Recent insights into physiological responses to nutrients by the cylindrospermopsin producing cyanobacterium, <italic style="font-style: italic">Cylindrospermopsis raciborskii</italic>

Michele A. BURFORD; Anusuya WILLIS; Ann CHUANG; Xiao MAN; Philip T. ORR

doi:10.1007/s00343-018-7179-5

Your Location：

Home >

Browse articles >

Recent insights into physiological responses to nutrients by the cylindrospermopsin producing cyanobacterium, Cylindrospermopsis raciborskii

Updated：2023-05-19

- Recent insights into physiological responses to nutrients by the cylindrospermopsin producing cyanobacterium, Cylindrospermopsis raciborskii
- Chinese Journal of Oceanology and Limnology Vol. 36, Issue 4, Pages: 1032-1039(2018)
- Affiliations：
  
  Australian Rivers Institute, Griffith University, Australia
- Author bio：
  
  Michele A. BURFORD, m.burford@griffith.edu.au
- Funds：
- DOI：10.1007/s00343-018-7179-5
  CLC：
- Received：21 June 2017，
  
  Accepted：28 July 2017，
  
  Online First：18 August 2017，
  
  Published：2018-07
- Accepted：
Scan QR Code
Michele A. BURFORD, Anusuya WILLIS, Ann CHUANG, et al. Recent insights into physiological responses to nutrients by the cylindrospermopsin producing cyanobacterium, Cylindrospermopsis raciborskii[J]. Chinese Journal of Oceanology and Limnology, 2018, 36(4): 1032-1039.
DOI：

Michele A. BURFORD, Anusuya WILLIS, Ann CHUANG, et al. Recent insights into physiological responses to nutrients by the cylindrospermopsin producing cyanobacterium, Cylindrospermopsis raciborskii[J]. Chinese Journal of Oceanology and Limnology, 2018, 36(4): 1032-1039. DOI： 10.1007/s00343-018-7179-5.

摘要

Abstract

The harmful cyanobacterium

Cylindrospermopsis raciborskii

is a widespread species increasingly being recorded in freshwater systems around the world. Studies have demonstrated some key attributes of this species which may explain its global dominance. It has a high level of flexibility with respect to light and nutrients

being capable of growth under low and variable light conditions. However

it is the strategy with respect to nutrient utilization that has received more attention. Unlike many bloom forming species

the dominance of this species is not simply linked to higher nutrient loads. In fact it appears that it is more competitive when phosphorus and nitrogen availability is low and/or variable. An important component of this flexibility appears to be the result of within-population strain variability in responses to nutrients

as well as key physiological adaptations. Strain variability also appears to have an effect on the population-level cell quota of toxins

specifically cylindrospermopsins (CYNs). Field studies in Australia showed that populations had the highest proportion of toxic strains when dissolved inorganic phosphorus was added

resulting in stoichiometrically balanced nitrogen and phosphorus within the cells. These strategies are part of an arsenal of responses to environmental conditions

making it a challenging species to manage. However

our ability to improve bloom prediction will rely on a more detailed understanding of the complex physiology and ecology of this species.

关键词

Keywords

references

Aguilera A, Aubriot L, Echenique R O, Salerno G L, Brena B M, Pírez M, Bonilla S. 2017. Synergistic effects of nutrients and light favor Nostocales over nonheterocystous cyanobacteria. Hydrobiologia, 794(1):241-255.

Amaral V, Bonilla S, Aubriot L. 2014. Growth optimization of the invasive cyanobacterium Cylindrospermopsis raciborskii in response to phosphate fluctuations.European Journal of Phycology, 49(1):134-141.

Ammar M, Comte K, Tran T D C, El Bour M. 2014. Initial growth phases of two bloom-forming cyanobacteria( Cylindrospermopsis raciborskii and Planktothrix agardhii ) in monocultures and mixed cultures depending on light and nutrient conditions. Annales de LimnologieInternational Journal of Limnology, 50(3):231-240.

Antunes J T, Leão P N, Vasconcelos V M. 2015. Cylindrospermopsis raciborskii :review of the distribution, phylogeography, and ecophysiology of a global invasive species. Frontiers in Microbiology, 6:473.

Bai F, Liu R, Yang Y J, Ran X F, Shi J Q, Wu Z X. 2014.Dissolved organic phosphorus use by the invasive freshwater diazotroph cyanobacterium, Cylindrospermopsis raciborskii . Harmful Algae, 39:112-120.

