The prokaryotic community of Chondrosia reniformis Nardo, 1847: from diversity to mercury detection

IF 1.6 3区 生物学 Q2 ZOOLOGY Zoology Pub Date : 2023-06-01 DOI:10.1016/j.zool.2023.126091
Camilla Roveta , Barbara Calcinai , Federico Girolametti , Joana Fernandes Couceiro , Stefania Puce , Anna Annibaldi , Rodrigo Costa
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Abstract

Microbial communities inhabiting sponges are known to take part in many metabolic pathways, including nutrient cycles, and possibly also in the bioaccumulation of trace elements (TEs). Here, we used high-throughput, Illumina sequencing of 16S rRNA genes to characterize the prokaryotic communities present in the cortex and choanosome, respectively the external and internal body region of Chondrosia reniformis, and in the surrounding seawater. Furthermore, we estimated the total mercury content (THg) in these body regions of the sponge and in the corresponding microbial cell pellets. Fifteen prokaryotic phyla were detected in association with C. reniformis, 13 belonging to the domain Bacteria and two to the Archaea. No significant differences between the prokaryotic community composition of the two regions were found. Three lineages of ammonium-oxidizing organisms (Cenarchaeum symbiosum, Nitrosopumilus maritimus, and Nitrosococcus sp.) co-dominated the prokaryotic community, suggesting ammonium oxidation/nitrification as a key metabolic pathway within the microbiome of C. reniformis. In the sponge fractions, higher THg levels were found in the choanosome compared to the cortex. In contrast, comparable THg levels found in the microbial pellets obtained from both regions were significantly lower than those observed in the corresponding sponge fractions. Our work provides new insights into the prokaryotic communities and TEs distribution in different body parts of a model organism relevant for marine conservation and biotechnology. In this sense, this study paves the way for scientists to deepen the possible application of sponges not only as bioindicators, but also as bioremediation tools of metal polluted environments.

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肾形软骨菌的原核生物群落,1847:从多样性到汞检测
已知海绵中的微生物群落参与许多代谢途径,包括营养循环,也可能参与微量元素(TE)的生物积累。在这里,我们使用16S rRNA基因的高通量Illumina测序来表征存在于皮层和choanosome中的原核群落,分别是肾形软骨藻的外部和内部身体区域,以及周围海水中。此外,我们估计了海绵的这些身体区域和相应的微生物细胞颗粒中的总汞含量(THg)。检测到15个与肾形梭菌相关的原核门,13个属于结构域细菌,2个属于古菌。两个区域的原核生物群落组成没有发现显著差异。铵氧化生物的三个谱系(Cenarchaeum symbiosum、Nitrosopumilus maritimus和Nitrosococcus sp.)共同主导原核生物群落,表明铵氧化/硝化作用是肾形梭菌微生物组中的关键代谢途径。在海绵组分中,与皮层相比,choanosome中的THg水平更高。相反,在从两个区域获得的微生物颗粒中发现的可比THg水平显著低于在相应的海绵级分中观察到的水平。我们的工作为与海洋保护和生物技术相关的模式生物的原核生物群落和TE在不同身体部位的分布提供了新的见解。从这个意义上说,这项研究为科学家深化海绵的可能应用铺平了道路,海绵不仅可以作为生物指示剂,还可以作为金属污染环境的生物修复工具。
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来源期刊
Zoology
Zoology 生物-动物学
CiteScore
3.90
自引率
0.00%
发文量
37
审稿时长
70 days
期刊介绍: Zoology is a journal devoted to experimental and comparative animal science. It presents a common forum for all scientists who take an explicitly organism oriented and integrative approach to the study of animal form, function, development and evolution. The journal invites papers that take a comparative or experimental approach to behavior and neurobiology, functional morphology, evolution and development, ecological physiology, and cell biology. Due to the increasing realization that animals exist only within a partnership with symbionts, Zoology encourages submissions of papers focused on the analysis of holobionts or metaorganisms as associations of the macroscopic host in synergistic interdependence with numerous microbial and eukaryotic species. The editors and the editorial board are committed to presenting science at its best. The editorial team is regularly adjusting editorial practice to the ever changing field of animal biology.
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