百岁老人肠道微生物群中的抗菌肽:生物合成的多样化和抗性基因的年轻化发展

Chunrong Lu, Xiaojun Wang, Pengpeng Ye, Zhilong Lu, Jie Ma, Weifei Luo, Shuai Wang, Xiaochun Chen
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引用次数: 0

摘要

抗菌肽(AMPs)因其抗菌特性而为抗生素危机提供了潜在的解决方案,人类肠道生物群可能是这些肽的来源。然而,对不同年龄组肠道微生物潜在的 AMPs 和抗菌肽抗性基因(AMPRGs)的评估还不够全面。在此,我们通过分析不同生命阶段健康人(CG:百岁老人组,n=20;OAG:老年人组,n=15;YG:年轻人组,n=15)的肠道元基因组数据,研究了不同年龄段肠道微生物组中 AMPs 的潜在发展和 AMPRGs 的分布模式。在肠道微生物组中观察到潜在的 AMPs 与年龄相关的增加,百岁老人显示出这些肽的更大多样性。不过,与 OAG 组相比,CG 组肠道微生物组中的 AMPRGs 水平较低,与 YG 组的水平相似。此外,传统益生菌菌株与某些潜在的 AMPs 呈显著的正相关,且抗性基因的检出率较低。此外,将潜在的 AMP 与现有库进行比较后发现,两者的相似性有限,这表明目前的机器学习模型可以识别肠道微生物群中的新型多肽。这些结果表明,长寿可能得益于AMPs的多样性和较低的抗性基因。我们的发现有助于解释百岁老人的年龄优势,并确定人类肠道微生物群中抗菌肽生物合成的潜力,为抗菌肽耐药性的发展和益生菌菌株的筛选提供启示。
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Antimicrobial peptides from the gut microbiome of the centenarians: diversification of biosynthesis and youthful development of resistance genes
Antimicrobial peptides (AMPs) offer a potential solution to the antibiotic crisis owing to their antimicrobial properties, and the human gut biome may be a source of these peptides. However, the potential AMPs and antimicrobial peptide resistance genes (AMPRGs) of gut microbes in different age groups has not been thoroughly assessed. Here, we investigated the potential development of AMPs and the distribution pattern of AMPRGs in the gut microbiome at different ages by analyzing the intestinal metagenomic data of healthy individuals at different life stages (CG: centenarians group n=20; OAG: older adults group n=15; YG: young group n=15). Age-related increases were observed in the potential AMPs within the gut microbiome, with centenarians showing a greater diversity of these peptides. However, the gut microbiome of the CG group had a lower level of AMPRGs compared to that of the OAG group, and it was similar to the level found in the YG group. Additionally, conventional probiotic strains showed a significant positive correlation with certain potential AMPs and were associated with a lower detection of resistance genes. Additionally, comparing potential AMPs with existing libraries revealed limited similarity, indicating that current machine-learning models can identify novel peptides in the gut microbiota. These results indicate that longevity may benefit from diversity of AMPs and lower resistance genes. Our findings help explain the age advantage of the centenarians and identify the potential for antimicrobial peptide biosynthesis in the human gut microbiome, offering insights into the development of antimicrobial peptide resistance and the screening of probiotic strains.
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