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Oral Treatment with Saccharomyces cerevisiae CNCM I-3856 Mitigates the Inflammatory Response Experimentally Induced by Salmonella enterica subsp. enterica Serovar Typhimurium in Mice
被引:0
|作者:
Campos, Lara L.
[1
]
Oliveira, Samantha R. M.
[1
]
Amaral, Maisa N. S.
[1
]
Gallotti, Bruno
[1
]
Oliveira, Aline F.
[1
]
Arantes, Rosa M. E.
[2
]
Ribeiro-Souza, Samantha
[3
]
Vital, Katia D.
[4
]
Fernandes, Simone O. A.
[4
]
Cardoso, Valbert N.
[4
]
Nicoli, Jacques R.
[1
]
Martins, Flaviano S.
[1
]
机构:
[1] Univ Fed Minas Gerais, Dept Microbiol, Inst Ciencias Biol, Belo Horizonte, MG, Brazil
[2] Univ Fed Minas Gerais, Dept Patol Geral, Inst Ciencias Biol, Belo Horizonte, MG, Brazil
[3] Univ Fed Ouro Preto, Dept Ciencias Biol, Ouro Preto, MG, Brazil
[4] Univ Fed Minas Gerais, Fac Farm, Dept Anal Clinicas & Toxicol, Belo Horizonte, MG, Brazil
关键词:
Probiotics;
Saccharomyces cerevisiae CNCM I-3856;
Salmonella Typhimurium;
Intestinal inflammation;
BACTERIAL TRANSLOCATION;
IMMUNE-SYSTEM;
GUT;
ENVIRONMENT;
MECHANISMS;
BOULARDII;
INFECTION;
PROTECT;
D O I:
10.1007/s12602-024-10359-4
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
Salmonella spp. are intracellular, Gram-negative pathogens responsible for a range of diarrheal diseases, which can present either as self-limited (gastroenteritis) or as a systemic form (typhoid fever), characterizing a serious public health problem. In this study, we investigated the therapeutic effects of oral administration of Saccharomyces cerevisiae CNCM I-3856 in a murine model infected with Salmonella Typhimurium (ST). This yeast species has previously demonstrated the potential to support immune function and reduce inflammation and the ability to exert antimicrobial activity, which is important considering the increasing prevalence of antibiotic-resistant bacteria. Our findings revealed that mice infected with ST and only treated with sterile saline exhibited a higher mortality rate and body weight loss. In contrast, mice treated with I-3856 showed a notable reduction in these adverse outcomes. The yeast demonstrated a high capacity for co-aggregation with the pathogen. Furthermore, the significant amounts of yeast found in the feces of treated mice suggest that intestinal colonization was effective, which was associated with several beneficial effects, including reduced intestinal permeability, which likely limits bacterial translocation to extraintestinal organs. Additionally, the administration of I-3856 reduced levels of sIgA and resulted in a decrease in the recruitment of neutrophils and eosinophils to infection sites, indicating a modulation of the inflammatory response. Histological analyses showed attenuated liver and intestinal lesions in the yeast-treated mice, corroborating the protective effects of the yeast. In conclusion, the results suggest that S. cerevisiae CNCM I-3856 has the potential to control the inflammatory response experimentally induced by S. Typhimurium when administered to mice.
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