Abstract

Picobirnaviruses (PBVs) have been detected in several species of animals worldwide; however, data pertaining to their presence in Australian wild and domestic animals are limited. Although PBVs are mostly found in faecal samples, their detection in blood and respiratory tract samples raises questions concerning their tropism and pathogenicity. We report here PBV detection in wild deer and cattle from southeastern Australia. Through metagenomics, the presence of PBV genogroups I (GI) and II (GII) were detected in deer serum and plasma. Molecular epidemiology studies targeting the partial RNA-dependent RNA polymerase gene were performed in a wide range of specimens (serum, faeces, spleen, lung, nasal swabs, and trachea) collected from wild deer and cattle, with PCR amplification obtained in all specimen types except lung and spleen. Our results reveal the predominance of GI and concomitant detection of both genogroups in wild deer and cattle. In concordance with other studies, the detected GI sequences displayed high genetic diversity, however in contrast, GII sequences clustered into three distinct clades. Detection of both genogroups in the upper respiratory tract (trachea and nasal swab) of deer in the present study gives more evidence about the respiratory tract tropism of PBV. Although much remains unknown about the epidemiology and tropism of PBVs, our study suggests a wide distribution of these viruses in southeastern Australia.

Highlights

  • Picobirnaviruses (PBVs) are members of the family Picobirnaviridae and have a nonenveloped bi-segmented double-stranded RNA genome measuring 35–40 nm in diameter

  • Further analysis of eukaryotic viral contigs revealed sequences identified as picobirnaviruses segment 2 in four deer samples with lengths ranging from 881 to 1719 nucleotides (Table 1)

  • Australia’s wild deer populations have increased in abundance and distribution during recent decades [40], and the close interactions between deer and livestock are a risk for pathogen transmission [41]

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Summary

Introduction

Picobirnaviruses (PBVs) are members of the family Picobirnaviridae and have a nonenveloped bi-segmented double-stranded RNA (dsRNA) genome measuring 35–40 nm in diameter. Based on the genetic variability of genomic segment 2, PBVs are classified into three genogroups [1]. PBVs have been reported in humans, invertebrates, environmental water samples, and a wide range of vertebrates worldwide [1,2,4,5]. There is only one published report of PBV detection in cervid (deer) species. 60% (42/70) of faeces collected from roe deer (Capreolus capreolus) in Slovenia tested positive for PBV GI by polymerase chain reaction (PCR) [6]. In Australia, PBVs have been previously detected by metagenomics in stool samples collected from humans [4], wild birds [7,8], European rabbits (Oryctolagus cuniculus) [9], and Tasmanian devils (Sarcophilus harrisii) [10]

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