Abstract

Nipah virus causes periodic livestock and human disease with high case fatality rate, and consequent major economic, social and psychological impacts. Fruit bats of the genus Pteropus are the natural reservoir. In this study, we used real time PCR to screen the saliva and urine of P. vampyrus from North Sumatera for Nipah virus genome. A conventional reverse transcriptase (RT-PCR) assay was used on provisionally positive samples to corroborate findings. This is the first report of Nipah virus detection in P. vampyrus in Sumatera, Indonesia.

Highlights

  • Nipah virus (NiV) is a novel paramyxovirus that is pathogenic to pigs and humans

  • In this paper we report the detection of Nipah virus genome in P. vampyrus in Sumatera, Indonesia using real time PCR

  • We targeted saliva and urine samples from Pteropus vampyrus in northern Sumatera based on the findings of Johara et al, 2001 [1] and Chua et al, 2002 [18], and adapting the methods of Wacharapluesadee et al, 2005, 2006 [11,20]

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Summary

Introduction

Nipah virus (NiV) is a novel paramyxovirus that is pathogenic to pigs and humans. The first attributed outbreak was reported in1998–9 in Malaysia, causing respiratory disease in pigs. Nipah virus (NiV) is a novel paramyxovirus that is pathogenic to pigs and humans. 2001 [1] suggested (based on their serologic findings) that flying-foxes were the likely natural reservoir of Nipah virus in Malaysia, and beyond. This contention was strengthened following the detection of Nipah virus genome in the urine and saliva of P. hypomelanus and P. vampyrus in Malaysia [2,4]. Nipah infection has subsequently been reported in Pteropus spp. across their global distribution, strongly suggesting that Nipah and related viruses have a long association with bats of this genus [5]

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