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Discriminating between JCPyV and BKPyV in Urinary Virome Data Sets.
Rita Mormando1, Alan J Wolfe2, Catherine Putonti1,2,3
1Bioinformatics Program, Loyola University Chicago, Chicago, IL 60660, USA.
JC virus (JCPyV) and BK virus (BKPyV) are common human polyomaviruses. Our study reveals that many reported JCPyV infections in the urinary tract are actually BKPyV, highlighting the need for precise viral identification.
Area of Science:
- Virology
- Human Microbiome
- Genomics
Background:
- Polyomaviruses, including JC virus (JCPyV) and BK virus (BKPyV), are widespread in the human body.
- Both JCPyV and BKPyV are frequently detected in the human urinary tract.
- These viruses share significant genomic similarity (75% nucleotide identity) and encode identical genes, complicating their differentiation.
Purpose of the Study:
- To compare the prevalence of JCPyV and BKPyV in the human urinary tract.
- To re-evaluate existing urinary virome data for accurate JCPyV and BKPyV identification.
- To establish reliable methods for distinguishing between closely related polyomaviruses.
Main Methods:
- Retrieved and analyzed publicly available shotgun metagenomic sequencing data from 165 urinary microbiome and virome studies.
- Specifically mined data for JCPyV and BKPyV sequences.
- Employed uniform genome coverage analysis to confirm viral identification and differentiate between closely related species.
Main Results:
- While approximately one-third of analyzed datasets showed hits to JCPyV, detailed investigation revealed most were misidentified BKPyV.
- Accurate differentiation confirmed BKPyV as the predominant polyomavirus in the analyzed urinary virome samples.
- The refined identification method ensures high confidence in taxonomic assignments for closely related viruses.
Conclusions:
- Many previous reports of JCPyV in the urinary tract likely represent BKPyV due to sequence similarity.
- Precise methods are crucial for accurate epidemiological studies of polyomaviruses.
- This study underscores the importance of rigorous bioinformatic approaches for distinguishing between highly homologous viral genomes.
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