Soborowski Andrew L, Hackley Rylee K, Hwang Sungmin, Zhou Guangyin, Dulmage Keely A, Schönheit Peter, Daniels Charles, Bisson-Filho Alexandre W, Marchfelder Anita, Maupin-Furlow Julie A, Allers Thorsten, Schmid Amy K
Department of Biology, Duke University, Durham, North Carolina, USA.
Computational Biology and Bioinformatics Graduate Program, Duke University, Durham, North Carolina, USA.
mSystems. 2025 Feb 18;10(2):e0108424. doi: 10.1128/msystems.01084-24. Epub 2025 Jan 10.
Archaeal molecular biology has been a topic of intense research in recent decades as their role in global ecosystems, nutrient cycles, and eukaryotic evolution comes to light. The hypersaline-adapted archaeal species and serve as important model organisms for understanding archaeal genomics, genetics, and biochemistry, in part because efficient tools enable genetic manipulation. As a result, the number of strains in circulation among the haloarchaeal research community has increased in recent decades. However, the degree of genetic divergence and effects on genetic integrity resulting from the creation and inter-lab transfer of novel lab stock strains remain unclear. To address this, we performed whole-genome re-sequencing on a cross-section of wild-type, parental, and knockout strains in both model species. Integrating these data with existing repositories of re-sequencing data, we identify mutations that have arisen in a collection of 60 strains, sampled from two species across eight different labs. Independent of sequencing, we construct strain lineages, identifying branch points and significant genetic events in strain history. Combining this with our sequencing data, we identify small clusters of mutations that definitively separate lab strains. Additionally, an analysis of gene knockout strains suggests that roughly one in three strains currently in use harbors second-site mutations of potential phenotypic impact. Overall, we find that divergence among lab strains is thus far minimal, though as the archaeal research community continues to grow, careful strain provenance and genomic re-sequencing are required to keep inter-lab divergence to a minimum, prevent the compounding of mutations into fully independent lineages, and maintain the current high degree of reproducible research between lab groups.
Archaea are a domain of microbial life whose member species play a critical role in the global carbon cycle, climate regulation, the human microbiome, and persistence in extreme habitats. In particular, hypersaline-adapted archaea are important, genetically tractable model organisms for studying archaeal genetics, genomics, and biochemistry. As the archaeal research community grows, keeping track of the genetic integrity of strains of interest is necessary. In particular, routine genetic manipulations and the common practice of sharing strains between labs allow mutations to arise in lab stocks. If these mutations affect cellular processes, they may jeopardize the reproducibility of work between research groups and confound the results of future studies. In this work, we examine DNA sequences from 60 strains across two species of archaea. We identify shared and unique mutations occurring between and within strains. Independently, we trace the lineage of each strain, identifying which genetic manipulations lead to observed off-target mutations. While overall divergence across labs is minimal so far, our work highlights the need for labs to continue proper strain husbandry.
近几十年来,古菌分子生物学一直是深入研究的课题,因为它们在全球生态系统、营养循环和真核生物进化中的作用逐渐显现出来。适应高盐环境的古菌物种和作为理解古菌基因组学、遗传学和生物化学的重要模式生物,部分原因是有效的工具能够实现基因操作。因此,近几十年来,古菌研究界流通的菌株数量有所增加。然而,新型实验室储备菌株的创建和实验室间转移所导致的遗传差异程度及其对遗传完整性的影响仍不清楚。为了解决这个问题,我们对两种模式物种的野生型、亲本和基因敲除菌株的横截面进行了全基因组重测序。将这些数据与现有的重测序数据存储库相结合,我们识别出从八个不同实验室的两个物种中采样的60株菌株中出现的突变。独立于测序,我们构建菌株谱系,识别菌株历史中的分支点和重大遗传事件。将此与我们的测序数据相结合,我们识别出明确区分实验室菌株的小突变簇。此外,对基因敲除菌株的分析表明,目前使用的菌株中大约三分之一含有可能具有表型影响的第二位点突变。总体而言,我们发现到目前为止实验室菌株之间的差异很小,不过随着古菌研究界的持续发展,需要仔细追踪菌株来源并进行基因组重测序,以将实验室间的差异降至最低,防止突变累积形成完全独立的谱系,并维持目前实验室小组之间高度可重复的研究。
古菌是微生物生命的一个领域,其成员物种在全球碳循环、气候调节、人类微生物组以及在极端栖息地的生存中发挥着关键作用。特别是,适应高盐环境的古菌是研究古菌遗传学、基因组学和生物化学的重要、易于进行基因操作的模式生物。随着古菌研究界的发展,跟踪感兴趣菌株的遗传完整性是必要的。特别是,常规的基因操作以及实验室之间共享菌株的普遍做法会使实验室储备菌株中出现突变。如果这些突变影响细胞过程,它们可能会危及研究小组之间工作的可重复性,并混淆未来研究的结果。在这项工作中,我们检查了来自两种古菌的60株菌株的DNA序列。我们识别出菌株之间和菌株内部出现的共享和独特突变。独立地,我们追踪每个菌株的谱系,识别哪些基因操作导致观察到的脱靶突变。虽然到目前为止各实验室之间的总体差异很小,但我们的工作强调了实验室继续妥善保存菌株的必要性。