ライフサイエンスコーパス: elementary body

1 e body, and an extracellular form called the elementary body.

2 tein) on the outer surface of the chlamydial elementary body.

3 noprecipitated with TARP from C. trachomatis elementary bodies.

4 only minimally packaged into the infectious elementary bodies.

5 ges that include the formation of infectious elementary bodies.

6 within these cells by generating infectious elementary bodies.

7 with DCs pulsed with inactivated chlamydial elementary bodies.

8 ere was a restricted production of infective elementary bodies.

9 s with no evidence of redifferentiation into elementary bodies.

10 gement of cell surface heparan sulfate by L2 elementary bodies.

11 lected late-stage proteins and transition to elementary bodies, a Chlamydia developmental form that i

12 condition is reversible, yielding infectious elementary bodies after removal of the inducers, includi

13 to lysosomes due to an intrinsic property of elementary bodies and (ii) an active modification of the

14 g of sedimented culture transport medium for elementary bodies and by TMA with 16S rRNA as a target.

15 cells infected with multiple C. trachomatis elementary bodies and cultivated at 32 degrees C for 24

16 IF) antibody titers to Chlamydia trachomatis elementary bodies and ELISA antibody to recombinant chla

17 icroscopy for the presence of C. trachomatis elementary bodies and for the presence and number of cel

18 mydia developmental transition to infectious elementary bodies and highlights the potential applicati

19 Here, in elementary bodies and in preparations of the outer membr

20 identified in purified Chlamydia trachomatis elementary bodies and in the chlamydial parasitophorous

21 dsF is concentrated in the outer membrane of elementary bodies and is surface exposed as a component

22 d imply that the cytotoxin is present in the elementary body and delivered to host cells very early d

23 ioning between the infectious, extracellular elementary body and the replicative, intracellular retic

24 ering the conversion of reticulate bodies to elementary bodies, and for translocation of lipid drople

25 e compared by testing C. pneumoniae purified elementary bodies, animal tissues, 228 peripheral blood

26 had increased CSF antibodies to C pneumoniae elementary body antigens as shown by enzyme-linked immun

27 lamydophila abortus or Chlamydophila pecorum elementary body antigens quantified antibodies against C

28 med by western blot assays of the CSF, using elementary body antigens.

29 noglobulin (Ig) reactivity with C pneumoniae elementary body antigens.

30 stence leads to attenuated production of new elementary bodies, appearance of morphologically aberran

31 In contrast to localization in RB, SEP in elementary bodies appears diffuse and irregular, suggest

32 The small size of infectious chlamydial elementary bodies (approximately 0.3 microm in diameter)

33 Elementary bodies are characterized by a condensed chrom

34 in synthesis inhibitors, vesicles containing elementary bodies are very slow to acquire lysosomal cha

35 42 h, they contained intermediate bodies and elementary bodies as well.

36 At 18 h after infection, only a few elementary bodies attached to cells were visible, as wer

37 hose of proteins identified in C. pneumoniae elementary bodies by matrix-assisted laser desorption io

38 ermined by diminished recovery of infectious elementary bodies, differed markedly among chlamydial st

39 -mer OmcB peptide that bound the surfaces of elementary bodies (EB) and by heparin-binding peptide cr

40 IgG antibodies to serovar D of chlamydia elementary bodies (EB) and IgG antibodies to CHSP60-1, C

41 We show that elementary bodies (EB) from two biovars of Chlamydia tra

42 t reduction in infectivity of C. trachomatis elementary bodies (EB) harvested from Desferal-exposed p

43 Serovar E elementary bodies (EB) metabolically radiolabeled with 3

44 A8-35 had a higher ratio of Abs to denatured elementary bodies (EB) over live EB, recognized more syn

45 her intranasally or intravaginally with live elementary bodies (EB).

46 lated outer membrane complexes of infectious elementary bodies (EB).

47 were immunized i.n. with C. trachomatis MoPn elementary bodies (EB).

