne

47 , we examined their binding specificities in bacterial adherence assays by using porcine brush border

48 es of S. epidermidis associated with initial bacterial adherence, biofilm formation, and intercellula

49 ype 1 pilus adhesin, FimH, mediates not only bacterial adherence, but also invasion of human bladder

50 esion interference and the susceptibility of bacterial adherence by these plasma preparations were al

51 neumoniae has been implicated as a factor in bacterial adherence, colonization, and invasion in the p

52 neumoniae has been implicated as a factor in bacterial adherence, colonization, and invasion in the p

53 the ability of elicited serum Abs to inhibit bacterial adherence compared with immunization with the

54 We conclude that Iha is a novel bacterial adherence-conferring protein and is contained

55 showed that this toxin-mediated increase in bacterial adherence correlated with an Stx-evoked increa

56 ory effects of CsrRS and environmental pH on bacterial adherence correlated with their effects on the

57 ated that glycan:glycan interaction-mediated bacterial adherence could be competitively inhibited by

58 BALB/c mice that were better able to inhibit bacterial adherence demonstrated an increase in Abs able

59 Proteins important in bacterial adherence deserve consideration as potential v

60 containing fibronectin, which is involved in bacterial adherence, from basolateral to the apical memb

61 milks on intestinal barrier function repair, bacterial adherence in Caco-2 and HEp-2 cells, intestina

62 Bacterial adherence in cellulose-binding assays was sign

63 ned beta1 integrin clustered at locations of bacterial adherence in porcine and bovine tissue.

64 ased the susceptibility of murine corneas to bacterial adherence in vivo.

65 h the time course of S. aureus invasion, and bacterial adherence induced the MAPK pathway.

66 mine whether stress and/or diet influence(s) bacterial adherence-induced changes in epithelial permea

67 gate the potential relations between mucosal bacterial adherence, intestinal mucus and mucin content,

68 disease, the absolute level of inhibition of bacterial adherence is insufficient to reduce the bacter

69 noclonal human IgA1 substrate and to enhance bacterial adherence, linking localization to enzyme func

70 To explore the relations between intestinal bacterial adherence, mucus bacterial binding, and bacter

71 There was no convincing evidence that bacterial adherence on the cornea was increased in Muc1

72 rnalization was associated with preferential bacterial adherence on the exposed enterocyte lateral su

73 rnalization was associated with preferential bacterial adherence on the exposed lateral surface of en

74 The variation in bacterial adherence only partially accounted for these d

75 l vaccine would induce antibodies to prevent bacterial adherence, promote opsonophagocytic killing by

76 ndings suggest that nucleolin is involved in bacterial adherence promoted by all intimin types and th

77 novo purine biosynthesis but did not impact bacterial adherence properties in vitro or in the bladde

78 These interactions affect bacterial adherence, resistance to serum killing and pha

79 g-Gly-Asp peptide, to TPBM culture inhibited bacterial adherence similarly to the inhibition previous

80 -8 and MCP-1 production was not dependent on bacterial adherence since similar results were obtained

81 he probes used in this study likely promoted bacterial adherence through two different mechanisms: th

82 y, we observed that PH mediated an increased bacterial adherence to alveolar epithelial cells in the

83 ) in Y. pestis KIM is required for efficient bacterial adherence to and internalization by cultured H

84 is a matricellular glycoprotein facilitating bacterial adherence to and invasion into eukaryotic cell

85 specifically block type 1 fimbriae-mediated bacterial adherence to bladder epithelial cells in situ

86 gen is believed to be important in promoting bacterial adherence to both intravascular catheters and

87 e for IRF-1 activation, which is enhanced by bacterial adherence to cells.

88 ding proteins, other than FnBPs, can mediate bacterial adherence to cells.

89 -mediated viral co-infection correlated with bacterial adherence to cells.

90 portant role in bacteriophage attachment and bacterial adherence to certain host cells, suggesting th

91 adhesin in HCG is called Cha, which mediates bacterial adherence to cultured human epithelial cells.

92 FHA mediates bacterial adherence to epithelial cells and macrophages

93 ustering of the DAF receptor at the sites of bacterial adherence to epithelial cells is proposed as a

94 cosphingolipid asialo-GM1 (aGM1) can mediate bacterial adherence to epithelial cells, but the steps s

95 and 3) to analyze the effect of HNP-1 on the bacterial adherence to epithelial cells.

96 Bacterial adherence to extracellular matrix proteins (EC

97 nant N23 effectively inhibited ClfB-mediated bacterial adherence to fibrinogen, and N123 caused some

98 specific attachment to fibronectin, blocked bacterial adherence to fibronectin-coated slides, and su

99 cal in meningococcal pathogenesis, mediating bacterial adherence to host cells, and modulating human

100 vidence that these ligands indeed do promote bacterial adherence to host cells, and with new insights

101 YadA deletion decreased bacterial adherence to host cells, whereas invasin delet

102 glycoprotein fibronectin, which facilitates bacterial adherence to host cells.

