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在人工养殖的无胃鱼,墨西哥鱵鱼(Atherinopsidae)中,肠道微生物多样性的丧失。

Loss of gut microbial diversity in the cultured, agastric fish, Mexican pike silverside (: Atherinopsidae).

机构信息

Instituto de Investigaciones Agropecuarias y Forestales (IIAF), Universidad Michoacana de San Nicolás de Hidalgo, Morelia, Michoacan, Mexico.

Centro de Investigación en Alimentación y Desarrollo, A.C. (CIAD), Mazatlán, Sinaloa, Mexico.

出版信息

PeerJ. 2022 Mar 7;10:e13052. doi: 10.7717/peerj.13052. eCollection 2022.

DOI:10.7717/peerj.13052
PMID:35282279
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8908885/
Abstract

Teleost fish are the most diverse group of extant vertebrates and have varied digestive anatomical structures and strategies, suggesting they also possess an array of different host-microbiota interactions. Differences in fish gut microbiota have been shown to affect host development, the process of gut colonization, and the outcomes of gene-environment or immune system-microbiota interactions. There is generally a lack of studies on the digestive mechanisms and microbiota of agastric short-intestine fish however, meaning that we do not understand how changes in gut microbial diversity might influence the health of these types of fish. To help fill these gaps in knowledge, we decided to study the Mexican pike silverside () which has a simplified alimentary canal (agastric, short-intestine, 0.7 gut relative length) to observe the diversity and metabolic potential of its intestinal microbiota. We characterized gut microbial populations using high-throughput sequencing of the V3 region in bacterial 16S rRNA genes while searching for population shifts resulting associated with fish development in different environments and cultivation methods. Microbiota samples were taken from the digesta, anterior and posterior intestine (the three different intestinal components) of fish that grew wild in a lake, that were cultivated in indoor tanks, or that were raised in outdoor ponds. Gut microbial diversity was significantly higher in wild fish than in cultivated fish, suggesting a loss of diversity when fish are raised in controlled environments. The most abundant phyla observed in these experiments were Firmicutes and Proteobacteria, particularly of the genera , , , and . Of the 14,161 OTUs observed in this experiment, 133 were found in all groups, and 17 of these, belonging to , , , and genera, were found in all samples suggesting the existence of a core microbiome. Functional metagenomic prediction of bacterial ecological functions using PICRUSt2 suggested that different intestinal components select for functionally distinct microbial populations with variation in pathways related to the metabolism of amino acids, vitamins, cofactors, and energy. Our results provide, for the first time, information on the bacterial populations present in an agastric, short-gut teleost with commercial potential and show that controlled cultivation of this fish reduces the diversity of its intestinal microbiota.

摘要

硬骨鱼类是现存脊椎动物中最多样化的群体,它们具有多样化的消化解剖结构和策略,这表明它们也拥有一系列不同的宿主-微生物相互作用。鱼类肠道微生物群的差异已被证明会影响宿主的发育、肠道定植过程以及基因-环境或免疫系统-微生物群相互作用的结果。然而,一般来说,关于胃短肠鱼类的消化机制和微生物群的研究很少,这意味着我们不了解肠道微生物多样性的变化如何影响这些类型鱼类的健康。为了帮助填补这些知识空白,我们决定研究墨西哥鱵(),它具有简化的消化道(胃、短肠、0.7 肠道相对长度),以观察其肠道微生物群的多样性和代谢潜力。我们使用高通量测序技术对细菌 16S rRNA 基因的 V3 区进行了测序,以表征肠道微生物种群,同时寻找与不同环境和养殖方法下鱼类发育相关的种群变化。从在湖泊中自然生长、在室内水箱中养殖或在室外池塘中养殖的鱼类的食糜、前肠和后肠(三个不同的肠道成分)中采集微生物群样本。野生鱼的肠道微生物多样性明显高于养殖鱼,这表明鱼类在受控环境中养殖时会丧失多样性。在这些实验中观察到的最丰富的门是厚壁菌门和变形菌门,特别是属、、、和。在本实验中观察到的 14161 个 OTUs 中,有 133 个在所有组中都有发现,其中 17 个属于属、、、和属,在所有样本中都有发现,这表明存在一个核心微生物群。使用 PICRUSt2 对细菌生态功能进行功能宏基因组预测表明,不同的肠道成分选择具有功能上不同的微生物种群,其变化与氨基酸、维生素、辅助因子和能量代谢有关的途径。我们的研究结果首次提供了具有商业潜力的胃短肠硬骨鱼类中存在的细菌种群信息,并表明这种鱼类的受控养殖会降低其肠道微生物群的多样性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b36/8908885/a862d9fb26cf/peerj-10-13052-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b36/8908885/e3fc4a5a2fca/peerj-10-13052-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b36/8908885/3afd8bf98801/peerj-10-13052-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b36/8908885/ea7a786aaddc/peerj-10-13052-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b36/8908885/4a702b7324f1/peerj-10-13052-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b36/8908885/a862d9fb26cf/peerj-10-13052-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b36/8908885/e3fc4a5a2fca/peerj-10-13052-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b36/8908885/3afd8bf98801/peerj-10-13052-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b36/8908885/ea7a786aaddc/peerj-10-13052-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b36/8908885/4a702b7324f1/peerj-10-13052-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b36/8908885/a862d9fb26cf/peerj-10-13052-g005.jpg

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