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1                                              V. parahaemolyticus displays additional phenotypic versa
2                                              V. parahaemolyticus lonS complemented E. coli lon mutant
3                                              V. parahaemolyticus serotype O6:K18 was isolated from th
4          This MLST scheme was applied to 100 V. parahaemolyticus strains isolated from geographically
5                              We sequenced 92 V. parahaemolyticus genomes and used the genome of strai
6                                            A V. parahaemolyticus gene that performed the function of
7 Because many effectors are injected during a V. parahaemolyticus infection, it is not surprising that
8 which genes were suitable for establishing a V. parahaemolyticus cgMLST scheme.
9 age-treated mice displayed protection from a V. parahaemolyticus infection and survived lethal oral a
10 odiesterase via restoration of motility in a V. parahaemolyticus strain previously shown to accumulat
11  responses, and effective protection against V. parahaemolyticus infection.
12  immunity, and strengthen resistance against V. parahaemolyticus in P. vannamei.
13  of SCFP enhanced disease resistance against V. parahaemolyticus.
14 y effects of SlAEW and AEW solutions against V. parahaemolyticus may be attributed to the changes in
15                             However, not all V. parahaemolyticus isolates swarm proficiently.
16 er resolution and discriminatory power among V. parahaemolyticus strains using WGS data.
17 ibrio species, V. mimicus, V. fluvialis, and V. parahaemolyticus, display lower MBCs of bile, DC, and
18 orum sensing represses TTS in V. harveyi and V. parahaemolyticus.
19 enterotoxigenic E. coli, S. typhimurium, and V. parahaemolyticus was produced and found immunogenic i
20 ning epitopes from ETEC, S. typhimurium, and V. parahaemolyticus was produced in plants cells and tri
21                   More than 12% of annotated V. parahaemolyticus genes are differentially expressed i
22                                         Both V. parahaemolyticus and E. coli Fur interacted with FcrX
23 showing sustained intestinal colonization by V. parahaemolyticus.
24 cytotoxicity when HeLa cells are infected by V. parahaemolyticus, while complementation of the Deltav
25 on for the selective pathogenic signaling by V. parahaemolyticus and reveal insight into a host's sus
26 mportant insights into the mechanism used by V. parahaemolyticus to cause disease.
27 y gene regions in four species (V. cholerae, V. parahaemolyticus, V. vulnificus, and V. mimicus).
28  species from the genus Vibrio: V. cholerae, V. parahaemolyticus, V. vulnificus, and V. mimicus.
29  attention, as the emergence of a new clone, V. parahaemolyticus O3:K6, has resulted in the first doc
30 sufficient for induction of autophagy during V. parahaemolyticus-mediated cell death and this effect
31 netic analysis of clinical and environmental V. parahaemolyticus originating largely from the Pacific
32 ltilocus sequence typing (MLST) database for V. parahaemolyticus was created in 2008, and a large num
33  Separate clonal complexes were observed for V. parahaemolyticus isolates originating from the Pacifi
34 ic processes to facilitate opportunities for V. parahaemolyticus to prolong infection within the host
35 e, we present a rapid detection platform for V. parahaemolyticus by combining loop-mediated isotherma
36 ral locus in Vibrio species, is required for V. parahaemolyticus fitness in vivo and for induction of
37 multilocus sequence typing (MLST) scheme for V. parahaemolyticus based on the internal fragment seque
38 d genetic markers thought to be specific for V. parahaemolyticus O3:K6 and its clonal derivatives.
39      The assay identified an additional four V. parahaemolyticus isolates among the other 119 isolate
40                     cpsQ encodes one of four V. parahaemolyticus homologs in the CsgD/VpsT family, me
41 iferation of intestinal cells and heightened V. parahaemolyticus' colonization and virulence.
42                         Genetic diversity in V. parahaemolyticus appears to be driven primarily by fr
43 oxRS to determine the role of these genes in V. parahaemolyticus RIMD2210633, an O3:K6 isolate, and s
44  they may be relative newcomers to growth in V. parahaemolyticus.
45 ative regulators modulates CPS production in V. parahaemolyticus.
