Randomized Clinical Trial Demonstrate the Safety Assessment of Dietzia natronolimnaea C79793-74 for Use as a Probiotic in Humans

1. Introduction

Probiotics have been defined as live microorganisms which when administered in sufficient quantities, have the capacity to enhance or restore the balance of the intestinal microbiota, resulting in various health benefits [1]. While the potential applications of probiotics in clinical settings are extensive, it is important to note that the range of clinical uses supported by evidence from rigorous clinical studies is comparatively limited [2].

Dietzia natronolimnaea C79793-74 is a nonpathogenic, non-toxin-producing bacterium that does not form spores. This microorganism belongs to the broader taxonomic group known as Dietzia sp. [3]. Strain and was originally obtained as a single colony isolate. was isolated from fecal material of a paratuberculosis sero- and fecal-positive cow [4].

Johne's disease is a chronic gastrointestinal ailment caused by Mycobacterium avium subspecies paratuberculosis (MAP) in ruminants. Crohn's disease, on the other hand, is a debilitating, chronic, and potentially life-threatening condition that shares significant clinical, pathological, and systemic similarities with Johne's disease. It is worth noting that the role of MAP in human intestinal inflammatory diseases, such as Crohn's disease and ulcerative colitis, remains a subject of debate [5]. There is a possibility that animals afflicted with Johne's disease may serve as a source of MAP infection underlying Crohn's disease in humans [6,7,8]. Moreover, MAP has been implicated in an increasingly long list of granulomatous and autoimmune diseases [9]

Hence, there is a pressing need for treatments targeting MAP in the context of Crohn’s disease. Previous research has suggested that D. natronolimnaea C79793-74 could be a promising probiotic supplement to assist patients suffering from inflammatory intestinal diseases like Crohn's disease [5,10]. Furthermore, the combination of gastric acid tolerance, bile salt tolerance, and resistance to lysozyme makes D. natronolimnaea C79793-74 a potential candidate for probiotic use. Nevertheless, comprehensive safety evaluations are imperative.

The primary objective of this study is to establish, through a safety clinical trial, that D. natronolimnaea C79793-74 can be categorized as a non-pathogenic and non-toxin-producing strain, rendering it suitable for use as a probiotic in humans.

2. Materials and Methods

2.1. Bacterial characterization

2.1.1. Bacterial strain

Dietzia natronolimnaea strain C79793-74 is a single colony isolate of a group of similar bacteria assembled under the taxon Dietzia natronolimnaea [11]. D. natronolimnaea C79793-74 was originally isolated from fecal samples material of a paratuberculosis sero- and fecal-positive cow in River Falls, Wisconsin. The strain is deposited at the American Type Culture Collection (ATCC), USA, under strain designation PTA-4125 with a BSL 1 in biosafety level classification [12,13].

2.1.2. Culture conditions of bacterial strain.

A single colony was used as the inoculum for the seed culture in 10 mL of of Brain-Heat Infusion broth (BHIB) and then incubated under aerobic conditions for 72 h. The seed culture was then diluted 1/10 into a larger volume of BHIB and incubated over a period of 3-5 days. Following this process, the bacterial cell mass is concentrated by centrifugation at 6,000 x g and the resulting wet cell mass was lyophilized and milled into a fine, dry powder. Bulk powder was stored in sealed mylar bags at -20 °C then encapsulated at 5 ± 0.1 billion CFU/capsule.

2.1.3. Genotypic characterization of the organism

Genotypic characterization of Dietzia natronolimnaea C79793-74. was carried out following 16S rRNA analysis and genomic sequencing. The C79793-74 strain was compared with ESB1503 strain.[3]. L. natronolimnaea C79793-74 was sequenced and annotated by EzBiome (www.ezbiocloud.net) using published and proprietary methods. Taxonomic analysis of the strain's genomic sequence was conducted using MiGA [14].

2.1.4. Antimicrobial susceptibility testing

Antimicrobial susceptibility testing (AST) was conducted, and results interpreted in accordance with the guidelines provided by the CLSI M100, 33rd. edition for the Disk Diffusion Method [15]. The following antimicrobials were used to assess the AST profile of D. natronolimnaea strain C79793-74.: ampicillin, vancomycin, gentamicin, kanamycin, streptomycin, erythromycin, clindamycin, tetracycline, and chloramphenicol.

