Sulcia muelleri

Sulcia muelleri
Scientific classification
Domain: Bacteria
Phylum: Bacteroidetes
Class: Flavobacteria
Order: Flavobacteriales
Family: Unclassified
Genus: Sulcia
Species: Muelleri
Binomial name
Sulcia muelleri 
 Moran et al 2005

The genetic and metabolic information on this page are derived from the Sulcia muelleri, Strain GWSS. The characteristics of different strands of Sulcia muelleri could vary. For more information about the other documented strains of Sulcia muelleri Redirect here.

Candidatus Sulcia muellleri is an aerobic, gram-negative, bacillus bacteria that is a part of the phylum Bacteroidetes.[1] Sulcia muelleri is an obligate and mutualistic symbiotic microbe commonly found occupying specialized cell compartments of sap-feeding insects called bacteriocytes.[1] A majority of the research done on Sulcia muelleri has detailed its relationship with the host, Homalodisca vitripennis.[2][3][4][5] Other studies have documented the nature of its residency in other insects like the maize leafhopper (Cicadulina) or the spittlebug (Cercopoidea).[5][6] Sulcia muelleri is noted for its exceptionally minimal genome and it is currently identified as having the smallest known, sequenced Bacteroidetes genome at only 245 kilobases.[5]

Discovery

Sulcia Muelleri was classified under microscope in 2005 by the evolutionary biologist, Nancy A. Moran.[1] The endosymbiont was found in the dissected bacteriocyte of the spittlebug (Calstopter arizonana).[1] The Genus Sulcia is named after Vytváření Karel Šulc, a Moravian embryologist who is responsible for being one of the first scientists to recognize that the insect bacteriome is an organ where bacteria reside.[1] The species, Muelleri, has been named in the honor of H.J. Muller, (not to be confused with Hermann Joseph Muller) whom speculated in 1960 that there was a parallel evolutionary history between endosymbionts and a select clade of insect hosts known as Auchenorrhyncha.[1] Sulcia muelleri is a member of the order Flavobacteriales. It is currently not classified as a member of any taxonomic family.[7]

Morphology

Not a whole lot of information has been documented about the morphology of Sulcia muelleri

Sulcia muelleri is a rod-shaped bacterium measuring 5-7 μm in length, .7 μm in diameter and 2-5 μm in width.[5] Because Sulcia muelleri lacks most of the genes responsible for cell division and membrane synthesis, it is sometimes observed to extend unusually long lengths during part of its life cycle; this extended length can range from 5-100 μm.[5]

Like all other Flavobacteriales, The Sulcia muelleri is gram-negative.

Phylogeny

The phylogeny of Sulcia muelleri has been discovered to follow the phylogeny of the Hemiptera clade, Auchenorrhyncha.[8] The first association between Sulcia muelleri and Auchenorrhyncha is estimated to have occurred sometime between 260-280 million years ago.[8][8] Further evidence supports the idea that Sulcia muelleri has coevolved with another symbiotic lineage from the taxonomic class Betaproteobacteria.[8] The result of this coevolution can be noticed through the fact that both Sulcia muelleri and its host leave cofactor and vitamin production to another member of the symbiotic relationship. Although Sulcia's co-residents are not always of the class Betaproteobacteria, contemporary analyses have shown that they often are.[4] The Betaproteobacteria ancestor is suggested to have diversified into the genera Zinderia, Nasuia and Vidania. [8]

There are currently 9 unique strains of Sulcia muelleri that have been identified through a complete genome sequence.[7] They can all be found Here .

Sulcia and the Flavobacteria

The tree below demonstrates the position of Sulcia muelleri with respect to some other members of the class Flavobacteria. The tree was constructed by comparing the peptide sequences of ten different types of proteins. The proteins used were the DNA polymerase III beta-subunit, initiation factor IF-2, leucyl-tRNA synthetase, the phenylalanine—tRNA ligase beta-subunit, VARS, elongation factor Tu, the RNA polymerase beta-subunit, and the ribosomal proteins L2, S5, and S11.[5] Where Sulcia Muelleri is found occupying the body of Auchenorrhyncha hosts, the other members of Flavobacteria are found residing in freshwater bodies and soils.[9] The inference for the long, isolated stretch of the Sulcia muelleri branch is that there has been a high frequency of base-pair substitution which has led to noticeable genetic differences between Sulcia muelleri and most other Flavobacteria.[5]


P. Irgensii


F. Johnsoniae

Flavo. BAL38

Flavo. BBFL7

Flavo. MED212

Cellulophaga

Sulcia muelleri



Genomics

The Sulcia muelleri, strain GWSS genome was completely sequenced at The Genome Institute using Illumina dye sequencing.[5] The genome is an exceptionally reduced genome, where the genetic range of Sulcia Muelleri is only 10% of that of Escherichia Coli's.[2] It is composed of one circular chromosome that measures 245,530 kilobases long. There are neither any plasmids nor any other mobile genetic elements.[10] The genome contains a total of 263 genes: 227 protein genes, 36 RNA genes and one pseudogene.[10] Of the 227 different polypeptides, 99 of them are enzymes and another 9 are transport proteins.[10] The GC-content is 22.4%.[10]

