Promastigote EPS secretion and haptomonad biofilm formation as evolutionary adaptations of trypanosomatid parasites for colonizing honeybee hosts.
Jéssica Carreira de PaulaPedro García OlmedoTamara Gómez-MorachoMaría Buendía-AbadMariano HigesRaquel Martín-HernándezAntonio OsunaLuis Miguel de PablosPublished in: NPJ biofilms and microbiomes (2024)
Bees are major pollinators involved in the maintenance of all terrestrial ecosystems. Biotic and abiotic factors placing these insects at risk is a research priority for ecological and agricultural sustainability. Parasites are one of the key players of this global decline and the study of their mechanisms of action is essential to control honeybee colony losses. Trypanosomatid parasites and particularly the Lotmaria passim are widely spread in honeybees, however their lifestyle is poorly understood. In this work, we show how these parasites are able to differentiate into a new parasitic lifestyle: the trypanosomatid biofilms. Using different microscopic techniques, we demonstrated that the secretion of Extracellular Polymeric Substances by free-swimming unicellular promastigote forms is a prerequisite for the generation and adherence of multicellular biofilms to solid surfaces in vitro and in vivo. Moreover, compared to human-infective trypanosomatid parasites our study shows how trypanosomatid parasites of honeybees increases their resistance and thus resilience to drastic changes in environmental conditions such as ultralow temperatures and hypoosmotic shock, which would explain their success thriving within or outside their hosts. These results set up the basis for the understanding of the success of this group of parasites in nature and to unveil the impact of such pathogens in honeybees, a keystones species in most terrestrial ecosystems.
Keyphrases
- plasmodium falciparum
- biofilm formation
- climate change
- candida albicans
- pseudomonas aeruginosa
- metabolic syndrome
- staphylococcus aureus
- cardiovascular disease
- physical activity
- escherichia coli
- endothelial cells
- type diabetes
- drug delivery
- adipose tissue
- gene expression
- depressive symptoms
- multidrug resistant
- antimicrobial resistance
- gram negative
- social support
- induced pluripotent stem cells
- drug release
- glycemic control