Spiroplasma Explained

Spiroplasma is a genus of Mollicutes, a group of small bacteria without cell walls. Spiroplasma shares the simple metabolism, parasitic lifestyle, fried-egg colony morphology and small genome of other Mollicutes, but has a distinctive helical morphology, unlike Mycoplasma. It has a spiral shape and moves in a corkscrew motion. Many Spiroplasma are found either in the gut or haemolymph of insects where they can act to manipulate host reproduction, or defend the host as endosymbionts. Spiroplasma are also disease-causing agents in the phloem of plants. Spiroplasmas are fastidious organisms, which require a rich culture medium. Typically they grow well at 30 °C, but not at 37 °C. A few species, notably Spiroplasma mirum, grow well at 37 °C (human body temperature), and cause cataracts and neurological damage in suckling mice. The best studied species of spiroplasmas are Spiroplasma poulsonii, a reproductive manipulator and defensive insect symbiont, Spiroplasma citri, the causative agent of citrus stubborn disease, and Spiroplasma kunkelii, the causative agent of corn stunt disease.

Human pathogenicity

There is some disputed evidence for the role of spiroplasmas in the etiology of transmissible spongiform encephalopathies (TSEs), due primarily to the work of Frank Bastian, summarized below. Other researchers have failed to replicate this work, while the prion model for TSEs has gained very wide acceptance.[1] A 2006 study appears to refute the role of spiroplasmas in the best small animal scrapie model (hamsters).[2] Bastian et al. (2007) have responded to this challenge with the isolation of a spiroplasma species from scrapie-infected tissue, grown it in cell-free culture, and demonstrated its infectivity in ruminants.[3]

Insect symbioses

Many Spiroplasma strains are vertically transmitted endosymbionts of Drosophila species, with a variety of host-altering mechanisms similar to Wolbachia. These strains are from the Spiroplasma poulsonii clade, and can have important effects on host fitness. The S. poulsonii strain of Drosophila neotestacea protects its host against parasitic nematodes. This interaction is an example of defensive symbiosis, where the fitness of the symbiont is intricately tied to the fitness of the host. The D. neotestacea S. poulsonii also defends its fly host from infestation by parasitic wasps.[4] [5] The mechanism through which S. poulsonii attacks nematodes and parasitic wasps relies on the presence of toxins called ribosome-inactivating proteins (RIPs), similar to Sarcin or Ricin.[6] These toxins depurinate a conserved adenine site in eukaryotic 28s ribosomal RNA called the Sarcin-Ricin loop by cleaving the N-glycosidic bond between the rRNA backbone and the adenine.[6] Spiroplasma associations highlight a growing movement to consider heritable symbionts as important drivers in patterns of evolution.[7] [8]

The S. poulsonii strain of Drosophila melanogaster can also attack parasitoid wasps, but is not regarded as a primarily defensive symbiont. This is because this D. melanogaster Spiroplasma (called MSRO) kills D. melanogaster eggs fertilized by Y-bearing sperm. This mode of reproductive manipulation benefits the symbiont as the female fly has a greater reproductive output than males. The genetic basis of this male-killing was discovered in 2018, solving a decades-old mystery of how the bacteria targeted male-specific cells.[9] In an interview with the Global Health Institute, Dr. Toshiyuki Harumoto said this discovery is the first example of a bacterial effector protein that affects host cellular machinery in a sex-specific manner, and the first endosymbiont factor identified to explain the cause of male-killing. Thus it should have a big impact on the fields of symbiosis, sex determination, and evolution.[10]

Beyond Drosophila, Spiroplasma of the ixodetis, apis, chrysopicola, citri, mirum, and poulsonii clades are found in many insects and arthropods, including ticks, spiders, bees, ants, beetles, and butterflies.[11] [12] [13] Male-killing is also found in the Spiroplasma of the ladybug Harmonia axyridis and the plain tiger butterfly. In the plain tiger butterfly, the consequences have led to speciation.[14]

