4.7 Article

Lianhuaqingwen capsule inhibits non-lethal doses of influenza virus-induced secondary Staphylococcus aureus infection in mice

期刊

JOURNAL OF ETHNOPHARMACOLOGY
卷 298, 期 -, 页码 -

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.jep.2022.115653

关键词

Lianhuaqingwen capsule; Influenza virus; Staphylococcus aureus; Anti-inflammatory; Antiviral; Antibacterial

资金

  1. National Key R & D Program of China [2021YFE0200300]
  2. Science and Technology Program of Guangzhou, China [202102100003]
  3. Science and Technology Program of Foshan, China [2020001000206]
  4. Science and Technology Projects in Guangzhou, China [202201010522]
  5. National Natural Science Foundation of China [82074311]

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Lianhuaqingwen capsule has been proven to have antiviral and antibacterial effects, reducing lung damage and inflammatory mediators like IL-6, IL-1 beta, IL-10, TNF-alpha, IFN-beta, MCP-1, and RANTES. It shows promise in treating influenza secondary bacterial infection.
Ethnopharmacological relevance: Lianhuaqingwen capsule (LH-C) is a traditional Chinese medicine (TCM), con-sisting of two prescriptions, Ma-xing-shi-gan-tang (MXSGT) and Yinqiao San. It has been proven to have anti-viral, antibacterial, and immunomodulatory effects in recent years. Clinically, it is commonly used in the treatment of respiratory tract infections. Aim of the study: It was demonstrated in our previous studies that LH-C has an effect of antivirus and inhibits influenza virus-induced bacterial adhesion to respiratory epithelial cells through down-regulation of cell adhe-sion molecules in vitro. However, LH-C's effect against influenza-induced secondary bacterial infection in animal studies remains unclear. Therefore, in the present study, we established a mouse model of infection with non-lethal doses of influenza virus(H1N1) and secondary infection of Staphylococcus aureus (S. aureus), to investi-gate the potential effects of LH-C. Methods: Experiments were carried out on BALB/c mice infecting non-lethal doses of H1N1 and non-lethal doses of S. aureus, and the viral, and bacterial doses were determined by observing and recording changes in the body weight, mortality, and pathological changes. Moreover, after LH-C treatment, the survival rate, body weight, lung index, viral titers, bacterial colonies, pathological changes, and the inflammatory cytokines in the mouse model have all been systematically determined. Results: In the superinfection models of H1N1 and S. aureus, the mortality rate was 100% in groups of mice infected with 20 PFU/50 mu L of H1N1 and 10(5) CFU/mL of S. aureus, 20 PFU/50 mu L of H1N1 and 10(6) CFU/mL of S. aureus, 4 PFU/50 mu L of H1N1 and 10(6) CFU/mL of S. aureus. The mortality rate was 50% in the group of mice infected with 4 PFU/50 mu L of H1N1 and 10(5) CFU/mL of S. aureus. The mortality rate was 37.5% in the group of mice infected with 20 PFU/50 mu L of H1N1 alone and in the group of mice infected with 2 PFU/50 mu L of H1N1 and 10(6) CFU/mL of S. aureus. The mortality rate in the group of mice infected with 2 PFU/50 mu L of H1N1 and 10(6 )CFU/mL of S. aureus was 30%. The infected mice of 2 PFU/50 mu L of H1N1 and 10(6) CFU/mL of S. aureus had a weight loss of nearly 10%. About the histopathological changes in the lung tissue of infection mice, severe lung lesions were found in the superinfection models. LH-C improved survival in the superinfected mice, significantly reduced lung index, lowered viral titers and bacterial loads, and alleviated lung damage. It reduced lung inflammation by down-regulating mRNA expression levels of inflammatory mediators like IL-6, IL-1 beta, IL-10, TNF-alpha, IFN-beta, MCP-1, and RANTES. Conclusions: We found that superinfection from non-lethal doses of S. aureus following non-lethal doses of H1N1 was equally fatal in mice, confirming the severity of secondary infections. The ability of LH-C to alleviate lung injury resulting from secondary S. aureus infection induced by H1N1 was confirmed. These findings provided a further assessment of LH-C, suggesting that LH-C may have good therapeutic efficacy in influenza secondary bacterial infection disease.

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