Learning from the unknown: exploring the range of bacterial functionality

Author:

Mahlich Yannick1ORCID,Zhu Chengsheng12,Chung Henri34,Velaga Pavan K1,De Paolis Kaluza M Clara5,Radivojac Predrag5ORCID,Friedberg Iddo34ORCID,Bromberg Yana167ORCID

Affiliation:

1. Department of Biochemistry and Microbiology, Rutgers University , 76 Lipman Dr, New Brunswick , NJ  08873, USA

2. Xbiome Inc. , 1 Broadway, 14th fl, Cambridge , MA  02142, USA

3. Department of Veterinary Microbiology and Preventive Medicine, Iowa State University , Ames , IA  50011, USA

4. Interdepartmental program in Bioinformatics and Computational Biology, Iowa State University , Ames , IA  50011, USA

5. Khoury College of Computer Sciences, Northeastern University , 177 Huntington Avenue, Boston , MA  02115, USA

6. Department of Biology, Emory University , 1510 Clifton Road NE, Atlanta , GA  30322, USA

7. Department of Computer Science, Emory University , 400 Dowman Drive, Atlanta , GA  30322, USA

Abstract

Abstract Determining the repertoire of a microbe's molecular functions is a central question in microbial biology. Modern techniques achieve this goal by comparing microbial genetic material against reference databases of functionally annotated genes/proteins or known taxonomic markers such as 16S rRNA. Here, we describe a novel approach to exploring bacterial functional repertoires without reference databases. Our Fusion scheme establishes functional relationships between bacteria and assigns organisms to Fusion-taxa that differ from otherwise defined taxonomic clades. Three key findings of our work stand out. First, bacterial functional comparisons outperform marker genes in assigning taxonomic clades. Fusion profiles are also better for this task than other functional annotation schemes. Second, Fusion-taxa are robust to addition of novel organisms and are, arguably, able to capture the environment-driven bacterial diversity. Finally, our alignment-free nucleic acid-based Siamese Neural Network model, created using Fusion functions, enables finding shared functionality of very distant, possibly structurally different, microbial homologs. Our work can thus help annotate functional repertoires of bacterial organisms and further guide our understanding of microbial communities.

Funder

National Science Foundation

NIH

NAI

Iowa State University's Translational Artificial Intelligence Center

Publisher

Oxford University Press (OUP)

Subject

Genetics

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