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Agrobacterium - Wikipedia
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Agrobacterium

Agrobacterium is a genus of Gram-negative bacteria established by H. J. Conn that uses horizontal gene transfer to cause tumors in plants. Agrobacterium tumefaciens is the most commonly studied species in this genus. Agrobacterium is well known for its ability to transfer DNA between itself and plants, and for this reason it has become an important tool for genetic engineering.

Agrobacterium
Scientific classification Edit this classification
Domain: Bacteria
Phylum: Pseudomonadota
Class: Alphaproteobacteria
Order: Hyphomicrobiales
Family: Rhizobiaceae
Genus: Agrobacterium
Conn 1942 (Approved Lists 1980)
Type species
Agrobacterium radiobacter
(Smith and Townsend 1907) Conn 1942 (Approved Lists 1980)
Species
Synonyms[1]
  • Polymonas Lieske 1928

Nomenclatural history

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Leading up to the 1990s, the genus Agrobacterium was used as a wastebasket taxon. With the advent of 16S sequencing, many Agrobacterium species (especially the marine species) were reassigned to genera such as Ahrensia, Pseudorhodobacter, Ruegeria, and Stappia.[2][3] The remaining Agrobacterium species were assigned to three biovars: biovar 1 (Agrobacterium tumefaciens), biovar 2 (Agrobacterium rhizogenes), and biovar 3 (Agrobacterium vitis). In the early 2000s, Agrobacterium was synonymized with the genus Rhizobium.[4] This move proved to be controversial.[5][6] The debate was finally resolved when the genus Agrobacterium was reinstated[7] after it was demonstrated that it was phylogenetically distinct from Rhizobium[8][9] and that Agrobacterium species were unified by a unique synapomorphy: the presence of the protelomerase gene, telA, which causes all members of the genus to have a linear chromid.[10] By this time, however, the three Agrobacterium biovars had become defunct; biovar 1 remained with Agrobacterium, biovar 2 was renamed Rhizobium rhizogenes, and biovar 3 was renamed Allorhizobium vitis.

Plant pathogen

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The large growths on these roots are galls induced by Agrobacterium sp.

Agrobacterium tumefaciens causes crown-gall disease in plants. The disease is characterised by a tumour-like growth or gall on the infected plant, often at the junction between the root and the shoot. Tumors are incited by the conjugative transfer of a DNA segment (T-DNA) from the bacterial tumour-inducing (Ti) plasmid. The closely related species, Agrobacterium rhizogenes, induces root tumors, and carries the distinct Ri (root-inducing) plasmid. Although the taxonomy of Agrobacterium is currently under revision it can be generalised that 3 biovars exist within the genus, Agrobacterium tumefaciens, Agrobacterium rhizogenes, and Agrobacterium vitis. Strains within Agrobacterium tumefaciens and Agrobacterium rhizogenes are known to be able to harbour either a Ti or Ri-plasmid, whilst strains of Agrobacterium vitis, generally restricted to grapevines, can harbour a Ti-plasmid. Non-Agrobacterium strains have been isolated from environmental samples which harbour a Ri-plasmid whilst laboratory studies have shown that non-Agrobacterium strains can also harbour a Ti-plasmid. Some environmental strains of Agrobacterium possess neither a Ti nor Ri-plasmid. These strains are avirulent.[11]

The plasmid T-DNA is integrated semi-randomly into the genome of the host cell,[12] and the tumor morphology genes on the T-DNA are expressed, causing the formation of a gall. The T-DNA carries genes for the biosynthetic enzymes for the production of unusual amino acids, typically octopine or nopaline. It also carries genes for the biosynthesis of the plant hormones, auxin and cytokinins, and for the biosynthesis of opines, providing a carbon and nitrogen source for the bacteria that most other micro-organisms can't use, giving Agrobacterium a selective advantage.[13] By altering the hormone balance in the plant cell, the division of those cells cannot be controlled by the plant, and tumors form. The ratio of auxin to cytokinin produced by the tumor genes determines the morphology of the tumor (root-like, disorganized or shoot-like).

