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基于CRISPR-Cas的适应性免疫介导牙周红色复合体病原体中的噬菌体抗性。

CRISPR-Cas-Based Adaptive Immunity Mediates Phage Resistance in Periodontal Red Complex Pathogens.

作者信息

Yadalam Pradeep Kumar, Arumuganainar Deepavalli, Anegundi Raghavendra Vamsi, Shrivastava Deepti, Alftaikhah Sultan Abdulkareem Ali, Almutairi Haifa Ali, Alobaida Muhanad Ali, Alkaberi Abdullah Ahmed, Srivastava Kumar Chandan

机构信息

Department of Periodontics, Saveetha Institute of Medical and Technical Sciences (SIMATS), Saveetha Dental College and Hospitals, Saveetha University, Chennai 600077, India.

Department of Periodontics, Ragas Dental College and Hospital, 2/102, East Coast Road, Uthandi, Chennai 600119, India.

出版信息

Microorganisms. 2023 Aug 11;11(8):2060. doi: 10.3390/microorganisms11082060.

Abstract

Periodontal diseases are polymicrobial immune-inflammatory diseases that can severely destroy tooth-supporting structures. The critical bacteria responsible for this destruction include red complex bacteria such as , and . These organisms have developed adaptive immune mechanisms against bacteriophages/viruses, plasmids and transposons through clustered regularly interspaced short palindromic repeats (CRISPR) and their associated proteins (Cas). The CRISPR-Cas system contributes to adaptive immunity, and this acquired genetic immune system of bacteria may contribute to moderating the microbiome of chronic periodontitis. The current research examined the role of the CRISPR-Cas system of red complex bacteria in the dysbiosis of oral bacteriophages in periodontitis. Whole-genome sequences of red complex bacteria were obtained and investigated for CRISPR using the CRISPR identification tool. Repeated spacer sequences were analyzed for homologous sequences in the bacteriophage genome and viromes using BLAST algorithms. The results of the BLAST spacer analysis for spacers had a 100% score (e value with a bacillus phage), and the results for and had a 56% score with a pectophage and cellulophage (e value: 0.21), respectively. The machine learning model of the identified red complex CRISPR sequences predicts with area an under the curve (AUC) accuracy of 100 percent, indicating phage inhibition. These results infer that red complex bacteria could significantly inhibit viruses and phages with CRISPR immune sequences. Therefore, the role of viruses and bacteriophages in modulating sub-gingival bacterial growth in periodontitis is limited or questionable.

摘要

牙周疾病是多微生物免疫炎症性疾病,可严重破坏牙齿支持结构。导致这种破坏的关键细菌包括红色复合体细菌,如牙龈卟啉单胞菌、福赛坦氏菌和齿垢密螺旋体。这些微生物通过成簇规律间隔短回文重复序列(CRISPR)及其相关蛋白(Cas),形成了针对噬菌体/病毒、质粒和转座子的适应性免疫机制。CRISPR-Cas系统有助于适应性免疫,细菌的这种获得性基因免疫系统可能有助于调节慢性牙周炎的微生物群。当前研究探讨了红色复合体细菌的CRISPR-Cas系统在牙周炎口腔噬菌体生态失调中的作用。获取红色复合体细菌的全基因组序列,并使用CRISPR识别工具研究其中的CRISPR。使用BLAST算法分析重复间隔序列在噬菌体基因组和病毒组中的同源序列。对16个间隔序列的BLAST分析结果显示,与一种芽孢杆菌噬菌体的匹配得分达100%(e值),而与果胶噬菌体和纤维噬菌体的匹配得分分别为56%(e值:0.21)。所识别的红色复合体CRISPR序列的机器学习模型预测曲线下面积(AUC)准确率为100%,表明具有噬菌体抑制作用。这些结果推断,红色复合体细菌可通过CRISPR免疫序列显著抑制病毒和噬菌体。因此,病毒和噬菌体在调节牙周炎龈下细菌生长中的作用有限或存疑。

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