Stigmatella aurantiaca

Stigmatella aurantiaca
Scientific classification
Domain:
Bacteria
Phylum:
Myxococcota
Class:
Myxococcia
Order:
Myxococcales
Family:
Myxococcaceae
Genus:
Stigmatella
Species:
S. aurantiaca
Binomial name
Stigmatella aurantiaca
Berkeley and Curtis 1875 [1]

Stigmatella aurantiaca is a member of myxobacteria, a group of gram-negative bacteria with a complex developmental life cycle.

Classification

The bacterial nature of this organism was recognized by Thaxter in 1892,[2] who grouped it among the Chrondromyces. It had been described several times before, but had been misclassified as a member of the fungi imperfecti.[3] More recent investigations have shown that, contrary to Thaxter's classification, this organism is not closely related to Chrondromyces, and Stigmatella is currently recognized as a separate genus.[3] Of the three major subgroups of the myxobacteria, Myxococcus, Nannocystis, and Chrondromyces, Stigmatella is most closely aligned with Myxococcus.[4][5]

Life cycle

Three species of myxobacteria: Chondromyces crocatus (figs. 7–11), Stigmatella aurantiaca (figs. 12–19) and Melittangium lichenicola (figs. 20–23).

S. aurantiaca, like other myxobacterial species, has a complex life cycle including social gliding (swarming), fruiting body formation, and predatory feeding behaviors. The bacteria do not swim, but glide on surfaces leaving slime trails, forming a mobile biofilm. It commonly grows on the surface of rotting soft woods or fungi, where it may form bright orange patches.

During the vegetative portion of their life cycles, swarming enables coordinated masses of myxobacteria to pool their secretions of extracellular digestive enzymes which are used to kill and consume prey microorganisms, a bacterial "wolfpack" effect.[6] The best studied of the myxobacteria, Myxococcus xanthus, has been shown to actively surround prey organisms, trapping them in pockets where they can be consumed. Roaming flares of M. xanthus can detect clumps of prey bacteria at a distance, making turns towards the clumps and moving directly towards them.[7]

Like other myxobacterial species, S. aurantiaca survives periods of starvation by undergoing a developmental process whereby the individuals of a swarm aggregate to form fruiting bodies (not to be confused with those in fungi). Within the fruiting bodies, a certain fraction of the cells differentiate into myxospores, which are dormant cells resistant to drying and temperatures up to 90 °C.[3] Differentiation into fruiting bodies appears to be mediated by contact-mediated signaling.[8][9]

Under laboratory growth conditions, the ability to undergo differentiation to form fruiting bodies is rapidly lost unless the cultures are regularly forced to fruit by transferring to starvation media. Shaker cultures of S. aurantiaca permanently lose the ability to fruit.[3]

The complex life cycle of myxobacteria is reminiscent of the life cycle of eukaryotic cellular slime molds.

Genome structure

Taxonomic identifier: 378806

See also: NCBI UniProtKB

S. aurantiaca DW4/3-1, a common laboratory strain, has been completely sequenced (See NCBI record link given above). Its circular DNA chromosome consists of 10.26 million base pairs and has a GC content of 67.5%. 8407 genes have been identified, coding for 8352 proteins.

Cell structure

The vegetative cells of S. aurantiaca are elongated rods typically measuring about 5–8 μm long and 0.7–0.8 μm wide. The fine structure resembles that of other gram negative bacteria. The cell surface consists of a cytoplasmic membrane with a typical triple layered organization and a cell wall. The cell wall consists of an outer triple layer and third dense monolayer in the periplasm.[10]

The myxospores are short, optically refractile rods measuring about 2.6–3.5 μm by 0.9–1.2 μm. The brightly colored, red or orange fruiting bodies comprise 1 to 20 spherical or ovoid cysts measuring 40–60 μm by 25–45 μm on top of a stalk measuring 60 to 140 μ high. Each red-brown cyst contains thousands of myxospores surrounded by thick, fibrous capsules.[11] Dispersal of cysts is thought to benefit myxobacteria by ensuring that cell growth is resumed with a group (swarm) of myxobacteria, rather than as isolated cells. The stalks consist mostly of tubules which may represent the debris of lysed swarm cells, as well as some unlysed cells; very little fibrous material interpretable as slime is seen.[11]

