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1.
Nat Commun ; 10(1): 5606, 2019 12 06.
Article in English | MEDLINE | ID: mdl-31811209

ABSTRACT

Feeding on unicellular photosynthetic organisms by unicellular eukaryotes is the base of the aquatic food chain and evolutionarily led to the establishment of photosynthetic endosymbionts/organelles. Photosynthesis generates reactive oxygen species and damages cells; thus, photosynthetic organisms possess several mechanisms to cope with the stress. Here, we demonstrate that photosynthetic prey also exposes unicellular amoebozoan and excavates predators to photosynthetic oxidative stress. Upon illumination, there is a commonality in transcriptomic changes among evolutionarily distant organisms feeding on photosynthetic prey. One of the genes commonly upregulated is a horizontally transferred homolog of algal and plant genes for chlorophyll degradation/detoxification. In addition, the predators reduce their phagocytic uptake while accelerating digestion of photosynthetic prey upon illumination, reducing the number of photosynthetic cells inside the predator cells, as this also occurs in facultative endosymbiotic associations upon certain stresses. Thus, some mechanisms in predators observed here probably have been necessary for evolution of endosymbiotic associations.


Subject(s)
Food Chain , Photosynthesis/physiology , Predatory Behavior/physiology , Symbiosis/physiology , Amoebozoa/physiology , Amoebozoa/radiation effects , Animals , Bacteria/metabolism , Bacterial Physiological Phenomena , Biological Evolution , Chlorophyll , Coculture Techniques , Eukaryota , Evolution, Molecular , Light/adverse effects , Naegleria/growth & development , Naegleria/physiology , Organelles/physiology , Oxidative Stress , Phagocytosis/physiology , Predatory Behavior/radiation effects , Protein Domains , Reactive Oxygen Species , Symbiosis/radiation effects , Transcriptome
2.
Nat Rev Microbiol ; 9(11): 791-802, 2011 Oct 03.
Article in English | MEDLINE | ID: mdl-21963801

ABSTRACT

Exposure to the shortest wavelengths in sunlight, ultraviolet light, constitutes a deleterious ecological factor for many microorganisms. The use of secondary metabolites as sunscreens has emerged as an important photoprotective mechanism in certain groups of large-celled microorganisms, such as cyanobacteria, fungi and many protists. In this Review, we describe our current understanding of microbial 'sunscreen' compounds, including scytonemin, the mycosporines and the naphthalene-based melanins. Study of these sunscreens has led to the discovery of new classes of compounds, new metabolic pathways, a deeper understanding of microbial photobiology and the potential for dermatological or biomedical applications.


Subject(s)
Amoebozoa/radiation effects , Cyanobacteria/radiation effects , Fungi/radiation effects , Sunscreening Agents/metabolism , Ultraviolet Rays , Amoebozoa/metabolism , Biosynthetic Pathways , Cyanobacteria/metabolism , Cyclohexanones/metabolism , Fungi/metabolism , Indoles/metabolism , Melanins/metabolism , Models, Biological , Phenols/metabolism
3.
Acta Trop ; 119(2-3): 138-43, 2011 Aug.
Article in English | MEDLINE | ID: mdl-21635868

ABSTRACT

The antimicrobial activity of simulated solar disinfection (SODIS) in the presence and absence of riboflavin against various protozoa and helminth organisms was investigated in this study. Assays were conducted in transparent 12 well microtitre plates containing a suspension of test organisms in the presence or absence of 250 µM riboflavin. Plates were exposed to simulated sunlight at an optical irradiance of 550 Wm(-2) (watts per square metre) delivered from a SUNTEST™ CPS+ solar simulator. Aliquots of the test suspensions were taken at set time points and the viability of the test organisms was determined by either culture, microscopy or flow cytometry where applicable. With Acanthamoeba, Naegleria, Entamoeba and Giardia exposure to SODIS at an optical irradiance of 550 Wm(-2) for up to 6h resulted in significant inactivation of these organisms. The addition of riboflavin to this system significantly increased the level of inactivation observed with cysts of A. castellanii. With Cryptosporidium oocysts and Ascaris ova exposure to SODIS in the presence and absence of riboflavin for 6-8h resulted in a negligible reduction in viability of both organisms. In this present study we have been able to show that SODIS is effective against a variety of previously untested waterborne organisms and with A. castellanii cysts the addition of micro-molar concentrations of riboflavin can enhance cyst inactivation. However, care must be taken as Ascaris larvae continue to develop inside the ova after exposure to SODIS and Cryptosporidium remain impermeable to propidium iodide staining indicating they may still be infectious.


Subject(s)
Amoebozoa/radiation effects , Disinfection/methods , Helminths/radiation effects , Sunlight , Amoebozoa/drug effects , Animals , Cell Survival/drug effects , Cell Survival/radiation effects , Flow Cytometry , Helminths/drug effects , Microscopy , Riboflavin/toxicity , Survival Analysis
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