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MGIT 960 中检测结核分枝杆菌生长以确定抗结核药物早期杀菌活性所需的时间。

Time to detection of the growth of Mycobacterium tuberculosis in MGIT 960 for determining the early bactericidal activity of antituberculosis agents.

机构信息

Department of Molecular Biology and Human Genetics, and MRC Centre for Molecular and Cellular Biology, DST/NRF Centre of Excellence for Biomedical TB Research, Faculty of Health Sciences, Stellenbosch University, Tygerberg, South Africa.

出版信息

Eur J Clin Microbiol Infect Dis. 2010 Dec;29(12):1561-5. doi: 10.1007/s10096-010-1043-7. Epub 2010 Sep 4.

Abstract

Evaluation of early bactericidal activity (EBA) by the determination of a fall in viable colony-forming units (CFU) of Mycobacterium tuberculosis in sputum is a first step in the clinical study of new antituberculosis agents. The time to detection (TTD) of growth in liquid media is more sensitive and could substitute for CFU counting on solid media. Overnight sputum samples collected during the evaluation of the novel agent TMC207 in comparison to isoniazid and rifampicin were studied. For the determination of CFU, we incubated 10-fold dilutions of homogenized sputum on selective 7H10 agar. The TTD was measured by incubating decontaminated sputum in the BACTEC MGIT 960 system. The fall in bacillary load over 7 days determined by CFU counting closely matched the prolongation of the TTD in the BACTEC MGIT 960 system. The CFU counts correlated significantly with the TTD. While the ranking of agents and different dosages of TMC207 was similar, the highest dose of TMC207 showed markedly better activity when measured by the TTD than CFU counting when compared to the activity of isoniazid. Automated TTD could augment, or, in future, replace, CFU counting to determine sputum bacillary load in EBA clinical trials pending a more formal evaluation of the correlation of the measurements.

摘要

评估早期杀菌活性(EBA)通过测定痰液中结核分枝杆菌活菌集落形成单位(CFU)的下降是新抗结核药物临床研究的第一步。液体培养基中生长的检测时间(TTD)更敏感,可以替代固体培养基上的 CFU 计数。在评估新型药物 TMC207 时,与异烟肼和利福平相比,研究了过夜痰液样本。为了确定 CFU,我们将均质化痰液的 10 倍稀释液接种在选择性 7H10 琼脂上。通过在 BACTEC MGIT 960 系统中孵育去污染的痰液来测量 TTD。通过 CFU 计数确定的 7 天内细菌负荷下降与 BACTEC MGIT 960 系统中 TTD 的延长密切相关。CFU 计数与 TTD 显著相关。虽然药物的排序和 TMC207 的不同剂量相似,但与异烟肼的活性相比,TTD 测量时,最高剂量的 TMC207 显示出明显更好的活性。在对测量相关性进行更正式评估之前,自动 TTD 可以增强或在未来取代 CFU 计数,以确定 EBA 临床试验中的痰细菌负荷。

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