کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5589488 | 1404644 | 2016 | 7 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
The NS3 and NS4A genes as the targets of RNA interference inhibit replication of Japanese encephalitis virus in vitro and in vivo
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کلمات کلیدی
DMEMNS3BVDVDENVhptRT-PCRshRNAPBSLD50hpi50% lethal dose - 50٪ مرگ و میرMOI - MERNA interference - RNA تداخل کنندهshort hairpin RNA - RNA موی سر کوتاهDulbecco's modification of Eagle's medium - اصلاح Dulbecco از محیط عقابJEV - جیوMin - حداقلminute - دقیقهHour - ساعتhours post infection - ساعت پس از عفونتphosphate buffer solution - محلول بافر فسفاتHCV - هپاتیت سیHepatitis C virus - هپاتیت سیplaque forming unit - واحد پالک تشکیل شده استreverse transcription-polymerase chain reaction - واکنش زنجیره ای رونویسی-پلیمراز معکوسJapanese encephalitis virus - ویروس آنسفالیت ژاپنیbovine viral diarrhea virus - ویروس اسهال ویروسی گاوDengue virus - ویروس دنگیMembrane protein - پروتئین غشائیEnvelope protein - پروتئین پاکتcapsid protein - پروتئین کپسیدpfu - پفوmultiplicity of infection - چندین عفونت
موضوعات مرتبط
علوم زیستی و بیوفناوری
بیوشیمی، ژنتیک و زیست شناسی مولکولی
ژنتیک
پیش نمایش صفحه اول مقاله
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چکیده انگلیسی
Japanese encephalitis virus (JEV) is a mosquito-borne flavivirus that can cause acute encephalitis with a high fatality rate. RNA interference (RNAi) is a powerful tool to silence gene expression and a potential therapy for virus infection. In this study, the antiviral ability of eight shRNA expression plasmids targeting different sites of the NS3 and NS4A genes of JEV was determined in BHK21 cells and mice. The pGP-NS3-3 and pGP-NS4A-4 suppressed 93.9% and 82.0% of JEV mRNA in cells, respectively. The virus titer in cells was reduced approximately 950-fold by pretreating with pGP-NS3-4, and 640-fold by pretreating with pGP-NS4A-4. The results of western blot and immunofluorescence analysis showed JEV E protein and viral load in cells were remarkably inhibited by shRNA expression plasmids. The viral load in brains of mice pretreated with pGP-NS3-4 or pGP-NS4A-4 were reduced approximately 2400-fold and 800-fold, respectively, and the survival rate of mice challenged with JEV were 70% and 50%, respectively. However, the antiviral ability of shRNA expression plasmids was decreased over time. This study indicates that RNAi targeting of the NS3 and NS4A genes of JEV can sufficiently inhibit the replication of JEV in vitro and in vivo, and NS3 and NS4A genes might be potential targets of molecular therapy for JEV infection.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Gene - Volume 594, Issue 2, 15 December 2016, Pages 183-189
Journal: Gene - Volume 594, Issue 2, 15 December 2016, Pages 183-189
نویسندگان
Lei Yuan, Rui Wu, Hanyang Liu, Xintian Wen, Xiaobo Huang, Yiping Wen, Xiaoping Ma, Qigui Yan, Yong Huang, Qin Zhao, Sanjie Cao,