Antimicrobial and Immunomodulating Activities of Two Endemic Nepeta Species and Their Major Iridoids Isolated from Natural Sources

Two Balkan Peninsula endemics, Nepeta rtanjensis and N. argolica subsp. argolica, both characterized by specialized metabolite profiles predominated by iridoids and phenolics, are differentiated according to the stereochemistry of major iridoid aglycone nepetalactone (NL). For the first time, the present study provides a comparative analysis of antimicrobial and immunomodulating activities of the two Nepeta species and their major iridoids isolated from natural sources—cis,trans-NL, trans,cis-NL, and 1,5,9-epideoxyloganic acid (1,5,9-eDLA), as well as of phenolic acid rosmarinic acid (RA). Methanol extracts and pure iridoids displayed excellent antimicrobial activity against eight strains of bacteria and seven strains of fungi. They were especially potent against food-borne pathogens such as L. monocytogenes, E. coli, S. aureus, Penicillium sp., and Aspergillus sp. Targeted iridoids were efficient agents in preventing biofilm formation of resistant P. aeruginosa strain, and they displayed additive antimicrobial interaction. Iridoids are, to a great extent, responsible for the prominent antimicrobial activities of the two Nepeta species, although are probably minor contributors to the moderate immunomodulatory effects. The analyzed iridoids and RA, individually or in mixtures, have the potential to be used in the pharmaceutical industry as potent antimicrobials, and in the food industry to increase the shelf life and safety of food products.


Introduction
The plant genus Nepeta L. (family Lamiaceae) comprises around 280 species native to Europe, Asia, and Africa, commonly known as catmints or catnips. These remarkable plants are widely used in folk medicine against a variety of diseases and disorders, as well as in traditional food production [1], and their antimicrobial potential against human pathogenic microorganisms and phytopathogens has been comprehensively documented [2][3][4]. The majority of reported studies highlight monoterpenoid iridoid nepetalactone (NL) as the main bioactive compound in Nepeta sp.
Nepetalactone is usually present in the form of 7S diastereoisomers, which can be found in species-specific amounts and ratios [1,5]. Some studies proved that, even though NL isomers differ only in the orientation of a single chemical bond, they still show differential bioactivities, including attractant effects on cats [6], sex pheromone activity in some aphids [7], as well as repellent activities against a variety of insects [8][9][10]. Antimicrobial activities of pure nepetalactones have only rarely been tested [3,11], and differential activity of the two NL isomers was confirmed against Helicobacter pylori [3]. On the other hand, Nepeta species are also a rich source of iridoid glucosides [12][13][14][15], which have been unjustifiably neglected and only rarely studied for their biological activities. A literature survey for data on the bioactivities of one of the most abundant iridoid compounds in Nepeta species, 1,5,9-epideoxyloganic acid (1,5,, revealed no results. Thus, the present study aimed to isolate trans,cis-NL, cis,trans-NL, and 1,5,9-eDLA from natural sources, and to comparatively analyze, for the first time, their antimicrobial activities with those of the crude methanol extracts of the two rare Nepeta species: (1) Nepeta rtanjensis Diklić & Milojević, a critically endangered perennial of Serbia, which is characterized by high amounts of trans,cis-NL, dehydronepetalactone (DNL), and 1,5,9-eDLA, while cis,trans-NL is present as a minor constituent [4,[16][17][18]; (2) Greek endemic N. argolica Bory & Chaub. subsp. argolica (syn. N. sibthorpii Bentham, Euro + Med PlantBase), a cis,trans-NLrich chemotype [17,18]. Antimicrobial activity was tested in microdilution assays against a series of food-borne and disease-causing bacteria and fungi. To supplement the knowledge on the mode of antimicrobial action, anti-biofilm activity and immunomodulatory effects of methanol extracts of the two model species and isolated compounds were analyzed. For the first time, antimicrobial interaction of targeted iridoid compounds and rosmarinic acid (RA) has been investigated within the present study.

