Sun Mingyue, Li Qian, Zhang Feiran, Yao Ding, Huang Wenhua, Lv Qingyu, Jiang Hua, Kong Decong, Ren Yuhao, Chen Shaolong, Jiang Yongqiang, Liu Peng
School of Basic Medical Sciences, Anhui Medical University, Hefei 230032, China.
State Key Laboratory of Pathogen and Biosecurity, Academy of Military Medical Sciences, Beijing 100072, China.
Microorganisms. 2025 Mar 20;13(3):694. doi: 10.3390/microorganisms13030694.
The isolation and characterization of novel probiotics from dairy products, fermented foods, and the gut have gained significant attention. In particular, shows promise for use in oral probiotic preparations. In this study, we isolated two strains of -S.82.15 and S.82.20-from the oral cavity of a healthy individual. These strains exhibited distinct antimicrobial profiles. We thoroughly assessed the morphology and growth patterns of both strains and confirmed auto-aggregation and hemolytic activity. Through comprehensive genomic analysis, we found notable strain differences within the same bacterial species isolated from the same individual. Notably, the presence or absence of plasmids varied between the two strains. The genome of S.82.15 spans 2,175,688 bps and contains 1994 coding DNA sequences (CDSs), while S.82.20 has a genome size of 2,414,610 bps, a GC content of 40.62%, and 2276 annotated CDSs. Both strains demonstrated antibacterial activity against Group A (GAS), , and . To investigate the antibacterial properties further, we identified a gene cluster of salivaricin 9 on the plasmid of S.82.20 and a gene family on the chromosomes of both S.82.15 and S.82.20. Moreover, the gene expression of the family was upregulated when the isolated strains were co-cultured with GAS.
从乳制品、发酵食品和肠道中分离和鉴定新型益生菌受到了广泛关注。特别是,[具体内容缺失]在口服益生菌制剂中显示出应用前景。在本研究中,我们从一名健康个体的口腔中分离出两株菌株——S.82.15和S.82.20。这些菌株表现出不同的抗菌谱。我们全面评估了这两株菌株的形态和生长模式,并证实了它们的自聚集和溶血活性。通过全面的基因组分析,我们发现从同一个体分离出的同一细菌物种内存在显著的菌株差异。值得注意的是,两株菌株之间质粒的有无情况不同。S.82.15的基因组跨度为2,175,688个碱基对,包含1994个编码DNA序列(CDS),而S.82.20的基因组大小为2,414,610个碱基对,GC含量为40.62%,有2276个注释的CDS。两株菌株均对A组链球菌(GAS)、[具体细菌缺失]和[具体细菌缺失]表现出抗菌活性。为了进一步研究其抗菌特性,我们在S.82.20的质粒上鉴定出一个唾液乳链菌肽9基因簇,以及在S.82.15和S.82.20的染色体上均存在一个[具体基因家族缺失]基因家族。此外,当分离出的菌株与GAS共培养时,[具体基因家族缺失]家族的基因表达上调。