ライフサイエンスコーパス: Vibrio parahaemolyticus

1 VopS-dependent manner during infection with Vibrio parahaemolyticus.

2 at ParP is integral to array localization in Vibrio parahaemolyticus.

3 odium hypochlorite (NaOCl) solutions against Vibrio parahaemolyticus.

4 present the crystal structure of a TrkH from Vibrio parahaemolyticus.

5 ome and stimulates motility and virulence of Vibrio parahaemolyticus.

6 nknown function from Pyrococcus furiosus and Vibrio parahaemolyticus.

7 ted by the lateral flagellar (laf) system in Vibrio parahaemolyticus.

8 S2 gene cluster found in a pandemic clone of Vibrio parahaemolyticus.

9 ter-regulator operons of Vibrio cholerae and Vibrio parahaemolyticus.

10 d encode a protein highly similar to NorM of Vibrio parahaemolyticus.

11 of P. aeruginosa is most similar to FlgM of Vibrio parahaemolyticus.

12 the sodium-powered polar flagellar motor in Vibrio parahaemolyticus.

13 Vibrio parahaemolyticus, a biofouling marine bacterium a

14 Vibrio parahaemolyticus, a causative agent of gastroente

15 hogenesis of the diarrheal disease caused by Vibrio parahaemolyticus, a leading cause of seafood-asso

16 Vibrio parahaemolyticus, a marine bacterium, is the caus

17 In Vibrio parahaemolyticus, a significant enteric pathogen

18 outer protein S) from the bacterial pathogen Vibrio parahaemolyticus and the human protein HYPE (hunt

19 ia, including the species Vibrio vulnificus, Vibrio parahaemolyticus and Vibrio cholerae, grow in war

20 Not unexpectedly, Vibrio parahaemolyticus and Vibrio vulnificus strains fo

21 Homologous clusters also exist in Vibrio parahaemolyticus and Vibrio vulnificus, and thus

22 at cause human diseases are Vibrio cholerae, Vibrio parahaemolyticus, and Vibrio vulnificus, the only

23 Of these 12, three species--Vibrio cholerae, Vibrio parahaemolyticus, and Vibrio vulnificus-account f

24 abdus luminescens, Aeromonas hydrophila, and Vibrio parahaemolyticus are also sensitive to mutations

25 swarming-proficient and virulent strains of Vibrio parahaemolyticus are silenced for the vibrio arch

26 ven different strains of the marine pathogen Vibrio parahaemolyticus as a model system.

27 The marine bacterium Vibrio parahaemolyticus causes gastroenteritis in humans

28 s of this nucleotide promote a more adhesive Vibrio parahaemolyticus cell type.

29 Vibrio parahaemolyticus differentiates from a polarly fl

30 Here we show that the Vibrio parahaemolyticus effector protein VopQ is a poten

31 The flaA locus of Vibrio parahaemolyticus encodes one of the four polar fl

32 Vibrio parahaemolyticus harbors two type III secretion s

33 Vibrio parahaemolyticus has dual flagellar systems adapt

34 controlling swarmer cell differentiation of Vibrio parahaemolyticus identified a novel three-gene op

35 egulatory cascade is poorly characterized in Vibrio parahaemolyticus, in part because swarming and vi

36 Vibrio parahaemolyticus infections are associated with c

37 In May and June 1998, reported Vibrio parahaemolyticus infections increased sharply in

38 to the seasonality of Vibrio vulnificus and Vibrio parahaemolyticus infections.

39 Vibrio parahaemolyticus is a common marine bacterium and

40 Vibrio parahaemolyticus is a Gram-negative bacterium res

41 Vibrio parahaemolyticus is a halophile that inhabits bra

42 Vibrio parahaemolyticus is a halophilic bacterium capabl

43 Vibrio parahaemolyticus is a marine microorganism that c

44 erial Na(+)/galactose cotransporter vSGLT of Vibrio parahaemolyticus is a member of the sodium:solute

45 Vibrio parahaemolyticus is a naturally occurring bacteri

46 Vibrio parahaemolyticus is a ubiquitous, gram-negative m

47 Vibrio parahaemolyticus is an emerging food- and waterbo

48 Vibrio parahaemolyticus is an important human foodborne

49 Vibrio parahaemolyticus is an important human pathogen w

50 Vibrio parahaemolyticus is an organism well adapted to c

51 Vibrio parahaemolyticus is the leading cause of bacteria

52 Vibrio parahaemolyticus is the leading cause of food-bor

53 Vibrio parahaemolyticus is the leading worldwide cause o

54 Vibrio parahaemolyticus is the most common cause of seaf

55 Vibrio parahaemolyticus isolates display variation in co

56 In this study, 77 clinical and 67 oyster Vibrio parahaemolyticus isolates from North America were

57 : Vibrio cholerae HapR, Vibrio harveyi LuxR, Vibrio parahaemolyticus OpaR and Vibrio vulnificus SmcR.

