Identification of Volatile Organic Compounds Emitted by Two Beneficial Endophytic Pseudomonas Strains from Olive Roots

The production of volatile organic compounds (VOCs) represents a promising strategy of plant-beneficial bacteria to control soil-borne phytopathogens. Pseudomonas sp. PICF6 and Pseudomonas simiae PICF7 are two indigenous inhabitants of olive roots displaying effective biological control against Verticillium dahliae. Additionally, strain PICF7 is able to promote the growth of barley and Arabidopsis thaliana, VOCs being involved in the growth of the latter species. In this study, the antagonistic capacity of these endophytic bacteria against relevant phytopathogens (Verticillium spp., Rhizoctonia solani, Sclerotinia sclerotiorum and Fusarium oxysporum f.sp. lycopersici) was assessed. Under in vitro conditions, PICF6 and PICF7 were only able to antagonize representative isolates of V. dahliae and V. longisporum. Remarkably, both strains produced an impressive portfolio of up to twenty VOCs, that included compounds with reported antifungal (e.g., 1-undecene, (methyldisulfanyl) methane and 1-decene) or plant growth promoting (e.g., tridecane, 1-decene) activities. Moreover, their volatilomes differed strongly in the absence and presence of V. dahliae. For example, when co incubated with the defoliating pathotype of V. dahliae, the antifungal compound 4-methyl-2,6-bis(2-methyl-2-propanyl)phenol was produced. Results suggest that volatiles emitted by these endophytes may differ in their modes of action, and that potential benefits for the host needs further investigation in planta.


Introduction
Soil-borne phytopathogens constitute a major threat affecting crops around the world, compromising global food production and security. Some of them can survive in soils for many years in the absence of host plants due to different resistance structures (i.e., microsclerotia, sclerotia, chlamydospores or oospores), hindering their effective control [1]. Examples of important soil-borne fungi causing serious yield losses in a broad crop range are some species of the genus Verticillium [2,3], Fusarium oxysporum (different formae speciales) [4,5], Rhizoctonia solani Kühn [6,7] or Sclerotinia sclerotiorum (Lib.) de Bary [8]. For instance, to name an example of particular interest in our study, Verticillium wilt (Verticillium dahliae Kleb.) is considered one of the most threatening biotic constrains for olive (Olea europaea L.) cultivation and the main limiting factor for olive oil production [9]. These phytopathogenic fungi were traditionally managed by crop rotations and soil treatments.

Assessment of In Vitro Antagonism against Selected Fungal Phytopathogens
Results from in vitro antagonism tests showed that Pseudomonas sp. PICF6 and P. simiae PICF7 only inhibited the growth of Verticillium longisporum ELV25 and V. dahliae V937I (Table 1 and Supplementary Figure S1). In contrast, Paenibacillus polymyxa PIC73, another beneficial olive rhizobacteria used in this study for comparative purposes due to its broad antagonist activity [24], effectively inhibited S. sclerotiorum, R. solani and V. longisporum ELV25 in both assayed media (Table 1 and Supplementary Figure S1). The only exception was F. oxysporum f. sp. lycopersici Fol 007 that was not inhibited in NA medium ( Table 1).

