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Published January 2022 | Submitted
Journal Article Open

The entomopathogenic nematode Steinernema hermaphroditum is a self-fertilizing hermaphrodite and a genetically tractable system for the study of parasitic and mutualistic symbiosis

Abstract

Entomopathogenic nematodes (EPNs), including Heterorhabditis and Steinernema, are parasitic to insects and contain mutualistically symbiotic bacteria in their intestines (Photorhabdus and Xenorhabdus, respectively) and therefore offer opportunities to study both mutualistic and parasitic symbiosis. The establishment of genetic tools in EPNs has been impeded by limited genetic tractability, inconsistent growth in vitro, variable cryopreservation, and low mating efficiency. We obtained the recently described Steinernema hermaphroditum strain CS34 and optimized its in vitro growth, with a rapid generation time on a lawn of its native symbiotic bacteria Xenorhabdus griffiniae. We developed a simple and efficient cryopreservation method. Previously, S. hermaphroditum isolated from insect hosts was described as producing hermaphrodites in the first generation. We discovered that CS34, when grown in vitro, produced consecutive generations of autonomously reproducing hermaphrodites accompanied by rare males. We performed mutagenesis screens in S. hermaphroditum that produced mutant lines with visible and heritable phenotypes. Genetic analysis of the mutants demonstrated that this species reproduces by self-fertilization rather than parthenogenesis and that its sex is determined chromosomally. Genetic mapping has thus far identified markers on the X chromosome and three of four autosomes. We report that S. hermaphroditum CS34 is the first consistently hermaphroditic EPN and is suitable for genetic model development to study naturally occurring mutualistic symbiosis and insect parasitism.

Additional Information

© The Author(s) 2021. Published by Oxford University Press on behalf of Genetics Society of America. This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model). Received: 25 August 2021; Accepted: 29 September 2021; Published: 11 October 2021; Corrected and typeset: 17 November 2021. We are overwhelmingly grateful for S. hermaphroditum as a generous gift from nature and a superb organism to explore scientific curiosities. We thank Adler Dillman of University of California Riverside for generously sharing the S. hermaphroditum-India strain CS34 and for comments on this manuscript. We also thank Heidi Goodrich-Blair and Jennifer Heppert of the University of Tennessee Knoxville for helpful discussions and editorial suggestions. We are also grateful for valuable suggestions from Zuzana Kocsisova. We appreciate our correspondence with Christine Griffin on the mode of reproduction of S. hermaphroditum-Indonesia. The monoclonal anti-MSP antibody 4A5 developed by David Greenstein of the University of Minnesota was obtained from the Developmental Studies Hybridoma Bank, created by the NICHD of the NIH and maintained at The University of Iowa Department of Biology. Bacterial strains HB101 and DA1877 were obtained from the Caenorhabditis Genetics Center (CGC), which is funded by the NIH Office of Research Infrastructure Programs (P40 OD010440). This work was also facilitated by WormBase and ParaSite, a knowledgebase for nematode research. Figures 2D and 5A are created with BioRender.com. This research was supported by National Institutes of Health (NIH) Ruth L. Kirschstein National Research Service Award (NRSA) Individual Postdoctoral Fellowship F32 5F32GM131570 (M.C.); National Science Foundation (NSF) Enabling Discovery through GEnomics (EDGE) grant 2128267, and the Center for Evolutionary Science at California Institute of Technology. Data availability: Strains described in this work are available upon request. 16S rRNA gene sequences of the X. griffiniae bacterial symbionts of the S. hermaphroditum isolate CS34 are available in the Genbank database. The accession numbers for 16S rRNA sequence (including HGB2511) are MZ913116–MZ913125. Supplemental material is available at figshare: https://doi.org/10.25386/genetics.16689217. The authors declare that there is no conflict of interest.

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Additional details

Created:
August 22, 2023
Modified:
December 22, 2023