46 hat quorum sensing can stimulate swarming in V. parahaemolyticus; it does so via an alternative pathw
47                   These data suggest that in V. parahaemolyticus, RpoN plays an important role in car
48 We show that quorum sensing regulates TTS in V. parahaemolyticus.
49 -frame deletion mutation in rpoN (VP2670) in V. parahaemolyticus RIMD2210633, a clinical serogroup O3
50        In some pathogenic Vibrios, including V. parahaemolyticus and V. cholerae, ToxR is required fo
51 arahaemolyticus and V. vulnificus, including V. parahaemolyticus pandemic strains.
52 omics-based method to distinguish individual V. parahaemolyticus strains on the basis of their protei
53  the clone carrying the luxR-like locus into V. parahaemolyticus dramatically affected colony morphol
54             Although not itself luminescent, V. parahaemolyticus produces autoinducer molecules capab
55      Application of this MLST scheme to more V. parahaemolyticus strains and by different laboratorie
56 ion profiles of a wild-type strain (NY-4) of V. parahaemolyticus with those of an ExsD deletion mutan
57       Comparative transcriptomic analysis of V. parahaemolyticus isolated from rabbit intestines and
58 l, the functional level, and, in the case of V. parahaemolyticus, the amino acid sequence or protein
59  This work initiates the characterization of V. parahaemolyticus biofilm formation in the OP and TR c
60 his cgMLST scheme to the characterization of V. parahaemolyticus strains provided by different labora
61                     In the pandemic clone of V. parahaemolyticus, a histone-like DNA-binding protein,
62 e unique biomarker for the pandemic clone of V. parahaemolyticus, it was possible to rationally desig
63 o the main U.S. West Coast clonal complex of V. parahaemolyticus (sequence type 36 [ST36]) causing oy
64 5 degrees C, providing specific detection of V. parahaemolyticus within 45 min at the detection limit
65 se results highlight the genetic dynamism of V. parahaemolyticus and aid in refining the genetic defi
66 y secreted lipase, is required for escape of V. parahaemolyticus from the host cells.
67            Here, we report a draft genome of V. parahaemolyticus strain 10329 of the O4:K12 serotype.
68   Whole-genome comparisons of 295 genomes of V. parahaemolyticus, including several traced to northea
69 lagella that inhibits the phage infection of V. parahaemolyticus.
70 ore-detailed pathogenicity investigations of V. parahaemolyticus.
71 ole of quorum signaling in the lifestyles of V. parahaemolyticus, the functional homolog of the gene
72              A portion of the tonB1 locus of V. parahaemolyticus was sequenced and found to encode pr
73 accumulation in a rabbit diarrhoeal model of V. parahaemolyticus infection.
74         We describe a recognized outbreak of V. parahaemolyticus infection associated with the consum
75 ted to one of the largest known outbreaks of V. parahaemolyticus in the United States.
76       Between 1973 and 1998, 40 outbreaks of V. parahaemolyticus infections were reported to the CDC,
77 ector proteins contribute to pathogenesis of V. parahaemolyticus infection.
78 lular machinery required for phagocytosis of V. parahaemolyticus during infection.
79 tive sigma factors in the stress response of V. parahaemolyticus RIMD2210633, an O3:K6 pandemic isola
80 s C (the theorized threshold for the risk of V. parahaemolyticus illness from the consumption of raw
81 n environmental study to identify sources of V. parahaemolyticus and contributors to the outbreak.
82 d in the first documented pandemic spread of V. parahaemolyticus.
83 Here we show that an AHPND-causing strain of V. parahaemolyticus contains a 70-kbp plasmid (pVA1) wit
84 nce different from those of other strains of V. parahaemolyticus.
85 recise identification of pandemic strains of V. parahaemolyticus.
86 ng the evolution and population structure of V. parahaemolyticus.
87  Vp1659 is specifically secreted by T3SS1 of V. parahaemolyticus, and Vp1659 is not required for the
88 machinery facilitates the virulence trait of V. parahaemolyticus.
89  potentially explaining the broad tropism of V. parahaemolyticus, and highlight the utility of genome
90 en for genes that contribute to viability of V. parahaemolyticus in vitro and in the mammalian intest
91  deletion of vopW abrogates the virulence of V. parahaemolyticus in several animal models of diarrhea
92  phage dramatically reduces the virulence of V. parahaemolyticus only when polar flagella were absent
93  four isolates, and all clustered with other V. parahaemolyticus sequences.
