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Bodo saltans

Bodo saltans
Scientific classification
Domain: Eukaryota
(unranked): Excavata
Phylum: Euglenozoa
Class: Kinetoplastida
Order: Bodonida
Genus: Bodo
Species: B. saltans
Binomial name
Bodo saltans
Ehrenberg
Synonyms

Pleuromonas jaculans


Pleuromonas jaculans

Bodo saltans, also known by the synonym Pleuromonas jaculans, is a free-living nonparasitic species of kinetoplastid flagellate protozoan that is distinguished by the organism's feeding upon bacteria. B. saltans can be found widely distributed throughout the world in both freshwater and marine environments.

B. saltans is a single-celled bean-shaped organism 4 to 5 micrometers in length. It has two flagella: a short anterior projecting flagellum and a longer posterior-projecting flagellum without hairs (acronematic) that extends beyond the length of the cell. B. saltans secures itself to the substrate of its aquatic habitat by the tip of a posterior flagellum. Flexing of the posterior flagellum results in a twitching, jumping movement that is characteristic of this species. This type of movement appears similar to the undulating membrane of the sexually-transmitted pathogen Trichomonas vaginalis and can result in a false-positive diagnosis in cases where B. saltans is a contaminant in test samples, especially if a nonsterile saline solution has been used.

Phylogenetic analysis of the RNA editing process and inferred protein sequences in B. saltans appear to show that B. saltans diverged early on from the evolutionary line of kinetoplastids and that this species of bodonid is more closely related to the trypanosomatids than at least two species of parasitic bodonids of the genus Cryptobia.

Analysis based on the sequence of the topoisomerase II (topo II) gene provides evidence that B. saltans is a predecessor of the trypanosomatids. Commonly, the molecules of in eukaryotes are circular and replication and transcription result in topological stress that is mitigated by enzymes called topoisomerases. Kinetoplastids possess a single mitochondrion with what is perhaps the most complex network of mitochondrial "kDNA" in small and large circular forms. As a consequence, mitochondrial genes for topoisomerases are available in high quantities that make it an attractive focus of genetic study. It is also the significance of the enzyme class of topoisomerases to the function of kinetoplastids that makes the topo genes a target for the medical treatment of trypanosomial and leishmanial diseases.


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