海水后生动物细胞的分离与遗传鉴定

IF 6.2 Q1 Agricultural and Biological Sciences
Haylea Power, Mitchell J. O'Brien, Miwa Takahashi, Henry Hui, Kathy Fuller, Darren Korbie, Oliver Berry, Simon Jarman
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引用次数: 0

摘要

环境DNA (eDNA)元条形码通常依赖于从环境样本中收集和描述混合的、碎片化的DNA池,以进行物种鉴定。在这里,我们引入了环境后生细胞(emCells),代表了大型生物进入水生生态系统的整个个体细胞,并报道了一种成功分离和扩增短扩增子以确定物种身份的方法。使用定制的鱼类探针和一种新型的多因子荧光激活细胞分选(FACS)方案,我们成功地富集了目标emCells,正如使用FACS和成像流式细胞术的人口密度变化所证实的那样。成像流式细胞术证实了整个单细胞的双重核和线粒体染色,而多重PCR测定(针对线粒体和核DNA)证实了鱼的emCells的有效富集,其中四分之一的分类细胞被鉴定为鱼。从分离的emCells中获得的序列与已知的中胚层物种相匹配,验证了我们的方法。尽管努力排除非靶细胞,但多种单细胞真核生物也得到了恢复,这突出了考虑到水生环境中存在的脱靶颗粒的丰富性和多样性,需要额外的策略来富集靶细胞,这对现实环境尤为重要。emCells的分离和分析可以通过提供通常需要从活生物体直接取样的基因组信息,为当前的eDNA方法提供一种通用的补充方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Isolation and Genetic Identification of Metazoan Cells From Seawater

Isolation and Genetic Identification of Metazoan Cells From Seawater

Environmental DNA (eDNA) metabarcoding typically relies on collecting and characterising a pool of mixed, fragmented DNA from environmental samples for species identification. Here, we introduce environmental metazoan cells (emCells), representing whole individual cells shed by macro-organisms into aquatic ecosystems, and report on a method to successfully isolate and amplifying short amplicons to determine species identity. Using a custom fish probe and a novel multi-factor fluorescence-activated cell sorting (FACS) protocol on mesocosm water samples, we successfully enriched for target emCells, as confirmed by shifts in population density using FACS and imaging flow cytometry. Imaging flow cytometry demonstrated dual nuclear and mitochondrial staining of whole single cells, while multiplexed PCR assays (targeting both mitochondrial and nuclear DNA) confirmed the effective enrichment of fish emCells, with one-quarter of sorted cells identified as fish. Sequences obtained from isolated emCells matched known species in the mesocosm, validating our approach. Despite efforts to exclude non-target cells, diverse single-cell eukaryotes were also recovered, highlighting the need for additional strategies to enrich for target emCells given the abundance and diversity of off-target particles present in aquatic environments, which will be especially important for real-world environments. Isolation and analysis of emCells could provide a versatile complementary approach to current eDNA methodologies by providing genomic information that normally requires direct sampling from live organisms.

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来源期刊
Environmental DNA
Environmental DNA Agricultural and Biological Sciences-Ecology, Evolution, Behavior and Systematics
CiteScore
11.00
自引率
0.00%
发文量
99
审稿时长
16 weeks
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