Single nucleotide polymorphism (SNP) marker-assisted breeding of Heterorhabditis bacteriophora for improvement of reproductive potential and stress tolerance

IF 1.2 4区 生物学 Q2 ZOOLOGY Nematology Pub Date : 2024-02-06 DOI:10.1163/15685411-bja10307
Christopher Ogaya, Michelle Ann B. Diano, Innocent Hategekimana, Verena Dörfler, Carlos Molina, Ralf-Udo Ehlers
{"title":"Single nucleotide polymorphism (SNP) marker-assisted breeding of Heterorhabditis bacteriophora for improvement of reproductive potential and stress tolerance","authors":"Christopher Ogaya, Michelle Ann B. Diano, Innocent Hategekimana, Verena Dörfler, Carlos Molina, Ralf-Udo Ehlers","doi":"10.1163/15685411-bja10307","DOIUrl":null,"url":null,"abstract":"\nThe entomopathogenic nematode (EPN), Heterorhabditis bacteriophora, is an efficient biological control agent against several economically important insect pests. Recent research has assessed the possibility to correlate desired beneficial traits with genotype data to pave a way for marker-assisted breeding approaches. A collection of H. bacteriophora WT inbred lines has been phenotyped in this framework for stress- and virulence-related traits. However, these traits are rarely combined in a single line. Thus, unifying these traits in commercial strains is of high priority. This investigation unified beneficial traits in hybrid pools through marker-assisted breeding using single nucleotide polymorphisms (SNPs) associated with reproductive potential, longevity, virulence and cold tolerance. Recombinant inbred lines (RILs) generated from a cross between a stress tolerant WT inbred line (XX21) and a line high in in vitro reproduction potential (IL3) were genotyped via SeqSNP and screened for SNP markers associated with beneficial traits. Thereafter, a genotypic pool (X21L3) comprising 22 ILs was formed. The X21L3 pool was subsequently evaluated for the target traits in comparison with the cross parents and a commercial strain HB4. An improvement of oxidative stress tolerance at 2°C (cold tolerance) was recorded with X21L3 surviving 1 day longer than the best performing parent (XX21). The hybrid pool also survived 1 day longer than the least performing parent IL3 for the trait longevity at 25°C under oxidative stress conditions. A higher dauer juvenile (DJ) recovery (58%) and DJ yield (209 000 DJ ml−1) than the least performing parent XX21 was recorded for the pool. The storage stability in diatomaceous earth formulation at 2°C and 7.5°C was also improved by 2 and 5 days, respectively, in comparison to the least performing parent XX21. This study depicts the potential of precision marker-assisted breeding for beneficial trait improvement of H. bacteriophora.","PeriodicalId":18928,"journal":{"name":"Nematology","volume":null,"pages":null},"PeriodicalIF":1.2000,"publicationDate":"2024-02-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nematology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1163/15685411-bja10307","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ZOOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The entomopathogenic nematode (EPN), Heterorhabditis bacteriophora, is an efficient biological control agent against several economically important insect pests. Recent research has assessed the possibility to correlate desired beneficial traits with genotype data to pave a way for marker-assisted breeding approaches. A collection of H. bacteriophora WT inbred lines has been phenotyped in this framework for stress- and virulence-related traits. However, these traits are rarely combined in a single line. Thus, unifying these traits in commercial strains is of high priority. This investigation unified