- Original article
- Open Access
Study of CFU for individual microorganisms in mixed cultures with a known ratio using MBRT
© Nandy and Venkatesh; licensee Springer 2014
Received: 18 February 2014
Accepted: 24 March 2014
Published: 5 April 2014
Determination of metabolically active cell count is an important step in designing, operating and controlling fermentation processes. It’s particularly relevant in processes involving mixed cultures, where multiple species contribute to the total growth. The motivation for the current study is to develop a methodology to estimate metabolically active cell counts for the individual species in a mixed culture with approximate equal numbers. Further, the methodology should indicate the presence of a contaminant in short time periods since in the agar plate methods used frequently it takes about 24 h. We present a methodology based on the rate of Methylene blue (MB) reduction to evaluate total count of metabolically active cells. The standard curve relating the slope of MB reduction and CFU of the individual species could be used to measure the metabolic activity of each species in the mixed culture. The slope of MB reduction could also be used to obtain the growth rate of individual species in a mixed culture and that of the total cell count. These measurements were achieved in less than 6 minutes during the growth of the cells. Evaluating the metabolic activity of individual species in a mixed culture is tedious, difficult and time consuming. The Methylene Blue dye Reduction Test (MBRT) presented here is capable of quickly estimating colony forming units (CFU) of individual species in a mixed culture if the ratio of the numbers of cells is known. The method was used to dynamically detect the occurrence of a contaminating microorganism during fermentation. The protocol developed here can be adapted to applications in processes involving mixed cultures.
Quantification of metabolic active cell is essential for design, operation and control of processes involving mixed cultures. Processes involving mixed cultures include biological waste treatment and food processing. Several methods have been used in the past to measure CFU including agar plating, imaging using microscope and fluorescence techniques, membrane filtration and flow cytometry. But, most of these methods are labor intensive, error prone, time consuming, instrumentation intensive and expensive (Auty et al. , Davey and Kell , Walley and Germida , Wright et al. ).
Thus, there is a need for fast and accurate method to enumerate metabolic active cell count of organisms present in a mixed culture. Metabolic active cell of pure culture is typically quantified using plate count assay such as streak and spread plate methods. However, these methods are time consuming although they are cheap and easy to perform. Enzyme activity specific to an organism has also been used to quantify metabolic active cell (Walley and Germida , Callaway et al. ). Imaging is another common technique that is used to evaluate metabolic active cell. This is achieved by staining the cells using acridine orange, propidium iodide or rhodamine (Wright et al. , Miller et al. ). Confocal scanning laser microscopy (CSLM) is a microscopic technique to determine metabolic active cell and is an accurate method (Schmidt et al. ). However, the method is expensive and requires operation and availability of the confocal microscope. For metabolic active count of cells in liquid medium, epifluorescence microscopy has been used in the past (Vaija et al. ). Flow cytometry is also a technique that yields accurate cell counts (Davey and Kell , Deere et al. ). The above methods are instrument dependent and expensive. The methods involving dyes are error prone as it is difficult to differentiate live from dead cells (Schmidt et al. ). Recently, our group has developed a protocol for fast estimation of cell count using the Methylene Blue Dye Reduction Test (MBRT) (Bapat et al. ). Methylene blue, a dye, is reduced by transmembrane reductases present on the cell membrane, which reduces methylene blue (MB) and thus the blue color disappears. The rate of disappearance of the color is correlated to the cell count of any aerobic organisms. This method can be used to obtain colony forming units in about 3 minutes (Bapat et al. ).
Although various methods exist for enumerating colony forming units or metabolic active cell for pure cultures, it is a difficult task to quantify metabolic active cell in a mixed culture. Since the individual metabolic active cell needs to be enumerated along with the total metabolic cell activity of a mixed culture. Agar plating using differential agar plates for specific organisms is commonly used to quantify metabolic active cell in mixed cultures. For example, MacConkey agar plates are commonly used to differentiate the number of Escherichia coli cells in a mixed culture (Fenlon and Wilson ). The bile salts and crystal violet dye presents in MacConkey agar inhibits the gram positive bacteria such as Bacillus subtilis. On the other hand phenyl ethyl alcohol agar plates are used to estimate gram positive organisms such as B. subtilis (DuTeau et al. ). Enzyme linked immunosorbant assay can be used to quantify specific organism in a biofilm or mixed cultures (Bauer-Kreisel et al. , David et al. ). Terminal-Restriction fragment length polymorphism has also been used to specifically quantify cells in cultures containing more than two cultures (Schmidt et al. ). Real time PCR based method has been used to enumerate Listeria monocytogenes in food samples at very high sensitivity (Schmidt et al. ). A laser integrated microarray scanner was used to quantify and compare the biomass of Burkholderia cepacia G4 alone in presence of phenol degrading community of microorganisms (Callister et al. ). This method could detect upto 103-104 cells ml−1. Hence, the methods are either expensive and accurate or cheap and error prone.
