Vibrio fischeri
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| Vibrio fischeri | ||||||||||||||
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| Vibrio fischeri |
Description and significance
Vibrio fischeri is a gram-negative marine bioluminescent bacterium that forms symbiosis with various species of fish and squid (Ruby, Oxygen). V. fischeri is a member of the Vibrionacea family of marine γ-proteobacteria which includes many species having symbiotic and pathogenic relationships with animals (Ruby, Complete genome). The bioluminescent bacteria chemically produces light in a reaction where a substrate molecule, luciferin is oxidized by an enzyme, luciferase. This process emits light energy rather than heat energy (Herring, Bioluminescence). The proteins necessary for the production of bioluminescence are encoded in a set of genes called the lux operon. The expression of the lux operon and other genes depend upon the presence of a signal molecule known as N-acyl homoserine lactone (AHL). The accumulation of the AHL is a function of population density and hence, bioluminescence can only occur after the bacterium reaches a critical population threshold. The expression of genes through the interaction of bacteria through a signal molecule is known as quorum sensing (NCBI). Intercellular communication via signal molecules has been shown to regulate genes whose products are needed for establishment of virulence, symbiosis, biofilm formation, plasmid transfer and morphogenesis in a variety of microorganisms (Wiley, Microbiology). Prior to its discovery in V. fischeri, quorum sensing and other mechanisms for bacterial cell communication was unknown. The particular symbiosis between a strain of V. fischeri and its host, the Hawian bobtail squid Euprmma scolopes, has been studied extensively. Comparative studies between symbiotic species, like V. fischeri, and human pathogenic species, like Vibrio cholerae, are being examined to elucidate the mechanisms for pathogenesis and pathogenic/host relationships (Ruby, complete).
Genome structure
To date, the complete genomes of two strains of V. fischeri, ES114 and MJII have been sequenced. Strain ES114 isolated from E.scolopes contains two circular chromosomes and a circular plasmid pES100. The genetic material is composed of DNA and the total genome is 4.284 Mbp in length. Chromosome 1, the larger of the two chromosomes contains 2586 genes, while Chromosome 2 and the plasmid contains 1175 and 57 genes respectively. The lux operon system, located on chromosome 2, contains luxI, luxR and luxCDABEG. LuxI encodes for AHL synthase, the enzyme that produces the autoinducer AHL. The Lux R gene produces the AHL dependent transcriptional activator protein that binds to the AHL and promotes the transcription of the lux operon. Luciferase, the enzyme responsible for catalyzing the light reaction, is encoded by luxA and lux B. LuxA produces the alpha chain subunit and luxB, the beta subunit of luciferase. LuxCDE are required for aldehyde synthesis (lux system,UK). LuxG encodes flavin mononucleotide reductase.
Cell structure and metabolism
Ecology
V. fischeri can be located in the microhabitats of its hosts’ light organs, but can also be found living freely as ‘marine snow’, in fecal pellets, as saprohytes (Herring, Bioluminescence), and amongst the microbial flora in the guts of marine animals. The bacterium is distributed in the pelagic zone of temperate and subtropical waters (Ruby, Oxygen). However, higher cell populations of V. fischeri is achieved when it is associated with its host. The symbiosis benefits E.scolopes by using the bioluminescent bacteria in a camouflage strategy called ‘counter-illumination’. The light produced by the bacterium is projected ventrally by the squid, which mimics down dwelling moonlight when viewed from below. The squid effectively projects no shadow, and it can regulate the amount of bacterial illumination with the light organ (Ruby, Oxygen). The squid provides housing and nutrients, especially carbon and nitrogen, in the form of proteins and peptides inside the crypts of the light organ (Serc). In providing a nutrient rich environment, the bacteria population increases to 1.09 cells of which 90-95% are expelled every morning by the squid. The remaining bacteria in the light organ are replenished daily, and the squid becomes a vehicle to produce an abundance of V. fischeri (Ruby, Oxygen). The symbiotic relationship between strains of V. fischeri and their particular hosts is highly specific (McFall-Ngai, Negotiation). Newly hatched squids are born without the bacterium and must acquire them from the surrounding seawaters. In waters inhabited by E.scolopes, the abundance of V. fischeri constitutes only 0.1% of total microbes per mL of seawater, yet only the specific strain of V. fischeri can effectively colonize and remain in the light organ of the squid (McFall-Ngai, Negotiation). The bacterium is housed inside the crypts of the light organ located in the squid’s mantle cavity (serc). Once the bacterium is acquired and colonizes the crypts, morphogenesis occurs for both the bacterium and its host (McFall-Ngai, Negotiation). The bacteria lose the flagella, and the cells decrease in size. As for the host, the ciliated fields used to obtain the bacterium undergo programmed cell death, and the light organ swells (McFall-Ngai, Negotiation). Colonization by the bacterium concurrently alters gene expression in the squid and the bacterium (Uconn).
Pathology
V. fischeri is non-pathogenic to humans but three other members of the Vibrios family are. These are; V. cholerae, V.parahaemolytus, V. vulnificus.