ライフサイエンスコーパス: parahaemolyticus

1 ella that inhibits the phage infection of V. parahaemolyticus.

2 the evolution and population structure of V. parahaemolyticus.

3 n the first documented pandemic spread of V. parahaemolyticus.

4 function from Pyrococcus furiosus and Vibrio parahaemolyticus.

5 the lateral flagellar (laf) system in Vibrio parahaemolyticus.

6 cluster found in a pandemic clone of Vibrio parahaemolyticus.

7 rce of oysters that caused illness due to V. parahaemolyticus.

8 show that quorum sensing regulates TTS in V. parahaemolyticus.

9 m sensing represses TTS in V. harveyi and V. parahaemolyticus.

10 different from those of other strains of V. parahaemolyticus.

11 ise identification of pandemic strains of V. parahaemolyticus.

12 ulator operons of Vibrio cholerae and Vibrio parahaemolyticus.

13 e a protein highly similar to NorM of Vibrio parahaemolyticus.

14 ey may be relative newcomers to growth in V. parahaemolyticus.

15 ve regulators modulates CPS production in V. parahaemolyticus.

16 aeruginosa is most similar to FlgM of Vibrio parahaemolyticus.

17 buted to this large multistate outbreak of V parahaemolyticus.

18 dium-powered polar flagellar motor in Vibrio parahaemolyticus.

19 ependent manner during infection with Vibrio parahaemolyticus.

20 is integral to array localization in Vibrio parahaemolyticus.

21 tinal tract by the streptomycin-resistant V. parahaemolyticus.

22 -detailed pathogenicity investigations of V. parahaemolyticus.

23 ypochlorite (NaOCl) solutions against Vibrio parahaemolyticus.

24 wing sustained intestinal colonization by V. parahaemolyticus.

25 the crystal structure of a TrkH from Vibrio parahaemolyticus.

26 stimulates motility and virulence of Vibrio parahaemolyticus.

27 vii (9 strains), V. mimicus (10 strains), V. parahaemolyticus (30 strains), and V. vulnificus (10 str

28 Vibrio parahaemolyticus, a biofouling marine bacterium and huma

29 Vibrio parahaemolyticus, a causative agent of gastroenteritis e

30 In the pandemic clone of V. parahaemolyticus, a histone-like DNA-binding protein, HU

31 is of the diarrheal disease caused by Vibrio parahaemolyticus, a leading cause of seafood-associated

32 Vibrio parahaemolyticus, a marine bacterium, is the causative a

33 In Vibrio parahaemolyticus, a significant enteric pathogen of huma

34 results highlight the genetic dynamism of V. parahaemolyticus and aid in refining the genetic definit

35 nvironmental study to identify sources of V. parahaemolyticus and contributors to the outbreak.

36 blooms may harbour high concentrations of V.parahaemolyticus and could serve as the foundation for a

37 rotein S) from the bacterial pathogen Vibrio parahaemolyticus and the human protein HYPE (huntingtin

38 e pathogenic vibrios tested, particularly V. parahaemolyticus and V. alginolyticus, are similar at th

39 ctivity for multiple-antibiotic-resistant V. parahaemolyticus and V. vulnificus, including V. parahae

40 luding the species Vibrio vulnificus, Vibrio parahaemolyticus and Vibrio cholerae, grow in warm, low-

41 Not unexpectedly, Vibrio parahaemolyticus and Vibrio vulnificus strains formed ou

42 Homologous clusters also exist in Vibrio parahaemolyticus and Vibrio vulnificus, and thus these g

43 tentially explaining the broad tropism of V. parahaemolyticus, and highlight the utility of genome-wi

44 e human diseases are Vibrio cholerae, Vibrio parahaemolyticus, and Vibrio vulnificus, the only member

45 e 12, three species--Vibrio cholerae, Vibrio parahaemolyticus, and Vibrio vulnificus-account for the

46 1659 is specifically secreted by T3SS1 of V. parahaemolyticus, and Vp1659 is not required for the suc

47 Genetic diversity in V. parahaemolyticus appears to be driven primarily by frequ

48 uminescens, Aeromonas hydrophila, and Vibrio parahaemolyticus are also sensitive to mutations that di

49 ng-proficient and virulent strains of Vibrio parahaemolyticus are silenced for the vibrio archetypal

50 ferent strains of the marine pathogen Vibrio parahaemolyticus as a model system.

