Current Protocols in Microbiology最新文献

{"title":"Psychological flexibility, temperament, and perceived stress.","authors":"Maria Cyniak-Cieciura","doi":"10.5114/cipp.2021.108685","DOIUrl":"10.5114/cipp.2021.108685","url":null,"abstract":"<p><strong>Background: </strong>Psychological flexibility (PF) is an ability to engage in meaningful actions regardless of the presence of difficult internal experiences. Higher psychological flexibility was found to be related not only to a lower level of the symptoms of psychopathology, but also with better functioning, lower stress levels and higher well-being. As temperament impacts preferred styles of action, data on the relationships between temperament, psychological flexibility and other criteria can provide ideas on how to improve the process of PF development. The aim of this study was to examine the relationships between psychological flexibility, temperament traits and perceived stress.</p><p><strong>Participants and procedure: </strong>A total of 254 people, aged 18-93, recruited directly by 13 pollsters from a local community sample, took part in the study. Temperamental traits were operationalized according to the regulative theory of temperament. Participants completed self-report measures.</p><p><strong>Results: </strong>Psychological flexibility was predicted by emotional reactivity and perseveration and it was a significant predictor of stress beyond and above temperamental traits. While the relationship between stress and two temperamental traits - emotional reactivity and perseveration - was partially mediated by psychological flexibility, activity was related to stress directly.</p><p><strong>Conclusions: </strong>Psychological flexibility is determined by temperamental traits to some extent. Further research on psychological flexibility and temperament needs to take an empirical design and test possible reciprocal effects.</p>","PeriodicalId":39967,"journal":{"name":"Current Protocols in Microbiology","volume":"44 1","pages":"306-315"},"PeriodicalIF":1.0,"publicationDate":"2021-10-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10655781/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86088773","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Programmable Gene Knockdown in Diverse Bacteria Using Mobile-CRISPRi","authors":"Amy B. Banta,&nbsp;Ryan D. Ward,&nbsp;Jennifer S. Tran,&nbsp;Emily E. Bacon,&nbsp;Jason M. Peters","doi":"10.1002/cpmc.130","DOIUrl":"10.1002/cpmc.130","url":null,"abstract":"<p>Facile bacterial genome sequencing has unlocked a veritable treasure trove of novel genes awaiting functional exploration. To make the most of this opportunity requires powerful genetic tools that can target all genes in diverse bacteria. CRISPR interference (CRISPRi) is a programmable gene-knockdown tool that uses an RNA-protein complex comprised of a single guide RNA (sgRNA) and a catalytically inactive Cas9 nuclease (dCas9) to sterically block transcription of target genes. We previously developed a suite of modular CRISPRi systems that transfer by conjugation and integrate into the genomes of diverse bacteria, which we call Mobile-CRISPRi. Here, we provide detailed protocols for the modification and transfer of Mobile-CRISPRi vectors for the purpose of knocking down target genes in bacteria of interest. We further discuss strategies for optimizing Mobile-CRISPRi knockdown, transfer, and integration. We cover the following basic protocols: sgRNA design, cloning new sgRNA spacers into Mobile-CRISPRi vectors, Tn<i>7</i> transfer of Mobile-CRISPRi to Gram-negative bacteria, and ICE<i>Bs1</i> transfer of Mobile-CRISPRi to Bacillales. © 2020 The Authors.</p><p><b>Basic Protocol 1</b>: sgRNA design</p><p><b>Basic Protocol 2</b>: Cloning of new sgRNA spacers into Mobile-CRISPRi vectors</p><p><b>Basic Protocol 3</b>: Tn<i>7</i> transfer of Mobile-CRISPRi to Gram-negative bacteria</p><p><b>Basic Protocol 4</b>: ICE<i>Bs1</i> transfer of Mobile-CRISPRi to Bacillales</p><p><b>Support Protocol 1</b>: Quantification of CRISPRi repression using fluorescent reporters</p><p><b>Support Protocol 2</b>: Testing for gene essentiality using CRISPRi spot assays on plates</p><p><b>Support Protocol 3</b>: Transformation of <i>E. coli</i> by electroporation</p><p><b>Support Protocol 4</b>: Transformation of CaCl₂-competent <i>E. coli</i></p>","PeriodicalId":39967,"journal":{"name":"Current Protocols in Microbiology","volume":"59 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2020-12-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpmc.130","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38724222","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Gene