Ecology

S. aurantiaca is found on rotting wood or fungi and is only rarely found in soil samples. Secreted and non-secreted proteins involved in their feeding behaviors, either identified directly or speculatively identified on the basis of proteome analysis, include enzymes capable of breaking down a wide selection of peptidoglycans, polysaccharides, proteins and other cellular detritus. Various other secreted compounds possibly involved in predation include antibiotics such as stigmatellin, which is toxic for yeast and filamentous fungi but not most bacteria,[12] and aurafuron A and B, which inhibits the growth of various filamentous fungi.[13]

Stigmatella species hence appear in nature to help decompose otherwise insoluble biological debris. It is only distantly related to the cellulolytic myxobacteria,[14] does not produce cellulases, and is strongly bacteriolytic.[3] Therefore, Stigmatella consumes organisms that feed on wood rather that feeding on wood directly. Besides bacteria, its production of antifungal antibiotics suggests that Stigmatella species may feed on yeasts and fungi as well, or alternatively, may suggest that Stigmatella competes with fungi for shared resources. By producing antimicrobial compounds, Stigmatella may play a role in maintaining the balance of the microbial population in its habitat.[15]

Current Research

Model system for development

Myxobacteria are distinguished from most bacteria by their remarkable range of social behaviors, and as a result, multiple laboratories have taken up studies of these bacteria as a prokaryotic paradigm for differentiation processes and signal transduction. Most studies on social behavior in the myxobacteria have focused on M. xanthus, which has provided an excellent system amenable to many classical genetic experimental approaches. The fruiting bodies of M. xanthus are relatively simple mounds, and the considerably more elaborate fruiting structures produced by S. aurantiaca has led to S. aurantiaca being considered an excellent complementary system to M. xanthus, especially given the advent of contemporary means of genomic analysis. Most of the 95 known M. xanthus development-specific genes are highly conserved in S. aurantiaca. Genes for entire signal transduction pathways important for fruiting body formation in M. xanthus are conserved in S. aurantiaca, whereas only a few are conserved in Anaeromyxobacter dehalogenans, a non-fruiting member of the order Myxococcales.[16]

Various genes have been identified in S. aurantiaca involved in the process of fruiting body formation, including fbfA, which encodes a polypeptide homologous to chitin synthases,[17] fbfB, a gene encoding a putative galactose oxidase,[18] various genes including those encoding tRNAAsp and tRNAVal located at the attB locus (a phage attachment site),[19] and so forth. These genes play a variety of roles in the developmental cycle. For example, in experiments where the fbFA gene was deactivated, the bacterium formed structured clumps instead of fruiting bodies.[17]

To control formation of the elaborate and spatially complex multicellular structure which is the fruiting body, the cells must exchange signals during the entire process. In M. xanthus, various signal molecules involved in this process have been identified. In S. aurantiaca, Stevens (1982) identified an extracellular, diffusible signaling molecule (pheromone) that could substitute for light in stimulating fruiting body maturation.[20] A few years later, the structure of this molecule, a hydroxy ketone named stigmolone, was determined by NMR and mass spectroscopy.[21]

Besides signaling via exchange of diffusible substances, cell-cell signaling can be mediated by contact through the activity of surface located macromolecules. An example of this in S. aurantiaca would be the csgA homolog to the M. xanthus gene, which is bound to the cell envelope. The csgA gene product helps the cells to stay together during development and regulates motility of the cells.[22]

Pxr sRNA is a regulatory RNA which downregulates genes responsible for the formation of fruiting bodies in M. xanthus, and a homolog has been noted in S. aurantiaca.[23] Another short nucleic acid that has been speculatively linked to cell–cell recognition is multicopy single-stranded DNA (msDNA). Sequence comparison of msDNAs from M. xanthus, S. aurantiaca,[24] and other bacteria reveal conserved and hypervariable domains reminiscent of conserved and hypervariable sequences found in allorecognition molecules.[25]

