Small Things that Make a Big Difference: Single-Cell Transcriptomic of Nanociliates Reveals Genes Potentially Involved in Mixotrophy.

IF 4 3区 生物学 Q2 ECOLOGY
Filomena Romano, Uwe John, Michele Laval-Peuto, Paraskevi Pitta
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Abstract

Nanociliates play an important role in the microbial food web of oligotrophic marine systems as grazers of picoplankton on one side, and as prey for microplankton, on the other. However, knowledge on their taxonomy, phylogeny, and trophic strategies is very limited, as well as their potential role as mixotrophs. In the present study, we investigated the transcriptomes of five marine planktonic nanociliates isolated from the Eastern Mediterranean Sea. Our aim was the following: (i) to characterize the phylogenetic placement of these cells using concatenated phylotranscriptomic and (ii) to identify genes potentially involved in mixotrophy by focusing on both photosynthesis and digestion-related genes (phagosome, lysosome). Phylogenetic reconstruction revealed that two cells clustered with Tintinnida, while the other three clustered with Oligotrichida. Reciprocal best hits (RHBs) BlastP analysis indicated the presence of genes related to photosynthesis across all the transcriptomes, while the detection of genes associated with phagosome, lysosome, and generic metabolic pathways provided a more informative insight into the mechanism of mixotrophy. These findings suggest that photosynthesis-related genes alone may not be sufficient indicators of mixotrophic potential in nanociliates and highlight the importance of considering additional cellular pathways involved in phagotrophy. Moreover, these transcriptomes will help to establish a basis for the evaluation of differential gene expression in Oligotrichida, Choreotrichida, and Tintinnida, and a step stone for mixotrophic investigation.

微小的事物产生巨大的差异:纳米纤毛虫的单细胞转录组学揭示了可能参与混合营养的基因。
纳米纤毛虫在低营养海洋系统的微生物食物网中扮演着重要的角色,一方面是微浮游生物的捕食者,另一方面是微浮游生物的猎物。然而,对它们的分类、系统发育和营养策略以及它们作为混合营养体的潜在作用的了解非常有限。在本研究中,我们研究了从东地中海分离的五种海洋浮游纳米纤毛虫的转录组。我们的目标是:(1)利用串联的系统转录组学来表征这些细胞的系统发育位置;(2)通过关注光合作用和消化相关基因(吞噬体、溶酶体)来鉴定可能参与混合营养的基因。系统发育重建显示,2个细胞与Tintinnida聚集在一起,另外3个细胞与Oligotrichida聚集在一起。互惠最佳匹配(RHBs) BlastP分析表明,在所有转录组中都存在与光合作用相关的基因,而与吞噬体、溶酶体和一般代谢途径相关的基因的检测为了解混合营养的机制提供了更丰富的信息。这些发现表明,单独的光合作用相关基因可能不足以作为纳米纤毛虫混合营养潜能的充分指标,并强调了考虑参与吞噬的其他细胞途径的重要性。此外,这些转录组将有助于为评估寡毛虫、Choreotrichida和Tintinnida的差异基因表达奠定基础,并为混合营养研究奠定基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Microbial Ecology
Microbial Ecology 生物-海洋与淡水生物学
CiteScore
6.90
自引率
2.80%
发文量
212
审稿时长
3-8 weeks
期刊介绍: The journal Microbial Ecology was founded more than 50 years ago by Dr. Ralph Mitchell, Gordon McKay Professor of Applied Biology at Harvard University in Cambridge, MA. The journal has evolved to become a premier location for the presentation of manuscripts that represent advances in the field of microbial ecology. The journal has become a dedicated international forum for the presentation of high-quality scientific investigations of how microorganisms interact with their environment, with each other and with their hosts. Microbial Ecology offers articles of original research in full paper and note formats, as well as brief reviews and topical position papers.
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