Haloquadratum walsbyi explained

Haloquadratum walsbyi is a species of Archaea in the genus Haloquadratum, known for its square shape and halophilic nature.[1]

First discovered in a brine pool in the Sinai peninsula of Egypt, H. walsbyi is noted for its flat, square-shaped cells, and its unusual ability to survive in aqueous environments with high concentrations of sodium chloride and magnesium chloride.[2] The species' genus name Haloquadratum translates from Greek and Latin as "salt square". This archaean is also commonly referred to as "Walsby's Square Bacterium" because of its identifying square shape which makes it unique.[3] In accordance with its name, Haloquadratum walsbyi are most abundantly observed in salty environments. Haloquadratum walsbyi is a phototrophic halophilic archaeon. It was the only recognized species of the genus Haloquadratum until 1999 when Haloarcula quadrata was reported as recovered from a brine pool. Haloquadratum walsbyi is very unusual because of its unique cellular structure that resembles an almost-perfectly flat-shaped figure.

The genus was first observed in 1980 by a British microbiologist, Prof. Anthony E. Walsby, from samples taken from the Sabkha Gavish, a brine lake in southern Sinai, Egypt. This discovery is formally described in 2007 by Burns et al. Attempts to cultivate the archaea were unsuccessful until 2004 and resulted in the identification of Haloarcula quadrata, another species of square archaea of the genus Haloarcula, distinct from H. walsbyi, less abundant and genetically quite different.

Description

Haloquadratum walsbyi cells size at 2 to 5 microns and 100 to 200 nanometers thick. The archaea generally contain granules of polyhydroxyalkanoates and hold a number of refractive vacuoles filled with gas that ensure buoyancy in an aqueous environment, and allow for maximum light absorption. These gas vacuoles were discovered by Wallaby in 1980 when determining the identity of intracellular refractive bodies in the archaean's structure. They gather in sheets up to 40 μm wide, but the connections between the cells are fragile and can easily be broken.[4]

These organisms can be found in any stretch of very salty water. During the evaporation of seawater, calcium carbonate (CaCO3) and calcium sulfate (CaSO4) precipitate first, leading to a brine rich in sodium chloride NaCl. If evaporation continues, NaCl precipitates in the form of halite, leaving a brine rich in magnesium chloride (MgCl2). H. walsbyi prospers during the final phase of the precipitation of halite, and can constitute 80% of the biomass of this medium. Haloquadratum walsbyi cells have been determined to be Gram-negative through staining and when grown in a laboratory the best determined conditions for growth is a media with 18% salts at a neutral pH.[5]

The genome of H. walsbyi has been completely sequenced, allowing access to a better understanding of the phylogenetic and taxonomic classification of this organism and its role in the ecosystem. A genomic comparison of Spanish and Australian isolates (strains HBSQ001 and C23T) strongly suggests a rapid global dispersion, as they are remarkably similar and have maintained the order of genes.

Its growth in the laboratory was obtained in a medium with very high chloride concentrations (greater than 2 mol · L−1 of MgCl2 and greater than 3 mol · L −1of NaCl), making this organism among the most haloresistant known. Its optimum growth temperature is, making this archaea a Mesophile.

Diversity

A surprisingly high amount of cells in salt brines around the world are Haloquadratum walsbyi, up to 80%. Experiments have been done to examine the genetic diversity in the salt brine environment. Seven different types of H. walsbyi's genomic island have been discovered in natural environments.[6] After examining the metogenomic fosmid library for H. walsbyi, two types of the cell-wall associated islands were identified. The genes in these islands include those responsible for the synthesis of surface layer structures such as glycoproteins and genes responsible for the synthesis of cell envelopes. Homologous recombination is responsible for the maintaining the genes mentioned above and also the diversity of the metagenome in its natural environment. Surface structures on different H. walsbyi cells help to differentiate sources of lineage for the population as a whole. These differing structures also increase the diversity of the cells in their natural environment. These changes in cell structure may be due to the cells' attempts to reduce their susceptibility to attack by viruses. In 2009 an experiment was conducted in Australia to determine the diversity of H. walsbyi in three distinct saltern crystallizer ponds. In all three of the pools that were located in different regions they all shared two 97%-OTU of both Haloquadratum and Halorubrum -like sequences.[7]

