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      DNA sequence of both chromosomes of the cholera pathogen Vibrio cholerae

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          Abstract

          Here we determine the complete genomic sequence of the Gram negative, γ-Proteobacterium Vibrio cholerae El Tor N16961 to be 4,033,460 base pairs (bp). The genome consists of two circular chromosomes of 2,961,146 bp and 1,072,314 bp that together encode 3,885 open reading frames. The vast majority of recognizable genes for essential cell functions (such as DNA replication, transcription, translation and cell-wall biosynthesis) and pathogenicity (for example, toxins, surface antigens and adhesins) are located on the large chromosome. In contrast, the small chromosome contains a larger fraction (59%) of hypothetical genes compared with the large chromosome (42%), and also contains many more genes that appear to have origins other than the γ-Proteobacteria. The small chromosome also carries a gene capture system (the integron island) and host ‘addiction’ genes that are typically found on plasmids; thus, the small chromosome may have originally been a megaplasmid that was captured by an ancestral Vibrio species. The V. cholerae genomic sequence provides a starting point for understanding how a free-living, environmental organism emerged to become a significant human bacterial pathogen.

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          The online version of this article (doi:10.1038/35020000) contains supplementary material, which is available to authorized users.

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          Genomic sequence of a Lyme disease spirochaete, Borrelia burgdorferi.

          The genome of the bacterium Borrelia burgdorferi B31, the aetiologic agent of Lyme disease, contains a linear chromosome of 910,725 base pairs and at least 17 linear and circular plasmids with a combined size of more than 533,000 base pairs. The chromosome contains 853 genes encoding a basic set of proteins for DNA replication, transcription, translation, solute transport and energy metabolism, but, like Mycoplasma genitalium, it contains no genes for cellular biosynthetic reactions. Because B. burgdorferi and M. genitalium are distantly related eubacteria, we suggest that their limited metabolic capacities reflect convergent evolution by gene loss from more metabolically competent progenitors. Of 430 genes on 11 plasmids, most have no known biological function; 39% of plasmid genes are paralogues that form 47 gene families. The biological significance of the multiple plasmid-encoded genes is not clear, although they may be involved in antigenic variation or immune evasion.
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            Epidemiology, genetics, and ecology of toxigenic Vibrio cholerae.

            Cholera caused by toxigenic Vibrio cholerae is a major public health problem confronting developing countries, where outbreaks occur in a regular seasonal pattern and are particularly associated with poverty and poor sanitation. The disease is characterized by a devastating watery diarrhea which leads to rapid dehydration, and death occurs in 50 to 70% of untreated patients. Cholera is a waterborne disease, and the importance of water ecology is suggested by the close association of V. cholerae with surface water and the population interacting with the water. Cholera toxin (CT), which is responsible for the profuse diarrhea, is encoded by a lysogenic bacteriophage designated CTXPhi. Although the mechanism by which CT causes diarrhea is known, it is not clear why V. cholerae should infect and elaborate the lethal toxin in the host. Molecular epidemiological surveillance has revealed clonal diversity among toxigenic V. cholerae strains and a continual emergence of new epidemic clones. In view of lysogenic conversion by CTXPhi as a possible mechanism of origination of new toxigenic clones of V. cholerae, it appears that the continual emergence of new toxigenic strains and their selective enrichment during cholera outbreaks constitute an essential component of the natural ecosystem for the evolution of epidemic V. cholerae strains and genetic elements that mediate the transfer of virulence genes. The ecosystem comprising V. cholerae, CTXPhi, the aquatic environment, and the mammalian host offers an understanding of the complex relationship between pathogenesis and the natural selection of a pathogen.
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              Cross-species induction of luminescence in the quorum-sensing bacterium Vibrio harveyi.

              Different species of bacteria were tested for production of extracellular autoinducer-like activities that could stimulate the expression of the luminescence genes in Vibrio harveyi. Several species of bacteria, including the pathogens Vibrio cholerae and Vibrio parahaemolyticus, were found to produce such activities. Possible physiological roles for the two V. harveyi detection-response systems and their joint regulation are discussed.
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                Author and article information

                Contributors
                gvc@tigr.org
                Journal
                Nature
                Nature
                Nature
                Nature Publishing Group UK (London )
                0028-0836
                1476-4687
                1 August 2000
                1 August 2000
                2000
                : 406
                : 6795
                : 477-483
                Affiliations
                [1 ]GRID grid.469946.0, The Institute for Genomic Research, ; 9712 Medical Center Drive, Rockville, 20850 Maryland USA
                [3 ]GRID grid.411024.2, ISNI 0000 0001 2175 4264, Center of Marine Biotechnology, University of Maryland Biotechnology Institute, ; 701 East Pratt Street, Baltimore, 21202 Maryland USA
                [2 ]GRID grid.164295.d, ISNI 0000 0001 0941 7177, Department of Cell and Molecular Biology, , University of Maryland, ; College Park, 20742 Maryland USA
                [4 ]GRID grid.38142.3c, ISNI 000000041936754X, Department of Microbiology and Molecular Genetics, , Harvard Medical School, ; 200 Longwood Avenue , Boston, 02115 Massachusetts USA
                [5 ]GRID grid.418124.a, ISNI 0000 0004 0462 1752, Present Address: Celera Genomics, ; 45 West Gude Drive, Rockville, Maryland 20850 USA
                Article
                BF35020000
                10.1038/35020000
                8288016
                10952301
                d58cdaf9-c0e5-475d-b134-cf51967598af
                © The Author(s) 2000

                This article is distributed under the terms of the Creative Commons Attribution-Non-Commercial-Share Alike licence ( http://creativecommons.org/licenses/by-nc-sa/3.0/), which permits distribution, and reproduction in any medium, provided the original author and source are credited. This licence does not permit commercial exploitation, and derivative works must be licensed under the same or similar licence.

                History
                : 3 April 2000
                : 18 May 2000
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                © Springer Nature Limited 2000

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