![[Feedback]](/icons/banner/feedbackACT.gif){kind=icon}
![[For Subscribers]](/icons/banner/subscriberACT.gif){kind=icon}
![[Archive]](/icons/banner/archiveACT.gif){kind=icon}
![[Search]](/icons/banner/searchACT.gif){kind=icon}
![[Contents]](/icons/banner/tocACT.gif){kind=icon}
,2*
Departamento de Genética y de Microbiología, Facultad de Ciencias,1 Instituto de Biotecnología y Biomedicina, Universidad Autónoma de Barcelona, 08193 Bellaterra (Barcelona), Spain2
Received 20 November 2001/ Returned for modification 21 January 2002/ Accepted 5 May 2002
 |
ABSTRACT |
|---|
 Top Abstract TextReferences |
|---|
|
TEXT |
|---|
|
TopAbstractTextReferences |
|---|
Cytochemical reactions in tubercle bacilli were studied in great depth in the 1940s and 1950s in order to find phenotypic markers correlated to virulence. The action of many basic dyes, such as Nile blue, methylene blue, neutral red, and methyl violet, on different Mycobacterium strains has been studied (5, 6, 7, 8). The most successful results were obtained with neutral red and Nile blue (6, 8). Dubos and Middlebrook reported that H37Rv, together with 22 M. tuberculosis and Mycobacterium bovis isolates, fixed neutral red in an alkaline aqueous environment and became red in color, whereas H37Ra cells did not (8). Two subsequent studies in which larger numbers of M. tuberculosis clinical isolates were used (about 200 strains in each) corroborated these findings (11, 15). At the same time, Desbordes and coworkers concluded that, unlike attenuated and avirulent strains, the virulent strain H37Rv strongly fixed basic dyes, such as Nile blue and neutral red, in their anionic forms (red and blue, respectively) in very alkaline environments.
In this work, we present an easy test for distinguishing H37Ra from H37Rv and from clinical isolates, developed by modifying previous cytochemical techniques and based on the variant behaviors of H37Ra, H37Rv, and clinical isolates when stained with neutral red or Nile blue.
M. tuberculosis strains, culture media, and growth conditions. Twenty-eight M. tuberculosis strains, including recent clinical isolates (Laboratory of Clinical Microbiology, Hospital "de la Santa Creu i Sant Pau," and Microbiology Service, "Germans Trias i Pujol" University Hospital, Barcelona, Spain), and the M. tuberculosis reference strains H37Rv (ATCC 27294) and H37Ra (ATCC 25177), both dissociated from H37 in 1934, were used in this study. M. tuberculosis clinical isolates were identified as M. tuberculosis complex by the AccuProbe assay (Gen-Probe Inc., San Diego, Calif.) (20) and as M. tuberculosis species by standard biochemical procedures (13, 21, 22). For cytochemical staining, colonies were grown on plates of Middlebrook 7H10 Bacto-agar enriched with oleic acid-albumin-dextrose-catalase (Difco Laboratories, Detroit, Mich.) at 37°C for 4 weeks.
Cytochemical staining of M. tuberculosis cells. H37Ra was distinguished from H37Rv and clinical isolates inside borosilicate glass screw-cap tubes by means of two cytochemical tests with two different basic dyes, neutral red and Nile blue. Neutral red staining was carried out as follows. A few colonies of mycobacteria were placed inside a screw-cap tube containing 5 ml of 50% aqueous methanol, mixed, and incubated for 1 h at 37°C. The fluid was then removed, and cells were washed again, as above, with aqueous methanol. Finally, 5 ml of 0.002% neutral red (Merck AG, Darmstadt, Germany) in barbital buffer (1% sodium barbital in 5% NaCl [pH 9.8]) was added and mixed with the washed cells, and the tubes were kept at room temperature. It is not necessary to centrifuge in order to eliminate the washing fluids, but it is important in each step to mix the cells well with the washing and staining solutions. Deionized water was used throughout the entire process.