Bonilla S, Aubriot L, Soares M C S, González-Piana M, Fabre A, Huszar V L M, Lürling M, Antoniades D, Padisák J, Kruk C. 2012. What drives the distribution of the bloomforming cyanobacteria Planktothrix agardhii and Cylindrospermopsis raciborskii ? FEMS Microbiology Ecology, 79(3):594-607.

Burford M A, Beardall J, Willis A, Orr P T, Magalhaes V F, Rangel L M, Azevedo S M F O E, Neilan B A. 2016.Understanding the winning strategies used by the bloomforming cyanobacterium Cylindrospermopsis raciborskii .Harmful Algae, 54:44-53.

Burford M A, Davis T W, Orr P T, Sinha R, Willis A, Neilan B A. 2014. Nutrient-related changes in the toxicity of field blooms of the cyanobacterium Cylindrospermopsis raciborskii . FEMS Microbiology Ecology, 89(1):135-148.

Burford M A, McNeale K L, McKenzie-Smith F J. 2006. The role of nitrogen in promoting toxic cyanophyte Cylindrospermopsis raciborskii in a subtropical water reservoir. Freshwater Biology, 51(11):2 143-2 153.

Byth S. 1980. Palm Island mystery disease. The Medical Journal of Australia, 2(1):40, 42.

Chislock M F, Sharp K L, Wilson A. 2014. Cylindrospermopsis raciborskii dominates under very low and high nitrogento-phosphorus ratios. Water Research, 49:207-214.

Dolman A M, Rücker J, Pick F R, Fastner J, Rohlack T, Mischke U, Wiedner C. 2012. Cyanobacteria and cyanotoxins:the influence of nitrogen versus phosphorus.PLoS One, 7(6):e38757.

Droop M R. 1983. 25 years of algal growth kinetics:a personal view. Botanica Marina, 26(3):99-112.

Falkner G, Wagner F, Small J V, Falkner R. 1995. Influence of fluctuating phosphate supply on the regulation of phosphate uptake by the blue-green alga Anacystzs nidulans . Journal of Phycology, 31(5):745-753.

Figueredo C C, Giani A, Bird D F. 2007. Does allelopathy contribute to Cylindrospermopsis raciborskii (Cyanobacteria) bloom occurrence and geographic expansion? Journal of Phycology, 43(2):256-265.

Glibert P M, Allen J I, Bouwman A F, Brown C W, Flynn K J, Lewitus A J, Madden C J. 2010. Modeling of HABs and eutrophication:status, advances, challenges. Journal of Marine Systems, 83(3-4):262-275.

Glibert P M, Burford M A. 2017. Globally changing nutrient loads and harmful algal blooms:recent advances, new paradigms, and continuing challenges. Oceanography, 30(1):58-69.

Gobler C J, Burkholder J M, Davis T W, Harke M J, Johengen T, Stow C A, Van de Waal D B. 2016. The dual role of nitrogen supply in controlling the growth and toxicity of cyanobacterial blooms. Harmful Algae, 54:87-97.

Hawkins P R, Runnegar M T C, Jackson A R B, Falconer I R. 1985. Severe hepatotoxicity caused by the tropical cyanobacterium (blue-green alga) Cylindrospermopsis raciborskii (Woloszynska) Seenaya and Subba Raju isolated from a domestic water supply reservoir. Applied and Environmental Microbiology, 50(5):1 292-1 295.

Hong Y, Burford M A, Ralph P J, Doblin M A. 2015. Subtropical zooplankton assemblage promotes the harmful cyanobacterium Cylindrospermopsis raciborskii in a mesocosm experiment. Journal of Plankton Research, 37(1):90-101.

Hong Y, Burford M A, Ralph P J, Udy J W, Doblin M A. 2013.The cyanobacterium Cylindrospermopsis raciborskii is facilitated by copepod selective grazing. Harmful Algae, 29:14-21.

Isvánovics V, Shafik H M, Présing M A, Juhos S. 2000. Growth and phosphate uptake kinetics of the cyanobacterium, Cylindrospermopsis raciborskii (Cyanophyceae) in throughflow cultures. Freshwater Biology, 43(2):257-275.

Kenesi G, Shafik H M, Kovács A W, Herodek S, Présing M. 2009. Effect of nitrogen forms on growth, cell composition and N 2 fixation of Cylindrospermopsis raciborskii in phosphorus-limited chemostat cultures. Hydrobiologica, 623(1):191-202.

Kokociński M, Soininen J. 2012. Environmental factors related to the occurrence of Cylindrospermopsis raciborskii (Nostocales, Cyanophyta) at the north-eastern limit of its geographical range. European Journal of Phycology, 47(1):12-21.

