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Paraprobiotic derived from Bacillus velezensis GV1 improves immune response and gut microbiota composition in cyclophosphamide-treated immunosuppressed mice.

Authors :
Lee HJ
Tran MTH
Le MH
Justine EE
Kim YJ
Source :
Frontiers in immunology [Front Immunol] 2024 Feb 22; Vol. 15, pp. 1285063. Date of Electronic Publication: 2024 Feb 22 (Print Publication: 2024).
Publication Year :
2024

Abstract

Paraprobiotics that benefit human health have the capacity to modulate innate and adaptive immune systems. In this study, we prepared the paraprobiotic from Bacillus velezensis GV1 using the heat-killing method and investigated its effects on immunity and gut microbiota in vitro and in vivo . The morphology of inactivated strain GV1 was observed using scanning electron microscopy. Treatment with GV1 promoted nitric oxide production and augmented cytokine (IL-6, IL-1β, and TNF-α) expression and secretion in RAW 264.7 macrophages. Moreover, the strain GV1 could alleviate cyclophosphamide monohydrate (CTX)-induced immunosuppression by reversing spleen damage and restoring the immune organ index, as well as by increasing the expression of immune-related cytokines (TNF-α, IL-1β, IFN-γ, and IL-2) in the spleen and thymus, respectively. Furthermore, GV1 treatment dramatically healed the CTX-damaged colon and regulated gut microbiota by increasing the relative abundance of beneficial bacterial families ( Lactobacillaceae , Akkermansiaceae , and Coriobacteriaceae ) and decreasing that of harmful bacterial families ( Desulfovibrionaceae , Erysipelotrichaceae , and Staphylococcaceae ). Thus, the heat-killed GV1 can be considered a potential immunoregulatory agent for use as a functional food or immune-enhancing medicine.<br />Competing Interests: Y-JK is affiliated with the company KDBio Corporation. The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2024 Lee, Tran, Le, Justine and Kim.)

Details

Language :
English
ISSN :
1664-3224
Volume :
15
Database :
MEDLINE
Journal :
Frontiers in immunology
Publication Type :
Academic Journal
Accession number :
38455053
Full Text :
https://doi.org/10.3389/fimmu.2024.1285063