New chemical method of viral inactivation for vaccine development based on membrane fusion inhibition

被引:5
|
作者
Stauffer, Fausto
De Miranda, Joari
Schechter, Marcos C.
Queiroz, Fernando A.
Santos, Nathalia O.
Alves, Ada M. B.
Da Poian, Andrea T. [1 ]
机构
[1] Univ Fed Rio de Janeiro, Inst Bioquim Med, BR-21941590 Rio De Janeiro, RJ, Brazil
[2] Fundacao Oswaldo Cruz, Inst Oswaldo Cruz, Lab Imunopatol, BR-21040900 Rio De Janeiro, RJ, Brazil
关键词
viral inactivation; diethylpyrocarbonate; vesicular stomatitis virus;
D O I
10.1016/j.vaccine.2007.09.025
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Membrane fusion is an essential step in the entry of enveloped viruses into their host cells. This process is triggered by conformational changes in viral surface glycoproteins. We have demonstrated previously that modification of vesicular stomatitis virus (VSV) with diethylpyrocarbonate (DEPC abolished the conformational changes on VSV glycoprotein and the fusion reaction induced by the virus. Moreover, we observed that viral treatment with DEPC inactivates the virus, preserving the conformational integrity of its surface proteins. In the present work, we evaluated the potential use of DEPC as a viral inactivating chemical agent for the development of useful vaccines. Pathogenicity and viral replication in Balb/c mice were abolished by viral treatment with 0.5 mM DEPC. In addition, antibodies elicited in mice after intraperitoneal immunization with DEPC-inactivated VSV mixed with adjuvants were able to recognize and neutralize the native virus and efficiently protected animals against the challenge with lethal doses of VSV. These results together suggest that viral inactivation with DEPC seems to be a suitable method for the development of safe vaccines. (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:7885 / 7892
页数:8
相关论文
共 50 条
  • [1] Viral Inactivation Based on Inhibition of Membrane Fusion: Understanding the Role of Histidine Protonation to Develop New Viral Vaccines
    Da Poian, A. T.
    Carneiro, F. A.
    Stauffer, F.
    PROTEIN AND PEPTIDE LETTERS, 2009, 16 (07): : 779 - 785
  • [2] Inactivation of vesicular stomatitis virus through inhibition of membrane fusion by chemical modification of the viral glycoprotein
    Stauffer, Fausto
    De Miranda, Joari
    Schechter, Marcos C.
    Carneiro, Fabiana A.
    Salgado, Leonardo T.
    Machado, Gisele F.
    Da Poian, Andrea T.
    ANTIVIRAL RESEARCH, 2007, 73 (01) : 31 - 39
  • [3] Delipidation of a hepadnavirus: Viral inactivation and vaccine development
    Cham, B. E.
    Vickery, K.
    Tohidi-Esfahani, R.
    Cossart, Y.
    JOURNAL OF VIROLOGICAL METHODS, 2006, 137 (01) : 160 - 163
  • [4] Mechanisms of viral membrane fusion and its inhibition
    Eckert, DM
    Kim, PS
    ANNUAL REVIEW OF BIOCHEMISTRY, 2001, 70 : 777 - 810
  • [5] Stabilisation of Viral Membrane Fusion Proteins in Prefusion Conformation by Structure-Based Design for Structure Determination and Vaccine Development
    Ebel, Henriette
    Benecke, Tim
    Vollmer, Benjamin
    VIRUSES-BASEL, 2022, 14 (08):
  • [6] Inhibition of Viral-Induced Membrane Fusion by Peptides
    Vitiello, Mariaterasa
    Galdiero, Marilena
    Galdiero, Massimiliano
    PROTEIN AND PEPTIDE LETTERS, 2009, 16 (07): : 786 - 793
  • [7] NEW APPROACHES IN VIRAL VACCINE DEVELOPMENT
    BROWN, F
    SCANDINAVIAN JOURNAL OF INFECTIOUS DISEASES, 1990, : 39 - 46
  • [8] Inhibition of Viral Membrane Fusion by Peptides and Approaches to Peptide Design
    Duezguenes, Nejat
    Fernandez-Fuentes, Narcis
    Konopka, Krystyna
    PATHOGENS, 2021, 10 (12):
  • [9] Viral membrane fusion: is glycoprotein G of rhabdoviruses a representative of a new class of viral fusion proteins?
    Da Poian, AT
    Carneiro, FA
    Stauffer, F
    BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH, 2005, 38 (06) : 813 - 823
  • [10] Effect of 25-hydroxycholesterol in viral membrane fusion: Insights on HIV inhibition
    Gomes, Barbara
    Goncalves, Sonia
    Disalvo, Anibal
    Hollmann, Axel
    Santos, Nuno C.
    BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2018, 1860 (05): : 1171 - 1178