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1.
Int J Environ Res Public Health ; 9(7): 2396-411, 2012 07.
Article in English | MEDLINE | ID: mdl-22851951

ABSTRACT

Cyanobacterial blooms represent one of the most conspicuous and widespread waterborne microbial hazards to human and ecosystem health. Investigation of a cyanobacterial bloom in a shallow brackish water recreational cable ski lake in south-eastern Queensland, Australia revealed the dominance of the toxigenic species Nodularia spumigena. The bloom spanned three months, during which time cell concentrations exceeded human guideline thresholds for recreational risk, and concentrations of the hepatotoxic cyanotoxin nodularin exceeded 200 µg L(-1). Cyanotoxin origin and identification was confirmed by amplification of the ndaF-specific PCR product and sequencing of the 16S rRNA gene. From the limited data available leading up to, and throughout the bloom, it was not possible to establish the set of causative factors responsible for its occurrence. However a combination of factors including salinity, hydraulic retention time and nutrient status associated with an extended period of drought are likely to have contributed. This was the first known occurrence of this species in bloom proportions from sub-tropical Australia and as such represents a hitherto uncharacterized risk to human and ecosystem health. It highlights the need for adaptive monitoring regimes to ensure a comprehensive understanding of the potentially toxic cyanobacteria likely to inhabit any given region. Such monitoring needs to recognize that cyanobacteria have a significant capacity for range expansion that has been facilitated by recent changes in global climate.


Subject(s)
Eutrophication , Nodularia/isolation & purification , Peptides, Cyclic/analysis , Humans , Lakes/analysis , Lakes/microbiology , Phytoplankton/isolation & purification , Public Health , Queensland , Recreation , Water Quality
2.
J Proteome Res ; 10(4): 1505-18, 2011 Apr 01.
Article in English | MEDLINE | ID: mdl-21226539

ABSTRACT

The relationship between aphids and their host plants is thought to be functionally analogous to plant-pathogen interactions. Although virulence effector proteins that mediate plant defenses are well-characterized for pathogens such as bacteria, oomycetes, and nematodes, equivalent molecules in aphids and other phloem-feeders are poorly understood. A dual transcriptomic-proteomic approach was adopted to generate a catalog of candidate effector proteins from the salivary glands of the pea aphid, Acyrthosiphon pisum. Of the 1557 transcript supported and 925 mass spectrometry identified proteins, over 300 proteins were identified with secretion signals, including proteins that had previously been identified directly from the secreted saliva. Almost half of the identified proteins have no homologue outside aphids and are of unknown function. Many of the genes encoding the putative effector proteins appear to be evolving at a faster rate than homologues in other insects, and there is strong evidence that genes with multiple copies in the genome are under positive selection. Many of the candidate aphid effector proteins were previously characterized in typical phytopathogenic organisms (e.g., nematodes and fungi) and our results highlight remarkable similarities in the saliva from plant-feeding nematodes and aphids that may indicate the evolution of common solutions to the plant-parasitic lifestyle.


Subject(s)
Aphids/chemistry , Gene Expression Profiling , Insect Proteins/analysis , Proteome/analysis , Proteomics/methods , Saliva/chemistry , Amino Acid Sequence , Animals , Aphids/metabolism , Electrophoresis, Gel, Two-Dimensional , Expressed Sequence Tags , Insect Proteins/classification , Insect Proteins/genetics , Mass Spectrometry/methods , Molecular Sequence Data , Phylogeny , Protein Sorting Signals/genetics , Sequence Alignment
3.
Environ Health ; 8: 52, 2009 Nov 19.
Article in English | MEDLINE | ID: mdl-19925679

ABSTRACT

Cyanobacteria can produce groups of structurally and functionally unrelated but highly potent toxins. Cyanotoxins are used in multiple research endeavours, either for direct investigation of their toxicologic properties, or as functional analogues for various biochemical and physiological processes. This paper presents occupational safety guidelines and recommendations for personnel working in field, laboratory or industrial settings to produce and use purified cyanotoxins and toxic cyanobacteria, from bulk harvesting of bloom material, mass culture of laboratory isolates, through routine extraction, isolation and purification. Oral, inhalational, dermal and parenteral routes are all potential occupational exposure pathways during the various stages of cyanotoxin production and application. Investigation of toxicologic or pharmacologic properties using in vivo models may present specific risks if radiolabelled cyanotoxins are employed, and the potential for occupational exposure via the dermal route is heightened with the use of organic solvents as vehicles. Inter- and intra-national transport of living cyanobacteria for research purposes risks establishing feral microalgal populations, so disinfection of culture equipment and destruction of cells by autoclaving, incineration and/or chlorination is recommended in order to prevent viable cyanobacteria from escaping research or production facilities.


Subject(s)
Bacterial Toxins/isolation & purification , Bacterial Toxins/toxicity , Cyanobacteria/isolation & purification , Environmental Monitoring/standards , Marine Toxins/isolation & purification , Marine Toxins/toxicity , Microcystins/isolation & purification , Microcystins/toxicity , Occupational Exposure/standards , Safety Management/standards , Cyanobacteria Toxins , Freeze Drying/standards , Occupational Exposure/prevention & control , Risk Assessment/standards , Toxicity Tests
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