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Horizontal Gene Transfer: Methods and Protocols PDF

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Methods in Molecular Biology 2075 Fernando de la Cruz Editor Horizontal Gene Transfer Methods and Protocols M M B ETHODS IN OLECULAR IO LO GY SeriesEditor JohnM.Walker School of Lifeand MedicalSciences University ofHertfordshire Hatfield, Hertfordshire, UK Forfurther volumes: http://www.springer.com/series/7651 For over 35 years, biological scientists have come to rely on the research protocols and methodologiesinthecriticallyacclaimedMethodsinMolecularBiologyseries.Theserieswas thefirsttointroducethestep-by-stepprotocolsapproachthathasbecomethestandardinall biomedicalprotocolpublishing.Eachprotocolisprovidedinreadily-reproduciblestep-by- step fashion, opening with an introductory overview, a list of the materials and reagents neededtocompletetheexperiment,andfollowedbyadetailedprocedurethatissupported with a helpful notes section offering tips and tricks of the trade as well as troubleshooting advice. These hallmark features were introduced by series editor Dr. John Walker and constitutethekeyingredientineachandeveryvolumeoftheMethodsinMolecularBiology series. Tested and trusted, comprehensive and reliable, all protocols from the series are indexedinPubMed. Horizontal Gene Transfer Methods and Protocols Edited by Fernando de la Cruz Instituto de Biomedicina y Biotecnología de Cantabria, Universidad de Cantabria-CSIC, Santander, Cantabria, Spain Editor FernandodelaCruz InstitutodeBiomedicinayBiotecnolog´ıadeCantabria UniversidaddeCantabria-CSIC Santander,Cantabria,Spain ISSN1064-3745 ISSN1940-6029 (electronic) MethodsinMolecularBiology ISBN978-1-4939-9876-0 ISBN978-1-4939-9877-7 (eBook) https://doi.org/10.1007/978-1-4939-9877-7 ©SpringerScience+BusinessMedia,LLC,partofSpringerNature2020 Thisworkissubjecttocopyright.AllrightsarereservedbythePublisher,whetherthewholeorpartofthematerialis concerned,specificallytherightsoftranslation,reprinting,reuseofillustrations,recitation,broadcasting,reproduction onmicrofilmsorinanyotherphysicalway,andtransmissionorinformationstorageandretrieval,electronicadaptation, computersoftware,orbysimilarordissimilarmethodologynowknownorhereafterdeveloped. Theuseofgeneraldescriptivenames,registerednames,trademarks,servicemarks,etc.inthispublicationdoesnotimply, evenintheabsenceofaspecificstatement,thatsuchnamesareexemptfromtherelevantprotectivelawsandregulations andthereforefreeforgeneraluse. Thepublisher,theauthors,andtheeditorsaresafetoassumethattheadviceandinformationinthisbookarebelievedto betrueandaccurateatthedateofpublication.Neitherthepublishernortheauthorsortheeditorsgiveawarranty, expressorimplied,withrespecttothematerialcontainedhereinorforanyerrorsoromissionsthatmayhavebeenmade. Thepublisherremainsneutralwithregardtojurisdictionalclaimsinpublishedmapsandinstitutionalaffiliations. ThisHumanaimprintispublishedbytheregisteredcompanySpringerScience+BusinessMedia,LLC,partofSpringer Nature. Theregisteredcompanyaddressis:233SpringStreet,NewYork,NY10013,U.S.A. Preface There is a fundamental difference between prokaryotes and eukaryotes in their evolution mechanisms and, consequently, in their genetic organization. Eukaryotes evolve within species, limited by sexual reproduction, while prokaryotes largely evolve by horizontal gene transfer (HGT), limited by the boundaries of gene exchange between species. In prokaryotes, HGT is pervasive, occurs contemporarily, and is an all-important mechanism of genetic originality. It can even be stated that bacterial genome structure and evolution cannotbeunderstoodunlesswecontemplatethedirecteffectsofHGT.Conversely,HGTin eukaryotes is an evolutionary mechanism that operates at a different timescale. Most eukaryoticspeciesareconfinedwithinthelimitsoftheirownspeciesbysexualreproduction. Consequently,andwithduerespecttoaffectedactors,activeinterspecificHGTispresently residual in eukaryotic organisms (not its cumulative effects, which are of extraordinary interest). Not surprisingly, therefore, the technologies used to study HGT in prokaryotes and eukaryotesarevastlydifferentandtheiraudiencesquiteseparate.Thisbookconcentrateson technologiesusedtostudyHGTinprokaryotes.TheelementsinvolvedinprokaryoticHGT are called mobile genetic elements (MGEs). There is a need for individualizing and func- tionallydescribingactiveMGEsifweattempttounderstandtheirstructure,epidemiology, andevolution.Inorder toachieveit,updatedmethodsfor theirdetectionandisolationare shownin PartI ofthisbook.Themain molecularprocesses involvedinHGTareconjuga- tion,transformation,andtransduction.PartIIdealswithmethodsinvolvedintheanalysisof these molecular processes. Again, quantitative description of these processes is required to attemptacomparative,functionaldescriptionofthedifferentprocesses.Thereisamyriadof MGEs,andeachonemusthavedifferentialspecificationsthatjustifytheirexistenceinever- evolving microbial ecosystems. Because of HGT, and the ups and downs of particular MGEs, bacterial populations adapt and evolve. Part III puts together a series of methods to analyze the adaptation and evolution of MGEs, with special attention to bioinformatics tools, as well as methods derived from the activity of MGEs that found utilities elsewhere. MethodsforthemetagenomicanalysisofMGEswillhopefullybethesubjectofalaterbook. Santander,Spain FernandodelaCruz v Contents Preface ..................................................................... v Contributors................................................................. xi PART I METHODS FOR THE DETECTION AND ISOLATION OF MOBILE GENETIC ELEMENTS 1 PlasmidDNAIsolationandVisualization:IsolationandCharacterization ofPlasmidsfromClinicalSamples......................................... 3 KaitlinA.Tagg,CarolaVenturini,MuhammadKamruzzaman, AndrewN.Ginn,andSallyR.Partridge 2 IsolationandVisualizationofPlasmidsfromGram-Positive BacteriaofInterestinPublicHealth....................................... 21 AnaR.Freitas,CarlaNovais,Luı´saPeixe,andTeresaM.Coque 3 Detection,Isolation,andCharacterizationofPlasmidsintheEnvironment .... 39 KhaldBlau,SvenJechalke,andKorneliaSmalla 4 BacteriophageIsolationandCharacterization:Phages ofEscherichiacoli ....................................................... 61 JuanJofreandMaiteMuniesa 5 DetectionandCharacterizationofTransposonsinBacteria................... 81 CatherineGuynet,PhanThaiNguyenLe,MichaelChandler, andBaoTon-Hoang PART II METHODS TO QUANTIFYAND CHARACTERIZE HORIZONTAL GENE TRANSFER 6 MeasuringPlasmidConjugationUsingAntibioticSelection.................. 93 JorgeRodriguez-GrandeandRaulFernandez-Lopez 7 MeasuringPlasmidConjugationUsingFluorescentReporters................ 99 CarolinaPalencia-Gandara,RaulRuiz,andRaulFernandez-Lopez 8 MethodstoQuantifyDNATransferinEnterococcus......................... 111 CarlaNovais,AnaR.Freitas,RicardoLe(cid:1)on-Sampedro,Luı´saPeixe, andTeresaM.Coque 9 QuantifyingandCharacterizingDistributiveConjugalTransfer inMycobacteriumsmegmatis.............................................. 123 RyanR.Clark,ToddA.Gray,andKeithM.Derbyshire 10 SpectrophotometricAssaystoQuantifytheActivityofT4SSATPases ......... 135 ElenaCabez(cid:1)onandIgnacioArechaga vii viii Contents 11 IdentificationofRelaxase-DNACovalentComplexesandDNAStrand TransferReactionProductsbyPolyacrylamideGelElectrophoresis ........... 145 Marı´aLucasandGabrielMoncalia´n 12 FirstBiochemicalStepsonBacterialTranspositionPathways ................. 157 CatherineGuynet,EmilienNicolas,BaoTon-Hoang,Jean-YvesBouet, andBernardHallet 13 NaturalTransformationinEscherichiacoli ................................. 179 YokoKomiyamaandSumioMaeda 14 IntegronIdentificationinBacterialGenomesandCassette RecombinationAssays................................................... 189 ClaireVit,Ce´lineLoot,Jose´AntonioEscudero,AleksandraNivina, andDidierMazel 15 MethodstoIdentifyandAnalyzeVesicle-ProtectedDNATransfer............ 209 AlbaBlesaandJose´Berenguer 16 MeasuringPlasmidStabilityinGram-NegativeBacteria...................... 223 Damia´nLobato-Ma´rquez 17 Methodsfor theAnalysisandCharacterizationofDefense MechanismsAgainstHorizontalGeneTransfer:CRISPRSystems ............ 235 AliciaCalvo-Villaman˜a´n,AudeBernheim,andDavidBikard PART III OMICS, BIOINFORMATICS, MATHEMATICAL MODELING, AND TECHNOLOGICAL APPLICATIONS OF HGT 18 TheMobilome:MetagenomicAnalysisofCircularPlasmids, Viruses,andOtherExtrachromosomalElements ........................... 253 PatrickDenisBrowne,WitoldKot,TueSparholtJørgensen, andLarsHestbjergHansen 19 IdentifyingConjugativePlasmidsandIntegrativeConjugative ElementswithCONJscan................................................ 