Results were read after 1 h, and a definitive reading was performed after 24 h. The reading may be done either in daylight or in artificial light.
Neutral red became yellow when added to barbital buffer, pH 9.8. However, the H37Rv cells and all 28 clinical isolates immediately took on a red coloration with the staining solution, while the H37Ra cells were not colored (Fig. 1A and B). No appreciable differences in the intensity of red coloration were observed among the clinical isolates. After the staining test was completed, H37Rv and clinical-isolate cells retained their coloration for several days. Special care must be taken to eliminate the maximum amount of washing solution after the second wash, because it is slightly acidic, and if it is not efficiently removed, the H37Ra cells can take on a pink coloration. After 24 h this pink coloration disappears completely. We therefore recommend that the definitive reading of results be done after 24 h. Another way of avoiding false positives due to the acidity of the washing solution is to carry out an additional wash with barbital buffer and without neutral red before adding the staining solution,. We studied the stability of the neutral red reaction over a 2-year period; during this time, the strains used in this work were passed in culture medium several times and retested every 4 weeks. H37Rv has proved to be very stable for this characteristic, and we observed no loss in the intensity of staining throughout the 2 years that the study lasted. Likewise, H37Ra showed itself consistently unable to take on the dye over the same period. However, in six clinical strains, after 7 or 8 passages, we observed a decrease in the intensity of neutral red fixation compared with that in H37Rv and the other clinical isolates. The cells of the strains that lost intensity became more pink than red when stained with neutral red and kept this coloration until the end of the study. In the remaining clinical isolates, no loss of intensity in the staining was observed. Therefore, this technique cannot be used on clinical isolates kept for long periods in the laboratory through several passages in culture medium. We recommend using H37Ra as the negative control and H37Rv or a recently tested clinical isolate as the positive control when testing clinical isolates by this technique.
|
When Nile blue was added to the very alkaline barbital buffer (pH 11.5), the staining solution took on a pink coloration. Subsequently, the staining solution became blue within a few minutes of reacting with H37Rv or clinical-isolate cells, while the solution reacting with H37Ra cells retained the pink coloration (Fig. 1C and D). No differences in the intensity of the reaction were observed among the clinical isolates. Unlike the neutral red staining, Nile blue did not stain the cells completely, and differences between positive and negative strains were better observed in the staining solution.
The six strains that after several passages showed a lower capacity to fix neutral red were the same ones that also turned the Nile blue staining solution to a weaker blue color. The other clinical strains, H37Ra, and H37Rv were stable to Nile blue staining over the 2-year period, as they were to neutral red staining.
The two stainings are equally clear and reproducible. To the naked eye the difference between the colors is very clear in both stainings, but when a photograph is taken, the difference between pink and blue is more difficult to capture correctly (Fig. 1). However, if we had to choose between the two stains, perhaps we would choose neutral red, because the cells become completely stained quite quickly and the difference in color between a positive and a negative strain lasts for several days. On the other hand, when Nile blue is used, the cells become only slightly stained, and the color difference between a positive and a negative isolate is most apparent in the supernatant during the first hour. After the first hour, the cells take on a more intense coloring but the staining loses its discriminative power.
Our results agree with those obtained 50 years ago by several authors (5-8, 11, 15): H37Rv and M. tuberculosis clinical isolates are able to absorb basic dyes (neutral red and Nile blue) in their anionic forms (red and blue, respectively), whereas H37Ra is not.
