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在琼脂平板上通过与产氢菌共培养来分离和培养 Methanobrevibacter smithii。

Isolation and culture of Methanobrevibacter smithii by co-culture with hydrogen-producing bacteria on agar plates.

机构信息

Aix-Marseille Université, IRD, APHM, MEPHI, IHU-Méditerranée Infection, Marseille, France.

Aix-Marseille Université, IRD, APHM, MEPHI, IHU-Méditerranée Infection, Marseille, France.

出版信息

Clin Microbiol Infect. 2019 Dec;25(12):1561.e1-1561.e5. doi: 10.1016/j.cmi.2019.04.008. Epub 2019 Apr 12.

Abstract

OBJECTIVES

Methanogenic Archaea are considered as extremely oxygen-sensitive organisms, and their culture is fastidious, requiring specific equipment. We report here conditions allowing the cultivation of Methanobrevibacter smithii in an anaerobic chamber without the addition of hydrogen.

METHODS

We first enriched the stool sample in an anaerobic liquid medium. To cultivate M. smithii with Bacteroides thetaiotaomicron and other hydrogen-producing bacteria on solid medium in an anaerobic chamber, we divided the agar plates into two compartments and seeded each strain on each compartment. Methane production was assessed by gas chromatography, and the growing colonies were authenticated by MALDI-TOF MS.

RESULTS

We successfully cultured M. smithii from a liquid culture medium inoculated with stool collected from a healthy donor in an anaerobic chamber. The isolation in pure culture permitted successful culture on agar medium by our performing a co-culture with B. thetaiotaomicron. We also successfully tested the co-cultivation of M. smithii with other known hydrogen-producing bacteria. Gas chromatographic tests showed that these strains produced hydrogen in different amounts. Agar colonies of methanogens were obtained by co-culture with these bacteria, and methane production was detected.

CONCLUSIONS

We propose a new approach to isolate and cultivate new strains of M. smithii by using a co-culture-based technique that can facilitate and make available the isolation of new methanogenic Archaea strains in clinical microbiology laboratories.

摘要

目的

产甲烷古菌被认为是对氧气极其敏感的生物,其培养条件苛刻,需要特定的设备。我们在此报告了一种在无需添加氢气的情况下,在厌氧室内培养甲烷短杆菌的条件。

方法

我们首先在厌氧液体培养基中对粪便样本进行富集。为了在厌氧室内的固体培养基上与拟杆菌属和其他产氢细菌共培养甲烷短杆菌,我们将琼脂平板分为两个隔室,并在每个隔室接种每种菌株。通过气相色谱法评估甲烷生成情况,并通过 MALDI-TOF MS 对生长的菌落进行鉴定。

结果

我们成功地从健康供体粪便接种的液体培养基中在厌氧室内培养了甲烷短杆菌。通过与拟杆菌属进行共培养,我们成功地在纯培养物中进行了分离,从而在琼脂培养基上成功培养了该菌。我们还成功地测试了甲烷短杆菌与其他已知产氢细菌的共培养。气相色谱测试表明,这些菌株产生了不同量的氢气。通过与这些细菌进行共培养获得了产甲烷菌的琼脂菌落,并检测到了甲烷的产生。

结论

我们提出了一种新的方法,通过基于共培养的技术来分离和培养新的甲烷短杆菌菌株,这可以促进和实现临床微生物学实验室中新的产甲烷古菌菌株的分离。

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