Subinhibitory concentrations of meropenem stimulate membrane vesicle production and modulate immune response in Bacteroides fragilis infection

IF 4.8 Q1 MICROBIOLOGY Current Research in Microbial Sciences Pub Date : 2024-01-01 DOI:10.1016/j.crmicr.2024.100294
Saniya Kozhakhmetova , Ayazhan Bekbayeva , Elena Zholdybayeva , Tatyana Krivoruchko , Natalya Dashevskaya , Zhanel Mukhanbetzhanova , Elizaveta Vinogradova , Almagul Kushugulova , Samat Kozhakhmetov
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Abstract

This study explores an adaptation mechanism of Bacteroides fragilis to subinhibitory concentrations of meropenem, characterized by an alteration in the production of membrane vesicles (MVs) and modulation of the host inflammatory response. Using a rat model of infection, we demonstrated a significant increase in the size of MVs accompanied by a nonsignificant increase in their number in the meropenem-treated group compared to the infected control. Both infected groups showed significantly altered hematological parameters and shifts in monocyte on day 8 (average increase of 21.5 %). At the same time, significant changes in neutrophils (decrease by 26 %) and eosinophils (increase by 3 %) were observed only in the infected group but not in the infected meropenem-treated group. On day 16, increased macrophage activation, neovascularization, and fibrosis were observed in the tissues of the antibiotic-treated group. Immunological profile analysis revealed a slight increase in the levels of pro-inflammatory cytokines (IL-5, IL-6, IFN-γ and G-CSF) on day 8 of the experiment, followed by a sharp decrease on day 16 in both infected groups compared to the negative control. At the same time, network analysis of correlations between these immunological factors showed complex changes in response to subinhibitory concentrations of meropenem. The bacterial load did not differ between the infected groups on days 8 and 16, but only in the meropenem-free group a significant decrease in the number of bacteria was observed on day 16 in all samples. These findings suggest that subinhibitory antibiotic concentrations can influence the pathophysiological progression of B. fragilis infection, modulating both the bacterial response and the host immune reaction, potentially leading to a more complex and chronic disease course.

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抑菌浓度以下的美罗培南可刺激膜泡生成并调节脆弱拟杆菌感染的免疫反应
本研究探讨了脆弱拟杆菌对亚抑制浓度美罗培南的适应机制,这种机制的特点是膜囊泡 (MV) 的产生发生了变化并调节了宿主的炎症反应。通过大鼠感染模型,我们发现与受感染的对照组相比,美罗培南处理组的膜囊泡体积显著增大,但数量却无明显增加。两个感染组在第 8 天都显示出明显的血液学参数变化和单核细胞变化(平均增加 21.5%)。同时,仅在感染组观察到中性粒细胞(减少 26%)和嗜酸性粒细胞(增加 3%)的明显变化,而在感染的美罗培南处理组则未观察到。第 16 天,在抗生素治疗组的组织中观察到巨噬细胞活化、新生血管和纤维化增加。免疫谱分析显示,与阴性对照组相比,两个感染组的促炎细胞因子(IL-5、IL-6、IFN-γ 和 G-CSF)水平在实验第 8 天略有上升,随后在第 16 天急剧下降。同时,这些免疫因子之间的相关网络分析显示了对亚抑制浓度美罗培南反应的复杂变化。感染组之间在第 8 天和第 16 天的细菌量没有差异,但只有不含美罗培南的感染组在第 16 天的所有样本中观察到细菌数量显著减少。这些研究结果表明,亚抑制浓度的抗生素可影响脆弱拟杆菌感染的病理生理进展,调节细菌反应和宿主免疫反应,从而可能导致更复杂的慢性病程。
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来源期刊
Current Research in Microbial Sciences
Current Research in Microbial Sciences Immunology and Microbiology-Immunology and Microbiology (miscellaneous)
CiteScore
7.90
自引率
0.00%
发文量
81
审稿时长
66 days
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