A Microbial Biorealm page on the genus Sodalis glossinidius
Higher order taxa
Bacteria; Proteobacteria; Gammaproteobacteria; Enterobacteriales; Enterobacteriaceae (1)
Sodalis glossinidius (1)
Description and significance
Describe the appearance, habitat, etc. of the organism, and why it is important enough to have its genome sequenced. Describe how and where it was isolated. Include a picture or two (with sources) if you can find them.
Sodalis glossinidius is a Gram-negative, rod-shaped, filamentous bacteria. It is one of three endosymbionts for the tsetse fly Glossina morsitans morsitansis. A secondary endosymbiont residing in the midgut, fat body and haemolymph of the insect. Though endosymbionts have proven to be difficult to culture, S. glossinidius was isolated and cultured from the haemolymph of G. m. morsitans in 1999. S. glossinidius can gros intracellularly in Aedes albopictus or axenically in media containing a nitrogen source. This microaerophilic bacterium grows optimally with 5% oxygen and 95% carbon dioxide at 25 °C. Colony morphology is uniform, with defined edges, and off-white. (7)
It is important to study S. glossinidius because it is an endosymbiont of two tsetse fly species which are vectors for Trypanosoma congolense,
Describe the size and content of the genome. How many chromosomes? Circular or linear? Other interesting features? What is known about its sequence? Does it have any plasmids? Are they important to the organism's lifestyle?
Though most organisms of the Family Enterobacteriaceae are able to produce catalase, S. glossinidius is not. This is thought to be why this microbe requires a microaerophilic environment. (7)
Strain M1T did produce a-galactosidase and b-N-acetylglucosaminidase. (7)
S. glossinidius has a relatively inactive biochemical profile compared to other organisms in the family Enterobacteriaceae, likely due to its path away from a free-existence. (7, and source one about degenerative)
Interestingly, chitinase production by this micro-organism has been postulated to account for an increase in trypanosome susceptibility in laboratory colonies of G. m. morsitans known to harbour large numbers of S-endosymbionts (Welburn & Maudlin, 1991). In addition to b-N-acetylglucosa (7)
Cell structure and metabolism
Describe any interesting features and/or cell structures; how it gains energy; what important molecules it produces.
Describe any interactions with other organisms (included eukaryotes), contributions to the environment, effect on environment, etc.
about if endosymbionts are gone, larvae cant develop
In the tsetse ¯y (Glossina spp.) P- and S-endosymbionts coexist in the gut lumen, with P-endosymbionts occupying specialized mycetocyte cells in the anterior portion of the insect gut and S-endosymbionts occupying midgut epithelial cells (Huebner & Davey, 1974; Pinnock & Hess, 1974). While the role of each micro-organism has not been clearly de®ned, collectively their presence is known to be essential for egg production and larval development in the insect (Nogge, 1981). Elimination of the bacterial endosymbionts with antibiotics, lysozyme and speci®c antibodies leads to reproductive abnormalities and growth retardation in the aposymbiotic host (Hill & Campbell, 1973; Nogge, 1976, 1978; Pinnock & Hess, 1974; Southwood et al., 1975). (7)
Sodalis glossinidius is one of three endosymbionts of the tsetse fly. 
How does this organism cause disease? Human, animal, plant hosts? Virulence factors, as well as patient symptoms.
Sodalis glossinidius does not cause any known diseases. bacterial uptake due to protein secretory system 
Sodalis glossinidius, a maternally transmitted endosymbiont of tsetse flies, maintains two phylogenetically distinct type-III secretion systems encoded by chromosomal symbiosis regions designated SSR-1 and SSR-2. Although both symbiosis regions are closely related to extant pathogenicity islands with similar gene inventories, SSR-2 has undergone novel degenerative adaptations in the transition to mutualism. Notably, SSR-2 lacks homologs of genes found in SSR-1
Application to Biotechnology
Does this organism produce any useful compounds or enzymes? What are they and how are they used?
Enter summaries of the most recent research here--at least three required
Some of the recent research on Sodalis glossinidius:
"The endosymbionts of tsetse flies: manipulating host–parasite interactions" 
1. "Sodalis glossinidius". NCBI Taxonomy Browser. 26 August 2007. 
2. Akman, L., Rio, R., Beard, C., and Aksoy, S. “Genome Size Determination and Coding Capacity of Sodalis glossinidius, an Enteric Symbiont of Tsetse Flies, as Revealed by Hybridization to Escherichia coli Gene Arrays.” Journal of Bacteriology. 2001. Volume 183.15 p. 4517-4525.
3. Dale, C., Jones, T., and Pontes, M. "Degenerative Evolution and Functional Diversification of Type-III Secretion Systems in the Insect Endosymbiont Sodalis glossinidius." Molecular Biology and Evolution. 2005. Volume 22.3 p. 758-766. 
4. Darby, A., Lagnel, J., Matthew, C., Bourtzis, K., Maudlin, I., and Welburn, S. "Extrachromosomal DNA of the Symbiont Sodalis glossinidius." Journal of Bacteriology. 2005. Volume 187.14 p. 5003-5007. 
5. Collazo, C., and Galán, J. "The invasion-associated type-III protein secretion system in Salmonella – a review." Gene. 1997. Volume 192.1 p. 51-59. 
6. Dale, C., and Welburn, S. "The endosymbionts of tsetse flies: manipulating host–parasite interactions." International Journal for Parasitology. http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6T7F-42WX3BM-11&_user=4429&_coverDate=05%2F01%2F2001&_rdoc=1&_fmt=&_orig=search&_sort=d&view=c&_acct=C000059602&_version=1&_urlVersion=0&_userid=4429&md5=32e639fc02894be83034e1718707992f ?????????????
7. Dale, C., and Maudlin, I. "Sodalis gen. nov. and Sodalis glossinidius sp. nov., a microaerophilic secondary endosymbiont of the tsetse fly Glossina morsitans morsitans." International Journal of Systematic Bacteriology. 1999. Volume 49 p. 267–275. 
8. Aksoy, S., and Rio, R. "Interactions among multiple genomes: Tsetse, its symbionts and trypanosomes." Insect Biochemistry and Molecular Biology. 2005. Volume 35.7 p. 691-698. 
Edited by Janet Melnyk, student of Rachel Larsen