We have made two contributions to these cytochemical staining techniques: first, by developing reproducible protocols and second, by rescuing them from oblivion. The first step in our study was to reproduce the previously reported protocols for neutral red and Nile blue staining (5-8). When these procedures were carried out, we encountered certain technical problems and made a series of observations. First, we noted that H37Ra differentiation by neutral red staining was not favorable at a pH of <9. At such pH values, the H37Ra strain fixed the dye and the cells took on a pale pink color. When staining was carried out at a pH of >9, H37Rv and clinical-isolate cells took on a purple-red coloration, whereas H37Ra cells became yellow, like the staining solution. We tried different concentrations of neutral red and we found that 0.002% was the most discriminative. On the other hand, when reproducing the neutral red staining reaction described by Desbordes et al. (7), we observed that the staining solution, made in saturated Na2CO3 (27.5 g of Na2CO3 in 96 ml of water) (10), was unstable. A colored precipitate was obtained a few minutes after the addition of neutral red. However, the neutral red staining solution in barbital buffer remained stable during the staining procedure. With the Nile blue test, the same problem occurred: when Desbordes' reaction was applied, a precipitate was formed in the staining solution when the dye was added to saturated Na2CO3. Dye precipitation was prevented by using a different alkaline environment (1% sodium barbital in 5% KCl adjusted at pH 11.5) and a very low dye concentration (0.0006%). pH was a critical parameter for optimal Nile blue staining results; the best differences in stain coloration were obtained at pH 11.5. With the modifications that we have introduced, both in the neutral red and in the Nile blue staining, there were no problems of precipitation, and clear differentiation of colors was observed both between H37Ra and H37Rv and between H37Ra and the clinical isolates.
We would encourage clinical laboratories currently using H37Rv or other M. tuberculosis strains as controls for identification of M. tuberculosis isolates to use H37Ra, since the techniques described here will allow them to carry out rapid screening and detect possible cross-contamination. Naturally, any clinical isolate giving negative results with neutral red or Nile blue staining would have to undergo spoligotyping or IS6110 genotyping in order to confirm the cross-contamination.
Another aspect to bear in mind is that the variant H37Ra was obtained from strain H37 in 1934 and then distributed to different laboratories throughout the world. During these 68 years, many variants may have been generated. Each laboratory will, therefore, have to acquire a strain of H37Ra which responds correctly to the cytochemical tests described.
One study correlated neutral red staining with the sulfolipid content in virulent M. tuberculosis strains (14). This correlation was doubtful, since some virulent strains were devoid of sulfolipids but were able to fix neutral red (14). Phospholipids and other acidic lipids have been proposed as additional possible structural components responsible for neutral red staining in strains lacking sulfolipids (9, 14). No clear explanation of this cytochemical staining has been obtained, and the component or components responsible for neutral red staining of virulent M. tuberculosis strains are not known with any certainty. Nile blue probably reacts to the same components as neutral red in the cell wall of M. tuberculosis, but no study has been published on this subject.
The technique described here would be useful in searching for the component that fixes neutral red and Nile blue. On the other hand, many studies are concerned with identifying the genomic differences between the virulent H37Rv strain and its attenuated variant H37Ra (2, 17-19). Furthermore, it is also common to study the differences between the abilities of virulent and attenuated (H37Rv and H37Ra) M. tuberculosis strains to invade and survive within cells of the immune system (12, 23). Many laboratories, therefore, work with these two variants, dissociated from the original M. tuberculosis H37 strain. In such laboratories, the possible exchange between these two strains requires evaluation. Thus, the application of the techniques described in this work could also be a very useful tool for control in mycobacterial research laboratories. Finally, this method of differentiating H37Ra from H37Rv and from clinical isolates is easy, inexpensive, reliable, and currently capable of being carried out in any laboratory.
|
ACKNOWLEDGMENTS |
|---|
|
FOOTNOTES |
|---|
Present address Departamento de Microbiología, Medicina Preventiva y Salud Pública, Universidad de Zaragoza, 50009 Zaragoza, Spain.
|
REFERENCES |
|---|
|
TopAbstractTextReferences |
|---|
This article has been cited by other articles:
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Antimicrob. Agents Chemother. | Clin. Microbiol. Rev. |
|---|---|
| Clin. Vaccine Immunol. | ALL ASM JOURNALS |
|---|
