白色念珠菌和牙龈卟啉单胞菌生物膜对吸入性肺炎3D模型上皮屏障功能的协同作用。

IF 4.6 2区 医学 Q2 IMMUNOLOGY
Frontiers in Cellular and Infection Microbiology Pub Date : 2025-03-07 eCollection Date: 2025-01-01 DOI:10.3389/fcimb.2025.1552395
Ewelina Wronowska, Ibeth Guevara-Lora, Aleksandra Brankiewicz, Grazyna Bras, Marcin Zawrotniak, Dorota Satala, Justyna Karkowska-Kuleta, Joanna Budziaszek, Joanna Koziel, Maria Rapala-Kozik
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引用次数: 0

摘要

包括白色念珠菌和牙龈卟啉单胞菌在内的多微生物感染是维持上皮屏障完整性的重大挑战。本研究利用气液界面(ALI)模型探讨了它们对上皮细胞的协同作用。方法:制备混合物种生物膜,分析其对上皮通透性和紧密连接蛋白的影响。评价生物膜上清液对IL-8分泌和氧化应激标志物的影响。使用gingipain-null突变体(ΔKΔRAB)与野生型菌株(W83)比较,评估了牙龈卟啉卟啉蛋白酶的作用。采用mellonella幼虫进行生存实验,研究双种生物膜的致病性。结果:混合物种生物膜显著增加了上皮通透性,破坏了紧密连接蛋白,证明了ZO-1和E-cadherin水平的降低。这些变化伴随着氧化应激,其特征是HO-1表达降低,Bax/Bcl-xL比值增加,表明促凋亡活性增加。双种生物膜的上清液对上皮细胞有明显的影响,调节IL-8的分泌,加剧氧化损伤。白色念珠菌被认为是促炎反应的主要驱动因素,而牙龈假单胞菌通过免疫调节和酶活性起作用,主要通过牙龈疼痛。与野生型相比,ΔKΔRAB突变生物膜引起的上皮破坏和氧化应激较少,突出了牙龈痛在发病机制中的关键作用。讨论:使用mellonella幼虫进行的生存实验支持了这些发现,强调了双物种生物膜与存活率降低相关,以及大剂量抗菌治疗减轻这种影响的潜力。这些结果强调了白色念珠菌和牙龈假单胞菌在破坏上皮屏障方面的合作机制,并强调了针对真菌和细菌成分的联合治疗在多微生物感染中的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synergistic effects of Candida albicans and Porphyromonas gingivalis biofilms on epithelial barrier function in a 3D aspiration pneumonia model.

Introduction: Polymicrobial infections involving Candida albicans and Porphyromonas gingivalis represent a significant challenge in maintaining epithelial barrier integrity. This study explores their synergistic effects on epithelial cells using an air-liquid interface (ALI) model.

Methods: Mixed-species biofilms were developed and analyzed for their impact on epithelial permeability and tight junction proteins. The effects of biofilm supernatants on IL-8 secretion and oxidative stress markers were also evaluated. The role of P. gingivalis proteases was assessed using a gingipain-null mutant (ΔKΔRAB) compared to the wild-type strain (W83). Survival experiments were conducted using Galleria mellonella larvae to examine the pathogenicity of dual-species biofilms.

Results: Mixed-species biofilms significantly increased epithelial permeability and disrupted tight junction proteins, as evidenced by reduced levels of ZO-1 and E-cadherin. These changes were accompanied by oxidative stress, characterized by decreased HO-1 expression and enhanced Bax/Bcl-xL ratios, indicating increased pro-apoptotic activity. Supernatants from dual-species biofilms demonstrated a pronounced effect on epithelial cells, modulating IL-8 secretion and exacerbating oxidative damage. C. albicans was identified as the dominant driver of pro-inflammatory responses, while P. gingivalis contributed through immune modulation and enzymatic activity, primarily via gingipains. The ΔKΔRAB mutant biofilms caused less epithelial disruption and oxidative stress compared to the wild-type, highlighting the critical role of gingipains in pathogenesis.

Discussion: Survival experiments using Galleria mellonella larvae supported these findings, highlighting the reduced survival associated with dual-species biofilms and the potential for high-dose antimicrobial therapies to mitigate this effect. These results emphasize the cooperative mechanisms of C. albicans and P. gingivalis in compromising epithelial barriers and underline the importance of combination therapies targeting both fungal and bacterial components in polymicrobial infections.

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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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