1. Introduction
The study and development of new technologies for the rapid screening of bacteria has been gaining traction in recent years due to their simplicity and efficiency for applications in the fields of medicine, biotechnology, and agriculture, among others. In epidemiology and public health, for example, the growing problem of antibiotic resistance can benefit from quick quantification of bacteria by helping clinicians administer suitable dosages of antibiotics to treat bacterial infections. In the case of upper urinary tract infections (UTI), it has been shown that prolonged administration of antibiotics is unnecessary for treatment [
1], yet, at the same time, improper targeting could potentially cause the infection to progress further. The current gold standard for quantification and detection of bacteria is the use of traditional culture methods, which is not always possible due to the required level of training, the need for high-end equipment, and, most importantly, time constraints. For UTI, timely diagnosis and treatment has been shown to be crucial in preventing death, especially in patients with sepsis [
2]. This becomes especially problematic in places such as the developing world, where resources to perform such analyses are scarce.
Rapid quantification of bacteria can also be crucial in the case of preventative healthcare and management. Taking pregnancy as an example, the presence of significant amounts of bacteria in urine (>10
5 CFU/mL) in the absence of UTI symptoms [
3], also known as asymptomatic bacteriuria (ASB), is often a precursor to UTI, which can in turn lead to adverse clinical outcomes [
4,
5]. In preventing the onset of UTI, the costs associated with routine screening for ASB through traditional culture procedures makes it difficult to achieve. One study revealed that routine screening for ASB was only cost-effective if rates were higher than 9% [
6]. Such cost-effectiveness dependency on incidence rate makes clinical management difficult to justify, further complicating efforts in the field of disease prevention.
Apart from medicine, other industries can also benefit from rapid quantification of bacteria. A study undertaken by Cavaiuolo and colleagues in 2013, for example, developed an optimized ELISA-based biochemical assay for the detection of
Listeria monocytogenes and
E. coli in fresh vegetables. The limit of detection (LOD), the lowest concentration that can be measured with statistical significance, was found to be approximately 10
3 CFU/g, with a bacteria isolation period of approximately 1–7 h. Such findings are significant in the food industry, as fresh vegetables tend to be contaminated with bacteria, and lengthy standard culture methods may render the vegetables unfit for consumption even before results are made available [
7]. Another recent study by Liao and colleagues looked at the use of a tetrazolium-based MTT-PMS portable biochemical reagent and device for the detection of
E. coli in water sources [
8]. The developed portable colorimetric device was similar in rationale in that there is a need for a convenient and easy-to-use tool in areas where access to clean water is scarce. The device had an LOD of approximately 3.43 × 10
5 CFU/mL in phosphate-buffered saline (PBS) and 1.41 × 10
6 CFU/mL in water in less than 15 min, making it a potential avenue for the immediate elimination of unsuitable water sources.
Similar to the Liao study [
8], the use of tetrazolium dye in biochemical and other applications is due to its unique ability to reduce into formazan, a brightly colored derivative with the potential to measure cells’ metabolic activity. The term owes itself to the salt’s chemical structure, a heterocyclic compound with four nitrogen atoms in the ring. Its reduction is enzymatic, where there is cleavage of the tetrazole ring, resulting in an intensely-colored formazan [
9]. MTT is a type of tetrazolium salt that was developed for use from 1957 onwards and has since been widely used in biochemical assays and other applications [
10]. For example, a study in 2001 looked at the use of an MTT-based biochemical assay as an alternative method to measure fungal spore viability [
11]. It was found that for a given number of viable cells, higher concentrations of MTT resulted in higher yields of formazan crystal, with the reduction based on the fungal spores’ dehydrogenase activity (DHA).
Grela, Kozlowska, and Grabowiecka provided a fresh perspective from multiple studies on the use of MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) tetrazolium assays as a means to assess culture viability through measurable enzymatic activity [
12]. Aside from Stentelaire’s 2001 MTT-based biochemical assay to measure fungal spore viability [
11], procedures involving MTT have also been used with mammalian cell lines. Mitochondrial membrane potentials, for example, have also been measured using MTT in conjunction with rhodamine B, making use of the tetrazole ring’s positive charge and differences in membrane potential [
13]. However, this only further supports MTT reduction and therefore its utility in eukaryotic cells. Despite this, Grela and colleagues argued that although MTT reduction in bacteria is still poorly understood [
14], it can still be utilized given proper optimization [
12]. A 2014 study by Brambilla and colleagues on
Streptococcus mutans, for example, found that their MTT assays produced accurate results that were similar to traditional plate counts following proper execution [
15], in addition to being much more rapid in producing results. One of the factors affecting MTT use on prokaryotes include the incubation period, which has been shown to turn into a colorless derivative upon prolonged incubation [
16]. The effectiveness of its use was demonstrated by the Liao study, successfully utilizing MTT-PMS based reagent to measure
E. coli metabolic activity following proper incubation period optimization [
8]. There is, therefore, potential for new applications in the use of MTT on prokaryotes, given properly implemented methodologies and optimizations.
