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用一种分泌型酯酶进行免疫可保护小鼠抵御A群的多种血清型(M1、M3和M28)。

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

作者信息

Zhang Xiaolan, Wei Deqin, Zhao Yuan, Zhong Zhaohua, Wang Yue, Song Yingli, Cai Minghui, Zhang Wenli, Zhao Jizi, Lv Chunmei, Zhu Hui

机构信息

College of Basic Medical Sciences, Harbin Medical University, Harbin, China.

出版信息

Front Microbiol. 2020 Apr 3;11:565. doi: 10.3389/fmicb.2020.00565. eCollection 2020.

Abstract

Streptococcal secreted esterase (Sse) is a platelet-activating factor acetylhydrolase that is critical for Group A (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) 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 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 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 can provide protection against M28 GAS infection even though its Sse and Sse have significant variations.

摘要

链球菌分泌酯酶(Sse)是一种血小板活化因子乙酰水解酶,对A组(GAS)皮肤侵袭和先天免疫逃逸至关重要。有两种Sse变体复合物,每个复合物内的同一性>98%,但复合物之间的氨基酸序列显示约37%的差异。Sse免疫可保护小鼠免受高毒力CovRS突变株MGAS5005皮下感染中的致死性感染和皮肤侵袭。然而,尚不清楚Sse免疫是否能有效抵御具有功能性CovRS的GAS感染,以及用一种变体复合物的Sse免疫是否能抵御产生另一种变体复合物Sse的GAS感染。本研究旨在解决这些问题。用重组M1 GAS的Sse(Sse)免疫小鼠,并用MGAS5005(血清型M1,CovS突变体,变体复合物I的Sse)、MGAS315(M3,CovS突变体,变体复合物I的Sse)、MGAS2221(M1,野生型CovRS,变体复合物I的Sse)和MGAS6180(M28,野生型CovRS,变体复合物II的Sse)进行攻击。Sse免疫显著提高了皮下MGAS5005和腹腔MGAS6180攻击中小鼠的存活率,并且在其他攻击中显示出持续更高或更长的存活率。在大多数攻击实验中,免疫小鼠在皮下感染中的皮肤损伤较小,中性粒细胞反应较高,在脾脏、肝脏和肾脏中的GAS负荷低于对照小鼠。Sse免疫增强了促炎反应。这些数据表明Sse免疫对不同菌株的GAS感染具有广泛益处,且这种益处可能归因于免疫增强的促炎反应。特别是,用Sse免疫可以抵御M28 GAS感染,尽管其Sse与其他Sse有显著差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a95/7145942/97003dd5e5eb/fmicb-11-00565-g001.jpg

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