Natto extract inhibits infection caused by the Aujeszky's disease virus in mice

Author:

Kobayashi Junya123,Wen Rongduo12,Nishikawa Takanobu4,Nunomura Yuka1,Suzuki Takehito4,Sejima Yudai4,Gokan Toshiya4,Furukawa Makio4,Yokota Tomoko1,Osawa Nanako12,Sato Yoko1,Nibu Yutaka56ORCID,Mizutani Tetsuya12,Oba Mami12ORCID

Affiliation:

1. Center for Infectious Diseases of Epidemiology and Prevention Research (CEPiR) Tokyo University of Agriculture and Technology Saiwai‐cho Tokyo Japan

2. Graduate School of Agriculture, Cooperative Division of Veterinary Science Tokyo University of Agriculture and Technology Tokyo Japan

3. Research Institute for Animal Science in Biochemistry and Toxicology (RIAS) Sagamihara Kanagawa Japan

4. Takanofoods Co., Ltd. Omitama Ibaraki Japan

5. The University Research Administration Center (URAC) Tokyo University of Agriculture and Technology Tokyo Japan

6. Institute for Glyco‐core Research (iGCORE) Nagoya University, Tokai National Higher Education and Research System Nagoya Japan

Abstract

AbstractAujeszky's disease virus (ADV), also known as Suid alphaherpesvirus 1, which mainly infects swine, causes life‐threatening neurological disorders. This disease is a serious global risk factor for economic losses in the swine industry. The development of new anti‐ADV drugs is highly anticipated and required. Natto, a traditional Japanese fermented food made from soybeans, is a well‐known health food. In our previous study, we confirmed that natto has the potential to inhibit viral infections by severe acute respiratory syndrome coronavirus 2 and bovine alphaherpesvirus 1 through their putative serine protease(s). In this study, we found that an agent(s) in natto functionally impaired ADV infection in cell culture assays. In addition, ADV treated with natto extract lost viral infectivity in the mice. We conducted an HPLC gel‐filtration analysis of natto extract and molecular weight markers and confirmed that Fraction No. 10 had ADV‐inactivating ability. Furthermore, the antiviral activity of Fraction No. 10 was inhibited by the serine protease inhibitor 4‐(2‐Aminoethyl) benzene sulfonyl fluoride hydrochloride (AEBSF). These results also suggest that Fraction No. 10, adjacent to the 12.5 kDa peak of the marker in natto extract, may inactivate ADV by proteolysis. Our findings provide new avenues of research for the prevention of Aujeszky's disease.

Publisher

Wiley

Subject

Virology,Immunology,Microbiology

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