ライフサイエンスコーパス: psittaci

1 inclusion conjunctivitis (GPIC) strain of C. psittaci.

2 e, particularly within the species Chlamydia psittaci.

3 contribute to the aggressive virulence of C. psittaci.

4 ally with the guinea pig strain of Chlamydia psittaci.

5 gen C. pneumoniae, and the zoonotic agent C. psittaci.

6 ates of C. pneumoniae, and 20 isolates of C. psittaci.

7 moniae, Chlamydia trachomatis, and Chlamydia psittaci.

8 C. pneumoniae strains, C. trachomatis, or C. psittaci.

9 birds from pet stores for infection with C. psittaci.

10 ains of C. trachomatis and two strains of C. psittaci.

11 ithin 1 h of infection of host cells with C. psittaci 6BC but that protein quantity peaks during the

12 C. psittaci 6BC infectious particles were electroporated wi

13 1000-fold difference in lethal dose of 2 C. psittaci 6BC strains in mice.

14 We report the genome sequences of C. psittaci 6BC, the prototype strain of the species, and C

15 C. trachomatis, is partially truncated in C. psittaci 6BC.

16 ologous recombination was investigated in C. psittaci 6BC.

17 Chlamydia pneumoniae (AR-39), and Chlamydia psittaci (6BC).

18 69 animal specimens; 98 were positive for C. psittaci (71.4% genotype A, 3.1% genotype B, 4.1% genoty

19 t the first genome sequence of Chlamydophila psittaci, an intracellular pathogen of birds and a human

20 d; however, two other chlamydial species, C. psittaci and C. abortus, are known zoonotic pathogens.

21 The 53% prevalence of low-level Chlamydia psittaci and C. pecorum genital infection detected in vi

22 sittacosis is a zoonosis caused by Chlamydia psittaci and is characterized by severe pneumonia and sy

23 h the species Chlamydia muridarum, Chlamydia psittaci, and Chlamydia caviae, which primarily infect n

24 minate among Chlamydia pneumoniae, Chlamydia psittaci, and Chlamydia trachomatis on the basis of the

25 homatis, Chlamydia pneumoniae, and Chlamydia psittaci as improved tests for sensitive diagnosis and r

26 and weak homologies were also detected in C. psittaci avian and feline pneumonitis strains, respectiv

27 ates, the synthetic peptides reacted with C. psittaci B577 antisera, but not with sera from specific-

28 2 region were strongly reactive with all C. psittaci B577 antisera.

29 were compared to those from the reference C. psittaci B577 elementary body (EB) ELISA and the Chlamyd

30 ms, were screened for antibodies by these C. psittaci B577 peptide ELISAs and an ELISA with recombina

31 The C. psittaci B577 peptide ELISAs, the LPS ELISA, and the EB

32 otein of C. psittaci serovar 1 (omp1 type C. psittaci B577).

33 Peptide antigens were identified with C. psittaci B577-immune sera by solid-phase scanning of ove

34 These results suggest that the C. psittaci B577-peptide and Chlamydia LPS ELISAs are super

35 developed to rapidly detect and genotype C. psittaci by light-upon-extension chemistry and high-reso

36 We analyzed avian strain 6BC of Chlamydia psittaci by polyacrylamide gel electrophoresis for the e

37 ng most similar to those originating from C. psittaci, C. felis and C. caviae.

38 the prototype strain of the species, and C. psittaci Cal10, a widely used laboratory strain.

39 man infection with Chlamydophila (Chlamydia) psittaci can lead to psittacosis, a disease that occasio

40 pathogenic association between Chlamydophila psittaci (Cp) and ocular adnexal marginal zone lymphoma

41 ment was exclusively targeting Chlamydophila psittaci (CP), using doxycycline in all but 2 studies.

42 to avian specimens increased the rate of C. psittaci detection.

43 le, a lambda expression library of Chlamydia psittaci DNA was differentially screened with convalesce

44 None of the OAL specimens harbored C psittaci DNA.

45 c chlamydial species in chickens, whereas C. psittaci dominates only in pigeons.

46 hat intranasal delivery of UV-inactivated C. psittaci EB formulated in Vibrio cholerae ghosts (VCG)-c

47 lved mixing recombinant EUO with a Chlamydia psittaci genomic library in a pBluescript plasmid vector

48 , whose sequence is 64% identical between C. psittaci GPIC and C. trachomatis, is partially truncated

49 of Chlamydophila caviae (formerly Chlamydia psittaci, GPIC isolate) (1 173 390 nt with a plasmid of

50 ng outbreaks of psittacosis to infer that C. psittaci had been transmitted from birds purchased in pe

51 Psittacid herpesvirus 1 (PsHV-1) is the causative agent

52 A single genetic variant (psittacid herpesvirus variant 1) amplified with all prim

53 19 bp of the UL16 open reading frame from 73 psittacid herpesviruses (PsHVs) from the United States a

54 ive than tissue culture for the detection of psittacid herpesviruses.

55 . trachomatis strains but not with Chlamydia psittaci hsp10 or Escherichia coli homolog GroES, sugges

56 ies against abortigenic strains of Chlamydia psittaci in livestock.

57 receptor are critical for defense against C. psittaci in mouse lung infection.

58 lymphomas has been associated with Chlamydia psittaci in some geographic areas.