Lagos N, Onodera H, Zagatto P A, Andrinolo D, Azevedo S M F Q, Oshima Y. 1999. The first evidence of paralytic shellfish toxins in the freshwater cyanobacterium Cylindrospermopsis raciborskii , isolated from Brazil.Toxicon, 37(10):1 359-1 373.

Lakeman M B, von Dassow P, Cattolico R A. 2009. The strain concept in phytoplankton ecology. Harmful Algae, 8(5):746-758.

Li R, Carmichael W W, Brittain S, Eaglesham G K, Shaw G R, Mahakhant A, Noparatnaraporn N, Yongmanitchai W, Kaya K, Watanabe M M. 2001. Isolation and identification of the cyanotoxin cylindrospermopsin and deoxycylindrospermopsin from a Thailand strain of Cylindrospermopsis raciborskii (Cyanobacteria). Toxicon, 39(7):973-980.

Marinho M M, Souza M B G, Lürling M. 2013. Light and phosphate competition between Cylindrospermopsis raciborskii and Microcystis aeruginosa is strain dependent. Microbial Ecology, 66(3):479-488.

Moisander P H, Cheshire L A, Braddy J, Calandrino E S, Hoffman M, Piehler M F, Paerl H W. 2012. Facultative diazotrophy increases Cylindrospermopsis raciborskii competitiveness under fluctuating nitrogen availability.FEMS Microbiology Ecology, 79(3):800-811.

Monod J. 1942. Recherches sur la Croissance des Cultures Bactériennes. Herman, Paris, France. p. 1-211.

Muhid P, Davis T W, Bunn S E, Burford M A. 2013. Effects of inorganic nutrients in recycled water on freshwater phytoplankton biomass and composition. Water Research, 47(1):384-394.

Neilan B A, Saker M L, Fastner J, Törökné A, Burns B P. 2003.Phylogeography of the invasive cyanobacterium Cylindrospermopsis raciborskii . Molecular Ecology, 12(1):133-140.

Oliver R L, Hamilton D P, Brookes J, Ganf G G. 2012. Physiology, blooms and prediction of planktonic cyanobacteria cyanobacteria. In : Whitton B A ed. Ecology of Cyanobacteria Ⅱ: Their Diversity in Space and Time. Springer, Dordrecht, Netherlands. p. 155-194.

Padisák J. 1997. Cylindrospermopsis raciborskii (Woloszynska) Seenayya et Subba Raju, an expanding, highly adaptive cyanobacterium:worldwide distribution and review of its ecology. Archiv für Hydrobiologie, 107(4):563-593.

Plominsky Á M, Delherbe N, Mandakovic D, Riquelme B, González K, Bergman B, Mariscal V, Vásquez M. 2015.Intercellular transfer along the trichomes of the invasive terminal heterocyst forming cyanobacterium Cylindrospermopsis raciborskii CS-505. FEMS Microbiology Letters, 362(5):fnu009.

PlominskyÁ M, Larsson J, Bergman B, Delherbe N, Osses I, Vásquez M. 2013. Dinitrogen fixation is restricted to the terminal heterocysts in the invasive cyanobacterium Cylindrospermopsis raciborskii CS-505. PLoS One, 8(2):e51682.

Posselt A J, Burford M A, Shaw G. 2009. Pulses of phosphate promote dominance of the toxic cyanophyte Cylindrospermopsis raciborskii in a subtropical water reservoir. Journal of Phycology, 45(3):540-546.

Prentice M J, O'Brien K R, Hamilton D P, Burford M A. 2015.High-and low-affinity phosphate uptake and its effect on phytoplankton dominance in a phosphate-depauperate lake. Aquatic Microbial Ecology, 75(2):139-153.

Redfield A C. 1958. The biological control of chemical factors in the environment. American Scientist, 46(3):205-222.

Richie R J, Trautman D A, Larkum A W D. 2001. Phosphate limited cultures of the cyanobacterium Synechococcus are capable of very rapid, opportunistic uptake of phosphate.New Phytologist, 152(2):189-201.

Rzymski P, Poniedziałek B, Kokociński M, Jurczak T, Lipski D, Wiktorowicz K. 2014. Interspecific allelopathy in cyanobacteria:cylindrospermopsin and Cylindrospermopsis raciborskii , effect on the growth and metabolism of Microcystis aeruginosa . Harmful Algae, 35:1-8.

Saker M L, Neilan B A. 2001. Varied diazotrophies, morphologies, and toxicities of genetically similar isolates of Cylindrospermopsis raciborskii (Nostocales, Cyanophyceae) from Northern Australia. Applied and Environmental Microbiology, 67(4):1 839-1 845.