Results and Discussion
Food-borne illnesses continue to be a frequent and severe threat to public health worldwide. Most food-borne diseases originate from bacterial or fungal pathogens that have contaminated the food at some point along the food chain from farm to fork. As the epidemiology of food-borne illnesses changes, with newly recognized pathogens emerging and well-recognized pathogens becoming associated with new food products, a growing number of synthetic additives and antibiotics are used to control infections. Given that the safety of synthetic antimicrobials has been questioned in recent years and that consumers demand more "green/organic" products, the imminent future of alternative food preservatives could be in bioactive molecules of plant origin.
Nepeta species are a promising source of effective antimicrobial agents for the food and pharmaceutical industries. The high content of monoterpenoid iridoids and phenolic compounds in Nepeta species is chiefly responsible for their prominent antimicrobial potential [3,4,16,19]. Although iridoid aglycones nepetalactones are highlighted as foremost responsible for the recorded bioactivities, iridoid glucosides, which represent significant contributors to the iridoids pool of Nepeta species, should not be neglected.
The present study aimed to test the bioactivity of two Nepeta species differing in the stereochemistry of major nepetalactones, N. rtanjensis and N. argolica subsp. argolica, and of their major bioactive principles. For this purpose, cis,trans-NL, trans,cis-NL, and 1,5,9-eDLA were isolated from natural sources, and their structures were determined by extensive analysis of NMR and mass data, as well as by comparison with those in the literature.

Isolation of cis,trans-and trans,cis-Nepetalactone
Semi-preparative HPLC/DAD chromatograms of N. rtanjensis EO revealed trans,cis-NL eluting at Rt = 20.263 min ( Figure 1A) and displaying absorption spectra with λ max = 225 nm ( Figure 1a). cis,trans-NL was visible as a peak at the N. cataria EO HPLC/DAD chro-matogram eluting at Rt = 19.764 min ( Figure 1D), and also showing λ max = 225 nm ( Figure 1d). Fractions containing cis,trans-NL (in 69% MeOH), and trans,cis-NL (70% MeOH) were separately combined, extracted with n-hexane, and evaporated to dryness at room temperature. The total yield of cis,trans-NL was 2 mg, and of trans,cis-NL it was 12 mg. A similar strategy to isolate NL stereoisomers from N. cataria EOs was previously adopted by Wang et al. [20].

Isolation of cis,trans-and trans,cis-Nepetalactone
Semi-preparative HPLC/DAD chromatograms of N. rtanjensis EO revealed trans,c NL eluting at Rt = 20.263 min ( Figure 1A) and displaying absorption spectra with λma 225 nm (Figure 1a). cis,trans-NL was visible as a peak at the N. cataria EO HPLC/DA chromatogram eluting at Rt = 19.764 min ( Figure 1D), and also showing λmax = 225 n ( Figure 1d). Fractions containing cis,trans-NL (in 69% MeOH), and trans,cis-NL (7 MeOH) were separately combined, extracted with n-hexane, and evaporated to dryn at room temperature. The total yield of cis,trans-NL was 2 mg, and of trans,cis-NL it w 12 mg. A similar strategy to isolate NL stereoisomers from N. cataria EOs was previou adopted by Wang et al. [20]. To confirm the identification of cis,trans-NL and trans,cis-NL, collected fractions w subjected to GC/MS analysis. The cis,trans-NL eluted at Rt = 18.837 min ( Figure 1B), wh trans,cis-NL was visible as a peak at Rt = 18.043 min on the GC/MS chromatogram (Figu 1E). GC/MS spectra of the two NL stereoisomers showed the similar fragmentati patterns, with slightly different intensities of the major daughter ions (Figure 1b,e).
Further characterization of cis,trans-and trans,cis-NL was performed, adopting UHPLC/DAD/(+)HESI−MS 2 instrument. The trans,cis-NL was visible on the UHPLC/M chromatogram as the molecular ion [M+H] + at m/z 167, which eluted at Rt = 6.73 m ( Figure 1C). cis,trans-NL was identified as the molecular ion [M+H] + at m/z 167, eluting Rt = 6.50 min ( Figure 1F). The product ion scanning (PIS) experiment of the MS instrume revealed that the two NL diastereoisomers showed similar (+)MS 2 fragmentation patter although the intensity of the fragments varied (Figure 1c  To confirm the identification of cis,trans-NL and trans,cis-NL, collected fractions were subjected to GC/MS analysis. The cis,trans-NL eluted at Rt = 18.837 min ( Figure 1B), while trans,cis-NL was visible as a peak at Rt = 18.043 min on the GC/MS chromatogram ( Figure 1E). GC/MS spectra of the two NL stereoisomers showed the similar fragmentation patterns, with slightly different intensities of the major daughter ions (Figure 1b,e).
Further characterization of cis,transand trans,cis-NL was performed, adopting a UHPLC/DAD/(+)HESI−MS 2 instrument. The trans,cis-NL was visible on the UHPLC/MS 2 chromatogram as the molecular ion [M+H] + at m/z 167, which eluted at Rt = 6.73 min ( Figure 1C). cis,trans-NL was identified as the molecular ion [M+H] + at m/z 167, eluting at Rt = 6.50 min ( Figure 1F). The product ion scanning (PIS) experiment of the MS instrument revealed that the two NL diastereoisomers showed similar (+)MS 2 fragmentation patterns, although the intensity of the fragments varied (Figure 1c,d), similarly as in Mišić et al. [17]. An unambiguous assignment of the NMR spectra of the two NL stereoisomers has been achieved using 1D ( 1 H and 13 C) and 2D (COSY, NOESY and HSQC) NMR techniques, and the results are shown in Supplementary Figures S1 and S2.

