CIGMH, Departamento de Ciências da Vida, Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, Caparica, Portugal.
CIGMH, Departamento de Ciências da Vida, Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, Caparica, Portugal; CENIMAT/I3N, Departamento de Ciência dos Materiais, Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, Caparica, Portugal.
Tuberculosis (Edinb). 2014 May;94(3):332-7. doi: 10.1016/j.tube.2013.12.009. Epub 2014 Jan 9.
Tuberculosis, still one of the leading human infectious diseases, reported 8.7 million new cases in 2011 alone. Also, the increasing rate of multidrug-resistant tuberculosis (MDRTB) and its treatment difficulties pose a serious public health threat especially in developing countries. Resistance to isoniazid and rifampicin, first line antibiotics, is commonly associated with point mutations in katG, inhA and rpoB genes of Mycobacterium tuberculosis complex (MTBC). Therefore, the development of cheap, fast and simple molecular methods to assess susceptibility profiles would have a huge impact in the capacity of early diagnosis and treatment of MDRTB. Gold nanoparticles functionalized with thiol-modified oligonucleotides (Au-nanoprobes) have shown the potential to provide a rapid and sensitive detection method for MTBC and single base mutations associated with antibiotic resistance, namely the characterization of the three most relevant codons in rpoB gene associated to rifampicin resistance. Here we extend the Au-nanoprobe approach towards discriminating specific mutations within inhA and rpoB genes in PCR amplified DNA from isolates. Using a multiplex PCR reaction for these two genes, it is possible to assess both loci in parallel, and extend the potential of the Au-nanoprobe method to MDRTB molecular characterization with special application in the most frequent Portuguese genotypes.
结核病仍然是主要的人类传染病之一,仅 2011 年就报告了 870 万例新发病例。此外,耐多药结核病(MDRTB)的发病率不断上升及其治疗困难对发展中国家的公共卫生构成了严重威胁。异烟肼和利福平耐药,一线抗生素,通常与结核分枝杆菌复合群(MTBC)的 katG、inhA 和 rpoB 基因的点突变有关。因此,开发廉价、快速和简单的分子方法来评估药敏谱将对早期诊断和治疗 MDRTB 产生巨大影响。巯基修饰的寡核苷酸功能化的金纳米颗粒(Au-纳米探针)已显示出提供一种快速和敏感的 MTBC 和与抗生素耐药性相关的单碱基突变检测方法的潜力,即鉴定与利福平耐药性相关的 rpoB 基因中三个最相关密码子的特征。在这里,我们将 Au-纳米探针方法扩展到区分来自分离株的 PCR 扩增 DNA 中 inhA 和 rpoB 基因内的特定突变。通过对这两个基因进行多重 PCR 反应,可以同时评估这两个基因座,并将 Au-纳米探针方法的应用扩展到 MDRTB 分子特征,特别是在葡萄牙最常见的基因型中的应用。