Suppr超能文献

氧化应激、基因表达与自然感染小瓜虫和溶藻弧菌的养殖真鲷组织病理学变化。

Oxidative stress, gene expression and histopathology of cultured gilthead sea bream (Sparus aurata) naturally co-infected with Ergasilus sieboldi and Vibrio alginolyticus.

机构信息

Department of Aquatic Animal Medicine and Management, Faculty of Veterinary Medicine, Cairo University, Giza, 12211, Egypt.

Department of Biochemistry and Chemistry of Nutrition, Faculty of Veterinary Medicine, Cairo University, Giza, 12211, Egypt.

出版信息

BMC Vet Res. 2023 Dec 16;19(1):277. doi: 10.1186/s12917-023-03840-9.

Abstract

BACKGROUND

Parasitic and bacterial co-infections have been associated with increasing fish mortalities and severe economic losses in aquaculture through the past three decades. The aim of this study was to evaluate the oxidative stress, histopathology, and immune gene expression profile of gilthead sea bream (Sparus aurata) co-infected with Ergasilus sieboldi and Vibrio alginolyticus.

RESULTS

Vibrio alginolyticus and Ergasilus sieboldi were identified using 16 S rRNA and 28 S rRNA sequencing, respectively. The collagenase virulence gene was found in all Vibrio alginolyticus isolates, and the multiple antimicrobial resistance index ranged from 0.286 to 0.857. Oxidant-antioxidant parameters in the gills, skin, and muscles of naturally infected fish revealed increased lipid peroxidation levels and a decrease in catalase and glutathione antioxidant activities. Moreover, naturally co-infected gilthead sea bream exhibited substantial up-regulation of il-1β, tnf-α, and cyp1a1. Ergasilus sieboldi encircled gill lamellae with its second antennae, exhibited severe gill architectural deformation with extensive eosinophilic granular cell infiltration. Vibrio alginolyticus infection caused skin and muscle necrosis in gilthead sea bream.

CONCLUSION

This study described some details about the gill, skin and muscle tissue defense mechanisms of gilthead sea bream against Ergasilus sieboldi and Vibrio alginolyticus co-infections. The prevalence of co-infections was 100%, and no resistant fish were detected. These co-infections imbalance the health status of the fish by hampering the oxidant-antioxidant mechanisms and proinflammatory/inflammatory immune genes to a more detrimental side. Our results suggest that simultaneous screening for bacterial and parasitic pathogens should be considered.

摘要

背景

在过去的三十年中,寄生虫和细菌的混合感染与水产养殖中的鱼类死亡率增加和严重的经济损失有关。本研究的目的是评估感染栉孔扇贝纤毛虫(Ergasilus sieboldi)和溶藻弧菌(Vibrio alginolyticus)的真鲷(Sparus aurata)的氧化应激、组织病理学和免疫基因表达谱。

结果

通过 16S rRNA 和 28S rRNA 测序分别鉴定出溶藻弧菌和栉孔扇贝纤毛虫。在所有溶藻弧菌分离株中均发现胶原酶毒力基因,多重抗生素耐药指数范围为 0.286 至 0.857。天然感染鱼的鳃、皮肤和肌肉中的氧化剂-抗氧化剂参数显示脂质过氧化水平升高,过氧化氢酶和谷胱甘肽抗氧化活性降低。此外,天然混合感染的真鲷表现出 il-1β、tnf-α 和 cyp1a1 的显著上调。栉孔扇贝纤毛虫用其二触角环绕鳃片,严重的鳃结构变形,伴有广泛的嗜酸性粒细胞浸润。溶藻弧菌感染导致真鲷的皮肤和肌肉坏死。

结论

本研究描述了真鲷鳃、皮肤和肌肉组织对栉孔扇贝纤毛虫和溶藻弧菌混合感染的防御机制的一些细节。混合感染的流行率为 100%,未检测到耐药鱼。这些混合感染通过干扰氧化应激-抗氧化机制和促炎/炎症免疫基因,使鱼类的健康状况更加恶化。我们的结果表明,应考虑同时筛选细菌和寄生虫病原体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e541/10724927/b732151da762/12917_2023_3840_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验