2.1.5. Antimicrobial resistance genes

To identify genes with high identity to previously published antibiotic resistance genes, the assembled genomes for C79793-74 were used to interrogate a curated database of antibiotic resistance genes (CARD) [16]. The database focused on acquired antibiotic resistance genes from the scientific literature and covers both Gram-positive and Gram-negative bacteria including pathogenic species.

2.1.6. Search Against the Virulence Factor Database

The assembled genome of D. natronolimnaea C79793-74 was also evaluated for the presence of known virulence factors, using the VFDB (Virulence Factor Database) [17] (http://www.mgc.ac.cn/VFs/). A total of 32,670 sequences were searched.

2.1.7. Hemolytic activity

Hemolytic activity (HA) was measured by hemoglobin release (HR) as described by Lefevre et al. [18]. Briefly, human blood obtained from healthy volunteers was centrifuged (3,000 x g for 5 min) to isolate the erythrocytes. The suspension of fresh erythrocytes obtained was washed and resuspended in 1mL of buffered phosphate solution (PBS). The concentration of the suspension was adjusted by adding PBS to obtain an absorbance of 0.7 at 490 nm was obtained by adding 1 mL of the standard to 14 mL of distilled water. For the hemolysis test, different concentrations of the compound to be tested were added to the erythrocytes. After 1h of incubation at room temperature, the samples were centrifuge, and the supernatant was added in the wells of a 96-well polystyrene. The supernatant of erythrocytes in PBS1X was used as negative control and supernatant of erythrocytes in distillate water was employed as positive control. Total released hemoglobin was measured at 490 nm using an automatic absorbance microplate reader (BioTek ELx800). The percentage of hemolysis was determined using at 100 % hemolysis the absorbance obtained in presence of water as follow:[19].

2.1.8. Cytotoxicity in Vero cells

Viable cells were quantified by the MTT colorimetric assay, which measures tetrazolium dye 3-(4, 5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide reduction by mitochondrial enzymes.[20]. Briefly, 100 µL of Vero cells were seeded at 105 cells into 96-well culture plates with serum-free Dulbecco's Modified Eagle's Medium (DMEM) (Sigma-Aldrich) and treated with different concentrations of Dietzia natronolimnaea C79793–74 and Control. After 30min incubation at 37ºC and 5% CO₂, 10 µl of MTT was added and the cells were incubated for three hours in similar conditions. Next, the crystals were dissolved with 100 µl DMSO and the absorbance was measured in an ELISA reader (MRX II, Dynex Technologies) at 550 nm with the 630 nm as reference. The % of Cellular Cytotoxicity (CC) was measured as CC % = ((Ac-At)/Ac) x100 where At is the absorbance of Dietzia treated cell and Ac is the absorbance of Control cells (Control are cells treated with the following excipients: calcium phosphate, magnesium stearate and colloidal silica, the excipients contained in bacteria capsule).

2.2. Human safety assessment

2.2.1. Study design

The present randomized, double blind, placebo controlled clinical trial study was conducted in adult, healthy volunteers. The study was designed to evaluate the safety of D. natronolimnaea C79793-74 for use as a probiotic in humans: This trial was conducted following to the Good Clinical Practice protocols as stated in the World Medical Association Declaration of Helsinki [21], and all procedures involving human subjects were approved under the Hermanos Ameijeiras Ethic Committee for Clinical Investigation and The Hermanos Ameijeiras Scientific Council. The D. natronolimnaea C79793-74 formulation was evaluated and approved for it use by the Ethical Committee at the National Institute of Nutrition of Cuba and The Cuba Ministry of Health.

The study enrolled 98 healthy individuals randomly assigned to either the Dietzia cohort or the Placebo group. The Dietzia cohort, consisting of 49 patients receiving the Dietzia test substance, while the Placebo group, consisted of 49 patients who were given a placebo. Table 1 provides an overview of the demographic and other baseline characteristics of the study population. Patients were randomly assigned to treatment groups using EpiData 3.1 software The software generated a list of random numbers for each group, which was used by pharmacy to assign individuals to their respective groups based on their compliance with the inclusion and signature criteria for informed consent. To ensure blinding, the products were dispensed in identical packaging.

2.2.2. Power and sample size consideration

The minimum required sample size for the study was estimated using a two-sided alpha of 0.05, a 95% confidence level, a standardized mean difference of 0.75, and a test power of 80%.

