Abstract

Some DNA viruses infect host animals usually by integrating their DNAs into the host genome. However, the mechanisms for integration remain largely unknown. Here, we find that Cotesia vestalis bracovirus (CvBV), a polydnavirus of the parasitic wasp C. vestalis (Haliday), integrates its DNA circles into host Plutella xylostella (L.) genome by two distinct strategies, conservatively and randomly, through high-throughput sequencing analysis. We confirmed that the conservatively integrating circles contain an essential “8+5” nucleotides motif which is required for integration. Then we find CvBV circles are integrated into the caterpillar’s genome in three temporal patterns, the early, mid and late stage-integration. We further identify that three CvBV-encoded integrases are responsible for some, but not all of the virus circle integrations, indeed they mainly participate in the processes of early stage-integration. Strikingly, we find two P. xylostella retroviral integrases (PxIN1 and PxIN2) are highly induced upon wasp parasitism, and PxIN1 is crucial for integration of some other early-integrated CvBV circles, such as CvBV_04, CvBV_12 and CvBV_24, while PxIN2 is important for integration of a late-integrated CvBV circle, CvBV_21. Our data uncover a novel mechanism in which CvBV integrates into the infected host genome, not only by utilizing its own integrases, but also by recruiting host enzymes. These findings will strongly deepen our understanding of how bracoviruses regulate and integrate into their hosts.

Highlights

  • DNA viruses use DNAs as their genetic material and generally infect and replicate in host cells

  • Polydnaviruses (PDVs) are a special kind of DNA virus associated parasitic wasps, which do not replicate in their infected caterpillar hosts

  • We identified 218 open reading frames (ORFs) including 13 gene families, which are shown in S2 Table

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Summary

Introduction

DNA viruses use DNAs as their genetic material and generally infect and replicate in host cells. PDV particles with multiple segments of double-stranded, superhelical DNAs, were firstly observed about 50 years ago [1,2] They were recognized as a virus family Polydnaviridae in 1991, which was classified into two genera, bracoviruses (BVs) and ichnoviruses (IVs), associated with the two largest parasitoid groups, Braconidae and Ichneumonidae, respectively [3]. PDV virions are injected into hosts (the caterpillars of Lepidopteramoth and butterfly, the second host of PDVs) during parasitoid oviposition. They are reported to infect most of host immune cells, and many other tissue cells as well [7,8,9], but PDVs do not replicate in host cells [10,11]

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