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The Dual Functions of a Bracovirus C-Type Lectin in Caterpillar Immune Response Manipulation

Parasitoids are widespread in natural ecosystems and normally equipped with diverse viral factors to defeat host immune responses. On the other hand, parasitoids can enhance the antibacterial abilities and improve the hypoimmunity traits of parasitized hosts that may encounter pathogenic infections....

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Autores principales: Wu, Xiaotong, Wu, Zhiwei, Ye, Xiqian, Pang, Lan, Sheng, Yifeng, Wang, Zehua, Zhou, Yuenan, Zhu, Jiachen, Hu, Rongmin, Zhou, Sicong, Chen, Jiani, Wang, Zhizhi, Shi, Min, Huang, Jianhua, Chen, Xuexin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9157488/
https://www.ncbi.nlm.nih.gov/pubmed/35663984
http://dx.doi.org/10.3389/fimmu.2022.877027
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author Wu, Xiaotong
Wu, Zhiwei
Ye, Xiqian
Pang, Lan
Sheng, Yifeng
Wang, Zehua
Zhou, Yuenan
Zhu, Jiachen
Hu, Rongmin
Zhou, Sicong
Chen, Jiani
Wang, Zhizhi
Shi, Min
Huang, Jianhua
Chen, Xuexin
author_facet Wu, Xiaotong
Wu, Zhiwei
Ye, Xiqian
Pang, Lan
Sheng, Yifeng
Wang, Zehua
Zhou, Yuenan
Zhu, Jiachen
Hu, Rongmin
Zhou, Sicong
Chen, Jiani
Wang, Zhizhi
Shi, Min
Huang, Jianhua
Chen, Xuexin
author_sort Wu, Xiaotong
collection PubMed
description Parasitoids are widespread in natural ecosystems and normally equipped with diverse viral factors to defeat host immune responses. On the other hand, parasitoids can enhance the antibacterial abilities and improve the hypoimmunity traits of parasitized hosts that may encounter pathogenic infections. These adaptive strategies guarantee the survival of parasitoid offspring, yet their underlying mechanisms are poorly understood. Here, we focused on Cotesia vestalis, an endoparasitoid of the diamondback moth Plutella xylostella, and found that C. vestalis parasitization decreases the number of host hemocytes, leading to disruption of the encapsulation reaction. We further found that one bracovirus C-type lectin gene, CvBV_28-1, is highly expressed in the hemocytes of parasitized hosts and participates in suppressing the proliferation rate of host hemocytes, which in turn reduces their population and represses the process of encapsulation. Moreover, CvBV_28-1 presents a classical bacterial clearance ability via the agglutination response in a Ca(2+)-dependent manner in response to gram-positive bacteria. Our study provides insights into the innovative strategy of a parasitoid-derived viral gene that has dual functions to manipulate host immunity for a successful parasitism.
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spelling pubmed-91574882022-06-02 The Dual Functions of a Bracovirus C-Type Lectin in Caterpillar Immune Response Manipulation Wu, Xiaotong Wu, Zhiwei Ye, Xiqian Pang, Lan Sheng, Yifeng Wang, Zehua Zhou, Yuenan Zhu, Jiachen Hu, Rongmin Zhou, Sicong Chen, Jiani Wang, Zhizhi Shi, Min Huang, Jianhua Chen, Xuexin Front Immunol Immunology Parasitoids are widespread in natural ecosystems and normally equipped with diverse viral factors to defeat host immune responses. On the other hand, parasitoids can enhance the antibacterial abilities and improve the hypoimmunity traits of parasitized hosts that may encounter pathogenic infections. These adaptive strategies guarantee the survival of parasitoid offspring, yet their underlying mechanisms are poorly understood. Here, we focused on Cotesia vestalis, an endoparasitoid of the diamondback moth Plutella xylostella, and found that C. vestalis parasitization decreases the number of host hemocytes, leading to disruption of the encapsulation reaction. We further found that one bracovirus C-type lectin gene, CvBV_28-1, is highly expressed in the hemocytes of parasitized hosts and participates in suppressing the proliferation rate of host hemocytes, which in turn reduces their population and represses the process of encapsulation. Moreover, CvBV_28-1 presents a classical bacterial clearance ability via the agglutination response in a Ca(2+)-dependent manner in response to gram-positive bacteria. Our study provides insights into the innovative strategy of a parasitoid-derived viral gene that has dual functions to manipulate host immunity for a successful parasitism. Frontiers Media S.A. 2022-05-18 /pmc/articles/PMC9157488/ /pubmed/35663984 http://dx.doi.org/10.3389/fimmu.2022.877027 Text en Copyright © 2022 Wu, Wu, Ye, Pang, Sheng, Wang, Zhou, Zhu, Hu, Zhou, Chen, Wang, Shi, Huang and Chen https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Wu, Xiaotong
Wu, Zhiwei
Ye, Xiqian
Pang, Lan
Sheng, Yifeng
Wang, Zehua
Zhou, Yuenan
Zhu, Jiachen
Hu, Rongmin
Zhou, Sicong
Chen, Jiani
Wang, Zhizhi
Shi, Min
Huang, Jianhua
Chen, Xuexin
The Dual Functions of a Bracovirus C-Type Lectin in Caterpillar Immune Response Manipulation
title The Dual Functions of a Bracovirus C-Type Lectin in Caterpillar Immune Response Manipulation
title_full The Dual Functions of a Bracovirus C-Type Lectin in Caterpillar Immune Response Manipulation
title_fullStr The Dual Functions of a Bracovirus C-Type Lectin in Caterpillar Immune Response Manipulation
title_full_unstemmed The Dual Functions of a Bracovirus C-Type Lectin in Caterpillar Immune Response Manipulation
title_short The Dual Functions of a Bracovirus C-Type Lectin in Caterpillar Immune Response Manipulation
title_sort dual functions of a bracovirus c-type lectin in caterpillar immune response manipulation
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9157488/
https://www.ncbi.nlm.nih.gov/pubmed/35663984
http://dx.doi.org/10.3389/fimmu.2022.877027
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