Interactions between bacterial vaginosis-associated microbiota and Trichomonas vaginalis modulate parasite-induced pathogenicity and host immune responses.

IF 3.5 2区 医学 Q1 PARASITOLOGY
Shu-Fang Chiu, Ching-Yun Huang, Chien-Yung Chen, Wei-Jane Hsu, Yuan-Ming Yeh, Ya-Wen Shih, Lichieh Julie Chu, Wei-Ning Lin, Kuo-Yang Huang
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引用次数: 0

Abstract

Background: Trichomoniasis, caused by Trichomonas vaginalis (Tv), is the most common nonviral sexually transmitted infection (STI). Bacterial vaginosis (BV) is characterized by a reduction in health-associated Lactobacillus and an overgrowth of anaerobes. Both BV-associated bacteria (BVB) and Tv are linked to adverse gynecologic outcomes. Herein, we aimed to investigate whether interactions between vaginal bacterial species and Tv could modulate Tv pathogenicity and Tv-induced host immune responses.

Methods: We established a co-culture system to evaluate the interaction between Tv and various vaginal bacteria, including Lactobacillus crispatus, Escherichia coli, Prevotella bivia, and Lactobacillus iners, in the context of polymicrobial infection in ectocervical cells (Ect1). The impact of the interactions between Tv and these bacterial species on Tv adhesion, Tv-induced cytotoxicity in Ect1 cells, and cytokine secretion were assessed. Additionally, the molecular mechanisms governing host inflammation following Tv-bacteria interactions were investigated.

Results: Our in vitro model showed that specific BVB, particularly P. bivia, enhanced the expression of Tv ap65 gene and promoted Tv adhesion to host cells. Additionally, Tv pretreated with P. bivia increased cytotoxicity and upregulated IL-6, IL-8, CXCL1, and IP-10 secretion in Ect1 cells. Furthermore, Ect1 cells stimulated with Tv pretreated with P. bivia also activated the PI3K, ERK, and p38 MAPK pathways, triggering epithelial-mesenchymal transition (EMT) events. These results demonstrate that this potential pathobiont enhances Tv pathogenicity, highlighting the impact of the vaginal microbiome on host cells during Tv infection.

Conclusions: This study significantly advances our understanding of the complex host-bacteria-parasite interactions in the vaginal ecosystem.

细菌性阴道病相关微生物群与阴道毛滴虫之间的相互作用调节寄生虫诱导的致病性和宿主免疫反应。
背景:阴道毛滴虫(Trichomonas vaginalis, Tv)引起的滴虫病是最常见的非病毒性性传播感染。细菌性阴道病(BV)的特点是与健康相关的乳酸菌减少和厌氧菌过度生长。细菌性阴道炎相关细菌(BVB)和细菌性阴道炎都与不良的妇科结果有关。在此,我们旨在研究阴道细菌种类与Tv之间的相互作用是否可以调节Tv致病性和Tv诱导的宿主免疫反应。方法:建立共培养体系,在宫颈外细胞(Ect1)多微生物感染的情况下,评价Tv与多种阴道细菌(包括crispatbacillus、Escherichia coli、provotella bivia和Lactobacillus iners)的相互作用。研究人员评估了Tv与这些细菌之间的相互作用对Tv粘附、Tv诱导的Ect1细胞毒性和细胞因子分泌的影响。此外,研究了电视细菌相互作用后控制宿主炎症的分子机制。结果:我们的体外模型显示,特异性BVB,特别是双胞弧菌,增强了Tv ap65基因的表达,促进了Tv对宿主细胞的粘附。此外,用双胞菌预处理Tv增加了Ect1细胞的细胞毒性,上调了IL-6、IL-8、CXCL1和IP-10的分泌。此外,用bivia p预处理Tv刺激的Ect1细胞也激活了PI3K、ERK和p38 MAPK通路,触发上皮-间质转化(EMT)事件。这些结果表明,这种潜在的病原体增强了Tv的致病性,突出了Tv感染期间阴道微生物组对宿主细胞的影响。结论:本研究显著提高了我们对阴道生态系统中复杂的宿主-细菌-寄生虫相互作用的理解。
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来源期刊
Parasites & Vectors
Parasites & Vectors 医学-寄生虫学
CiteScore
6.30
自引率
9.40%
发文量
433
审稿时长
1.4 months
期刊介绍: Parasites & Vectors is an open access, peer-reviewed online journal dealing with the biology of parasites, parasitic diseases, intermediate hosts, vectors and vector-borne pathogens. Manuscripts published in this journal will be available to all worldwide, with no barriers to access, immediately following acceptance. However, authors retain the copyright of their material and may use it, or distribute it, as they wish. Manuscripts on all aspects of the basic and applied biology of parasites, intermediate hosts, vectors and vector-borne pathogens will be considered. In addition to the traditional and well-established areas of science in these fields, we also aim to provide a vehicle for publication of the rapidly developing resources and technology in parasite, intermediate host and vector genomics and their impacts on biological research. We are able to publish large datasets and extensive results, frequently associated with genomic and post-genomic technologies, which are not readily accommodated in traditional journals. Manuscripts addressing broader issues, for example economics, social sciences and global climate change in relation to parasites, vectors and disease control, are also welcomed.
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