Another means for intercellular signaling could be via the exchange of outer membrane vesicles (OMVs). These vesicles are produced from the outer membrane of myxobacterial cells and are found in large quantities within bacterial biofilms. OMVs appear to play a variety of roles in myxobacterial swarming, predation, and development.[26]

Natural secondary metabolites

Natural products have been the source of most of the active ingredients in medicine, and continue to be an important source despite the advent of automated high-throughput screening methods for drug discovery in synthetic compounds.[27]

Historically, actinomycetes and fungi have been the major source of microbial secondary metabolites found useful as starting points for the development of new drugs, but the last several decades have seen myxobacteria come to the forefront of drug research. The pharmaceutical interest in these organisms comes from their production of a wide variety of structurally unique metabolites with interesting biological activities.[28] The epothilones, derived from the myxobacterium Sporangium cellulosum, represent a new, recently approved class of cancer drugs. Other myxobacterial compounds of potential pharmaceutical interest include disorazol, tubulysin, rhizopodin, chondramid, the aurafurons, tuscolid, tuscuron, and dawenol, chivosazol, soraphen, myxochelin, and the leupyrrins.[28]

S. aurantiaca has been the source of several of these bioactive compounds, including myxothiazol, an inhibitor of the electron transport chain,[29] dawenol, a polyene metabolite,[30] stigmatellin, an antifungal agent,[12] the antifungals aurafuron A and B,[13] and the iron siderophores myxochelin A and B.[31]

