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Biology subjects

Blackburn, G.

Publications and source records attributed to Blackburn, G..

5 recordsLinked to original sources

Comparative lipidomic profiling of the livestock pathogens Trypanosoma congolense and Trypanosoma brucei

African Animal Trypanosomosis (AAT) is a disease affecting domestic animals, in particular cattle, in sub-Saharan Africa, resulting in billion-dollar losses annually. New drugs to combat and control AAT are urgently required, yet few treatment candidates are currently on the horizon. This can be attributed, in part, to the relative challenges associated with culturing the clinically relevant parasite species in a laboratory environment. Particularly, effective culture of bloodstream form Trypanosoma congolense, the trypanosome species responsible for a large proportion of AAT disease in cattle, requires the use of goat serum, whilst T. brucei is typically cultured in FBS-supplemented culture. This constrains in vitro studies on biology, especially comparative analyses between AAT-causing species. The differing serum supplementation requirements of these two trypanosome species point to metabolic distinctions, which may be important considerations in developing experimental systems to enable the identification and design of novel, pan-species therapies. In this study, untargeted LC-MS lipidomics analyses were conducted to determine the relative lipidomic profiles of T. congolense and T. brucei bloodstream form parasites. Employing a new media formulation that permits effective in vitro culture of both species, it was possible to establish that their global lipidomic profiles are distinct. Notably, T. congolense exhibits a relatively low abundance of ether phospholipids compared to T. brucei, whilst also possessing an enrichment of long-chain polyunsaturated fatty acids (PUFAs). These observations indicate that there are significant differences in the ways these parasites synthesise and remodel their lipid complement, highlighting an evolutionary divergence between the species that likely carries implications for host-pathogen interactions as well as trypanosome membrane biology. Furthermore, this study demonstrates that fine-tuning fatty acid supplementation may aid in optimising a universal medium suited for multiple species of AAT parasites. SummaryMultiple species of protozoan parasites can cause African Animal Trypanosomosis (AAT) in livestock and other animals. However, AAT research has largely centred on a single species, Trypanosoma brucei, partially due to the comparative difficulties in sustaining the other economically important parasite species - Trypanosoma congolense and Trypanosoma vivax - in laboratory culture. In this work, we aimed to determine whether distinctions in use of lipids between T. brucei and T. congolense explains their differing in vitro culture requirements. Using a newly designed media formulation, it was possible to culture mammalian-infective forms of both parasite species under identical conditions, enabling direct comparison of their lipidome - a complete inventory of the different fats and lipids the cells contain. We demonstrate that the T. congolense lipidome significantly differs from that of T. brucei, and that T. congolense shows a preference for longer, more unsaturated lipids. These differences are likely to underlie species-specific differences observed during host infections. Furthermore, our work demonstrates that understanding the lipid biology of protozoan parasites aids in optimisation of laboratory culturing conditions, thereby facilitating further research into these understudied pathogens, including the development of new therapies.

microbiology↗

Microbiota reduce Drosophila triacylglyceride density by providing pantothenate

Metabolism follows ground-rules that evolved in ancient bacteria: as a legacy, animal gut microbiota have abundant opportunity to modulate host metabolism, via conserved mechanisms. When these effects are beneficial, natural selection should favour hosts that reciprocally support bacterial growth. Whether microbes simply nourish hosts or more profoundly reprogram host metabolism remains to be established. Here we show that Acetobacter promote Drosophila coenzyme A, an ancient signalling metabolite, reprogramming host metabolism and generating a state that reciprocally supports bacterial growth. Impairing pathways from bacterial pantothenate to host coenzyme A increases host lipid storage, reduces nitrogen excretion, and diminishes bacterial load. These processes correspond to reprogrammed host carbohydrate handling and tissue-specific acyl-CoA pools, but live bacteria and short-chain fatty acids are dispensable. These results outline a simple microbial basis for complex host metabolic effects, via mechanisms that precede the origins of metazoa, facilitating metabolic and symbiotic homeostasis.

physiology↗

Anthropogenic noise affects vocalisation properties of the territorial song of Western Australian magpies

Anthropogenic noise is considered one of the most serious forms of pollution globally and has been shown to have negative effects on the distribution, behaviour, cognition and reproductive success of animal species worldwide. One of the most well researched impacts of anthropogenic noise is its effect on acoustic communication. Animals may adjust the rate, amplitude, duration, and/or frequency of their acoustic signals to better maintain communication when anthropogenic noise is present. In this study, we combine behavioural focals, amplitude measurements and audio recordings to investigate how female Western Australian magpies (Gymnorhina tibicen dorsalis) alter the acoustic features of their territorial song (known as a carol) when anthropogenic noise is present. Magpies reduced the rate at which they carolled when loud anthropogenic noise was present, and increased their peak frequency during anthropogenic noise, but, contrary to our hypotheses did not alter the amplitude, duration, or other frequency parameters of their carols. Results from this study add to the growing body of literature documenting changes to the vocal behaviour of wildlife in the presence of anthropogenic noise and highlights the importance of investigating multiple acoustic parameters to understand how species adjust their vocalisations in response to this pollutant.

animal behavior and cognition↗

Artificial light at night shifts the circadian system but still leads to physiological disruption in a wild bird

Globally increasing levels of artificial light at night (ALAN) are associated with shifts in circadian rhythms of behaviour in many wild species. However, it is still unclear whether changes in behavioural timing are underlined by parallel shifts in the molecular clock, and whether such internal shifts may differ between different tissues and physiological pathways, which could highlight circadian disruption. We tackled these questions in a comprehensive study that integrated behavioural, gene expression and metabolomic analyses. We exposed captive male great tits (Parus major) to three ALAN intensities or to dark nights, recorded their activity rhythms and obtained mid-day and midnight samples of brain, liver, spleen and blood. ALAN advanced wake-up time, and this shift was paralleled by an advance in the expression of the clock gene BMAL1 in all tissues, suggesting close links of brain and peripheral clock gene expression with activity rhythms. However, several metabolic and immune genes were desynchronised the shifted BMAL1 expression, suggesting circadian disruption of behaviour and physiology. This result was reinforced by untargeted metabolomic profiling, which showed that only 9.7% of the 755 analysed metabolites followed the behavioural shift. We suggest circadian as a key mediator of the health impacts of ALAN on wild animals.

zoology↗

Nanotopography reveals metabolites that maintain the immunosuppressive phenotype of mesenchymal stem cells

Mesenchymal stem cells (MSCs) are multipotent stem cells that are immunosuppressive and thus of considerable therapeutic potential in transplant operations. However, MSCs rapidly differentiate once in culture, making their large-scale expansion for use in immunosuppressive therapies challenging. Although the differentiation mechanisms of MSCs have been extensively investigated using materials, little is known about how materials can modulate paracrine activities of MSCs. Here, we show for the first time that nanotopography can control the immunomodulatory capacity of MSCs through decreased intracellular tension increasing oxidative glycolysis. We also use the nanotopography to identify bioactive metabolites that modulate intracellular tension, growth and immunomodulatory phenotype of MSCs in standard culture. Our findings show a novel route to support large-scale expansion of functional MSCs for therapeutic purposes

bioengineering↗