Objective: To detect the immunogenicity of enterotoxigenic Escherichia coli heat-labile enterotoxin B subunit (LTB) and evaluate the immune effect of enterovirus 71 (EV71) capsid protein VP1 together with LTB by the intranasal route.
Methods: The LTB gene was cloned into the plasmid pET32a. The 6×His-LTB fusion protein was purified with Ni(2+)-NTA resin and used to vaccinate the New Zealand white rabbits to prepare the LTB-specific antiserum. The titer was determined by ELISA. BALB/c mice were immunized with normal saline, purified EV71 VP1 alone and EV71 VP1 together with LTB by the intranasal drip respectively. The sera as well as lung and intestinal mucosa lavage fluids were collected and determined for IgG and secretory IgA (sIgA) by indirect ELISA.
Results: Recombinant plasmid pET32a-LTB was constructed successfully. The expressed fusion protein 6×His-LTB, with a relative molecular mass of about 30 000, existed mostly in a form of inclusion body. The serum antibody titer induced with it was 1:125 000 in the New Zealand white rabbits. The levels of specific IgG and sIgA in mice immunized with EV71 VP1 plus LTB were significantly higher than those in the ones with EV71 VP1 alone and normal saline.
Conclusion: Fusion protein 6×His-LTB was successfully expressed in E.coli BL21 (DE3) and showed both good immunogenicity and adjuvant activity. The LTB can efficiently enhance specific serum antibody response and induce mucosal immune response by intranasal drip.
Download full-text PDF |
Source |
---|
J Transl Med
June 2024
School of Pharmaceutical, Department of Laboratory Medicine of Fenyang College, Shanxi Medical University, Taiyuan, Shanxi Province, 030001, China.
Background: Astragaloside IV (AST-IV), as an effective active ingredient of Astragalus membranaceus (Fisch.) Bunge. It has been found that AST-IV inhibits the replication of dengue virus, hepatitis B virus, adenovirus, and coxsackievirus B3.
View Article and Find Full Text PDFVirol Sin
August 2024
Center for Emerging Infectious Diseases, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan, Hubei, 430071, China; Hubei Jiangxia Laboratory, Wuhan, Hubei, 430200, China. Electronic address:
Increasing evidences suggest that the methyltransferase NSUN2 catalyzes 5-methylcytosine (m5C) modifications on viral RNAs, which are essential for the replication of various viruses. Despite the function of m5C deposition is well characterized, other potential roles of NSUN2 in regulating viral replication remain largely unknown. In this study, the m5C modified residues catalyzed by NSUN2 on enterovirus 71 (EV71) RNAs were mapped.
View Article and Find Full Text PDFFront Public Health
May 2024
Zhejiang Provincial Center for Disease Control and Prevention, Hangzhou, Zhejiang, China.
Vaccine
June 2024
School of Bioresources and Technology, King Mongkut's University of Technology Thonburi, Bangkok, Thailand; Pilot Plant Development and Training Institute, King Mongkut's University of Technology Thonburi, Bangkok, Thailand. Electronic address:
Hand, foot, and mouth disease (HFMD) poses a significant public health threat primarily caused by four major enteroviruses: enterovirus 71 (EV71), coxsackieviruses A16, A10, and A6. Broadly protective immune responses are essential for complete protection against these major enteroviruses. In this study, we designed a new tetravalent immunogen for HFMD, validated it in silico, in vivo evaluated the immunogenicity of the DNA-based tetravalent vaccine in mice, and identified immunogenic B-cell and T-cell epitopes.
View Article and Find Full Text PDFAutophagy
July 2024
State Key Laboratory for Animal Disease Control and Prevention, College of Veterinary Medicine, Lanzhou University, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, China.
Many viruses, including foot-and-mouth disease virus (FMDV), can promote the degradation of host proteins through macroautophagy/autophagy, thereby promoting viral replication. However, the regulatory mechanism between autophagy and innate immune responses is not fully understood during FMDV infection. Here, we found that the host GTPBP4/NOG1 (GTP binding protein 4) is a negative regulator of innate immune responses.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!