beneficial traits in hybrid pools through marker-assisted breeding using single nucleotide polymorphisms (SNPs) associated with reproductive potential, longevity, virulence and cold tolerance. Recombinant inbred lines (RILs) generated from a cross between a stress tolerant WT inbred line (XX21) and a line high in in vitro reproduction potential (IL3) were genotyped via SeqSNP and screened for SNP markers associated with beneficial traits. Thereafter, a genotypic pool (X21L3) comprising 22 ILs was formed. The X21L3 pool was subsequently evaluated for the target traits in comparison with the cross parents and a commercial strain HB4. An improvement of oxidative stress tolerance at 2°C (cold tolerance) was recorded with X21L3 surviving 1 day longer than the best performing parent (XX21). The hybrid pool also survived 1 day longer than the least performing parent IL3 for the trait longevity at 25°C under oxidative stress conditions. A higher dauer juvenile (DJ) recovery (58%) and DJ yield (209 000 DJ ml−1) than the least performing parent XX21 was recorded for the pool. The storage stability in diatomaceous earth formulation at 2°C and 7.5°C was also improved by 2 and 5 days, respectively, in comparison to the least performing parent XX21. This study depicts the potential of precision marker-assisted breeding for beneficial trait improvement of H. bacteriophora.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
单核苷酸多态性(SNP)标记辅助细菌杂环虫育种以提高繁殖潜力和抗逆性
昆虫病原线虫(EPN)--细菌异habditis bacteriophora--是一种高效的生物防治剂,可防治多种具有重要经济价值的害虫。最近的研究评估了将所需的有益性状与基因型数据相关联的可能性,从而为标记辅助育种方法铺平道路。在这一框架下,已对一系列菌核病 WT 近交系进行了压力和毒力相关性状的表型分析。然而,这些性状很少结合在一个品系中。因此,在商业品系中统一这些性状是当务之急。这项研究通过使用与繁殖潜力、寿命、毒力和耐寒性相关的单核苷酸多态性(SNPs)进行标记辅助育种,统一了杂交种池中的有益性状。通过 SeqSNP 对抗逆性强的 WT 近交系(XX21)和体外繁殖潜力高的品系(IL3)杂交产生的重组近交系(RIL)进行基因分型,并筛选与有益性状相关的 SNP 标记。之后,形成了一个由 22 个 IL 组成的基因型库(X21L3)。随后,通过与杂交亲本和商业菌株 HB4 的比较,对 X21L3 基因库的目标性状进行了评估。结果表明,X21L3 比表现最好的亲本(XX21)多存活 1 天,从而提高了在 2°C 下的氧化应激耐受性(耐寒性)。在 25°C 的氧化胁迫条件下,杂种池的寿命也比表现最差的亲本 IL3 长 1 天。与表现最差的亲本 XX21 相比,该杂交种池的 Dauer 幼虫(DJ)恢复率(58%)和 DJ 产量(209 000 DJ ml-1)都更高。与性能最差的亲本 XX21 相比,硅藻土制剂在 2°C 和 7.5°C 下的储存稳定性也分别提高了 2 天和 5 天。这项研究展示了精确标记辅助育种在改良菌核病有益性状方面的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Nematology
Nematology 生物-动物学
CiteScore
2.60
自引率
33.30%
发文量
67
审稿时长
3 months
期刊介绍: Nematology is an international journal for the publication of all aspects of nematological research (with the exception of vertebrate parasitology), from molecular biology to field studies. Papers on nematode parasites of arthropods, and on soil free-living nematodes, and on interactions of these and other organisms, are particularly welcome. Research on fresh water and marine nematodes is also considered when the observations are of more general interest. Nematology publishes full research papers, short communications, Forum articles (which permit an author to express a view on current or fundamental subjects), perspectives on nematology, and reviews of books and other media.
期刊最新文献
Redescription of two species of the genus Tricirronema Siddiqi, 1993 (Rhabditida, Bicirronematidae) from Vietnam, including SEM study for both species Unveiling novel and known Cryptaphelenchus species from China and USA Skrjabinomermis pirnaimi sp. n. (Nematoda: Mermithidae) from Iran: A morphological and molecular phylogenetic study Delving into the diversity of genus Ironus Bastian, 1865 with special reference to Ironus dentifurcatus Argo & Heyns, 1972 (Ironidae: Enoplida), collected from coal mines Description of Longidorus sanlitanensis n. sp. (Dorylaimida: Longidoridae) from the rhizosphere of Melilotoides ruthenica and Chamaerhodos erecta in China
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1