Generation and characterization of recombinant vaccinia viruses expressing a hepatitis C virus Core protein, genotype 1b, individually or as a polyprotein

نویسندگان

  • Liz Alvarez-Lajonchere
  • Ivis Guerra
  • Yalena Amador-Cañizares
  • Roberto Frías
  • Dania Vazquez-Blomquist
  • Juan Morales
  • Santiago Dueñas-Carrera
چکیده

Hepatitis C virus Core is an intriguing protein with important roles in life cycle of this pathogen. In the present work, recombinant vaccinia viruses expressing a genotype 1b HCV Core protein, individually (vvCore) or as a polyprotein Core-E1-E2 (vvRE), were generated and characterized. In general, viral titer of recombinant vaccinia viruses expressing the Core protein in BSC40 infected cells was similar to the one detected in BSC40 cells infected with the Western Reserve vaccinia virus control. Additionally, intraperitonial inoculation of BALB/c mice with 10 plaque forming units (pfu) of vvCore or vvRE effectively infected animals. Viral load detected in ovaries of infected mice was similar for recombinant viruses or vaccinia virus control. Moreover, up to 10 pfu of recombinant vaccinia viruses were inoculated to BALB/c mice without lethal consequences. Remarkably, after single inoculation of recombinant vaccinia viruses, specific antibodies or IFN-gamma secreting cells against the HCV Core antigen were not detectable. The generated recombinant vaccinia viruses, expressing the HCV Core, are valuable instruments for the development of surrogate challenge models and for the future investigation of in vitro and in vivo aspects related to this viral antigen.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

The Full Length Hepatitis C Virus Polyprotein and Interactions with the Interferon-Beta Signalling Pathways in vitro

Background: Hepatitis C is a global health problem. The exact mechanisms by which hepatitis C virus (HCV) can evade the host immune system have become controversial. Whether HCV polyproteins modulate IFN signalling pathways or HCV proteins are responsible for such a property is the subject of interest. Therefore, an efficient baculovirus delivery system was developed to introduce the whole geno...

متن کامل

Suppression of host immune response by the core protein of hepatitis C virus: possible implications for hepatitis C virus persistence.

Hepatitis C virus (HCV) is a major human pathogen causing mild to severe liver disease worldwide. This positive strand RNA virus is remarkably efficient at establishing chronic infections. Although a high rate of genetic variability may facilitate viral escape and persistence in the face of Ag-specific immune responses, HCV may also encode proteins that facilitate evasion of immunological surve...

متن کامل

Enhanced Immune Responses of a Hepatitis C Virus core DNA Vaccine by co-Inoculating Interleukin-12 Expressing Vector in Mice

Background: Hepatitis C (HCV) is a worldwide problem without an effective vaccine with more than 170 million chronically infected people worldwide. DNA vaccines expressing antigenic portions of the virus with adjutants have recently been developed as a novel vaccination technology. Objectives: In the present study, a DNA vaccine expressing HCV core protein was developed with IL12 as a genetic a...

متن کامل

Overexpression of Full-Length Core Protein of Hepatitis C Virus by Escherichia coli Cultivated in Stirred Tank Fermentor

The mature core protein of the Hepatitis C virus (HCVC173) carrying pelB as a signal peptide (PelB::core) was overexpressed in Escherichia coli as 18% and 23.3% of the host’s total protein, in flask and fermentor cultivation, respectively. A final specific yield of 25 ± 1 mg HCVC173/g dry cell weight and an overallproductivity of 51±1 mg HCVC173/l/h were obtained in the stirred-tank ferme...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2008