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1 tinal tract by the streptomycin-resistant V. parahaemolyticus.
2 -detailed pathogenicity investigations of V. parahaemolyticus.
3 wing sustained intestinal colonization by V. parahaemolyticus.
4  the crystal structure of a TrkH from Vibrio parahaemolyticus.
5  stimulates motility and virulence of Vibrio parahaemolyticus.
6 the evolution and population structure of V. parahaemolyticus.
7 n the first documented pandemic spread of V. parahaemolyticus.
8 function from Pyrococcus furiosus and Vibrio parahaemolyticus.
9 the lateral flagellar (laf) system in Vibrio parahaemolyticus.
10  cluster found in a pandemic clone of Vibrio parahaemolyticus.
11 rce of oysters that caused illness due to V. parahaemolyticus.
12 show that quorum sensing regulates TTS in V. parahaemolyticus.
13 m sensing represses TTS in V. harveyi and V. parahaemolyticus.
14  different from those of other strains of V. parahaemolyticus.
15 hinery facilitates the virulence trait of V. parahaemolyticus.
16 ise identification of pandemic strains of V. parahaemolyticus.
17 ulator operons of Vibrio cholerae and Vibrio parahaemolyticus.
18 e a protein highly similar to NorM of Vibrio parahaemolyticus.
19 ey may be relative newcomers to growth in V. parahaemolyticus.
20 ve regulators modulates CPS production in V. parahaemolyticus.
21 aeruginosa is most similar to FlgM of Vibrio parahaemolyticus.
22 buted to this large multistate outbreak of V parahaemolyticus.
23 dium-powered polar flagellar motor in Vibrio parahaemolyticus.
24 l pathogens, followed by Shigella and Vibrio parahaemolyticus.
25  SCFP enhanced disease resistance against V. parahaemolyticus.
26 ic Necrosis Disease (AHPND) caused by Vibrio parahaemolyticus.
27 COD homologs from Vibrio cholerae and Vibrio parahaemolyticus.
28  mortality rates after the challenge with V. parahaemolyticus.
29 to combat the causative agent of EMS, Vibrio parahaemolyticus.
30  via long term exposure to the pathogenic V. parahaemolyticus.
31 ypochlorite (NaOCl) solutions against Vibrio parahaemolyticus.
32 ella that inhibits the phage infection of V. parahaemolyticus.
33 ependent manner during infection with Vibrio parahaemolyticus.
34  is integral to array localization in Vibrio parahaemolyticus.
35 vii (9 strains), V. mimicus (10 strains), V. parahaemolyticus (30 strains), and V. vulnificus (10 str
36 elding a limit of detection of 62 CFU Vibrio parahaemolyticus, 86 CFU Salmonella Typhimurium, and 82
37                                       Vibrio parahaemolyticus, a biofouling marine bacterium and huma
38                                       Vibrio parahaemolyticus, a causative agent of gastroenteritis e
39                  In the pandemic clone of V. parahaemolyticus, a histone-like DNA-binding protein, HU
40 is of the diarrheal disease caused by Vibrio parahaemolyticus, a leading cause of seafood-associated
41                                   For Vibrio parahaemolyticus, a marine bacterium and pathogen, iron
42                                       Vibrio parahaemolyticus, a marine bacterium, is the causative a
43                                    In Vibrio parahaemolyticus, a significant enteric pathogen of huma
44 results highlight the genetic dynamism of V. parahaemolyticus and aid in refining the genetic definit
45 nvironmental study to identify sources of V. parahaemolyticus and contributors to the outbreak.
46  blooms may harbour high concentrations of V.parahaemolyticus and could serve as the foundation for a
47                                      Both V. parahaemolyticus and E. coli Fur interacted with FcrX, a
48 for the selective pathogenic signaling by V. parahaemolyticus and reveal insight into a host's suscep
49 rotein S) from the bacterial pathogen Vibrio parahaemolyticus and the human protein HYPE (huntingtin
50 e pathogenic vibrios tested, particularly V. parahaemolyticus and V. alginolyticus, are similar at th
51     In some pathogenic Vibrios, including V. parahaemolyticus and V. cholerae, ToxR is required for b
52 ctivity for multiple-antibiotic-resistant V. parahaemolyticus and V. vulnificus, including V. parahae
53 luding the species Vibrio vulnificus, Vibrio parahaemolyticus and Vibrio cholerae, grow in warm, low-
54                     Not unexpectedly, Vibrio parahaemolyticus and Vibrio vulnificus strains formed ou
55     Homologous clusters also exist in Vibrio parahaemolyticus and Vibrio vulnificus, and thus these g
56 ogenic non-cholera Vibrio spp., e.g., Vibrio parahaemolyticus and Vibrio vulnificus, cause gastroente
57 a Typhimurium, Staphylococcus aureus, Vibrio parahaemolyticus) and their mixtures in water and milk.