E. coli cells can be regarded as systems of dehydrogenases, making MTT a potential tool in the measurement of their viability (
Figure 1). A study by Oh and Hong in 2021 found that their MTT assay showed sufficient sensitivity to early growth phase bacterial cells compared to the plate counting method [
17]. Moreover, it was found that MTT reached peak reduction within 15–30 min, and underwent no further reduction after 60 min, further supporting Liao’s procedure, and highlighting MTT’s potential for bacterial rapid screening capabilities in clinical settings. Despite its utility in rapid screening, however, biochemical assays are still problematic in terms of convenience due to the need for high-end equipment and trained personnel.
The advent of paper-based analytical devices provides many opportunities for the development of point-of-care diagnostic tools that require minimal to no resources to achieve their objectives. Highlighting the importance of early intervention for the treatment of UTI, Shih and colleagues utilized a paper-based ELISA for the rapid detection of
E. coli [
18]. Analysis was performed through colorimetric analysis using a smartphone camera. Similarly, Wang and colleagues developed a turntable paper-based ELISA to produce results within 5 h [
19], incorporating Whatman Fusion Paper 5
TM in its design. Both studies capitalized on biochemical assays’ rapid screening potential, along with paper-based diagnostic devices’ convenience, with significant reductions in cost.
A study by Tsao and colleagues in 2020 looked at the feasibility of paper based MTT-PMS strips for point-of-care semen analysis [
20], combining the MTT’s propensity for colorimetric analysis, and paper-based analytical devices’ ease of use and convenience. Using MTT-PMS embedded in a test pad on paper ribbon, Tsao and colleagues utilized the tetrazolium’s reductive property to infer sperm motility. Their rationale was to develop a convenient device that can be used as a cheap, routine screening tool for private, in-home assessment through visual cues.
This study therefore sought to assess the feasibility of paper-based MTT-PMS strips in the rapid screening of bacterial concentration through colorimetric analysis for potential clinical, agricultural, and the environmental applications, among others, in the future. This builds on the already established potential use of MTT strips in point-of-care semen analysis.
4. Discussion
Based on simple colorimetric detection and analysis, there was sufficient evidence to suggest that there is potential for the MTT-PMS strips to be used in distinguishing concentrations of bacteria in a sample. Linear modeling of the relationship between the average standardized greyscale value against the log of bacteria concentration showed a statistical measure of fit (R2) of approximately 98%. This suggests that there was enough evidence to suggest that variations in the average standardized greyscale value can be sufficiently explained by differences in the log of bacteria concentration. Moreover, an F-test of the coefficients of the model was conducted against a null of no model predictive capability and was found to be statistically significant at p < 0.001. This suggests that there was sufficient statistical evidence to suggest a relationship between average standardized grayscale values and the log of bacteria concentration, further supporting the viability of the MTT-PMS strips and their simplistic mode of detection.
Early tests also revealed an optimal incubation period of 20 min (
Figure 6). This is somewhat consistent with a 1995 study by Stowe and colleagues, where it was found that prolonged formazan incubation can result in transformation to a colorless derivative [
16], potentially causing a misinterpretation of results in a colorimetric analysis. This is further supported by the findings of Wang and colleagues in the development of an improved MTT reduction assay for the evaluation of viable
E. coli cells, where rapid formazan crystal formation was found within the first 20 min of incubation, after which the speed of its formation began to deteriorate [
25]. This makes it an optimal period of incubation and hence why it was chosen for the standard procedure.
