Streptomyces sp. BI87 from human gut: potent anticancer activities and divergence from known Streptomyces lineages.

IF 3.8 2区 生物学 Q2 MICROBIOLOGY
Microbiology spectrum Pub Date : 2025-10-07 Epub Date: 2025-08-13 DOI:10.1128/spectrum.00858-25
Yu-Hui Wang, Hong-Tao Xu, Miao-Wei Liu, Bao-Juan Yuan, Xin-Yu Gao, Xing-Hua Zhang, Hong-Da Tian, Hao Yu, Jin-Ru Lai, Liang Liu, Randal N Johnston, Gui-Rong Liu, Shu-Lin Liu
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Abstract

Cancer is among the deadliest diseases with few truly curative therapies. Recent studies have shown that the human intestinal microbiota contains bacteria that exhibit potent suppressive effects on cancer or coordinate anticancer functions with the immune system. However, whether the peculiar anticancer trait was acquired stochastically by a strain of a non-anticancer bacterial species or an intrinsic property of a phylogenetic lineage of bacteria remained unclear. In this study, we compared a human gut isolate Streptomyces sp. BI87, which had highly effective anticancer activities, with the type strain of Streptomyces albidoflavus, DSM 40455T, which was most closely related to BI87 among 30 type strains of the genus Streptomyces but did not show any detectable anticancer activities. We found that, although BI87 and DSM 40455T had >99% 16S rDNA sequence similarity, they are phylogenetically separated by a genetic boundary into distinct natural species as evaluated by the 3Cs definition of bacterial species based on the ratio of common genes with zero sequence degeneracy. In addition to the anticancer activities, BI87 encodes several biological characteristics different from DSM 40455T, including those of antibacterial and antiviral spectra, secondary metabolites, structural composition in the cell wall, and major cellular fatty acids. Based on the genomic and phenotypic distinctions of BI87 from closely related Streptomyces strains, we propose that the anticancer bacterial strain BI87 represents a new lineage at the natural species level within the genus Streptomyces.IMPORTANCEThe characterization of the anticancer bacterial strain, Streptomyces sp. BI87, isolated from a healthy human, suggests the prevalent existence of anticancer microbes in the gut microbiome of humans, which may be nurtured and harnessed for cancer prevention or treatment without the need for the introduction of engineered and non-indigenous microbes to a person or the use of radio- or chemo-therapies. Also important is the finding that a close relative of BI87, Streptomyces albidoflavus DSM40455T, does not express appreciable anticancer properties in the same in vitro and in vivo experiments, demonstrating that Streptomyces sp. BI87 represents a novel bacterial lineage with selective suppressive activities on cancer, at the phylogenetic level of natural species. Genomic comparisons between BI87 and DSM40455T demonstrate that phylogenetic delineation of closely related bacteria needs to be conducted at the level of natural species rather than OTUs, as an OTU may contain phenotypically or even phylogenetically radically distinct bacteria.

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来自人类肠道的链霉菌sp. BI87:有效的抗癌活性和与已知链霉菌谱系的分化。
癌症是最致命的疾病之一,几乎没有真正有效的治疗方法。最近的研究表明,人类肠道微生物群中含有的细菌对癌症表现出强有力的抑制作用,或与免疫系统协调抗癌功能。然而,这种特殊的抗癌特性是由一种非抗癌细菌物种随机获得的,还是细菌系统发育谱系的固有特性,目前尚不清楚。在本研究中,我们将一株具有高效抗癌活性的人肠道分离株Streptomyces sp. BI87与在30株Streptomyces属链霉菌中与BI87亲缘关系最密切但未显示出任何抗癌活性的黄色链霉菌(Streptomyces albidoflavus)型菌株DSM 40455T进行了比较。我们发现,尽管BI87和DSM 40455T的16S rDNA序列相似度高达99%,但根据基于零序列退化的共同基因比例的细菌物种的3s定义,它们在系统发育上被遗传边界分隔为不同的自然物种。除了抗癌活性外,BI87还编码了一些不同于DSM 40455T的生物学特性,包括抗菌和抗病毒光谱、次级代谢物、细胞壁结构组成和主要细胞脂肪酸。基于BI87与近缘链霉菌的基因组和表型差异,我们认为抗癌菌株BI87代表了链霉菌属自然种水平上的一个新谱系。从健康人体中分离出的抗癌菌株Streptomyces sp. BI87的特性表明,人类肠道微生物群中普遍存在抗癌微生物,可以培养和利用抗癌微生物来预防或治疗癌症,而不需要将工程和非本地微生物引入人体,也不需要使用放射或化疗。同样重要的是,研究人员发现BI87的近亲白黄链霉菌(Streptomyces albidoflavus) DSM40455T在体外和体内实验中都没有表现出明显的抗癌特性,这表明在自然物种的系统发育水平上,BI87代表了一种具有选择性抑制癌症活性的新型细菌谱系。BI87和DSM40455T之间的基因组比较表明,密切相关细菌的系统发育描述需要在自然物种水平上进行,而不是在OTU水平上进行,因为OTU可能包含表型上甚至系统发育上完全不同的细菌。
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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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