2.2.3. Subjects

The study included healthy individuals, both men and women, aged over 18 years, without distinction of sex or skin color, and with hematological, clinical chemistry, and hemodynamic parameters within normal ranges. Before participating in the study, all volunteers provided signed, written informed consent. Exclusion criteria included individuals suffering from any comorbidity or showing alterations in their hematological, clinical, or hemodynamic parameters.

A total of 98 healthy volunteers were randomly allocated to either the Dietzia natronolimnaea (Dietzia) or Placebo groups, with 49 individuals in each group. The assignment to treatment groups was randomized using the Epidemiological Analysis from Tabulated Data (EpiData 3.1) software (Figure 1).

2.2.4. Trial Intervention

The study spanned a total duration of 8 weeks with RPCEC registry number RPCEC00000421. All participants were instructed to orally consume one capsule daily while fasting, 40 minutes before their breakfast. They were assigned to either the D. natronolimnaea C79793-74 (Dietzia) test substance or a Placebo. Sample packages, each containing 60 capsules, were distributed over the 8-week study period. During this period, subjects in the treated group (n=50) ingested one capsule of Dietzia natronolimnaea C79793–74, which contained 5 x 109 bacteria per capsule mixed with the excipients consisting of calcium phosphate, magnesium stearate, and colloidal silica. Participants in the Placebo group (n=50) were provided with capsules containing only the excipient mix.

Hemodynamic parameters, encompassing arterial pressure and heart rate, were assessed on the first day of the study, prior to probiotic consumption, and at the conclusion of the study, at week 8. Additionally, a health questionnaire was administered at the baseline day preceding the commencement of the trials (week 1) and at the end of the study (week 8). (Cuestionario de Salud SF-36 (version 2)) Vilagut [23].

2.2.5. Sample Collection, Processing, and Data Management

Participants underwent sample collection, supplement delivery, and clinical evaluation at the beginning (week 1) and the end of the study (week 8). Samples were collected by venipuncture, then properly identified with the inclusion number, processed, and aliquoted within one hour for storage and future use. All records were maintained in a dedicated database. Access to these records was limited to study and clinical staff responsible for patient care. The HHA was responsible for managing the security of the information technology infrastructure.

2.3. Safety assessment

2.3.1. Clinical Determinations

Hematology parameters for obtaining standard complete blood count data were assessed through the utilization of a hematologic complex autoanalyzer XN-350 (Roche Diagnostics). This analysis was performed in strict adherence to the manufacturer's guidelines, with blood samples collected in K3 EDTA tubes at the baseline (one week before the study commencement) and at the study's conclusion (week 8).

For the evaluation of clinical chemistry parameters, a Cobas 600 modular immunochemical autoanalyzer (Roche Diagnostics) was employed. The analysis was performed on serum samples, following the manufacturer's recommended protocols.

2.3.2. Occurrence of adverse events determination

The occurrence of adverse events was documented by the investigators in the case report forms for each subject adhering to the framework outlined by Lefvre et al. [18]. The relationship between each adverse event and the subject's involvement in the study was assessed and categorized as improbable, possible, probable, or definite. Additionally, the investigators ranked the severity of each adverse event as mild (with no impediment to daily activities), moderate (resulting in partial limitations to daily activities), or severe (rendering daily activities unattainable).

2.3.3. Statistical Analyses

All clinical data collected were analyzed using Statistical Package for Social Sciences (SPSS) version 23.0. Descriptive statistics were used to characterize the samples. Qualitative variables were summarized in absolute numbers and percentages, while quantitative variables were summarized as mean and standard deviation (SD) for normally distributed data. To compare differences between groups according to qualitative variables, the chi-square test (χ2) or Fisher's exact test was used, while the Student’s t-test was used for age and Body Mass Index (BMI (quantitative variable).

The number of subjects with at least one adverse effect and the association of adverse events with study participation, were compared between the Dietzia and placebo groups using the Fisher's exact test. The Kappa Test was applied to evaluate the congruence in the responses to the health questionary (SF-36) in each group, at both time periods (before-after).

3. Results

3.1. Species and strain identification

Dietzia natronolimnaea strain C79793-74 was identified using 16s rRNA gene as the phylogenetic marker. D. natronolimnaea strain C79793-74 can be distinguished from other closely related species of the genus Dietzia based on 16S rRNA sequence analysis. D. natronolimnaea strain C79793-74 showed closest homology at 97.74% with 100% coverage to D. natronolimnaea strain IL4-1.