In humans

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Although generally seen as an infection in plants, Agrobacterium can be responsible for opportunistic infections in humans with weakened immune systems,[14][15] but has not been shown to be a primary pathogen in otherwise healthy individuals. One of the earliest associations of human disease caused by Agrobacterium radiobacter was reported by Dr. J. R. Cain in Scotland (1988).[16] A later study suggested that Agrobacterium attaches to and genetically transforms several types of human cells by integrating its T-DNA into the human cell genome. The study was conducted using cultured human tissue and did not draw any conclusions regarding related biological activity in nature.[17]

Uses in biotechnology

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See also: Horizontal gene transfer

The ability of Agrobacterium to transfer genes to plants and fungi is used in biotechnology, in particular, genetic engineering for plant improvement. Genomes of plants and fungi can be engineered by use of Agrobacterium for the delivery of sequences hosted in T-DNA binary vectors. A modified Ti or Ri plasmid can be used. The plasmid is 'disarmed' by deletion of the tumor inducing genes; the only essential parts of the T-DNA are its two small (25 base pair) border repeats, at least one of which is needed for plant transformation.[18][19] The genes to be introduced into the plant are cloned into a plant binary vector that contains the T-DNA region of the disarmed plasmid, together with a selectable marker (such as antibiotic resistance) to enable selection for plants that have been successfully transformed. Plants are grown on media containing antibiotic following transformation, and those that do not have the T-DNA integrated into their genome will die. An alternative method is agroinfiltration.[20][21]

 
Plant (S. chacoense) transformed using Agrobacterium. Transformed cells start forming calluses on the side of the leaf pieces

Transformation with Agrobacterium can be achieved in multiple ways. Protoplasts or alternatively leaf-discs can be incubated with the Agrobacterium and whole plants regenerated using plant tissue culture. In agroinfiltration the Agrobacterium may be injected directly into the leaf tissue of a plant. This method transforms only cells in immediate contact with the bacteria, and results in transient expression of plasmid DNA.[22]

Agroinfiltration is commonly used to transform tobacco (Nicotiana). A common transformation protocol for Arabidopsis is the floral dip method:[23] An inflorescence is dipped in a suspension of Agrobacterium, and the bacterium transforms the germline cells that make the female gametes. The seeds can then be screened for antibiotic resistance (or another marker of interest). Plants that have not integrated the plasmid DNA will die when exposed to the antibiotic.[20]

Agrobacterium is listed as being the vector of genetic material that was transferred to these USA GMOs:[24]

The transformation of fungi using Agrobacterium is used primarily for research purposes,[25][26] and follows similar approaches as for plant transformation. The Ti plasmid system is modified to include DNA elements to select for transformed fungal strains, after co-incubation of Agrobacterium strains carrying these plasmids with fungal species.

Genomics

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The Agrobacterium genome consists of three parts: a circular chromosome, a linear chromosome/chromid, and (in some species) a Ti plasmid.[27]

The sequencing of the genomes of several species of Agrobacterium has permitted the study of the evolutionary history of these organisms and has provided information on the genes and systems involved in pathogenesis, biological control and symbiosis. One important finding is the possibility that chromosomes are evolving from plasmids in many of these bacteria. Another discovery is that the diverse chromosomal structures in this group appear to be capable of supporting both symbiotic and pathogenic lifestyles. The availability of the genome sequences of Agrobacterium species will continue to increase, resulting in substantial insights into the function and evolutionary history of this group of plant-associated microbes.[28]

History

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Marc Van Montagu and Jozef Schell at the University of Ghent (Belgium) discovered the gene transfer mechanism between Agrobacterium and plants, which resulted in the development of methods to alter Agrobacterium into an efficient delivery system for gene engineering in plants.[18][19] A team of researchers led by Mary-Dell Chilton were the first to demonstrate that the virulence genes could be removed without adversely affecting the ability of Agrobacterium to insert its own DNA into the plant genome (1983).[29]

