Ebola Virus Produces Discrete Small Noncoding RNAs Independently of the Host MicroRNA Pathway Which Lack RNA Interference Activity in Bat and Human Cells

Author:

Prasad Abhishek N.123ORCID,Ronk Adam J.123,Widen Steven G.4,Wood Thomas G.4,Basler Christopher F.5,Bukreyev Alexander1623

Affiliation:

1. Department of Pathology, The University of Texas Medical Branch, Galveston, Texas, USA

2. Galveston National Laboratory, The University of Texas Medical Branch, Galveston, Texas, USA

3. The University of Texas Medical Branch, Galveston, Texas, USA

4. Department of Biochemistry and Molecular Biology, The University of Texas Medical Branch, Galveston, Texas, USA

5. Center of Microbial Pathogenesis, Institute of Biomedical Sciences, Georgia State University, Atlanta, Georgia, USA

6. Department of Microbiology and Immunology, The University of Texas Medical Branch, Galveston, Texas, USA

Abstract

Here, we report the discovery, via deep sequencing, of numerous noncoding RNAs (ncRNAs) derived from both EBOV and MARV during infection of both bat and human cell lines. In addition to identifying several novel ncRNAs from both viruses, we identified two EBOV ncRNAs in our sequencing data that were near-matches to computationally predicted viral miRNAs reported in the literature. Using molecular and immunological techniques, we assessed the potential of EBOV ncRNAs to function as viral miRNAs. Importantly, we found little evidence supporting this hypothesis. Our work is significant because it represents the first rigorous assessment of the potential for EBOV to encode viral miRNAs and provides evidence contrary to the existing paradigm regarding the biological role of computationally predicted EBOV ncRNAs. Moreover, our work highlights further avenues of research regarding the nature and function of EBOV ncRNAs.

Funder

DOD | Defense Threat Reduction Agency

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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