Bacillus subtilis partially inhibits African swine fever virus infection in vivo and in vitro based on its metabolites arctiin and genistein interfering with the function of viral topoisomerase II

Author:

Lv Changjie12ORCID,Yang Jingyu3,Zhao Li3,Zou Zhong4,Kang Chao4,Zhang Qiang5,Wu Chao4,Yang Li12,Cheng Chuxing4,Zhao Ya12,Liao Qi4,Hu Xiaotong12,Li Chengfei12,Sun Xiaomei12,Jin Meilin12ORCID

Affiliation:

1. College of Veterinary Medicine, Huazhong Agricultural University , Wuhan, China

2. State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University , Wuhan, China

3. State Key Laboratory of Biocatalysis and Enzyme Engineering, College of Life Sciences, Hubei University , Wuhan, China

4. Research Institute of Wuhan Keqian Biology Co., Ltd , Wuhan, China

5. College of Biomedicine and Health, Huazhong Agricultural University , Wuhan, China

Abstract

ABSTRACT African swine fever virus (ASFV) is an infectious disease with a mortality rate of nearly 100% in pigs; however, no safe commercial vaccines or antiviral drugs are currently available, which seriously threatens the global pig industry. Therefore, effective biologics against ASFV are urgently needed. Here, we screened 138 Bacillus subtilis strains, four of which evidently inhibited ASFV replication in vitro . Pigs fed with biologics of different types from the four B. subtilis strains showed reduced pathological changes and viral loads in tissues, with a survival rate of up to 100%. The antiviral activity of B. subtilis was attributed to small-molecule metabolites, rather than to secretory proteins. A total of 169 small molecules were obtained from the metabolites of B. subtilis using liquid chromatograph mass spectrometer/mass spectrometer (LC-MS/MS), arctiin, and genistein, which showed the highest inhibition efficiency, suppressing ASFV proliferation at the mid-stage of infection. These molecules acted as competitive inhibitors by complexing the ATP-binding domain of viral topoisomerase II, as demonstrated using molecular docking, biolayer interferometry binding, and a competitive decatenation assay, thereby disrupting the catalytic activity of the enzyme and inhibiting ASFV replication. Furthermore, pigs administered arctiin and genistein orally showed decreased mortality and tissue damage. Collectively, these results suggest that the four B. subtilis strains screened may be preventative biologics against ASFV infection. Our findings pave the way for ASFV prevention and control strategies in the pig industry to curb the economic losses caused by the disease. IMPORTANCE African swine fever virus (ASFV) is a highly fatal swine disease that severely affects the pig industry. Although ASFV has been prevalent for more than 100 years, effective vaccines or antiviral strategies are still lacking. In this study, we identified four Bacillus subtilis strains that inhibited ASFV proliferation in vitro . Pigs fed with liquid biologics or powders derived from four B. subtilis strains mixed with pellet feed showed reduced morbidity and mortality when challenged with ASFV. Further analysis showed that the antiviral activity of B. subtilis was based on its metabolites arctiin and genistein interfering with the function of viral topoisomerase II. Our findings offer a promising new strategy for the prevention and control of ASFV that may significantly alleviate the economic losses in the pig industry.

Funder

MOST | National Key Research and Development Program of China

Department of Science and Technology, Hubei Provincial People's Government

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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