The Probiotic Bacillus hwajinpoensis Colonizes the Digestive System of Crassostrea gigas Larvae and Protects Them from Vibrio alginolyticus Infection

Author:

Zheng Yu-Dong12,Huang Bo-Wen123ORCID,Zhang Xiang12,Liu Chen-Feng12,Xin Lu-Sheng123ORCID,Wang Chong-Ming123ORCID,Bai Chang-Ming123ORCID

Affiliation:

1. State Key Laboratory of Mariculture Biobreeding and Sustainable Goods, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao 266071, China

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

3. Key Laboratory of Maricultural Organism Disease Control, Qingdao Key Laboratory of Mariculture Epidemiology and Biosecurity, Ministry of Agriculture, Qingdao 266071, China

Abstract

The Pacific oyster Crassostrea gigas is one of the most important cultured marine species around the world. Production of Pacific oysters in China has depended primarily on hatchery produced seeds since 2016, with the successful introduction and development of triploid oysters. However, the seed supply of Pacific oysters is threatened by recurring mass mortality events in recent years. Vibriosis is the most commonly encountered disease associated with intensive oyster culture in hatcheries and nurseries. Vibrio alginolyticus and Bacillus hwajinpoensis were the two strains with pathogenic and probiotic effects, respectively, identified during the Pacific oyster larvae production. To monitor their colonization process in Pacific oyster larvae, green fluorescent protein (GFP) and red fluorescent protein (RFP) were labeled to the pathogenic V. alginolyticus and the probiotic B. hwajinpoensis stain, respectively. The pathogenic and probiotic effects of the two strains during the colonization process were then assessed. Stabile expression of GFP and RFP were observed in corresponding stains, and the capabilities of growth, biofilm formation and in vitro adhesion of GFP- and RFP- tagged stains were not significantly different from those of the wild-type strains. Usage of probiotics of 105 CFU/mL significantly inhibited the growth of pathogenic V. alginolyticus and reduced the mortality of D-sharped larvae. Both the pathogenic and probiotic strains employed a similar route to enter and colonize the oyster larvae, which indicates that competing with pathogens for binding and spreading sites were one of the mechanisms of B. hwajinpoensis to provide the probiotic effects to oyster larvae. In summary, employment of fluorescence-tagged pathogenic and probiotic strains simultaneously provides us with an excellent bioassay model to investigate the potential mechanisms of probiotics.

Funder

Central Public-interest Scientific Institution Basal Research Fund, CAFS

The earmarked fund for CARS

Postdoctoral Innovation Project of Shandong Province

Publisher

MDPI AG

Subject

Virology,Microbiology (medical),Microbiology

Reference68 articles.

1. Bayne, B. (2017). Biology of Oysters, Academic Press.

2. Use and exchange of genetic resources in molluscan aquaculture;Guo;Rev. Aquacult.,2009

3. China Agriculture Research System-Mollusk (2021). Developemnt report of oyster industry in China. China Fish., 6, 20–31.

4. An evolution of oyster mariculture industry in China: New knowledge, variety and product;Zhang;Oceanol. Limnol. Sin.,2020

5. Analysis of agglomeration characteristics of Chinese oyster breeding industry;Jiang;Chin. Fish. Econ.,2021

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