See also

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References

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  1. ^ Buchanan RE (1965). "Proposal for rejection of the generic name Polymonas Lieske 1928". International Bulletin of Bacteriological Nomenclature and Taxonomy. 15 (1): 43–44. doi:10.1099/00207713-15-1-43.
  2. ^ Uchino Y, Yokota A, Sugiyama J (August 1997). "Phylogenetic position of the marine subdivision of Agrobacterium species based on 16S rRNA sequence analysis". The Journal of General and Applied Microbiology. 43 (4): 243–247. doi:10.2323/jgam.43.243. PMID 12501326.
  3. ^ Uchino Y, Hirata A, Yokota A, Sugiyama J (June 1998). "Reclassification of marine Agrobacterium species: Proposals of Stappia stellulata gen. nov., comb. nov., Stappia aggregata sp. nov., nom. rev., Ruegeria atlantica gen. nov., comb. nov., Ruegeria gelatinovora comb. nov., Ruegeria algicola comb. nov., and Ahrensia kieliense gen. nov., sp. nov., nom. rev". The Journal of General and Applied Microbiology. 44 (3): 201–210. doi:10.2323/jgam.44.201. PMID 12501429.
  4. ^ Young JM, Kuykendall LD, Martínez-Romero E, Kerr A, Sawada H (January 2001). "A revision of Rhizobium Frank 1889, with an emended description of the genus, and the inclusion of all species of Agrobacterium Conn 1942 and Allorhizobium undicola de Lajudie et al. 1998 as new combinations: Rhizobium radiobacter, R. rhizogenes, R. rubi, R. undicola and R. vitis". International Journal of Systematic and Evolutionary Microbiology. 51 (Pt 1): 89–103. doi:10.1099/00207713-51-1-89. PMID 11211278.
  5. ^ Farrand SK, van Berkum PB, Oger P (September 2003). "Agrobacterium is a definable genus of the family Rhizobiaceae". International Journal of Systematic and Evolutionary Microbiology. 53 (Pt 5): 1681–1687. doi:10.1099/ijs.0.02445-0. PMID 13130068.
  6. ^ Young JM, Kuykendall LD, Martínez-Romero E, Kerr A, Sawada H (September 2003). "Classification and nomenclature of Agrobacterium and Rhizobium". International Journal of Systematic and Evolutionary Microbiology. 53 (Pt 5): 1689–1695. doi:10.1099/ijs.0.02762-0. PMID 13130069.
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  10. ^ Ramírez-Bahena MH, Vial L, Lassalle F, Diel B, Chapulliot D, Daubin V, Nesme X, Muller D (2014). "Single acquisition of protelomerase gave rise to speciation of a large and diverse clade within the Agrobacterium/Rhizobium supercluster characterized by the presence of a linear chromid". Mol Phylogenet Evol. 73: 202–207. doi:10.1016/j.ympev.2014.01.005. PMID 24440816.
  11. ^ Sawada H, Ieki H, Oyaizu H, Matsumoto S (October 1993). "Proposal for rejection of Agrobacterium tumefaciens and revised descriptions for the genus Agrobacterium and for Agrobacterium radiobacter and Agrobacterium rhizogenes". International Journal of Systematic Bacteriology. 43 (4): 694–702. doi:10.1099/00207713-43-4-694. PMID 8240952.
  12. ^ Francis KE, Spiker S (February 2005). "Identification of Arabidopsis thaliana transformants without selection reveals a high occurrence of silenced T-DNA integrations". The Plant Journal. 41 (3): 464–77. doi:10.1111/j.1365-313X.2004.02312.x. PMID 15659104.
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  19. ^ a b Joos H, Timmerman B, Montagu MV, Schell J (1983). "Genetic analysis of transfer and stabilization of Agrobacterium DNA in plant cells". The EMBO Journal. 2 (12): 2151–60. doi:10.1002/j.1460-2075.1983.tb01716.x. PMC 555427. PMID 16453483.
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  22. ^ Shamloul M, Trusa J, Mett V, Yusibov V (April 2014). "Optimization and utilization of Agrobacterium-mediated transient protein production in Nicotiana". Journal of Visualized Experiments (86). doi:10.3791/51204. PMC 4174718. PMID 24796351.
  23. ^ Clough SJ, Bent AF (December 1998). "Floral dip: a simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana". The Plant Journal. 16 (6): 735–43. doi:10.1046/j.1365-313x.1998.00343.x. PMID 10069079. S2CID 410286.
  24. ^ The FDA List of Completed Consultations on Bioengineered Foods Archived May 13, 2008, at the Wayback Machine
  25. ^ Michielse CB, Hooykaas PJ, van den Hondel CA, Ram AF (July 2005). "Agrobacterium-mediated transformation as a tool for functional genomics in fungi". Current Genetics. 48 (1): 1–17. doi:10.1007/s00294-005-0578-0. PMID 15889258. S2CID 23959400.
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  27. ^ Zhang, Linshuang; Li, Xiangyang; Zhang, Feng; Wang, Gejiao (2 January 2014). "Genomic analysis of Agrobacterium radiobacter DSM 30147T and emended description of A. radiobacter (Beijerinck and van Delden 1902) Conn 1942 (Approved Lists 1980) emend. Sawada et al. 1993". Standards in Genomic Sciences. 9 (3): 574–584. doi:10.4056/sigs.4688352.
  28. ^ Setubal JC, Wood D, Burr T, Farrand SK, Goldman BS, Goodner B, Otten L, Slater S (2009). "The Genomics of Agrobacterium: Insights into its Pathogenicity, Biocontrol, and Evolution". In Jackson RW (ed.). Plant Pathogenic Bacteria: Genomics and Molecular Biology. Caister Academic Press. pp. 91–112. ISBN 978-1-904455-37-0.
  29. ^ Chilton, Mary-Dell (2001). "Agrobacterium. A Memoir". Plant Physiology. 125 (1): 9–14. doi:10.1104/pp.125.1.9. ISSN 0032-0889. PMC 1539314. PMID 11154285.

Further reading

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