Centro de Pesquisas em Biologia Molecular e Funcional (CPBMF), Instituto de Pesquisas Biomédicas, Instituto Nacional de Ciência e Tecnologia em Tuberculose (INCT-TB), Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS), Porto Alegre, Brazil; Programa de Pós-Graduação em Biologia Celular e Molecular, PUCRS, Porto Alegre, Brazil.
Centro de Pesquisas em Biologia Molecular e Funcional (CPBMF), Instituto de Pesquisas Biomédicas, Instituto Nacional de Ciência e Tecnologia em Tuberculose (INCT-TB), Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS), Porto Alegre, Brazil.
Microb Pathog. 2018 Jun;119:60-64. doi: 10.1016/j.micpath.2018.03.056. Epub 2018 Mar 30.
Purine nucleoside phosphorylase from Mycobacterium tuberculosis (MtPNP), encoded by deoD gene (Rv3307), is an enzyme from the purine salvage pathway, which has been widely studied as a molecular target for the development of inhibitors with potential antimycobacterial activity. However, the role of MtPNP in tuberculosis pathogenesis and dormancy is still unknown. The present work aims to construct a deoD knockout strain from M. tuberculosis, to evaluate the role of MtPNP in the growth of M. tuberculosis under oxygenated condition and in a dormancy model, and to assess whether deoD gene is important for M. tuberculosis invasion and growth in macrophages. The construction of a knockout strain for deoD gene was confirmed at DNA level by PCR and protein level by Western blot and LC-MS/MS. The deoD gene is not required for M. tuberculosis growth and survival under oxygenated and hypoxic conditions. The disruption of deoD gene did not affect mycobacterial ability to invade and grow in RAW 264.7 cells under the experimental conditions employed here.
结核分枝杆菌(Mycobacterium tuberculosis)中的嘌呤核苷磷酸化酶(Purine nucleoside phosphorylase from Mycobacterium tuberculosis,MtPNP)由 deoD 基因(Rv3307)编码,是嘌呤补救途径中的一种酶,已被广泛研究作为开发具有潜在抗分枝杆菌活性的抑制剂的分子靶标。然而,MtPNP 在结核病发病机制和休眠中的作用仍不清楚。本工作旨在构建结核分枝杆菌 deoD 基因敲除株,评估 MtPNP 在有氧条件下和休眠模型中分枝杆菌生长中的作用,并评估 deoD 基因是否对分枝杆菌在巨噬细胞中的入侵和生长重要。通过 PCR 从 DNA 水平和 Western blot 和 LC-MS/MS 从蛋白质水平确认 deoD 基因敲除株的构建。deoD 基因对于有氧和缺氧条件下结核分枝杆菌的生长和存活不是必需的。在本实验条件下,deoD 基因的破坏不影响分枝杆菌在 RAW 264.7 细胞中的入侵和生长能力。