48 matis standards ranging from 32 to 1,048,576 elementary bodies (EB)/ml of urine exhibited a linear co

49 e investigated immune responses to Chlamydia elementary body (EB) and 3 genotypically variant heat sh

50 rized by an infectious cell type known as an elementary body (EB) and an intracellular replicative fo

51 n a regulated fashion between the infectious elementary body (EB) and the replicative reticulate body

52 to those from the reference C. psittaci B577 elementary body (EB) ELISA and the Chlamydia complement

53 The infectious chlamydial elementary body (EB) is metabolically inactive yet posse

54 at low or undetectable levels at the time of elementary body (EB) to reticulate body conversion early

55 transition between two forms: the infectious elementary body (EB), and the rapidly dividing reticulat

56 g between two distinct forms: the infectious elementary body (EB), and the replicative but non-infect

57 acellular chlamydial infectious particle, or elementary body (EB), is enveloped by an intra- and inte

58 We used a Chlamydia trachomatis elementary body (EB)-based enzyme-linked immunosorbent a

59 ial cell-surface GAGs, as well as chlamydial elementary body (EB)-surface GAGs, were investigated.

60 nvironmentally resistant cell type called an elementary body (EB).

61 not a function of infection by more than one elementary body (EB).

62 ajor outer membrane protein (MOMP) and whole elementary bodies (EBs) from the 4 predominant serovars

63 hasic developmental cycle whereby infectious elementary bodies (EBs) invade host epithelial cells and

64 The chromatin of chlamydial elementary bodies (EBs) is stabilized by proteins with s

65 t full-length CT153 (p91) was present in the elementary bodies (EBs) of 15 C. trachomatis reference s

66 lity to recognize the immunizing peptide and elementary bodies (EBs) of C. pneumoniae by enzyme-linke

67 Elementary bodies (EBs) of C. trachomatis, serovar E (BO

68 lfate receptor for binding C. trachomatis L2 elementary bodies (EBs) prior to entry into HeLa cells.

69 In this study, C pneumoniae elementary bodies (EBs) rapidly activated p44/p42 mitoge

70 ated the presence of a type III apparatus on elementary bodies (EBs) that might function early in inf

71 vity to formalin-fixed Chlamydia trachomatis elementary bodies (EBs) to address whether these associa

72 he susceptibilities of Chlamydia trachomatis elementary bodies (EBs) to human defensin HNP-2 and porc

73 entiation of infectious, metabolically inert elementary bodies (EBs) to larger, metabolically active

74 nifested by the transformation of infectious elementary bodies (EBs) to larger, non-infectious reticu

75 crophages at low MOIs but yielded few viable elementary bodies (EBs) when macrophages were infected a

76 ection (after 20 h) when RBs reorganize into elementary bodies (EBs), and is absent in infectious EBs

77 keleton in the internalization of chlamydial elementary bodies (EBs).

78 ed absorption studies with viable chlamydial elementary bodies (EBs).

79 attenuates the production of new, infectious elementary bodies (EBs).

80 rected at formalin-fixed purified chlamydial elementary bodies (EBs).

81 Using elementary body ELISA, we demonstrated approximately 1 i

82 Chlamydia trachomatis elementary body enzyme-linked immunosorbent assay (ELISA

83 t RAM can detect as few as 10 C. trachomatis elementary bodies in less than 2 h, comparable to result

84 esponse occurs both with the introduction of elementary bodies into the host and early replication of

85 fectious reticulate bodies (RBs) and back to elementary bodies, into a state of persistence.

86 d significantly decreased incorporation into elementary bodies of both C. trachomatis and Chlamydophi

87 tocol for the growth and harvest of purified elementary bodies of Chlamydia pneumoniae is presented.

88 , to label proteins in the outer membrane of elementary bodies of Chlamydia trachomatis LGV serovar L

89 Western blot analyses of purified elementary bodies showed that 11 of the 21 Pmps were det

90 odies generated to the Chlamydia trachomatis elementary bodies stained Chlamydia-infected cells, but

91 infected with multiple Chlamydia trachomatis elementary bodies, they are internalized by endocytosis

92 etween infectious but metabolically inactive elementary bodies to metabolically active but noninfecti

93 Exposure of C. pneumoniae elementary bodies to periodate, but not elevated tempera

94 Conversion of C. trachomatis elementary bodies to reticulate bodies and cell division

95 Differentiation of elementary bodies to reticulate bodies is accompanied by

96 iption, as well as initial transformation of elementary bodies to reticulate bodies, were detected ea

97 the maturation of the reticulate body to the elementary body, TTS genes expressed in the later stages

98 ation of rCPAF and UV-inactivated chlamydial elementary bodies (UV-EB) against vaginal chlamydial cha

99 n PMNs were depleted, the number of released elementary bodies was significantly greater as determine

100 n a dose-dependent manner; were not toxic to elementary bodies; were cidal at a concentration of > or