MICROBIAL TEST STANDARD FOR USE IN INFRARED SPECTROMETRY

Abstract

The invention relates to a microbial test standard for use in infrared spectrometry which has at least two resealable vessels which are liquid-tight when closed, each of which contains a predefined amount of dried biomass of a microorganism. The microorganisms in the different vessels differ in at least one characteristic, which is selected in particular from the group comprising species, subspecies, strain, serovar, pathovar, toxivar and variety, and the difference manifests itself in a predefined intermicrobial spectral distance. The disclosure furthermore comprises a method of using the microbial test standard.

Claims

1. A microbial test standard for use in infrared spectrometry which has at least two resealable vessels which are liquid-tight when closed, each of which contains a predefined amount of dried biomass of a microorganism, where the microorganisms in the different vessels differ in at least one characteristic and the difference manifests itself in a predefined intermicrobial spectral distance.

2. The microbial test standard according to claim 1, wherein the at least one characteristic is selected from the group: species, subspecies, strain, serovar, pathovar, toxivar and variety.

3. The microbial test standard according to claim 1, wherein the dried biomass is sterilized.

4. The microbial test standard according to claim 1, wherein the dried biomass is comprised of vacuum-dried pellets.

5. The microbial test standard according to claim 1, wherein the microorganisms belong to different strains of one bacterial species.

6. The microbial test standard according to claim 1, wherein the vessels have screw caps.

7. A method of using the microbial test standard according to claim 1, comprising: provision of a sample support for infrared spectrometry which has an array of sample spots, re-suspension of the biomass in the vessels by adding a solvent, removal of a predetermined quantity of the suspension from each vessel, which is then deposited on a predetermined number of sample spots, drying of the suspension on the sample spots, acquisition of infrared spectra from the sample spots; calculation of intermicrobial spectral distances between spectral signatures in the infrared spectra of the different sample spots; and determination of whether the spectral distances are outside a predetermined range.

8. The method according to claim 7, wherein the spectral distances are computed from the microbial spectral signatures in a predetermined wave number range and correspond to a predetermined distance.

9. The method according to claim 8, wherein the predetermined wave number range is between around 1,300 and 800 cm-1.

10. The method according to claim 7, wherein the intramicrobial spectral distances between the spectral signatures of the infrared spectra of the different sample spots are computed to examine the spectral reproducibility.

11. The method according to claim 10, wherein the predetermined range of the intramicrobial spectral distance extends to a maximum distance A, which is a measure for the reproducibility of the acquisitions, and the predetermined range of the intermicrobial spectral distance extends from a minimum distance B, which is a measure for the spectral specificity in the acquisitions.

12. The method according to claim 7, wherein the solvent for the re-suspension contains distilled and/or deionized water.

13. The method according to claim 7, wherein the re-suspension is promoted by agitating the vessels or by mix-pipetting.

14. The method according to claim 7, wherein a (warning) tag is attached to the IR spectra when a spectral distance is outside the predetermined range.

15. The method according to claim 7, wherein a plurality of replicates of the microorganism suspensions are applied to the sample support.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0028] The invention can be better understood by referring to the following illustrations. The elements in the illustrations are not necessarily to scale, but are intended primarily to illustrate the principles of the invention (mainly schematically). In the illustrations, the same reference numbers designate corresponding elements in the different views.

[0029] FIG. 1A is a schematic representation of the first part of an example use of a microbial test standard.

[0030] FIG. 1B provides a schematic illustration of an IR spectrometric measurement in transmission through dried samples with corresponding example of an extinction spectrum.

[0031] FIG. 1C gives a schematic illustration of the different processing steps of an extinction spectrum which are carried out before the evaluation.

[0032] FIG. 2 provides a schematic illustration of the possible result of a spectral distance determination for replicates of two bacterial strains in a two-dimensional principal component space.

DETAILED DESCRIPTION

[0033] While the invention has been illustrated and explained with reference to a number of different embodiments thereof, those skilled in the art will acknowledge that various changes in form and detail may be made to it without departing from the scope of the technical teaching as defined in the appended claims.

[0034] The dried biomass for the microbial IR test standard can be produced in the following way: The different reference microorganisms are cultured overnight on a two-dimensional culture medium (e.g. Columbia sheep blood agar). The cultured cells are inoculated into several hundred milliliters of nutrient broth (e.g. LBlysogeny broth) before they are allowed to grow again at 37 C. with slight agitation of a few hundred rpm for several hours (e.g. 12 to 24 hours). The broth thus enriched can then be divided between a number of centrifuge vessels and centrifuged at several thousand g for several minutes. The supernatant is disposed of, and the microbial pellet left behind is re-suspended in water to remove the residual nutrient broth. Renewed centrifugation and renewed re-suspension in water, supplemented by the addition of a protic solvent such as ethanol, if necessary, produce a suspension whose microorganism content can be determined by measuring the optical density (e.g. in accordance with the McFarland standard). If the concentration of the suspended microorganisms is sufficient, the suspension can be aliquoted into plastic vessels and dried therein, for example in a vacuum at slightly raised temperatures, in order to form a ready-to-use pellet, from which the liquid has been removed, in the vessel itself.

[0035] FIGS. 1A to 1C outline a possible procedure for using a microbial test standard.