References

  1. ↑ Skerman, V. B. D.; McGowan, V.; Sneath, P. H. A. (1980). "Approved Lists of Bacterial Names". International Journal of Systematic Bacteriology. 30: 225–420. doi:10.1099/00207713-30-1-225.
  2. ↑ Thaxter, R. (1892). "On the Myxobacteriaceae, a new order of Schizomycetes". Botanical Gazette. 17 (12): 389–406. doi:10.1086/326866. JSTOR 2464109.
  3. 1 2 3 4 5 Reichenbach, H.; Dworkin, M. (1969). "Studies on Stigmatella aurantiaca (Myxobacterales)" (PDF). J. Gen. Microbiol. 58 (1): 3–14. doi:10.1099/00221287-58-1-3. Retrieved 8 September 2013.
  4. ↑ Shimkets, L.; Woese, C. R. (1992). "A phylogenetic analysis of the myxobacteria: Basis for their classification". Proc. Natl. Acad. Sci. USA. 89 (20): 9459–9463. doi:10.1073/pnas.89.20.9459. PMC 50151. PMID 1384053.
  5. ↑ Spröer, Cathrin; Reichenbach, Hans; Stackebrand, Erko (1999). "The correlation between morphological and phylogenetic classification of myxobacteria" (PDF). International Journal of Systematic Bacteriology. 49 (3): 1255–1262. doi:10.1099/00207713-49-3-1255. PMID 10425789. Retrieved 8 September 2013.
  6. ↑ Berleman, James E.; Kirby, John R. (September 2009). "Deciphering the hunting strategy of a bacterial wolfpack". FEMS Microbiol. Rev. 33 (5): 942–957. doi:10.1111/j.1574-6976.2009.00185.x. PMC 2774760. PMID 19519767.
  7. ↑ Shapiro, James A. (June 1988). "Bacteria as Multicellular Organisms" (PDF). Scientific American. 258 (6): 82–89. doi:10.1038/scientificamerican0688-82. Retrieved 8 September 2013.
  8. ↑ Kiskowski MA, Jiang Y, Alber MS (2004). "Role of streams in myxobacteria aggregate formation". Phys Biol. 1 (3–4): 173–83. doi:10.1088/1478-3967/1/3/005. PMID 16204837.
  9. ↑ Sozinova O, Jiang Y, Kaiser D, Alber M (2005). "A three-dimensional model of myxobacterial aggregation by contact-mediated interactions". Proc Natl Acad Sci USA. 102 (32): 11308–12. doi:10.1073/pnas.0504259102. PMC 1183571. PMID 16061806.
  10. ↑ Reichenbach, Hans; Voelz, Herbert; Dworkin, Martin (1969). "Structural Changes in Stigmatella aurantiaca During Myxospore Induction" (PDF). J. Bacteriol. 97 (2): 905–911. doi:10.1128/jb.97.2.905-911.1969. PMC 249776. PMID 5773035. Retrieved 8 September 2013.
  11. 1 2 Voelz, Herbert; Reichenbach, Hans (1969). "Fine Structure of the Fruiting Bodies of Stigmatella aurantiaca (Myxobacterales)" (PDF). Journal of Bacteriology. 99 (3): 856–866. doi:10.1128/jb.99.3.856-866.1969. PMC 250104. PMID 5370282. Retrieved 8 September 2013.
  12. 1 2 Kunze, B.; Kemmer, T.; Höfle, G.; Reichenbach, H. (1984). "Stigmatellin, a new antibiotic from Stigmatella aurantiaca (Myxobacterales). I. Production, physico-chemical and biological properties". J. Antibiot. (Tokyo). 37 (5): 454–461. doi:10.7164/antibiotics.37.454. PMID 6429114.
  13. 1 2 Kunze, B.; Reichenbach, H.; Müller, R.; Höfle, G. (2005). "Aurafuron a and B, New Bioactive Polyketides from Stigmatella aurantiaca and Archangium gephyra (Myxobacteria)". The Journal of Antibiotics. 58 (4): 244–251. doi:10.1038/ja.2005.28. PMID 15981410.
  14. ↑ Yan, Z. C.; Wang, B.; Li, Y. Z.; Gong, X.; Zhang, H. Q.; Gao, P. J. (2003). "Morphologies and Phylogenetic Classification of Cellulolytic Myxobacteria". Systematic and Applied Microbiology. 26 (1): 104–109. doi:10.1078/072320203322337380. PMID 12747417.
  15. ↑ Dworkin, Martin (2007). "Lingering Puzzles about Myxobacteria" (PDF). Microbe. 2 (1): 18–23. Retrieved 11 September 2013.
  16. ↑ Huntley, S.; Hamann, N.; Wegener-Feldbrugge, S.; Treuner-Lange, A.; Kube, M.; Reinhardt, R.; Klages, S.; Muller, R.; Ronning, C. M.; Nierman, W. C.; Sogaard-Andersen, L. (2010). "Comparative Genomic Analysis of Fruiting Body Formation in Myxococcales". Molecular Biology and Evolution. 28 (2): 1083–1097. doi:10.1093/molbev/msq292. PMID 21037205.
