{"title":"Molecular Characterization of Superoxide Dismutase and Its Putative Relationship With Drug Resistance in Eimeria Tenella","authors":"Xinrui Xie, Yu Yu, Guilin Liu, Qiping Zhao, Shunhai Zhu, Jinwen Wang, Jiayu Bai, Wenqi Han, Hui Dong, Hongyu Han","doi":"10.1111/jeu.70057","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>Avian coccidiosis, an intestinal parasitic disease caused by <i>Eimeria</i> spp., remains one of the most economically significant diseases in poultry. Although anticoccidial drugs have been effective in controlling coccidiosis, the emergence of drug resistance in <i>Eimeria</i> poses a persistent challenge to disease management. Our previous study revealed differential expression of superoxide dismutase (<i>Et</i>SOD) between drug-sensitive (DS) and drug-resistant <i>Eimeria tenella</i> strains. In this study, qPCR and western blot analyses demonstrated that <i>Et</i>SOD expression was significantly upregulated in diclazuril-resistant (DZR) and maduramicin-resistant (MRR) strains compared to the DS strain, with a progressive increase corresponding to higher drug concentrations. Enzyme activity assays further confirmed that SOD activity was elevated in both resistant strains. Additionally, qPCR results indicated higher <i>Et</i>SOD mRNA levels in second-generation merozoites and unsporulated oocysts than in sporulated oocysts and sporozoites. Indirect immunofluorescence revealed that fluorescence intensity increased during parasite development within host cells. Notably, <i>Et</i>SOD was predominantly localized on the surface of sporozoites and merozoites, as well as on the parasitophorous vacuole membrane (PVM) post-invasion of DF-1 cells, suggesting its potential role in host–parasite interactions and immune evasion. Collectively, these findings imply that <i>Et</i>SOD may contribute to drug resistance and facilitate parasite growth and development within host cells.</p>\n </div>","PeriodicalId":15672,"journal":{"name":"Journal of Eukaryotic Microbiology","volume":"73 1","pages":""},"PeriodicalIF":3.3000,"publicationDate":"2025-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Eukaryotic Microbiology","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/jeu.70057","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Avian coccidiosis, an intestinal parasitic disease caused by Eimeria spp., remains one of the most economically significant diseases in poultry. Although anticoccidial drugs have been effective in controlling coccidiosis, the emergence of drug resistance in Eimeria poses a persistent challenge to disease management. Our previous study revealed differential expression of superoxide dismutase (EtSOD) between drug-sensitive (DS) and drug-resistant Eimeria tenella strains. In this study, qPCR and western blot analyses demonstrated that EtSOD expression was significantly upregulated in diclazuril-resistant (DZR) and maduramicin-resistant (MRR) strains compared to the DS strain, with a progressive increase corresponding to higher drug concentrations. Enzyme activity assays further confirmed that SOD activity was elevated in both resistant strains. Additionally, qPCR results indicated higher EtSOD mRNA levels in second-generation merozoites and unsporulated oocysts than in sporulated oocysts and sporozoites. Indirect immunofluorescence revealed that fluorescence intensity increased during parasite development within host cells. Notably, EtSOD was predominantly localized on the surface of sporozoites and merozoites, as well as on the parasitophorous vacuole membrane (PVM) post-invasion of DF-1 cells, suggesting its potential role in host–parasite interactions and immune evasion. Collectively, these findings imply that EtSOD may contribute to drug resistance and facilitate parasite growth and development within host cells.
期刊介绍:
The Journal of Eukaryotic Microbiology publishes original research on protists, including lower algae and fungi. Articles are published covering all aspects of these organisms, including their behavior, biochemistry, cell biology, chemotherapy, development, ecology, evolution, genetics, molecular biology, morphogenetics, parasitology, systematics, and ultrastructure.