| Taxonomy Citation ID | Reference | ||||
|---|---|---|---|---|---|
| 11928 |
Thompson FL,
Hoste B,
Vandemeulebroecke K,
Swings J,
( 2003 ) Reclassification of Vibrio hollisae as Grimontia hollisae gen. nov., comb. nov. PMID : 13130058 DOI : 10.1099/ijs.0.02660-0 Abstract >>
The taxonomic positions of three representative strains of Vibrio hollisae (LMG 17719(T), LMG 21416 and LMG 21538) were investigated by means of 16S rDNA sequences and phenotypic data. V. hollisae strains (GenBank/EMBL accession nos AJ514909-AJ514911) shared 99.5 % 16S rDNA sequence similarity, but had only 94.6 % similarity to their closest phylogenetic neighbour, Enterovibrio norvegicus. 16S rDNA sequence similarity of V. hollisae and Vibrio cholerae was only 91 %. These results suggest that V. hollisae should be placed into a novel genus, for which the name Grimontia gen. nov. is proposed.
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| 12506 | De Vos, P., and Truper, H.G. "Judicial Commission of the International Committee on Systematic Bacteriology IXth International (IUMS) Congress of Bacteriology and Applied Microbiology. Minutes of the meetings, 14, 15 and 18 August 1999, Sydney, Australia." Int. J. Syst. Evol. Microbiol. (2000) 50:2239-2244. (Note: Because the description cites ony a single culture collection accession (LMG 17719), the name Grimontia hollisae is not validly published although the type strain is known to be in other culture collections as well). | 6711 |
Hickman FW,
Farmer JJ,
Hollis DG,
Fanning GR,
Steigerwalt AG,
Weaver RE,
Brenner DJ,
( 1982 ) Identification of Vibrio hollisae sp. nov. from patients with diarrhea. PMID : 7076812 PMC : PMC272106 Abstract >>
The name Vibrio hollisae (synonym = Special Bacteriology group EF-13) is proposed for a new group of 16 strains that occurred in stool cultures of patients with diarrhea. V. hollisae is a small gram-negative rod, which is motile with a single polar flagellum. No lateral or peritrichous flagella were observed, even when it was grown on a solid medium. Sodium chloride is required for growth, so V. hollisae is a halophilic vibrio. Strains were positive (36 degrees C, 24 or 48 h) for oxidase (Kovacs), indole production, nitrate reduction to nitrite, and fermentation of D-glucose (acid, no gas), L-arabinose, D-galactose, and D-mannose. Strains were negative for the following tests often used in enteric bacteriology: lipase (corn oil); deoxyribonuclease; gelatinase; methyl red; Voges-Proskauer; utilization of citrate, acetate, and malonate; L-lysine decarboxylase (M?llers); L-ornithine decarboxylase (M?llers); L-arginine dihydrolase (M?llers); growth in KCN medium; and acid production from D-adonitol, D-arabitol, cellobiose, dulcitol, erythritol, glycerol (25% delayed positive at 7 days), i-(myo)-inositol, lactose, maltose, D-mannitol, melibiose, alpha-methyl-D-glucoside, mucate, raffinose, L-rhamnose, salicin, D-sorbitol, sucrose, trehalose, and D-xylose. None of the strains was motile (semisolid medium) at 36 degrees C at 48 h, but by 7 days 88% were motile. The strains did not grow within 2 days when plated on thiosulfate-citrate-bile salts-sucrose (TCBS) agar or MacConkey agar, but they grew on sheep blood agar and marine agar. By DNA-DNA hybridization (75 degrees C, hydroxyapatite with (32)P), V. hollisae was only 0 to 4% related to 21 named species in Vibrio and Photobacterium. The type strain is designated ATCC 33564, which has a mean guanineplus-cytosine content in DNA of 50 mol%. With the disk diffusion method V. hollisae had relatively large zones of inhibition around penicillin, ampicillin, carbenicillin, cephalothin, colistin, polymyxin B, streptomycin, kanamycin, gentamicin, tetracycline, chloramphenicol, and sulfadiazine. Future studies should focus on the isolation of this new vibrio and its ecology and relationship to human diseases.
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4945 |
( 1990 ) 5S ribosomal RNA sequences of Vibrio adaptatus, V. cyclosites, V. hollisae and V. neocistes; three of these eubacteria may not be true members of the Vibrionaceae. PMID : 2326202 DOI : 10.1093/nar/18.6.1636 PMC : PMC330542 Abstract >>
N/A
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| 12505 | VALIDATION LIST No. 9. Int. J. Syst. Bacteriol. (1982) 32:384-385. |