Isolation of 1,5,9-Epideoxyloganic Acid
Iridoid glucoside, 1,5,9-eDLA, was isolated from a methanol extract of N. rtanjensis. UPLC/Q-TOF MS analysis of the extract revealed that 1,5,9-eDLA, eluting at Rt = 4.86 min (Figure 2A), was visible in a negative mode of the instrument, and it displayed the pseudomolecular ion [M−H] − at m/z 359.1368. Its MS 2 fragmentation pattern ( Figure 2a) revealed a base peak at 197 m/z (loss of hexose, 162 Da) and MS 3 base peak at 153 m/z (further loss of CO 2 , 44 Da). The loss of another molecule of CO 2 resulted in a secondary MS 3 peak at 109 m/z. Finally, fragmentation of the MS 3 base peak (153 m/z) resulted in an MS 4 base peak (135 m/z) by the loss of one water molecule (18 Da). The proposed fragmentation pattern of 1,5,9-eDLA is presented in Figure 2B. An unambiguous assignment of the NMR spectra of the two NL stereoisomers has been achieved using 1D ( 1 H and 13 C) and 2D (COSY, NOESY and HSQC) NMR techniques, and the results are shown in Supplementary Figures S1 and S2.

Isolation of 1,5,9-Epideoxyloganic Acid
Iridoid glucoside, 1,5,9-eDLA, was isolated from a methanol extract of N. rtanjensis. UPLC/Q-TOF MS analysis of the extract revealed that 1,5,9-eDLA, eluting at Rt = 4.86 min (Figure 2A), was visible in a negative mode of the instrument, and it displayed the pseudomolecular ion [M−H] -at m/z 359.1368. Its MS 2 fragmentation pattern ( Figure 2a) revealed a base peak at 197 m/z (loss of hexose, 162 Da) and MS 3 base peak at 153 m/z (further loss of CO2, 44 Da). The loss of another molecule of CO2 resulted in a secondary MS 3 peak at 109 m/z. Finally, fragmentation of the MS 3 base peak (153 m/z) resulted in an MS 4 base peak (135 m/z) by the loss of one water molecule (18 Da). The proposed fragmentation pattern of 1,5,9-eDLA is presented in Figure 2B. Following preparative isolation of 1,5,9-epideoxyloganic acid from methanol extract, its structural characterization included UHPLC/MS 2 analysis. UHPLC/qqqMS 2 chromatogram (C) and corresponding (−)MS 2 spectrum (c) are presented.

