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Pavoncello, V.

Publications and source records attributed to Pavoncello, V..

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The microbiota affects energy production, nitrogen excretion and sterol metabolism in mosquito larvae

Mosquito larvae rely on a living microbiota for normal development because the microbiota supplies essential nutrients, particularly vitamins. Beyond vitamin provision, transcriptomic data suggest that the microbiota also supports other key nutritional processes. Here, we explored these roles by conducting a metabolomics analysis on Aedes aegypti third instar larvae following microbiota depletion. We sampled larvae and dissected guts 12- and 20-hours post-decolonization and analysed methanol-soluble metabolites using untargeted gas chromatography-mass spectrometry. Our findings reveal a pronounced impact of gut microbial presence on several metabolites involved in the tricarboxylic acid cycle and the uricolytic pathway. Germ-free larvae also had a lower quantity of cholesterol in guts and their long-chain fatty acid profile was altered in guts and whole larvae. Sterols, including cholesterol, are essential precursors for the production of the moulting hormone 20-hydroxyecdysone. We therefore tested how supplementing exogenous cholesterol affects the development of germ-free larvae. The effects proved to be highly concentration-dependent, ranging from a marginally significant increase in successful development to adulthood at low concentrations to a pronounced developmental impairment at higher concentrations. Moreover, bacteria deficient in fatty acids beta-oxidation had a significantly lower ability to support larval development. Together, the observed alterations suggest that microbiota-deprived larvae exhibit a downregulation of metabolic processes related to energy production, nitrogen excretion and sterol metabolism, likely due to the absence of microbiota-derived vitamins essential for these central metabolic functions. ImportanceMosquito larvae depend on gut microbiota for normal growth because microbes supply essential nutrients, particularly B vitamins. To explore microbial roles beyond vitamin provision, we analysed metabolic changes in Aedes aegypti larvae after microbiota removal using gas chromatography-mass spectrometry. Germ-free larvae exhibited decreased metabolites associated with the tricarboxylic acid cycle and uricolytic pathway, indicating a general slowdown in metabolic activity and nitrogen waste processing. Additionally, the absence of a microbiota affected cholesterol and fatty acid metabolism. To validate these findings, we found that supplementing germ-free larvae with low levels of cholesterol modestly improved their development. In contrast, larvae colonized with bacteria deficient in fatty acid metabolism exhibited significantly reduced developmental success. Overall, the findings show that removing the microbiota downregulates key metabolic pathways related to energy production, nitrogen excretion, and sterol metabolism, highlighting that bacterial vitamins and fatty acid degradation are vital for mosquito larval development and successful transformation into adults.

microbiology↗

The essential role of 2,4-dienoyl-CoA reductase for degradation of complex fatty acid mixtures

Fatty acids (FAs) can be used as carbon and energy source by most bacteria. FAs are very diverse and show variations in aliphatic chain length, degree and kind of branching, and number of double bonds. After their activation by a thioester link to Coenzyme A, FAs are degraded by the {beta}-oxidation machinery. The core enzymes of the {beta}-oxidation machinery can degrade most FAs, except for those that bear an unsaturation at even-numbered carbons. Such FAs include arachidonic acid or linoleic acid, which are essential FAs of the mammalian diet. We studied the role of the 2,4-dienoyl-CoA reductase FadH in E. coli FA metabolism. We showed that fadH is essential for growth on linoleic acid and that Cys residues connecting FadH-bound [Fe-S] cluster are essential for activity in vivo. Moreover, we showed that when mixed with other FAs, linoleic acid prevents growth of the fadH mutant. These results underline the key role of FadH in complex environments like the gut containing diverse FAs. Eukaryotes also use 2,4-dienoyl-CoA reductases for {beta}-oxidation in mitochondria, but these enzymes belong to a different family than FadH, with different co-factors equipment and mechanism. Yet, we showed that eukaryotic 2,4-dienoyl-CoA reductases DECR can complement the E. coli fadH mutant for growth on linoleic acid and for relief of linoleate mediated jamming of the {beta}-oxidation, paving the way to search for chemicals targeting DECR activity. Altogether these studies demonstrate the key role of prokaryotic and eukaryotic 2,4-dienoyl-CoA reductases in complex environments containing mixtures of saturated and unsaturated FAs. IMPORTANCEBacteria and eukaryotes can harness energy from fatty acids (FAs) through the process of {beta}-oxidation. However, information on the {beta}-oxidation in bacteria stems from studies in which degradation of only a limited set of saturated or monounsaturated FAs were investigated, far from reflecting the wide chemical diversity of FAs found in Nature. Here we evidenced the physiological importance of dienoyl-CoA reductase enzymes required for the degradation of specific unsaturated fatty acids in complex mixtures of fatty acids, and how their absence leads to the congestion of the {beta}-oxidation machinery. These results will permit to better understand the impact of FA degradation in enterobacteria, living in the complex gut environment where FAs are available from the diet or from host lipids. Furthermore, we showed that eukaryotic enzymes can replace the prokaryotic ones, opening the possibility of biomedical application in structure/function studies of the eukaryotic dienoyl-CoA reductases.

microbiology↗