Sinha R, Pearson L, Davis T W, Muenchhoff J, Pratama R, Jex A, Burford M A, Neilan B. 2014. Comparative genomics of Cylindrospermopsis raciborskii strains with differential toxicities. BMC Genomics, 15:83.

Soares M C S, Huszar V L M, Miranda M N, Mello M M, Roland F, Lürling M. 2013. Cyanobacterial dominance in Brazil:distribution and environmental preferences.Hydrobiologia, 717(1):1-12.

Stucken K, John U, Cembella A, Soto-Liebe K, Vásquez M. 2014. Impact of nitrogen sources on gene expression and toxin production in the diazotroph Cylindrospermopsis raciborskii CS-505 and non-diazotroph Raphidiopsis brookii D9. Toxins, 6(6):1 896-1 915.

Willis A, Adams M P, Chuang A W, Orr P T, O'Brien K R, Burford M A. 2015. Constitutive toxin production under various nitrogen and phosphorus regimes of three ecotypes of Cylindrospermopsis raciborskii ((Wołoszyńska) Seenayya et Subba Raju). Harmful Algae, 47:27-34.

Willis A, Chuang A W, Burford M A. 2016b. Nitrogen fixation by the reluctant diazotroph Cylindrospermopsis raciborskii (Cyanophyceae). Journal of Phycology, 52(5):854-862.

Willis A, Chuang A W, Woodhouse J N, Neilan B A, Burford M A. 2016a. Intraspecific variation in growth, morphology and toxin quotas for the cyanobacterium, Cylindrospermopsis raciborskii. Toxicon, 119:307-310.

Willis A, Posselt A J, Burford M A. 2017. Variations in carbonto-phosphorus ratios of two Australian strains of Cylindrospermopsis raciborskii . European Journal of Phycology, 52(3):303-310.

Wimmer K M, Strangman W K, Wright J L C. 2014. 7-Deoxydesulfo-cylindrospermopsin and 7-deoxy-desulfo-12-acetylcylindrospermopsin:two new cylindrospermopsin analogs isolated from a Thai strain of Cylindrospermopsis raciborskii . Harmful Algae, 37:203-206, https://doi.org/10.1016/j.hal.2014.06.006.

Wood S A, Stirling D J. 2003. First identification of the cylindrospermopsin-producing cyanobacterium Cylindrospermopsis raciborskii in New Zealand. New Zealand Journal of Marine and Freshwater Research, 37(4):821-828.

Wu Z X, Zeng B, Li R H, Song L R. 2012. Physiological regulation of Cylindrospermopsis raciborskii (Nostocales, Cyanobacteria) in response to inorganic phosphorus limitation. Harmful Algae, 15:53-58.

Xiao M, Willis A, Burford M A. 2017. Differences in cyanobacterial strain responses to light and temperature reflect species plasticity. Harmful Algae, 62:84-93.

Views

Downloads

CSCD

Alert me when the article has been cited

Submit

Tools

Publicity Resources

Effect of enclosure and nutrient enrichment onMicrocystis blooms in Donghu Lake

Biogeochemical characteristics of nitrogen and phosphorus in Jiaozhou Bay sediments

Nitrogen and phosphorus budgets of the Changjiang River estuary

Sewage pollution in Negril, Jamaica: effects on nutrition and ecology of coral reef macroalgae

Effect of nitrogen to phosphorus ratios on cell proliferation in marine micro algae

Related Author

Tang Huijuan

Xie Ping

Xie Liqiang

Chen Feizhou

Xuegang Li

Jinming Song

Huamao Yuan

Jicui Dai

Related Institution

Donghu Experimental Station of Lake Ecosystems Institute of Hydrobiology The Chinese Academy of Sciences

School of Animal Science South China Agricultural University

The Graduate School Chinese Academy of Sciences

Institute of Oceanology Chinese Academy of Sciences

Graduate University of Chinese Academy of Sciences

Address：Editorial Office of JOL, 88 Haijun Rd. Qingdao, 266000, China
Tel：+86-532-82898754 Email：jol@qdio.ac.cn
Technical support is provided by Beijing Founder electronics co., LTD 京ICP备09064830号-19 京公网安备11010802024621
It is recommended to read the content of this site in Chrome&IE9+. Please switch to extreme mode in browser 360.
Cookies We use cookies to help provide and enhance our service and tailor content. By continuing, you agree to the use of cookies.

⁰

Recent insights into physiological responses to nutrients by the cylindrospermopsin producing cyanobacterium, Cylindrospermopsis raciborskii

DOI：10.1007/s00343-018-7179-5

摘要

Abstract

关键词

Keywords

references