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Brazilian Journal of Microbiology

Print version ISSN 1517-8382

Braz. J. Microbiol. vol.44 no.1 São Paulo  2013

http://dx.doi.org/10.1590/S1517-83822013000100042 

MEDICAL MICROBIOLOGY
SHORT COMMUNICATION

 

Measuring of Mycobacterium tuberculosis growth. A correlation of the optical measurements with colony forming units

 

 

Katia Peñuelas-UrquidesI,II; Licet Villarreal-TreviñoII; Beatriz Silva-RamírezIII; Liliana Rivadeneyra-EspinozaIV; Salvador Said-FernándezV; Mario Bermúdez de LeónI

ILaboratorio de Biología Molecular, Centro de Investigación Biomédica del Noreste, Instituto Mexicano del Seguro Social, Monterrey, NL, México
IIPosgrado en Microbiología, Facultad de Ciencias Biológicas, Universidad Autónoma de Nuevo León, San Nicolás de los Garza, NL, México
IIIDivisión de Genética, Centro de Investigación Biomédica del Noreste, Instituto Mexicano del Seguro Social, Monterrey, NL, México
IVDivisión de Biología Celular y Molecular, Centro de Investigación Biomédica del Noreste, Instituto Mexicano del Seguro Social, Monterrey, NL, México
VDepartamento de Bioquímica y Medicina Molecular, Facultad de Medicina, Universidad Autónoma de Nuevo León, Monterrey, NL México

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ABSTRACT

The quantification of colony forming units (cfu), turbidity, and optical density at 600 nm (OD600) measurements were used to evaluate Mycobacterium tuberculosis growth. Turbidity and OD600 measurements displayed similar growth curves, while cfu quantification showed a continuous growth curve. We determined the cfu equivalents to McFarland and OD600 units.

Key words: bacterial growth, colony forming units, McFarland, Mycobacterium tuberculosis, optical density.


 

 

The McFarland standards are a series of references of different densities used to estimate the concentration of cells in microbial cultures (Versalovic et al., 2011). The turbidity of these standards is compared to a defined number of Escherichia coli microorganisms per mL (Perilla et al., 2003), and frequently has been used to estimate the density of Mycobacterium tuberculosis cultures (Bergmann et al., 2000; Bollela et al., 1999; Elbir et al., 2008; Leonard et al., 2008; Syre et al., 2003). It is commonly assumed that E. coli and M. tuberculosis cultures with equivalent concentrations have equivalent turbidities (Bollela et al., 1999; Elbir et al., 2008). This assumption has not been validated and could be contributing to erroneous quantifications. Another method for quantifying the concentration of microbial cultures includes measuring the optical density at 600 nm (OD600); though measuring M. tuberculosis concentrations using OD is controversial (Iona et al., 2007; Taneja and Tyagi, 2007). The method considered the most reliable for measuring the concentration of viable microorganisms in culture is the quantification of colony-forming units (cfu) per unit volume of culture (Davey et al., 2004). However, this approach is laborious, and for M. tuberculosis,requires lengthy time periods to obtain results (Damato et al., 1983; von Groll et al., 2010). The aim of this study was to define the number of viable M. tuberculosis cells equivalent to McFarland and OD600 measurements in liquid cultures and to compare the reliability of these methods in estimating M. tuberculosis concentrations in suspension.

M. tuberculosis cultures (strain H37Rv, ATCC 27294) were inoculated in Lowenstein-Jensen slants and incubated at 37 ºC in 5% CO2 atmosphere for 2 weeks. A portion of the mycobacterial colonies was transferred to Middlebrook 7H9 medium (Difco, Becton Dickinson, Le Pont de Claix, France) supplemented with 10% OADC (oleic acid, albumin, dextrose and catalase, Becton Dickinson and Company, Sparks, MD. USA.). The cultures were incubated at 37 ºC in 5% CO2 atmosphere until they reached a turbidity equivalent to the McFarland standard No. 1. A 100 µL aliquot was inoculated in 10 mL of Middlebrook 7H9 medium (Becton Dickinson) supplemented with 10% OADC (Becton Dickinson and Company). To avoid clump formation the cultures were incubated in constant shaking at 300 rpm.

The turbidity, OD600 and cfu per milliliter (cfu/mL) of 1 mL aliquots of mycobacteria cultures were measured every three days for 21 days. Data obtained with cfu/mL counting were compared with McFarlands and OD600 measurements. The turbidity of the aliquots was measured using a nephelometer (ATB 1550, BioMérieux, France). Prior to measuring the OD600 using a spectrophotometer (DU 800 Beckman Coulter, CA, USA), cultures were inactivated with 10% (v/v) formaldehyde (Sigma-Aldrich, Steinheim, Germany) and adjusted to the appropriate dilution. Before formaldehyde addition, cultures were serially diluted 10-fold (from 10-2 to 10-8) to quantify cfu/mL. 100 µL aliquots from these dilutions were inoculated on Middlebrook 7H10 agar media (Difco, Becton Dickinson, Le Pont de Claix, France) and incubated as described above until colonies were visible. The M. tuberculosis colonies were counted and adjusted according to the dilution factor. The generation time was calculated using cfu/mL counting by the following equation: Log(N) = log(N0) + Kt, where N = final number of microorganisms, N0 = inoculum, K = slope, and t = incubation time.

