ライフサイエンスコーパス: C. psittaci

1 ay contribute to the aggressive virulence of C. psittaci.

2 solates of C. pneumoniae, and 20 isolates of C. psittaci.

3 er C. pneumoniae strains, C. trachomatis, or C. psittaci.

4 thogen C. pneumoniae, and the zoonotic agent C. psittaci.

5 ead birds from pet stores for infection with C. psittaci.

6 strains of C. trachomatis and two strains of C. psittaci.

7 ig inclusion conjunctivitis (GPIC) strain of C. psittaci.

8 d within 1 h of infection of host cells with C. psittaci 6BC but that protein quantity peaks during t

9 C. psittaci 6BC infectious particles were electroporated

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

11 We report the genome sequences of C. psittaci 6BC, the prototype strain of the species, an

12 homologous recombination was investigated in C. psittaci 6BC.

13 nd C. trachomatis, is partially truncated in C. psittaci 6BC.

14 d 169 animal specimens; 98 were positive for C. psittaci (71.4% genotype A, 3.1% genotype B, 4.1% gen

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

16 ng and weak homologies were also detected in C. psittaci avian and feline pneumonitis strains, respec

17 plates, the synthetic peptides reacted with C. psittaci B577 antisera, but not with sera from specif

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

19 As were compared to those from the reference C. psittaci B577 elementary body (EB) ELISA and the Chla

20 blems, were screened for antibodies by these C. psittaci B577 peptide ELISAs and an ELISA with recomb

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

22 protein of C. psittaci serovar 1 (omp1 type C. psittaci B577).

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

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

25 een developed to rapidly detect and genotype C. psittaci by light-upon-extension chemistry and high-r

26 being most similar to those originating from C. psittaci, C. felis and C. caviae.

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

28 PCR to avian specimens increased the rate of C. psittaci detection.

29 emic chlamydial species in chickens, whereas C. psittaci dominates only in pigeons.

30 Srp, whose sequence is 64% identical between C. psittaci GPIC and C. trachomatis, is partially trunca

31 uring outbreaks of psittacosis to infer that C. psittaci had been transmitted from birds purchased in

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

33 trachomatis IncA is structurally similar to C. psittaci IncA and is also localized to the inclusion

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

35 ci, uniquely targets the nuclear envelope of C. psittaci-infected cells and uninfected neighboring ce

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

37 Notably, C. psittaci-infected cells were lysed with greater effic

38 e cells migrated identically to that seen in C. psittaci-infected cells, indicating the host cell was

39 ted lysis differ between C. trachomatis- and C. psittaci-infected cells.

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

41 onstrated that these proteins are present in C. psittaci-infected HeLa cells but are absent or below

42 rescently labelled anti-IncA antibodies into C. psittaci-infected HeLa cells resulted in immunostaini

43 C. psittaci is currently grouped into seven avian genoty

44 the interpretation of results obtained with C. psittaci models of infection and immune resolution, p

45 C. psittaci modulates virulence by alteration of host im

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

47 ith Chlamydia trachomatis inclusions but not C. psittaci or C. pneumoniae inclusions.

48 The C. psittaci plasmid was also sequenced.

49 three species of Chlamydiaceae; LcrH-2 from C. psittaci reacted with LcrE from C. pneumoniae but not

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

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

52 antiserum raised against a recombinant ovine C. psittaci strain POMP, and two possessed surface-expos

53 None of the C. trachomatis serovars, C. psittaci strains, other organisms, or human DNAs test

54 on at the periphery of aberrant RB, while in C. psittaci, treatment causes SEP to localize to distinc

55 ment of the 16S rRNA gene were observed when C. psittaci was electroporated with the recombination su

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

57 TETR-PCR for C. psittaci with primer set CPS 100-CPS 101 showed subst