58 tentially explaining the broad tropism of V. parahaemolyticus, and highlight the utility of genome-wi
59 microbial activity for fish pathogen, Vibrio parahaemolyticus, and identified surfactin as the key an
60 form each group) were challenged with Vibrio parahaemolyticus, and survival rates were subsequently a
61 e human diseases are Vibrio cholerae, Vibrio parahaemolyticus, and Vibrio vulnificus, the only member
62 e 12, three species--Vibrio cholerae, Vibrio parahaemolyticus, and Vibrio vulnificus-account for the
63 1659 is specifically secreted by T3SS1 of V. parahaemolyticus, and Vp1659 is not required for the suc
64                      Genetic diversity in V. parahaemolyticus appears to be driven primarily by frequ
65 uminescens, Aeromonas hydrophila, and Vibrio parahaemolyticus are also sensitive to mutations that di
66 ng-proficient and virulent strains of Vibrio parahaemolyticus are silenced for the vibrio archetypal
67                   Some bacteria, like Vibrio parahaemolyticus, are social and swarm in groups on surf
68 ferent strains of the marine pathogen Vibrio parahaemolyticus as a model system.
69  somni at tyrosine 32 or by VopS from Vibrio parahaemolyticus at threonine 35.
70 tilocus sequence typing (MLST) scheme for V. parahaemolyticus based on the internal fragment sequence
71 is work initiates the characterization of V. parahaemolyticus biofilm formation in the OP and TR cell
72 we present a rapid detection platform for V. parahaemolyticus by combining loop-mediated isothermal a
73                 Thus, we demonstrate that V. parahaemolyticus can invoke a programme of gene control
74 n exotoxin of the food-borne pathogen Vibrio parahaemolyticus, can be exported through the type III s
75                  The marine bacterium Vibrio parahaemolyticus causes gastroenteritis in humans and en
76 is nucleotide promote a more adhesive Vibrio parahaemolyticus cell type.
77 ch genes were suitable for establishing a V. parahaemolyticus cgMLST scheme.
78 d between 1997 and 2005 revealed that the V. parahaemolyticus chromosome 2 type III secretion system
79                      The success of a Vibrio parahaemolyticus clone (VpST3) in Latin America- the fir
80 o the global expansion of this successful V. parahaemolyticus clone into regions with different clima
81    We identified genes that contribute to V. parahaemolyticus colonization of the intestine independe
82 ration of intestinal cells and heightened V. parahaemolyticus' colonization and virulence.
83 e we show that an AHPND-causing strain of V. parahaemolyticus contains a 70-kbp plasmid (pVA1) with a
84 )-like fold highly similar to that of Vibrio parahaemolyticus CpxA as determined by X-ray crystallogr
85                                       Vibrio parahaemolyticus differentiates from a polarly flagellat
86 io species, V. mimicus, V. fluvialis, and V. parahaemolyticus, display lower MBCs of bile, DC, and SD
87                                           V. parahaemolyticus displays additional phenotypic versatil
88 e clone carrying the luxR-like locus into V. parahaemolyticus dramatically affected colony morphology
89 ar machinery required for phagocytosis of V. parahaemolyticus during infection.
90                 Here we show that the Vibrio parahaemolyticus effector protein VopQ is a potent inhib
91 the actin-binding repeat (ABR) of the Vibrio parahaemolyticus effector VopV binds to cytoplasmic acti
92                     The flaA locus of Vibrio parahaemolyticus encodes one of the four polar flagellin
93  locus in Vibrio species, is required for V. parahaemolyticus fitness in vivo and for induction of T3
94 ecreted lipase, is required for escape of V. parahaemolyticus from the host cells.
