Cargando…

Penetrance of symbiont-mediated parthenogenesis is driven by reproductive rate in a parasitoid wasp

Trichogramma wasps are tiny parasitoids of lepidopteran eggs, used extensively for biological control. They are often infected with the bacterial symbiont Wolbachia, which converts Trichogramma to an asexual mode of reproduction, whereby females develop from unfertilized eggs. However, this Wolbachi...

Descripción completa

Detalles Bibliográficos
Autores principales: Lindsey, Amelia R.I., Stouthamer, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5490460/
https://www.ncbi.nlm.nih.gov/pubmed/28663939
http://dx.doi.org/10.7717/peerj.3505
_version_ 1783246987990138880
author Lindsey, Amelia R.I.
Stouthamer, Richard
author_facet Lindsey, Amelia R.I.
Stouthamer, Richard
author_sort Lindsey, Amelia R.I.
collection PubMed
description Trichogramma wasps are tiny parasitoids of lepidopteran eggs, used extensively for biological control. They are often infected with the bacterial symbiont Wolbachia, which converts Trichogramma to an asexual mode of reproduction, whereby females develop from unfertilized eggs. However, this Wolbachia-induced parthenogenesis is not always complete, and previous studies have noted that infected females will produce occasional males in the lab. The conditions that reduce penetrance of the parthenogenesis phenotype are not well understood. We hypothesized that more ecologically relevant conditions of limited host access will sustain female-biased sex ratios. After restricting access to host eggs, we found a strong relationship between reproductive rate and sex ratio. By limiting reproduction to one hour a day, wasps could sustain up to 100% effective parthenogenesis for one week, with no significant impact on total fecundity. Reproductive output in the first 24-hours appears to be critical to the total sex ratio of the entire brood. Limiting oviposition in that period resulted in more effective parthenogenesis after one week, again without any significant impact on total fecundity. Our data suggest that this phenomenon may be due to the depletion of Wolbachia when oviposition occurs continuously, whereas Wolbachia titers may recover when offspring production is limited. In addition to the potential to improve mass rearing of Trichogramma for biological control, findings from this study help elucidate the context-dependent nature of a pervasive symbiotic relationship.
format Online
Article
Text
id pubmed-5490460
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher PeerJ Inc.
record_format MEDLINE/PubMed
spelling pubmed-54904602017-06-29 Penetrance of symbiont-mediated parthenogenesis is driven by reproductive rate in a parasitoid wasp Lindsey, Amelia R.I. Stouthamer, Richard PeerJ Ecology Trichogramma wasps are tiny parasitoids of lepidopteran eggs, used extensively for biological control. They are often infected with the bacterial symbiont Wolbachia, which converts Trichogramma to an asexual mode of reproduction, whereby females develop from unfertilized eggs. However, this Wolbachia-induced parthenogenesis is not always complete, and previous studies have noted that infected females will produce occasional males in the lab. The conditions that reduce penetrance of the parthenogenesis phenotype are not well understood. We hypothesized that more ecologically relevant conditions of limited host access will sustain female-biased sex ratios. After restricting access to host eggs, we found a strong relationship between reproductive rate and sex ratio. By limiting reproduction to one hour a day, wasps could sustain up to 100% effective parthenogenesis for one week, with no significant impact on total fecundity. Reproductive output in the first 24-hours appears to be critical to the total sex ratio of the entire brood. Limiting oviposition in that period resulted in more effective parthenogenesis after one week, again without any significant impact on total fecundity. Our data suggest that this phenomenon may be due to the depletion of Wolbachia when oviposition occurs continuously, whereas Wolbachia titers may recover when offspring production is limited. In addition to the potential to improve mass rearing of Trichogramma for biological control, findings from this study help elucidate the context-dependent nature of a pervasive symbiotic relationship. PeerJ Inc. 2017-06-27 /pmc/articles/PMC5490460/ /pubmed/28663939 http://dx.doi.org/10.7717/peerj.3505 Text en ©2017 Lindsey and Stouthamer http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Ecology
Lindsey, Amelia R.I.
Stouthamer, Richard
Penetrance of symbiont-mediated parthenogenesis is driven by reproductive rate in a parasitoid wasp
title Penetrance of symbiont-mediated parthenogenesis is driven by reproductive rate in a parasitoid wasp
title_full Penetrance of symbiont-mediated parthenogenesis is driven by reproductive rate in a parasitoid wasp
title_fullStr Penetrance of symbiont-mediated parthenogenesis is driven by reproductive rate in a parasitoid wasp
title_full_unstemmed Penetrance of symbiont-mediated parthenogenesis is driven by reproductive rate in a parasitoid wasp
title_short Penetrance of symbiont-mediated parthenogenesis is driven by reproductive rate in a parasitoid wasp
title_sort penetrance of symbiont-mediated parthenogenesis is driven by reproductive rate in a parasitoid wasp
topic Ecology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5490460/
https://www.ncbi.nlm.nih.gov/pubmed/28663939
http://dx.doi.org/10.7717/peerj.3505
work_keys_str_mv AT lindseyameliari penetranceofsymbiontmediatedparthenogenesisisdrivenbyreproductiverateinaparasitoidwasp
AT stouthamerrichard penetranceofsymbiontmediatedparthenogenesisisdrivenbyreproductiverateinaparasitoidwasp