265 JeanCury,SophieS.Abby,OliviaDoppelt-Azeroual,BertrandNe´ron, andEduardoP.C.Rocha 20 PlasmidFinderandInSilicopMLST:IdentificationandTyping ofPlasmidRepliconsinWhole-GenomeSequencing(WGS) ................. 285 AlessandraCarattoliandHenrikHasman 21 MOBscan:AutomatedAnnotationofMOBRelaxases....................... 295 M.PilarGarcilla´n-Barcia,SantiagoRedondo-Salvo,LuisVielva, andFernandodelaCruz 22 PlasmidTypingandClassification......................................... 309 LauraVillaandAlessandraCarattoli 23 PlasmidReconstructionfromNext-GenData:ADetailedProtocol for theUseofPLACNETwfor theReconstructionofPlasmids fromWGSDatasets..................................................... 323 Marı´adeToro,ValF.Lanza,LuisVielva,SantiagoRedondo-Salvo, andFernandodelaCruz Contents ix 24 StatisticalAnalysisofAccessoryGenome................................... 341 MiguelD.Ferna´ndez-de-Bobadilla,TeresaM.Coque, andValF.Lanza 25 InferringHorizontalGeneTransfer withDarkHorse,Phylomizer, andETEToolkits....................................................... 355 LuisDelaye,CarlosVargas,AmparoLatorre,andAndre´sMoya 26 MethodstoStudyFitnessandCompensatoryAdaptation inPlasmid-CarryingBacteria............................................. 371 JavierDelaFuente,JeronimoRodriguez-Beltran,andAlvaro SanMillan 27 ABroadHostRangePlasmid-BasedRoadmapforssDNA-Based RecombineeringinGram-NegativeBacteria................................ 383 Toma´sAparicio,Vı´ctordeLorenzo,andEstebanMartı´nez-Garcı´a 28 ConjugativeAssemblyGenomeEngineering(CAGE)....................... 399 MarcGu¨ell Index ...................................................................... 411 Contributors SOPHIES.ABBY (cid:1) Universite´GrenobleAlpes,CNRS,GrenobleINP,TIMC-IMAG,Grenoble, France TOMA´SAPARICIO (cid:1) SystemsandSyntheticBiologyProgram,CentroNacionaldeBiotecnologı´a (CNB-CSIC),Madrid,Spain IGNACIO ARECHAGA (cid:1) DepartamentodeBiologı´aMolecular,InstitutodeBiomedicinay Biotecnologı´adeCantabria(IBBTEC),UniversidaddeCantabria-CSIC,Santander, Spain JOSE´ BERENGUER (cid:1) CentrodeBiologı´aMolecularSeveroOchoa,UniversidadAut(cid:1)onomade Madrid-ConsejoSuperiordeInvestigacionesCientı´ficas,Madrid,Spain AUDEBERNHEIM (cid:1) SyntheticBiologyGroup,MicrobiologyDepartment,InstitutPasteur, Paris,France;E´coleDoctoraleFIRE—ProgrammeBettencourt,CentredeRecherches Interdisciplinaires,Paris,France;MicrobialEvolutionaryGenomics,Departmentof GenomesandGenetics,InstitutPasteur,Paris,France;AgroParisTech,Paris,France DAVIDBIKARD (cid:1) SyntheticBiologyGroup,MicrobiologyDepartment,InstitutPasteur,Paris, France KHALDBLAU (cid:1) InstituteforEpidemiologyandPathogenDiagnostics,JuliusKu¨hn-Institut (JKI),FederalResearchCentreforCultivatedPlants,Braunschweig,Germany ALBABLESA (cid:1) CentrodeBiologı´aMolecularSeveroOchoa,UniversidadAut(cid:1)onomade Madrid-ConsejoSuperiordeInvestigacionesCientı´ficas,Madrid,Spain;Departmentof Biotechnology,FacultyofExperimentalSciences,UniversidadFranciscodeVitoria, Madrid,Spain JEAN-YVESBOUET (cid:1) LaboratoiredeMicrobiologieetGe´ne´tiqueMole´culaires,Centrede BiologieInte´grative(CBI),CentreNationaldelaRechercheScientifique(CNRS), Universite´deToulouse,UPS,Toulouse,France PATRICKDENIS BROWNE (cid:1) DepartmentofEnvironmentalScience,AarhusUniversity, Roskilde,Denmark;DepartmentofPlantandEnvironmentalSciences, UniversityofCopenhagen,Frederiksberg,Denmark ELENACABEZO´N (cid:1) DepartamentodeBiologı´aMolecular,InstitutodeBiomedicinay Biotecnologı´adeCantabria(IBBTEC),UniversidaddeCantabria-CSIC,Santander, Spain ALICIA CALVO-VILLAMAN˜A´N (cid:1) SyntheticBiologyGroup,MicrobiologyDepartment,Institut Pasteur,Paris,France;E´coleDoctoraleFIRE—ProgrammeBettencourt,Centrede RecherchesInterdisciplinaires,Paris,France ALESSANDRACARATTOLI (cid:1) DepartmentofMolecularMedicine,SapienzaUniversityofRome, Rome,Italy MICHAELCHANDLER (cid:1) LaboratoiredeMicrobiologieetGe´ne´tiqueMole´culaires,Centrede BiologieInte´grative(CBI),CentreNationaldelaRechercheScientifique(CNRS), Universite´deToulouse,UPS,Toulouse,France;DepartmentofBiochemistry,Molecularand CellularBiology,GeorgetownUniversityMedicalCenter,Washington,DC,USA RYANR.CLARK (cid:1) NewYorkStateDepartmentofHealth,WadsworthCenter,Albany,NY, USA xi

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