Chemical Composition of N. rtanjensis and N. argolica Subsp. argolica Methanol Extracts
According to the literature, the extracts of plants of the genus Nepeta contain a wide variety of phytochemicals; the most common are monoterpenoids, among which glycosides and aglycones of iridoids predominate [5,21]. Phenolics from the groups of phenolic acids and flavonoids, both aglycones and glycosides, are also very abundant in Nepeta species [5,17,19].
The present study gives insight into the profile of polyphenolics and iridoids of Nepeta argolica subsp. argolica and N. rtanjensis methanol extracts using non-targeted and targeted metabolomics approaches. UHPLC-LTQ OrbiTrap XL fingerprinting resulted in identifying 49 compounds (Table 1) in analyzed samples. The tentative identification of compounds was based on high-resolution mass spectrometry (HRMS) and MS 4 fragmentation, as well as literature data [13,17,22,23]. All identified compounds could be divided into four major groups: (1) phenolic acids and derivatives (20 compounds); (2) flavonoid glycosides and aglycones (12 compounds); (3) iridoid glycosides (13 compounds); and (4) 4 compounds belonging to other classes (Table 1). Data were acquired only in the negative ionization mode of the UHPLC-LTQ OrbiTrap MS instrument; thus, no iridoid aglycones were recorded.
Four hexosyl derivatives of hydroxybenzoic acids (compounds 1, 2, 4, and 5) were identified in the examined samples (Table 1). All other phenolic acid derivatives belonged to hydroxycinnamic acid groups. The MS 2 base peak of compound 8, found at retention time 7.03 min and displaying pseudomolecular ion [M−H] − at 369 m/z, was identified at 191 m/z (deprotonated quinic acid). In this case, the neutral loss was found at 178 m/z, which most likely corresponds to the trihydroxycinnamoyl residue. However, the hydroxyl group's exact position on the benzene nucleus of this compound could not be defined based only on LC/MS n data. Further fragmentation of 191 m/z confirmed the presence of quinic acid. Supplementary Figure S4 presents the proposed structural formula and fragmentation pathway of trihydroxy-cinnamoylquinic acid (8). A literature survey revealed that such a compound has not previously been identified in Nepeta species. Caffeic acid (13) derivatives are common in Nepeta species [17,24]. Caffeoylquinic acid derivatives (3, 9, 10, 15, and 16) and rosmarinic acid (17) were the most abundant phenolic acids in both Nepeta species analyzed within the present study. Compound 18, found at Rt = 9.38 min and 313 m/z, could be tentatively identified as nepetoidin A or nepetoidin B. Nepetoidin B was previously isolated from root cultures of Nepeta teydea [23].
The analysis was targeted towards some of the major phenolic compounds, including phenolic acids (9,13,17) and flavonoids (21,22,25). The most abundant phenolic compound in methanol extracts of N. rtanjensis and N. argolica was 5-O-caffeoylquinic acid (9) ( Figure 3B,C). The second most abundant phenolic compound in both analyzed samples was RA (17) ( Figure 3C). Other analyzed phenolic acids and flavonoids were much less abundant in the analyzed samples.

Antimicrobial Activity
Antimicrobial activity of N. rtanjensis and N. argolica subsp. argolica methanol extracts and their major iridoid (trans,cis-NL, cis,trans-NL, and eDLA) and phenolic constituents (RA) were comparatively tested against eight bacterial (B. cereus, S. aureus, M. flavus, L. monocytogenes, E. faecalis, P. aeruginosa, E. coli and S. typhimurium) and seven fungal food-borne pathogens (A. fumigatus, A. ochraceus, A. versicolor, A. niger, P. funiculosum, P. ochlochloron and P. v. cylopium) ( Table 2). Although two analyzed Nepeta species displayed differential qualitative and quantitative content of nepetalactones (Table 1, Figure 3 [4]. This endemic species is well characterized for antimicrobial effects of its EOs and extracts [4,16]. On the other hand, literature dealing with antimicrobial activities of N. argolica is rather scarce, and no records on the activity of methanol extracts are reported. N. argolica subsp. dyrphia essential oil and pure nepetalactones were effective against 25 clinically isolated and commercial strains of Helicobacter pylori [3]. previous studies [17,18,27], the positive ion HESI mode of the UHPLC/DAD/qqqMS instrument was found to be the ionization method of choice for iridoid aglycones (cis,trans-NL, trans,cis-NL, and DNL), while iridoid glycoside 1,5,9-eDLA was analyzed in negative mode. The most abundant iridoid compounds in N. rtanjensis sample were 41, 50, and 52, while in N. argolica subsp. argolica methanol extracts, compounds 41 and 51 predominated ( Figure 3A,C). This was in accordance with our previous studies [17,18]. The analysis was targeted towards some of the major phenolic compounds, including phenolic acids (9,13,17) and flavonoids (21,22,25). The most abundant phenolic compound in methanol extracts of N. rtanjensis and N. argolica was 5-O-caffeoylquinic acid (9) (Figure 3B,C). The second most abundant phenolic compound in both analyzed samples was RA (17) ( Figure 3C). Other analyzed phenolic acids and flavonoids were much less abundant in the analyzed samples.

