Neuraminidase in Virus-like Particles Contributes to the Protection against High Dose of Avian Influenza Virus Challenge Infection

Neuraminidase is an important target for influenza vaccination. In this study, we generated avian influenza VLPs, expressing hemagglutinin (HA), neuraminidase (NA), HA and NA co-expressed (HANA), to evaluate the protective role of NA against a high (10LD<sub>50</sub>) and low (2LD<sub...

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Main Authors: Hae-Ji Kang, Ki-Back Chu, Keon-Woong Yoon, Gi-Deok Eom, Jie Mao, Min-Ju Kim, Su-Hwa Lee, Eun-Kyung Moon, Fu-Shi Quan
Format: Article
Language:English
Published: MDPI AG 2021-10-01
Series:Pathogens
Subjects:
Online Access:https://www.mdpi.com/2076-0817/10/10/1291
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author Hae-Ji Kang
Ki-Back Chu
Keon-Woong Yoon
Gi-Deok Eom
Jie Mao
Min-Ju Kim
Su-Hwa Lee
Eun-Kyung Moon
Fu-Shi Quan
author_facet Hae-Ji Kang
Ki-Back Chu
Keon-Woong Yoon
Gi-Deok Eom
Jie Mao
Min-Ju Kim
Su-Hwa Lee
Eun-Kyung Moon
Fu-Shi Quan
author_sort Hae-Ji Kang
collection DOAJ
description Neuraminidase is an important target for influenza vaccination. In this study, we generated avian influenza VLPs, expressing hemagglutinin (HA), neuraminidase (NA), HA and NA co-expressed (HANA), to evaluate the protective role of NA against a high (10LD<sub>50</sub>) and low (2LD<sub>50</sub>) dose of avian influenza virus challenge infections. A single immunization with HANA VLPs elicited the highest level of virus-specific IgG, IgG1, and IgG2a responses from the sera post-vaccination and the lungs post-challenge-infection. Potent antibody-secreting cell responses were observed from the spleens and lungs of HANA-VLP-immunized mice post-challenge-infection. HANA VLPs induced the highest CD4<sup>+</sup> T cell, CD8<sup>+</sup> T cell, and germinal center B cells, while strongly limiting inflammatory cytokine production in the lungs compared to other VLP immunization groups. In correlation with these findings, the lowest bodyweight losses and lung virus titers were observed from HANA VLP immunization, and all of the immunized mice survived irrespective of the challenge dose. Contrastingly, VLPs expressing either HA or NA alone failed to elicit complete protection. These results indicated that NA in VLPs played a critical role in inducing protection against a high dose of the challenge infection.
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spelling doaj.art-ee32a697a6454ce2bfc780a5563e71a22023-11-22T19:33:44ZengMDPI AGPathogens2076-08172021-10-011010129110.3390/pathogens10101291Neuraminidase in Virus-like Particles Contributes to the Protection against High Dose of Avian Influenza Virus Challenge InfectionHae-Ji Kang0Ki-Back Chu1Keon-Woong Yoon2Gi-Deok Eom3Jie Mao4Min-Ju Kim5Su-Hwa Lee6Eun-Kyung Moon7Fu-Shi Quan8Department of Biomedical Science, Graduate School, Kyung Hee University, Seoul 02447, KoreaDepartment of Biomedical Science, Graduate School, Kyung Hee University, Seoul 02447, KoreaDepartment of Biomedical Science, Graduate School, Kyung Hee University, Seoul 02447, KoreaDepartment of Biomedical Science, Graduate School, Kyung Hee University, Seoul 02447, KoreaDepartment of Biomedical Science, Graduate School, Kyung Hee University, Seoul 02447, KoreaDepartment of Biomedical Science, Graduate School, Kyung Hee University, Seoul 02447, KoreaDepartment of Biomedical Science, Graduate School, Kyung Hee University, Seoul 02447, KoreaDepartment of Medical Zoology, School of Medicine, Kyung Hee University, Seoul 02447, KoreaDepartment of Medical Zoology, School of Medicine, Kyung Hee University, Seoul 02447, KoreaNeuraminidase is an important target for influenza vaccination. In this study, we generated avian influenza VLPs, expressing hemagglutinin (HA), neuraminidase (NA), HA and NA co-expressed (HANA), to evaluate the protective role of NA against a high (10LD<sub>50</sub>) and low (2LD<sub>50</sub>) dose of avian influenza virus challenge infections. A single immunization with HANA VLPs elicited the highest level of virus-specific IgG, IgG1, and IgG2a responses from the sera post-vaccination and the lungs post-challenge-infection. Potent antibody-secreting cell responses were observed from the spleens and lungs of HANA-VLP-immunized mice post-challenge-infection. HANA VLPs induced the highest CD4<sup>+</sup> T cell, CD8<sup>+</sup> T cell, and germinal center B cells, while strongly limiting inflammatory cytokine production in the lungs compared to other VLP immunization groups. In correlation with these findings, the lowest bodyweight losses and lung virus titers were observed from HANA VLP immunization, and all of the immunized mice survived irrespective of the challenge dose. Contrastingly, VLPs expressing either HA or NA alone failed to elicit complete protection. These results indicated that NA in VLPs played a critical role in inducing protection against a high dose of the challenge infection.https://www.mdpi.com/2076-0817/10/10/1291avian influenzavirus-like particleneuraminidaseprotection
spellingShingle Hae-Ji Kang
Ki-Back Chu
Keon-Woong Yoon
Gi-Deok Eom
Jie Mao
Min-Ju Kim
Su-Hwa Lee
Eun-Kyung Moon
Fu-Shi Quan
Neuraminidase in Virus-like Particles Contributes to the Protection against High Dose of Avian Influenza Virus Challenge Infection
Pathogens
avian influenza
virus-like particle
neuraminidase
protection
title Neuraminidase in Virus-like Particles Contributes to the Protection against High Dose of Avian Influenza Virus Challenge Infection
title_full Neuraminidase in Virus-like Particles Contributes to the Protection against High Dose of Avian Influenza Virus Challenge Infection
title_fullStr Neuraminidase in Virus-like Particles Contributes to the Protection against High Dose of Avian Influenza Virus Challenge Infection
title_full_unstemmed Neuraminidase in Virus-like Particles Contributes to the Protection against High Dose of Avian Influenza Virus Challenge Infection
title_short Neuraminidase in Virus-like Particles Contributes to the Protection against High Dose of Avian Influenza Virus Challenge Infection
title_sort neuraminidase in virus like particles contributes to the protection against high dose of avian influenza virus challenge infection
topic avian influenza
virus-like particle
neuraminidase
protection
url https://www.mdpi.com/2076-0817/10/10/1291
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