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DNA sequence of both chromosomes of the cholera pathogen Vibrio cholerae

TLDR
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.
Abstract
Here we determine the complete genomic sequence of the Gram negative, g-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 g-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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Biodiversity of Vibrios

TL;DR: Vibrios harbour a wealth of diverse genomes as revealed by different genomic techniques including amplified fragment length polymorphism, multilocus sequence typing, repetetive extragenic palindrome PCR, ribotyping, and whole-genome sequencing, which are probably important driving forces in the evolution and speciation of vibrios.
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A small RNA regulates the expression of genes involved in iron metabolism in Escherichia coli.

TL;DR: RyhB provides a mechanism for the cell to down-regulate iron-storage proteins and nonessential ironcontaining proteins when iron is limiting, thus modulating intracellular iron usage to supplement mechanisms for iron uptake directly regulated by Fur.
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Genomic islands in pathogenic and environmental microorganisms

TL;DR: Recent lessons that have been learned from pathogenicity islands in pathogenic microorganisms are discussed and how they apply to the role of genomic islands in commensal, symbiotic and environmental bacteria are discussed.
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Integrons: agents of bacterial evolution

TL;DR: The basic biology of integrons and superintegrons, their evolutionary history and the evidence for the existence of a novel recombination pathway is reviewed.
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The Small RNA Chaperone Hfq and Multiple Small RNAs Control Quorum Sensing in Vibrio harveyi and Vibrio cholerae

TL;DR: It is proposed that Hfq, together with four candidate sRNAs, creates an ultrasensitive regulatory switch that controls the critical transition into the high cell density, quorum-sensing mode.
References
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Journal ArticleDOI

Survival strategies of bacteria in the natural environment.

TL;DR: The heterotrophic plate count has come under increasing criticism because it is inefficient, at best, for enumerating viable bacteria present in marine and estuarine systems.
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Lysogenic conversion by a filamentous phage encoding cholera toxin.

TL;DR: The emergence of toxigenic V. cholerae involves horizontal gene transfer that may depend on in vivo gene expression, and is shown here to be encoded by a filamentous bacteriophage (designated CTXΦ), which is related to coliphage M13.
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Global Climate and Infectious Disease: The Cholera Paradigm*

TL;DR: The association of Vibrio cholerae with plankton, notably copepods, provides further evidence for the environmental origin of cholera, as well as an explanation for the sporadic and erratic occurrence of Cholera epidemics.
Journal ArticleDOI

Microbial gene identification using interpolated Markov models

TL;DR: A new system, GLIMMER, is described, which is more flexible and more powerful than fixed-order Markov methods, which have previously been the primary content-based technique for finding genes in microbial DNA.
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