ライフサイエンスコーパス: biovar

1 localized to C. trachomatis inclusions in a biovar-specific manner.

2 ith the agent of mouse pneumonitis (MoPn), a biovar of Chlamydia trachomatis.

3 The genome of a biovar I strain, A. tumefaciens C58, has been previously

4 1 was biotyped as a typical rough B. abortus biovar 1 (not strain 19) after animal passage or a high

5 tus strain RB51, 57 identified as B. abortus biovar 1, 15 identified as B. abortus bv.2, 1 identified

6 OmcBc processing and release occurred in all biovars of C. trachomatis.

7 representing all known Brucella species and biovars.

8 s of two isolates of the "classical" antiqua biovar, strains Antiqua and Nepal516.

9 The antiqua biovar was the most diverse, with four alleles observed

10 posal to group classical Brucella species as biovars of Brucella melitensis, the commonly recognized

11 account for this close relationship between biovar orientalis strains and the antiqua Nicholisk 51 i

12 n part or as a whole both within and between biovars.

13 wo Chlamydia trachomatis strains (L2/434/Bu [biovar LGV] and E/DK20/ON [biovar trachoma]) to induce p

14 rigin of the pathogen is Japan or Korea, but biovar 3, which is responsible for the global outbreak,

15 of an anthrax-causing agent, Bacillus cereus biovar anthracis, in a tropical rainforest have severe c

16 duration of infection with either chlamydial biovar was significantly increased in the C3H strain of

17 strains belong to one of the three classical biovars, they represent separate lineages defined by rec

18 ce was compared with that of Y. pestis CO92, biovar Orientalis, revealing homologous sequences but a

19 distinct groups consistent with the current biovar classification system of F. tularensis.

20 a large collection of isolates of different biovars and geographical origins.

21 d Y. pseudotuberculosis strains of different biovars and serogroups, respectively, were tested for th

22 Y. enterocolitica biovar 1B additionally has a distinct chromosomal locus,

23 ene expression patterns of Y. enterocolitica biovar 1B through the course of an in vitro infection, t

24 Yersinia enterocolitica biovar 1B contains two type III secretion systems (TTSSs

25 Yersinia enterocolitica biovar 1B employs two type three secretion systems (T3SS

26 Yersinia enterocolitica biovar 1B maintains three distinct type III secretion (T

27 4 strains successfully grouped isolates from biovar orientalis and most of the antiqua and mediaevali

28 sely related serovars Dublin and Gallinarum (biovars Gallinarum and Pullorum) revealed several genomi

29 Most Shewanella alga organisms (Gilardi biovar 2; Centers for Disease Control and Prevention [CD

30 , Shewanella putrefaciens organisms (Gilardi biovars 1 and 3; CDC biotype 1) were more often associat

31 gainst ocular challenge of mice with a human biovar of C. trachomatis.

32 (C57) and C3H/HeN (C3H) mice with the human biovar of Chlamydia trachomatis, serovar E, and, in sele

33 ecognized epitopes of either murine or human biovars of C. trachomatis.

34 y against challenge with either of two human biovars.

35 ne to challenge with either of the two human biovars.

36 tic of the glpD version found exclusively in biovar orientalis strains.

37 r B isolates were less diverse than those in biovar A, possibly reflecting the history of tularemia i

38 a mouse-adapted clinical Ureaplasma isolate (biovar 2) or sham inoculated with 10B broth.

39 The strain KIM, biovar Mediaevalis, is associated with the second pandem

40 KR223, from Lactococcus lactis subsp. lactis biovar diacetylactis KR2 encodes two distinct bacterioph

41 ) system of Lactococcus lactis subsp. lactis biovar diacetylactis KR2 was determined.

42 The pyrE gene of Rhizobium leguminosarum biovar trifolii (Rl) was subcloned and its sequence is p

43 Rhizobium leguminosarum biovar viciae strain 3841 is a motile alpha-proteobacter

44 he inner membrane of Rhizobium leguminosarum biovar viciae was analysed using a series of gene fusion

45 trachoma and lymphogranuloma venereum (LGV) biovars from temporally and geographically diverse sourc

46 with strains representative of the two major biovars of Chlamydia trachomatis has been studied to det

47 Interestingly, a Manchurian biovar antiqua strain Nicholisk 51 displayed a genotypin

48 trains, while the orientalis and mediaevalis biovars exhibited five alleles in 21 strains and three a

49 ioneer oral streptococci Streptococcus mitis biovar 1 and Streptococcus oralis, the late oral coloniz

50 Streptococcus oralis and Streptococcus mitis biovar 1 strains but were cleaved to various degrees by

51 to inoculation with the C. trachomatis MoPn biovar is dependent on the surface beta-2 integrin molec

52 infection with the mouse pneumonitis (MoPn) biovar of Chlamydia trachomatis, mice were challenged in

53 esistant to cleavage by both human and mouse biovars.

54 viously infected with either human or murine biovars produced broadly cross-reactive T cells that rec

55 sequences derived from the glycerol-negative biovar orientalis strain CO92, a set of 27 locus-specifi

56 d by the VC1216 gene from Vibrio cholerae O1 biovar El Tor str.

57 of the FLEXGene clone set for V. cholerae O1 biovar eltor str.

58 51 displayed a genotyping pattern typical of biovar orientalis isolates.

