Surveillance, isolation and genomic characterization of Pteropine orthoreovirus of probable bat origin among patients with acute respiratory infection in Malaysia

Author:

Tee Kok Keng123ORCID,Chan Po Qhuan1,Loh Alson Mun‐Khin4,Singh Sarbhan3,Teo Chee How5,Iyadorai Thevambiga1,Chook Jack Bee2ORCID,Ng Kim Tien6,Takebe Yutaka17,Chan Kok Gan89,Sam I‐Ching1ORCID,Voon Kenny410

Affiliation:

1. Department of Medical Microbiology, Faculty of Medicine Universiti Malaya Kuala Lumpur Malaysia

2. Department of Medical Sciences, School of Medical and Life Sciences Sunway University Bandar Sunway Selangor Darul Ehsan Malaysia

3. Special Resource Centre, Institute for Medical Research Ministry of Health Shah Alam Malaysia

4. School of Medicine, Pathology Division International Medical University Kuala Lumpur Malaysia

5. Centre for Research in Biotechnology for Agriculture (CEBAR) Universiti Malaya Kuala Lumpur Malaysia

6. Institute of Molecular and Cell Biology, Agency for Science Technology and Research (A*STAR) Singapore Singapore

7. AIDS Research Center National Institute of Infectious Diseases Tokyo Japan

8. Division of Genetics and Molecular Biology, Institute of Biological Sciences, Faculty of Science Universiti Malaya Kuala Lumpur Malaysia

9. International Genome Centre Jiangsu University Zhenjiang China

10. School of Pharmacy University of Nottingham Malaysia Semenyih Malaysia

Abstract

AbstractPteropine orthoreovirus (PRV), an emerging bat‐borne virus, has been linked to cases of acute respiratory infections (ARI) in humans. The prevalence, epidemiology and genomic diversity of PRV among ARI of unknown origin were studied. Among 632 urban outpatients tested negative for all known respiratory viruses, 2.2% were PRV‐positive. Patients mainly presented with moderate to severe forms of cough, sore throat and muscle ache, but rarely with fever. Phylogenetic analysis revealed that over 90% of patients infected with the Melaka virus (MelV)‐like PRV, while one patient infected with the Pulau virus previously found only in fruit bats. Human oral keratinocytes and nasopharyngeal epithelial cells were susceptible to clinical isolates of PRV, including the newly isolated MelV‐like 12MYKLU1034. Whole genome sequence of 12MYKLU1034 using Nanopore technique revealed a novel reassortant strain. Evolutionary analysis of the global PRV strains suggests the continuous evolution of PRV through genetic reassortment among PRV strains circulating in human, bats and non‐human primate hosts, creating a spectrum of reassortant lineages with complex evolutionary characteristics. In summary, the role of PRV as a common etiologic agent of ARI is evident. Continuous monitoring of PRV prevalence, pathogenicity and diversity among human and animal hosts is important to trace the emergence of novel reassortants.

Funder

Ministry of Higher Education, Malaysia

Publisher

Wiley

Subject

Infectious Diseases,Virology

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