Cost-effective complete genome sequencing using the MinION platform for identification of recombinant enteroviruses

Author:

Chien Yeh-Sheng1,Chen Feng-Jui12,Wu Han-Chieh1,Lin Chieh-Hua3ORCID,Chang Wen-Chiung1,Perera David4,Yang Jyh-Yuan5,Lee Min-Shi1ORCID,Liao Yu-Chieh3ORCID

Affiliation:

1. National Institute of Infectious Diseases and Vaccinology, National Health Research Institutes , Zhunan, Taiwan

2. Department of Biological Science and Technology, National Yang Ming Chiao Tung University , Hsinchu, Taiwan

3. Institute of Population Health Sciences, National Health Research Institutes , Zhunan, Taiwan

4. Institute of Health and Community Medicine, Universiti Malaysia Sarawak , Sarawak, Malaysia

5. Research and Diagnosis Center, Centers for Disease Control , Taipei, Taiwan

Abstract

ABSTRACT Enteroviruses (EVs) are a group of viruses that cause various human illnesses. While the CODEHOP (COnsensus-DEgenerate Hybrid Oligonucleotide Primer) method can generate VP1 gene fragments for enterovirus genotyping, it is unable to detect recombinant strains. Recent advances in viral genome sequencing using next-generation sequencing technologies have enabled comprehensive analyses. However, the high cost poses a challenge for widespread adoption. To address this issue, this study proposes a cost-effective approach for generating complete enterovirus genome sequences using the Oxford Nanopore MinION sequencer. This protocol not only facilitates the generation of accurate genome sequences for various enterovirus strains but also allows for the differentiation of co-infections from viral isolates. In addition, the method can generate polyprotein sequences as well as peptide sequences of the upstream ORF (uORF) whose expression can impact virus infection. Through the analysis of complete enterovirus genomes, this study successfully identified seven enterovirus A71 isolates obtained during the 2018 enterovirus outbreak in Malaysia and Taiwan as recombinants between enterovirus A71 and coxsackievirus A2. Furthermore, our study has made a significant discovery by establishing a strong correlation between uORF trees and the epidemics of EVA71. This finding highlights the potential of uORF sequences as valuable indicators for monitoring and understanding the spread of EVA71 infections. We also identified notable amino acid changes in the transmembrane domain of the uORF protein within a newly identified lineage. These findings provide crucial insights into the molecular characteristics and evolutionary dynamics of EVA71, offering valuable information for future research and intervention strategies. IMPORTANCE By employing a cost-effective approach for complete genome sequencing, the study has enabled the identification of novel enterovirus strains and shed light on the genetic exchange events during outbreaks. The success rate of genome sequencing and the scalability of the protocol demonstrate its practical utility for routine enterovirus surveillance. Moreover, the study’s findings of recombinant strains of EVA71 and CVA2 contributing to epidemics in Malaysia and Taiwan emphasize the need for accurate detection and characterization of enteroviruses. The investigation of the whole genome and upstream ORF sequences has provided insights into the evolution and spread of enterovirus subgenogroups. These findings have important implications for the prevention, control, and surveillance of enteroviruses, ultimately contributing to the understanding and management of enterovirus-related illnesses.

Funder

National Health Research Institutes

Ministry of Health and Welfare

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Cell Biology,Microbiology (medical),Genetics,General Immunology and Microbiology,Ecology,Physiology

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