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利用等位基因特异性环介导等温扩增技术对单核苷酸突变进行单细胞基因分型。

Single-Cell Genotyping of Single-Nucleotide Mutations Using Allele-Specific Loop-Mediated Isothermal Amplification.

机构信息

College of Biomass Science and Engineering, Healthy Food Evaluation Research Center, Sichuan University, Chengdu 610065, Sichuan, China.

Research Center for Analytical Science, College of Chemistry, Nankai University, Tianjin 300071, China.

出版信息

ACS Sens. 2023 Nov 24;8(11):4315-4322. doi: 10.1021/acssensors.3c01679. Epub 2023 Oct 20.

Abstract

Single-nucleotide mutations (SNMs) in the bacterial genome may cause antibiotic resistance. The visualization of SNMs can indicate antibiotic resistance phenotypes at the single-cell level but remains challenging. Herein, we proposed an allele-specific isothermal amplification proceeded inside cells, allowing us to image bacterial genes with single-nucleotide resolution. The primer for loop-mediated isothermal amplification (LAMP) was designed with artificial mismatch bases to serve as an allele-specific probe, endowing LAMP to specifically amplify genes with SNMs. Due to the high amplification efficiency of LAMP, the method termed AlleLAMP can generate high gain for imaging SNMs and precisely quantify mutated quinolone-resistant in bacterial mixture. We utilized AlleLAMP to survey the selection of antibiotic resistance under the preservative stress and found that the mutant quinolone-resistant strain owned a survival advantage over the wild-type quinolone-sensitive strain under the stress of preservatives. AlleLAMP can serve as a single-cell tool for analyzing the relationship between bacterial genotype and phenotype.

摘要

细菌基因组中的单核苷酸突变(SNMs)可能导致抗生素耐药性。SNMs 的可视化可以在单细胞水平上指示抗生素耐药表型,但仍然具有挑战性。在此,我们提出了一种在细胞内进行的等位基因特异性等温扩增方法,使我们能够以单核苷酸分辨率成像细菌基因。环介导等温扩增(LAMP)的引物设计有人工错配碱基,用作等位基因特异性探针,使 LAMP能够特异性扩增具有 SNMs 的基因。由于 LAMP 的高扩增效率,该方法称为 AlleLAMP,可以为成像 SNMs 产生高增益,并精确量化细菌混合物中突变的喹诺酮耐药基因。我们利用 AlleLAMP 研究了在防腐剂应激下抗生素耐药性的选择,发现突变的喹诺酮耐药菌株在防腐剂的应激下比野生型喹诺酮敏感菌株具有生存优势。AlleLAMP 可以作为一种单细胞工具,用于分析细菌基因型和表型之间的关系。

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