[0036] The dried biomass (2) for the two reference microorganisms can be supplied in plastic containers (4) with screw caps (6). To prepare a reference sample, the screw cap (6) is removed and a quantity of solvent such as distilled or de-ionized water is added to re-suspend the dry pellets (2). After the vessels (4) have been resealed, this procedure can be assisted by light shaking or, additionally or alternatively, by repeatedly drawing liquid into a pipette tip and forcing it out again (mix-pipetting) without forming any bubbles (not shown).

[0037] After a few minutes, when the solid biomass has dissolved and is no longer visible, the caps (6) can be removed again and a quantity of the microbial suspension (8) removed from the vessels (4) and applied to a number of sample spots (A-H; 1-12) on an IR spectrometry sample support (10). This can be done in duplicates, triplicates or a larger number of replicates, as is shown schematically for two sample supports (10) with a 96 sample spot array (eight rows A-H, twelve columns 1-12). In general, the statistical basis of the spectral distance determination can be improved by increasing the number of replicates of the test standard, but only at the expense of a correspondingly smaller number of sample spots for the analytical samples that are actually to be identified on the sample support. The latter are not shown here for reasons of clarity. The droplets of the test standard suspension are dried, assisted where necessary by thermal irradiation at a temperature slightly higher than room temperature and/or a stream of air.

[0038] The microorganisms of the reference standard (#1, #2) are then measured in the same run as the actual sample with an IR spectrometer (12a, 12b), preferably in transmission, as shown. One example for such a spectrometer is the TENSOR II FT-IR from Bruker Optik GmbH. The result of such a measurement is an extinction spectrum, as shown at the bottom of FIG. 1B by way of example. The optical density (O.D.) is plotted as a function of the wave number, as is usual in spectrometry. The spectra acquired are differentiated twice and smoothed in each case over a specific number of data points. A wave number range is then chosen in which the absorption bands of microbial cells, which are caused in particular by carbohydrates and proteins, stand out best with respect to background effects, such as water absorption bands, and therefore provide the best signal-to-background ratio. The range between around 1,300 and 800 cm.sup.1 is particularly suitable for this; FIG. 1C.

[0039] A vector normalization prepares the selected spectral range for the subsequent evaluation with regard to the spectral distance measures. One option to determine the spectral distance from the microorganism-specific extinction signals is a principal component analysis. The crucial issue here is that the microorganisms for the different vessels are selected such that they can be represented in different components with reliable, slight but clear differences. Although the intermicrobial spectral distance is defined essentially by a lower limit, it should not be set too high in order to enable an assessment to be made about the spectral specificity at the performance limit of the infrared spectrometer. Nor should it be too low in order to counteract the danger of a variance-induced, random overlapping of the principal component data clouds, which exhibit a certain variance from measurement to measurement.

[0040] FIG. 2 is a schematic representation, by way of example, of a result of a principal component analysis on the basis of IR spectra of two bacterial strains. The intramicrobial spectral distance between the replicates of the same microorganism must not exceed a certain peak value A, because then it would not be possible to confirm the identity, which would cast doubt on the quality of the measurement. In addition, the intermicrobial spectral distance between the different replicates of the different microorganisms used must not fall below a certain lower limit B, because then the spectral specificity of the measurement was not sufficient. The larger the number of replicates of the individual microorganism suspensions, the more statistically reliable the assessments derived from them. However, the space available for the actual microbial measuring samples on the sample support has to be taken into account.

[0041] As can be seen in FIG. 2, two separate data clouds, shown in outline, form in the two-dimensional principal component space when the same microorganisms are measured again. These clouds are in close proximity to each other with regard to the individual replicates of one organism, but are a significant distance from the replicates of the other organism in each case (in the example shown>0.15 arbitrary units). Since the microbial test standard is investigated in the same measurement run as the real microbial samples, this distance in the computed principal components allows an assessment to be made about the spectral specificity of the IR spectrometer. At the same time, the reproducibility of the IR measurement can be assessed by means of the intramicrobial spectral distances of the individual replicates of the same microorganism with respect to each other and among themselves. If individual data points from the replicates of the same organism exceed the maximum permissible distance A, this would be regarded as an indication of a problem with the reproducibility of the measurements. The parallel measurements of real samples can then be tagged accordingly. If it is even the case that the data clouds of the different microorganisms spill over into each other, the spectral specificity would not be adequate. This reduces the quality of the identification, and it may even be necessary to label the identification/characterization result from the sample support in question as unreliable under the given measurement conditions.

[0042] The use of a principal component analysis above shall not be understood as a limitation, but as an illustrative example. Principles of the present disclosure can also be carried out with alternative methods of determining spectral distances, for example with the native Euclidian distances and/or with the aid of hierarchical cluster analyses. The test spectra could also be classified with ANN (artificial neural network analysis) appropriately trained in advance, PLS-DA (partial least-square discriminant analysis), or SVM (support vector machines).

[0043] Above, the principles of the invention have been explained with the aid of two spectrally distinguishable microorganisms. Those skilled in the art will recognize, however, that more than two suitable microorganisms can also be used to provide a microbial test standard for infrared spectrometry. The fundamental idea can be expanded as desired in this respect.

[0044] The invention has been described above with reference to different, specific example embodiments. It is understood, however, that various aspects or details of the embodiments described can be modified without deviating from the scope of the invention. In particular, characteristics and measures disclosed in connection with different embodiments can be combined as desired if this appears practicable to a person skilled in the art. Moreover, the above description serves only as an illustration of the invention and not as a limitation of the scope of protection, which is exclusively defined by the appended claims, taking into account any equivalents which may possibly exist.