Co-frequency or contrary? The effects of Qiwei Baizhu Powder and its bioactive compounds on mucosa-associated microbiota of mice with antibiotic-associated diarrhea.

IF 4.6 2区 医学 Q2 IMMUNOLOGY
Frontiers in Cellular and Infection Microbiology Pub Date : 2024-10-28 eCollection Date: 2024-01-01 DOI:10.3389/fcimb.2024.1483048
Zeli Zhang, Yan Yang, Yingsi Zhang, Guozhen Xie
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引用次数: 0

Abstract

Qiwei Baizhu Powder (QWBZP) has been proven effective in treating antibiotic-associated diarrhea (AAD), and the mechanism is associated with regulating the gut microbiota. However, the role of the bioactive compounds of QWBZP in regulating the gut microbiota is still unclear. In this study, 24 mice were divided into a normal control group (N), a model group (R), a QWBZP decoction group (TW), and a QWBZP-TG group (TG). AAD mouse models were established by mixed antibiotic administration. After modeling, mice in the TW group and TG group were treated with QWBZP decoction and QWBZP-TG, respectively. Mice in the N group and R group were gavaged with sterile water. 16S rRNA gene sequencing was used to investigate the changes of mucosa-associated microbiota (MAM) in the small intestine of mice. Moreover, the levels of diamine oxidase (DAO), D-Lactate, secretory immunoglobulin A (sIgA), interleukin 6 (IL-6), IL-10, and tumor necrosis factor-α (TNF-α) were detected using enzyme-linked immunosorbent assay (ELISA) kits. The results showed that QWBZP-TG significantly altered the diversity, structure, and abundance of MAM in the AAD mice. QWBZP-TG exerted a stronger suppression effect on Escherichia and Clostridium compared with QWBZP decoction. Meanwhile, QWBZP-TG downregulated the abundance of Lactobacillus, which elicited an opposite effect to QWBZP decoction. Prevotella was the signature bacteria that responded to the QWBZP-TG intervention. Furthermore, both QWBZP decoction and QWBZP-TG decreased the levels of DAO, D-Lactate, sIgA, IL-6, and TNF-α in the AAD mice. The role of glycosides is to help QWBZP ameliorate diarrhea symptoms by inhibiting the proliferation of diarrhea-associated bacteria, reducing inflammation and regulating immunity.

同频还是相反?七味白术粉及其生物活性化合物对抗生素相关性腹泻小鼠黏膜相关微生物群的影响
七味白术散(QWBZP)已被证实能有效治疗抗生素相关性腹泻(AAD),其机制与调节肠道微生物群有关。然而,QWBZP 的生物活性化合物在调节肠道微生物群方面的作用仍不清楚。本研究将 24 只小鼠分为正常对照组(N)、模型组(R)、QWBZP 煎剂组(TW)和 QWBZP-TG 组(TG)。AAD 小鼠模型通过混合抗生素给药建立。建模后,TW 组和 TG 组小鼠分别接受 QWBZP 煎剂和 QWBZP-TG 治疗。N 组和 R 组小鼠用无菌水灌胃。采用 16S rRNA 基因测序法研究小鼠小肠粘膜相关微生物群(MAM)的变化。此外,还使用酶联免疫吸附试验(ELISA)试剂盒检测了二胺氧化酶(DAO)、D-乳酸盐、分泌型免疫球蛋白 A(sIgA)、白细胞介素 6(IL-6)、IL-10 和肿瘤坏死因子-α(TNF-α)的水平。结果表明,QWBZP-TG能显著改变AAD小鼠体内MAM的多样性、结构和丰度。与QWBZP煎剂相比,QWBZP-TG对埃希氏菌和梭状芽孢杆菌有更强的抑制作用。同时,QWBZP-TG 降低了乳酸杆菌的数量,与 QWBZP 煎剂的效果相反。Prevotella 是对 QWBZP-TG 干预产生反应的标志性细菌。此外,QWBZP煎剂和QWBZP-TG都能降低AAD小鼠体内DAO、D-乳酸、sIgA、IL-6和TNF-α的水平。苷的作用是通过抑制腹泻相关细菌的增殖、减轻炎症反应和调节免疫力来帮助 QWBZP 改善腹泻症状。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
1817
审稿时长
14 weeks
期刊介绍: Frontiers in Cellular and Infection Microbiology is a leading specialty journal, publishing rigorously peer-reviewed research across all pathogenic microorganisms and their interaction with their hosts. Chief Editor Yousef Abu Kwaik, University of Louisville is supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Cellular and Infection Microbiology includes research on bacteria, fungi, parasites, viruses, endosymbionts, prions and all microbial pathogens as well as the microbiota and its effect on health and disease in various hosts. The research approaches include molecular microbiology, cellular microbiology, gene regulation, proteomics, signal transduction, pathogenic evolution, genomics, structural biology, and virulence factors as well as model hosts. Areas of research to counteract infectious agents by the host include the host innate and adaptive immune responses as well as metabolic restrictions to various pathogenic microorganisms, vaccine design and development against various pathogenic microorganisms, and the mechanisms of antibiotic resistance and its countermeasures.
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