Elucidation of the Volatilomes of Strains PICF6 and PICF7
Analysis by Headspace Solid Phase Microextraction (HS-SPME) Gas Chromatography-Mass Spectrometry (GC-MS) of VOCs profiles of Pseudomonas sp. PICF6 and P. simiae PICF7 cultivated alone or in the presence of V. dahliae V937I, as well as the VOCs profile of this representative of the defoliating (highly-virulent) pathotype causing severe VWO, indicated that both the endohytic bacteria and the pathogen are able to produce diverse compounds (Table 2 and Supplementary Figure S2).
On the one hand, four VOCs, namely 2-methyl-1-propanol, 3-methyl-1-butanol, 2methyl-1-butanol and 2-phenylethanol were exclusively detected in the VOC profile of V. dahliae V937I. On the other hand, several compounds were emitted by the endophytic BCAs here studied and their production varied depending on the experimental conditions (i.e., presence/absence of V. dahliae). Indeed, fourteen compounds were detected when Pseudomonas sp. PICF6 was cultivated alone. However, in the presence of the pathogen, 20 compounds were detected for this olive endophyte, 13 of them being produced in both conditions ( Table 2). Some of them (e.g., dimethyltrisulfane, tridecane, 1-decene, 1,10-undecadiene, etc.) have been earlier described in the literature for their antimicrobial activity or for their involvement in plant growth promotion (Table 2). For P. simiae PICF7, 15 different VOCs were identified. Twelve of these compounds were also produced when this BCA was incubated in the presence of V. dahliae V937I. However, other compounds such as bis(methylsulfanyl)methane, 4-methyl-2-pentanone and 2-decyloxiranese (produced by PICF7 but not by PICF6) were identified only when the bacterium was incubated alone, while 4-methyl-2,6-bis(2-methyl-2-propanyl)phenol was identified when PICF7 was incubated in the presence of isolate V937I (Table 2). Results showed that strains PICF6 and PICF7 shared 12 VOCs when they were incubated alone. However, in the presence of V. dahliae V937I, only 11 VOCs were emitted. 4-methyl-2-pentanone was produced by PICF7 but not by PICF6, regardless of whether or not the latter BCA was incubated alone or in the presence of V. dahliae V937I. In addition, bis(methylsulfanyl)methane and 2-decyloxirane were produced by PICF6, but only in the absence of the pathogen. 2,6,11-trimethyldodecane and methyl thiocyanate were exclusively produced by strain PICF6, independently of the absence or presence of the pathogen. 1-tridecyne, 2-undecanone (antifungal activity), 2-undecanol (antifungal and nematicidal activity), 2-nonanol (nematicidal activity) and 10-methyl-1-undecene were only identified when strain PICF6 was incubated with V. dahliae V937I ( Table 2). Interestingly, tridecane (a compound related to plant growth promotion), (3Z)-3-dodecene and 2,5-dimethylpyrazine (antifungal activity) were produced by PICF6 and PICF7 only when they were incubated alone. However, these compounds were only detected for strain PICF6 when incubated with the pathogen. Finally, 4-methyl-2,6-bis (2-methyl-2-propanyl)phenol (antifungal activity) and 3,7-dimethyl-1-octene were only detected when each BCA was grown in the presence of V937I (Table 2).

Evaluation of the Antagonistic Effect of VOCs Emitted by Pseudomonas sp. PICF6 and Pseudomonas simiae PICF7 against Verticillium dahliae
The Two Clamp VOCs Assay (TCVA) performed revealed that bacterial volatiles were not involved in the observed in vitro antagonistic effect of strains PICF6 and PICF7 against the defoliating pathotype of V. dahliae. Indeed, V. dahliae colonies confronted with these root endophytes showed a similar size to that scored for control plates. Statistical analysis showed no significant differences among treatments, either on potato dextrose agar (PDA) or nutrient agar (NA) culturing media (Table 3).

