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dc.contributor.authorCan-Sahna, Kezban
dc.contributor.authorAbaylı, Hasan
dc.contributor.authorÖzbek, Remziye
dc.contributor.authorTonbak, Sukm
dc.contributor.authorBulut, Hakan
dc.date.accessioned2022-05-11T14:42:22Z
dc.date.available2022-05-11T14:42:22Z
dc.date.issued2020
dc.identifier.issn0253-8318
dc.identifier.issn2074-7764
dc.identifier.urihttps://doi.org/10.29261/pakvetj/2020.051
dc.identifier.urihttps://hdl.handle.net/20.500.11776/9347
dc.description.abstractInfectious laryngotracheitis (ILT) is an economically important respiratory disease affecting the poultry industry worldwide. The aim of this study was to characterize the Turkish ILT virus (ILTV) isolates by sequencing and polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). ILTV isolates obtained from laying hens in Turkey in 2003 and 2018 were used in this study. The isolates were analyzed for ICP4, gG, gE and TK gene regions by PCR. The amplification products were used in RFLP analysis to determine the differences among the isolates. Sequence analyses of TK and ICP4 regions were carried out and a phylogenetic tree was formed by using the Maximum Likelihood method. Nucleotide identity values were then calculated among five isolates and other strains/isolates in Genbank. In addition, about 200 amino acid sequences of the start and end regions of the ICP4 gene were compared to other strains in Genbank. PCR-RFLP analysis indicated that Turkish ILTV isolates were low-virulent. In general, the nucleotide sequence similarities of the TK and ICP4 gene regions among Turkish isolates and others was more than 95% (lower in some Egyptian and Bangladeshi strains, 41 and 45% respectively); in the amino acid sequence, it was close to 100%. As a result, PCR-RFLP results were similar in many gene regions. However, evolutionary analysis of ICP4 and TK gene regions did not yield reliable results based on geographic distribution or pathogenicity levels. For this purpose, different methods, such as Bayesian analysis or the involvement of samples from different gene regions can yield more reliable results, just like whole-genome sequences. (C) 2020 PVJ. All rights reserveden_US
dc.description.sponsorshipScientific Research Projects Coordination Unit of Firat UniversityFirat University [VF18.07]en_US
dc.description.sponsorshipThis work was supported by the project number VF18.07 by the Scientific Research Projects Coordination Unit of Firat University.en_US
dc.language.isoengen_US
dc.publisherUniv Agriculture, Fac Veterinary Scienceen_US
dc.identifier.doi10.29261/pakvetj/2020.051
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectILTVen_US
dc.subjectPCR-RFLPen_US
dc.subjectsequence analysisen_US
dc.subjectTurkeyen_US
dc.subjectFragment-Length-Polymorphismen_US
dc.subjectPolymerase-Chain-Reactionen_US
dc.subjectVaccine Strainsen_US
dc.subjectFielden_US
dc.subjectDifferentiationen_US
dc.subjectStrategiesen_US
dc.subjectRegionsen_US
dc.subjectIltven_US
dc.titleCharacterization of Infectious Laryngotracheitis Virus Isolates from Turkey by Molecular and Sequence Analysisen_US
dc.typearticleen_US
dc.relation.ispartofPakistan Veterinary Journalen_US
dc.departmentFakülteler, Veteriner Fakültesi, Klinik Öncesi Bilimler Bölümü, Viroloji Ana Bilim Dalıen_US
dc.authorid0000-0003-2116-105X
dc.authorid0000-0003-2822-560X
dc.authorid0000-0002-5811-2588
dc.identifier.volume40en_US
dc.identifier.issue3en_US
dc.identifier.startpage337en_US
dc.identifier.endpage342en_US
dc.institutionauthorBulut, Hakan
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorscopusid24597452800
dc.authorscopusid57103691500
dc.authorscopusid57217233918
dc.authorscopusid8896086300
dc.authorscopusid7003605484
dc.authorwosidAbayli, Hasan/W-1858-2018
dc.authorwosidtonbak, sukru/W-2199-2018
dc.authorwosidErtan, Asli/AAE-6201-2021
dc.authorwosidBulut, Hakan/ABA-1433-2020
dc.identifier.wosWOS:000555954700011en_US
dc.identifier.scopus2-s2.0-85090277269en_US


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