59 achomatis IncA is structurally similar to C. psittaci IncA and is also localized to the inclusion mem

60 Infection of HEK 293 cells with C. psittaci increased IFN-gammaR expression only in cells e

61 uniquely targets the nuclear envelope of C. psittaci-infected cells and uninfected neighboring cells

62 The lysis of C. psittaci-infected cells was characterized further and co

63 Notably, C. psittaci-infected cells were lysed with greater efficien

64 tment of Chlamydia trachomatis- or Chlamydia psittaci-infected cells with gamma interferon (IFN-gamma

65 ells migrated identically to that seen in C. psittaci-infected cells, indicating the host cell was re

66 lysis differ between C. trachomatis- and C. psittaci-infected cells.

67 additional higher M(r) forms are found in C. psittaci-infected cells.

68 trated that these proteins are present in C. psittaci-infected HeLa cells but are absent or below the

69 cently labelled anti-IncA antibodies into C. psittaci-infected HeLa cells resulted in immunostaining

70 Association with Chlamydia psittaci infection is examined in 57 tumor specimens.

71 were 10(5)-fold more resistant to Chlamydia psittaci infection than DBA/2J mice by LD(100) determina

72 outh Florida, OALs are not associated with C psittaci infections.

73 Chlamydia psittaci is a highly prevalent avian pathogen and the ca

74 C. psittaci is currently grouped into seven avian genotypes

75 lls with Chlamydia trachomatis and Chlamydia psittaci is shown in the present studies to upregulate m

76 (formerly the abortion subtype of Chlamydia psittaci) is an important cause of late gestation aborti

77 ddition to a phage associated with Chlamydia psittaci isolated from an ornithosis infection in ducks

78 aphylatoxin C3a receptor (C3aR) in Chlamydia psittaci lung infection and elucidated C3a-dependent ada

79 e interpretation of results obtained with C. psittaci models of infection and immune resolution, part

80 C. psittaci modulates virulence by alteration of host immun

81 Overall our findings demonstrate that C. psittaci-negative ocular adnexal EMZL exhibit biased usa

82 gene usage and mutations in 67 Chlamydophila psittaci-negative ocular adnexal EMZL.

83 Chlamydia trachomatis inclusions but not C. psittaci or C. pneumoniae inclusions.

84 This study investigates the role of the psittacid (parrot) central nucleus of the lateral neostr

85 The C. psittaci plasmid was also sequenced.

86 ial treatment of patients with Chlamydophila psittaci-positive lymphoma before considering more aggre

87 Chlamydia psittaci produces a collection of proteins, termed IncA,

88 ution in Chlamydia trachomatis and Chlamydia psittaci RB.

89 ree species of Chlamydiaceae; LcrH-2 from C. psittaci reacted with LcrE from C. pneumoniae but not fr

90 s) of the major outer membrane protein of C. psittaci serovar 1 (omp1 type C. psittaci B577).

91 EUO, a previously described ORF of avian C. psittaci strain 6BC which is preferentially transcribed

92 ollowing intranasal inoculation of Chlamydia psittaci strain B577 were modulated by 7-day i.p. admini

93 3, omp2 and srp gene homologs from Chlamydia psittaci strain GPIC was determined.

94 pstream of the omp3-omp2 operon of Chlamydia psittaci strain GPIC was obtained, revealing four signif

95 Four genes of Chlamydia psittaci strain guinea pig inclusion conjunctivitis (GPI

96 iserum raised against a recombinant ovine C. psittaci strain POMP, and two possessed surface-exposed,

97 Chlamydia psittaci (strain GPIC) produces a 39 kDa protein (IncA)

98 None of the C. trachomatis serovars, C. psittaci strains, other organisms, or human DNAs tested

99 ia trachomatis, serovar E, and Chlamydophila psittaci, Texas turkey, were also cloned in the two-hybr

100 e outer membrane of the subtype of Chlamydia psittaci that causes ovine enzootic abortion (strain S26

101 o that the intracellular growth of Chlamydia psittaci, trachomatis, and Legionella pneumophila is reg

102 at the periphery of aberrant RB, while in C. psittaci, treatment causes SEP to localize to distinct p

103 in of the avian and human pathogen Chlamydia psittaci, uniquely targets the nuclear envelope of C. ps

104 o determine the mechanism by which Chlamydia psittaci up-regulates IFN-gammaR expression and evaluate

105 t of the 16S rRNA gene were observed when C. psittaci was electroporated with the recombination subst

106 Chlamydia psittaci was found to modulate receptor expression for t

107 ly upstream open reading frame) of Chlamydia psittaci was previously found to be transcribed better a

108 homatis, Chlamydia pneumoniae, and Chlamydia psittaci were analyzed for evidence of intragenic recomb

109 Additionally, target cells infected with C. psittaci were lysed by C. trachomatis-elicited immune sp

110 r serovar C, genital serovar D, or Chlamydia psittaci, whereas the titers of anti-Chlamydia pneumonia

111 apy and antibiotic therapy against Chlamydia psittaci, which has been associated with the pathogenesi

112 TETR-PCR for C. psittaci with primer set CPS 100-CPS 101 showed substant

113 s, closely related to the zoonotic Chlamydia psittaci, with some strains associated with cases of hum