59 ased strictly on the classical definition of biovars (predicated upon two biochemical assays) does no

60 rains (L2/434/Bu [biovar LGV] and E/DK20/ON [biovar trachoma]) to induce putative host defense respon

61 var I strains, one biovar II strain, and one biovar III strain of A. tumefaciens displayed between 0.

62 inoculation with three biovar I strains, one biovar II strain, and one biovar III strain of A. tumefa

63 ella and not one of the classical species or biovars invading new host species.

64 pathogens, specifically Brucella species or biovars.

65 raphically diverse members of the orientalis biovar formed a homogeneous group with identical genotyp

66 lycerol-negative phenotype of the orientalis biovar.

67 Orientalis strains from other biovars.

68 ose bacteria, Ureaplasma urealyticum (parvum biovar), which is also a mucosal pathogen of humans.

69 Pathogenic biovars of Yersinia enterocolitica maintain the well-stu

70 h increased virulence and with the Y. pestis biovar responsible for the current (third) plague pandem

71 romosomal element (CUS-2) in Yersinia pestis biovar orientalis is integrated at the same relative loc

72 Strains from all epidemic plague biovars were similarly affected, implicating Hfq, and li

73 The classic three plague biovars did not have single identifying alleles, althoug

74 ts (IFU) of C. trachomatis mouse pneumonitis biovar (MoPn) and were euthanized at 10 days postinfecti

75 the Chlamydia trachomatis mouse pneumonitis biovar (MoPn).

76 infection induced with the mouse pneumonitis biovar of Chlamydia trachomatis (MoPn) elicits a short-l

77 vaginal infection with the mouse pneumonitis biovar of Chlamydia trachomatis (MoPn).

78 enital infections with the mouse pneumonitis biovar of Chlamydia trachomatis (MoPn).

79 ed intravaginally with the mouse pneumonitis biovar of Chlamydia trachomatis became infertile and sus

80 the Chlamydia trachomatis mouse pneumonitis biovar.

81 during infection with the murine pneumonitis biovar of Chlamydia trachomatis.

82 , strains belonging to the glycerol-positive biovar antiqua showed a variety of fingerprinting profil

83 e of B. abortus 2308, the virulent prototype biovar 1 strain, and its comparison to the two other hum

84 n should be considered members of a separate biovar.

85 rts chromosomal differences between species, biovars, serotypes, and strains of Y. pestis and Y. pseu

86 In this study, biovar B isolates were less diverse than those in biovar

87 its certain pathogenic agrobacteria, and the biovar III strain A. vitis S4, a narrow-host-range strai

88 In this study, the genomes of the biovar II strain A. radiobacter K84, a commercially avai

89 Moreover, strains of the biovar medievalis (also glycerol positive) clustered tog

90 hism analysis method for differentiating the biovars of this species that reveals five patterns among

91 that the latter represents a variant of this biovar with restored ability to ferment glycerol.

92 re challenged by stem inoculation with three biovar I strains, one biovar II strain, and one biovar I

93 cterium strains have been divided into three biovars, based on physiological and biochemical properti

94 ase, whose presence is apparently limited to biovar 1 strains, acts via a cleavage-and-religation mec

95 e binding by heparin was saturable, trachoma biovar organisms bound twice the amount of heparin than

96 With trachoma biovar strain DK20, a small increase in the initial entr

97 t groups: (i) Chlamydia trachomatis trachoma biovars (serovars A to H), (ii) C. trachomatis lymphogra

98 id-cured derivatives of human C. trachomatis biovars exhibit similar phenotypic characteristics, they

99 r selected genital and ocular C. trachomatis biovars provides a means for investigating genomic diffe

100 Although for two C. trachomatis biovars the binding by heparin was saturable, trachoma b

101 l genomic differences, Chlamydia trachomatis biovars exhibit diverse disease manifestations and diffe

102 a virulent clinical isolate of F. tularensis biovar A (NMFTA1).

103 e from intranasal infection by F. tularensis biovar A.

104 tularensis biovar tularensis, F. tularensis biovar novicida, and F. philomiragia.

105 nsis strains but not Fx1, Fx2, F. tularensis biovar novicida, or F. philomiragia; serum from either p

106 The inhalation of Francisella tularensis biovar A causes pneumonic tularemia associated with high

107 la strains, including Francisella tularensis biovar tularensis, F. tularensis biovar novicida, and F.

108 demonstrate the differences between the two biovar antiqua lineages and support the notion that grou

109 in vitro root inoculation bioassays with two biovar I strains of A. tumefaciens, transgenic Arabidops

110 Infection of epithelial cells by two biovars of Chlamydia trachomatis results in the tyrosine

111 We show that elementary bodies (EB) from two biovars of Chlamydia trachomatis recruit fibronectin to

112 U. urealyticum can be divided into two biovars comprising 14 serovars.

113 asma genitalium (MG), Ureaplasma urealyticum biovar 2 (UU-2), and Trichomonas vaginalis (TV) using nu

114 unt of heparin than lymphogranuloma venereum biovar organisms.

115 With lymphogranuloma venereum biovar strain 434, little difference in the influx of re

116 (ii) C. trachomatis lymphogranuloma venereum biovars (serovars L1 to L3), (iii) C. muridarum, and (iv

117 orynebacterium diphtheriae strains; six were biovar mitis, which were associated with recent travel a

118 e identified between Y. pestis strains, with biovar Antiqua and Mediaevalis strains showing most dive

119 s, although there were allelic biases within biovar categories.