High‐resolution phylogeographical surveillance of Hantaan orthohantavirus using rapid amplicon‐based Flongle sequencing, Republic of Korea

Author:

Kim Jongwoo12,Park Kyungmin12,Kim Kijin34,Noh Juyoung12,Kim Seong‐Gyu12,Yang Eunyoung12,Cho Hee‐Kyung12,Lee Seung‐Ho5,No Jin Sun6,Lee Geum‐Young1,Lee Daesang5,Song Dong‐Hyun5,Gu Se Hun5,Park Man‐Seong127,Cho Nam‐Hyuk89,Jeong Seong Tae5,Kim Won‐Keun1011ORCID,Song Jin‐Won12

Affiliation:

1. Department of Microbiology Korea University College of Medicine Seoul Republic of Korea

2. BK21 Graduate Program Korea University College of Medicine Seoul Republic of Korea

3. Centre for Infectious Disease Genomics and One Health, Faculty of Health Sciences Simon Fraser University Burnaby British Columbia Canada

4. Department of Molecular Biology and Biochemistry Simon Fraser University Burnaby British Columbia Canada

5. Chem‐Bio Technology Center Agency for Defense Development Daejeon Republic of Korea

6. Division of High‐Risk Pathogens, Bureau of Infectious Diseases Diagnosis Control Korea Disease Control and Prevention Agency Cheongju Republic of Korea

7. Department of Microbiology, Institute for Viral Diseases, College of Medicine Korea University Seoul Republic of Korea

8. Department of Microbiology and Immunology, College of Medicine Seoul National University Seoul Republic of Korea

9. Department of Biomedical Sciences, College of Medicine Seoul National University Seoul Republic of Korea

10. Department of Microbiology Hallym University Chuncheon Republic of Korea

11. Institute of Medical Research Hallym University Chuncheon Republic of Korea

Abstract

AbstractOrthohantaviruses, etiological agents of hemorrhagic fever with renal syndrome (HFRS) and hantavirus cardiopulmonary syndrome, pose a critical public health threat worldwide. Hantaan orthohantavirus (HTNV) outbreaks are particularly endemic in Gyeonggi Province in northern area of the Republic of Korea (ROK). Small mammals were collected from three regions in the Gyeonggi Province during 2017 and 2018. Serological and molecular prevalence of HTNV was 25/201 (12.4%) and 10/25 (40%), respectively. A novel nanopore‐based diagnostic assay using a cost‐efficient Flongle chip was developed to rapidly and sensitively detect HTNV infection in rodent specimens within 3 h. A rapid phylogeographical surveillance of HTNV at high‐resolution phylogeny was established using the amplicon‐based Flongle sequencing. In total, seven whole‐genome sequences of HTNV were newly obtained from wild rodents collected in Paju‐si (Gaekhyeon‐ri) and Yeoncheon‐gun (Hyeonga‐ri and Wangnim‐ri), Gyeonggi Province. Phylogenetic analyses revealed well‐supported evolutionary divergence and genetic diversity, enhancing the resolution of the phylogeographic map of orthohantaviruses in the ROK. Incongruences in phylogenetic patterns were identified among HTNV tripartite genomes, suggesting differential evolution for each segment. These findings provide crucial insights into on‐site diagnostics, genome‐based surveillance, and the evolutionary dynamics of orthohantaviruses to mitigate hantaviral outbreaks in HFRS‐endemic areas in the ROK.

Publisher

Wiley

Subject

Infectious Diseases,Virology

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