Transcriptomic profile of the zoonotic parasite Anisakis pegreffii upon in vitro exposure to human dendritic cells.

IF 4.8 2区 医学 Q2 IMMUNOLOGY
Frontiers in Cellular and Infection Microbiology Pub Date : 2025-09-15 eCollection Date: 2025-01-01 DOI:10.3389/fcimb.2025.1646537
Marialetizia Palomba, Aurelia Rughetti, Tiziana Castrignanò, Chiara Napoletano, Xavier Roca-Geronès, Valentina Pinna, Franco Liberati, Daniele Canestrelli, Simonetta Mattiucci
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Abstract

Anisakis pegreffii is a zoonotic marine nematode whose life-cycle involves marine organisms-small crustaceans, fish and squids as intermediate/paratenic hosts, and marine mammals, mainly cetaceans-as definitive ones. When its third-stage larvae (L3) are accidentally ingested by humans with the consumption of raw or undercooked parasitized fish and/or squids, the parasite fails to complete its life cycle, leading to human anisakiasis. Despite increasing interest in understanding the molecular basis of pathogenic effects in human anisakiasis, the transcriptomic response of A. pegreffii L3 to interaction with human immune cells, remains poorly understood. Thus, in this study, the transcriptomic profile of A. pegreffii L3 larvae under in vitro exposure to human dendritic cells (DCs) was performed for the first time. A total of 3914 differentially expressed genes (DEGs) were identified in A. pegreffii L3 after exposure to immature DCs (iDCs), by RNA-seq, allowing to detect 1868 upregulated and 2046 downregulated transcripts. Upregulated genes were significantly enriched in pathways related to energy metabolism, oxidative stress response and structural maintenance, suggesting active metabolic and structural adaptation to immune-induced stress. Conversely, genes involved in cytoskeletal organization and intracellular trafficking were downregulated, potentially reflecting the parasite's developmental arrest in an unsuitable host such as humans. These findings provide novel insights into the molecular response pathways activated by this zoonotic parasite during the early stages of interaction with the human immune system.

人畜共患寄生虫异尖线虫在体外暴露于人类树突状细胞后的转录组学特征。
pegreffii异尖线虫是一种人畜共患的海洋线虫,其生命周期涉及海洋生物——小型甲壳类动物、鱼类和鱿鱼作为中间/副宿主,以及海洋哺乳动物,主要是鲸类动物——作为最终宿主。当它的第三阶段幼虫(L3)被人类误食生的或未煮熟的寄生鱼和/或鱿鱼时,寄生虫无法完成其生命周期,导致人类异丝虫病。尽管人们对了解人类异根线虫病致病作用的分子基础越来越感兴趣,但对A. pegreffii L3与人类免疫细胞相互作用的转录组反应仍然知之甚少。因此,在本研究中,首次进行了A. pegreffii L3幼虫在体外暴露于人树突状细胞(DCs)下的转录组学分析。通过RNA-seq,在暴露于未成熟dc (iDCs)后的A. pegreffii L3中共鉴定出3914个差异表达基因(DEGs),可以检测到1868个上调转录本和2046个下调转录本。在与能量代谢、氧化应激反应和结构维持相关的通路中,表达上调的基因显著富集,表明对免疫诱导的应激有积极的代谢和结构适应。相反,参与细胞骨架组织和细胞内运输的基因被下调,这可能反映了寄生虫在不合适的宿主(如人类)中发育迟缓。这些发现为了解这种人畜共患寄生虫在与人类免疫系统相互作用的早期阶段激活的分子反应途径提供了新的见解。
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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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