Plant diseases

Spiroplasma citri is the causative agent of Citrus stubborn disease, a plant disease affecting species in the genus Citrus.[15] It infects the phloem of the affected plant, causing fruit deformities. Spiroplasma kunkelii is also referred to as Corn Stunt Spiroplasma as it is the causative agent of Corn stunt disease, a disease of corn and other grasses that stunts plant growth. Spiroplasma kunkelii represents a major economic risk, as corn production in the United States is an industry worth over $50 billion.[16] Both Spiroplasma citri and Spiroplasma kunkelii are transmitted by leafhoppers.[17] [18]

Phylogeny

The currently accepted taxonomy is based on the List of Prokaryotic names with Standing in Nomenclature (LPSN)[19] and National Center for Biotechnology Information (NCBI)[20]

See also

External links

Notes and References

  1. Leach . R.H. . Matthews . W.B. . Will . R. . Creutzfeldt-Jakob disease . Journal of the Neurological Sciences . June 1983 . 59 . 3 . 349–353 . 10.1016/0022-510x(83)90020-5 . 6348215 . 3558955 .
  2. Alexeeva . I. . Elliott . E. J. . Rollins . S. . Gasparich . G. E. . Lazar . J. . Rohwer . R. G. . Absence of Spiroplasma or Other Bacterial 16S rRNA Genes in Brain Tissue of Hamsters with Scrapie . Journal of Clinical Microbiology . 3 January 2006 . 44 . 1 . 91–97 . 10.1128/JCM.44.1.91-97.2006 . 16390954 . 1351941 .
  3. Bastian . Frank O. . Sanders . Dearl E. . Forbes . Will A. . Hagius . Sue D. . Walker . Joel V. . Henk . William G. . Enright . Fred M. . Elzer . Philip H. . Spiroplasma spp. from transmissible spongiform encephalopathy brains or ticks induce spongiform encephalopathy in ruminants . Journal of Medical Microbiology . 1 September 2007 . 56 . 9 . 1235–1242 . 10.1099/jmm.0.47159-0 . 17761489 . free .
  4. Jaenike . J. . Unckless . R. . Cockburn . S. N. . Boelio . L. M. . Perlman . S. J. . Adaptation via Symbiosis: Recent Spread of a Drosophila Defensive Symbiont . Science . 8 July 2010 . 329 . 5988 . 212–215 . 10.1126/science.1188235 . 20616278 . 2010Sci...329..212J . 206526012 .
  5. Haselkorn . Tamara S. . Jaenike . John . Macroevolutionary persistence of heritable endosymbionts: acquisition, retention and expression of adaptive phenotypes in . Molecular Ecology . July 2015 . 24 . 14 . 3752–3765 . 10.1111/mec.13261 . 26053523 . 206182327 .
  6. Ballinger . Matthew J. . Perlman . Steve J. . Hurst . Greg . Generality of toxins in defensive symbiosis: Ribosome-inactivating proteins and defense against parasitic wasps in Drosophila . PLOS Pathogens . 6 July 2017 . 13 . 7 . e1006431 . 10.1371/journal.ppat.1006431 . 28683136 . 5500355 . free .
  7. Jaenike . John . Stahlhut . Julie K. . Boelio . Lisa M. . Uncless . Robert L. . Association between Wolbachia and Spiroplasma within Drosophila neotestacea: an emerging symbiotic mutualism? . Molecular Ecology . January 2010 . 19 . 2 . 414–425 . 10.1111/j.1365-294X.2009.04448.x . 20002580 . 46063874 . free . 2010MolEc..19..414J .
  8. Koch . Hauke . Schmid-Hempel . Paul . Socially transmitted gut microbiota protect bumble bees against an intestinal parasite . Proceedings of the National Academy of Sciences of the United States of America . 29 November 2011 . 108 . 48 . 19288–19292 . 10.1073/pnas.1110474108 . 22084077 . 3228419 . 2011PNAS..10819288K . free .
  9. Harumoto . Toshiyuki . Lemaitre . Bruno . Male-killing toxin in a bacterial symbiont of Drosophila . Nature . May 2018 . 557 . 7704 . 252–255 . 10.1038/s41586-018-0086-2 . 29720654 . 5969570 . 2018Natur.557..252H .