  17. 1 2 Silakowski, B.; Pospiech, A.; Neumann, B.; Schairer, U. (1996). "Stigmatella aurantiaca Fruiting Body Formation Is Dependent on the fbfA Gene Encoding a Polypeptide Homologous to Chitin Synthases" (PDF). J. Bacteriol. 178 (23): 6706–6713. doi:10.1128/jb.178.23.6706-6713.1996. PMC 178565. PMID 8955286. Retrieved 9 September 2013.
  18. ↑ Silakowski, Barbara; Ehret, Heidi; Schairer, Hans Ulrich (1998). "fbfB, a Gene Encoding a Putative Galactose Oxidase, Is Involved in Stigmatella aurantiaca Fruiting Body Formation". J. Bacteriol. 180 (5): 1241–1247. doi:10.1128/JB.180.5.1241-1247.1998. PMC 107013. PMID 9495764.
  19. ↑ Muller, S.; Shen, H.; Hofmann, D.; Schairer, H. U.; Kirby, J. R. (2006). "Integration into the Phage Attachment Site, attB, Impairs Multicellular Differentiation in Stigmatella aurantiaca". Journal of Bacteriology. 188 (5): 1701–1709. doi:10.1128/JB.188.5.1701-1709.2006. PMC 1426541. PMID 16484181.
  20. ↑ Stephens, K.; Hegeman, G. D.; White, D. (1982). "Pheromone produced by the myxobacterium Stigmatella aurantiaca" (PDF). J. Bacteriol. 149 (2): 739–747. doi:10.1128/jb.149.2.739-747.1982. PMC 216567. PMID 6276369. Retrieved 9 September 2013.
  21. ↑ Plaga, W.; Stamm, I.; Schairer, H. U. (1998). "Intercellular signaling in Stigmatella aurantiaca: Purification and characterization of stigmolone, a myxobacterial pheromone". Proceedings of the National Academy of Sciences. 95 (19): 11263–11267. doi:10.1073/pnas.95.19.11263. PMC 21630. PMID 9736724.
  22. ↑ Milosevic, Ana (2003). CsgA, A Putative Signal Molecule of the Myxobacterium Stigmatella aurantiaca Involved in Fruiting: Characterization of the csgA gene and influence of csgA inactivation on development. Ph.D. Dissertation (PDF). Rupertus Carola University of Heidelberg, Germany.
  23. ↑ Yu, Y. T. N.; Yuan, X.; Velicer, G. J. (2010). "Adaptive Evolution of an sRNA That Controls Myxococcus Development". Science. 328 (5981): 993. doi:10.1126/science.1187200. PMC 3027070. PMID 20489016.
  24. ↑ Dhundale, A.; Lampson, B.; Furuichi, T.; Inouye, M.; Inouye, S. (1987). "Structure of msDNA from myxococcus xanthus: Evidence for a long, self-annealing RNA precursor for the covalently linked, branched RNA". Cell. 51 (6): 1105–1112. doi:10.1016/0092-8674(87)90596-4. PMID 2446773. S2CID 21762469.
  25. ↑ Sherman, L. A.; Chattopadhyay, S. (1993). "The Molecular Basis of Allorecognition". Annual Review of Immunology. 11: 385–402. doi:10.1146/annurev.iy.11.040193.002125. PMID 8476567.
  26. ↑ Whitworth, D. E. (2011). Myxobacterial vesicles death at a distance?. Advances in Applied Microbiology. Vol. 75. pp. 1–31. doi:10.1016/B978-0-12-387046-9.00001-3. ISBN 9780123870469. PMID 21807244.
  27. ↑ Harvey, A. (2008). "Natural products in drug discovery". Drug Discovery Today. 13 (19–20): 894–901. doi:10.1016/j.drudis.2008.07.004. PMID 18691670.
  28. 1 2 Bode, H. B.; Müller, R. (2006). "Analysis of myxobacterial secondary metabolism goes molecular". Journal of Industrial Microbiology & Biotechnology. 33 (7): 577–588. doi:10.1007/s10295-006-0082-7. PMID 16491362. S2CID 26415438.
  29. ↑ Silakowski, B.; Schairer, H. U.; Ehret, H.; Kunze, B.; Weinig, S.; Nordsiek, G.; Brandt, P.; Blöcker, H.; Höfle, G.; Beyer, S.; Müller, R. (1999). "New Lessons for Combinatorial Biosynthesis from Myxobacteria. THE MYXOTHIAZOL BIOSYNTHETIC GENE CLUSTER OF Stigmatella aurantiaca DW4/3-1". Journal of Biological Chemistry. 274 (52): 37391–37399. doi:10.1074/jbc.274.52.37391. PMID 10601310.
  30. ↑ Soker, Udo; Kunze, Brigette; Reichenbach, Hans; Hofle, Gerhard (2003). "Dawenol, a New Polyene Metabolite from the Myxobacterium Stigmatella aurantiaca" (PDF). Z. Naturforsch. 58b (10): 1024–1026. doi:10.1515/znb-2003-1015. S2CID 102657249.
  31. ↑ Silakowski, B.; Kunze, B.; Nordsiek, G.; Blöcker, H.; Höfle, G.; Müller, R. (2000). "The myxochelin iron transport regulon of the myxobacterium Stigmatella aurantiaca Sg a15". European Journal of Biochemistry. 267 (21): 6476–6485. doi:10.1046/j.1432-1327.2000.01740.x. PMID 11029592.
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