Abstract

Bats are implicated as the natural reservoirs for several highly pathogenic viruses that can infect other animal species, including man. Here, we investigate the potential for two recently discovered bat rubulaviruses, Achimota virus 1 (AchPV1) and Achimota virus 2 (AchPV2), isolated from urine collected under urban bat (Eidolon helvum) roosts in Ghana, West Africa, to infect small laboratory animals. AchPV1 and AchPV2 are classified in the family Paramyxoviridae and cluster with other bat derived zoonotic rubulaviruses (i.e. Sosuga, Menangle and Tioman viruses). To assess the susceptibility of AchPV1 and AchPV2 in animals, infection studies were conducted in ferrets, guinea pigs and mice. Seroconversion, immunohistological evidence of infection, and viral shedding were identified in ferrets and guinea pigs, but not in mice. Infection was associated with respiratory disease in ferrets. Viral genome was detected in a range of tissues from ferrets and guinea pigs, however virus isolation was only achieved from ferret tissues. The results from this study indicate Achimota viruses (AchPVs) are able to cross the species barrier. Consequently, vigilance for infection with and disease caused by these viruses in people and domesticated animals is warranted in sub-Saharan Africa and the Arabian Peninsula where the reservoir hosts are present.

Highlights

  • The recently discovered rubulaviruses, Achimota virus 1 and Achimota virus 2 (AchPV1 and AchPV2), were isolated from bat (Eidolon helvum) urine samples collected beneath urban bat roosts in Ghana, West Africa[15]

  • We investigated the potential of the two recently discovered bat rubulaviruses, AchPV1 and AchPV2, to infect laboratory animals representing three species

  • Seroconversion to both Achimota viruses in ferrets and guinea pigs indicated these animals were susceptible to infection, mice did not seroconvert to either virus

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Summary

Introduction

The recently discovered rubulaviruses, Achimota virus 1 and Achimota virus 2 (AchPV1 and AchPV2), were isolated from bat (Eidolon helvum) urine samples collected beneath urban bat roosts in Ghana, West Africa[15]. Despite being discovered in the same study, the AchPVs are not nearest-phylogenetic relatives and share only 31 to 64% protein amino acid identities[15] Their relationship to each other is similar to their relationships with other bat rubulaviruses such as Sosuga (SosPV), Menangle (MenPV) and Tioman (TioPV) viruses (sharing 58–70% N protein amino acid sequence identities), which have been shown to cause human infection. Based on what is known of these closely related bat rubulaviruses, the potential of AchPV1 and AchPV2 to infect and cause disease in other species is worthy of further investigation. Time course studies were performed using AchPV2 to obtain data on viral replication sites and potential routes of transmission

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