51 tilocus sequence typing (MLST) scheme for V. parahaemolyticus based on the internal fragment sequence

52 is work initiates the characterization of V. parahaemolyticus biofilm formation in the OP and TR cell

53 Thus, we demonstrate that V. parahaemolyticus can invoke a programme of gene control

54 The marine bacterium Vibrio parahaemolyticus causes gastroenteritis in humans and en

55 is nucleotide promote a more adhesive Vibrio parahaemolyticus cell type.

56 ch genes were suitable for establishing a V. parahaemolyticus cgMLST scheme.

57 d between 1997 and 2005 revealed that the V. parahaemolyticus chromosome 2 type III secretion system

58 We identified genes that contribute to V. parahaemolyticus colonization of the intestine independe

59 e we show that an AHPND-causing strain of V. parahaemolyticus contains a 70-kbp plasmid (pVA1) with a

60 Vibrio parahaemolyticus differentiates from a polarly flagellat

61 io species, V. mimicus, V. fluvialis, and V. parahaemolyticus, display lower MBCs of bile, DC, and SD

62 V. parahaemolyticus displays additional phenotypic versatil

63 e clone carrying the luxR-like locus into V. parahaemolyticus dramatically affected colony morphology

64 ar machinery required for phagocytosis of V. parahaemolyticus during infection.

65 Here we show that the Vibrio parahaemolyticus effector protein VopQ is a potent inhib

66 The flaA locus of Vibrio parahaemolyticus encodes one of the four polar flagellin

67 locus in Vibrio species, is required for V. parahaemolyticus fitness in vivo and for induction of T3

68 3, 50, 65, 135 and 417) demonstrates that V. parahaemolyticus gastroenteritis in the Pacific Northwes

69 Here, we used RNA-Seq to profile V. parahaemolyticus gene expression in infected infant rabb

70 A V. parahaemolyticus gene that performed the function of V.

71 More than 12% of annotated V. parahaemolyticus genes are differentially expressed in t

72 We sequenced 92 V. parahaemolyticus genomes and used the genome of strain R

73 Vibrio parahaemolyticus harbors two type III secretion systems

74 Our analyses also suggest that V. parahaemolyticus has access to glucose or other preferre

75 Vibrio parahaemolyticus has dual flagellar systems adapted for

76 . cholerae and P. aeruginosa, whereas the V. parahaemolyticus homolog of one of these regulators, Fla

77 cpsQ encodes one of four V. parahaemolyticus homologs in the CsgD/VpsT family, membe

78 ance was a significant correlate of total V. parahaemolyticus; however, the prevalence of genes commo

79 H gene are highly similar to the Haemophilus parahaemolyticus hphIMC , hphIMA and hphIR gene products

80 lling swarmer cell differentiation of Vibrio parahaemolyticus identified a novel three-gene operon th

81 (the theorized threshold for the risk of V. parahaemolyticus illness from the consumption of raw oys

82 letion of vopW abrogates the virulence of V. parahaemolyticus in several animal models of diarrheal d

83 to one of the largest known outbreaks of V. parahaemolyticus in the United States.

84 for genes that contribute to viability of V. parahaemolyticus in vitro and in the mammalian intestine

85 ry cascade is poorly characterized in Vibrio parahaemolyticus, in part because swarming and virulence

86 hole-genome comparisons of 295 genomes of V. parahaemolyticus, including several traced to northeaste

87 ria and enhances the phage infectivity to V. parahaemolyticus, indicating that polar flagella play an

88 -treated mice displayed protection from a V. parahaemolyticus infection and survived lethal oral and

89 We describe a recognized outbreak of V. parahaemolyticus infection associated with the consumpti

90 ause many effectors are injected during a V. parahaemolyticus infection, it is not surprising that th

91 or proteins contribute to pathogenesis of V. parahaemolyticus infection.

