Abstract
Heavy metal pollution in waters causes serious stress to aquatic ecosystems. Several autotrophs with strong tolerance are extensively used to adsorb heavy metals, but their use may be limited by the specific conditions of polluted waters due to their single nutrition mode. By contrast, mixotrophs possess strong environmental adaptability due to their plastic metabolic modes. However, studies focusing on mixotroph's resistance and its underlying mechanism in response to heavy metals and their bioremediation potentials are currently lacking. In this study, we investigated the population, phytophysiological, and transcriptomic (RNA-Seq) responses of a typical and common mixotrophic organism, Ochromonas, to cadmium exposure and then evaluated their capacity to remove cadmium under mixotrophic condition. Compared with autotrophy, mixotrophic Ochromonas enhanced photosynthetic performances under short-time cadmium exposure and subsequently shifted to stronger resistance with increasing exposure time. Transcriptomic analyses suggested that the genes related to photosynthesis, ATP production, ECM components, and scavenging of reactive oxygen species and damaged organelles were upregulated to boost mixotrophic Ochromonas resistance to cadmium. Consequently, the harm of metal exposure was eventually reduced and cellular stability was maintained. Approximately, 70% of cadmium at 2.4 mg L(-1) cadmium was removed by mixotrophic Ochromonas in the end, benefiting from upregulated genes associated with the transport of metal ions. Hence, mixotrophic Ochromonas tolerance to cadmium can be attributed to multiple pathways of energy metabolism and effective transport of metal ions. Collectively, this study advanced a better understanding of the unique mechanism of heavy metal resistance in mixotrophs and their potential use in recovering cadmium-contaminated aquatic ecosystems. IMPORTANCE Mixotrophs widely living in aquatic ecosystems possess unique ecological roles and strong environmental adaptability due to their plastic metabolic modes; however, little is known about their underlying resistance mechanism and bioremediation potential in response to environmental stresses. For the first time, this work investigated how mixotrophs respond to metal pollutants through physiological, population dynamics, and transcriptional regulation, and highlighted the unique underlying mechanism of mixotrophs to resist and remove heavy metal, thereby advancing our understanding of the potentials of mixotrophs in recovering metal-contaminated aquatic environments. These unique properties in mixotrophs are essential for the long-term functional stability of aquatic ecosystems.