Discussion
A relevant outcome of this study was to demonstrate that the two selected endophytic Pseudomonas strains from olive roots can produce an impressive portfolio of VOCs including those with antifungal, nematicidal and plant growth promoting effects. In addition, under in vitro experimental conditions, PICF6 and PICF7 were only able to inhibit the growth of V. dahliae V937I and V. longisporum ELV25 to some extent. Nevertheless, their effectiveness as true BCA against V. longisporum will need further in planta confirmation, in contrast to the abundant information available regarding biocontrol of VWO exerted by these strains [28,30,32,35]. This result suggested that in vitro antagonism of both olive root endophytes was specific and effective only against representatives of Verticillium spp.
Volatile compounds released by beneficial rhizobacteria have been identified as a mechanism to antagonize soil-borne pathogens without physical contact between the BCA and its target [42,48]. Additionally, some VOCs produced by microorganisms are also able to stimulate the plant's growth and to induce systemic disease resistance ( [65], and references therein). In the present study, we characterized for the first time the volatilomes of the olive root endophytes PICF6 and PICF7. Many of the VOCs produced by these strains have been earlier described either for their antifungal activity or the capacity to promote plant growth. The use of these natural substances produced at large scale could be a promising alternative to the traditional use of synthetic fungicides, thereby contributing to more sustainable strategies for the control of phytopathogens [48]. For instance, direct application of some of these compounds (e.g., S-methyl ethanethioate, (methyldisulfanyl)methane, dimethyltrisulfane and 1-undecene), which are produced by PICF6 and PICF7, was earlier proven to be effective against Alternaria alternata, Botrytis cinerea, Cochliobolus heterostrophus, Phytophthora infestans, Ralstonia solanacearum or R. solani [47,54,55,60,66,67]. Moreover, (methyldisulfanyl)methane (also known as dimethyl disulfide) elicited a protective response in tobacco and corn plants against B. cinerea and C. heterostrophus under greenhouse conditions [55], and was able to promote growth of A. thaliana [47]. Remarkably, 4-methyl-2,6-bis(2-methyl-2-propanyl) phenol (also known as butylated hydroxytoluene) was detected in the olive rhizobacteria tested here, but only when they were co-incubated with V. dahliae. Recently, it has been shown that this compound, also produced by P. polymyxa CF05, presented a strong inhibitory effect against the pathogenic fungus Rhizopus stolonifera [61]. It is worth mentioning that the emission of different compounds when a BCA and a pathogen are co-incubated may be related to species-specific responses when both microorganisms share the same (micro)habitat [68]. The implications of these pathogen-induced alterations on the olive rhizobacteria volatilomes deserve further in-depth analysis.
Concerning VOCs that were shown to be specifically produced by strain PICF6, four compounds (2-undecanone, methyl thiocyanate, 2-undecanol and 2-nonanol) were detected in the presence of V. dahliae. Among them, 2-undecanone might be of interest because of its antifungal activity. Indeed, the volatilomes of different strains of Burkholderia ambifaria showed the presence of 2-undecanone. In vitro experiments demonstrated that high concentrations of this compound affect the growth of A. alternata and R. solani when pure 2-undecanone was used [47]. Similarly, methyl thiocyanate produced by Pseudomonas donghuensis has been reported to be involved, among other VOCs, in the strong antimicrobial activity exerted by this bacterium against the fungal pathogens Fusarium culmorum PV, R. solani and V. dahliae JR, and the oomycete Pythium ultimum P17 [54]. Mycelial growth of V. dahliae and F. oxysporum was inhibited by 2-undecanol produced by P. polymyxa KM2501-1 or Bacillus velezensis CT32 which is also one of the most active compounds, along with 2-nonanol, against the pathogenic nematode Meloidogyne incognita [63,64].
Several VOCs (i.e., tridecane, 2,5-dimethylpyrazine, 1-decene or 2-decyloxirane) produced by P. simiae PICF7 have been earlier reported to display antimicrobial activity against different phytopathogens (e.g., Pseudomonas syringae pv. maculicola ES4326, Penicillium italicum, Sclerotinia minor, Pythium ultimum, R. solani or B. cinerea) [51,57,58]. Despite the fact that different compounds that are potentially implicated in plant pathogen control were identified in the volatilomes of strains PICF6 and PICF7, the involvement of VOCs produced by these root endophytes in the antagonism towards V. dahliae could not be proven by the implemented Two Clamp VOCs Assay (Table 3). We thus conclude that growth inhibition of Verticillium spp. must be a consequence of bacterial metabolites that diffuse through the medium (Table 1 and Supplementary Figure S1), instead of bioactive VOCs. However, some relevant aspects need to be considered that may influence/alter VOCs emission by the endophytes tested here. For example, Zhang et al. [50] showed that the antifungal action of volatiles emitted by P. chlororaphis subsp. aureofaciens SPS-41 against Ceratocystis fimbriata was strongly influenced by the initial bacteria concentration. These authors evaluated the effect of different inoculation strategies and concentrations of strain SPS-41 on the antifungal activity of the VOCs towards the pathogen C. fimbriata which causes black rot disease in sweet potato tuber roots. Their study revealed that the antifungal activity of the VOCs was augmented after the inoculum concentration and the inoculation volume of strain SPS-41 were increased [50]. Therefore, we cannot completely rule out that the observed lack of inhibition towards V. dahliae by PICF6 and PICF7 volatilomes could be due to insufficient bacterial biomass needed to produce inhibitory amounts of a specific VOCs. It would thus be interesting to test some of these VOCs individually and at a higher concentration against V. dahliae. Besides, different studies have shown that the production of certain VOCs is highly dependent on the culturing medium, thereby resulting in the characterization of an unique volatilome produced under specific growing conditions [69,70]. This may have important consequences for their activity in terms of pathogen inhibition and/or plant growth promotion. For instance, significant changes in VOCs-mediated pathogen inhibition by Lysobacter spp. due to the culturing media used have been reported. VOCs emitted by Lysobacter antibioticus, L. capsici, L. enzymogenes and L. gummosus grown on NA inhibited the mycelial growth of Phytophthora infestans. Conversely, when PDA was used, the VOCs produced by these Lysobacter spp. did not affect the growth of the oomycete [71]. Therefore, it would be interesting to explore whether the lack of inhibitory effect of PICF6 and PICF7 against V. dahliae through VOCs can be overcome when the olive rhizobacteria are grown in culturing media other than the ones utilized in our study.
Regarding the potential involvement of VOCs produced by PICF6 and PICF7 in plant growth promotion, 1-decene, a compound elsewhere reported to increase the fresh weight of A. thaliana [59], was found in the volatilomes of both strains (Table 2). Interestingly, Desrut et al. [36] have recently reported the ability to promote the growth of A. thaliana Plants 2022, 11, 318 7 of 14 seedlings by volatiles (not determined) emitted by strain PICF7. As mentioned above for the case of pathogen inhibition, attention should be called here since results may also vary depending on the culturing medium used. In the latter study, Murashige and Skoog (MS) medium was used. However, Blom et al. [69] did not observe growth promotion of A. thaliana by P. chlororaphis or Pseudomonas putida ISOf through the action of volatiles when MS medium was employed. In contrast, plant growth was enhanced when Luria-Bertani (LB) and Methyl Red Vogues Proskauer (MR-VP) were used, media that favored the production of the volatile butanediol. Whether 1-decene is produced by strain PICF7 in MS medium (as here reported for NA and PDA media), and whether this compound is the responsible of the growth of A. thaliana seedlings [36] remains to be elucidated.
In summary, results here reported confirmed that Pseudomonas sp. PICF6 and P. simiae PICF7 only antagonized Verticillium spp. suggesting that the mechanisms involved in in vitro antagonism of strains PICF6 and PICF7 are specific to a certain degree, or at least more effective, against representatives of this genus. Moreover, the characterization of the volatilomes of strains PICF6 and PICF7 allowed the identification of several compounds with known antimicrobial activity against different phytopathogens. However, the TCVA experiments indicated that none of the bacterial strains were able to inhibit the growth of V. dahliae by the action of volatiles, at least under our experimental conditions. Nevertheless, it must be stressed that the TCVA shows the effect of the total volatilome of bacterial strains and does not dissect the effect of individual compounds. From an agro-biotechnological point of view, and considering the antecedents available in the literature, the potential inhibitory effect against Verticillium spp. of specific compounds detected in the volatilomes of these beneficial rhizobacteria deserves further in-depth analysis.

