Using Next Generation Sequencing to Identify and Quantify the Genetic Composition of Resistance-Breaking Commercial Isolates of Cydia pomonella Granulovirus

Viruses. 2017 Sep 4;9(9):250. doi: 10.3390/v9090250.

Abstract

The use of Cydia pomonella granulovirus (CpGV) isolates as biological control agents of codling moth (CM) larvae is important in organic and integrated pome fruit production worldwide. The commercially available isolates CpGV-0006, CpGV-R5, and CpGV-V15 have been selected for the control of CpGV resistant CM populations in Europe. In infection experiments, CpGV-0006 and CpGV-R5 were able to break type I resistance and to a lower extent also type III resistance, whereas CpGV-V15 overcame type I and the rarely occurring type II and type III resistance. The genetic background of the three isolates was investigated with next generation sequencing (NGS) tools by comparing their nucleotide compositions to whole genome alignments of five CpGV isolates representing the known genetic diversity of the CpGV genome groups A to E. Based on the distribution of single nucleotide polymorphisms (SNPs) in Illumina sequencing reads, we found that the two isolates CpGV-0006 and CpGV-R5 have highly similar genome group compositions, consisting of about two thirds of the CpGV genome group E and one third of genome group A. In contrast, CpGV-V15 is composed of equal parts of CpGV genome group B and E. According to the identified genetic composition of these isolates, their efficacy towards different resistance types can be explained and predictions on the success of resistance management strategies in resistant CM populations can be made.

Keywords: Baculoviridae; codling moth; genome composition; genome diversity; granulovirus; resistance; resistance management; resistance testing; single nucleotide polymorphism (SNP).

MeSH terms

  • Animals
  • Europe
  • Genetic Variation
  • Genome, Viral*
  • Granulovirus / genetics*
  • Granulovirus / isolation & purification
  • Granulovirus / pathogenicity
  • Granulovirus / physiology*
  • High-Throughput Nucleotide Sequencing / methods*
  • Larva / virology
  • Moths / virology*
  • Pest Control, Biological
  • Polymorphism, Single Nucleotide