| Literature DB >> 28528278 |
Federica Verna1, Federica Giorda1, Ilaria Miceli1, Giovanna Rizzo1, Alessandra Pautasso1, Angelo Romano1, Barbara Iulini1, Maria Domenica Pintore1, Walter Mignone2, Carla Grattarola1, Elena Bozzetta1, Katia Varello1, Alessandro Dondo1, Cristina Casalone1, Maria Goria3.
Abstract
Morbillivirus genus comprises several members related to specific hosts, such as canine distemper virus (CDV) and cetacean morbillivirus (CeMV) in which the dolphin morbillivirus (DMV) is included. Both CDV and DMV are able to cause serious outbreak associated with high morbidity and mortality representing an important conservation threat for terrestrial and aquatic mammalian species. This paper describes a new RT-PCR RFLP technique based on a RT-PCR with degenerate primers targeting a 287 bp fragment located on the conserved N terminus of the morbillivirus NP gene, followed by MseI RFLP, in order both to confirm the detection of the virus and to distinguish DMV from CDV. Both carnivores and cetaceans tissues (brain, lung and lymph node) presenting evidence of morbillivirus infection (MI) were analyzed. RT-PCR positive samples were typed by RFLP analysis and then sequenced to confirm the RFLP results. This method was applied during the last morbillivirus cetacean die-off occurred in the Mediterranean basin in 2013, when there was the urgent need of a rapid and economic method to investigate among causes of death on stranded cetaceans. This new technique has proved to be a valuable, reliable, simple and relatively inexpensive diagnostic tool easily applicable also in limited-resource laboratories.Entities:
Keywords: Canine distemper virus; Carnivore; Cetacean; Dolphin morbillivirus; RFLP; RT-PCR
Mesh:
Year: 2017 PMID: 28528278 DOI: 10.1016/j.jviromet.2017.05.009
Source DB: PubMed Journal: J Virol Methods ISSN: 0166-0934 Impact factor: 2.014