Similarly, Analysis of the strain identified as C79793-74 using whole genome sequences to interrogate the NCBI database and using the BLASTN algorithm [24] revealed that Dietzia natronolimnaea C79793-74 is most closely related to D. natronolimnaea as reported by Yumoto et al. [25].

The MiGA analysis [26] revealed that strain C79793-74 is closest (97.77%) to the sequence of the strain of Dietzia natronolimnaea strain ILA-1 (DSM 44820 – NCBI tax ID 139021). A total of 67 contigs, representing 100% of the genome of 3,029,571 base pairs were analyzed, with very low level of contamination level (3.8%) and excellent quality (81%). The G+C content was determined to be 46.6231% with a G-C skew of 2.1581% and an A-T skew of 0.2951% Analysis of the assembled genome revealed a total of 2,897 predicted proteins with an average length of 297.3783 amino acids. The genome has a coding density of 85.3096%. The G+C observed agreed with that reported by Yumoto et al. [3] for the type-strain ILA-1 (69.7 mol%)

3.2. Antimicrobial resistance and Virulence factors

The results, reported in Table 2, indicate that Dietzia natronolimnaea strain C79793-74. Based on the reference strain results and cited susceptibility breakpoints the Dietzia natronolimnaea, strain C79793-74 is fully susceptible to all the antibiotics tested, which are class representatives as follows: Ampicillin (beta-lactam class); Chloramphenicol (phenicol class); Clindamycin (lincosamide class); Erythromycin (macrolide class); Gentamicin and Kanamycin (aminoglycoside class); Streptomycin (Streptomycin class); tetracycline (tetracycline class including doxycycline and minocycline); and Vancomycin (glycopeptide class).

Genomic analysis using the CARD database detected a 59.63% identity match to the Mycobacterium tuberculosis folC. Point mutations in the dihydrofolate synthetase folC gene, chromosomally located, [27], and has been shown to confer resistance to p-aminosalicylic acid or other aminosalicylates [28].

The analysis of Virulence Factor Database in D. natronolimnaea C79793-74, showed that only two sequences had significant alignments. These genes were located on the chromosome and identified as follows: VFG052054 (embC) and VFG023381 (eccD3). There was no evidence of mobile elements in the flanking regions of the above-mentioned antimicrobial resistance gene.

3.3. Hemolytic activity and cytotoxicity

The hemolytic activity (HA) of D. natronolimnaea C79793-74 was concentration dependent as shown in Figure 2. The maximum concentration (400mg) showed the 100% of HA similar to that of the positive control. No appreciable HA was detected at concentration less than 128 mg/mL.

The Cellular Cytotoxicity of D. natronolimnaea C79793-74 as measured in Vero cells showed a high % cytotoxicity at concentrations at and above 40 mg/mL (90.1%), however this effect decreases considerably at 10 mg/ml and less. (Figure 3B)

3.4. Clinical determinations

Clinical and hematological determinations, as well as hemodynamic parameters showed normal ranges in all individuals, and no differences were found between the probiotic Dietzia and Placebo cohorts (Table 2).

Table 2. Clinical, hematological determinations and hemodynamic parameters.

Table 2. Clinical, hematological determinations and hemodynamic parameters.

3.5. Occurrence of Adverse Effect determination

The study involved a total of 98 individuals, 49 in each study group. The majority of individuals, 88.8% (n=87) did not show any adverse effects (AE) (Table 3). Of these, 83.7% belonged to the Dietzia cohort (n=41) and 93.9% to the Placebo cohort (n=46). No significant differences were observed between treated group and placebo according to the development of AE (p= 0.199) (Table 3).

Three of the cases with AE belonged to the Placebo group. Two of them stated that they had looser stools than usual. The AE in the third case (edema) coincides with the debut of a dengue infection [29], so probably it could be associate to this arbovirus.

Of the cases that received the Dietzia probiotic capsule, 8 individuals (16.3%) manifested some AE. The AE described were gastrointestinal pain or discomfort (n=5), gas (n=10), anxiety, depression (n= 2), bruising (n=1), dizziness and nausea (n=4), headache (n=2), pain followed by capsule consumption (n=4), insomnia (n=2) (Table 4).

The research comprised 67 females and 31 males. Most adverse events (AE) were observed in females (7 out of 67), in contrast to males (4 out of 31). Among the females in the Placebo group, one person (7%) experienced moderate-intensity AE, starting with a dengue infection, while the remaining individuals reported no significant impact on their daily activities, indicating mild-intensity effects. Furthermore, the effect diminished over the course of the treatment period.

