4.6 Article

Effects of glycyrrhizin on the growth cycle and ATPase activity of PRRSV-2-infected MARC-145 cells

Journal

RESEARCH IN VETERINARY SCIENCE
Volume 138, Issue -, Pages 30-38

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.rvsc.2021.05.011

Keywords

Porcine reproductive and respiratory syndrome; virus (PRRSV); Glycyrrhizin; MARC-145 cell; Cell cycle; ATPase activity

Funding

  1. National Natural Science Foundation of China [31702235]
  2. Doctoral Scientific Research Startup Foundation from Henan University of Technology [2016BS007]
  3. Innovative Funds Plan of Henan University of Technology [2020ZKCJ25]

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PRRS is a viral infectious disease caused by PRRSV, which has a significant impact on the swine industry. Glycyrrhizin inhibits the proliferation of PRRSV-2 in MARC-145 cells by affecting the cell cycle and ATPase activity.
Porcine reproductive and respiratory syndrome (PRRS) is a viral infectious disease caused by the porcine reproductive and respiratory syndrome virus (PRRSV) and is devastating the swine industry. MARC-145 cells, an African green monkey kidney cell line, are sensitive to PRRSV-2, and are often used for in vitro studies on PRRSV2. Preliminary research has shown that glycyrrhizin, an important active component extracted from traditional Chinese medicinal licorice, significantly inhibits the proliferation of PRRSV-2 in MARC-145 cells; however, the in-depth molecular mechanism remains unclear. By determining the cell growth cycle, this study found that PRRSV-2 infection first increased the content of G1-phase MARC-145 cells and then decreased the content of G1phase cells. Moreover, glycyrrhizin affected the role of PRRSV-2 in regulating the cell cycle. Furthermore, PRRSV-2 had the highest proliferation titer in G0/G1-phase MARC-145 cells, and glycyrrhizin reduced the content of PRRSV-2 in synchronized MARC-145 cells. According to the results of ATPase detection, PRRSV-2 infection weakened the Na+/K+-ATPase and Ca2+/Mg2+-ATPase activities in MARC-145 cells, while glycyrrhizin significantly enhanced their activities in PRRSV-2-infected MARC-145 cells. The above results provide theoretical support toward clarifying the mechanism by which glycyrrhizin inhibits the proliferation of PRRSV-2 in MARC-145 cells. Moreover, these results offer references for the development and use of glycyrrhizin and the clinical treatment of PRRSV-2 infection.

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