Production of Polyclonal Antiserum using Recombinant Coat Protein of Passiflora mottle virus Infecting Passion Fruit in Vietnam

Received: 28-09-2020

Accepted: 16-12-2020

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Cuong, H., Tuyet, L., Ha, T., Huy, N., & Dung, D. (2024). Production of Polyclonal Antiserum using Recombinant Coat Protein of Passiflora mottle virus Infecting Passion Fruit in Vietnam. Vietnam Journal of Agricultural Sciences, 19(2), 195–205. http://testtapchi.vnua.edu.vn/index.php/vjasvn/article/view/788

Production of Polyclonal Antiserum using Recombinant Coat Protein of Passiflora mottle virus Infecting Passion Fruit in Vietnam

Ha Viet Cuong (*) 1, 2, 3 , Le Thi Tuyet 2 , Tran Nguyen Ha 2 , Nguyen Duc Huy 2 , Do Tan Dung 2

  • 1 Trung tâm Nghiên cứu Bệnh cây Nhiệt đới, Học viện Nông nghiệp Việt Nam
  • 2 Khoa Nông học, Học viện Nông nghiệp Việt Nam
  • 3 Bộ môn Bệnh cây, Khoa Nông học, Học viện Nông nghiệp Việt Nam
  • Keywords

    Passifloramottlevirus, potyvirus, DIBA, ELISA, passionfruit, Vietnam

    Abstract


    ThemajoraimofthisworkwastoproducepolyclonalantibodiesfordiagnosisofPassifloramottlevirus(PaMoV),aputativenovelpotyvirus(thegenusPotyvirus,thefamilyPotyviridae),whichwasfirstdiscoveredfrompassionfruit(Passifloraedulis)andnamedinVietnam.Theentiregeneencodingcoatprotein(CP)ofPaMoVwasclonedonpET28avectorandtheexpressionofthisproteinwasevaluatedintheEscherichiacoli(E.coli)strainRosetta(DE3).ThedenaturedrecombinantPaMoVCPproteinwasusedasan antigenforrabbitinjection.ThetiterandspecificityoftherabbitantiserumwereevaluatedbyDot-ImmunobindingAssay(DIBA)andPlateTrappedAntigenEnzyme-LinkedImmunosorbentAssay(PTA-ELISA).Theexperimental resultsshowed: (i) Rosetta(DE3)wasasuitablehoststrainforexpressionofthePaMoVCPprotein, (ii) thePaMoV CP antiserumdidnotreactwithhealthypassionfruitsapanddetected easily cognate inpassionfruitleaves, and (iii) the antiserumalsoreactedwithtwopotyviruses,Telosmamosaicvirus(TelMV)andEastAsianpassifloravirusstrainIB(EAPV-IB),bothareinfectingpassionfruitinVietnam.

    References

    AbdEl-AzizM.H.(2019).Threemodernserologicalmethodstodetectplantviruses.JournalofPlantScienceandPhytopathology.3:101-106.

    Abdel-SalamA.M.,El-AttarA.K.&SolimanA.M.(2013).TheuseofnativeanddenaturedrecombinantcoatproteinformsforinductionofgoodqualityantiseraforPotatovirusXandPotatoleafrollvirus.AmericanJournalofResearchCommunication.1(17):70-86.

    CostaS.,AlmeidaA.,CastroA.&DominguesL.(2014).Fusiontagsforproteinsolubility,purificationandimmunogenicityinEscherichiacoli:thenovelFh8system.Frontiersinmicrobiology.5:63.

    GadhaveK.R.,GautamS.,RasmussenD.A.&SrinivasanR.(2020).AphidTransmissionofPotyvirus:TheLargestPlant-InfectingRNAVirusGenus.Viruses.12(7):773.

    GrintzalisK.,GeorgiouC.D.&SchneiderY.-J.(2015).AnaccurateandsensitiveCoomassieBrilliantBlueG-250-basedassayforproteindetermination.Analyticalbiochemistry.480:28-30.

    HaV.C.,TranN.H.,DoT.D.,NguyenD.H.,WeiS.F.,QinW.&LyuR.H.(2019).Productionofpolyclonalantiserafordiagnosisofriceyellowstuntvirus(RYSV)inVietnam.JournalofSouthernAgriculture.50(7):1472:1482.

    LimaJ.A.A.,NascimentoA.K.Q.,RadaelliP.&PurcifullD.E.(2012).Serologyappliedtoplantvirology.Serologicaldiagnosisofcertainhuman,animalandplantdiseases.Rijeka,Croatia:InTech.1:71-94.

    PengD.,ZhengG.,ZhengZ.,TongQ.&MingY.(2018).HighvariabilityintheNterminusofcoatproteinamongpotyvirusesanditsadvantageinproducingaspecificantibody.EuropeanJournalofPlantPathology.152(2):385-393.

    QIAgenesE.coliHandbook(2009).QIAgenesexpressionkitE.coliforhigh-LevelexpressionofHis-taggedproteinsinE.colisystems.

    RosanoG.L.&CeccarelliE.A.(2014).RecombinantproteinexpressioninEscherichiacoli:advancesandchallenges.Frontiersinmicrobiology.5:172.

    SastryK.S.(2013).DiagnosisandDetectionofPlantVirusandViroidDiseases.In:PlantVirusandViroidDiseasesintheTropics.Springer. pp.233-353.

    ShuklaD.D.,LauricellaR.&WardC.W.(1992).Serologyofpotyviruses:currentproblemsandsomesolutions.In:PotyvirusTaxonomy.pp. 57-69.

    ShuklaD.D.,TribbickG.,MasonT.,HewishD.R.,GeysenH.&WardC.W.(1989).Localizationofvirus-specificandgroup-specificepitopesofplantpotyvirusesbysystematicimmunochemicalanalysisofoverlappingpeptidefragments.ProceedingsoftheNationalAcademyofSciences.86(21):8192-8196.

    SouiriA.,ZemzamiM.,AmzaziS.&EnnajiM.M.(2014).Polyclonalandmonoclonalantibody-basedmethodsfordetectionofplantviruses.EuropeanJournalofScientificResearch.123(3):281-295.

    VanRegenmortelM.H.(1992).Theconformationalspecificityofviralepitopes.FEMSmicrobiologyletters.100(1-3):483-487.

    VanRegenmortelM.H.(2014).Specificity,polyspecificityandheterospecificityofantibody-antigenrecognition.JournalofMolecularRecognition.27(11):627-639.

    WylieS.J.,AdamsM.,ChalamC.,KreuzeJ.,López-MoyaJ.J.,OhshimaK.,PraveenS.,RabensteinF.,StengerD.&WangA.(2017).ICTVvirustaxonomyprofile:Potyviridae.TheJournalofgeneralvirology.98(3):352.

    XieL.,GaoF.,ZhengS.,ZhangX.,ZhangL.&LiT.(2019).Molecularcharacterizationofanewpotyvirusinfectingpassionfruit.Archivesofvirology.164(7):1903-1906.

    ZellnerM.,WinklerW.,HaydenH.,DiestingerM.,EliasenM.,GesslbauerB.,MillerI.,ChangM.,KunglA.&RothE.(2005).Quantitativevalidationofdifferentproteinprecipitationmethodsinproteomeanalysisofbloodplatelets.Electrophoresis.26(12):2481-2489.