Here, we extend the MBRT to quantify metabolic active cells in mixed cultures. The method yields the total metabolic active cell and CFU of individual cells present in the mixed cultures. We have developed and standardized the method by monitoring and relating the dye reduction rate to the metabolic active cell count of E. coli and B. Subtilis. The MBRT test correlates with Colony Forming Units (CFU) up to a 1000 live cells as established by plating. Developed MBRT test is very simple, fast (200 s) and inexpensive as compared to available techniques. The protocol was also used to predict the presence of a contaminant during growth of pure culture.
Materials and methods
Escherichia coli K12 (MTCC 1302) and Bacillus subtilis 168trpC2 (Nandy et al. ) were used throughout the study. The E. coli K12 strain was obtained from MTCC, IMTECH Chandigarh, India and B. subtilis 168trpC2 was a gift from the lab of Prof. K.K. Rao, School of Biosciences and Bioengineering, IIT Bombay. Both of the strains were maintained on Luria broth agar slants. A loopful of the culture from the slant was subculture before each test and transferred into 100 ml of sterile Luria broth (Hi-media, Mumbai, India; Cat. No. M1245) and grown for 6 h at 37°C at 240 rpm. The 10% (v/v) of this seed was then added to 100 ml sterile Luria broth and grown for another 24 to 36 h for kinetic analysis.
Luria broth, Luria agar (LA), MacConkey agar and Phenyl ethyl Alcohol Hiveg™ Agar (Hi-media, Mumbai, India) were used throughout the experiments to grow the organism, maintain culture on slant and for obtaining metabolic active cell count using spread plate method, respectively. Methylene blue dye was obtained from E. Merck, India.
Methylene blue dye reduction test
Methylene blue dye was prepared by dissolving 1 g of the dye in 100 ml double distilled water. This 1% dye was used throughout the study. Spectrophotometer was used to obtain the rate of disappearance of blue color at 700 nm for 200 s. Cuvettes containing metabolic active cells were used to get the rate of decoloration. Methylene blue is reduced by respiratory cells, and thus the rate of decoloration could be correlated to metabolically active cell counts.
During the time course measurement in a spectrophotometer, cuvettes were covered with a plastic lid to prevent fresh oxygen dissolution into the culture. In the dye reduction test dead bacterial cells were used as a negative control. The quartz cuvettes were used instead of plastic to minimize error caused by the adhesion of methylene blue dye over a period of time. Further, the MB dye concentration and the blue color intensity was also linear in the range of 0.1-1.0 g l−1 of methylene blue indicating that any concentration in this range can be used for the assay (Bapat et al. ).
E. coli and B. subtilis were grown separately for 8 h in shake flasks at 240 rpm and at 37°C. The whole broth was centrifuged at 10,000 rpm (Remi C-24 centrifuge, India) (after 6–8 h of incubation). Cells from each culture flasks were resuspended in 10 ml PBS of pH 8. The cells were further either diluted or concentrated to yield various concentrations of initial cell number in PBS. The cell number varied from 1014-102 cells/ml of both E. coli and B. subtilis. The test-tubes containing equal number of E. coli and B. subtilis were mixed in equal quantity (5 ml each) to obtain mixed culture of the two strains containing equal number of the metabolic active cells. The sample containing the highest cell number (i.e. 1014 cells/ml) was diluted to various degrees using PBS as a diluent. The procedure thus yielded two ways of obtaining equal number of the two organisms but with different initial concentrations. Each of these tubes were used to obtain optical density (1 ml) using spectrophotometer (at 600 nm, Model V530, Jasco corporation, Japan), CFU using spread plate technique (0.1 ml) by incubating for 24 h at 37°C and rate of decoloration using MBRT. In the spread plate technique, at least 4 different dilutions were used to obtain an average colony forming units. The samples from the dilutions were also used to obtain individual colonies of E. coli and B. subtilis. Differential agar plates were used to differentiate the two organisms. MacConkey agar plate was used to quantify E. coli, while phenyl ethyl alcohol Hiveg™ agar was used to quantify B. subtilis. Thus, the MBRT slope was related to the OD of mixed culture, CFU of mixed culture, CFU of E. coli in mixed culture and CFU of B. subtilis in mixed culture. MBRT could be linearly related to all of the above measurements. However, it should be noted that for measurements less than 1000 cells, the sensitivity of MBRT reduced resulting in a nonlinear relationship (below an OD of 0.05). The sample growth rate was evaluated by obtaining the slope of linear profile using the plot of CFU in the log scale. Similarly, slope of the profile obtained using the log of the MBRT slope also yielded the specific growth rate since the slope of MBRT was directly related to the CFU.
