Rotavirus Disease and Genotype Diversity in Older Children and Adults in Australia

Author:

Donato Celeste M123ORCID,Roczo-Farkas Susie1,Kirkwood Carl D124,Barnes Graeme L125,Bines Julie E125

Affiliation:

1. Enteric Diseases Group, Murdoch Children’s Research Institute, Parkville, Australia

2. Department of Paediatrics, The University of Melbourne, Parkville, Australia

3. Biomedicine Discovery Institute and Department of Microbiology, Monash University, Melbourne, Australia

4. Enteric and Diarrheal Diseases, Global Health, Bill & Melinda Gates Foundation, Seattle, Washington, USA

5. Department of Gastroenterology and Clinical Nutrition, Royal Children’s Hospital, Parkville, Australia

Abstract

Abstract Background Rotavirus is a major cause of gastroenteritis in children <5 years of age. The disease burden in older children, adults, and the elderly is underappreciated. This study describes rotavirus disease and genotypic diversity in the Australian population comprising children ≥5 years of age and adults. Methods Rotavirus positive fecal samples were collected from laboratories Australia-wide participating in the Australian Rotavirus Surveillance Program between 2010 and 2018. Rotavirus samples were genotyped using a heminested multiplex reverse-transcription polymerase chain reaction. Notification data from the National Notifiable Diseases Surveillance System were also analyzed. Results Rotavirus disease was highest in children aged 5–9 years and adults ≥85 years. G2P[4] was the dominant genotype in the population ≥5 years of age. Genotype distribution fluctuated annually and genotypic diversity varied among different age groups. Geographical differences in genotype distribution were observed based on the rotavirus vaccine administered to infants <1 year of age. Conclusions This study revealed a substantial burden of rotavirus disease in the population ≥5 years of age, particularly in children 5–9 years and the elderly. This study highlights the continued need for rotavirus surveillance across the population, despite the implementation of efficacious vaccines.

Funder

Australian National Health and Medical Research Council

Australian Government Department of Health

Victorian Government’s Operational Infrastructure

GlaxoSmithKline

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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