Deciphering interactions between the marine dinoflagellate Prorocentrum lima and the fungus Aspergillus pseudoglaucus.
Olivier BerryEnora BriandAlizé BagotMaud ChaignéLaurence Meslet-CladièreJulien WangOlivier GrovelJeroen J JansenNicolas RuizThibaut Robiou du PontYves François PouchusPhilipp HessSamuel BertrandPublished in: Environmental microbiology (2022)
The comprehension of microbial interactions is one of the key challenges in marine microbial ecology. This study focused on exploring chemical interactions between the toxic dinoflagellate Prorocentrum lima and a filamentous fungal species, Aspergillus pseudoglaucus, which has been isolated from the microalgal culture. Such interspecies interactions are expected to occur even though they were rarely studied. Here, a co-culture system was designed in a dedicated microscale marine-like condition. This system allowed to explore microalgal-fungal physical and metabolic interactions in presence and absence of the bacterial consortium. Microscopic observation showed an unusual physical contact between the fungal mycelium and dinoflagellate cells. To delineate specialized metabolome alterations during microalgal-fungal co-culture metabolomes were monitored by high-performance liquid chromatography coupled to high-resolution mass spectrometry. In-depth multivariate statistical analysis using dedicated approaches highlighted (1) the metabolic alterations associated with microalgal-fungal co-culture, and (2) the impact of associated bacteria in microalgal metabolome response to fungal interaction. Unfortunately, only a very low number of highlighted features were fully characterized. However, an up-regulation of the dinoflagellate toxins okadaic acid and dinophysistoxin 1 was observed during co-culture in supernatants. Such results highlight the importance to consider microalgal-fungal interactions in the study of parameters regulating toxin production.
Keyphrases
- cell wall
- high performance liquid chromatography
- high resolution mass spectrometry
- escherichia coli
- physical activity
- microbial community
- induced apoptosis
- mass spectrometry
- tandem mass spectrometry
- liquid chromatography
- oxidative stress
- cell death
- ultra high performance liquid chromatography
- high resolution
- data analysis