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Neutralizing Antibody Response to Genotypically Diverse Measles Viruses in Clinically Suspected Measles Cases

The neutralizing antibody (Nt-Ab) response to vaccine and wild-type measles viruses (MeV) was studied in suspected measles cases reported during the years 2012–2016. The neutralization activity against MeV A, D4 and D8 genotypes was studied on sera (Panel A; n = 68 (measles-immunized) and Panel B; n...

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Autores principales: Vaidya, Sunil R., Kumbhar, Neelakshi S., Andhare, Gargi K., Pawar, Nilesh, Walimbe, Atul M., Kinikar, Meenal, Kasibhatla, Sunitha M., Kulkarni-Kale, Urmila
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10674322/
https://www.ncbi.nlm.nih.gov/pubmed/38005920
http://dx.doi.org/10.3390/v15112243
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author Vaidya, Sunil R.
Kumbhar, Neelakshi S.
Andhare, Gargi K.
Pawar, Nilesh
Walimbe, Atul M.
Kinikar, Meenal
Kasibhatla, Sunitha M.
Kulkarni-Kale, Urmila
author_facet Vaidya, Sunil R.
Kumbhar, Neelakshi S.
Andhare, Gargi K.
Pawar, Nilesh
Walimbe, Atul M.
Kinikar, Meenal
Kasibhatla, Sunitha M.
Kulkarni-Kale, Urmila
author_sort Vaidya, Sunil R.
collection PubMed
description The neutralizing antibody (Nt-Ab) response to vaccine and wild-type measles viruses (MeV) was studied in suspected measles cases reported during the years 2012–2016. The neutralization activity against MeV A, D4 and D8 genotypes was studied on sera (Panel A; n = 68 (measles-immunized) and Panel B; n = 50 (unvaccinated)) that were either laboratory confirmed or not confirmed by the presence of IgM antibodies. Additionally, the Nt-Ab response in Panel A was measured against the MeV vaccine and four wild-type viruses. Neutralization results were compared using homology modeling and molecular dynamics simulation (MDS) of MeV-hemagglutinin (H) and fusion (F) proteins. Overall, the Nt-Ab titres for MeV-A were found to be significantly lower than MeV-D4 and MeV-D8 viruses for Panel A. No major difference was noted in Nt-Ab titres between MeV-D8 viruses (Jamnagar and New Delhi), whereas MeV-D4 (Sindhudurg and Bagalkot (BGK) viruses) showed significant differences between Nt-Ab titres for Panel B. Interestingly, the substitutions observed in epitopes of H-protein, L249P and G316A are observed to be unique to MeV-BGK. MDS of H-protein revealed significant fluctuations in neutralizing epitopes due to L249P substitution. The majority of the clinically suspected cases showed Nt-Abs to MeV wild-types. Higher IgG antibody avidity and Nt-Ab titres were noted in IgM-negatives than in IgM-positives cases, indicating reinfection or breakthrough. MDS revealed reduced neutralization due to decreased conformational flexibility in the H-epitope.
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spelling pubmed-106743222023-11-10 Neutralizing Antibody Response to Genotypically Diverse Measles Viruses in Clinically Suspected Measles Cases Vaidya, Sunil R. Kumbhar, Neelakshi S. Andhare, Gargi K. Pawar, Nilesh Walimbe, Atul M. Kinikar, Meenal Kasibhatla, Sunitha M. Kulkarni-Kale, Urmila Viruses Article The neutralizing antibody (Nt-Ab) response to vaccine and wild-type measles viruses (MeV) was studied in suspected measles cases reported during the years 2012–2016. The neutralization activity against MeV A, D4 and D8 genotypes was studied on sera (Panel A; n = 68 (measles-immunized) and Panel B; n = 50 (unvaccinated)) that were either laboratory confirmed or not confirmed by the presence of IgM antibodies. Additionally, the Nt-Ab response in Panel A was measured against the MeV vaccine and four wild-type viruses. Neutralization results were compared using homology modeling and molecular dynamics simulation (MDS) of MeV-hemagglutinin (H) and fusion (F) proteins. Overall, the Nt-Ab titres for MeV-A were found to be significantly lower than MeV-D4 and MeV-D8 viruses for Panel A. No major difference was noted in Nt-Ab titres between MeV-D8 viruses (Jamnagar and New Delhi), whereas MeV-D4 (Sindhudurg and Bagalkot (BGK) viruses) showed significant differences between Nt-Ab titres for Panel B. Interestingly, the substitutions observed in epitopes of H-protein, L249P and G316A are observed to be unique to MeV-BGK. MDS of H-protein revealed significant fluctuations in neutralizing epitopes due to L249P substitution. The majority of the clinically suspected cases showed Nt-Abs to MeV wild-types. Higher IgG antibody avidity and Nt-Ab titres were noted in IgM-negatives than in IgM-positives cases, indicating reinfection or breakthrough. MDS revealed reduced neutralization due to decreased conformational flexibility in the H-epitope. MDPI 2023-11-10 /pmc/articles/PMC10674322/ /pubmed/38005920 http://dx.doi.org/10.3390/v15112243 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Vaidya, Sunil R.
Kumbhar, Neelakshi S.
Andhare, Gargi K.
Pawar, Nilesh
Walimbe, Atul M.
Kinikar, Meenal
Kasibhatla, Sunitha M.
Kulkarni-Kale, Urmila
Neutralizing Antibody Response to Genotypically Diverse Measles Viruses in Clinically Suspected Measles Cases
title Neutralizing Antibody Response to Genotypically Diverse Measles Viruses in Clinically Suspected Measles Cases
title_full Neutralizing Antibody Response to Genotypically Diverse Measles Viruses in Clinically Suspected Measles Cases
title_fullStr Neutralizing Antibody Response to Genotypically Diverse Measles Viruses in Clinically Suspected Measles Cases
title_full_unstemmed Neutralizing Antibody Response to Genotypically Diverse Measles Viruses in Clinically Suspected Measles Cases
title_short Neutralizing Antibody Response to Genotypically Diverse Measles Viruses in Clinically Suspected Measles Cases
title_sort neutralizing antibody response to genotypically diverse measles viruses in clinically suspected measles cases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10674322/
https://www.ncbi.nlm.nih.gov/pubmed/38005920
http://dx.doi.org/10.3390/v15112243
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