94  the pathogenic vibrios tested, particularly V. parahaemolyticus and V. alginolyticus, are similar at
95       Our results indicate that the pathogen V. parahaemolyticus perceives nitrite as a host-derived
96                         During pathogenesis, V. parahaemolyticus secretes effector proteins that usur
97 r whether these assays detect all pathogenic V. parahaemolyticus strains since a clear correlation be
98 ent via long term exposure to the pathogenic V. parahaemolyticus.
99                                   To prevent V. parahaemolyticus infections, persons should avoid con
100             Here, we used RNA-Seq to profile V. parahaemolyticus gene expression in infected infant r
101  We confirmed that deletion of rpoN rendered V. parahaemolyticus nonmotile, and it caused reduced bio
102 nfectivity for multiple-antibiotic-resistant V. parahaemolyticus and V. vulnificus, including V. para
103 odel against a multiple-antibiotic-resistant V. parahaemolyticus pandemic strain infection.
104 cially for the multiple-antibiotic-resistant V. parahaemolyticus pandemic strain.
105 ection using a multiple-antibiotic-resistant V. parahaemolyticus pandemic strain.
106 testinal tract by the streptomycin-resistant V. parahaemolyticus.
107          Between 1988 and 1997, 345 sporadic V. parahaemolyticus infections were reported: 59% were g
108 ikovii (9 strains), V. mimicus (10 strains), V. parahaemolyticus (30 strains), and V. vulnificus (10
109 into the global expansion of this successful V. parahaemolyticus clone into regions with different cl
110   The LAMP reactions using primers targeting V. parahaemolyticus toxR gene were optimized at an isoth
111 t appears to infect at much lower doses than V. parahaemolyticus strains with these same determinants
112                             We conclude that V. parahaemolyticus, V. vulnificus, V. cholerae and subp
113                    Thus, we demonstrate that V. parahaemolyticus can invoke a programme of gene contr
114                    The data demonstrate that V. parahaemolyticus senses the S signal using SscL and S
115 ST43, 50, 65, 135 and 417) demonstrates that V. parahaemolyticus gastroenteritis in the Pacific North
116                           It is evident that V. parahaemolyticus population structure in the Pacific
117 he data reported in this study indicate that V. parahaemolyticus is genetically diverse with a semicl
118               Our analyses also suggest that V. parahaemolyticus has access to glucose or other prefe
119                                          The V. parahaemolyticus polar flaC flagellin gene was poorly
120                                          The V. parahaemolyticus transcriptional response to in vivo
121  so far that these phages can lysogenize the V. parahaemolyticus strain 16 host.
122   We determined the crystal structure of the V. parahaemolyticus PirA and PirB (PirA(vp) and PirB(vp)
123 ion flow through the central elements of the V. parahaemolyticus quorum pathway is proven for the fir
124 s, correctly identified more than 90% of the V. parahaemolyticus strains.
125 cted between 1997 and 2005 revealed that the V. parahaemolyticus chromosome 2 type III secretion syst
126  compared to the functions attributed to the V. parahaemolyticus TDH and TRH proteins.
127 e, dbToxRp is structurally homologous to the V. parahaemolyticus VtrA periplasmic domain.
128 n V. cholerae and P. aeruginosa, whereas the V. parahaemolyticus homolog of one of these regulators,
129       We identified genes that contribute to V. parahaemolyticus colonization of the intestine indepe
130 source of oysters that caused illness due to V. parahaemolyticus.
131 cteria and enhances the phage infectivity to V. parahaemolyticus, indicating that polar flagella play
132 undance was a significant correlate of total V. parahaemolyticus; however, the prevalence of genes co
133 n assay between the DeltatoxRS and wild-type V. parahaemolyticus strains marked with the beta-galacto
134 nowledge of additional factors that underlie V. parahaemolyticus pathogenicity is limited.
135  The 3 commonly reported Vibrio species were V. parahaemolyticus, V. vulnificus, and V. alginolyticus
136            The regulatory mechanism by which V. parahaemolyticus ToxR activates expression of T3SS2 r
137 wer mortality rates after the challenge with V. parahaemolyticus.
138 tality during the shrimp challenge test with V. parahaemolyticus was observed in shrimp fed SCFP 0.35

 
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