95 3, 50, 65, 135 and 417) demonstrates that V. parahaemolyticus gastroenteritis in the Pacific Northwes
96          Here, we used RNA-Seq to profile V. parahaemolyticus gene expression in infected infant rabb
97                                         A V. parahaemolyticus gene that performed the function of V.
98                More than 12% of annotated V. parahaemolyticus genes are differentially expressed in t
99                           We sequenced 92 V. parahaemolyticus genomes and used the genome of strain R
100 mple sets of Escherichia/Shigella and Vibrio parahaemolyticus genomes, we show that iterative-PopPUNK
101                                       Vibrio parahaemolyticus harbors two type III secretion systems
102            Our analyses also suggest that V. parahaemolyticus has access to glucose or other preferre
103                                       Vibrio parahaemolyticus has dual flagellar systems adapted for
104 . cholerae and P. aeruginosa, whereas the V. parahaemolyticus homolog of one of these regulators, Fla
105                  cpsQ encodes one of four V. parahaemolyticus homologs in the CsgD/VpsT family, membe
106 ance was a significant correlate of total V. parahaemolyticus; however, the prevalence of genes commo
107 H gene are highly similar to the Haemophilus parahaemolyticus hphIMC , hphIMA and hphIR gene products
108 lling swarmer cell differentiation of Vibrio parahaemolyticus identified a novel three-gene operon th
109  (the theorized threshold for the risk of V. parahaemolyticus illness from the consumption of raw oys
110 munity, and strengthen resistance against V. parahaemolyticus in P. vannamei.
111 ities, and disease resistance against Vibrio parahaemolyticus in Pacific white shrimp (Penaeus vannam
112 letion of vopW abrogates the virulence of V. parahaemolyticus in several animal models of diarrheal d
113  to one of the largest known outbreaks of V. parahaemolyticus in the United States.
114 for genes that contribute to viability of V. parahaemolyticus in vitro and in the mammalian intestine
115 ry cascade is poorly characterized in Vibrio parahaemolyticus, in part because swarming and virulence
116 hole-genome comparisons of 295 genomes of V. parahaemolyticus, including several traced to northeaste
117 ria and enhances the phage infectivity to V. parahaemolyticus, indicating that polar flagella play an
118 -treated mice displayed protection from a V. parahaemolyticus infection and survived lethal oral and
119      We describe a recognized outbreak of V. parahaemolyticus infection associated with the consumpti
120 ause many effectors are injected during a V. parahaemolyticus infection, it is not surprising that th
121 or proteins contribute to pathogenesis of V. parahaemolyticus infection.
122 umulation in a rabbit diarrhoeal model of V. parahaemolyticus infection.
123 sponses, and effective protection against V. parahaemolyticus infection.
124                                       Vibrio parahaemolyticus infections are associated with consumpt
125        In May and June 1998, reported Vibrio parahaemolyticus infections increased sharply in Texas.
126    Between 1973 and 1998, 40 outbreaks of V. parahaemolyticus infections were reported to the CDC, an
127       Between 1988 and 1997, 345 sporadic V. parahaemolyticus infections were reported: 59% were gast
128                                To prevent V. parahaemolyticus infections, persons should avoid consum
129  seasonality of Vibrio vulnificus and Vibrio parahaemolyticus infections.
130                                       Vibrio parahaemolyticus is a common marine bacterium and a lead
131                                       Vibrio parahaemolyticus is a facultative intracellular pathogen
132                                       Vibrio parahaemolyticus is a Gram-negative bacterium responsibl
133                                       Vibrio parahaemolyticus is a halophile that inhabits brackish w
134                                       Vibrio parahaemolyticus is a halophilic bacterium capable of ca
135                                       Vibrio parahaemolyticus is a marine microorganism that causes a
136 a(+)/galactose cotransporter vSGLT of Vibrio parahaemolyticus is a member of the sodium:solute sympor
137                                       Vibrio parahaemolyticus is a naturally occurring bacterium comm
138                                       Vibrio parahaemolyticus is a ubiquitous, gram-negative marine b
139                                       Vibrio parahaemolyticus is an emerging food- and waterborne pat
140                                       Vibrio parahaemolyticus is an important human foodborne pathoge
141                                       Vibrio parahaemolyticus is an important human pathogen whose tr
142                                       Vibrio parahaemolyticus is an organism well adapted to communal
143 data reported in this study indicate that V. parahaemolyticus is genetically diverse with a semiclona
