Discovery of a High-Efficient Algicidal Bacterium against Microcystis aeruginosa Based on Examinations toward Culture Strains and Natural Bloom Samples.
He ZhangYan XieRongzhen ZhangZhongliang ZhangXinglong HuYao ChengRuozhen GengZengling MaRenhui LiPublished in: Toxins (2023)
Harmful cyanobacterial blooms occur worldwide and pose a great threat to aquatic ecosystems and public health. The application of algicidal bacteria represents an eco-friendly strategy for controlling harmful cyanobacterial blooms; thus, searching for a high efficiency of algicidal bacteria has been becoming an important and continuous task in science. Herein, we identified a bacterial strain coded Streptomyces sp. HY with a highly algicidal activity, and investigated its algicidal efficiency and mechanism against Microcystis aeruginosa . The strain HY displayed high algicidal activity toward Microcystis aeruginosa cells, with a removal rate of 93.04% within 2 days via indirect attack. Streptomyces sp. HY also showed the ability to lyse several genera of cyanobacterial strains, including Dolichospermum , Pseudanabaena , Anabaena , and Synechocystis , whereas it showed a minor impact on the green alga Scenedesmus obliquus , demonstrating its selectivity specially for targeting cyanobacteria. Its algicidal mechanism involved damages to the photosynthesis system, morphological injury of algal cells, oxidative stress, and dysfunction of the DNA repair system. Furthermore, HY treatment reduced the expression levels of genes ( mcyB and mcyD ) related to microcystin biosynthesis and decreased the total content of microcystin-leucine-arginine by 79.18%. Collectively, these findings suggested that the algicidal bacteria HY is a promising candidate for harmful cyanobacterial bloom control.
Keyphrases
- public health
- induced apoptosis
- oxidative stress
- dna repair
- high efficiency
- dna damage
- cell cycle arrest
- nitric oxide
- escherichia coli
- poor prognosis
- endoplasmic reticulum stress
- climate change
- dna methylation
- genome wide
- high throughput
- cell death
- small molecule
- replacement therapy
- ischemia reperfusion injury
- transcription factor
- heat shock protein
- high resolution
- pi k akt
- heat stress
- drug delivery