A high-throughput behavioral screening platform for measuring chemotaxis by C. elegans.

IF 9.8 1区 生物学 Q1 Agricultural and Biological Sciences
PLoS Biology Pub Date : 2024-06-27 eCollection Date: 2024-06-01 DOI:10.1371/journal.pbio.3002672
Emily Fryer, Sujay Guha, Lucero E Rogel-Hernandez, Theresa Logan-Garbisch, Hodan Farah, Ehsan Rezaei, Iris N Mollhoff, Adam L Nekimken, Angela Xu, Lara Selin Seyahi, Sylvia Fechner, Shaul Druckmann, Thomas R Clandinin, Seung Y Rhee, Miriam B Goodman
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引用次数: 0

Abstract

Throughout history, humans have relied on plants as a source of medication, flavoring, and food. Plants synthesize large chemical libraries and release many of these compounds into the rhizosphere and atmosphere where they affect animal and microbe behavior. To survive, nematodes must have evolved the sensory capacity to distinguish plant-made small molecules (SMs) that are harmful and must be avoided from those that are beneficial and should be sought. This ability to classify chemical cues as a function of their value is fundamental to olfaction and represents a capacity shared by many animals, including humans. Here, we present an efficient platform based on multiwell plates, liquid handling instrumentation, inexpensive optical scanners, and bespoke software that can efficiently determine the valence (attraction or repulsion) of single SMs in the model nematode, Caenorhabditis elegans. Using this integrated hardware-wetware-software platform, we screened 90 plant SMs and identified 37 that attracted or repelled wild-type animals but had no effect on mutants defective in chemosensory transduction. Genetic dissection indicates that for at least 10 of these SMs, response valence emerges from the integration of opposing signals, arguing that olfactory valence is often determined by integrating chemosensory signals over multiple lines of information. This study establishes that C. elegans is an effective discovery engine for determining chemotaxis valence and for identifying natural products detected by the chemosensory nervous system.

用于测量秀丽隐杆线虫趋化性的高通量行为筛选平台
纵观历史,人类一直依赖植物作为药物、调味品和食物的来源。植物会合成大量化学物质,并将其中许多化合物释放到根瘤菌圈和大气中,影响动物和微生物的行为。为了生存,线虫必须进化出分辨植物制造的小分子(SMs)的感官能力,这些小分子是有害的、必须避免的,而那些是有益的、应该寻找的。这种根据化学线索的价值对其进行分类的能力是嗅觉的基础,也是包括人类在内的许多动物所共有的能力。在这里,我们展示了一个基于多孔板、液体处理仪器、廉价光学扫描仪和定制软件的高效平台,它能有效地确定模式线虫秀丽隐杆线虫体内单个 SM 的价态(吸引或排斥)。利用这个硬件-软件-软件集成平台,我们筛选了 90 种植物 SM,发现 37 种能吸引或排斥野生型动物,但对化学感觉传导缺陷突变体没有影响。基因分析表明,至少有 10 种 SM 的反应价位是通过整合对立信号而产生的,这表明嗅觉价位往往是通过整合多种信息的化学感觉信号而决定的。这项研究证明,草履虫是一种有效的发现引擎,可用于确定趋化性价位和鉴定由化学感觉神经系统检测到的天然产品。
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来源期刊
PLoS Biology
PLoS Biology BIOCHEMISTRY & MOLECULAR BIOLOGY-BIOLOGY
CiteScore
15.40
自引率
2.00%
发文量
359
审稿时长
3-8 weeks
期刊介绍: PLOS Biology is the flagship journal of the Public Library of Science (PLOS) and focuses on publishing groundbreaking and relevant research in all areas of biological science. The journal features works at various scales, ranging from molecules to ecosystems, and also encourages interdisciplinary studies. PLOS Biology publishes articles that demonstrate exceptional significance, originality, and relevance, with a high standard of scientific rigor in methodology, reporting, and conclusions. The journal aims to advance science and serve the research community by transforming research communication to align with the research process. It offers evolving article types and policies that empower authors to share the complete story behind their scientific findings with a diverse global audience of researchers, educators, policymakers, patient advocacy groups, and the general public. PLOS Biology, along with other PLOS journals, is widely indexed by major services such as Crossref, Dimensions, DOAJ, Google Scholar, PubMed, PubMed Central, Scopus, and Web of Science. Additionally, PLOS Biology is indexed by various other services including AGRICOLA, Biological Abstracts, BIOSYS Previews, CABI CAB Abstracts, CABI Global Health, CAPES, CAS, CNKI, Embase, Journal Guide, MEDLINE, and Zoological Record, ensuring that the research content is easily accessible and discoverable by a wide range of audiences.
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