92 Vibrio parahaemolyticus infections are associated with consumpt

93 In May and June 1998, reported Vibrio parahaemolyticus infections increased sharply in Texas.

94 Between 1973 and 1998, 40 outbreaks of V. parahaemolyticus infections were reported to the CDC, an

95 Between 1988 and 1997, 345 sporadic V. parahaemolyticus infections were reported: 59% were gast

96 To prevent V. parahaemolyticus infections, persons should avoid consum

97 seasonality of Vibrio vulnificus and Vibrio parahaemolyticus infections.

98 Vibrio parahaemolyticus is a common marine bacterium and a lead

99 Vibrio parahaemolyticus is a Gram-negative bacterium responsibl

100 Vibrio parahaemolyticus is a halophile that inhabits brackish w

101 Vibrio parahaemolyticus is a halophilic bacterium capable of ca

102 Vibrio parahaemolyticus is a marine microorganism that causes a

103 a(+)/galactose cotransporter vSGLT of Vibrio parahaemolyticus is a member of the sodium:solute sympor

104 Vibrio parahaemolyticus is a naturally occurring bacterium comm

105 Vibrio parahaemolyticus is a ubiquitous, gram-negative marine b

106 Vibrio parahaemolyticus is an emerging food- and waterborne pat

107 Vibrio parahaemolyticus is an important human foodborne pathoge

108 Vibrio parahaemolyticus is an important human pathogen whose tr

109 Vibrio parahaemolyticus is an organism well adapted to communal

110 data reported in this study indicate that V. parahaemolyticus is genetically diverse with a semiclona

111 Vibrio parahaemolyticus is the leading cause of bacterial seafo

112 Vibrio parahaemolyticus is the leading cause of food-borne illn

113 Vibrio parahaemolyticus is the leading worldwide cause of seafo

114 Vibrio parahaemolyticus is the most common cause of seafood-bor

115 Comparative transcriptomic analysis of V. parahaemolyticus isolated from rabbit intestines and fro

116 The assay identified an additional four V. parahaemolyticus isolates among the other 119 isolates.

117 Vibrio parahaemolyticus isolates display variation in colony mo

118 this study, 77 clinical and 67 oyster Vibrio parahaemolyticus isolates from North America were examin

119 parate clonal complexes were observed for V. parahaemolyticus isolates originating from the Pacific a

120 However, not all V. parahaemolyticus isolates swarm proficiently.

121 nique biomarker for the pandemic clone of V. parahaemolyticus, it was possible to rationally design s

122 quorum sensing can stimulate swarming in V. parahaemolyticus; it does so via an alternative pathway

123 V. parahaemolyticus lonS complemented E. coli lon mutants t

124 ffects of SlAEW and AEW solutions against V. parahaemolyticus may be attributed to the changes in cel

125 ficient for induction of autophagy during V. parahaemolyticus-mediated cell death and this effect is

126 confirmed that deletion of rpoN rendered V. parahaemolyticus nonmotile, and it caused reduced biofil

127 enetic markers thought to be specific for V. parahaemolyticus O3:K6 and its clonal derivatives.

128 tention, as the emergence of a new clone, V. parahaemolyticus O3:K6, has resulted in the first docume

129 age dramatically reduces the virulence of V. parahaemolyticus only when polar flagella were absent bo

130 o cholerae HapR, Vibrio harveyi LuxR, Vibrio parahaemolyticus OpaR and Vibrio vulnificus SmcR.

131 mechanisms of environmental persistence of V.parahaemolyticus or an accurate early warning system for

132 ic analysis of clinical and environmental V. parahaemolyticus originating largely from the Pacific No

133 l against a multiple-antibiotic-resistant V. parahaemolyticus pandemic strain infection.

134 lly for the multiple-antibiotic-resistant V. parahaemolyticus pandemic strain.

135 ion using a multiple-antibiotic-resistant V. parahaemolyticus pandemic strain.

