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Immunization With a Secreted Esterase Protects Mice Against Multiple Serotypes (M1, M3, and M28) of Group A Streptococcus

Streptococcal secreted esterase (Sse) is a platelet-activating factor acetylhydrolase that is critical for Group A Streptococcus (GAS) skin invasion and innate immune evasion. There are two Sse variant complexes that share >98% identity within each complex but display about 37% variation between...

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Autores principales: Zhang, Xiaolan, Wei, Deqin, Zhao, Yuan, Zhong, Zhaohua, Wang, Yue, Song, Yingli, Cai, Minghui, Zhang, Wenli, Zhao, Jizi, Lv, Chunmei, Zhu, Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7145942/
https://www.ncbi.nlm.nih.gov/pubmed/32308652
http://dx.doi.org/10.3389/fmicb.2020.00565
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author Zhang, Xiaolan
Wei, Deqin
Zhao, Yuan
Zhong, Zhaohua
Wang, Yue
Song, Yingli
Cai, Minghui
Zhang, Wenli
Zhao, Jizi
Lv, Chunmei
Zhu, Hui
author_facet Zhang, Xiaolan
Wei, Deqin
Zhao, Yuan
Zhong, Zhaohua
Wang, Yue
Song, Yingli
Cai, Minghui
Zhang, Wenli
Zhao, Jizi
Lv, Chunmei
Zhu, Hui
author_sort Zhang, Xiaolan
collection PubMed
description Streptococcal secreted esterase (Sse) is a platelet-activating factor acetylhydrolase that is critical for Group A Streptococcus (GAS) skin invasion and innate immune evasion. There are two Sse variant complexes that share >98% identity within each complex but display about 37% variation between the complexes in amino acid sequences. Sse immunization protects mice against lethal infection and skin invasion in subcutaneous infection with the hypervirulent CovRS mutant strain, MGAS5005. However, it is not known whether Sse immunization provides significant protection against infection of GAS with functional CovRS and whether immunization with Sse of one variant complex provides protection against infection of GAS that produces Sse of another variant complex. This study was designed to address these questions. Mice were immunized with recombinant Sse of M1 GAS (Sse(M1)) and challenged with MGAS5005 (serotype M1, CovS mutant, and Sse of variant complex I), MGAS315 (M3, CovS mutant, and Sse of variant complex I), MGAS2221 (M1, wild-type CovRS, and Sse of variant complex I), and MGAS6180 (M28, wild-type CovRS, and Sse of variant complex II). Sse(M1) immunization significantly increased survival rates of mice in subcutaneous MGAS5005 and intraperitoneal MGAS6180 challenges and showed consistently higher or longer survival in the other challenges. Immunized mice had smaller skin lesion and higher neutrophil responses in subcutaneous infections and lower GAS burdens in spleen, liver, and kidney in most of the challenge experiments than control mice. Sse(M1) immunization enhanced proinflammatory responses. These data suggest that Sse immunization has a broad benefit against GAS infections that can vary in extent from strain to strain and that the benefit may be due to the immunization-enhanced proinflammatory responses. In particular, immunization with Sse(M1) can provide protection against M28 GAS infection even though its Sse and Sse(M1) have significant variations.
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spelling pubmed-71459422020-04-18 Immunization With a Secreted Esterase Protects Mice Against Multiple Serotypes (M1, M3, and M28) of Group A Streptococcus Zhang, Xiaolan Wei, Deqin Zhao, Yuan Zhong, Zhaohua Wang, Yue Song, Yingli Cai, Minghui Zhang, Wenli Zhao, Jizi Lv, Chunmei Zhu, Hui Front Microbiol Microbiology Streptococcal secreted esterase (Sse) is a platelet-activating factor acetylhydrolase that is critical for Group A Streptococcus (GAS) skin invasion and innate immune evasion. There are two Sse variant complexes that share >98% identity within each complex but display about 37% variation between the complexes in amino acid sequences. Sse immunization protects mice against lethal infection and skin invasion in subcutaneous infection with the hypervirulent CovRS mutant strain, MGAS5005. However, it is not known whether Sse immunization provides significant protection against infection of GAS with functional CovRS and whether immunization with Sse of one variant complex provides protection against infection of GAS that produces Sse of another variant complex. This study was designed to address these questions. Mice were immunized with recombinant Sse of M1 GAS (Sse(M1)) and challenged with MGAS5005 (serotype M1, CovS mutant, and Sse of variant complex I), MGAS315 (M3, CovS mutant, and Sse of variant complex I), MGAS2221 (M1, wild-type CovRS, and Sse of variant complex I), and MGAS6180 (M28, wild-type CovRS, and Sse of variant complex II). Sse(M1) immunization significantly increased survival rates of mice in subcutaneous MGAS5005 and intraperitoneal MGAS6180 challenges and showed consistently higher or longer survival in the other challenges. Immunized mice had smaller skin lesion and higher neutrophil responses in subcutaneous infections and lower GAS burdens in spleen, liver, and kidney in most of the challenge experiments than control mice. Sse(M1) immunization enhanced proinflammatory responses. These data suggest that Sse immunization has a broad benefit against GAS infections that can vary in extent from strain to strain and that the benefit may be due to the immunization-enhanced proinflammatory responses. In particular, immunization with Sse(M1) can provide protection against M28 GAS infection even though its Sse and Sse(M1) have significant variations. Frontiers Media S.A. 2020-04-03 /pmc/articles/PMC7145942/ /pubmed/32308652 http://dx.doi.org/10.3389/fmicb.2020.00565 Text en Copyright © 2020 Zhang, Wei, Zhao, Zhong, Wang, Song, Cai, Zhang, Zhao, Lv and Zhu. http://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 Microbiology
Zhang, Xiaolan
Wei, Deqin
Zhao, Yuan
Zhong, Zhaohua
Wang, Yue
Song, Yingli
Cai, Minghui
Zhang, Wenli
Zhao, Jizi
Lv, Chunmei
Zhu, Hui
Immunization With a Secreted Esterase Protects Mice Against Multiple Serotypes (M1, M3, and M28) of Group A Streptococcus
title Immunization With a Secreted Esterase Protects Mice Against Multiple Serotypes (M1, M3, and M28) of Group A Streptococcus
title_full Immunization With a Secreted Esterase Protects Mice Against Multiple Serotypes (M1, M3, and M28) of Group A Streptococcus
title_fullStr Immunization With a Secreted Esterase Protects Mice Against Multiple Serotypes (M1, M3, and M28) of Group A Streptococcus
title_full_unstemmed Immunization With a Secreted Esterase Protects Mice Against Multiple Serotypes (M1, M3, and M28) of Group A Streptococcus
title_short Immunization With a Secreted Esterase Protects Mice Against Multiple Serotypes (M1, M3, and M28) of Group A Streptococcus
title_sort immunization with a secreted esterase protects mice against multiple serotypes (m1, m3, and m28) of group a streptococcus
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7145942/
https://www.ncbi.nlm.nih.gov/pubmed/32308652
http://dx.doi.org/10.3389/fmicb.2020.00565
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