ライフサイエンスコーパス: pathovar

1 er adhesin that is conserved within the ETEC pathovar.

2 hat some antigens are restricted to the ETEC pathovar.

3 0%), but absent in the other major X. oryzae pathovar.

4 ree Secretion System in Pseudomonas syringae pathovars.

5 d that blurs the distinction between E. coli pathovars.

6 issue specificity for individual species and pathovars.

7 dividual host species coevolving with single pathovars.

8 but not complete, overlap between these two pathovars.

9 to (Pto) representing particularly divergent pathovars.

10 tors that contribute to the formation of new pathovars.

11 to diverse TAL effectors from both X. oryzae pathovars.

12 lmonella enterica serovar Typhi or Paratyphi pathovars A, B or C(1).

13 e" confirmed the diverse history of the ETEC pathovar and provides a finer resolution of the E. coli

14 o reference genomes from each of the E. coli pathovars and Shigella species.

15 fector suites from two sequenced P. syringae pathovars and show that type III effector protein suites

16 cluster but before the divergence of modern pathovars and that some EELs underwent transpositions yi

17 Although these two pathovars are highly similar at the physiological level,

18 e often classified into pathogenic variants (pathovars) based on their virulence gene content.

19 sed by uropathogenic Escherichia coli (UPEC) pathovars belong to the most frequent infections in huma

20 sed by uropathogenic Escherichia coli (UPEC) pathovars belong to the most frequent infections in huma

21 reduced virulence of Xanthomonas campestris pathovar campestris (Xcc).

22 Six distinct E. coli pathovars can be distinguished using molecular or phenot

23 ar japonica (Psj) or Xanthomonas translucens pathovar cerealis (Xtc).

24 wever, the recently emerged ST313 lineage II pathovar commonly causes systemic bacteremia in sub-Saha

25 cterium Pseudomonas syringae is divided into pathovars differing in host specificity, with P. syringa

26 he family of agn alleles in Escherichia coli pathovars encodes autotransporters that have been implic

27 nts and unique features of three unsequenced pathovars, enterotoxigenic E. coli, enteropathogenic E.

28 It has also been proposed that this pathovar has the ability to produce a second siderophore

29 phenotypic markers, but only two of the six pathovars have been subjected to any genome sequencing p

30 protein in the T3SS of different P. syringae pathovars, hrpP from P. syringae pv. syringae 61 and P.

31 stence and virulence potential of an E. coli pathovar hybrid that blurs the distinction between E. co

32 other distinguishing feature between the two pathovars is their distinctive sets of transposable elem

33 f infection with either Pseudomonas syringae pathovar japonica (Psj) or Xanthomonas translucens patho

34 rast, the resistance to Pseudomonas syringae pathovar maculicola (RPM1) bacterial resistance gene is

35 ation with HR-eliciting Pseudomonas syringae pathovars measured by laser photoacoustic detection was

36 ultiple effector proteins from an individual pathovar more frequently and more intensely than host sp

37 e majority of deaths are attributable to one pathovar of E. coli, namely, enterotoxigenic E. coli.

38 The ST313 pathovar of Salmonella enterica serovar Typhimurium cont

39 Among the pathovars of diarrheagenic E. coli that cause significan

40 newly analyzed and eight known PFPs from 12 pathovars of P. syringae, which belong to four genomospe

41 ction of type III effector proteins from two pathovars of P. syringae.

42 id-encoded phytotoxin synthesized by several pathovars of phytopathogenic Pseudomonas syringae.

43 ned 171 effector-encoding genes from several pathovars of Pseudomonas and Ralstonia.

44 ne (COR) is a phytotoxin produced by several pathovars of Pseudomonas syringae and consists of corona

45 t only compromised nonhost resistance to few pathovars of Pseudomonas syringae and Xanthomonas campes

46 Several pathovars of Pseudomonas syringae produce the phytotoxin

47 portant virulence factor produced by several pathovars of the bacterial pathogen Pseudomonas syringae

48 ance to another race of H. parasitica and to pathovars of the bacterial pathogen Pseudomonas syringae

49 The two pathovars of this economically important species of plan

50 i (ETEC) is an important pathogenic variant (pathovar) of E. coli in developing countries from a huma

51 e analyses with a phylogenetically divergent pathovar, P. syringae pv. tomato DC3000, revealed a stro

52 hF gene was cloned from Pseudomonas syringae pathovar phaseolicola (PPH:) races 5 and 7, based on its

53 major clades, which includes the P. syringae pathovar phaseolicola.

54 tomato hrpW were found in other P. syringae pathovars, Pseudomonas viridiflava, Ralstonia (Pseudomon

55 The rice pathogens Xanthomonas oryzae pathovar (pv.) oryzae and pv. oryzicola produce numerous

56 psis thaliana pathogens Pseudomonas syringae pathovar (pv.) tomato and pv. maculicola were made by in

57 (serotypes A-C) and two sexually transmitted pathovars; serotypes D-K and lymphogranuloma venereum (L

58 able to identify genes that were isolate and pathovar specific.

59 Fewer pathovar-specific genes were identified than anticipated

60 lmonella Typhimurium isolates, 42 of 43 were pathovar ST313.

61 ess and its prevalence in many X. campestris pathovars suggests that the Bs2 gene may be durable in t

62 most cases are more similar to other E. coli pathovars than to text modification AEEC.

63 invasive Escherichia coli (EIEC) is a unique pathovar that has a pathogenic mechanism nearly indistin

64 ative Hrp pathways from Pseudomonas syringae pathovars that produce these proteins.

65 were more resistant to Pseudomonas syringae pathovar tomato (Pst) DC3000 infection implicating SCD1

66 During Pseudomonas syringae pathovar tomato (Pst) DC3000 infection of Arabidopsis, a

67 pe Pi-0 is resistant to Pseudomonas syringae pathovar tomato (Pst) strain DC3000 expressing the T3S e

68 In 1991, a P. syringae pathovar tomato (Pst) strain, DC3000, was reported to in

69 the bacterial pathogens Pseudomonas syringae pathovar tomato and Erwinia amylovora, respectively, and

70 odel bacterial pathogen Pseudomonas syringae pathovar tomato DC3000 (DC3000), which is pathogenic on

71 of the foliar pathogen, Pseudomonas syringae pathovar tomato DC3000 (hereafter PstDC3000), into the p

72 the bacterial pathogen Pseudomonas syringae pathovar tomato requires Pto and Prf.

73 s in the plant pathogen Pseudomonas syringae pathovar tomato strain DC3000 possess characteristic pat

74 lence protein AvrPto of Pseudomonas syringae pathovar tomato, the agent of bacterial speck disease, a

75 ce of the avrE locus of Pseudomonas syringae pathovar tomato.

76 e resistance in response to Pto (P. syringae pathovars tomato) DC3000(avrB), but not against Pto DC30

77 dentified as putative orthologs in these two pathovars using a reciprocal best-hit method, with 3,941

78 We have found within-species, within-pathovar variation for defense-eliciting activity of fla

79 virulence factor from Xanthomonas campestris pathovar vesicatoria (Xcv) that is translocated into tom

80 ype III effector from Xanthomonas campestris pathovar vesicatoria (Xcv), suppresses symptom productio

81 -dependent promoters of Pseudomonas syringae pathovars were identified with a consensus sequence of 5

82 tional strains representing nine P. syringae pathovars were isolated and sequenced.

83 ted AvrBs2 proteins from the two Xanthomonas pathovars were strongly conserved and had predicted sequ