136 haemolyticus and V. vulnificus, including V. parahaemolyticus pandemic strains.

137 ledge of additional factors that underlie V. parahaemolyticus pathogenicity is limited.

138 e determined the crystal structure of the V. parahaemolyticus PirA and PirB (PirA(vp) and PirB(vp)) p

139 The V. parahaemolyticus polar flaC flagellin gene was poorly ex

140 It is evident that V. parahaemolyticus population structure in the Pacific Nor

141 Vibrio parahaemolyticus possesses dual flagellar systems adapte

142 Vibrio parahaemolyticus possesses two types of flagella, polar

143 Although not itself luminescent, V. parahaemolyticus produces autoinducer molecules capable

144 flow through the central elements of the V. parahaemolyticus quorum pathway is proven for the first

145 intracellular cyclic-di-GMP pools in Vibrio parahaemolyticus revealed that these genes also altered

146 ame deletion mutation in rpoN (VP2670) in V. parahaemolyticus RIMD2210633, a clinical serogroup O3:K6

147 S to determine the role of these genes in V. parahaemolyticus RIMD2210633, an O3:K6 isolate, and show

148 e sigma factors in the stress response of V. parahaemolyticus RIMD2210633, an O3:K6 pandemic isolate.

149 These data suggest that in V. parahaemolyticus, RpoN plays an important role in carbon

150 The Vibrio parahaemolyticus Scr system modulates decisions pertinen

151 In Vibrio parahaemolyticus, scrC participates in controlling the d

152 Vibrio parahaemolyticus senses surfaces via impeded rotation of

153 Vibrio parahaemolyticus sequence type 36 (ST36) strains that ar

154 he main U.S. West Coast clonal complex of V. parahaemolyticus (sequence type 36 [ST36]) causing oyste

155 ur isolates, and all clustered with other V. parahaemolyticus sequences.

156 This is the first reported outbreak of V parahaemolyticus serotype O3:K6 infection in the United

157 ol specimens from affected persons yielded V parahaemolyticus serotype O3:K6 isolates.

158 V. parahaemolyticus serotype O6:K18 was isolated from the m

159 The crystal structure of the Vibrio parahaemolyticus SGLT showed that residue Gln(428) inter

160 a solute-sodium symporter (SSS) from Vibrio parahaemolyticus, shares a common structural fold with L

161 The crystal structure of TrkH from Vibrio parahaemolyticus showed that TrkH resembles a K(+) chann

162 e solute sodium symporters (SSS), the Vibrio parahaemolyticus sodium/galactose symporter (vSGLT).

163 the external face of a cysteine-less Vibrio parahaemolyticus sodium/glucose cotransporter for expres

164 The Vibrio parahaemolyticus sodium/glucose transporter (vSGLT) is a

165 Here, we report a draft genome of V. parahaemolyticus strain 10329 of the O4:K12 serotype.

166 far that these phages can lysogenize the V. parahaemolyticus strain 16 host.

167 esterase via restoration of motility in a V. parahaemolyticus strain previously shown to accumulate c

168 Application of this MLST scheme to more V. parahaemolyticus strains and by different laboratories w

169 Recently isolated Vibrio parahaemolyticus strains have displayed multiple antibio

170 The present method of characterizing Vibrio parahaemolyticus strains involves serotyping or detectio

171 This MLST scheme was applied to 100 V. parahaemolyticus strains isolated from geographically di

172 ssay between the DeltatoxRS and wild-type V. parahaemolyticus strains marked with the beta-galactosid

173 cs-based method to distinguish individual V. parahaemolyticus strains on the basis of their protein p

174 cgMLST scheme to the characterization of V. parahaemolyticus strains provided by different laborator

175 hether these assays detect all pathogenic V. parahaemolyticus strains since a clear correlation betwe

176 resolution and discriminatory power among V. parahaemolyticus strains using WGS data.

177 ppears to infect at much lower doses than V. parahaemolyticus strains with these same determinants fr

178 correctly identified more than 90% of the V. parahaemolyticus strains.