103 ) have been reported to significantly reduce bacterial adherence to host cells.

104 rmeability and acid sensitivity, and reduced bacterial adherence to host cells.

105 urface-exposed PepO-C1q interaction mediates bacterial adherence to host epithelial cells.

106 Bacterial adherence to host tissue involves specific mic

107 that these proteinaceous fibers are used for bacterial adherence to host tissues and for the establis

108 nt increase in the inflammatory response and bacterial adherence to human ciliated epithelial culture

109 of the serum from immunized mice to inhibit bacterial adherence to human salivary agglutinin by a BI

110 lar metabolic processes, this toxin promotes bacterial adherence to intestinal epithelial cells.

111 Bacterial adherence to intravenous catheters may be medi

112 patients and those with retinal detachments, bacterial adherence to lenses, prophylactic measures, an

113 ling activity of neutrophils, and preventing bacterial adherence to lung epithelial cells.

114 loss-of-function mutations in pilU increased bacterial adherence to ME-180 human epithelial cells eig

115 ised to purified rabbit SI complex inhibited bacterial adherence to microvilli.

116 LXA4 stable analogs did not alter bacterial adherence to nor internalization by epithelia,

117 The disruption of hfq did not affect bacterial adherence to or invasion of host cells but did

118 However, loss of Scl-1 did not alter bacterial adherence to or invasion of skin keratinocytes

119 The SpaA pili are known to mediate bacterial adherence to pharyngeal epithelial cells.

120 P4-mediated bacterial adherence to pharynx, type II alveolar, and br

121 In vitro, bacterial adherence to platelets, fibrin matrices, or fi

122 Paramyxoviruses augmented bacterial adherence to primary bronchial epithelial cell

123 We found that Hap promotes bacterial adherence to purified fibronectin, laminin, an

124 After bacterial adherence to receptors on the mammalian cell m

125 sted their effect in a colonization model of bacterial adherence to respiratory epithelial cells in c

126 asopharynx, a process that likely depends on bacterial adherence to respiratory epithelial cells.

127 dhesins are homologous proteins that promote bacterial adherence to respiratory epithelium and are th

128 athogenesis of K. kingae disease begins with bacterial adherence to respiratory epithelium, which is

129 In contrast, SP-A and SP-D effects on bacterial adherence to SAEC differed between the two str

130 may be indispensable in establishing stable bacterial adherence to saliva-coated surfaces in the ora

131 It is possible that bacterial adherence to salivary pellicle occurs as a cum

132 ificant difference in the ability to inhibit bacterial adherence to salivary-agglutinin-coated hydrox

133 -aspartate repeat protein SdrC promotes both bacterial adherence to surfaces and biofilm formation.

134 in O-glycans contribute to the prevention of bacterial adherence to the apical surface of corneal epi

135 tributed, at least in part, to inhibition of bacterial adherence to the bladder surface by s-FimH1-25

136 SP-A can provide innate immunity by blocking bacterial adherence to the ciliated epithelium.

137 related to pathogenetic events subsequent to bacterial adherence to the damaged endocardium.

138 eraction increases avidity, thus stabilizing bacterial adherence to the epithelial surface, despite p

139 een the duration of protein malnutrition and bacterial adherence to the intestinal mucosa (r = 0.62,

140 equently, studies focusing on the biology of bacterial adherence to the intestinal mucosa likely are

141 function are characterized by depressed IgA, bacterial adherence to the intestinal mucosa, and permea

142 on was evaluated by measuring secretory IgA, bacterial adherence to the intestinal mucosa, and transe

143 ignificantly impairs secretory IgA, promotes bacterial adherence to the mucosa, and results in increa

144 Evidence documents the involvement of bacterial adherence to the plasma membrane of the endoth

145 meric autotransporter subfamily and mediates bacterial adherence to the respiratory epithelium.

146 eading frame (ORF) in GBS strain 515 reduced bacterial adherence to VK2 vaginal epithelial cells in v

147 HL-60 cells were compared for differences in bacterial adherence, type III secretion induction, and E

148 of complement, specific IgA induced minimal bacterial adherence, uptake, and killing.

149 Bacterial adherence was also reduced.

150 Finally, increased bacterial adherence was observed when apical secretion o

151 Bacterial adherence was restored by incubation of postex

152 aken together, PepO facilitates C1q-mediated bacterial adherence, whereas its localized release consu

153 le acid responsiveness enables tight mucosal bacterial adherence while also allowing an effective esc