A distinct feature of the Sulcia muelleri genome is the presence of three unique rRNA sequences at the positions of (486-504), (1001-1016), (1418-1431). The implications of these unique sequences are not identified.[1]

Reduced Genome

The Sulcia muelleri genome is what scientists refer to as a reduced genome; it is categorized by the apparent evolutionary loss of many ostensibly essential genes related to processes like DNA repair, translation or cell membrane biosynthesis.[5] The conditions required for genome reduction can be multifaceted, however they often involve some form of stability.[11] The occurrence of genome reduction raises interesting questions about what are the minimal requirements for a functioning genome. Scientists are currently testing their hypotheses about the matter by engineering their own reduced genomes.[12]

Symbiosis

Sulcia Muelleri is a symbiont for a group of insects classified under the suborder Auchenorrhyncha.[3] Usual hosts are cicadas, leafhoppers, treehoppers, spittlebugs, and planthoppers.[1] Sulcia Muelleri is always found co-residing its host with another bacterial endosymbiont from the phylum Proteobacteria.[5] For example, Sulcia Muelleri and candidatus Zinderia insecticola are both found to live in the bacteriome of select species of the spittlebug.[5]

Insect-associated symbionts have been found to share a similar set of features. All symbionts appear to possess a reduced genome, have a high GC-content and bear a more frequent Base-pair substitution rate compared to their free-living ancestors.[5]

Because of symbiosis, hosts may be able to utilize metabolic pathways they might not be able to use if their endosymbionts were absent; one relevant example is the ability for sap-feeding insects to survive off of relatively nutrient-poor food sources, e.g. xylem and phloem.[5]

Symbiosis with the Glassy-winged sharpshooter

Most of the contemporary research concerning the nature of the symbiosis between Sulcia and its hosts has been conducted on the Glassy-winged sharpshooter.[2][3][4][5] Sulcia Muelleri is always found inside the bacteriocyte of a host along with at least one other endosymbiont; The GSWW strain of Sulcia Muelleri is found within the Glassy-winged sharpshooter along with the Gammaproteobacterium, Baumannia cicadellinicola.[5] Genomic analysis has revealed the respective metabolic roles for each other members of this symbiotic triangle.[5] The Glassy-winged sharpshooter, which feeds on the xylem of plants, supplies simple amino acids and carbon sources for the two endosymbionts. In return, Sulcia Muelleri uses the basic materials to synthesize complex amino acids like homoserine or L-threonine.[2] The Baumannia cicadellinicolais reported to provide most of the cofactors and vitamins for the system.[5]

One unanswered question about this symbiotic relationship asks how the endosymbionts receive a sufficient amount nitrogen. This speculation arises due to the dilute and nutrient-poor character of xylem.[5] Although nitrogen assimilation was hypothesized, genomic analysis suggests that Sulcia Muelleri lacks the ability to perform this function.[5]

Metabolic exchange

Listed below is a model of the symbiotic metabolic exchange based on the metabolites that are used by Sulcia Muelleri and the metabolites that are produced by Sulcia Muelleri.[2] The Glassy-winged sharpshooter is mostly responsible for providing Sulcia Muelleri with nutrients and basic amino acids received from the xylem it feeds on. The Sulcia Muelleri, in return, produces more complex substrates.

Produced by Sulcia Muelleri Received from 'Glassy-winged sharpshooter' Received from Baumannia cicadellinicola
2-ketovaline cysteine Erythrose 4-phosphate
L-threonine L-serine Phosphoenolpyruvic acid
homoserine L-aspartate Ribose 5-phosphate
L-Lysine Erythrose 4-phosphate octaprenyl-diphosphate
LL-2,6-diaminoheptanedioate Ribose 5-phosphate Oxaloacetic acid

Biology and Metabolism

Sulcia Muelleri is found in the bacteriocytes of their insect hosts.[1] The only time when the bacterial cells are not found in the bacteriocyte compartments is when they are transferred vertically from the host to their host's offspring.[3]

Evidence suggests that Sulcia Muelleri utilizes aerobic respiration.[5] ATP is synthesized by way of a cytochrome c oxidase catalyzed termination.[5] The cytochrome is of the type cbb-3.[5]

The electron donor for Sulcia Muelleri is implied to be some carbon source retrieved from the sap-feeding diet of its host.[5] Some examples are glutamate, malate and glucose; all of which are found in xylem sap. [5]

The symbiont harvests reducing power in the form of NADH. [5]

The analysis of Sulcia Muelleri, strand GWSS's reduced genome suggests that a proportionate amount of the genes preserved over its evolution are dedicated to amino acid biosynthesis. 21.3% of its protein-coding genes are dedicated to creating amino acids, while another 33% is dedicated to translation-related processes.[5] Sulcia Muelleri is usually capable of synthesizing 8 of its essential amino acids: leucine, valine, threonine, isoleucine, lysine, arginine, phenylalanine, and tryptophan. Some strains of Sulcia Muelleri are incapable of making the amino acid, tryptophan.[4] It receives its other two amino acids - methionine and histidine from either its host or its co-symbiont.[5] Sulcia Muelleri is responsible for making two complex amino acids for its host: homoserine and 2-ketovaline.[5] Sulcia Muelleri lacks a full set of Aminoacyl tRNA synthetases; surprisingly, however, it possesses all of the genes necessary to code for all 20 amino acids.[5]