144                                       Vibrio parahaemolyticus is one of only two marine pathogens whe
145                                       Vibrio parahaemolyticus is one of the most important foodborne
146                                       Vibrio parahaemolyticus is the leading cause of bacterial seafo
147                                       Vibrio parahaemolyticus is the leading cause of food-borne illn
148                                       Vibrio parahaemolyticus is the leading cause of seafood-borne d
149                                       Vibrio parahaemolyticus is the leading worldwide cause of seafo
150                                       Vibrio parahaemolyticus is the most common cause of seafood-bor
151    Comparative transcriptomic analysis of V. parahaemolyticus isolated from rabbit intestines and fro
152   The assay identified an additional four V. parahaemolyticus isolates among the other 119 isolates.
153                                       Vibrio parahaemolyticus isolates display variation in colony mo
154 this study, 77 clinical and 67 oyster Vibrio parahaemolyticus isolates from North America were examin
155 parate clonal complexes were observed for V. parahaemolyticus isolates originating from the Pacific a
156                          However, not all V. parahaemolyticus isolates swarm proficiently.
157            When exposure challenge of Vibrio parahaemolyticus, it is indicated that the PI3K-AKT, MAP
158 nique biomarker for the pandemic clone of V. parahaemolyticus, it was possible to rationally design s
159  quorum sensing can stimulate swarming in V. parahaemolyticus; it does so via an alternative pathway
160                                           V. parahaemolyticus lonS complemented E. coli lon mutants t
161 ffects of SlAEW and AEW solutions against V. parahaemolyticus may be attributed to the changes in cel
162 ficient for induction of autophagy during V. parahaemolyticus-mediated cell death and this effect is
163  confirmed that deletion of rpoN rendered V. parahaemolyticus nonmotile, and it caused reduced biofil
164 enetic markers thought to be specific for V. parahaemolyticus O3:K6 and its clonal derivatives.
165 tention, as the emergence of a new clone, V. parahaemolyticus O3:K6, has resulted in the first docume
166 age dramatically reduces the virulence of V. parahaemolyticus only when polar flagella were absent bo
167 o cholerae HapR, Vibrio harveyi LuxR, Vibrio parahaemolyticus OpaR and Vibrio vulnificus SmcR.
168 mechanisms of environmental persistence of V.parahaemolyticus or an accurate early warning system for
169 ic analysis of clinical and environmental V. parahaemolyticus originating largely from the Pacific No
170 l against a multiple-antibiotic-resistant V. parahaemolyticus pandemic strain infection.
171 lly for the multiple-antibiotic-resistant V. parahaemolyticus pandemic strain.
172 ion using a multiple-antibiotic-resistant V. parahaemolyticus pandemic strain.
173 haemolyticus and V. vulnificus, including V. parahaemolyticus pandemic strains.
174 ledge of additional factors that underlie V. parahaemolyticus pathogenicity is limited.
175    Our results indicate that the pathogen V. parahaemolyticus perceives nitrite as a host-derived sig
176 e determined the crystal structure of the V. parahaemolyticus PirA and PirB (PirA(vp) and PirB(vp)) p
177                                       The V. parahaemolyticus polar flaC flagellin gene was poorly ex
178                        It is evident that V. parahaemolyticus population structure in the Pacific Nor
179                                       Vibrio parahaemolyticus possesses dual flagellar systems adapte
180                                       Vibrio parahaemolyticus possesses two types of flagella, polar
181          Although not itself luminescent, V. parahaemolyticus produces autoinducer molecules capable
182 red for normal flagellar synthesis in Vibrio parahaemolyticus, Pseudomonas putida, and Shewanella put
183  flow through the central elements of the V. parahaemolyticus quorum pathway is proven for the first
184  intracellular cyclic-di-GMP pools in Vibrio parahaemolyticus revealed that these genes also altered
185 ame deletion mutation in rpoN (VP2670) in V. parahaemolyticus RIMD2210633, a clinical serogroup O3:K6
186 S to determine the role of these genes in V. parahaemolyticus RIMD2210633, an O3:K6 isolate, and show
187 e sigma factors in the stress response of V. parahaemolyticus RIMD2210633, an O3:K6 pandemic isolate.
