Literature DB >> 29212944

The Neutralizing Linear Epitope of Human Herpesvirus 6A Glycoprotein B Does Not Affect Virus Infectivity.

Aika Wakata1, Satoshi Kanemoto1, Huamin Tang1,2, Akiko Kawabata1, Mitsuhiro Nishimura1, Chyntia Jasirwan3, Nora Fahmy Mahmoud1,4, Yasuko Mori5.   

Abstract

Human herpesvirus 6A (HHV-6A) glycoprotein B (gB) is a glycoprotein consisting of 830 amino acids and is essential for the growth of the virus. Previously, we reported that a neutralizing monoclonal antibody (MAb) called 87-y-13 specifically reacts with HHV-6A gB, and we identified its epitope residue at asparagine (Asn) 347 on gB. In this study, we examined whether the epitope recognized by the neutralizing MAb is essential for HHV-6A infection. We constructed HHV-6A bacterial artificial chromosome (BAC) genomes harboring substitutions at Asn347, namely, HHV-6A BACgB(N347K) and HHV-6A BACgB(N347A). These mutant viruses could be reconstituted and propagated in the same manner as the wild type and their revertants, and MAb 87-y-13 could not inhibit infection by either mutant. In a cell-cell fusion assay, Asn at position 347 on gB was found to be nonessential for cell-cell fusion. In addition, in building an HHV-6A gB homology model, we found that the epitope of the neutralizing MAb is located on domain II of gB and is accessible to solvents. These results indicate that Asn at position 347, the linear epitope of the neutralizing MAb, does not affect HHV-6A infectivity.IMPORTANCE Glycoprotein B (gB) is one of the most conserved glycoproteins among all herpesviruses and is a key factor for virus entry. Therefore, antibodies targeted to gB may neutralize virus entry. Human herpesvirus 6A (HHV-6A) encodes gB, which is translated to a protein of about 830 amino acids (aa). Using a monoclonal antibody (MAb) for HHV-6A gB, which has a neutralizing linear epitope, we analyzed the role of its epitope residue, N347, in HHV-6A infectivity. Interestingly, this gB linear epitope residue, N347, was not essential for HHV-6A growth. By constructing a homology model of HHV-6A gB, we found that N347 was located in the region corresponding to domain II. Therefore, with regard to its neutralizing activity against HHV-6A infection, the epitope on gB might be exposed to solvents, suggesting that it might be a target of the immune system.
Copyright © 2018 American Society for Microbiology.

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Keywords:  HHV-6; epitope; gB; neutralizing antibodies

Mesh:

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Year:  2018        PMID: 29212944      PMCID: PMC5809734          DOI: 10.1128/JVI.02074-17

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  56 in total

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Journal:  J Virol       Date:  2013-07-24       Impact factor: 5.103

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  2 in total

1.  Humanization of Murine Neutralizing Antibodies against Human Herpesvirus 6B.

Authors:  Bochao Wang; Mitsuhiro Nishimura; Yuji Maekawa; Toshiya Kotari; Toshiomi Okuno; Yasuko Mori
Journal:  J Virol       Date:  2019-05-01       Impact factor: 5.103

2.  The Combination of gQ1 and gQ2 in Human Herpesvirus 6A and 6B Regulates the Viral Tetramer Function for Their Receptor Recognition.

Authors:  Aika Wakata; Lidya Handayani Tjan; Mitsuhiro Nishimura; Akiko Kawabata; Anna Lystia Poetranto; Chisato Yamamoto; Jun Arii; Yasuko Mori
Journal:  J Virol       Date:  2020-12-09       Impact factor: 5.103

  2 in total

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