Limits of detection (LODs) of the MTT-PMS strips were also inferred based on average standardized greyscale value of the strips in sterilized PBS. Calculations based on a multiple of three standard deviations showed that LOD was approximately 2.05 × 10
4 CFU/mL, suggesting that there was sufficient evidence to potentially screen bacteria concentrations of above 2.05 × 10
4 CFU/mL. Although this is not to be confused with accurate quantification, the sufficiently accurate screening capability of such a device can potentially be used in applications where rapid diagnosis is crucial. In the case of asymptomatic bacteriuria, for example, the presence of more than 1 × 10
5 CFU/mL of bacteria in the absence of symptoms of upper urinary tract infections can be classified as such. In the case of water and food safety, in Egypt, for example, it is known that the standard acceptable bacterial count for fresh chilled fish is approximately 10
6 CFU/mL [
26]. At the current device’s LOD, there is also potential for its use in the preliminary elimination of unacceptable produce prior to consumption.
The use of the MTT-PMS strips for this purpose has significant implications. Clinically, one of them being its potential utility in preventing the development of pyelonephritis during pregnancy. As was seen in a previous 1967 study, early clinical management of asymptomatic bacteriuria was shown to be an effective strategy in the prevention of pyelonephritis [
27], which has been found to be detrimental during pregnancy [
5]. However, due to the significant amount of time and skill required for testing, it was also found to be non-cost-effective, further complicating efforts in its prevention [
6]. Since each MTT-PMS strip costs less than 1 USD to make, it has the potential to significantly cut down on costs. Moreover, it also has the potential to ensure that, in combination with clinician’s expertise, only cases that warrant further testing can be referred to more sophisticated and detailed laboratory testing, potentially allowing more scope for early detection, treatment, and prevention of UTI’s. This is a significant improvement to gold-standard bacteria screening and detection procedures, where culturing may require up to 72 h in a laboratory with highly skilled personnel.
Similarly, in terms of water and food safety, there is an industrial need for improvements in rapid detection methods to guarantee the safety of produce for consumers, especially in ready-to-consume cut vegetables, such as leafy greens [
28]. Standard culture methods that aim to detect the contamination of fresh vegetables can render them unfit for consumption even before results are made available. The study by Cavaiuolo and colleagues had a sensitivity of approximately 10
3 CFU/g, but still at a significant cost in time and required a significant amount of laboratory resources and trained personnel to perform [
7]. The use of paper-based MTT-PMS has the potential to cut down on time, with further advantages in terms of convenience and ease of use, albeit with some sacrifice in sensitivity. Nonetheless, its utilization can preliminarily eliminate produce that is potentially unfit for consumption. A quick summary of relevant biochemical analytical tools is listed in
Table 2.
Comparing the MTT-PMS strips with other modes of pathogenic detection, the MTT-PMS strip fared quite well, especially considering the amount of time required to obtain results. At an LOD of approximately 10
4–10
5 CFU/mL, the strips performed comparatively well compared to Liao and colleagues’ MTT-based portable reagent at 10
5–10
6 CFU/mL. This suggests that, other than the portability of both tetrazolium-based analytical detection tools, both devices are able to screen for similar concentrations of bacteria [
8]. Moreover, although the MTT-PMS strips were found to be limited in terms of LOD, compared to Cavaiuolo and colleagues’ indirect ELISA [
7], the short time it takes to perform a test is comparable to the advantages offered by Shih and colleagues’ paper-based ELISA [
18], where its paper-based mode of detection is more similar in technique to the current strips. Similar to Liao and colleagues, the current MTT-PMS strips only require a 20-min period of incubation to produce reliable results (
Figure 6). In fact, prolonged incubation may even result in the formation of a colorless derivative, making colorimetric reading inaccurate [
16]. This further highlights the strips’ advantage in terms of accessibility, convenience, and speed.
It is important to note that the method is still not superior to standard culture methods. The utility of the strips is limited to quantitative screening and does not differentiate between different pathogens, limiting its use to applications where screening is paramount. Moreover, as in the study by Tsao and colleagues, although the strips may not be able to accurately quantify bacteria concentration, they have the potential to estimate an average range based on colorimetric data. Therefore, given their ease of use, as well as their ability to operate with minimal sophisticated equipment, this study has shown that the strips can potentially be utilized as an early, alternative screening tool in clinical, environmental, and agricultural applications, among others. The results of this study has created openings for further studies to investigate the utility of paper-based tetrazolium derivatives in the quantification of other pathogens, for applications in food safety, such as
Listeria monocytogenes as investigated by Cavaiuolo and colleagues’ [
7], for water safety applications, such as Liao and colleagues [
8], or even in general clinical samples, such as urine and other bodily fluids in comparison with standard culture procedures. Whatever the application, convenient and rapid screening of bacteria concentration will not only be beneficial in clinical care, but also in other fields such as agriculture and biotechnology.