Page 45 - E-Tez Bülteni Mart 2026, Sayı 5
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                                    MASTER’S THESIS
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                     Department of Molecular Biotechnology
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                 Biologıcal Control Of Cotton Pest Helicoverpa Armigera
                 B i o l o g ı c a l   C o n t r o l   O f   C o t t o n   P e s t   H e l i c o v e r p a   A r m i g e r a
                         Using Rna Interference (Rnai) Technology
                         U s i n g   R n a   I n t e r f e r e n c e   ( R n a i )   T e c h n o l o g y
                                     H a l i m e   K A R A T E K E
                                     Halime KARATEKE
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                        T Thesis Supervisor: Prof. Dr. Remziye NALÇACIOĞLU
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                                     Thesis Summary
        Helicoverpa armigera (Hübner, 1808) is a member of the lepidopteran order of the Noctuidae family. It is an effective polyphagous
        species that causes serious damage to agricultural crops in many parts of the world. Control is generally achieved with synthetic
        insecticides. The development of resistance in insects to synthetic insecticides, coupled with the harm they cause to humans and other
        non-target  organisms,  has  necessitated  the  development  and  use  of  alternative  biological  control  preparations.  RNA  interference
        (RNAi) is an alternative method for controlling pest populations. This method provides a species-specific control method by silencing
        vital genes in target insects. Chitin, an important biological polymer, is found in all arthropods, including insects. Furthermore, chitin and
        the enzymes involved in its synthesis are not found in plants or humans.  This study aimed to silence the expression of the Chitin
        synthase B (CHSB) gene, which is involved in chitin synthesis, using double stranded RNA (dsRNA) technology. For this purpose, the
        CHSB gene from H. armigera larvae was amplified by polymerase chain reaction and subsequently cloned into a dsRNA synthesis
        vector  (L4440).  dsRNA  synthesis  was  performed  in  a  bacterial  system  (E.  coli  HT115  (DE3)  strain).  Subsequently,  both  the  dsRNA-
        expressing bacterial suspension and the total RNA purified from these cells were mixed with separate feed and fed to H. armigera
        larvae.  The  effects  of  dsRNA  on  insects  were  investigated  through  bioassay  experiments.  Both  dsRNAexpressing  E.  coli  cells  and
        RNA’s isolated from these cells induced significant mortality in thirdinstar H. armigera larvae, reaching 40% and 35%, respectively,
        whereas control treatments exhibited negligible effects.
                       Keywords: dsRNA, Chitin Synthase B, RNA interference, Helicoverpa armigera
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