IJSEM Visit JGV Online
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Int J Syst Bacteriol 43 (1993), 8-19; DOI 10.1099/00207713-43-1-8
© 1993 Society for General Microbiology
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kita-Tsukamoto, K.
Right arrow Articles by Simidu, U.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Kita-Tsukamoto, K.
Right arrow Articles by Simidu, U.
Agricola
Right arrow Articles by Kita-Tsukamoto, K.
Right arrow Articles by Simidu, U.

Phylogenetic Relationships of Marine Bacteria, Mainly Members of the Family Vibrionaceae, Determined on the Basis of 16S rRNA Sequences

Kumiko Kita-Tsukamoto1,*, Hiroshi Oyaizu2, Kenji Nanba1 and Usio Simidu1

1Ocean Research Institute, University of Tokyo, Minamidai, Nakano, Tokyo 164, Japan
2Faculty of Agriculture, University of Tokyo, Hongo, Bunkyou, Tokyo 113, Japan

* Corresponding author.

ABSTRACT

The phylogenetic relationships of 50 reference strains, mostly marine bacteria which require Na+ for growth, were determined on the basis of 600 16S rRNA nucleotides by using reverse transcriptase sequencing. Strains belonging to 10 genera were included (four genera of the family Vibrionaceae, the genus Aeromonas of the family Aeromonadaceae, and the genera Alteromonas, Marinomonas, Shewanella, Pseudomonas, and Deleya). The sequences were alligned, the similarity values and evolutionary distance values were determined, and a phylogenetic tree was constructed by using the neighbor-joining method. On the basis of our results, the family Vibrionaceae was separated into at least seven groups (genera and families). Vibrio marinus clearly was on a line of descent that was remote from other vibrios. As determined by the similarity and evolutionary distance values, V. marinus is more distantly related to the family Vibrionaceae than the members of the Aeromonadaceae are. Also, Vibrio cholerae strains formed a separate group with Vibrio mimicus at the genus level. Of 30 species of the Vibrionaceae, 17 formed a large phylogenetic cluster. The genus Listonella was found to be a heterogeneous group, and the species were distributed in various subgroups of the Vibrionaceae. The separation of the family Aeromonadaceae from the family Vibrionaceae and the separation of the genera Marinomonas and Shewanella from the genus Alteromonas were confirmed in this phylogenetic study. However, a marine Pseudomonas species, Pseudomonas nautica, was clearly separated from two terrestrial Pseudomonas species. Each group that was separated by the phylogenetic analysis had characteristic 16S rRNA sequence patterns that were common only to species in that group. Therefore, the characteristic sequences described in this paper may be useful for identification purposes.




This article has been cited by other articles:


Home page
Appl. Environ. Microbiol.Home page
D. E. Hunt, D. Gevers, N. M. Vahora, and M. F. Polz
Conservation of the Chitin Utilization Pathway in the Vibrionaceae
Appl. Envir. Microbiol., January 1, 2008; 74(1): 44 - 51.
[Abstract] [Full Text] [PDF]


Home page
J. Bacteriol.Home page
T. Sawabe, K. Kita-Tsukamoto, and F. L. Thompson
Inferring the Evolutionary History of Vibrios by Means of Multilocus Sequence Analysis
J. Bacteriol., November 1, 2007; 189(21): 7932 - 7936.
[Abstract] [Full Text] [PDF]


Home page
J BiochemHome page
C. Suadee, S. Nijvipakul, J. Svasti, B. Entsch, D. P. Ballou, and P. Chaiyen
Luciferase from Vibrio campbellii is more thermostable and binds reduced FMN better than its homologues
J. Biochem., October 1, 2007; 142(4): 539 - 552.
[Abstract] [Full Text] [PDF]


Home page
J Med MicrobiolHome page
R. Chakraborty, S. Sinha, A. K. Mukhopadhyay, M. Asakura, S. Yamasaki, S. K. Bhattacharya, G. B. Nair, and T. Ramamurthy
Species-specific identification of Vibrio fluvialis by PCR targeted to the conserved transcriptional activation and variable membrane tether regions of the toxR gene
J. Med. Microbiol., June 1, 2006; 55(6): 805 - 808.
[Full Text] [PDF]


Home page
Appl. Environ. Microbiol.Home page
G. P. Richards, M. A. Watson, and S. Parveen
Development of a Simple and Rapid Fluorogenic Procedure for Identification of Vibrionaceae Family Members
Appl. Envir. Microbiol., July 1, 2005; 71(7): 3524 - 3527.
[Abstract] [Full Text] [PDF]