188                These data suggest that in V. parahaemolyticus, RpoN plays an important role in carbon
189                                   The Vibrio parahaemolyticus Scr system modulates decisions pertinen
190                                    In Vibrio parahaemolyticus, scrC participates in controlling the d
191                      During pathogenesis, V. parahaemolyticus secretes effector proteins that usurp t
192                            Pathogenic Vibrio parahaemolyticus senses bile acids and induce pathogenes
193                                       Vibrio parahaemolyticus senses surfaces via impeded rotation of
194                 The data demonstrate that V. parahaemolyticus senses the S signal using SscL and SscS
195                                       Vibrio parahaemolyticus sequence type 36 (ST36) strains that ar
196 he main U.S. West Coast clonal complex of V. parahaemolyticus (sequence type 36 [ST36]) causing oyste
197 ur isolates, and all clustered with other V. parahaemolyticus sequences.
198     This is the first reported outbreak of V parahaemolyticus serotype O3:K6 infection in the United
199 ol specimens from affected persons yielded V parahaemolyticus serotype O3:K6 isolates.
200                                           V. parahaemolyticus serotype O6:K18 was isolated from the m
201          The crystal structure of the Vibrio parahaemolyticus SGLT showed that residue Gln(428) inter
202  a solute-sodium symporter (SSS) from Vibrio parahaemolyticus, shares a common structural fold with L
203    The crystal structure of TrkH from Vibrio parahaemolyticus showed that TrkH resembles a K(+) chann
204 e solute sodium symporters (SSS), the Vibrio parahaemolyticus sodium/galactose symporter (vSGLT).
205  the external face of a cysteine-less Vibrio parahaemolyticus sodium/glucose cotransporter for expres
206                                   The Vibrio parahaemolyticus sodium/glucose transporter (vSGLT) is a
207         Here, we report a draft genome of V. parahaemolyticus strain 10329 of the O4:K12 serotype.
208  far that these phages can lysogenize the V. parahaemolyticus strain 16 host.
209 esterase via restoration of motility in a V. parahaemolyticus strain previously shown to accumulate c
210   Application of this MLST scheme to more V. parahaemolyticus strains and by different laboratories w
211                     Recently isolated Vibrio parahaemolyticus strains have displayed multiple antibio
212  The present method of characterizing Vibrio parahaemolyticus strains involves serotyping or detectio
213       This MLST scheme was applied to 100 V. parahaemolyticus strains isolated from geographically di
214 ssay between the DeltatoxRS and wild-type V. parahaemolyticus strains marked with the beta-galactosid
215 cs-based method to distinguish individual V. parahaemolyticus strains on the basis of their protein p
216  cgMLST scheme to the characterization of V. parahaemolyticus strains provided by different laborator
217 hether these assays detect all pathogenic V. parahaemolyticus strains since a clear correlation betwe
218 resolution and discriminatory power among V. parahaemolyticus strains using WGS data.
219 ppears to infect at much lower doses than V. parahaemolyticus strains with these same determinants fr
220 correctly identified more than 90% of the V. parahaemolyticus strains.
221                                   The Vibrio parahaemolyticus T3SS effector VopQ targets host-cell V-
222  is conserved only in V. cholerae and Vibrio parahaemolyticus T3SS-positive strains and has not been
223 chnology with the cytotoxicity of two Vibrio parahaemolyticus T3SSs (T3SS1 and T3SS2) to identify hum
224 +)/galactose cotransporter (vSGLT) of Vibrio parahaemolyticus, tagged with C-terminal hexahistidine,
225 mpared to the functions attributed to the V. parahaemolyticus TDH and TRH proteins.
226 gent penaeid shrimp disease caused by Vibrio parahaemolyticus that has already led to tremendous loss
227      VopL is an effector protein from Vibrio parahaemolyticus that nucleates actin filaments.
228 cteria, such as Vibrio vulnificus and Vibrio parahaemolyticus, that have syp-like loci and conserved
229 the functional level, and, in the case of V. parahaemolyticus, the amino acid sequence or protein lev
230  of quorum signaling in the lifestyles of V. parahaemolyticus, the functional homolog of the gene enc
231                                    In Vibrio parahaemolyticus, the leading cause of bacterial seafood
232                                       Vibrio parahaemolyticus, the leading cause of seafood-associate
233 rtant insights into the mechanism used by V. parahaemolyticus to cause disease.
234         Biofilm formation and adherence of V.parahaemolyticus to chitin is mediated by the ability of
235 processes to facilitate opportunities for V. parahaemolyticus to prolong infection within the host.
