EAGER: Collaborative Research: Mechanisms of Establishing and Maintaining an Algal Endosymbiont in a Vertebrate Host
EAGER: Collaborative Research: Mechanisms of Establishing and Maintaining an Algal Endosymbiont in a Vertebrate Host
批准号:
1428062
负责人:
Ryan Kerney
金额:
$3.34万
依托单位:
依托单位国家:
美国
项目类别:
Standard Grant
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-06-01 至 2016-05-31
中文摘要
研究人员最近发现了第一个有益的共生藻类进入脊椎动物宿主细胞的例子。宿主是北美东部常见的斑点蝾螈(Ambystoma maculatum)。绿藻共生体进入蝾螈胚胎的组织和细胞后,他们开始在临时的春季池发育。该项目将使用多种实验方法,包括细胞共培养、mRNA测序和基于激光的细胞分选,以确定藻类细胞进入蝾螈宿主的机制以及这种独特关联的生理含义。该项目的成功完成也将为在藻类共生体和蝾螈宿主中引入外源基因(转基因)提供新的工具,这将使进一步研究这种密切联系的细胞和分子机制成为可能。该项目将包括对葛底斯堡学院本科生的培训,培训内容包括多种蝾螈的实地取样,以及细胞培养、细胞分选和下一代测序方面的先进技术。该项目还将通过美国自然历史博物馆(AMNH)支持一个博物馆视频展览,并资助该博物馆的博士后研究员。本项目概述了几个高风险高回报的实验,这些实验将显著促进我们对这种密切联系的分子机制的理解,并为未来的研究提供一套研究工具。实现这些目标将采用的方法包括:从纽约州、宾夕法尼亚州和华盛顿州收集蝾螈胚胎;培养两种蝾螈的胚胎及其藻类,并在宿主之间切换共生体;藻类内共生寄主细胞的解离和荧光活化细胞分选转录组学和伴随的生物信息学来确定宿主+内共生细胞群体中的差异表达基因;建立寄主内胚层细胞与藻类共生体体外共培养的方法利用在密切相关的模式生物中建立的协议和载体进行宿主和共生体细胞培养的试点转基因转化。这项工作的结果将揭示宿主如何?S对有益共生体的反应可能不同于已知脊椎动物对进入宿主细胞的有害病原体的反应。
英文摘要
The investigators have recently discovered the first example of a beneficial, symbiotic alga entering cells of a vertebrate host. The host in this association is the common spotted salamander (Ambystoma maculatum) from Eastern North America. The green algal symbiont enters tissues and cells of the salamander embryos soon after they begin development in temporary vernal pools. The project will use several experimental approaches, including cell co-culturing, mRNA sequencing, and laser-based cell sorting, to determine the mechanisms of algal cell entry into the salamander host and the physiological implications of this unique association. The successful completion of this project will also make new tools available for introducing foreign genes (transgenics) in both the algal symbiont and salamander host, which will allow further investigation into the cellular and molecular mechanisms that enable this intimate association. The project will include training of undergraduate students from Gettysburg College in both field sampling of multiple salamander species as well as advanced techniques in cell culture, cell sorting, and next generation sequencing. The project will also support a museum video exhibit through the American Museum of Natural History (AMNH), and fund a post-doctoral researcher at the museum. This project outlines several high-risk high-reward experiments that will significantly advance our understanding of the molecular mechanisms of this intimate association and provide a suite of research tools for future investigations. The methods that will be employed to accomplish these goals include: Collecting salamander embryos from New York, Pennsylvania and Washington State; Culturing embryos and their algae from two salamander species and switching symbionts between hosts; Dissociation and fluorescence-activated cell sorting (FACS) of host cells containing algal endosymbionts; Transcriptomics and accompanying bioinformatics to determine differentially expressed genes in the host+endosymbiont cell population; Establishing host endoderm cell culture for in vitro co-culturing with algal symbionts; Pilot transgene transformation of both host and symbiont cell cultures using protocols and vectors established in closely related model organisms. The results from this work will reveal how a host?s response to a beneficial symbiont can differ from known vertebrate reactions to harmful pathogens that enter host cells.
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