利用全基因组测序对临床肺炎链球菌分离株进行比较基因组分析,发现31个新的独特耐药snp

H. Jindal, Babu Ramanathan, C. Le, Ranganath Gudimella, R. Manikam, S. Sekaran
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摘要

利用全基因组测序对马来西亚某医院收集的10株临床肺炎链球菌进行比较基因组分析,发现31个新的独特耐药snp。肺炎链球菌是全球呼吸道感染的主要原因,特别是社区获得性肺炎。由于抗生素的过度使用,肺炎链球菌对多种抗菌药物产生了高度耐药性。在这项研究中,我们对10株具有不同抗生素耐药水平的肺炎球菌临床分离株进行了全基因组测序(WGS)。主要目的是调查与肺炎链球菌抗生素耐药性相关的遗传变化。我们的研究结果表明,与敏感菌株相比,耐药菌株在毒力因子编码基因中含有更高的非同义单核苷酸多态性(snp),这表明耐药性本质上是由snp的发生而不是毒力基因的存在与否决定的。此外,还鉴定出耐药菌株特有的90个snp。在这90个snp中,31个是独一无二的,以前没有报道过。检测与抗生素耐药性相关的snp对于未来使用基因组测序来预测临床微生物学中的抗生素敏感性和开发新的抗肺炎球菌药物至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative Genomic Analysis of Clinical Streptococcus Pneumoniae Isolates Reveal 31 New Unique Drug Resistant SNPs Using Whole Genome Sequencing
Comparative genomic analysis of ten clinical Streptococcus pneumoniae collected from a Malaysian hospital reveal 31 new unique drug-resistant SNPs using whole genome sequencing. Abstract Streptococcus pneumoniae is the leading cause of respiratory infections worldwide, specifically community-acquired pneumonia. Due to the overuse of antibiotics, S. pneumoniae has developed a high degree of resistance to a wide range of antibacterial drugs. In this study, we performed whole genome sequencing (WGS) for ten pneumococcal clinical isolates with different levels of antibiotic resistance. The key objective is to investigate genetic changes associated with antibiotic resistance in S. pneumoniae . Our results showed that resistant isolates contain higher non-synonymous single nucleotide polymorphisms (SNPs) within genes coding for virulence factors as compared to susceptible isolates, suggesting that drug resistance is essentially determined by the occurrence of SNPs rather than the presence or absence of virulent genes. In addition, 90 SNPs were identified that were unique to resistant isolates. Out of these 90 SNPs, 31 were unique and have not been reported previously. Detection of SNPs associated with antibiotic resistance is crucial for the future use of genome sequencing to predict antibiotic susceptibility in clinical microbiology and for developing new anti-pneumococcal drugs.
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