Genomes of the entomopathogenic nematode Steinernema hermaphroditum and its associated bacteria.

IF 5.1 3区 生物学 Q2 GENETICS & HEREDITY
Genetics Pub Date : 2025-08-27 DOI:10.1093/genetics/iyaf170
Erich M Schwarz, Anil Baniya, Jennifer K Heppert, Hillel T Schwartz, Chieh-Hsiang Tan, Igor Antoshechkin, Paul W Sternberg, Heidi Goodrich-Blair, Adler R Dillman
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引用次数: 0

Abstract

As an entomopathogenic nematode (EPN), Steinernema hermaphroditum parasitizes insect hosts and harbors symbiotic Xenorhabdus griffinae bacteria. In contrast to other Steinernematids, S. hermaphroditum has hermaphroditic genetics, offering the experimental scope found in Caenorhabditis elegans. To enable study of S. hermaphroditum, we have assembled and analyzed its reference genome. This genome assembly has five chromosomal scaffolds and 83 unassigned scaffolds totaling 90.7 Mb, with 19,426 protein-coding genes having a BUSCO completeness of 88.0%. Its autosomes show higher densities of strongly conserved genes in their centers, as in C. elegans, but repetitive elements are evenly distributed along all chromosomes, rather than with higher arm densities as in C. elegans. Either when comparing protein motif frequencies between nematode species or when analyzing gene family expansions during nematode evolution, we observed two categories of genes preferentially associated with the origin of Steinernema or S. hermaphroditum: orthologs of venom genes in S. carpocapsae or S. feltiae; and some types of chemosensory G protein-coupled receptors, despite the tendency of parasitic nematodes to have reduced numbers of chemosensory genes. Three-quarters of venom orthologs occurred in gene clusters, with the larger clusters comprising functionally diverse gene groups rather than paralogous repeats of a single venom gene. While assembling S. hermaphroditum, we coassembled bacterial genomes, finding sequence data for not only the known symbiont, X. griffinae, but also for eight other bacterial genera. All eight genera have previously been observed to be associated with Steinernema species or the EPN Heterorhabditis, and may constitute a "second bacterial circle" of EPNs.

昆虫病原线虫雌雄同体及其伴生细菌的基因组。
雌雄斯坦纳线虫是一种昆虫病原线虫,寄生于昆虫宿主体内,并携带共生的格里菲纳异芽孢杆菌。与其他隐杆线虫相比,S. hermaphroditum具有雌雄同体的遗传,为秀丽隐杆线虫提供了实验范围。为了便于对雌雄同体的研究,我们对其参考基因组进行了组装和分析。该基因组装配有5个染色体支架和83个未分配支架,总长度为90.7 Mb,包含19426个蛋白质编码基因,BUSCO完整性为88.0%。与秀丽隐杆线虫一样,它的常染色体在其中心显示出更高密度的强保守基因,但重复元件均匀分布在所有染色体上,而不像秀丽隐杆线虫那样具有更高的臂密度。无论是比较不同线虫物种之间的蛋白质基序频率,还是分析线虫进化过程中基因家族的扩展,我们都观察到两类基因优先与Steinernema或S. hermaphroditum的起源相关:S. carpocapsae或S. feltiae的毒液基因同源;以及某些类型的化学感觉G蛋白偶联受体,尽管寄生线虫倾向于减少化学感觉基因的数量。四分之三的毒液同源基因发生在基因簇中,较大的簇由功能不同的基因群组成,而不是单个毒液基因的同源重复。在组装S. hermaphroditum的同时,我们还组装了细菌基因组,不仅找到了已知的共生体X. griffinae的序列数据,还找到了其他8个细菌属的序列数据。所有8个属以前都被观察到与Steinernema种或EPN Heterorhabditis有关,并且可能构成EPN的“第二细菌圈”。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Genetics
Genetics GENETICS & HEREDITY-
CiteScore
6.90
自引率
6.10%
发文量
177
审稿时长
1.5 months
期刊介绍: GENETICS is published by the Genetics Society of America, a scholarly society that seeks to deepen our understanding of the living world by advancing our understanding of genetics. Since 1916, GENETICS has published high-quality, original research presenting novel findings bearing on genetics and genomics. The journal publishes empirical studies of organisms ranging from microbes to humans, as well as theoretical work. While it has an illustrious history, GENETICS has changed along with the communities it serves: it is not your mentor''s journal. The editors make decisions quickly – in around 30 days – without sacrificing the excellence and scholarship for which the journal has long been known. GENETICS is a peer reviewed, peer-edited journal, with an international reach and increasing visibility and impact. All editorial decisions are made through collaboration of at least two editors who are practicing scientists. GENETICS is constantly innovating: expanded types of content include Reviews, Commentary (current issues of interest to geneticists), Perspectives (historical), Primers (to introduce primary literature into the classroom), Toolbox Reviews, plus YeastBook, FlyBook, and WormBook (coming spring 2016). For particularly time-sensitive results, we publish Communications. As part of our mission to serve our communities, we''ve published thematic collections, including Genomic Selection, Multiparental Populations, Mouse Collaborative Cross, and the Genetics of Sex.
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