E. coli and B. subtilis were separately grown in shake flask at 240 rpm and at 37°C. The cells (1% v/v) of each of the organism were inoculated into another 100 ml sterile Luria broth and grown for 25 h. MBRT, total CFU, CFU of E. coli and CFU of B. subtilis were evaluated at regular intervals.
It is clear from the figure that all the four protocol can be used to estimate the CFUs within the error (Maximum 12%). This indicated that the standard curves from pure culture could be used to obtain the total CFU (protocol ‘D’), using slope of MB reduction slope from a mixed culture, demonstrating the utility of the methodology. The reason for the applicability of MBRT slope of mixed culture using standard curves of pure culture may be due to the dominance of one microorganism over the other at any given time (See Figure 3a).
The above experiments demonstrated that MBRT can be used to quantify not only the total cell count but also the individual CFUs of different organisms in the mixed culture (Nandy et al. , Nandy et al. , Nandy and Venkatesh , Nandy and Venkatesh ) with approximately same known initial cell concentration. Thus, the next step was to use the methodology to monitor fermentations which is exhibited in Figure 5.
We have presented here a methodology for quantification of metabolic active cell in mixed culture using Methylene Blue dye Reduction Test (MBRT). The slope of the rate of reduction of Methylene Blue was correlated to the metabolically active cell count. This was compared to CFU obtained using agar plate method to demonstrate the utility of the test. Further, starting from the approximately same initial cell concentration of different species, the MBRT was also used to quantify the metabolically active cell count for the individual cells in a mixed culture, of E. coli and B. subtilis. It was noted that the standard curve relating the slope of MB reduction and CFU for the individual cells could be used to measure the metabolic activity of each species.. The individual growth rates were evaluated at the end of the growth experiment itself as MBRT yielded the metabolic active cell count in less than 6 minutes at each time point. Thus, by the end of the exponential growth rate (i.e. about 12 h in case of initial cell count of 102 cells/ml) the individual growth rate could also be estimated, whereas in case of the agar plate method, one needs to streak the cells on differential plates for E. coli and B. subtilis at the end of 8 h and obtain the cell count only after 24-30 h of incubation. This demonstrated the strength of the method reported here. Initial known cell concentration is only the limitation of this method. It is possible to add an unknown species with initial cell concentration in a known culture concentration; then one could calculate the number of cell by MBRT but would need to take MBRT slope before and after addition. The difference in slope may exhibit the addition of cell concentration in the culture. It will be a challenge for future work to estimate unknown individual initial cell concentrations in a mixed culture.
Further, we have also demonstrated that the slope of decoloration of methylene blue can be used to monitor fermentations online. Since the slope obtained from MBRT is indicative of the total metabolic active cell, a standard profile for normal operation can be established. During operation deviations from the normal profile may indicate contamination or abnormal behavior. Since the metabolic active cell count increased in case of contamination, the MBRT slope would be higher than the MBRT slope for normal operation. If the MBRT slope obtained during monitoring is less than that of the normal profile, abnormalities such as failure in temperature or pH control, oxygen limitation or inhibitors in the medium, may be the cause for decrease in metabolic active cell. Thus, MBRT can be used for fault diagnosis through online measurement of slope of MB decoloration.
The evaluation of the total metabolic active cell count and the individual metabolic active cell counts starting with an equal cell numbers of different species present in a mixed culture offers a quantification which would be helpful in designing, operating and controlling processes using mixed cultures. Further, the evaluation of growth rates of the individual species during the growth of mixed culture in a process offers insights into the operation of such processes. Thus, the protocol developed here can be adapted to applications in processes involving mixed cultures.
We thank to Morten Kielland-Brandt, Professor in Systems biology department, Technical University of Denmark for some useful suggestions to improve the manuscript.
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