人感染伤寒沙门氏菌血清型体内诱导蛋白抗原的鉴定。

Yong Hu, YanGuang Cong, Shu Li, XianCai Rao, Gang Wang, FuQuan Hu
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引用次数: 17

摘要

在传染病发作期间,病原体表达不同的毒力因子亚群,使它们能够适应不同的环境。因此,体内表达或上调的基因与发病机制有关。采用体内诱导抗原技术(IVIAT)鉴定了伤寒沙门氏菌血清型感染过程中表达的抗原。我们鉴定了7种体内诱导(IVI)抗原,包括BcfD(一种纤维结构亚基)、GrxC(一种glutaredoxin 3)、SapB(一种abc型运输系统)、T3663(一种abc型未表征的运输系统)、T3816(一种推测的罗丹斯岛相关硫转移酶)、T1497(一种可能的tonb依赖性受体)和T3689(功能未知)。7种抗原中,5种抗原在健康对照血清中无交叉免疫反应性。这5种包括BcfD、GrxC、SapB、T3663和T3689。本研究确定的抗原是药物和疫苗开发的潜在靶点,可能用作诊断试剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of in vivo induced protein antigens of Salmonella enterica serovar Typhi during human infection.

During infectious disease episodes, pathogens express distinct subsets of virulence factors which allow them to adapt to different environments. Hence, genes that are expressed or upregulated in vivo are implicated in pathogenesis. We used in vivo induced antigen technology (IVIAT) to identify antigens which are expressed during infection with Salmonella enterica serovar Typhi. We identified 7 in vivo induced (IVI) antigens, which included BcfD (a fimbrial structural subunit), GrxC (a glutaredoxin 3), SapB (an ABC-type transport system), T3663 (an ABC-type uncharacterized transport system), T3816 (a putative rhodanese-related sulfurtransferase), T1497 (a probable TonB-dependent receptor) and T3689 (unknown function). Of the 7 identified antigens, 5 antigens had no cross-immunoreactivity in adsorbed control sera from healthy subjects. These 5 included BcfD, GrxC, SapB, T3663 and T3689. Antigens identified in this study are potential targets for drug and vaccine development and may be utilized as diagnostic agents.

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