Insights into the fatty acid binding protein of Pacific white shrimp (Litopenaeus vannamei) suffering acute hepatopancreatic necrosis disease infection
Gu, Xiaoqian1,3,4; Wang, Baojie1,3; Jiang, Keyong1,3; Liu, Mei2,5; Wang, Lei1,3,4,6
刊名AQUACULTURE
2023-09-15
卷号574页码:12
关键词Fatty acid binding protein AHPND Immunofluorescence localization Blocking assay Neutralization assay Transcriptome analysis
ISSN号0044-8486
DOI10.1016/j.aquaculture.2023.739719
通讯作者Liu, Mei(mliu_msrisd@126.com) ; Wang, Lei(leiwang@qdio.ac.cn)
英文摘要Acute hepatopancreatic necrosis disease (AHPND) has a significant economic impact on aquaculture worldwide. However, the molecular mechanism responsible for AHPND remains unknown. Our previous study demonstrated that the Litopenaeus vannamei fatty acid binding protein (LvFABP) interacted with the Vibrio parahaemolyticus toxin PirB, and that silencing LvFABP using RNA interference improved AHPND resistance in shrimp. Polyclonal antibodies against recombinant LvFABP and PirBvp toxin were produced to further elucidate the role of LvFABP in AHPND resistance. Immunofluorescence localization showed that LvFABP was abundant throughout the cytoplasm of the hepatopancreas cells, and a co-localization assay revealed that PirBvp directly interacted with LvFABP. Antibodies against LvFABP were able to partially block the binding of LvFABP to PirBvp in vitro and inhibited AHPND infection in vivo. Exogenous recombinant LvFABP had a partially neutralizing effect against AHPND and gave L. vannamei significant protection against infection. In addition, recombinant LvFABP treatment of L. vannamei significantly reduced the morphological damage to the shrimp following pathogen challenge. The transcriptomes of the L. vannamei hepatopancreas with and without V. parahaemolyticus infection after silencing of LvFABP by RNA interference were also explored. The results showed that AHPND infection could affect the health of L. vannamei via functional changes in carbohydrate metabolism, lipid metabolism, and transport and catabolism. Furthermore, silencing LvFABP could effectively protect metabolism, transport and catabolic homeostasis, thus enabling adaptation to further or prolonged AHPND infections. These findings provided a unique and important dataset that deepened our understanding of the pathological mechanism of AHPND and may help in the development of strategies to prevent and ameliorate the effects of bacterial diseases.
资助项目Yellow River Delta Industry Leading Talent Project ; National Key Ramp;D Program of China[2019YFD0900401]
WOS关键词DIFFERENTIALLY EXPRESSED GENES ; SPOT SYNDROME VIRUS ; VIBRIO-PARAHAEMOLYTICUS ; TRANSCRIPTOME ANALYSIS ; PPAR-ALPHA ; AHPND ; DEFICIENT
WOS研究方向Fisheries ; Marine & Freshwater Biology
语种英语
出版者ELSEVIER
WOS记录号WOS:001012431100001
内容类型期刊论文
源URL[http://ir.qdio.ac.cn/handle/337002/182339]  
专题海洋研究所_实验海洋生物学重点实验室
通讯作者Liu, Mei; Wang, Lei
作者单位1.Chinese Acad Sci, Inst Oceanol, Ctr Ocean Mega Sci, Shandong Prov Key Lab Expt Marine Biol, Qingdao, Peoples R China
2.Marine Sci Res Inst Shandong Prov, Shandong Key Lab Dis Control Mariculture, Qingdao, Peoples R China
3.Chinese Acad Sci, Inst Oceanol, Ctr Ocean Mega Sci, CAS, Qingdao, Peoples R China
4.Univ Chinese Acad Sci, Beijing, Peoples R China
5.Marine Sci Res Inst Shandong Prov, 7 Youyun Rd, Qingdao 266104, Peoples R China
6.Chinese Acad Sci, Inst Oceanol, 7 Nanhai Rd, Qingdao 266071, Peoples R China
推荐引用方式
GB/T 7714
Gu, Xiaoqian,Wang, Baojie,Jiang, Keyong,et al. Insights into the fatty acid binding protein of Pacific white shrimp (Litopenaeus vannamei) suffering acute hepatopancreatic necrosis disease infection[J]. AQUACULTURE,2023,574:12.
APA Gu, Xiaoqian,Wang, Baojie,Jiang, Keyong,Liu, Mei,&Wang, Lei.(2023).Insights into the fatty acid binding protein of Pacific white shrimp (Litopenaeus vannamei) suffering acute hepatopancreatic necrosis disease infection.AQUACULTURE,574,12.
MLA Gu, Xiaoqian,et al."Insights into the fatty acid binding protein of Pacific white shrimp (Litopenaeus vannamei) suffering acute hepatopancreatic necrosis disease infection".AQUACULTURE 574(2023):12.
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