State Key Laboratory of Food Science and Technology, Jiangnan University, Wuxi, Jiangsu, 214122, PR China; School of Food Science and Technology, Jiangnan University, Wuxi, Jiangsu, 214122, PR China.
State Key Laboratory of Food Science and Technology, Jiangnan University, Wuxi, Jiangsu, 214122, PR China; School of Food Science and Technology, Jiangnan University, Wuxi, Jiangsu, 214122, PR China; National Engineering Research Center for Functional Food, Jiangnan University, Wuxi, Jiangsu, 214122, PR China.
Food Chem Toxicol. 2020 Jan;135:110934. doi: 10.1016/j.fct.2019.110934. Epub 2019 Nov 1.
The novel commensal strain of Bacteroides fragilis HCK-B3 isolated from a healthy Chinese donor was discovered beneficial effects of attenuating lipopolysaccharides-induced inflammation. In order to contribute to the development of natural next-generation probiotic strains, the safety assessment was carried out with in vitro investigations of its morphology, potential virulence genes and antimicrobial resistance, and an in vivo acute toxicity study based on both healthy and immunosuppressed mice by cyclophosphamide injection. Consequently, the potential virulence genes in the genome of B. fragilis HCK-B3 have yet been identified as toxicity-associated. The absence of plasmids prevents the possibility of transferring antibiotic resistance features to other intestinal commensals. No intracorporal pathogenic properties were observed according to the body weight, hematological and liver parameters, cytokine secretions and tissue integrity. In addition, B. fragilis HCK-B3 performed alleviations on part of the side effects caused by the cyclophosphamide treatment. Thus, the novel strain of B. fragilis HCK-B3 was confirmed to be non-toxigenic and did not display adverse effects in both healthy and immune-deficient mice at a routinely applicable dose.
从一名健康的中国捐赠者中分离出的新型共生脆弱拟杆菌 HCK-B3 菌株具有减轻脂多糖诱导的炎症的有益作用。为了为天然下一代益生菌菌株的开发做出贡献,对其形态、潜在毒力基因和抗生素耐药性进行了体外研究,并通过环磷酰胺注射对健康和免疫抑制小鼠进行了体内急性毒性研究。因此,脆弱拟杆菌 HCK-B3 基因组中的潜在毒力基因尚未被确定为与毒性相关。不存在质粒可防止将抗生素耐药性特征转移到其他肠道共生菌的可能性。根据体重、血液学和肝脏参数、细胞因子分泌和组织完整性,未观察到体内致病性。此外,脆弱拟杆菌 HCK-B3 减轻了环磷酰胺治疗引起的部分副作用。因此,新型脆弱拟杆菌 HCK-B3 菌株在常规应用剂量下,在健康和免疫缺陷小鼠中均被证实无毒性,且无不良反应。