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Biology subjects

Petrova, E.

Publications and source records attributed to Petrova, E..

3 recordsLinked to original sources

Cultivation and genomic characterisation of novel methanogens from a desert biocrust

Methanogens are strictly anaerobic archaea capable of energy conservation by methane production, yet their presence in oxic and arid environments challenges existing paradigms. In this study, we enriched and genomically characterised seven methanogenic cultures from desert biocrusts, affiliated with the genera Methanobacterium, Methanosarcina, and Methanocella. Six of these new cultures represent new species. Nonetheless, phylogenomic analyses revealed close genetic relationships with organisms from anoxic environments, indicating the absence of an evolutionary distinction. Comparative genomics exposed diverse though non-unique repertories of antioxidant (e.g. catalase, superoxide dismutase and desulfoferrodoxin), and desiccation-resistance genes (including genes for maintaining osmotic pressure and repair of cell wall and membrane), with Methanobacterium spp. possessing the lowest gene abundance and diversity for oxygen and desiccation tolerance. Nevertheless, the occurrence of a Class I methanogen such as Methanobacterium in arid soils challenges the notion that members of this class are less oxygen tolerant than Class II. Pangenome analysis further uncovered unique genes enriched in membrane-associated functions and potentially non-functional stress-related genes. Via a global metagenomic survey, we find that methanogens are underdetected in dryland soils, likely due to sequencing depth limitations. Our findings highlight previously overlooked methanogen diversity and ecological plasticity in oxic and desiccated habitats, and emphasise the need for further studies to elucidate their survival strategies.

microbiology↗

Engineering multivalent Fc display for FcγR blockade

Autoimmune diseases, driven by Fc{gamma} receptor (Fc{gamma}R) activation through autoantibody immune complexes (IC), present a complex therapeutic challenge of achieving pharmacological blockade of Fc{gamma}R without triggering receptor activation. The assembly of ICs into polydisperse, higher-order structures is required for Fc{gamma}R activation. However, engineered multimeric, monodisperse Fc assemblies have been reported to prevent Fc{gamma}R activation, suggesting that Fc spatial organization determines Fc{gamma}R activation. In this study, we engineered a functional single-chain Fc domain protein (scFc) for unidirectional, multivalent presentation by virus-like particles (VLPs), used as a display platform. We found that the multivalent display of scFc on the VLPs elicited distinct cellular responses compared with monovalent scFc, highlighting the importance of the structural context of scFc on its function. scFc-VLPs had minimal impact on the nanoscale spatial organization of Fc{gamma}R at the cell membrane and caused limited receptor activation and internalization. In contrast, the monovalent scFc acted as an Fc{gamma}R agonist, inducing receptor clustering, activation, and internalization. Increasing scFc valency in scFc-VLPs was associated with increased binding to monocytes, reaching a plateau at high valencies. Notably, the ability of scFc-VLPs to block IC-mediated phagocytosis in vitro increased with scFc valency. In a murine model of passive immune thrombocytopenia (ITP), a high valency scFc-VLP variant with a desirable immunogenicity profile induced attenuation of thrombocytopenia. Here we show that multivalent presentation of an engineered scFc on a display platform can be tailored to promote suppression of IC-mediated phagocytosis while preventing Fc{gamma}R activation. This work introduces a new paradigm that can contribute to the development of therapies for autoimmune diseases.

bioengineering↗

A microfluidic biodisplay

Synthetically engineered cells are powerful and potentially useful biosensors, but it remains problematic to deploy such systems due to practical difficulties and biosafety concerns. To overcome these hurdles, we developed a microfluidic device that serves as an interface between an engineered cellular system, environment, and user. We created a biodisplay consisting of 768 individually programmable biopixels and demonstrated that it can perform multiplexed, continuous sampling. The biodisplay detected 10 {micro}g/l sodium-arsenite in tap water using a research grade fluorescent microscope, and reported arsenic contamination down to 20 {micro}g/l with an easy to interpret \"skull and crossbones\" symbol detectable with a low-cost USB microscope or by eye. The biodisplay was designed to prevent release of chemical or biological material to avoid environmental contamination. The microfluidic biodisplay thus provides a practical solution for the deployment and application of engineered cellular systems.

synthetic biology↗