  10. News: Papageorgiou . Nik . Mystery solved: The bacterial protein that kills male fruit flies . 5 July 2018 .
  11. Duron . Olivier . Bouchon . Didier . Boutin . Sébastien . Bellamy . Lawrence . Zhou . Liqin . Engelstädter . Jan . Hurst . Gregory D. . The diversity of reproductive parasites among arthropods: Wolbachiado not walk alone . BMC Biology . 24 June 2008 . 6 . 1 . 27 . 10.1186/1741-7007-6-27. free . 18577218 . 2492848 .
  12. Binetruy . Florian . Bailly . Xavier . Chevillon . Christine . Martin . Oliver Y. . Bernasconi . Marco V. . Duron . Olivier . Phylogenetics of the Spiroplasma ixodetis endosymbiont reveals past transfers between ticks and other arthropods . Ticks and Tick-borne Diseases . 1 April 2019 . 10 . 3 . 575–584 . 10.1016/j.ttbdis.2019.02.001. free . 30744948 .
  13. Tsushima . Yusuke . Nakamura . Kayo . Tagami . Yohsuke . Miura . Kazuki . Mating rates and the prevalence of male-killing Spiroplasma in Harmonia axyridis (Coleoptera: Coccinellidae) . Entomological Science . April 2015 . 18 . 2 . 217–220 . 10.1111/ens.12113 . 83582284 .
  14. Jiggins . F. M. . Hurst . G. D. D. . Jiggins . C. D. . Schulenburg . J. H. G. v d . Majerus . M. E. N. . The butterfly Danaus chrysippus is infected by a male-killing Spiroplasma bacterium . Parasitology . 2000 . 120 . 5 . 439–446 . 10.1017/S0031182099005867 . 10840973 . 34436795 .
  15. Yokomi . Raymond K. . Mello . Alexandre F. S. . Saponari . Maria . Fletcher . Jacqueline . Polymerase Chain Reaction-Based Detection of Spiroplasma citri Associated with Citrus Stubborn Disease . Plant Disease . February 2008 . 92 . 2 . 253–260 . 10.1094/PDIS-92-2-0253 . 30769379 . free .
  16. Web site: Use of Spectral Vegetation Indices for Detection of European Corn Borer Infestation in Iowa Corn Plots | Science Inventory | US EPA . Cfpub.epa.gov . 2019-02-12.
  17. Bové . Joseph M. . Renaudin . Joël . Saillard . Colette . Foissac . Xavier . Garnier . Monique . 2003 . Spiroplasma citri, a Plant Pathogenic Mollicute: Relationships with Its Two Hosts, the Plant and the Leafhopper Vector . Annual Review of Phytopathology . en . 41 . 1 . 483–500 . 10.1146/annurev.phyto.41.052102.104034 . 12730387 . 0066-4286.
  18. Özbek . Elvan . Miller . Sally A . Meulia . Tea . Hogenhout . Saskia A . 2003-03-01 . Infection and replication sites of Spiroplasma kunkelii (Class: Mollicutes) in midgut and Malpighian tubules of the leafhopper Dalbulus maidis . Journal of Invertebrate Pathology . 82 . 3 . 167–175 . 10.1016/S0022-2011(03)00031-4 . 12676553 . 0022-2011.
  19. Web site: A.C. Parte. Spiroplasmataceae. 2022-09-09. List of Prokaryotic names with Standing in Nomenclature (LPSN). et al..
  20. Web site: Sayers. Spiroplasmataceae. 2022-09-09. National Center for Biotechnology Information (NCBI) taxonomy database. et al..
  21. Web site: The LTP . 20 November 2023.
  22. Web site: LTP_all tree in newick format. 20 November 2023.
  23. Web site: LTP_08_2023 Release Notes. 20 November 2023.
  24. Web site: GTDB release 08-RS214 . Genome Taxonomy Database. 10 May 2023.
  25. Web site: bac120_r214.sp_label . Genome Taxonomy Database. 10 May 2023.
  26. Web site: Taxon History . Genome Taxonomy Database. 10 May 2023.
  27. Ramírez . A. S. . Rosas . A. . Hernández-Beriain . J. A. . Orengo . J. C. . Saavedra . P. . de la Fe . C. . Fernández . A. . Poveda . J. B. . Relationship between rheumatoid arthritis and Mycoplasma pneumoniae: a case–control study . Rheumatology . July 2005 . 44 . 7 . 912–914 . 10.1093/rheumatology/keh630 . 15814575 . free .

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