236         The regulatory mechanism by which V. parahaemolyticus ToxR activates expression of T3SS2 rese
237 he LAMP reactions using primers targeting V. parahaemolyticus toxR gene were optimized at an isotherm
238                                       The V. parahaemolyticus transcriptional response to in vivo gro
239  that the BPD of the newly identified Vibrio parahaemolyticus Type III effector VopR is unfolded in s
240                                   The Vibrio parahaemolyticus type III effector VopS is implicated in
241 c bile acid sensor that activates the Vibrio parahaemolyticus type III secretion system adopts an obl
242                   Herein we show that Vibrio parahaemolyticus uses the type III effector VopQ (Vibrio
243 evidence supporting that the pathogen Vibrio parahaemolyticus uses transertion to assemble its type I
244  alginolyticus, Vibrio fluvialis, and Vibrio parahaemolyticus utilized heme and hemoglobin as iron so
245                The bacterial pathogen Vibrio parahaemolyticus utilizes a type III secretion system to
246                                       Vibrio parahaemolyticus (V. para) is a Gram-negative bacterium
247                                       Vibrio parahaemolyticus (V. para), a Gram-negative halophilic b
248  reaction for the prevalence of total Vibrio parahaemolyticus, V. vulnificus and V. cholerae and sele
249 e 3 commonly reported Vibrio species were V. parahaemolyticus, V. vulnificus, and V. alginolyticus; b
250 ene regions in four species (V. cholerae, V. parahaemolyticus, V. vulnificus, and V. mimicus).
251 ecies from the genus Vibrio: V. cholerae, V. parahaemolyticus, V. vulnificus, and V. mimicus.
252                          We conclude that V. parahaemolyticus, V. vulnificus, V. cholerae and subpopu
253 ation of the polar flagellar genes of Vibrio parahaemolyticus, Vibrio cholerae, and Pseudomonas aerug
254 ies, with a focus on Vibrio cholerae, Vibrio parahaemolyticus, Vibrio vulnificus and Vibrio fischeri.
255 he structure of the first W domain of Vibrio parahaemolyticus VopL cross-linked to actin Cys374 and s
256 e of these pathogens, disease-causing Vibrio parahaemolyticus (VP(AHPND)) which induces acute hepatop
257 ned to have a complementary region in Vibrio parahaemolyticus (VP) genome and to make different hybri
258 st structure of a bacterial ATL, from Vibrio parahaemolyticus (vpAtl).
259 the sodium/galactose transporter from Vibrio parahaemolyticus (vSGLT), consisting of molecular dynami
260 dbToxRp is structurally homologous to the V. parahaemolyticus VtrA periplasmic domain.
261                    We discovered that Vibrio parahaemolyticus VtrC, along with VtrA and VtrB, are req
262 locus sequence typing (MLST) database for V. parahaemolyticus was created in 2008, and a large number
263 ity during the shrimp challenge test with V. parahaemolyticus was observed in shrimp fed SCFP 0.35 an
264 erotoxigenic E. coli, S. typhimurium, and V. parahaemolyticus was produced and found immunogenic in m
265 g epitopes from ETEC, S. typhimurium, and V. parahaemolyticus was produced in plants cells and trigge
266           A portion of the tonB1 locus of V. parahaemolyticus was sequenced and found to encode prote
267     In Gram-negative enteric pathogen Vibrio parahaemolyticus, we found that polar flagella can reduc
268 phages of an environmental isolate of Vibrio parahaemolyticus were isolated and sequenced.
269 ing the pathogens Vibrio cholerae and Vibrio parahaemolyticus, were found to produce such activities.
270 rities to the TDH and TRH proteins of Vibrio parahaemolyticus, where they have been shown to contribu
271  the closely related marine bacterium Vibrio parahaemolyticus, which is a human pathogen, shows that
272 on of an effector protein secreted by Vibrio parahaemolyticus, which is an enteric pathogen found in
273 otoxicity when HeLa cells are infected by V. parahaemolyticus, while complementation of the Deltavp16
274 s have implications in the pathogenesis of V.parahaemolyticus, whose invasion of intestinal epithelia
275  profiles of a wild-type strain (NY-4) of V. parahaemolyticus with those of an ExsD deletion mutant (
276 egrees C, providing specific detection of V. parahaemolyticus within 45 min at the detection limit of

 
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