I am Gabriel Lovate and I come from Brazil. I studied Pharmacy and Biochemistry as a bachelor, and then obtained a master in Biochemistry, at the University of São Paulo, Brazil. As an undergraduate student, I was involved in the field of Synthetic Biology, working on the development of bacterial-based biosensors. During my master’s studies I tried to better understand how antibiotic resistance is distributed in clinical settings, employing functional genomic characterization of bacterial pathogens.
During this training period, I was deeply interested in using computational tools to describe and understand biology. Following this drive, in February 2021, I joined the Friedrich Schiller University in Jena, Germany, to develop methods and tools for the analysis of RNA structure in viruses. Under the supervision of Prof. Dr. Marz, I am decided to embark on the challenge of deciphering the RNA genome packaging code of influenza A viruses.
I am always chaotically reading 3 or more books at the same time, always some kind of Sci-Fi/dystopia, biography, or science outreach. Another pleasure for me is going on hikes and camping.
Friedrich Schiller University Jena (FSU), Germany
Prof. Dr. Manja Marz (FSU Jena)
Prof. Dr. Andreas Henke (Jena University Hospital)
Rithu Paul Stansilaus (ESR 2)
WP 1.4 Virus regulation
WP 2.1 Microevolution: Virus quasispecies
WP 2.2 Macroevolution: Natural selection of viruses
Currently, bioinformatical tools are not specifically designed for viruses. However, viruses bring unique features, which require specific bioinformatical tools to trace virus-host interaction. For example, the number of sequences in a quasispecies is massively high due to their high mutation rate, but only a few interact again with the host cells. Some viruses, such as IAV or as used by AG, are segmented RNA viruses, which urgently require tools with specific features: RNA viruses should include standardised secondary structure predictions, leading to RNA-RNA interaction prediction necessary for the packaging of segmented RNA viruses.
Therefore the precise aims of this project are
- Development of a bioinformatical tool to predict RNA-RNA interactions as packaging signal for segmented viruses, such as IAV. The tool will also consider the 3D arrangement of the RNA molecules being essential to understand the nature of packaged viruses.
- Development of a virus-specific full genome multiple sequence alignment algorithm to track the quasispecies. We will combine this tool with secondary structure information being available from literature and ESR 2 to build more accurate alignments.
- Establishment of RNA-RNA interaction sets and more importantly non-interaction sets. The result will be used by ESR 2 to explore the reassortment space of IAVs. This understanding is essential for a prediction of future Flu outbreaks.
- Application of the tool for at least 30 different viruses in other projects in VIROINF.