Canine distemper virus isolated from a monkey efficiently replicates on Vero cells expressing non-human primate SLAM receptors but not human SLAM receptor

BMC Vet Res. 2016 Aug 2;12(1):160. doi: 10.1186/s12917-016-0757-x.

Abstract

Background: In 2008, an outbreak of canine distemper virus (CDV) infection in monkeys was reported in China. We isolated CDV strain (subsequently named Monkey-BJ01-DV) from lung tissue obtained from a rhesus monkey that died in this outbreak. We evaluated the ability of this virus on Vero cells expressing SLAM receptors from dog, monkey and human origin, and analyzed the H gene of Monkey-BJ01-DV with other strains.

Results: The Monkey-BJ01-DV isolate replicated to the highest titer on Vero cells expressing dog-origin SLAM (10(5.2±0.2) TCID50/ml) and monkey-origin SLAM (10(5.4±0.1) TCID50/ml), but achieved markedly lower titers on human-origin SLAM cells (10(3.3±0.3) TCID50/ml). Phylogenetic analysis of the full-length H gene showed that Monkey-BJ01-DV was highly related to other CDV strains obtained during recent CDV epidemics among species of the Canidae family in China, and these Monkey strains CDV (Monkey-BJ01-DV, CYN07-dV, Monkey-KM-01) possessed a number of amino acid specific substitutions (E276V, Q392R, D435Y and I542F) compared to the H protein of CDV epidemic in other animals at the same period.

Conclusions: Our results suggested that the monkey origin-CDV-H protein could possess specific substitutions to adapt to the new host. Monkey-BJ01-DV can efficiently use monkey- and dog-origin SLAM to infect and replicate in host cells, but further adaptation may be required for efficient replication in host cells expressing the human SLAM receptor.

Keywords: Canine distemper virus (CDV); H protein; Monkey; SLAM.

MeSH terms

  • Animals
  • China
  • Chlorocebus aethiops / virology
  • Distemper Virus, Canine / isolation & purification*
  • Distemper Virus, Canine / physiology*
  • Dogs
  • Host-Pathogen Interactions / genetics
  • Humans
  • Lung / virology
  • Monkey Diseases / virology*
  • Receptors, Cell Surface / genetics*
  • Vero Cells
  • Virus Replication / physiology*

Substances

  • Receptors, Cell Surface