瘤胃主要细菌在三种不同厌氧培养基上的选择性培养和富集。

IF 3.8 2区 生物学 Q2 MICROBIOLOGY
Alice M Buckner, Laura Glendinning, Juan M Palma Hidalgo, Jolanda M van Munster, Mark Stevens, Mick Watson, C Jamie Newbold
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引用次数: 0

摘要

反刍动物在全球粮食安全中发挥着重要作用,但也会排放甲烷,导致全球变暖。瘤胃微生物强烈影响宿主植物性饮食的能量保留效率,并产生甲烷作为副产物。虽然从宏基因组序列数据中已经组装了数千种新的微生物基因组,但它们的可培养性尚不明确。在这里,使用不同的培养基(Med10、Med2和MedTC)从瘤胃液中分离微生物共培养物。共鉴定出34个OTUs,归属于杆菌门(75.28±6.34%)、拟杆菌门(19.99±4.85%)、假单胞菌门(2.46±2.01%)和放线菌门(2.09±1.07%)。丰度最高的属为硒单胞菌(28.08±11.71%)、链球菌(22.67±6.06%)、普雷沃氏菌(18.71±4.02%)和未分类毛螺科(11.50±2.54%),其中31个属在至少一种培养基上显著富集,每种培养基成功培养了不同范围的微生物。源瘤胃液的组成与培养瘤胃液有很大的不同。以拟杆菌门(52.53±5.10%)为主,杆菌门(41.00±3.96%)、甲烷菌门(5.12±1.94%)、假单胞菌门(1.22±0.78%)、放线菌门(0.12±0.08%)次之。数量最多的属分别为普雷沃菌属(29.13±4.16%)、丁酸弧菌属(18.21±2.08%)、丁酸弧菌属(15.57±5.03%)、拟杆菌属(13.91±1.67%)和普雷沃菌科(9.50±2.01%)。这些数据进一步强调了使用定义培养基选择不同微生物类群的重要性。这对于了解瘤胃微生物的复杂工作机制以提高消化效率和减少可能被宿主利用的能量损失至关重要。这项研究表明,使用一系列含有多种底物的培养基可以培养关键的瘤胃微生物。了解这些微生物中的哪一种在每种培养基上被选择性富集,对于了解如何在共培养中培养这些微生物以及如何在纯培养中分离它们以进行进一步研究至关重要。此外,本研究表明,在共培养中生长的瘤胃微生物数量与瘤胃本身的微生物数量之间存在明显差异。这进一步表明需要一种有针对性的方法来培养和分离这些微生物。了解这些微生物对不同营养成分培养基的反应将有助于更好地了解瘤胃微生物群,并且本研究为选择性培养基如何针对不同微生物的富集提供了有价值的见解。这一知识将有助于提高反刍动物的消化效率和减少甲烷的产生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The selective culture and enrichment of major rumen bacteria on three distinct anaerobic culture media.

Ruminants play an important part in global food security, but also emit methane, which contributes to global warming. Rumen microbes strongly influence the energy retention efficiency from the host's plant-based diet and produce methane as a by-product. While thousands of novel microbial genomes have been assembled from metagenomic sequence data, their culturability is ill-defined. Here, different media (Med10, Med2, and MedTC) were used to isolate co-cultures of microbes from rumen fluid. Thirty-four OTUs were identified belonging to the phyla Bacillota (75.28 ± 6.34%), Bacteroidota (19.99 ± 4.85%), Pseudomonadota (2.46 ± 2.01%), and Actinomycetota (2.09 ± 1.07%). The most abundant genera were Selenomonas (28.08 ± 11.71%), Streptococcus (22.67 ± 6.06%), Prevotella (18.71 ± 4.02%), and unclassified Lachnospiraceae (11.50 ± 2.54%), and 31 significantly enriched on at least one medium, with each medium successfully culturing a distinct range of microbes. The composition of the source rumen fluid was vastly different from those cultured. Bacteroidota (52.53 ± 5.10%) predominated, with Bacillota (41.00 ± 3.96%), Methanobacteriota (5.12 ± 1.94%), Pseudomonadota (1.22 ± 0.78%), and Actinomycetota (0.12 ± 0.08%) comprising the rest. The most abundant genera were Prevotella (29.13 ± 4.16%), Butyrivibrio (18.21 ± 2.08%), Succiniclasticum (15.57 ± 5.03%), unclassified Bacteroidetes (13.91 ± 1.67%), and unclassified Prevotellaceae (9.50 ± 2.01%). These data further emphasize the importance of using defined media to select for different microbial taxa. This is essential to understand the complex workings of the rumen microbes to enhance digestion efficiency and reduce the loss of energy that could potentially be utilized by the host.IMPORTANCEThis research demonstrates that using a range of culture media, containing a wide variety of substrates, can lead to the culture of key rumen microbes. The knowledge of which of these microbes is selectively enriched on each medium is essential to understand how to grow these microbes in co-culture and isolate them in pure culture for further investigation. In addition, this research shows the stark disparity between the population of rumen microbes grown in co-culture and those found in the rumen itself. This further demonstrates the need for a targeted approach to growing and isolating these microbes. Learning how these microbes respond to culture media with different nutritional compositions will lead to a better understanding of the rumen microbiota, and this research provides a valuable insight into how selective media can target the enrichment of different microbes. This knowledge will contribute to increasing ruminant digestion efficiency and reducing methane production.

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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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