Editing in Dimorphic Fungi Using CRISPR/Cas9","authors":"Gregory C. Kujoth,&nbsp;Thomas D. Sullivan,&nbsp;Bruce S. Klein","doi":"10.1002/cpmc.132","DOIUrl":"10.1002/cpmc.132","url":null,"abstract":"<p>Dimorphic fungi in the genera <i>Blastomyces</i>, <i>Histoplasma</i>, <i>Coccidioides</i>, and <i>Paracoccidioides</i> are important human pathogens that affect human health in many countries throughout the world. Understanding the biology of these fungi is important for the development of effective treatments and vaccines. Gene editing is a critically important tool for research into these organisms. In recent years, gene targeting approaches employing RNA-guided DNA nucleases, such as clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated nuclease 9 (Cas9), have exploded in popularity. Here, we provide a detailed description of the steps involved in applying CRISPR/Cas9 technology to dimorphic fungi, with <i>Blastomyces dermatitidis</i> in particular as our model fungal pathogen. We discuss the design and construction of single guide RNA and Cas9-expressing targeting vectors (including multiplexed vectors) as well as introduction of these plasmids into <i>Blastomyces</i> using <i>Agrobacterium</i>-mediated transformation. Finally, we cover the outcomes that may be expected in terms of gene-editing efficiency and types of gene alterations produced. © 2020 Wiley Periodicals LLC.</p><p><b>Basic Protocol 1</b>: Construction of CRISPR/Cas9 targeting vectors</p><p><b>Support Protocol 1</b>: Choosing protospacers in the target gene</p><p><b>Basic Protocol 2</b>: <i>Agrobacterium</i>-mediated transformation of <i>Blastomyces</i></p><p><b>Support Protocol 2</b>: Preparation of electrocompetent <i>Agrobacterium</i></p><p><b>Support Protocol 3</b>: Preparation and recovery of <i>Blastomyces</i> frozen stocks</p>","PeriodicalId":39967,"journal":{"name":"Current Protocols in Microbiology","volume":"59 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2020-12-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpmc.132","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38707319","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Vibrio parahaemolyticus: Basic Techniques for Growth, Genetic Manipulation, and Analysis of Virulence Factors","authors":"Suneeta Chimalapati,&nbsp;Alexander E. Lafrance,&nbsp;Luming Chen,&nbsp;Kim Orth","doi":"10.1002/cpmc.131","DOIUrl":"10.1002/cpmc.131","url":null,"abstract":"<p><i>Vibrio parahaemolyticus</i> is a Gram-negative, halophilic bacterium and opportunistic pathogen of humans and shrimp. Investigating the mechanisms of <i>V. parahaemolyticus</i> infection and the multifarious virulence factors it employs requires procedures for bacterial culture, genetic manipulation, and analysis of virulence phenotypes. Detailed protocols for growth assessment, generation of mutants, and phenotype assessment are included in this article. © 2020 Wiley Periodicals LLC.</p><p><b>Basic Protocol 1</b>: Assessment of growth of <i>V. parahaemolyticus</i></p><p><b>Alternate Protocol 1</b>: Assessment of growth of <i>V. parahaemolyticus</i> using a plate reader</p><p><b>Basic Protocol 2</b>: Swimming/swarming motility assay</p><p><b>Basic Protocol 3</b>: Genetic manipulation</p><p><b>Alternate Protocol 2</b>: Natural transformation</p><p><b>Basic Protocol 4</b>: Secretion assay and sample preparation for mass spectrometry analysis</p><p><b>Basic Protocol 5</b>: Invasion assay (gentamicin protection assay)</p><p><b>Basic Protocol 6</b>: Immunofluorescence detection of intracellular <i>V. parahaemolyticus</i></p><p><b>Basic Protocol 7</b>: Cytotoxicity assay for T3SS2</p>","PeriodicalId":39967,"journal":{"name":"Current Protocols in Microbiology","volume":"59 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2020-12-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpmc.131","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38343047","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"3D Oral and Cervical Tissue Models for Studying Papillomavirus Host-Pathogen Interactions","authors":"Robert Jackson,&nbsp;Jason D. Maarsingh,&nbsp;Melissa M. Herbst-Kralovetz,&nbsp;Koenraad Van Doorslaer","doi":"10.1002/cpmc.129","DOIUrl":"10.1002/cpmc.129","url":null,"abstract":"<p>Human papillomavirus (HPV) infection occurs in differentiating epithelial tissues. Cancers caused by high-risk types (e.g., HPV16 and HPV18) typically occur at oropharyngeal and anogenital