4.7 Article

In Vivo and In Vitro Antiviral Activity of Phlorizin Against Bovine Viral Diarrhea Virus

Journal

JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
Volume 70, Issue 47, Pages 14841-14850

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jafc.2c05934

Keywords

phlorizin; BVDV; autophagy; innate immune receptors; biotype specificity

Funding

  1. Heilongjiang Bayi Agricultural University Support Program [ZRCQC202203, TDJH202002]
  2. Postdoctoral Research Foundation of Heilongjiang Province [2032030150]
  3. Scholarship, Talent Research Fund of Heilongjiang Bayi Agricultural University [2031011079]

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Phlorizin, extracted from apple tree, has been found to inhibit the replication of BVDV and improve the histopathological changes caused by the infection. It works by regulating immune-related molecules, promoting interferon levels, and suppressing the expression of inflammatory cytokines.
Bovine viral diarrhea virus (BVDV) is one of the most serious pathogens affecting the cattle industry worldwide. Phlorizin, a kind of flavonoids extracted from apple tree roots, leaves, and fruits, has a variety of biological functions and has been widely used as a herbal supplement and food additive. Here, BALB/c mouse and Madin-Darby bovine kidney (MDBK) cells were used to explore the effect and mechanism of phlorizin against BVDV infection. The results showed that phlorizin significantly inhibited CP BVDV replication and improved the histopathological changes of duodenum and spleen in mice. In vitro studies also confirmed the activity of phlorizin against CP BVDV. Exploration on its potential mechanism suggested that phlorizin inhibited CP BVDV-induced beclin-1 level and the conversion rate of LC3B-I to LC3B-II. Interestingly, although phlorizin also showed a protective effect on MDBK cells, which were treated with 3-methyladenine A (3-MA), the effect was significantly weakened. Furthermore, phlorizin suppressed the stage of BVDV replication but showed no effect on stages of attachment and internalization. Our data further indicated that phlorizin promoted IFN-alpha and IFN-beta levels, decreased IL-1 beta and IL-6 expression, and regulated RIG-I, MDA5, TLR3, and NLRP3 levels. Similar to CP BVDV results, in vivo and in vitro, phlorizin inhibited NCP BVDV (NY-1 and YNJG2020 strains) infection. These results were the first to be discovered that phlorizin might be used as a new dietary strategy for controlling BVDV infection.

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