Kim S, Schuler B, Terekhov A, Auer J, Mauer L J, Perry L, Applegate B
Department of Food Science, Purdue University, 745 Agriculture Mall Drive, West Lafayette, IN 47907-2009, USA.
J Microbiol Methods. 2009 Oct;79(1):18-22. doi: 10.1016/j.mimet.2009.07.011. Epub 2009 Jul 21.
A bioluminescence-based assay for enumeration of lytic bacteriophage was developed. The assay consists of a bioluminescent Escherichia coli as the host bacterium, the lytic bacteriophage T4 and an automated luminometer measuring luminescence over time. The assay is based on the decrease in luminescence as the bioluminescent host cells are lysed by T4. The T4 concentration, bioluminescent E. coli concentration, phage suspension medium, and temperature (25 degrees C and 37 degrees C) were varied. There was a strong negative correlation between bioluminescence intensities and T4 phage concentrations at both room temperature (R(2)=0.993) and 37 degrees C (R(2)=0.970). Phage was detected more rapidly at 37 degrees C than at 25 degrees C. The detection limit was also lower when the assay was performed at 37 degrees C with a minimum detection level of 2.4 log CFU/ml compared to 3.4 log CFU/ml for 25 degrees C. The assay was used to determine thermal inactivation using T4 phages heated at 70 degrees C for 0 to 30 min, and phage concentrations were determined using the bioluminescence assay and a standard plaque assay. There was no significant difference between the two enumeration methods (P>0.01). This study suggests the bioluminescence-based assay can be used as an alternative for quantitatively monitoring phage infectivity, instead of conventional standard plaque assays.
开发了一种基于生物发光的裂解性噬菌体计数测定法。该测定法由作为宿主细菌的生物发光大肠杆菌、裂解性噬菌体T4和一台随时间测量发光的自动发光计组成。该测定法基于生物发光宿主细胞被T4裂解时发光的降低。改变了T4浓度、生物发光大肠杆菌浓度、噬菌体悬浮培养基和温度(25℃和37℃)。在室温(R² = 0.993)和37℃(R² = 0.970)下,生物发光强度与T4噬菌体浓度之间均存在很强的负相关。在37℃下比在25℃下能更快地检测到噬菌体。当在37℃下进行测定时检测限也更低,最低检测水平为2.4 log CFU/ml,而25℃时为3.4 log CFU/ml。该测定法用于使用在70℃加热0至30分钟的T4噬菌体来确定热失活,并使用生物发光测定法和标准噬菌斑测定法来确定噬菌体浓度。两种计数方法之间没有显著差异(P>0.01)。这项研究表明,基于生物发光的测定法可作为定量监测噬菌体感染性的替代方法,以取代传统的标准噬菌斑测定法。