Microorganisms and Growth Conditions
Olive root endophytic bacteria and fungal pathogens used in this study, including main features and references/source, are compiled in Table 4. Starting cultures of Pseudomonas sp. PICF6, P. simiae PICF7 and P. polymyxa PIC73 (Table 4), which belong to the culture collection of the Laboratory of Plant-Microorganism Interactions, Crop Protection Department, Institute for Sustainable Agriculture (IAS, Córdoba, Spain), were grown as described by Montes-Osuna et al. [35]. In all cases, inocula were spectrophotometrically (A600 nm) adjusted at 1·10 8 cfu/mL. Fungi were previously grown at 25 • C in the dark in PDA medium (Oxoid, Basingstoke, UK).

In Vitro Antagonism Assays
Pseudomonas sp. PICF6 and P. simiae PICF7 were tested against several relevant soilborne fungal pathogens (Table 4). In addition, P. polymyxa PIC73 (Table 4) was included in the assays as reference due to its known broad-spectrum antagonistic activity against different plant pathogens [24]. Mycelial plugs (3-mm diameter) of each phytopathogen were obtained from 7-day-old colonies grown on PDA and placed in the center of Petri dishes (9 cm of diameter) with PDA or NA (Oxoid, Basingstoke, UK) media. Subsequently, four equidistant (2.5 cm from the center of the plate) 10 µL-drops of overnight cultures of each tested bacteria were inoculated around each pathogen. Additionally, Petri dishes inoculated only with mycelial plugs of each phytopathogen were used as controls. Plates were incubated at 25 • C until the pathogen covered the distance between microorganisms in the control plates (approximately 4 days for R. solani and S. sclerotiorum, 6 days for F. oxysporum f. sp. lycopersici Fol 007 and 14 days for V. longisporum ELV25 and V. dahliae V937I). The percentage of pathogen growth inhibition (relative inhibition index, PI) was calculated according to Gómez-Lama Cabanás et al. [25]. Experiments were performed twice with three biological replicates per each interaction and used medium.

