Establishment of a gill cell line from yellowfin seabream (Acanthopagrus latus) for studying Amyloodinium ocellatum infection of fish

© 2024 John Wiley & Sons Ltd.

Détails bibliographiques
Publié dans:Journal of fish diseases. - 1998. - 47(2024), 5 vom: 11. Mai, Seite e13923
Auteur principal: Li, Zhicheng (Auteur)
Autres auteurs: Zhuang, Jingyu, Chen, Jiaming, Cao, Jizhen, Han, Qing, Luo, Zhi, Wang, Baotun, Wang, Hebing, Li, Anxing
Format: Article en ligne
Langue:English
Publié: 2024
Accès à la collection:Journal of fish diseases
Sujets:Journal Article Acanthopagrus latus Amyloodinium ocellatum cell line in vitro infection
Description
Résumé:© 2024 John Wiley & Sons Ltd.
Amyloodinium ocellatum is among the most devastating protozoan parasites, causing huge economic losses in the mariculture industry. However, the pathogenesis of amyloodiniosis remains unknown, hindering the development of targeted anti-parasitic drugs. The A. ocellatum in vitro model is an indispensable tool for investigating the pathogenic mechanism of amyloodiniosis at the cellular and molecular levels. The present work developed a new cell line, ALG, from the gill of yellowfin seabream (Acanthopagrus latus). The cell line was routinely cultured at 28°C in Dulbecco's modified Eagle medium (DMEM) supplemented with 15% fetal bovine serum (FBS). ALG cells were adherent and exhibited an epithelioid morphology; the cells were stably passed over 30 generations and successfully cryopreserved. The cell line derived from A. latus was identified based on partial sequence amplification and sequencing of cytochrome B (Cyt b). The ALG was seeded onto transwell inserts and found to be a platform for in vitro infection of A. ocellatum, with a 37.23 ± 5.75% infection rate. Furthermore, scanning electron microscopy (SEM) revealed that A. ocellatum parasitizes cell monolayers via rhizoids. A. ocellatum infection increased the expression of apoptosis and inflammation-related genes, including caspase 3 (Casp 3), interleukin 1 (IL-1), interleukin 10 (IL-10), tumour necrosis factor-alpha (TNF-α), in vivo or in vitro. These results demonstrated that the in vitro gill cell monolayer successfully recapitulated in vivo A. latus host responses to A. ocellatum infection. The ALG cell line holds great promise as a valuable tool for investigating parasite-host interactions in vitro
Description:Date Completed 11.04.2024
Date Revised 11.04.2024
published: Print-Electronic
RefSeq: MN413448.1
Citation Status MEDLINE
ISSN:1365-2761
DOI:10.1111/jfd.13923