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Identification and prioritization of macrolideresistance genes with hypothetical annotation inStreptococcus pneumoniae

机译:肺炎链球菌中带有假想注释的大环内酯酶抗性基因的鉴定和优先排序

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摘要

Macrolide resistant Streptococcus pneumoniae infections have limited treatment options. While some resistance mechanisms are well established, ample understanding is limited by incomplete genome annotation (hypothetical genes). Some hypothetical genes encode a domain of unknown function (DUF), a conserved protein domain with uncharacterized function. Here, we identify and confirm macrolide resistance genes. We further explore DUFs from macrolide resistance hypothetical genes to prioritize them for experimental characterization. We found gene similarities between two macrolide resistance gene signatures from untreated and either erythromycin- or spiramycin-treated resistant Streptococcus pneumoniae. We confirmed the association of these gene sets with macrolide resistance through comparison to gene signatures from (i) second erythromycin resistant Streptococcus pneumoniae strain, and (ii) erythromycin-treated sensitive Streptococcus pneumoniae strain, both from non-overlapping datasets. Examination into which cellular processes these macrolide resistance genes belong found connections to known resistance mechanisms such as increased amino acid biosynthesis and efflux genes, and decreased ribonucleotide biosynthesis genes, highlighting the predictive ability of the method used. 22 genes had hypothetical annotation with 10 DUFs associated with macrolide resistance. DUF characterization could uncover novel co-therapies that restore macrolide efficacy across multiple macrolide resistant species. Application of the methods to other antibiotic resistances could revolutionize treatment of resistant infections
机译:对大环内酯类耐药的肺炎链球菌感染的治疗选择有限。尽管已经建立了一些抗性机制,但由于不完整的基因组注释(假设的基因),对充分的理解受到了限制。一些假设的基因编码一个功能未知的域(DUF),这是一个功能未知的保守蛋白域。在这里,我们确定并确认大环内酯类耐药基因。我们进一步从大环内酯抗性假设基因中探索DUF,以将其优先用于实验表征。我们发现未经治疗的和对红霉素或螺旋霉素治疗的肺炎链球菌的两个大环内酯类耐药基因签名之间的基因相似性。我们通过与来自非重叠数据集的(i)第二种抗红霉素的肺炎链球菌菌株和(ii)红霉素治疗的敏感的肺炎链球菌菌株的基因签名进行比较,证实了这些基因组与大环内酯类药物的抗药性相关。这些大环内酯类抗性基因属于细胞过程的研究发现与已知的抗性机制有关,例如增加的氨基酸生物合成和外排基因,以及减少的核糖核苷酸生物合成基因,突出了所用方法的预测能力。假设有22个基因与10个与大环内酯类药物耐药相关的DUF注释。 DUF表征可能会发现新颖的联合疗法,可在多种抗大环内酯类药物中恢复大环内酯的疗效。将该方法应用于其他抗生素耐药性可能会彻底改变耐药性感染的治疗方法

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