Localization and Tissue Tropism of Ostreid Herpesvirus 1 in Blood Clam Anadara broughtonii

Author:

Li Ya-Nan12,Zhang Xiang2,Huang Bo-Wen2ORCID,Xin Lu-Sheng2ORCID,Wang Chong-Ming23ORCID,Bai Chang-Ming23ORCID

Affiliation:

1. College of Ocean and Biology Engineering, Yancheng Teachers University, Yancheng 224007, China

2. Key Laboratory of Maricultural Organism Disease Control, Ministry of Agriculture, Qingdao Key Laboratory of Mariculture Epidemiology and Biosecurity, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao 266071, China

3. Laboratory for Marine Fisheries Science and Food Production Processes, Qingdao National Laboratory for Marine Science and Technology, Qingdao 266237, China

Abstract

OsHV-1 caused detrimental infections in a variety of bivalve species of major importance to aquaculture worldwide. Since 2012, there has been a notable increase in the frequency of mass mortality events of the blood clam associated with OsHV-1 infection. The pathological characteristics, tissue and cellular tropisms of OsHV-1 in A. broughtonii remain unknown. In this study, we sought to investigate the distribution of OsHV-1 in five different organs (mantle, hepatopancreas, gill, foot, and adductor muscle) of A. broughtonii by quantitative PCR, histopathology and in situ hybridization (ISH), to obtain insight into the progression of the viral infection. Our results indicated a continuous increase in viral loads with the progression of OsHV-1 infection, reaching a peak at 48 h or 72 h post-infection according to different tissues. Tissue damage and necrosis, as well as colocalized OsHV-1 ISH signals, were observed primarily in the connective tissues of various organs and gills. Additionally, minor tissue damage accompanied by relatively weak ISH signals was detected in the foot and adductor muscle, which were filled with muscle tissue. The predominant cell types labeled by ISH signals were infiltrated hemocytes, fibroblastic-like cells, and flat cells in the gill filaments. These results collectively illustrated the progressive alterations in pathological confusion and OsHV-1 distribution in A. broughtonii, which represent most of the possible responses of cells and tissues to the virus.

Funder

National Natural Science Foundation of China

Postdoctoral Innovation Project of Shandong Province

Central Public-interest Scientific Institution Basal Research Fund, CAFS

Central Public-interest Scientific Institution Basal Research Fund, YSFRI

earmarked fund for CARS

Publisher

MDPI AG

Reference65 articles.

1. Oyster herpes-type virus;Farley;Science,1972

2. Viruses and virus-like lesions in marine mollusks;Farley;Mar. Fish. Rev.,1978

3. Herpes-like virus infecting Pacific-oyster larvae, Crassostrea gigas;Nicolas;Bull. Eur. Assoc. Fish. Pathol.,1992

4. Herpesviruses associated with mortalities among hatchery-reared larval Pacific oysters, Crassostrea-gigas;Hine;Dis. Aquat. Organ.,1992

5. A novel class of herpesvirus with bivalve hosts;Davison;J. Gen. Virol.,2005

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