Genomics and structure

H. walsbyi is classified as an oligotrophic microorganism, as it grows in nutrient deficient conditions where concentrations of organic substances are minimal. The high surface to volume ratio of H. walsbyi, due to its flattened shape, helps maximize nutrient uptake and overcome this limitation. Because of their square shape, they are more capable of flattening than spherical shaped microorganisms are. H. walsbyi can flatten an extreme amount of about 0.1-0.5μm. The overall size of the cell structure ranges from 1.5 to 11 μm. However, larger cells have been observed. The largest recorded H. walsbyi cell was measured as 40 x 40 μm.[8]

The square shape of H. walsbyi has been the focus of many studies. It is able to maintain this structure due to its adaptive traits. These traits can be found in both H. walsbyi's genome composition as well as its protein sequences. For example, H.walsbyi’s expression of the halomucin protein creates an aqueous protective layering that helps prevent desiccation of the cells.[9] These adaptations allow H. walsbyi to thrive in environments such as saturated brines while also maintaining a defined square structure.

H. walsbyi’s cellular structure consists of highly refractive gas vesicles, poly-β-hydroxyalkanoate granules, and a unique cellular wall. This microbe has displayed cell walls that range from 15 to 25 nm in thickness. The genome of H.walsbyi encodes S-layered glycoproteins of the cell wall. Additionally, photoactive retinal proteins are also encoded for the membrane. The HBSQ001 strain, discovered in 2004, showed these same internal cellular structures. However, this specific strain showed a complex trichotomous structured cell wall.

The strain HBSQ001, DSM 16790 of H. walsbyi has a 3,132,494 bp chromosome. H. walsbyi is distinguished by the abnormally low Guanine-Cytosine (GC) content compared to other haloarchaea. H. walsbyi has an average of 47.9% GC content compared to the expected 60-70%. Additionally, the proteins encoded are highly conserved specifically in the amino acid sequence. It is understood that H. walsbyi evolved from a typical GC rich, moderately conserving ancestor.

History

The Haloquadratum walsbyi archaea was first discovered in 1980 by a microbiology professor Anthony E. Walsby.[10] The microbe was initially named after him as “Walsby's square bacterium," as it was discovered before the archaea domain was acknowledged in full.[11] It is now formally known as Haloquadratum walsbyi, and considered a well known halophilic archaea. Additionally, it is accredited to be one of first archaea discovered with a square cellular shape.[12]

Upon the observation of the unique shape of H. walsbyi, cultivation has been a goal for scientists studying the species. Hyper-saline media has been found to be a substantial medium to maintain the pure cultures.[13] H. walsbyi remains one of the largest prokaryotes known today and contains roughly 3 million basepairs.

As mentioned earlier, the location site of this distinctive microbe's discovery was in the transcontinental country of Egypt within the Sinai peninsula. However, with this discovery also came an extended period that consisted of intensive trial and error attempts to achieve complete isolation of H. walsbyi. Because of how difficult it was to fully isolate this microorganism, there existed a vast gap in known information on H. walsbyi's physiological processes and genomic composition. However in 2004, two strains of H. walsbyi were successfully isolated and able to be sequenced. The second strain was an Australian isolate, called C23. Five strains were additionally isolated, totaling in seven total isolates of H. walsbyi.[14] In a specific hypersaline environment, Lake Tyrrell, Haloquadratum walsbyi made up nearly 38% of the community of archaea found when the ecosystem was cultured.[15]

