Morphological and molecular analyses of season-specific responses of freshwater ciliate communities to top-down and bottom-up experimental manipulations.

IF 4.6 2区 生物学 Q1 MICROBIOLOGY
mSystems Pub Date : 2025-09-23 Epub Date: 2025-08-15 DOI:10.1128/msystems.00304-25
Usman Asghar, Indranil Mukherjee, Bettina Sonntag, Caio César Pires de Paula, Vojtěch Kasalický, Paul-Adrian Bulzu, Anusha Priya Singh, Tanja Shabarova, Kasia Piwosz, Karel Šimek
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引用次数: 0

Abstract

In aquatic microbial food webs, ciliates represent an important trophic link in the energy transfer from prokaryotes, algae, and heterotrophic nanoflagellates (HNFs) to higher trophic levels. However, the trophic role of abundant small ciliates (<20 µm) is not clearly understood. To unveil their trophic linkages, we conducted two experiments manipulating both top-down and bottom-up controlling factors, thus modulating the trophic cascading and bacterial prey availability for protists during contrasting spring and summer seasons with samples collected from a freshwater meso-eutrophic reservoir. Water samples were size fractionated to modify food web complexity, i.e., 10 µm, 20 µm, and unfiltered control and amended with bacterial prey additions. The samples were analyzed by morphological and sequencing techniques. The bacterial amendments triggered strong ciliate growth following the peaks of HNFs in the 10 and 20 µm treatments, reflecting a trophic cascading from HNFs to raptorial prostome ciliates (Balanion planctonicum and Urotricha spp.) in spring. In summer, HNFs and ciliates peaked simultaneously, suggesting the important trophic cascade also from bacteria to bacterivorous scuticociliates (Cyclidium glaucoma and Cinetochilum margaritaceum) and HNFs. In spring, unfiltered treatments showed stronger ciliate top-down control by zooplankton than in summer. The sequence analysis revealed season-specific manipulation-induced shifts in ciliate communities and their large cryptic diversity. However, morphological and molecular analyses also revealed considerable discrepancies in the abundance of major ciliate taxa. The ciliate communities responded to our experimental manipulations in season-specific fashions, thereby highlighting the different roles of ciliates as an intermediate trophic link between prokaryotes and higher trophic levels.

Importance: Ciliates represent an important trophic link in aquatic microbial food webs. In this study, we used the food web manipulation techniques to reveal their complex trophic interactions during seasonally different plankton scenarios occurring in spring and summer. Manipulating top-down controlling factors (grazing pressure of micro- and metazooplankton grazers) and bottom-up factors (an availability of bacterial prey) shaped distinctly the complexity and dynamics of natural plankton communities and thus yielded significant changes in ciliate community dynamics. The experimentally simplified plankton and ciliate communities responded to our manipulations in season-specific fashions, reflected in different roles of ciliates as an intermediate trophic link between prokaryotes and higher trophic levels. This study also demonstrates that the combination of molecular and morphological analyses is essential to gain more realistic insights into the structure of ciliate community and for providing robust, ecologically meaningful results.

Abstract Image

Abstract Image

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淡水纤毛虫群落对自上而下和自下而上实验操作的季节特异性响应的形态学和分子分析。
在水生微生物食物网中,纤毛虫是原核生物、藻类和异养纳米鞭毛虫(hnf)向更高营养水平转移能量的重要营养环节。然而,丰富的小纤毛虫(Balanion plantonicum和Urotricha spp)在春季的营养作用。在夏季,hnf和纤毛虫同时达到峰值,表明重要的营养级联也从细菌到细菌寄生的scuticociates (Cyclidium glaucoma和Cinetochilum margaritaceum)和hnf。春季未过滤处理浮游动物对纤毛虫自上而下的控制强于夏季处理。序列分析揭示了季节特异性操纵引起的纤毛虫群落变化及其巨大的隐多样性。然而,形态学和分子分析也揭示了主要纤毛虫类群的丰度存在相当大的差异。纤毛虫群落以特定季节的方式响应我们的实验操作,从而突出了纤毛虫作为原核生物和更高营养水平之间的中间营养环节的不同作用。重要性:纤毛虫是水生微生物食物网中重要的营养环节。在本研究中,我们利用食物网操纵技术揭示了它们在春夏季不同季节浮游生物情景下复杂的营养相互作用。自上而下的控制因素(微浮游动物和中游浮游动物的放牧压力)和自下而上的控制因素(细菌猎物的可利用性)的操纵,明显地塑造了天然浮游生物群落的复杂性和动态,从而导致了纤毛虫群落动态的显著变化。实验简化的浮游生物和纤毛虫群落以特定季节的方式响应我们的操作,反映了纤毛虫作为原核生物和更高营养水平之间的中间营养环节的不同作用。该研究还表明,分子和形态分析的结合对于获得对纤毛虫群落结构的更现实的见解以及提供可靠的、有生态意义的结果至关重要。
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
mSystems
mSystems Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
10.50
自引率
3.10%
发文量
308
审稿时长
13 weeks
期刊介绍: mSystems™ will publish preeminent work that stems from applying technologies for high-throughput analyses to achieve insights into the metabolic and regulatory systems at the scale of both the single cell and microbial communities. The scope of mSystems™ encompasses all important biological and biochemical findings drawn from analyses of large data sets, as well as new computational approaches for deriving these insights. mSystems™ will welcome submissions from researchers who focus on the microbiome, genomics, metagenomics, transcriptomics, metabolomics, proteomics, glycomics, bioinformatics, and computational microbiology. mSystems™ will provide streamlined decisions, while carrying on ASM''s tradition of rigorous peer review.
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