3.6. Health questionnaire analysis

The survey questions related to the physical and emotional health status of the study subjects were analyzed (SF-36, Questions 1, 6, 7 and 11). In both groups, the behavior of the answers to these questions was very similar. Both the placebo group and the treatment group maintained similar responses at both times (Kappa ~1, p=0.000). The significant p values represent that the agreement between the responses of the two moments is high in both evaluated groups.

4. Discussion

Dietzia natronolimnaea C79793-74 is a promising probiotic bacterium with various potential applications for Crohn's disease in humans [5,30]. However, before considering its use as a probiotic in humans, it is essential to conduct a thorough safety evaluation [31]. This safety assessment encompasses in vitro and in vivo parameters, providing a comprehensive evaluation of the strain’s safety.

Morphological and cultural techniques confirmed that the strain D. natronolimnaea C79793-74 represented a pure culture exhibiting characteristics akin to those of other members within the Dietzia genus. [32]. The colonies of different Dietzia strains are characterized by their small size, circular shape, and convex form. [33]. This is in concordance with D. natronolimnaea C79793-74 and confirm that this bacterium is a nonpathogenic, non-toxicogenic non-spore spore-forming bacterium. [3].

The genotypic characterization of Dietzia natronolimnaea C79793-74 was made based on 16s RNA [33], whole genome analysis, including using the Microbial Genomes Atlas (MiGA) [14] for comparison, classification, and analysis of the genome of D. natronolimnaea C79793-74, to assess its diversity, evolutionary relationships, and functional potential. Both analytic methods were in concordance to strain C79793-74 and is closest to the sequence of the strain of Dietzia natronolimnaea. strain ILA-1 (DSM 44820 – NCBI tax ID 139021). This results also was confirmed by the determination of mol G+C%. [14,34] The homology-based bioinformatics framework MyTaxa [35] also showed that de strain C79793-74 falls well within the expected taxonomic affiliation for the genus Dietzia and in concordance with that of other Dietzia natronolimnaea strains.

The safety assessment for a potential probiotic strain must consider its potential to transfer antimicrobial resistance to other bacteria or to express virulence or toxin genes [31]. As an integral part of this assessment, the genome of D. natronolimnaea C79793-74 was used to interrogate the CARD [36] database for the presence of any genetic elements in its genome that showed Perfect or Strict matches to antimicrobial genes therein.

The analysis of the D. natronolimnaea C79793-74 genome revealed a 59.63% identity match to the Mycobacterium tuberculosis folC. Point mutations in the dihydrofolate synthetase folC gene shown clinically to confer resistance to p-aminosalicylic acid (PAS) or other amino salicylates. Mutations in folC C inhibit bioactivation of PAS and thus confer resistance [28]. This gene is chromosomally located [27] and it is unlikely to be transferred to other bacteria. While chromosomal DNA segments can be transferred via transformation and transduction, this transfer is inefficient and random [37].

Phenotypic expression of antimicrobial resistance genes was also evaluated using the disk diffusion test for the presence of antimicrobial resistance traits as recommended by CLSI M100 guidelines ([15]. The results of this evaluation revealed no phenotypic resistance traits against the antimicrobials tested, which represented a broad spectrum of antimicrobial classes. These results were congruent with those obtained from the genome analysis using the CARD database. Based on these observations it is safe to state that based on the results reported herein, that D. natronolimnaea C79793-74 poses little or no risk of transmission of antimicrobial resistance and as such safe for use in food and supplements for humans [38].

The search for virulence genes using the VFDB within the D. natronolimnaea C79793-74 genome revealed the presence of two important genes: embC, which involved in the biosynthesis of mycolic acids, and eccD3, a component of the ESX-3 secretion system [39,40]. These genes are of significance as they contribute to the bacterium's cell wall integrity, protection against environmental stresses, and potential interactions with the host [41,42,43]. On the other hand, as there is no evidence of mobile elements in the flanking regions of the above-mentioned antimicrobial resistance gene, D. natronolimnaea. C79793-74 does not contain any sequences/genes in the genome that are risk associated, thus confirming the safety of the strain through the genome-based approach. [43,44].

The cytotoxicity of probiotic strains is a distinctive attribute. Most probiotic strains either demonstrate cytotoxic effects or do not, based on their characteristic targeted mode of action as a probiotic strain [45,46,47,48]. This property is particularly notable in probiotics like Bacillus subtilis and B. indicus, [49], and L. casei strains [50], all of which hold promise as candidates for colorectal cancer management. This targeted cytotoxic effect seen in goats and cattle after 60-day of D. natronolimnaea C797793-74 treatment for paratuberculosis could explain the therapeutic benefit observed after ingestion of D. natronolimnaea [51].