Normal microbiota

The Archaeon Haloquadratum walsbyi is abundant in red brines, in salt lakes and solar salter crystallizer ponds,[16] shallow ponds that are connected to each other and increase in salinity.[17] Bacteriorhodopsin, a membrane protein that uses energy from light to drive the hydrogen-ion pump,[18] which are found in Haloquadratum walsbyi absorbs energy from light and are found in communities within these brines. The use of these bacteriorhodopsin shows the photoheterotroph nature of Haloquadratum walsbyi. The salt saturated environments that this archaean inhabits, along with being rich in magnesium chloride, have very low activity within the water which causes desiccation stress. These salt saturated environments can have a salinity of more than ten-times that of average seawater. The magnesium saturation in these ecosystems, what is also referred to as bitterns, are most often found with very little to no life present.[19] This environment is very hostile and H. walsbyi is only able to survive in it due to its unique genomic make up and while other organisms would perish in similar conditions.

Further reading

External links

Notes and References

  1. Bolhuis H, Palm P, Wende A, Falb M, Rampp M, Rodriguez-Valera F, Pfeiffer F, Oesterhelt D . 6 . The genome of the square archaeon Haloquadratum walsbyi : life at the limits of water activity . BMC Genomics . 7 . 169 . July 2006 . 16820047 . 1544339 . 10.1186/1471-2164-7-169 . free .
  2. Oren A, Ventosa A, Gutiérrez MC, Kamekura M . July 1999 . Haloarcula quadrata sp. nov., a square, motile archaeon isolated from a brine pool in Sinai (Egypt) . International Journal of Systematic Bacteriology . 10425773 . 10.1099/00207713-49-3-1149 . free . 49 . 3 . 1149–1155 . Square bacteria were first observed in 1980 by Walsby in the Gavish Sabkha, a coastal brine pool in the Sinai peninsula, Egypt (Parkes & Walsby, 1981; Walsby, 1980). Walsby recognized these extremely thin, square-shaped structures as prokaryotes....
  3. Web site: Oesterhelt D . 2022 . Haloquadratum walsbyi - overview . 2022-11-16 . Max Planck Institute of Biochemistry . Max-Planck-Gesellschaft . en.
  4. Sublimi Saponetti M, Bobba F, Salerno G, Scarfato A, Corcelli A, Cucolo A . Morphological and structural aspects of the extremely halophilic archaeon Haloquadratum walsbyi . PLOS ONE . 6 . 4 . e18653 . April 2011 . 21559517 . 3084702 . 10.1371/journal.pone.0018653 . free . 2011PLoSO...618653S .
  5. Burns DG, Janssen PH, Itoh T, Kamekura M, Li Z, Jensen G, Rodríguez-Valera F, Bolhuis H, Dyall-Smith ML . 6 . Haloquadratum walsbyi gen. nov., sp. nov., the square haloarchaeon of Walsby, isolated from saltern crystallizers in Australia and Spain . International Journal of Systematic and Evolutionary Microbiology . 57 . Pt 2 . 387–392 . February 2007 . 17267984 . 10.1099/ijs.0.64690-0 . free .
  6. Martin-Cuadrado AB, Pašić L, Rodriguez-Valera F . Diversity of the cell-wall associated genomic island of the archaeon Haloquadratum walsbyi . BMC Genomics . 16 . 1 . 603 . August 2015 . 26268990 . 4535781 . 10.1186/s12864-015-1794-8 . free .
  7. Oh D, Porter K, Russ B, Burns D, Dyall-Smith M . Diversity of Haloquadratum and other haloarchaea in three, geographically distant, Australian saltern crystallizer ponds . Extremophiles . 14 . 2 . 161–169 . March 2010 . 20091074 . 2832888 . 10.1007/s00792-009-0295-6 .