179 is conserved only in V. cholerae and Vibrio parahaemolyticus T3SS-positive strains and has not been

180 chnology with the cytotoxicity of two Vibrio parahaemolyticus T3SSs (T3SS1 and T3SS2) to identify hum

181 +)/galactose cotransporter (vSGLT) of Vibrio parahaemolyticus, tagged with C-terminal hexahistidine,

182 mpared to the functions attributed to the V. parahaemolyticus TDH and TRH proteins.

183 gent penaeid shrimp disease caused by Vibrio parahaemolyticus that has already led to tremendous loss

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

185 cteria, such as Vibrio vulnificus and Vibrio parahaemolyticus, that have syp-like loci and conserved

186 the functional level, and, in the case of V. parahaemolyticus, the amino acid sequence or protein lev

187 of quorum signaling in the lifestyles of V. parahaemolyticus, the functional homolog of the gene enc

188 Vibrio parahaemolyticus, the leading cause of seafood-associate

189 rtant insights into the mechanism used by V. parahaemolyticus to cause disease.

190 Biofilm formation and adherence of V.parahaemolyticus to chitin is mediated by the ability of

191 The regulatory mechanism by which V. parahaemolyticus ToxR activates expression of T3SS2 rese

192 The V. parahaemolyticus transcriptional response to in vivo gro

193 that the BPD of the newly identified Vibrio parahaemolyticus Type III effector VopR is unfolded in s

194 The Vibrio parahaemolyticus type III effector VopS is implicated in

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

196 alginolyticus, Vibrio fluvialis, and Vibrio parahaemolyticus utilized heme and hemoglobin as iron so

197 The bacterial pathogen Vibrio parahaemolyticus utilizes a type III secretion system to

198 Vibrio parahaemolyticus (V. para) is a Gram-negative bacterium

199 reaction for the prevalence of total Vibrio parahaemolyticus, V. vulnificus and V. cholerae and sele

200 e 3 commonly reported Vibrio species were V. parahaemolyticus, V. vulnificus, and V. alginolyticus; b

201 ene regions in four species (V. cholerae, V. parahaemolyticus, V. vulnificus, and V. mimicus).

202 ecies from the genus Vibrio: V. cholerae, V. parahaemolyticus, V. vulnificus, and V. mimicus.

203 We conclude that V. parahaemolyticus, V. vulnificus, V. cholerae and subpopu

204 ation of the polar flagellar genes of Vibrio parahaemolyticus, Vibrio cholerae, and Pseudomonas aerug

205 ies, with a focus on Vibrio cholerae, Vibrio parahaemolyticus, Vibrio vulnificus and Vibrio fischeri.

206 he structure of the first W domain of Vibrio parahaemolyticus VopL cross-linked to actin Cys374 and s

207 ned to have a complementary region in Vibrio parahaemolyticus (VP) genome and to make different hybri

208 st structure of a bacterial ATL, from Vibrio parahaemolyticus (vpAtl).

209 the sodium/galactose transporter from Vibrio parahaemolyticus (vSGLT), consisting of molecular dynami

210 We discovered that Vibrio parahaemolyticus VtrC, along with VtrA and VtrB, are req

211 locus sequence typing (MLST) database for V. parahaemolyticus was created in 2008, and a large number

212 A portion of the tonB1 locus of V. parahaemolyticus was sequenced and found to encode prote

213 In Gram-negative enteric pathogen Vibrio parahaemolyticus, we found that polar flagella can reduc

214 phages of an environmental isolate of Vibrio parahaemolyticus were isolated and sequenced.

215 ing the pathogens Vibrio cholerae and Vibrio parahaemolyticus, were found to produce such activities.

216 rities to the TDH and TRH proteins of Vibrio parahaemolyticus, where they have been shown to contribu

217 the closely related marine bacterium Vibrio parahaemolyticus, which is a human pathogen, shows that

218 otoxicity when HeLa cells are infected by V. parahaemolyticus, while complementation of the Deltavp16

219 profiles of a wild-type strain (NY-4) of V. parahaemolyticus with those of an ExsD deletion mutant (