Deconstructing and Reconstructing Cheese Rind Microbiomes for Experiments in Microbial Ecology and Evolution
Casey M. Cosetta, Benjamin E. Wolfe
下载PDF
{"title":"Deconstructing and Reconstructing Cheese Rind Microbiomes for Experiments in Microbial Ecology and Evolution","authors":"Casey M. Cosetta, Benjamin E. Wolfe","doi":"10.1002/cpmc.95","DOIUrl":null,"url":null,"abstract":"<p>Cheese rind microbiomes are useful model systems for identifying the mechanisms that control microbiome diversity. Here, we describe the methods we have optimized to first deconstruct in situ cheese rind microbiome diversity and then reconstruct that diversity in laboratory environments to conduct controlled microbiome manipulations. Most cheese rind microbial species, including bacteria, yeasts, and filamentous fungi, can be easily cultured using standard lab media. Colony morphologies of taxa are diverse and can often be used to distinguish taxa at the phylum and sometimes even genus level. Through the use of cheese curd agar medium, thousands of unique community combinations or microbial interactions can be assessed. Transcriptomic experiments and transposon mutagenesis screens can pinpoint mechanisms of interactions between microbial species. Our general approach of creating a tractable synthetic microbial community from cheese can be easily applied to other fermented foods to develop other model microbiomes. © 2019 by John Wiley & Sons, Inc.</p><p><b>Basic Protocol 1</b>: Isolation of cheese rind microbial communities</p><p><b>Support Protocol 1</b>: Preparation of plate count agar with milk and salt</p><p><b>Basic Protocol 2</b>: Identification of cheese rind bacterial and fungal isolates using 16S and ITS sequences</p><p><b>Basic Protocol 3</b>: Preparation of experimental glycerol stocks of yeasts and bacteria</p><p><b>Basic Protocol 4</b>: Preparation of experimental glycerol stocks of filamentous fungi</p><p><b>Basic Protocol 5</b>: Reconstruction of cheese rind microbial communities in vitro</p><p><b>Support Protocol 2</b>: Preparation of lyophilized and powdered cheese curd</p><p><b>Support Protocol 3</b>: Preparation of 10% cheese curd agar plates and tubes</p><p><b>Basic Protocol 6</b>: Interaction screens using responding lawns</p><p><b>Support Protocol 4</b>: Preparation of liquid 2% cheese curd</p><p><b>Basic Protocol 7</b>: Experimental evolution</p><p><b>Basic Protocol 8</b>: Measuring community function: pH/acidification</p><p><b>Basic Protocol 9</b>: Measuring community function: Pigment production</p><p><b>Basic Protocol 10</b>: RNA sequencing of cheese rind biofilms</p>","PeriodicalId":39967,"journal":{"name":"Current Protocols in Microbiology","volume":"56 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpmc.95","citationCount":"21","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Microbiology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpmc.95","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 21
引用
批量引用
Abstract
Cheese rind microbiomes are useful model systems for identifying the mechanisms that control microbiome diversity. Here, we describe the methods we have optimized to first deconstruct in situ cheese rind microbiome diversity and then reconstruct that diversity in laboratory environments to conduct controlled microbiome manipulations. Most cheese rind microbial species, including bacteria, yeasts, and filamentous fungi, can be easily cultured using standard lab media. Colony morphologies of taxa are diverse and can often be used to distinguish taxa at the phylum and sometimes even genus level. Through the use of cheese curd agar medium, thousands of unique community combinations or microbial interactions can be assessed. Transcriptomic experiments and transposon mutagenesis screens can pinpoint mechanisms of interactions between microbial species. Our general approach of creating a tractable synthetic microbial community from cheese can be easily applied to other fermented foods to develop other model microbiomes. © 2019 by John Wiley & Sons, Inc.
Basic Protocol 1 : Isolation of cheese rind microbial communities
Support Protocol 1 : Preparation of plate count agar with milk and salt
Basic Protocol 2 : Identification of cheese rind bacterial and fungal isolates using 16S and ITS sequences
Basic Protocol 3 : Preparation of experimental glycerol stocks of yeasts and bacteria
Basic Protocol 4 : Preparation of experimental glycerol stocks of filamentous fungi
Basic Protocol 5 : Reconstruction of cheese rind microbial communities in vitro
Support Protocol 2 : Preparation of lyophilized and powdered cheese curd
Support Protocol 3 : Preparation of 10% cheese curd agar plates and tubes
Basic Protocol 6 : Interaction screens using responding lawns
Support Protocol 4 : Preparation of liquid 2% cheese curd
Basic Protocol 7 : Experimental evolution
Basic Protocol 8 : Measuring community function: pH/acidification
Basic Protocol 9 : Measuring community function: Pigment production
Basic Protocol 10 : RNA sequencing of cheese rind biofilms
在微生物生态学和进化实验中解构和重建奶酪外皮微生物组
奶酪皮微生物组是识别控制微生物组多样性机制的有用模型系统。在这里,我们描述了我们优化的方法,首先解构原位奶酪皮微生物群多样性,然后在实验室环境中重建多样性,以进行受控的微生物群操作。大多数干酪皮微生物种类,包括细菌、酵母和丝状真菌,可以很容易地用标准实验室培养基培养。分类群的群体形态是多样的,通常可以用来在门甚至属水平上区分分类群。通过使用奶酪凝乳琼脂培养基,可以评估数千种独特的群落组合或微生物相互作用。转录组学实验和转座子突变筛选可以查明微生物物种之间相互作用的机制。我们从奶酪中创建可处理的合成微生物群落的一般方法可以很容易地应用于其他发酵食品以开发其他模型微生物组。©2019 by John Wiley &基本方案1:干酪皮微生物群落的分离支持方案1:用牛奶和盐制备平板计数琼脂基本方案2:用16S和ITS序列鉴定干酪皮细菌和真菌分离基本方案3:酵母和细菌实验甘油储备的制备基本方案4:丝状真菌实验甘油储备的制备基本方案5:体外重建奶酪皮微生物群落支持方案2:制备冻干和粉状奶酪凝乳支持方案3:制备10%奶酪凝乳琼脂板和管基本方案6:使用响应laws的相互作用屏幕支持方案4:制备液态2%奶酪凝乳基本方案7:实验进化基本方案8:测量群落功能:pH/酸化基本方案9:测量群落功能:色素生产基本方案10:干酪皮生物膜的RNA测序
本文章由计算机程序翻译,如有差异,请以英文原文为准。
来源期刊
期刊介绍:
Current Protocols in Microbiology provides detailed, step-by-step instructions for analyzing bacteria, animal and plant viruses, fungi, protozoans and other microbes. It offers updated coverage of emerging technologies and concepts, such as biofilms, quorum sensing and quantitative PCR, as well as proteomic and genomic methods. It is the first comprehensive source of high-quality microbiology protocols that reflects and incorporates the new mandates and capabilities of this robust and rapidly evolving discipline.