Identification of the Volatilomes of Strains PICF6 and PICF7
The volatilomes of the olive root endophytes Pseudomonas sp. PICF6 and P. simiae PICF7 were identified by HS-SPME GC-MS. Moreover, VOCs produced by these bacterial strains in the presence of V. dahliae V937I (co-incubated with the fungus in separated vials) were also determined to assess potential differences due to the presence of the target pathogen. In the latter case, and in order to discard possible compounds produced by V. dahliae V937I in the dual cultures, VOCs exclusively emitted by this fungal isolate were examined separately and used as control. Mycelial plugs (3 mm diameter) of V. dahliae V937I were placed in headspace vials (20 mL; 75.5 × 22.5 mm; Chromtech, Idstein, Germany) previously filled with 8 mL of PDA medium ( Figure 1A). Bacterial isolates were streaked out in vials containing NA medium in parallel lines to assure equal distribution ( Figure 1B). Vials with the BCA were connected to vials with the pathogen by the top of the container and sealed in this area with parafilm ( Figure 1C). Three replicated vials were used for each BCA/pathogen combination, BCA or pathogen sample. In order to detect compounds that exclusively originated from the culturing media, vials filled only with PDA or NA were analyzed under the same conditions and used as controls. Vials were incubated at 25 • C for 5 days. Separation and detection of VOCs were performed on a system combining a GC 7890A with a quadrupol MS 5975C (Agilent Technologies GmbH, Waldbronn, Germany) as described by Mülner et al. [42]. For identification of microbial VOCs, the NIST MS Search 2.2 included in the Software-Package of the NIST 2014 database was used. Further verification was done by calculating the Kovats index (KI) and comparing it to database entries in the online database Chemspider (http://www.chemspider.com/, accessed on 17 February 2021).
Vials were incubated at 25 °C for 5 days. Separation and detection of VOCs were per-formed on a system combining a GC 7890A with a quadrupol MS 5975C (Agilent Technologies GmbH, Waldbronn, Germany) as described by Mülner et. al. [42]. For identification of microbial VOCs, the NIST MS Search 2.2 included in the Software-Package of the NIST 2014 database was used. Further verification was done by calculating the Kovats index (KI) and comparing it to database entries in the online database Chemspider (http://www.chemspider.com/, accessed on 17 February 2021).

Effect of Bacterial Volatiles on Mycelial Growth of Verticillium dahliae V937I
The ability of Pseudomonas sp. PICF6 and P. simiae PICF7 to inhibit the mycelial growth of V. dahliae V937I was examined by using the Two Clamp VOCs Assay (TCVA), according to Cernava et. al. [74]. Petri dish bottoms of a 6-well plate (Greiner Bio-One, Frickenhausen, Germany) were filled with 4 mL of either PDA or NA per well. Mycelial plugs (3 mm diameter) obtained from 7-day-old colonies grown on PDA were placed in the center of the wells of a 6-well plate containing PDA medium (Figure 2A). Subsequently, each bacterial sample was streaked out on the same position of a 6-well plate placed opposite to the plate with the pathogen ( Figure 2B). Under this setup, the bacteria were tested on two different media, PDA and NA. A silicone perforated foil was placed between both 6-well plates to facilitate their fixing in combination with the usual clamps as shown in Figure 2C. As a control, wells containing V. dahliae were connected to wells filled only with PDA or NA (without any bacteria). Plates were incubated at 25 °C for 6 days. Subsequently, the largest and smallest diameters of the V. dahliae colonies were measured. Six replicates per each Verticillium-bacteria and Verticillium-medium (control) combination were performed.