anatomical sites. The HPV life cycle is differentiation-dependent, requiring tissue culture methodology that is able to recapitulate the three-dimensional (3D) stratified epithelium. Here we report two distinct and complementary methods for growing differentiating epithelial tissues that mimic many critical morphological and biochemical aspects of in vivo tissue. The first approach involves growing primary human epithelial cells on top of a dermal equivalent consisting of collagen fibers and living fibroblast cells. When these cells are grown at the liquid-air interface, differentiation occurs and allows for epithelial stratification. The second approach uses a rotating wall vessel bioreactor. The low-fluid-shear microgravity environment inside the bioreactor allows the cells to use collagen-coated microbeads as a growth scaffold and self-assemble into 3D cellular aggregates. These approaches are applied to epithelial cells derived from HPV-positive and HPV-negative oral and cervical tissues. The second part of the article introduces potential downstream applications for these 3D tissue models. We describe methods that will allow readers to start successfully culturing 3D tissues from oral and cervical cells. These tissues have been used for microscopic visualization, scanning electron microscopy, and large omics-based studies to gain insights into epithelial biology, the HPV life cycle, and host-pathogen interactions. © 2020 Wiley Periodicals LLC.</p><p><b>Basic Protocol 1</b>: Establishing human primary cell–derived 3D organotypic raft cultures</p><p><b>Support Protocol 1</b>: Isolation of epithelial cells from patient-derived tissues</p><p><b>Support Protocol 2</b>: Growth and maintenance of primary human epithelial cells in monolayer culture</p><p><b>Support Protocol 3</b>: PCR-based HPV screening of primary cell cultures</p><p><b>Basic Protocol 2</b>: Establishing human 3D cervical tissues using the rotating wall vessel bioreactor</p><p><b>Support Protocol 4</b>: Growth and maintenance of human A2EN cells in monolayer culture</p><p><b>Support Protocol 5</b>: Preparation of the slow-turning lateral vessel bioreactor</p><p><b>Support Protocol 6</b>: Preparation of Cytodex-3 microcarrier beads</p><p><b>Basic Protocol 3</b>: Histological assessment of 3D organotypic raft tissues</p><p><b>Basic Protocol 4</b>: Spatial analysis of protein expression in 3D organotypic raft cultures</p><p><b>Basic Protocol 5</b>: Immunofluorescence imaging of RWV-derived 3D tissues</p><p><b>Basic Protocol 6</b>: Ultrastructural visualization and imaging of RWV-derived 3D tissues</p><p><b>Basic Protocol 7</b>: Characterization of gene expression by RT-qPCR</p>","PeriodicalId":39967,"journal":{"name":"Current Protocols in Microbiology","volume":"59 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2020-11-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpmc.129","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38640518","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Dissecting the Biology of the Fungal Wheat Pathogen Zymoseptoria tritici: A Laboratory Workflow","authors":"Wagner C. Fagundes,&nbsp;Janine Haueisen,&nbsp;Eva H. Stukenbrock","doi":"10.1002/cpmc.128","DOIUrl":"10.1002/cpmc.128","url":null,"abstract":"<p>The fungus <i>Zymoseptoria tritici</i> is one of the most devastating pathogens of wheat. Aside from its importance as a disease-causing agent, this species has emerged as a powerful model system for evolutionary genetic studies of crop-infecting fungal pathogens. <i>Z. tritici</i> exhibits exceptionally high levels of genetic and phenotypic diversity as well as morphological plasticity, which can make experimental studies and comparability of results obtained in different laboratories, e.g., from infection assays, challenging. Therefore, standardized experimental methods are crucial for research on <i>Z. tritici</i> biology and the interaction of this fungus with its wheat host. Here, we describe a suite of well-tested and optimized protocols ranging from isolation of <i>Z. tritici</i> field specimens to analyses of virulence assays under controlled conditions. Several biological and technical aspects of working with <i>Z. tritici</i> under laboratory conditions are considered and carefully described in each protocol. © 2020 The Authors.