Home page
Microbiol. Mol. Biol. Rev.Home page
F. L. Thompson, T. Iida, and J. Swings
Biodiversity of Vibrios
Microbiol. Mol. Biol. Rev., September 1, 2004; 68(3): 403 - 431.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Microbiol.Home page
S. F. Gonzalez, M. J. Krug, M. E. Nielsen, Y. Santos, and D. R. Call
Simultaneous Detection of Marine Fish Pathogens by Using Multiplex PCR and a DNA Microarray
J. Clin. Microbiol., April 1, 2004; 42(4): 1414 - 1419.
[Abstract] [Full Text] [PDF]


Home page
Int. J. Syst. Evol. Microbiol.Home page
M. K. Nishiguchi and V. S. Nair
Evolution of symbiosis in the Vibrionaceae: a combined approach using molecules and physiology
Int J Syst Evol Microbiol, November 1, 2003; 53(6): 2019 - 2026.
[Abstract] [Full Text] [PDF]


Home page
Clin. Microbiol. Rev.Home page
E. K. Lipp, A. Huq, and R. R. Colwell
Effects of Global Climate on Infectious Disease: the Cholera Model
Clin. Microbiol. Rev., October 1, 2002; 15(4): 757 - 770.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Microbiol.Home page
B. Nandi, R. K. Nandy, S. Mukhopadhyay, G. B. Nair, T. Shimada, and A. C. Ghose
Rapid Method for Species-Specific Identification of Vibrio cholerae Using Primers Targeted to the Gene of Outer Membrane Protein OmpW
J. Clin. Microbiol., November 1, 2000; 38(11): 4145 - 4151.
[Abstract] [Full Text]


Home page
MicrobiologyHome page
C. A. Clark, L. Purins, P. Kaewrakon, T. Focareta, and P. A. Manning
The Vibrio cholerae O1 chromosomal integron
Microbiology, October 1, 2000; 146(10): 2605 - 2612.
[Abstract] [Full Text]


Home page
Appl. Environ. Microbiol.Home page
V. Vuddhakul, T. Nakai, C. Matsumoto, T. Oh, T. Nishino, C.-H. Chen, M. Nishibuchi, and J. Okuda
Analysis of gyrB and toxR Gene Sequences of Vibrio hollisae and Development of gyrB- and toxR-Targeted PCR Methods for Isolation of V. hollisae from the Environment and Its Identification
Appl. Envir. Microbiol., August 1, 2000; 66(8): 3506 - 3514.
[Abstract] [Full Text]


Home page
J. Clin. Microbiol.Home page
C. Matsumoto, J. Okuda, M. Ishibashi, M. Iwanaga, P. Garg, T. Rammamurthy, H.-C. Wong, A. Depaola, Y. B. Kim, M. J. Albert, et al.
Pandemic Spread of an O3:K6 Clone of Vibrio parahaemolyticus and Emergence of Related Strains Evidenced by Arbitrarily Primed PCR and toxRS Sequence Analyses
J. Clin. Microbiol., February 1, 2000; 38(2): 578 - 585.
[Abstract] [Full Text]


Home page
J. Clin. Microbiol.Home page
Y. B. Kim, J. Okuda, C. Matsumoto, N. Takahashi, S. Hashimoto, and M. Nishibuchi
Identification of Vibrio parahaemolyticus Strains at the Species Level by PCR Targeted to the toxR Gene
J. Clin. Microbiol., April 1, 1999; 37(4): 1173 - 1177.
[Abstract] [Full Text]


Home page
Appl. Environ. Microbiol.Home page
P. A. Sobecky, T. J. Mincer, M. C. Chang, A. Toukdarian, and D. R. Helinski
Isolation of Broad-Host-Range Replicons from Marine Sediment Bacteria
Appl. Envir. Microbiol., August 1, 1998; 64(8): 2822 - 2830.
[Abstract] [Full Text]


Home page
ScienceHome page
D. Mazel, B. Dychinco, V. A. Webb, and J. Davies
A Distinctive Class of Integron in the Vibrio cholerae Genome
Science, April 24, 1998; 280(5363): 605 - 608.
[Abstract] [Full Text]


Home page
J. Bacteriol.Home page
P. M. Fidopiastis, S. v. Boletzky, and E. G. Ruby
A New Niche for Vibrio logei, the Predominant Light Organ Symbiont of Squids in the Genus Sepiola
J. Bacteriol., January 1, 1998; 180(1): 59 - 64.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 1993 by the International Union of Microbiological Societies.