Retrospective Detection and Complete Genomic Sequencing of Canine morbillivirus in Eurasian Otter (Lutra lutra) Using Nanopore Technology

Viruses. 2022 Jun 29;14(7):1433. doi: 10.3390/v14071433.

Abstract

The Eurasian otter (Lutra lutra) is a piscivorous apex predator in aquatic habitats, and a flagship species of conservation biology throughout Europe. Despite the wide distribution and ecological relevance of the species, there is a considerable lack of knowledge regarding its virological and veterinary health context, especially in Central Europe. Canine morbillivirus (Canine distemper virus (CDV)) is a highly contagious viral agent of the family Paramyxoviridae with high epizootic potential and veterinary health impact. CDV is present worldwide among a wide range of animals; wild carnivores are at particular risk. As part of a retrospective study, lung-tissue samples (n = 339) from Eurasian otters were collected between 2000 and 2021 throughout Hungary. The samples were screened for CDV using a real-time RT-PCR method. Two specimens proved positive for CDV RNA. In one sample, the complete viral genome was sequenced using a novel, pan-genotype CDV-specific amplicon-based sequencing method with Oxford Nanopore sequencing technology. Both viral sequences were grouped to a European lineage based on the hemagglutinin-gene phylogenetic classification. In this article, we present the feasibility of road-killed animal samples for understanding the long-term dynamics of CDV among wildlife and provide novel virological sequence data to better understand CDV circulation and evolution.

Keywords: MinION; Mustelidae; NGS; conservation biology; enzootic; third generation sequencing.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Distemper Virus, Canine* / genetics
  • Distemper*
  • Dogs
  • Genomics
  • Nanopores*
  • Otters* / genetics
  • Phylogeny
  • Retrospective Studies
  • Technology

Grants and funding

The research was financed by the Higher Education Institutional Excellence Program of the Ministry for Innovation and Technology in Hungary, within the framework of the “Innovation for a sustainable life and environment” thematic program of the University of Pécs (TUDFO/47138/2019-ITM). J.L. was supported by the TKP2020-IKA-12 project. The project was supported by the ÚNKP-20-3-I-PTE-579 New National Excellence Program of the Ministry for Innovation and Technology. Z.L. was supported by the Biological and Sportbiological Doctoral School of the University of Pécs, Hungary. GK was supported by the Janos Bolyai Research Scholarship of the Hungarian Academy of Sciences. This work was supported by the National Laboratory of Virology, grant number: RRF-2.3.1-21-2022-00010.