Response of Salmonella enterica serovar Typhimurium to alginate oligosaccharides fermented with fecal inoculum: integrated transcriptomic and metabolomic analyses

被引:10
|
作者
Cheng, Jiaying [1 ]
Xiao, Mengshi [1 ]
Ren, Xinmiao [1 ]
Secundo, Francesco [2 ]
Yu, Ying [1 ]
Nan, Shihao [3 ]
Chen, Weimiao [4 ]
Zhu, Changliang [1 ]
Kong, Qing [1 ]
Huang, Youtao [1 ]
Fu, Xiaodan [3 ]
Mou, Haijin [1 ]
机构
[1] Ocean Univ China, Coll Food Sci & Engn, Qingdao 266003, Peoples R China
[2] CNR, Ist Sci & Tecnol Chim Giulio Natta, I-20131 Milan, Italy
[3] Nanchang Univ, State Key Lab Food Sci & Technol, China Canada Joint Lab Food Sci & Technol Nanchang, Key Lab Bioact Polysaccharides Jiangxi Prov, Nanchang 330047, Peoples R China
[4] Ocean Univ China, Sch Med & Pharm, Qingdao 266003, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Alginate oligosaccharides; Gut microbiota; Metabolite; Salmonella enterica serovar Typhimurium; Metabolomics; Transcriptomic; ANTIOXIDANT CAPACITY; VIRULENCE FACTORS; PERFORMANCE; METABOLITES; MICROBIOTA; SUPPLEMENTATION; COLONIZATION; MICROFLORA; MODEL; TYPHI;
D O I
10.1007/s42995-023-00176-z
中图分类号
Q17 [水生生物学];
学科分类号
071004 ;
摘要
Alginate oligosaccharides (AOS), extracted from marine brown algae, are a common functional feed additive; however, it remains unclear whether they modulate the gut microbiota and microbial metabolites. The response of Salmonella enterica serovar Typhimurium, a common poultry pathogen, to AOS fermented with chicken fecal inocula was investigated using metabolomic and transcriptomic analyses. Single-strain cultivation tests showed that AOS did not directly inhibit the growth of S. Typhimurium. However, when AOS were fermented by chicken fecal microbiota, the supernatant of fermented AOS (F-AOS) exhibited remarkable antibacterial activity against S. Typhimurium, decreasing the abundance ratio of S. Typhimurium in the fecal microbiota from 18.94 to 2.94%. Transcriptomic analyses showed that the 855 differentially expressed genes induced by F-AOS were mainly enriched in porphyrin and chlorophyll metabolism, oxidative phosphorylation, and Salmonella infection-related pathways. RT-qPCR confirmed that F-AOS downregulated key genes involved in flagellar assembly and the type III secretory system of S. Typhimurium, indicating metabolites in F-AOS can influence the growth and metabolism of S. Typhimurium. Metabolomic analyses showed that 205 microbial metabolites were significantly altered in F-AOS. Among them, the increase in indolelactic acid and 3-indolepropionic acid levels were further confirmed using HPLC. This study provides a new perspective for the application of AOS as a feed additive against pathogenic intestinal bacteria.
引用
收藏
页码:242 / 256
页数:15
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