破译与虎尾海马(Hippocampus comes)相关的微生物群落的分类和功能模式。

IF 2.5 4区 生物学 Q3 CELL BIOLOGY
Physiological genomics Pub Date : 2024-08-01 Epub Date: 2024-07-08 DOI:10.1152/physiolgenomics.00039.2024
Chinee Surita Padasas-Adalla, Rose Chinly Mae Ortega-Kindica, Rodelyn Dalayap, Joey Genevieve Martinez, Olive Amparado, Carlo Stephen Moneva, Carlos O Lomelí-Ortega, Sharon Rose Tabugo, José Luis Balcázar
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引用次数: 0

摘要

深入了解微生物群落的多样性、结构和代谢功能,对于理解它们在宿主健康和生态系统动态中的作用至关重要。然而,尽管这些濒危鱼类在全球范围内面临着越来越大的人类压力,但有关海马相关微生物群落的研究仍然有限。在这里,我们利用霰弹枪元基因组学和生物信息学探索了虎尾海马(Hippocampus comes)皮肤和肠道及其周围环境的微生物多样性和代谢功能。假单胞菌门的成员在皮肤微生物组中占主导地位,而类杆菌在肠道中占主导地位。在与海马相关的微生物组中还检测到芽孢杆菌属、放线菌属和担子菌属。统计分析表明,两者之间存在明显差异(pMoraxellaceae 科在皮肤上占优势,而 Bacteroidaceae 科在肠道中占优势)。此外,周围环境(水或沉积物)对海马微生物组的组成没有直接影响。与肠道微生物组相比,皮肤微生物组中与能量、脂质、氨基酸代谢以及萜类化合物和多酮类化合物代谢、异种生物降解和代谢相关的功能基因丰度更高。尽管各类微生物之间存在差异,但肠道微生物群和皮肤微生物群中细菌素的总丰度相似。更好地了解海马微生物组有利于保护和可持续水产养殖工作,为栖息地保护、疾病管理和优化水产养殖环境提供见解,从而促进海马的健康和福利,同时最大限度地减少对环境的影响,提高水产养殖的可持续性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Deciphering taxonomic and functional patterns of microbial communities associated with the tiger tail seahorse (Hippocampus comes).

Gaining insight into the diversity, structure, and metabolic functions of microbial communities is essential for understanding their roles in host health and ecosystem dynamics. However, research on the seahorse-associated microbiome remains limited, despite these threatened fish facing increasing human pressures worldwide. Here, we explored the microbial diversity and metabolic functions of the skin and gut of the tiger tail seahorse (Hippocampus comes) and its surrounding environment using shotgun metagenomics and bioinformatics. Members of the Pseudomonadota phylum were dominant in the skin microbiome, whereas Bacteroidota was dominant in the gut. Bacillota, Actinomycetota, and Planctomycetota were also detected in the seahorse-associated microbiome. Statistical analysis revealed significant differences (P < 0.01) in species diversity between skin and gut microbiomes, with members belonging to the Moraxellaceae family being dominant on the skin and the Bacteroidaceae family in the gut. Moreover, the surrounding environment (water or sediment) did not have a direct effect on the seahorse microbiome composition. The skin microbiome exhibited a higher abundance of functional genes related to energy, lipid, and amino acid metabolism as well as terpenoids and polyketides metabolism, xenobiotics biodegradation, and metabolism compared with the gut. Despite differences among classes, the total abundance of bacteriocins was similar in both gut and skin microbiomes, which is significant in shaping microbial communities due to their antimicrobial properties. A better knowledge of seahorse microbiomes benefits conservation and sustainable aquaculture efforts, offering insights into habitat protection, disease management, and optimizing aquaculture environments, thereby promoting seahorse health and welfare while minimizing environmental impact and enhancing aquaculture sustainability.NEW & NOTEWORTHY To the best of our knowledge, this study represents the first comprehensive examination of the taxonomic and functional patterns of the skin and gut microbiome in the tiger tail seahorse. These findings have the potential to significantly enhance our understanding of the seahorse-associated microbiome, thereby contributing to the prediction and control of bacterial infections in seahorses, which are a leading cause of high mass mortality rates in seahorse aquaculture and other fish species.

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来源期刊
Physiological genomics
Physiological genomics 生物-生理学
CiteScore
6.10
自引率
0.00%
发文量
46
审稿时长
4-8 weeks
期刊介绍: The Physiological Genomics publishes original papers, reviews and rapid reports in a wide area of research focused on uncovering the links between genes and physiology at all levels of biological organization. Articles on topics ranging from single genes to the whole genome and their links to the physiology of humans, any model organism, organ, tissue or cell are welcome. Areas of interest include complex polygenic traits preferably of importance to human health and gene-function relationships of disease processes. Specifically, the Journal has dedicated Sections focused on genome-wide association studies (GWAS) to function, cardiovascular, renal, metabolic and neurological systems, exercise physiology, pharmacogenomics, clinical, translational and genomics for precision medicine, comparative and statistical genomics and databases. For further details on research themes covered within these Sections, please refer to the descriptions given under each Section.
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