Effect of Bacterial Volatiles on Mycelial Growth of Verticillium dahliae V937I
The ability of Pseudomonas sp. PICF6 and P. simiae PICF7 to inhibit the mycelial growth of V. dahliae V937I was examined by using the Two Clamp VOCs Assay (TCVA), according to Cernava et al. [74]. Petri dish bottoms of a 6-well plate (Greiner Bio-One, Frickenhausen, Germany) were filled with 4 mL of either PDA or NA per well. Mycelial plugs (3 mm diameter) obtained from 7-day-old colonies grown on PDA were placed in the center of the wells of a 6-well plate containing PDA medium ( Figure 2A). Subsequently, each bacterial sample was streaked out on the same position of a 6-well plate placed opposite to the plate with the pathogen ( Figure 2B). Under this setup, the bacteria were tested on two different media, PDA and NA. A silicone perforated foil was placed between both 6-well plates to facilitate their fixing in combination with the usual clamps as shown in Figure 2C. As a control, wells containing V. dahliae were connected to wells filled only with PDA or NA (without any bacteria). Plates were incubated at 25 • C for 6 days. Subsequently, the largest and smallest diameters of the V. dahliae colonies were measured. Six replicates per each Verticillium-bacteria and Verticillium-medium (control) combination were performed. Plants 2022, 11, x FOR PEER REVIEW 10 of 14

Data Analysis
Analysis of variance (ANOVA) was performed to determine statistical differences using the ANOVA module of Statistix 10 program (NH Analytical Software, Roseville, MN, USA). Data were tested for normality, homogeneity of variances and subjected to whiskers and graphic boxes in order to detect the outlier, which proved their suitability for the statistical analysis in all experiments. When analysis of variance showed significant differences among treatments, means were compared according to Tukey honestly-significant-difference (HSD) test at p = 0.05.

Supplementary Materials:
The following are available online at www.mdpi.com/xxx/s1, Figure S1. In vitro antagonistic activity of Pseudomonas sp. PICF6 and Pseudomonas simiae PICF7 against Verticillium longisporum ELV25, Figure S2. Representative gas chromatography spectra of Pseudomonas sp. PICF6 and Pseudomonas simiae PICF7 (alone and in the presence of Verticillium dahliae V937I), V. dahliae 937I, PDA and NA media. Funding: This research was funded by the Spanish Ministerio de Economía, Industria y Competitividad/Agencia Estatal de Investigación, grant number AGL2016-75729-C2-1-R, and Junta de Andalucía (Consejería de Economía, Innovación y Ciencia), grant number P12-AGR-0667, both co-financed by the European Regional Development Fund (ERDF). The international short-term stay performed by N-M.-O at Institute of Environmental Biotechnology in Graz University of Technology (Technische Universität Graz) was supported by the University of Córdoba ("Ayudas de movilidad internacional para el fomento de tesis con mención internacional o en régimen de cotutela").

Institutional Review Board Statement: Not applicable.
Informed Consent Statement: Not applicable.

Data Analysis
Analysis of variance (ANOVA) was performed to determine statistical differences using the ANOVA module of Statistix 10 program (NH Analytical Software, Roseville, MN, USA). Data were tested for normality, homogeneity of variances and subjected to whiskers and graphic boxes in order to detect the outlier, which proved their suitability for the statistical analysis in all experiments. When analysis of variance showed significant differences among treatments, means were compared according to Tukey honestly-significantdifference (HSD) test at p = 0.05.

Supplementary Materials:
The following are available online at https://www.mdpi.com/article/ 10.3390/plants11030318/s1, Figure S1. In vitro antagonistic activity of Pseudomonas sp. PICF6 and Pseudomonas simiae PICF7 against Verticillium longisporum ELV25, Figure S2. Representative gas chromatography spectra of Pseudomonas sp. PICF6 and Pseudomonas simiae PICF7 (alone and in the presence of Verticillium dahliae V937I), V. dahliae 937I, PDA and NA media. Funding: This research was funded by the Spanish Ministerio de Economía, Industria y Competitividad/Agencia Estatal de Investigación, grant number AGL2016-75729-C2-1-R, and Junta de Andalucía (Consejería de Economía, Innovación y Ciencia), grant number P12-AGR-0667, both co-financed by the European Regional Development Fund (ERDF). The international short-term stay performed by N-M.-O at Institute of Environmental Biotechnology in Graz University of Technology (Technische Universität Graz) was supported by the University of Córdoba ("Ayudas de movilidad internacional para el fomento de tesis con mención internacional o en régimen de cotutela").

Institutional Review Board Statement: Not applicable.
Informed Consent Statement: Not applicable. Data Availability Statement: All data required to reproduce the results presented in this study can be found in the article.