Though the samples measured by each method in the study were processed from the same M. tuberculosis cultures, under comparable conditions, cfu/mL and McFarlands growth curves showed a longer lag phase than observed at OD600.The logarithmic growth phase lasted nine days in all cases, conserving the starting delay. The stationary phase was observed by day 15 in growth curves using the McFarland method and OD600, whereas the cfu/mL curve did not have a stationary phase within the 21 days of incubation (Figure 1). The discrepancy observed between the McFarland and OD600 curves could be due to a higher threshold of detection for the nephelometer (BioMérieux) as compared to the spectrophotometer (Beckman Coulter). When the multidrug resistant clinical isolate CIBIN:UMF:15:99 (Molina-Salinas et al., 2006) of M. tuberculosis was used to evaluate the equivalents of McFarland and OD600 measurements, we did not observe a correlation with the growth curve of H37Rv reference strain (data not shown).

 

 

In quantifying cfu/mL by colony counting, colonies were not observed until the 9th day of incubation. During log phase, the generation time was calculated in 24.91 h. Figure 2 shows the correlation of the growth curves generated from the different methods. The correlation between cfu/mL quantification and OD600 measurement was the lowest (R2 = 0.8913, Figure 2A), followed by the correlation between cfu/mL quantification and turbidity measurement (R2 = 0.9252, Figure 2B). OD600 and turbidity measurements were highly correlated (R2 = 0.9823, Figure 2C). We determined in M. tuberculosis H37Rv ATCC 27294 that 1 McFarland unit is equivalent to either 1.97 x 106 cfu/mL or 0.39 OD600, and an OD600 measurement of 1 is equivalent to either 3.13 x 107 cfu/mL or 3.66 McFarland units.

 



 

Quantification of M. tuberculosis in liquid cultures is difficult as this microorganism is prone to clump formation (Lambrecht et al., 1988). Results from this study show that turbidity and optical density measurements yield similar growth curves, with lag, log and stationary phases clearly defined (Figure 1). Though these methods are easy to perform and the equipment is readily available, these methods do not distinguish between live and dead microorganisms. Thus, the measurements do not reflect the concentration of actively growing cells. In addition, turbidity measurement by nephelometry uses versatile equipment that can be maintained in biosafety rooms, but the real mycobacterial number equivalent to the McFarland standards is not known with certainty (Kitchen et al., 1998; Martin-Casabona et al., 1997; Raut et al., 2008).

In this study, we compare turbidity and OD600 measurements to cfu/mL quantification. Our results demonstrate there is a relationship between turbidity and OD600 lectures and cfu/mL quantification. These measurements are not quite as precise, since M. tuberculosis tends to form clumps. Nevertheless, we have established equivalents of McFarland and OD600 units for a defined number of viable cells in M. tuberculosis H37Rv ATCC 27294 cultures. The lack of correlation of McFarland and OD600 equivalents found between a multidrug-resistant clinical isolate and H37Rv strain of M. tuberculosis could be explained by its high rate of clumping and the slower growing. On the other hand, McFarland standards for Escherichia coli cultures (Perilla et al., 2003) are not comparable with those of M. tuberculosis because they have different physical properties such as cell size, sedimentation, and light scattering. For example, the bacterial size for E. coli is 1-2 /m length (Zobell and Cobet, 1962) vs. 3.5-4 /mof M. tuberculosis (Will et al., 1951); M. tuberculosis has a higher sedimentable mass than E. coli, as well as a suspension of E. coli scatters the light more intensely than M. tuberculosis (Jaiswal and Panda, 2009). These data support the idea of an erroneous quantification when McFarland equivalents in E. coli are used to evaluate the growth of M. tuberculosis, which lead to a misinterpretation of results in liquid cultures. Other methods such as respiration rate (Gomez-Flores et al., 1995), resazurin reduction (Sanchotene et al., 2008; von Groll et al., 2010), as well as protein and ATP measurements (Meyers et al., 1998) have measured the growth kinetics of M. tuberculosis, but all of these methods require further incubation time and analysis resulting in a delay of additional assays. In conclusion, OD600 measuring is the most sensible method for the evaluation of M. tuberculosis growth in liquid cultures, whereas the growth curve is more consistent using McFarland method, particularly between 9-15 days.

 

Acknowledgments

This work was supported by a grant from CONACyT (99792-M)

 

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Send correspondence to:
M.B. León
Laboratorio de Biología Molecular, Centro de Investigación Biomédica del Noreste, Instituto Mexicano del Seguro Social
Ave 2 de Abril 501, Col. Independencia
C.P. 64720, Monterrey, N.L., México
E-mail: mario.bermudez@imss.gob.mx

Submitted: September 21, 2011
Approved: July 2, 2012.

 

 

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