Kargupta Roli, Puttaswamy Sachidevi, Lee Aiden J, Butler Timothy E, Li Zhongyu, Chakraborty Sounak, Sengupta Shramik
Department of Bioengineering, University of Missouri, 252 Agricultural Engineering Building, 1406 E. Rollins Street, Columbia, MO, 65211, USA.
Department of Statistics, University of Missouri, Columbia, MO, USA.
Biol Res. 2017 Jun 10;50(1):21. doi: 10.1186/s40659-017-0126-7.
Multiple techniques exist for detecting Mycobacteria, each having its own advantages and drawbacks. Among them, automated culture-based systems like the BACTEC-MGIT™ are popular because they are inexpensive, reliable and highly accurate. However, they have a relatively long "time-to-detection" (TTD). Hence, a method that retains the reliability and low-cost of the MGIT system, while reducing TTD would be highly desirable.
Living bacterial cells possess a membrane potential, on account of which they store charge when subjected to an AC-field. This charge storage (bulk capacitance) can be estimated using impedance measurements at multiple frequencies. An increase in the number of living cells during culture is reflected in an increase in bulk capacitance, and this forms the basis of our detection. M. bovis BCG and M. smegmatis suspensions with differing initial loads are cultured in MGIT media supplemented with OADC and Middlebrook 7H9 media respectively, electrical "scans" taken at regular intervals and the bulk capacitance estimated from the scans. Bulk capacitance estimates at later time-points are statistically compared to the suspension's baseline value. A statistically significant increase is assumed to indicate the presence of proliferating mycobacteria.
Our TTDs were 60 and 36 h for M. bovis BCG and 20 and 9 h for M. smegmatis with initial loads of 1000 CFU/ml and 100,000 CFU/ml respectively. The corresponding TTDs for the commercial BACTEC MGIT 960 system were 131 and 84.6 h for M. bovis BCG and 41.7 and 12 h for M smegmatis, respectively.
Our culture-based detection method using multi-frequency impedance measurements is capable of detecting mycobacteria faster than current commercial systems.
存在多种检测分枝杆菌的技术,每种技术都有其自身的优缺点。其中,像BACTEC - MGIT™这样基于自动化培养的系统很受欢迎,因为它们价格低廉、可靠且高度准确。然而,它们的“检测时间”(TTD)相对较长。因此,一种既能保留MGIT系统的可靠性和低成本,又能缩短TTD的方法将非常理想。
活细菌细胞具有膜电位,因此在受到交流电场作用时会储存电荷。这种电荷储存(总体电容)可以通过在多个频率下的阻抗测量来估计。培养过程中活细胞数量的增加反映在总体电容的增加上,这构成了我们检测的基础。分别在添加了OADC的MGIT培养基和Middlebrook 7H9培养基中培养具有不同初始载量的牛分枝杆菌卡介苗(M. bovis BCG)和耻垢分枝杆菌(M. smegmatis)悬浮液,定期进行电“扫描”,并从扫描结果中估计总体电容。将后期时间点的总体电容估计值与悬浮液的基线值进行统计学比较。统计学上的显著增加被认为表明存在增殖的分枝杆菌。
对于初始载量分别为1000 CFU/ml和100,000 CFU/ml的牛分枝杆菌卡介苗,我们的TTD分别为60小时和36小时,对于耻垢分枝杆菌分别为20小时和9小时。商业BACTEC MGIT 960系统对牛分枝杆菌卡介苗的相应TTD分别为131小时和84.6小时,对耻垢分枝杆菌分别为41.7小时和12小时。
我们基于培养的多频阻抗测量检测方法能够比当前商业系统更快地检测分枝杆菌。