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Diversity of Xanthomonas spp. population - pepper pathogens in Serbia

dc.contributor.advisorObradović, Aleksa
dc.contributor.otherBalaž, Jelica
dc.contributor.otherMilošević, Mirjana
dc.contributor.otherGvozdenović-Varga, Jelica
dc.contributor.otherIvanović, Milan
dc.creatorIgnjatov, Maja V.
dc.date.accessioned2016-01-05T12:09:11Z
dc.date.available2016-01-05T12:09:11Z
dc.date.available2020-07-03T08:59:31Z
dc.date.issued2013-11-22
dc.identifier.urihttps://nardus.mpn.gov.rs/handle/123456789/2570
dc.identifier.urihttp://eteze.bg.ac.rs/application/showtheses?thesesId=1169
dc.identifier.urihttps://fedorabg.bg.ac.rs/fedora/get/o:8030/bdef:Content/download
dc.identifier.urihttp://vbs.rs/scripts/cobiss?command=DISPLAY&base=70036&RID=512066013
dc.description.abstractTokom 2008, 2009 i 2010. godine prikupljeni su uzorci obolelog lišća paprike sa simptomima bakteriozne pegavosti iz različitih lokaliteta Republike Srbije. Izolacijom iz zaraženih listova dobijeno je 116 sojeva bakterija. Proučavanja patogenih, biohemijsko-fizioloških odlika ukazuju da proučavani sojevi pripadaju vrsti Xanthomonas euvesicatoria. Primenom dva serološka testa (DAS - ELISA i test aglutinacije) potvrđena je antigena uniformnost proučavanih sojeva, kao i serološka sličnost sa bakterijom X. c. pv. vesicatoria. Diferencijacija Xanthomonas spp. prouzrokovača bakteriozne pegavosti paprike izvršena je primenom dve molekularne metode. Prvi metod zasnivao se na restrikcionoj analizi - RFLP (Restriction Fragment Lenght Polymorphism) fragmenta hrp gena (HrpB regiona) nakon digestije (sečenja) dobijenih proizvoda restrikcionim enzimima (CfoI, TaqI i HaeIII). Poređenjem restrikcionih profila proučavanih sojeva sa kontrolnim sojevima, potvrđena je sličnost sa vrstom X. euvesicatoria. Drugi molekularni metod je lančana reakcija polimeraze primenom specifičnih prajmera koji amplifikuju proizvode različite veličine specifične za: X. euvesicatoria – 173 bp; X. vesicatoria – 138 bp; X. perforans – 197 bp i X. gardneri – 154 bp. Kod svih proučavanih sojeva, uključujući i kontrolni soj X. euvesicatoria KFB (189) detektovani su fragmenti DNK veličine 173 bp, koji odgovaraju vrsti X. euvesicatoria. Utvrđeno je da je prag detekcije ove metode 0,4 x 103 CFU/ml. Proučeno je dejstvo bakar-sulfata (CuSO4), antibiotika streptomicina i kasugamicina, pri različitim koncentracijama, na razvoj bakterijskih ćelija u in vitro uslovima. U podlogu su dodati filterom sterilisani rastvori bakar-sulfata do konačne koncentracije od 100 i 200 ppm tj. aktivne komponente navedenih antibiotika do konačne koncentracije od 50, 100 i 200 ppm. Sojevi rezistentni na streptomicin nisu detektovani ovim istraživanjima. Rezistentnost prema 50 ppm kasugamicina utvrđena je kod 6 sojeva, a 19 sojeva je bilo rezistentno na 200 ppm bakar-sulfata. Dobijeni rezultati ukazuju na opasnost od razvoja rezistentnosti bakterija prema ovim jedinjenjima...sr
dc.description.abstractDuring 2008, 2009 and 2010 samples of diseased pepper leaves with bacterial spot symptoms were collected from different localities in Republic of Serbia. Total of 116 strains of bacteria were obtained by isolation from infected leaves. Studies of pathogenic, biochemical and physiological traits showed that tested strains belong to species Xanthomonas euvesicatoria. Two serological tests (DAS - ELISA and agglutination test) confirmed antigenic identity of tested bacterial isolates and serological similarity to bacteria X. c. pv. vesicatoria. Differentiation of Xantomonas spp. causal agent of bacterial spot of pepper was performed using two molecular methods. The first method was based on restriction analysis – RFLP (Restriction Fragment Length Polymorphism) of the hrp gene fragment (HrpB region) after digestion of obtained products by restriction enzymes (CfoI, TaqI and HaeIII). Comparison of restriction profiles of studied strains to control strains confirmed the similarity with the X. euvesicatoria. The other molecular method is polymerase chain reaction of specific primers which allow amplification of different size products sprecific for: X. euvesicatoria – 173 bp; X. vesicatoria – 138 bp; X. perforans – 197 bp and X. gardneri – 154 bp. As a result, DNA fragments of 173 bp which belong to species X. euvesicatoria were detected at all studied strains, including test strain Xe KFB (189). Threshold of detection was confirmed to be 0.4x103 CFU/ml. The effects of copper-sulphate (CuSO4), antibiotics streptomycin and kasugamycin on the development of bacterial cells were studied. The sensitivity of strains to bactericides was studied in vitro by culturing bacteria on sucrose pepton agar (SPA) plates, amended with filter-sterilized aqueous solution of streptomycin and kasugamycin (50, 100, 200 ppm) or copper-sulphate (100, 200 ppm). Streptomycin resistant strains were not detected, but 6 strains were resistant to kasugamycin (50 ppm) and 19 strains to copper-sulphate (200 ppm), indicating bacterial resistance development...en
dc.formatapplication/pdf
dc.languagesr
dc.publisherУниверзитет у Београду, Пољопривредни факултетsr
dc.relationinfo:eu-repo/grantAgreement/MESTD/Technological Development (TD or TR)/31030/RS//
dc.rightsopenAccessen
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceУниверзитет у Београдуsr
dc.subjectXanthomonas euvesicatoriasr
dc.subjectXanthomonas euvesicatoriaen
dc.subjectbakteriozna pegavostsr
dc.subjectkarakterizacijasr
dc.subjectmolekularna identifikacijasr
dc.subjectfiziološke rasesr
dc.subjectosetljivost genotipovasr
dc.subjectantibioticisr
dc.subjectbakteriofagisr
dc.subjectbacterial spoten
dc.subjectcharacterizationen
dc.subjectmolecular identificationen
dc.subjectracesen
dc.subjectsusceptibility of genotypeen
dc.subjectantibioticsen
dc.subjectbacteriophagesen
dc.titleDiverzitet populacije Xanthomonas spp. patogena paprike u Srbijisr
dc.titleDiversity of Xanthomonas spp. population - pepper pathogens in Serbiaen
dc.typedoctoralThesisen
dc.rights.licenseBY-NC-ND
dcterms.abstractОбрадовић, Aлекса; Милошевић, Мирјана; Балаж, Јелица; Ивановић, Милан; Гвозденовић-Варга, Јелица; Игњатов, Маја В.;
dc.identifier.fulltexthttps://nardus.mpn.gov.rs/bitstream/id/12592/Disertacija.pdf
dc.identifier.fulltexthttp://nardus.mpn.gov.rs/bitstream/id/12592/Disertacija.pdf
dc.identifier.rcubhttps://hdl.handle.net/21.15107/rcub_nardus_2570


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