Other proteins that Sulcia Muelleri makes include a couple of transport proteins; the microbe creates organic cation transport proteins, antibiotic-related transporters and heavy-metal ion transporters.[5]

Sulcia Muelleri is marked down for containing only two genes dedicated to cofactor or vitamin production; these genes code for the synthesis of menaquinone. Sulcia Muelleri receives most of its cofactors or vitamins from its cosymbiont.[5]

Sulcia Muelleri has a minimal set of genes assigned for DNA housekeeping purposes.[5] The only genes it has for DNA repair are the mutL and mutS genes.[5]

See also

References

  1. 1 2 3 4 5 6 7 8 9 Moran, Nancy A.; Tran, Phat; Gerardo, Nicole M. (December 2005). "Symbiosis and Insect Diversification: an Ancient Symbiont ofSap-Feeding Insects from the Bacterial PhylumBacteroidetes". Applied and Environmental Microbiology 71 (12): 8802–8810. doi:10.1128/aem.71.12.8802-8810.2005.
  2. 1 2 3 4 5 Cottret, L; Milreu, PV; Acuña, V; Marchetti-Spaccamela, A; Stougie, L; Charles, H; Sagot, MF (2 September 2010). "Graph-based analysis of the metabolic exchanges between two co-resident intracellular symbionts, Baumannia cicadellinicola and Sulcia muelleri, with their insect host, Homalodisca coagulata.". PLOS Computational Biology 6 (9): e1000904. doi:10.1371/journal.pcbi.1000904. PMID 20838465.
  3. 1 2 3 4 Wu, D; Daugherty, SC; Van Aken, SE; Pai, GH; Watkins, KL; Khouri, H; Tallon, LJ; Zaborsky, JM; Dunbar, HE; Tran, PL; Moran, NA; Eisen, JA (June 2006). "Metabolic complementarity and genomics of the dual bacterial symbiosis of sharpshooters.". PLOS Biology 4 (6): e188. doi:10.1371/journal.pbio.0040188. PMC 1472245. PMID 16729848.
  4. 1 2 3 4 McCutcheon, JP; Moran, NA (2010). "Functional convergence in reduced genomes of bacterial symbionts spanning 200 My of evolution.". Genome biology and evolution 2: 708–18. doi:10.1093/gbe/evq055. PMC 2953269. PMID 20829280.
  5. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 McCutcheon, JP; Moran, NA (4 December 2007). "Parallel genomic evolution and metabolic interdependence in an ancient symbiosis.". Proceedings of the National Academy of Sciences of the United States of America 104 (49): 19392–7. doi:10.1073/pnas.0708855104. PMID 18048332.
  6. ↑ Chang, HH; Cho, ST; Canale, MC; Mugford, ST; Lopes, JR; Hogenhout, SA; Kuo, CH (29 January 2015). "Complete Genome Sequence of "Candidatus Sulcia muelleri" ML, an Obligate Nutritional Symbiont of Maize Leafhopper (Dalbulus maidis).". Genome announcements 3 (1): e01483–14. doi:10.1128/genomeA.01483-14. PMID 25635014.
  7. 1 2 "Candidatus Sulcia muelleri GWSS". KEGG Genome.
  8. 1 2 3 4 5 Bennett, GM; Moran, NA (2013). "Small, smaller, smallest: the origins and evolution of ancient dual symbioses in a Phloem-feeding insect.". Genome biology and evolution 5 (9): 1675–88. doi:10.1093/gbe/evt118. PMID 23918810.
  9. ↑ Welker, Thomas; Shoemaker, Craig; Arias, Codovanga; Kelsius, Phillip (28 February 2005). "Transmission and Detection of Flavobacterium Columnare in Channel Catfish, Ictalurus Punctatus". Diseases of Aquatic Organisms 63: 129–132. doi:10.3354/dao063129.
  10. 1 2 3 4 Subhraveti, Pallavi; Ong, Quang; Holland, Tim; Kothari, Anamika; Ingrid, Keseler; Caspi, Ron; Karp, Peter D. "Summary of Candidatus Sulcia muelleri, Strain GWSS, version 19.0". BioCyc.
  11. ↑ McCutcheon, JP; Moran, NA (8 November 2011). "Extreme genome reduction in symbiotic bacteria.". Nature reviews. Microbiology 10 (1): 13–26. doi:10.1038/nrmicro2670. PMID 22064560.
  12. ↑ Lee, Jun; Sung, Bong; Kim, Mi; Blattner, Frederick R; Yoon, Byoung; Kim, Jung; Kim, Sun (2009). "Metabolic engineering of a reduced-genome strain of Escherichia coli for L-threonine production". Microbial Cell Factories 8 (1): 2. doi:10.1186/1475-2859-8-2.

External links

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