</p><p><b>Basic Protocol 1</b>: Purification of <i>Z. tritici</i> field isolates from leaf material</p><p><b>Basic Protocol 2</b>: Molecular identification of <i>Z. tritici</i> isolates</p><p><b>Support Protocol 1</b>: Rapid extraction of <i>Z. tritici</i> genomic DNA</p><p><b>Support Protocol 2</b>: Extraction of high-quality <i>Z. tritici</i> genomic DNA</p><p><b>Basic Protocol 3</b>: In vitro culture and long-term storage of <i>Z. tritici</i> isolates</p><p><b>Basic Protocol 4</b>: Analysis of <i>Z. tritici</i> virulence in wheat</p><p><b>Support Protocol 3</b>: Preparation of <i>Z. tritici</i> inoculum</p>","PeriodicalId":39967,"journal":{"name":"Current Protocols in Microbiology","volume":"59 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2020-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpmc.128","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38685020","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Counter-Selection Method for Markerless Allelic Exchange in Bordetella bronchiseptica Based on sacB Gene From Bacillus subtilis","authors":"Nicolás Ambrosis,&nbsp;Julieta Fernández,&nbsp;Federico Sisti","doi":"10.1002/cpmc.125","DOIUrl":"10.1002/cpmc.125","url":null,"abstract":"<p><i>Bordetella bronchiseptica</i> is a gram-negative bacterium that causes respiratory tract infections. It is a natural pathogen of a wide variety of mammals, including some used as laboratory models. This makes <i>B. bronchiseptica</i> an ideal organism to study pathogen–host interactions in order to unveil molecular mechanisms behind pathogenic processes. Even though genetic engineering is an essential tool in this area, there are just a few reports about genome manipulation techniques in this organism. In this article we describe an allelic exchange protocol based on double crossover recombination facilitated by the <i>Bacillus subtilis sacB</i> gene that can be applied for partial or complete gene knockouts, single-nucleotide mutations, or even introduction of coding sequences for transcriptional fusions. In contrast to previously employed techniques, this protocol renders genetically manipulated chromosomes without foreign DNA and enables the construction of successive genome manipulation using the same vector backbone. The entire procedure has been developed for fast and reliable manipulations with a total duration of 2 weeks. © 2020 Wiley Periodicals LLC.</p><p><b>Basic Protocol 1</b>: Setting up strains</p><p><b>Basic Protocol 2</b>: Homologous recombination (first crossing-over)</p><p><b>Alternate Protocol</b>: <i>B. bronchiseptica</i> electroporation</p><p><b>Basic Protocol 3</b>: Screening for sucrose-sensitive clones</p><p><b>Basic Protocol 4</b>: Homologous recombination (second crossing-over)</p><p><b>Basic Protocol 5</b>: PCR screening of putative marker-exchange mutants</p><p><b>Support Protocol</b>: Electrocompetent cell preparation</p>","PeriodicalId":39967,"journal":{"name":"Current Protocols in Microbiology","volume":"59 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2020-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpmc.125","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38581996","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"A Mouse Model of Sublethal Leptospirosis: Protocols for Infection with Leptospira Through Natural Transmission Routes, for Monitoring Clinical and Molecular Scores of Disease, and for Evaluation of the Host Immune Response","authors":"Nisha Nair,&nbsp;Maria Gomes-Solecki","doi":"10.1002/cpmc.127","DOIUrl":"10.1002/cpmc.127","url":null,"abstract":"<p>Leptospirosis is a zoonotic disease caused by pathogenic <i>Leptospira</i> species that are maintained in sylvatic and domestic environments by transmission among rodents and other carriers. Humans become infected after contact of breached skin or mucosa with contaminated water or soil. Understanding persistent or sublethal infection in a host is critical for controlling human risk of exposure to pathogenic <i>Leptospira</i>. Animal models that recapitulate disease progression after infection via natural transmission routes are more appropriate for validation of vaccines and therapeutics. Furthermore, the ability to measure shedding of live <i>Leptospira</i> in urine of reservoir and carrier hosts can be used to develop new diagnostic assays and sensors to evaluate human risk of exposure. We developed inbred mouse models of Leptospirosis, that bypass survival as a criterion, in which we can analyze both pathogen and host factors affecting sublethal infection (&lt;1 month), including shedding of <i>Leptospira</i> in urine. Mice are infected with pathogenic <i>Leptospira</i> using a physiologic route, and the clinical, histological, and molecular scores of disease are measured. Furthermore, the host immune response to <i>Leptospira</i> is evaluated. This mouse model also provides a tool in which to test fundamental hypotheses related to host-pathogen interactions and the immune mechanisms engaged in protective and pathogenic immune responses. © 2020 Wiley Periodicals LLC</p><p><b>Basic Protocol 1</b>: Culture and maintenance of virulent <i>Leptospira</i></p><p><b>Basic Protocol 2</b>: Infection of mice through a physiologic route and collection of clinical scores and biological samples</p><p><b>Basic Protocol 3</b>: Analysis of pathogenesis after <i>Leptospira</i> infection</p>","PeriodicalId":39967,"journal":{"name":"Current Protocols in Microbiology","volume":"59 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2020-11-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpmc.127","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38665020","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Monitoring Inflammasome Priming and Activation in Response to Candida albicans","authors":"Darian J. Santana,&nbsp;Faith M. Anderson,&nbsp;Teresa R. O'Meara","doi":"10.1002/cpmc.124","DOIUrl":"10.1002/cpmc.124","url":null,"abstract":"<p><i>Candida albicans</i> is a common mucosal colonizer, as well as a cause of lethal invasive fungal infections. The major predisposing factor for invasive fungal disease is a compromised immune system. One component of the host immune response to fungal infection is the activation of the inflammasome, a multimeric protein complex that is critical for regulating host pro-inflammatory responses. Here, we describe methods for investigating the interactions between <i>C. albicans</i> and host macrophages, with a focus on the inflammasome. <i>C. albicans</i> isolates differ in the degree to which they activate the inflammasome due to differences in internalization, morphogenic switching, and inflammasome priming. Therefore, we include protocols for identifying these factors. This simple in vitro model can be used to elucidate the contributions of specific <i>C. albicans</i> strains or mutants to different aspects of interactions with macrophages. © 2020 Wiley Periodicals LLC.</p><p><b>Basic Protocol 1</b>: Measuring inflammasome priming in response to <i>Candida albicans</i></p><p><b>Basic Protocol 2</b>: Measuring inflammasome activation in response to <i>Candida albicans</i></p><p><b>Support Protocol</b>: Controlling for phagocytosis</p>","PeriodicalId":39967,"journal":{"name":"Current Protocols in Microbiology","volume":"59 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2020-10-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpmc.124","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38627675","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Yersinia pseudotuberculosis: Cultivation, Storage, and Methods for Introducing DNA","authors":"Robert K. Davidson,&nbsp;Kimberly M. Davis","doi":"10.1002/cpmc.122","DOIUrl":"10.1002/cpmc.122","url":null,"abstract":"<p><i>Yersinia pseudotuberculosis</i> has been studied for many decades, and research on this microbe has taught us a great deal about host-pathogen interactions, bacterial manipulation of host cells, virulence factors, and the evolution of pathogens. This microbe should not be cultivated at 37°C because this is a trigger that the bacterium uses to sense its presence within a mammalian host and results in expression of genes necessary to colonize a mammalian host. Prolonged growth at this temperature can result in accumulation of mutations that reduce the virulence of the strain, so all protocols need to be modified for growth at room temperature, or 26°C. This article describes protocols for cultivating this microbe and for its long-term storage and its genetic manipulation by transformation and conjugation. © 2020 Wiley Periodicals LLC.</p><p><b>Basic Protocol 1</b>: Growth of <i>Y. pseudotuberculosis</i> from a stock</p><p><b>Basic Protocol 2</b>: Growth of <i>Y. pseudotuberculosis</i> in liquid medium from a single colony</p><p><b>Basic Protocol 3</b>: Freezing <i>Y. pseudotuberculosis</i> in glycerol for long-term storage</p><p><b>Basic Protocol 4</b>: Transformation of <i>Y. pseudotuberculosis</i> by electroporation</p><p><b>Basic Protocol 5</b>: Tri-parental mating/conjugation</p>","PeriodicalId":39967,"journal":{"name":"Current Protocols in Microbiology","volume":"59 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2020-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpmc.122","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38508627","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}