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改良的海洋弧菌培养介质,提高其分离效率。

A modified culture medium for improved isolation of marine vibrios.

机构信息

IAS-CNR, Campobello di Mazara, Italy.

Department of Biological, Chemical and Pharmaceutical Sciences and Technologies (STEBICEF), University of Palermo, Palermo, Italy.

出版信息

Microbiologyopen. 2019 Sep;8(9):e00835. doi: 10.1002/mbo3.835. Epub 2019 Jul 18.

Abstract

Marine Vibrio members are of great interest for both ecological and biotechnological research, which often relies on their isolation. Whereas many efforts have been made for the detection of food-borne pathogenic species, much less is known about the performances of standard culture media toward environmental vibrios. We show that the isolation/enumeration of marine vibrios using thiosulfate-citrate-bile salts-sucrose agar (TCBS) as selective medium may be hampered by the variable adaptability of different taxa to the medium, which may result even in isolation failure and/or in substantial total count underestimation. We propose a modified TCBS as isolation medium, adjusted for marine vibrios requirements, which greatly improved their recovery in dilution plate counts, compared with the standard medium. The modified medium offers substantial advantages over TCBS, providing more accurate and likely estimations of the actual presence of vibrios. Modified TCBS allowed the recovery of otherwise undetected vibrios, some of which producing biotechnologically valuable enzymes, thus expanding the isolation power toward potentially new enzyme-producers Vibrio taxa. Moreover, we report a newly designed Vibrio-specific PCR primers pair, targeting a unique rpoD sequence, useful for rapid confirmation of isolates as Vibrio members and subsequent genetic analyses.

摘要

海洋弧菌成员对于生态和生物技术研究具有重要意义,而这些研究往往依赖于它们的分离。虽然已经做出了许多努力来检测食源性病原体,但对于环境弧菌,人们对标准培养基的性能知之甚少。我们表明,使用硫代硫酸盐-柠檬酸盐-胆汁盐-蔗糖琼脂(TCBS)作为选择性培养基进行海洋弧菌的分离/计数可能会受到不同分类群对培养基适应性变化的阻碍,这甚至可能导致分离失败和/或总计数的大量低估。我们提出了一种改良的 TCBS 作为分离培养基,根据海洋弧菌的要求进行了调整,与标准培养基相比,大大提高了其在稀释平板计数中的回收率。改良的 TCBS 提供了比 TCBS 更显著的优势,可更准确和可能地估计实际存在的弧菌数量。改良的 TCBS 允许回收原本无法检测到的弧菌,其中一些弧菌产生具有生物技术价值的酶,从而扩大了潜在新的酶产生弧菌分类群的分离能力。此外,我们报告了一对新设计的针对独特 rpoD 序列的霍乱弧菌特异性 PCR 引物,可用于快速确认分离株是否为弧菌成员,并进行后续的遗传分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73bc/6741135/2e789a699ec1/MBO3-8-e00835-g001.jpg

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