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1 three TonB systems within the human pathogen Vibrio vulnificus.
2 idase (PGI-LysAP) activity was identified in Vibrio vulnificus.
3 ansferase, termed Bpt, in the human pathogen Vibrio vulnificus.
4 lding pathway of the adenine riboswitch from Vibrio vulnificus.
5 in from the highly lethal foodborne pathogen Vibrio vulnificus.
6 nesis of an encapsulated, virulent strain of Vibrio vulnificus 1003(O) led to the identification of f
8 n applied to a collection of 120 isolates of Vibrio vulnificus, a water-born species common in shellf
9 ibrio cholerae, Vibrio parahaemolyticus, and Vibrio vulnificus-account for the majority of Vibrio inf
10 , we established a conformational map of the Vibrio vulnificus add adenine riboswitch that reveals fi
11 mily toxins are produced by Vibrio cholerae, Vibrio vulnificus, Aeromonas hydrophila and other Gram-n
16 ficient mice with the siderophilic bacterium Vibrio vulnificus and found that hepcidin deficiency res
18 gh October, mostly due to the seasonality of Vibrio vulnificus and Vibrio parahaemolyticus infections
19 useful insights into other bacteria, such as Vibrio vulnificus and Vibrio parahaemolyticus, that have
21 charide (CPS) is a major virulence factor in Vibrio vulnificus, and encapsulated strains have an opaq
23 rs also exist in Vibrio parahaemolyticus and Vibrio vulnificus, and thus these genes may represent a
24 brio spp., e.g., Vibrio parahaemolyticus and Vibrio vulnificus, cause gastroenteritis, septicemia, an
29 that the active site of a phospholipase from Vibrio vulnificus employs the anion in place of the comm
30 erential translation of a subset of mRNAs in Vibrio vulnificus, enabling the rapid adaptation of bact
52 xtracellular capsule polysaccharide (CPS) of Vibrio vulnificus is a primary virulence factor which al
66 from two different effector domains from the Vibrio vulnificus MARTX toxin restored RID activity, ind
70 ocessing repeats-in-toxin (MARTXVv) toxin of Vibrio vulnificus plays a significant role in the pathog
74 structure of a complex of EspI and EpsJ from Vibrio vulnificus represents the first atomic resolution
77 ot unexpectedly, Vibrio parahaemolyticus and Vibrio vulnificus strains formed out-groups; we also ide
78 ibrio cholerae, Vibrio parahaemolyticus, and Vibrio vulnificus, the only members of the Vibrionaceae
81 (MARTX) toxin-effector domain DUF5(Vv) from Vibrio vulnificus to be a site-specific endopeptidase th
82 the first time the antibacterial activity of Vibrio vulnificus Type 6 secretion systems in vivo, reve
83 nse to iron in the broad-range host pathogen Vibrio vulnificus under the hypothesis that iron is one
84 effects of urban interface wildfire ashes on Vibrio vulnificus (V. vulnificus) growth and gene expres
85 ram-negative bacteria, including the species Vibrio vulnificus, Vibrio parahaemolyticus and Vibrio ch
86 nce for L-ornithine, whereas the enzyme from Vibrio vulnificus (VvL/ODC) had dual specificity functio
87 x genes of the only known luminous strain of Vibrio vulnificus, VVL1 (ATCC 43382), were evolutionaril
88 se gene sequence shows 80% homology with the Vibrio vulnificus VvpD type 4 prepilin peptidase require
92 Pseudomonas aeruginosa, Vibrio cholerae and Vibrio vulnificus, which adopt a hexapeptide repeat fold
93 e and elucidated the structure of VvPL2 from Vibrio vulnificus YJ016, which represents a transitional