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Conradi, F. D.

Publications and source records attributed to Conradi, F. D..

2 recordsLinked to original sources

Flocculation of a cyanobacterium confers defense against bacterial predation

Many cyanobacteria, including unicellular species, are capable of flocculation: the formation of floating linked assemblages of many thousands of cells. Flocculation is a highly regulated process requiring both type IV pilus activity and the production of extracellular polysaccharides. Under standard laboratory conditions flocculation often slows culture growth, and its physiological advantages remain unclear. Proposed benefits include self-shading as protection from excess light exposure and flotation in the water column. Here, we determine whether flocculation can serve as a method of defense against bacterial predation. Using the unicellular cyanobacterium Synechocystis sp. PCC 6803, we show that flocculation is strongly triggered by exposure to live cells of "foreign" bacteria, including the opportunistic pathogen Pseudomonas aeruginosa. The established P. aeruginosa virulence arsenal includes bacterial warfare systems for competition for resources and acquisition of nutrients by way of interbacterial competition. Here, we establish the use of these strategies for direct predation, via the use of Type VI Secretion Systems. Comparisons of P. aeruginosa co-cultures with either wild type Synechocystis or a non-flocculating mutant revealed that Synechocystis flocculation minimizes both growth of P. aeruginosa and cell lysis of Synechocystis. This in turn reduces the impact of P. aeruginosa on Synechocystis growth by mechanistically limiting the photosynthetic products that P. aeruginosa can access. From these data, we propose that the type VI secretion system of P. aeruginosa can be used for predation and that the primary function of cyanobacterial flocculation is for defense against microbial predation. IMPORTANCEBacteria in the environment rarely, if ever, grow in isolation. Some phenotypic traits can only be understood in the context of interspecies interactions. Here, we examine interactions between two bacterial species with very different modes of metabolism. Synechocystis sp. PCC 6803 is a freshwater cyanobacterium that grows photosynthetically using light, water, CO2 and minerals. Pseudomonas aeruginosa is a soil bacterium and an opportunistic pathogen that depends on a supply of organic molecules for survival. When P. aeruginosa is co-cultured with Synechocystis in mineral medium, it lyses Synechocystis cells, using its Type VI secretion system to access nutrients via predation. The presence of P. aeruginosa (and other foreign bacteria) triggers a Synechocystis response in which it aggregates to form floating assemblages or flocs. Floc formation creates a defensive barrier to P. aeruginosa predation, and we suggest this complex behavior is best understood as a defense against microbial predation in the wild.

microbiology↗

Development of a highly sensitive luciferase-based reporter system to study two-step protein secretion in cyanobacteria

Cyanobacteria, ubiquitous oxygenic photosynthetic bacteria, interact with the environment and their surrounding microbiome through the secretion of a variety of small molecules and proteins. The release of these compounds is mediated by sophisticated multi-protein complexes, also known as secretion systems. Genomic analyses indicate that protein and metabolite secretion systems are widely found in cyanobacteria; however little is known regarding their function, regulation and secreted effectors. One such system, the type IVa pilus system (T4aPS), is responsible for the assembly of dynamic cell surface appendages, type IVa pili (T4aP), that mediate ecologically relevant processes such as phototactic motility, natural competence and adhesion. Several studies have suggested that the T4aPS can also act as a two-step protein secretion system in cyanobacteria akin to the homologous type II secretion system in heterotrophic bacteria. To determine whether the T4aP are involved in two-step secretion of non-pilin proteins, we developed a NanoLuc-based quantitative secretion reporter for the model cyanobacterium Synechocystis sp. PCC 6803. The NLuc reporter presented a wide dynamic range with at least one order of magnitude more sensitivity than traditional immunoblotting. Application of the reporter to a collection of Synechocystis T4aPS mutants demonstrated that two-step protein secretion in cyanobacteria is independent of T4aP. In addition, our data suggest that secretion differences typically observed in T4aPS mutants are likely due to a disruption of cell envelope homeostasis. This study opens the door to explore protein secretion in cyanobacteria further. ImportanceProtein secretion allows bacteria to interact and communicate with the external environment. Secretion is also biotechnologically relevant, where it is often beneficial to target proteins to the extracellular space. Due to a shortage of quantitative assays, many aspects of protein secretion are not understood. Here we introduce a NanoLuc (NLuc)-based secretion reporter in cyanobacteria. NLuc is highly sensitive and can be assayed rapidly and in small volumes. The NLuc reporter allowed us to clarify the role of type IVa pili in protein secretion and identify mutations that increase secretion yield. This study expands our knowledge on cyanobacterial secretion and offers a valuable tool for future studies of protein secretion systems in cyanobacteria.

microbiology↗