African Journal of
Biotechnology

  • Abbreviation: Afr. J. Biotechnol.
  • Language: English
  • ISSN: 1684-5315
  • DOI: 10.5897/AJB
  • Start Year: 2002
  • Published Articles: 12487

Full Length Research Paper

Use of remote sensing and molecular markers to detect toxic cyanobacterial hyperscum crust: A case study on Lake Hartbeespoort, South Africa

  P. J. Oberholster1,2* and A. M. Botha3  
  1CSIR Natural Resources and the Environment, P.O. Box 320, Stellenbosch 7599, South Africa. 2Department of Paraclinical Sciences, Faculty of Veterinary Science, University of Pretoria, P/Bag X04, Onderstepoort 0110, South Africa. 3Department of Genetics, University of Stellenbosch, Matieland 7601, South Africa.  
Email: [email protected]

  •  Accepted: 02 November 2010
  •  Published: 20 December 2010

Abstract

 

In this study, we monitored the formation of cyanobacterial hyperscum and crust formation in Lake Hartbeespoort using satellite images and ground monitoring. The hyperscum that formed near the reservoir wall was characterised by a distinctive white surface layer of crust. Hyperscum is the result of exposure of the cells to high radiation, inflicting irreversible damage to the genetic constitution of the upper layer of Microcystis aeruginosa cells. Under the 3 mm thick layer of crust, dark (<0.93 µmol of photons m-2s-1) anaerobic conditions (0.4 mg/l, 3% saturation) prevailed with high levels of microcystin (12,300 µg/l) in the absence of sunlight irradiation and photolysis by UV light. Real time polymerase chain reaction (PCR) analysis indicated low levels of transcription of the mcyAmcyB and mcyD genes which are responsible for synthesis of cyanotoxins under these low light intensity conditions. At other sampling sites where cyanobacterial scum occurred and hyperscum crust was absent, only the mcyB and mcyD genes were transcribed. A plausible explanation for the transcription of the mcyA gene in the hyperscum and not at the other sampling sites, was the presence of environmental stress-inducing factors, e.g. low light intensity (0.93 µmol of photon m-2 s-1) and pH 6.1. At the sampling site where no cyanobacterial scum was visible on the satellite images, low cell abundance (2.4 x 104 µg/l) and chlorophyll a (12.2 µg/l) was measured in comparison with sites where cyanobacterial scum was visible on the satellite images.

 

Key words: Hyperscum crust, reverse-transcription PCR, mcyA levels, microcystin, satellite imaging, cyanobacteria.

Abbreviation

Abbreviation: ELISA, Enzyme-linked immunosorbent assay; chl-a, chlorophyll a;PCR, polymerase chain reaction.