Suppr超能文献

媒体事务,考察历史和现代增长媒体以及它们影响的实验。

Media Matters, Examining Historical and Modern Growth Media and the Experiments They Affect.

机构信息

Department of Immunobiology, University of Arizona, Tucson, AZ, United States.

BIO5 Institute, University of Arizona, Tucson, AZ, United States.

出版信息

Front Cell Infect Microbiol. 2021 Mar 23;11:613623. doi: 10.3389/fcimb.2021.613623. eCollection 2021.

Abstract

While some bacteria can thrive for generations in minerals and salts, many require lavish nutrition and specific chemicals to survive to the point where they can be observed and researched. Although researchers once boiled and rendered animal flesh and bones to obtain a media that facilitated bacterial growth, we now have a plethora of formulations and manufacturers to provide dehydrated flavors of historical, modified, and modern media. The purpose of media has evolved from simple isolation to more measured study. However, in some instances, media formulated to aid the metabolic, nutritional, or physical properties of microbes may not be best suited for studying pathogen behavior or resilience as a function of host interactions. While there have been comparative studies on handfuls of these media in , this review focuses on describing both the historical and modern composition of common complex (Todd Hewitt and M17), semi-defined (Adams and Roe), and defined pneumococcal media (RPMI and Van de Rijn and Kessler), key components discovered/needed for cultivation/growth enhancement, and effects these different media have on bacterial phenotypes and experimental outcomes. While many researchers find the best conditions to grow and experiment on their bacteria of choice, the reasons for some researchers to use a specific medium is at best, not discussed, and at worst, arbitrary. As such, the goal of this review is to highlight the differences in pneumococcal media to encourage investigators to challenge their decisions on why they use a given medium, discuss the recipe, and explain their reasoning.

摘要

虽然有些细菌可以在矿物质和盐中繁殖多代,但许多细菌需要丰富的营养和特定的化学物质才能存活下来,以便被观察和研究。尽管研究人员曾经煮沸和处理动物的肉和骨头,以获得促进细菌生长的培养基,但我们现在有大量的配方和制造商提供历史、改良和现代培养基的脱水口味。培养基的目的已经从简单的分离进化到更有针对性的研究。然而,在某些情况下,为了促进微生物的代谢、营养或物理特性而设计的培养基可能并不适合研究病原体的行为或作为宿主相互作用的功能的弹性。虽然已经有一些关于这些培养基的比较研究,但本综述重点描述了常见复杂(Todd Hewitt 和 M17)、半定义(Adams 和 Roe)和定义的肺炎球菌培养基(RPMI 和 Van de Rijn 和 Kessler)的历史和现代组成,关键的发现/需要用于培养/生长增强的成分,以及这些不同的培养基对细菌表型和实验结果的影响。虽然许多研究人员找到了最佳的条件来培养和实验他们选择的细菌,但一些研究人员使用特定培养基的原因,最多只是没有讨论,最坏的情况是任意的。因此,本综述的目的是强调肺炎球菌培养基的差异,以鼓励研究人员质疑他们使用特定培养基的决定,讨论配方,并解释他们的推理。

相似文献

5
Streptococcus pneumoniae infection: a Canadian perspective.肺炎链球菌感染:加拿大视角。
Expert Rev Anti Infect Ther. 2013 Aug;11(8):781-91. doi: 10.1586/14787210.2013.814831.
7
Proteomic response of Streptococcus pneumoniae to iron limitation.肺炎链球菌对铁限制的蛋白质组反应。
Int J Med Microbiol. 2018 Aug;308(6):713-721. doi: 10.1016/j.ijmm.2018.02.001. Epub 2018 Feb 13.

引用本文的文献

1
The global proteome of EF3030 under nutrient-defined conditions.营养成分确定条件下EF3030的全球蛋白质组。
Front Cell Infect Microbiol. 2025 Jul 11;15:1606161. doi: 10.3389/fcimb.2025.1606161. eCollection 2025.
3
Antibacterial effects of Kampo products against pneumonia causative bacteria.汉方药产品对肺炎致病菌的抗菌作用。
PLoS One. 2024 Oct 28;19(10):e0312500. doi: 10.1371/journal.pone.0312500. eCollection 2024.
5
Insights into the enigma of oral streptococci in carcinogenesis.口腔链球菌致癌之谜的研究进展。
Microbiol Mol Biol Rev. 2024 Jun 27;88(2):e0009523. doi: 10.1128/mmbr.00095-23. Epub 2024 Mar 20.

本文引用的文献

7
Carbon source regulates polysaccharide capsule biosynthesis in .碳源调节. 多糖荚膜生物合成。
J Biol Chem. 2019 Nov 15;294(46):17224-17238. doi: 10.1074/jbc.RA119.010764. Epub 2019 Oct 8.
10
Role of Pneumococcal NanA Neuraminidase Activity in Peripheral Blood.肺炎链球菌 NanA 神经氨酸酶活性在血液中的作用。
Front Cell Infect Microbiol. 2019 Jun 26;9:218. doi: 10.3389/fcimb.2019.00218. eCollection 2019.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验