The results illustrated in Figure 3 indicate that the cytotoxicity of D. natronolimnaea C79793-74 extract on both Vero cells and erythrocytes, is dose dependent, with notable cytotoxicity at 400 mg/mL on erythrocytes and at 40 mg/mL in Vero cells. These cytotoxic concentrations exceed the dose of approximately 15 mg daily (~ 5 billion CFUs) used in this study. These results support the hypothesis that at the recommended levels, D. natronolimnaea C79793-74 is safe from cytotoxic effects. This observation is supported by the lack of moderate or serious adverse events reported during this study (Table 4).

It is generally recognized that microorganisms used as nutritional supplements must be evaluated for safety in a controlled clinical trial such the one reported here. Even though Dietzia is generally regarded as nonpathogenic and a safety level 1 organism, certain species of this genus have been identified as a potential human pathogen in immunocompetent individuals and immunocompromised patients [30,52]. None of these reports, however, identify AE associated with D. natronolimnaea. However, most reports recognize the useful application of Dietzia in many industries, especially the medical, chemical and food industries.[5,30,53,54]. Taking in to account the potential role of Dietzia spp. as opportunistic pathogens, this clinical trial was designed to evaluate the safety of daily consumption of D. natronolimnaea. C79793–74 (5 x10⁹ CFU/day – 15 mg dry cell weight) for 60 days [55,56].

The demographic characteristic of the volunteers, the duration of study and the compliance to product consumption were similar for Dietzia and Placebo groups. The clinical and hematological determinations reported in Table 2 indicated that all clinical and hematological paraments remained within the generally accepted normal range in both cohorts throughout the study. These results confirmed the healthy status of all participants and thus, supports the hypothesis that D. natronolimnaea C79793-74 is safe for human consumption at the recommended level, at least in immunocompetent adults and could be used as a safe probiotic supplement.

Lack of understanding regarding the mechanism of action of probiotic microbes has been recognized as a hindrance to ensuring the safety of their applications [57]. However, based on the similarities of Johne´s Disease in ruminants and Crohn´s Disease in humans, the role of MAP in the pathogenesis of both of these inflammatory diseases, the inhibition of growth of MAP by Dietzia under specific culture condition and the safe used of Dietzia of cattle [5,51,53,58], provide supportive evidence for the safe and effective use of Dietzia in the treatment of Crohn´s and other humans inflammatory bowel diseases (IBD) [30,54,59,60]. To date, there is insufficient evidence to demonstrate that the administration of probiotics existing in the market can be helpful in maintaining remission in patients with IBD.[31,57].

The principally reported serious AE of probiotics are systemic infections, gastrointestinal side effects, skin complications, inflammation of endocardium, gene transfer from probiotics to the normal microbiota , metabolic harmful impacts of probiotics, and immune system stimulation [57].

The analysis of adverse events (AE) and their intensity in this study revealed that two individuals who consumed the probiotic capsules experienced gastrointestinal discomfort, gas, and pain during weeks 1 and week 3. Although they reported a decrease in the intensity of these symptoms from week 1 to week 3, they chose to discontinue the study. On the other hand, the remaining individuals in the Dietzia cohort reporting AE (Table 4) described their AE as mild and indicated that the symptoms improved within a few days. Furthermore, they reported benefits from taking the test substance, including the regulation of daily stool frequency with softer stools, improvements in low back pain, and the absence of migraines. All participants reported feeling better after receiving treatment.

The analyses conducted using health surveys administered before and after capsule consumption indicated that the overall health status of the Dietzia group was not adversely affected as compared to the Placebo group. This is consistent with the few adverse effects that were observed.

5. Conclusions

This study marks the first clinical trial conducted to assess the safety and security of Dietzia species, specifically Dietzia natronolimnaea C79793–74. Our findings demonstrate that the consumption of D. natronolimnaea C79793–74 was well-tolerated and safe for nearly all the volunteer participants involved in the study. Importantly, there were no AE associated with the consumption of D. natronolimnaea C79793–74 when compared to the placebo group. Based on the sum total of all the data obtained in this study it can be inferred that D. natronolimnaea strain C79793-74 is safe as a nutritional supplement for humans.