58 Vibrio parahaemolyticus possesses dual flagellar systems

59 Vibrio parahaemolyticus possesses two types of flagella,

60 o alter intracellular cyclic-di-GMP pools in Vibrio parahaemolyticus revealed that these genes also a

61 The Vibrio parahaemolyticus Scr system modulates decisions p

62 In Vibrio parahaemolyticus, scrC participates in controllin

63 Vibrio parahaemolyticus senses surfaces via impeded rota

64 Vibrio parahaemolyticus sequence type 36 (ST36) strains

65 The crystal structure of the Vibrio parahaemolyticus SGLT showed that residue Gln(428

66 vSGLT), a solute-sodium symporter (SSS) from Vibrio parahaemolyticus, shares a common structural fold

67 The crystal structure of TrkH from Vibrio parahaemolyticus showed that TrkH resembles a K(+

68 r of the solute sodium symporters (SSS), the Vibrio parahaemolyticus sodium/galactose symporter (vSGL

69 ed into the external face of a cysteine-less Vibrio parahaemolyticus sodium/glucose cotransporter for

70 The Vibrio parahaemolyticus sodium/glucose transporter (vSGL

71 Recently isolated Vibrio parahaemolyticus strains have displayed multiple

72 The present method of characterizing Vibrio parahaemolyticus strains involves serotyping or d

73 _1663), is conserved only in V. cholerae and Vibrio parahaemolyticus T3SS-positive strains and has no

74 ting technology with the cytotoxicity of two Vibrio parahaemolyticus T3SSs (T3SS1 and T3SS2) to ident

75 The Na(+)/galactose cotransporter (vSGLT) of Vibrio parahaemolyticus, tagged with C-terminal hexahist

76 ly emergent penaeid shrimp disease caused by Vibrio parahaemolyticus that has already led to tremendo

77 VopL is an effector protein from Vibrio parahaemolyticus that nucleates actin filaments.

78 ther bacteria, such as Vibrio vulnificus and Vibrio parahaemolyticus, that have syp-like loci and con

79 Vibrio parahaemolyticus, the leading cause of seafood-as

80 reveal that the BPD of the newly identified Vibrio parahaemolyticus Type III effector VopR is unfold

81 The Vibrio parahaemolyticus type III effector VopS is implic

82 Herein we show that Vibrio parahaemolyticus uses the type III effector VopQ

83 Vibrio alginolyticus, Vibrio fluvialis, and Vibrio parahaemolyticus utilized heme and hemoglobin as

84 The bacterial pathogen Vibrio parahaemolyticus utilizes a type III secretion sy

85 Vibrio parahaemolyticus (V. para) is a Gram-negative bac

86 e chain reaction for the prevalence of total Vibrio parahaemolyticus, V. vulnificus and V. cholerae a

87 l regulation of the polar flagellar genes of Vibrio parahaemolyticus, Vibrio cholerae, and Pseudomona

88 io species, with a focus on Vibrio cholerae, Vibrio parahaemolyticus, Vibrio vulnificus and Vibrio fi

89 mined the structure of the first W domain of Vibrio parahaemolyticus VopL cross-linked to actin Cys37

90 y designed to have a complementary region in Vibrio parahaemolyticus (VP) genome and to make differen

91 the first structure of a bacterial ATL, from Vibrio parahaemolyticus (vpAtl).

92 udy of the sodium/galactose transporter from Vibrio parahaemolyticus (vSGLT), consisting of molecular

93 We discovered that Vibrio parahaemolyticus VtrC, along with VtrA and VtrB,

94 In Gram-negative enteric pathogen Vibrio parahaemolyticus, we found that polar flagella ca

95 acteriophages of an environmental isolate of Vibrio parahaemolyticus were isolated and sequenced.

96 including the pathogens Vibrio cholerae and Vibrio parahaemolyticus, were found to produce such acti

97 similarities to the TDH and TRH proteins of Vibrio parahaemolyticus, where they have been shown to c

98 nome of the closely related marine bacterium Vibrio parahaemolyticus, which is a human pathogen, show