Abstract

Indian fruit bats, flying fox Pteropus medius was identified as an asymptomatic natural host of recently emerged Nipah virus, which is known to induce a severe infectious disease in humans. The absence of P. medius genome sequence presents an important obstacle for further studies of virus–host interactions and better understanding of mechanisms of zoonotic viral emergence. Generation of the high-quality genome sequence is often linked to a considerable effort associated to elevated costs. Although secondary scaffolding methods have reduced sequencing expenses, they imply the development of new tools for the integration of different data sources to achieve more reliable sequencing results. We initially sequenced the P. medius genome using the combination of Illumina paired-end and Nanopore sequencing, with a depth of 57.4x and 6.1x, respectively. Then, we introduced the novel scaff2link software to integrate multiple sources of information for secondary scaffolding, allowing to remove the association with discordant information among two sources. Different quality metrics were next produced to validate the benefits from secondary scaffolding. The P. medius genome, assembled by this method, has a length of 1,985 Mb and consists of 33,613 contigs and 16,113 scaffolds with an NG50 of 19 Mb. At least 22.5% of the assembled sequences is covered by interspersed repeats already described in other species and 19,823 coding genes are annotated. Phylogenetic analysis demonstrated the clustering of P. medius genome with two other Pteropus bat species, P. alecto and P. vampyrus, for which genome sequences are currently available. SARS-CoV entry receptor ACE2 sequence of P. medius was 82.7% identical with ACE2 of Rhinolophus sinicus bats, thought to be the natural host of SARS-CoV. Altogether, our results confirm that a lower depth of sequencing is enough to obtain a valuable genome sequence, using secondary scaffolding approaches and demonstrate the benefits of the scaff2link application. The genome sequence is now available to the scientific community to (i) proceed with further genomic analysis of P. medius, (ii) to characterize the underlying mechanism allowing Nipah virus maintenance and perpetuation in its bat host, and (iii) to monitor their evolutionary pathways toward a better understanding of bats’ ability to control viral infections.

Highlights

  • Bats have been reported to be the natural reservoir of several zoonotic viruses that cause severe human diseases, including Marburg, Ebola, Nipah, Hendra, SARS, and MERS viruses (Wang and Anderson, 2019)

  • Pteropus medius DNA was extracted from cultured primary bat cells and sequenced using both paired-end Illumina and Nanopore sequencing, generating 114.5 Gb of Illumina DNASeq data

  • We report here that the process of secondary scaffolding is beneficial in terms of assembly quality (6.1x of Nanopore long-reads and 57.4x Illumina paired-end) with sequencing cost that remains relatively moderate, making this approach rather attractive

Read more

Summary

Introduction

Bats have been reported to be the natural reservoir of several zoonotic viruses that cause severe human diseases, including Marburg, Ebola, Nipah, Hendra, SARS, and MERS viruses (Wang and Anderson, 2019). Nipah virus is a recently emerged zoonotic Paramyxovirus, capturing the attention of both scientific and public health communities due to its high lethality rate, up to 90% in Bangladesh and India epidemics, associated with human-to-human transmission (Mathieu and Horvat, 2015; Arunkumar et al, 2019). This virus is highly pathogenic in humans and numerous other mammalian species, it is asymptomatic in its natural host, fruit bats (Enchéry and Horvat, 2017). Recent outbreaks of numerous pathogenic viruses from bats, including SARS coronavirus (Hu et al, 2015), urge improved comprehension and characterizations of bat species

Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.