Mesman Annelies W, Baek Seung-Hun, Huang Chuan-Chin, Kim Young-Mi, Cho Sang-Nae, Ioerger Thomas R, Barreda Nadia N, Calderon Roger, Sassetti Christopher M, Murray Megan B
Gemeentelijke Gezondheidsdiensten en Geneeskundige Hulpverleningsorganisaties in de Regio Nederland, 3524 SJ Utrecht, The Netherlands.
Department of Microbiology and Institute for Immunology and Immunological Diseases, College of Medicine, Yonsei University, Seoul 16995, Korea.
J Clin Med. 2021 Jul 23;10(15):3249. doi: 10.3390/jcm10153249.
An estimated 15-20% of patients who are treated for pulmonary tuberculosis (TB) are culture-negative at the time of diagnosis. Recent work has focused on the existence of differentially detectable () bacilli that do not grow under routine solid culture conditions without the addition of supplementary stimuli. We identified a cohort of TB patients in Lima, Peru, in whom acid-fast bacilli could be detected by sputum smear microscopy, but from whom could not be grown in standard solid culture media. When we attempted to re-grow from the frozen sputum samples of these patients, we found that 10 out of 15 could be grown in a glycerol-poor/lipid-rich medium. These fell into the following two groups: a subset that could be regrown in glycerol after "lipid-resuscitation", and a group that displayed a heritable glycerol-sensitive phenotype that were unable to grow in the presence of this carbon source. Notably, all of the glycerol-sensitive strains were found to be multidrug resistant. Although whole-genome sequencing of the lipid-resuscitated strains identified 20 unique mutations compared to closely related strains, no single genetic lesion could be associated with this phenotype. In summary, we found that lipid-based media effectively fostered the growth of from a series of sputum smear-positive samples that were not culturable in glycerol-based Lowenstein-Jensen or 7H9 media, which is consistent with 's known preference for non-glycolytic sources during infection. Analysis of the recovered strains demonstrated that both genetic and non-genetic mechanisms contribute to the observed differential capturability, and suggested that this phenotype may be associated with drug resistance.
估计有15%至20%接受肺结核(TB)治疗的患者在诊断时培养结果为阴性。最近的研究聚焦于存在差异可检测的()杆菌,这些杆菌在不添加补充刺激的常规固体培养条件下无法生长。我们在秘鲁利马确定了一组肺结核患者,他们的痰涂片显微镜检查可检测到抗酸杆菌,但在标准固体培养基中无法培养出()。当我们试图从这些患者的冷冻痰样本中重新培养()时,发现15个样本中有10个可以在甘油含量低/脂质丰富的培养基中生长。这些样本分为以下两组:一组在“脂质复苏”后可以在甘油中重新生长,另一组表现出可遗传的甘油敏感表型,在有这种碳源的情况下无法生长。值得注意的是,所有甘油敏感菌株均被发现对多种药物耐药。尽管与密切相关菌株相比,脂质复苏菌株的全基因组测序鉴定出20个独特突变,但没有单一基因损伤与该表型相关。总之,我们发现基于脂质的培养基有效地促进了一系列在基于甘油的罗-琴培养基或7H9培养基中不可培养的痰涂片阳性样本中()的生长,这与()在感染期间对非糖酵解来源的已知偏好一致。对回收菌株的分析表明,遗传和非遗传机制都导致了观察到的差异捕获能力,并表明这种表型可能与耐药性有关。