We've updated our Privacy Policy to make it clearer how we use your personal data.

We use cookies to provide you with a better experience. You can read our Cookie Policy here.

Fungi Get Viral Infections Too

Fungi Get Viral Infections Too

Fungi Get Viral Infections Too

Fungi Get Viral Infections Too

Read time:

Want a FREE PDF version of This News Story?

Complete the form below and we will email you a PDF version of "Fungi Get Viral Infections Too"

First Name*
Last Name*
Email Address*
Company Type*
Job Function*
Would you like to receive further email communication from Technology Networks?

Technology Networks Ltd. needs the contact information you provide to us to contact you about our products and services. You may unsubscribe from these communications at any time. For information on how to unsubscribe, as well as our privacy practices and commitment to protecting your privacy, check out our Privacy Policy

Researchers from the University of Tsukuba have used an advanced technique to screen fungi for RNA viruses with unique sequences dissimilar to those previously identified.

We've all suffered from viruses, but did you know that they are also a problem for mushrooms and molds? Mycoviruses are viruses that specifically infect fungi and have the potential to impact ecology, agriculture, food security, and public health. Understanding the nature of these viruses, including their number and evolution, can help us understand their origins and inform our understanding of viruses in general.

Previous research into RNA mycoviruses has relied on their sequence similarity to viruses that have already been described. However, this approach leaves viruses with different genetic structures or sequences undiscovered. Using an advanced technological approach called Fragmented and Primer Ligated Double Stranded RNA sequencing, or FLDS for short, researchers from the University of Tsukuba were able to identify viral sequences that were previously overlooked.

Summarizing the importance of this work, Professor Hagiwara said: "The current approaches used to identify RNA viruses mean that their genetic diversity has been underestimated. Using FLDS, we were able to study RNA viruses without relying on sequence similarity, which allows us to identify RNA viral sequences that are dissimilar to those previously identified."

Using FLDS, Professors Urayama and Hagiwara, and their colleagues, identified 19 RNA viruses in a fungus called Aspergillus. Highlighting the value of this approach, 9 of the 19 viruses identified had been undetected using conventional methods of examination. Moreover, 42% of identified viruses had genomes that were segmented, or spread throughout the host genome, and others identified had novel genome architectures.

RNA-dependent RNA polymerase (RdRp) is an essential gene found in all RNA viruses and allows RNA genome replication from an RNA template. It was commonly understood that all RNA viruses encode RdRp as a single, continuous gene.

"Unexpectedly, we found that viruses within a certain clade of Narnaviridae encode an RdRp gene lacking the catalytic domains," Professor Urayama explains, "but we also found a different open reading frame containing the missing domains." Although some RdRp sequences lacking the catalytic domains have been described previously, those viral genomes also lack the catalytic domains and produce imperfect RdRp proteins. The functional, yet divided, RdRp described by Professors Urayama and Hagiwara, and their colleagues, indicates that researchers should reconsider the structural plasticity of RdRp.

This research shows that FLDS is a powerful approach that should be widely applied to identify high quality viral genomes and is a powerful tool for expanding the current understanding of RNA virus genome diversity.

Reference: Chiba Y, Oiki S, Yaguchi T, Urayama SI, Hagiwara D. Discovery of divided RdRp sequences and a hitherto unknown genomic complexity in fungal viruses. Virus Evolution. 2020. doi:10.1093/ve/veaa101

This article has been republished from the following materials. Note: material may have been edited for length and content. For further information, please contact the cited source.