Genome-wide identification and immune response analysis to vibrio for heme peroxidase in the blood clam Anadara granosa

IF 2.2 2区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Yazhuo Hu , Chengtian Zhang , Zongming Wu , Sufang Wang , Yongbo Bao
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引用次数: 0

Abstract

Heme peroxidases (HPs), an essential class of oxidoreductases that may have an important role in molluscan immune defense, remain inadequately studied in mollusks. In this study, HPs in Anadara granosa (AgHPs) were comprehensively analyzed on a genome-wide scale and their immune responses under stress from three species of Vibrio were investigated. A total of 18 AgHPs were identified in the genome of A. granosa, unequally distributed in four subfamilies, peroxinectin (Pxt), prostaglandin G/H synthase (PGHS), dual oxidases (DuOx) and peroxidasin (Pxd). AgHPs were mainly expressed in gills and mantle, with AgHP6 being the only member expressed in hemocytes. The immune response of A. granosa to Vibrio stress demonstrated dynamic alterations in gene expression, characterized by prominent upregulation of AgHP3 and AgHP4 in both gills and mantle, alongside significant downregulation of several other genes; these expression changes likely underpin antimicrobial immunity in A. granosa and suggest distinct regulatory mechanisms and functional roles. Further analyses suggest that AgHP11 (Pxt) may enhance cell adhesion when invaded by exogenous bacteria, and AgHP3 (PGHS) and AgHP4 (PGHS) contribute to the immunity by synthesizing various prostaglandins. AgHP6 (DuOx) and AgHP7 (DuOx) may activate epithelial immunity by reducing expression levels. Additionally, during the anti-Vibrio process, hemoglobin may substitute for ROS-producing HPs to provide antimicrobial defense in A. granosa. This study represents the first genome-wide identification and immune response analysis of HPs in A. granosa, laying a foundation for future research into the immune functions of HPs in mollusks.
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来源期刊
CiteScore
5.10
自引率
3.30%
发文量
69
审稿时长
33 days
期刊介绍: Comparative Biochemistry & Physiology (CBP) publishes papers in comparative, environmental and evolutionary physiology. Part D: Genomics and Proteomics (CBPD), focuses on “omics” approaches to physiology, including comparative and functional genomics, metagenomics, transcriptomics, proteomics, metabolomics, and lipidomics. Most studies employ “omics” and/or system biology to test specific hypotheses about molecular and biochemical mechanisms underlying physiological responses to the environment. We encourage papers that address fundamental questions in comparative physiology and biochemistry rather than studies with a focus that is purely technical, methodological or descriptive in nature.
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