Genomic patterns of strain-specific genetic structure, linkage, and selection across fall armyworm populations.

IF 3.7 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY BMC Genomics Pub Date : 2025-02-07 DOI:10.1186/s12864-025-11214-8
Ashley E Tessnow, Rodney N Nagoshi, Robert L Meagher, Todd M Gilligan, Ben M Sadd, Yves Carrière, Holly N Davis, Shelby J Fleischer, Kelly Richers, John C Palumbo, Patrick Porter, Jose Carlos Verle Rodrigues, Gregory A Sword
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Abstract

Background: Molecular genetic approaches have become vital to understanding the evolutionary processes that act on insect pest populations. From mapping the development of resistance to monitoring and predicting pest movement, genomic tools can inform and enhance pest management programs. Here, we used whole genome sequencing population genomics to unravel novel patterns of population structure, linkage, and selection across the genome of a notorious agricultural pest, the fall armyworm.

Results: Our data strongly support the existence of two genetically distinct strains of fall armyworm in North America, which have previously been referred to as the C-strain and the R-strain. Although these strains have diverged genetically, we find that differentiation is not uniform across the genome. The Z-chromosome appears to drive divergence between strains with high levels of linkage observed across this chromosome. We also show that a region of the Z-chromosome containing a circadian clock gene implicated in allochronic reproductive isolation is under strain-specific selection. Our data indicates that strains differ in their geographic distributions and exhibit distinct patterns of geographic sub-structuring indicative of unique dispersal patterns. We provide the first evidence for nuclear genomic differentiation between the two major overwintering populations of fall armyworm in the US. Finally, our data reveal population-specific patterns of selection on genomic regions containing putative insecticide resistance alleles, which could relate to their biogeography.

Conclusions: Our results support the existence of the fall armyworm as a pest dyad in the US, with genetically-distinct strains differing in their population structure, dispersal patterns, and genomic signatures of selection on regions likely involved reproductive isolation and insecticide resistance. These differences should be considered when devising and implementing management strategies.

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品系特异性遗传结构、连锁和秋粘虫种群选择的基因组模式。
背景:分子遗传学方法对于理解作用于害虫种群的进化过程已经变得至关重要。从绘制耐药性的发展到监测和预测害虫的移动,基因组工具可以为害虫管理计划提供信息并加强它们。在这里,我们使用全基因组测序种群基因组学来揭示一种臭名昭著的农业害虫——秋粘虫的种群结构、连锁和选择的新模式。结果:我们的数据强烈支持北美存在两种遗传上不同的秋粘虫菌株,这两种菌株以前被称为c株和r株。虽然这些菌株在遗传上有分歧,但我们发现分化在整个基因组中并不均匀。在z染色体上观察到的高水平连锁似乎驱动了菌株之间的分化。我们还发现,z染色体上含有一个与异速生殖隔离有关的生物钟基因的区域处于菌株特异性选择之下。我们的数据表明,菌株在地理分布上存在差异,并表现出明显的地理亚结构模式,表明其独特的扩散模式。我们提供了美国两个主要秋粘虫越冬种群之间核基因组分化的第一个证据。最后,我们的数据揭示了含有假定杀虫剂抗性等位基因的基因组区域的种群特异性选择模式,这可能与它们的生物地理有关。结论:我们的研究结果支持了秋粘虫在美国作为一种害虫二联体的存在,其种群结构、传播模式和基因组特征的遗传差异可能与生殖隔离和杀虫剂抗性有关。在设计和实施管理战略时应考虑到这些差异。
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来源期刊
BMC Genomics
BMC Genomics 生物-生物工程与应用微生物
CiteScore
7.40
自引率
4.50%
发文量
769
审稿时长
6.4 months
期刊介绍: BMC Genomics is an open access, peer-reviewed journal that considers articles on all aspects of genome-scale analysis, functional genomics, and proteomics. BMC Genomics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
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