  8. Zenke R, von Gronau S, Bolhuis H, Gruska M, Pfeiffer F, Oesterhelt D . Fluorescence microscopy visualization of halomucin, a secreted 927 kDa protein surrounding Haloquadratum walsbyi cells . Frontiers in Microbiology . 6 . 249 . 2015 . 25870593 . 10.3389/fmicb.2015.00249 . 4378361 . free .
  9. Sublimi Saponetti M, Bobba F, Salerno G, Scarfato A, Corcelli A, Cucolo A . Morphological and structural aspects of the extremely halophilic archaeon Haloquadratum walsbyi . PLOS ONE . 6 . 4 . e18653 . April 2011 . 21559517 . 3084702 . 10.1371/journal.pone.0018653 . 2011PLoSO...618653S . free .
  10. Bolhuis H, Martín-Cuadrado AB, Rosselli R, Pašić L, Rodriguez-Valera F . Transcriptome analysis of Haloquadratum walsbyi: vanity is but the surface . BMC Genomics . 18 . 1 . 510 . July 2017 . 28673248 . 5496347 . 10.1186/s12864-017-3892-2 . free .
  11. Legault BA, Lopez-Lopez A, Alba-Casado JC, Doolittle WF, Bolhuis H, Rodriguez-Valera F, Papke RT . Environmental genomics of "Haloquadratum walsbyi" in a saltern crystallizer indicates a large pool of accessory genes in an otherwise coherent species . BMC Genomics . 7 . 1 . 171 . July 2006 . 16820057 . 1560387 . 10.1186/1471-2164-7-171 . free .
  12. Lobasso S, Lopalco P, Mascolo G, Corcelli A . Lipids of the ultra-thin square halophilic archaeon Haloquadratum walsbyi . Archaea . 2 . 3 . 177–183 . December 2008 . 19054744 . 2685597 . 10.1155/2008/870191 . free .
  13. Bolhuis H, Poele EM, Rodriguez-Valera F . Isolation and cultivation of Walsby's square archaeon . Environmental Microbiology . 6 . 12 . 1287–1291 . December 2004 . 15560825 . 10.1111/j.1462-2920.2004.00692.x .
  14. Podell S, Ugalde JA, Narasingarao P, Banfield JF, Heidelberg KB, Allen EE . Assembly-driven community genomics of a hypersaline microbial ecosystem . PLOS ONE . 8 . 4 . e61692 . 2013-04-18 . 23637883 . 3630111 . 10.1371/journal.pone.0061692 . 2013PLoSO...861692P . free .
  15. Ghai R, Pašić L, Fernández AB, Martin-Cuadrado AB, Mizuno CM, McMahon KD, Papke RT, Stepanauskas R, Rodriguez-Brito B, Rohwer F, Sánchez-Porro C, Ventosa A, Rodríguez-Valera F . 6 . New abundant microbial groups in aquatic hypersaline environments . Scientific Reports . 1 . 135 . 2011-10-31 . 22355652 . 3216616 . 10.1038/srep00135 . 2011NatSR...1E.135G .
  16. Oren A . The microbiology of red brines . Advances in Applied Microbiology . 113 . 57–110 . 2020 . 32948267 . 10.1016/bs.aambs.2020.07.003 . 978-0-12-820709-3 . 221797864 .
  17. Antón J, Rosselló-Mora R, Rodríguez-Valera F, Amann R . Extremely halophilic bacteria in crystallizer ponds from solar salterns . Applied and Environmental Microbiology . 66 . 7 . 3052–3057 . July 2000 . 10877805 . 92110 . 10.1128/aem.66.7.3052-3057.2000 . 2000ApEnM..66.3052A .
  18. Henderson R, Schertler GF . The structure of bacteriorhodopsin and its relevance to the visual opsins and other seven-helix G-protein coupled receptors . Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences . 326 . 1236 . 379–389 . January 1990 . 1970644 . 10.1098/rstb.1990.0019 . 1990RSPTB.326..379H .
  19. Oren A . Diversity of halophilic microorganisms: environments, phylogeny, physiology, and applications . Journal of Industrial Microbiology & Biotechnology . 28 . 1 . 56–63 . January 2002 . 11938472 . 10.1038/sj/jim/7000176 . 24223243 .