Antimicrobial Activity
Antimicrobial activity of N. rtanjensis and N. argolica subsp. argolica methanol extracts and their major iridoid (trans,cis-NL, cis,trans-NL, and eDLA) and phenolic constituents (RA) were comparatively tested against eight bacterial (B. cereus, S. aureus, M. flavus, L. monocytogenes, E. faecalis, P. aeruginosa, E. coli and S. typhimurium) and seven fungal foodborne pathogens (A. fumigatus, A. ochraceus, A. versicolor, A. niger, P. funiculosum, P. ochlochloron and P. v. cylopium) ( Table 2). Although two analyzed Nepeta species displayed differential qualitative and quantitative content of nepetalactones (Table 1, Figure 3), there was no considerable difference in antimicrobial activity between their methanol extracts. The formation of biofilm is the initial step that leads to the overgrowth of food-borne bacteria, and in the food industry biofilms create a persistent contamination source. The examined Nepeta sp. extracts/compounds have shown significant potential in inhibiting the growth of a resistant strain of bacterial pathogen P. aeruginosa ( Figure 4A). This opportunistic pathogen is used as a model system for biofilm formation due to its ability to establish biofilms on different surfaces and because it is frequently present in water, dairy products, meat, and food of plant origin [28]. Pure compounds have shown more promising activity than extracts, with MIC values of 0.0375-0.05 mg mL −1 and MBC values of 0.075-0.1 mg mL −1 . Table 2. Antimicrobial activities of N. rtanjensis, N. argolica subsp. argolica, and of cis,trans-nepetalactone (cis,trans-NL), trans,cis-nepetalactone (trans,cis-NL), 1,5,9-epideoxyloganic acid (1,5,9-eDLA) and rosmarinic acid (RA). Values for minimal inhibitory (MIC) and lethal concentration (MBC-bactericidal and MFC-fungicidal concentration) are presented as mg of extract/compound per mL (mg mL −1 ). Among tested extracts and pure compounds, the most substantial antibiofilm potential could be observed for trans,cis-NL ( Figure 4B). The application of this compound in a concentration equal to previously determined MIC caused 54.8% inhibition while one-half of the MIC reduced biofilm biomass formation by 41.4%. The other two iridoid compounds, cis,trans-NL and 1,5,9-eDLA, also displayed significant antibiofilm potential, inducing around 41.8% and 32.2% inhibition when applied with MICs, respectively. The efficiency of RA, which induced 57.8% inhibition with MIC, was drastically reduced to 3.4% with one-half MIC. Likewise, antibiofilm activity of N. nuda tincture, rich in eDLA, has been demonstrated against E. faecalis biofilm formation [29].

Antibacterial Activity
To determine potential antimicrobial interactions of the major compounds found in N. rtanjensis leaf extracts against P. aeruginosa, three combinations of compounds (RA+1,5,9-eDLA; RA+trans,cis-NL, and 1,5,9-eDLA+trans,cis-NL) were examined. The results have shown that all three compound combinations have an additive effect on P. aeruginosa growth inhibition ( Figure 4C), which might, at least partially, be responsible for the pronounced antimicrobial activity of N. rtanjensis methanol extracts. Taking into account the recorded iridoid and phenolic profiles in methanol extracts (Table 1) and the known antimicrobial activities for some of the compounds which are available in the literature [1,5], the contribution of minor constituents of methanol extracts to the overall antimicrobial activity should not be neglected. The formation of biofilm is the initial step that leads to the overgrowth of food-borne bacteria, and in the food industry biofilms create a persistent contamination source. The examined Nepeta sp. extracts/compounds have shown significant potential in inhibiting the growth of a resistant strain of bacterial pathogen P. aeruginosa ( Figure 4A). This opportunistic pathogen is used as a model system for biofilm formation due to its ability to establish biofilms on different surfaces and because it is frequently present in water, dairy products, meat, and food of plant origin [28]. Pure compounds have shown more promising activity than extracts, with MIC values of 0.0375-0.05 mg mL -1 and MBC values of 0.075-0.1 mg mL -1 . Among tested extracts and pure compounds, the most substantial antibiofilm potential could be observed for trans,cis-NL ( Figure 4B). The application of this compound in a concentration equal to previously determined MIC caused 54.8% inhibition while onehalf of the MIC reduced biofilm biomass formation by 41.4%. The other two iridoid compounds, cis,trans-NL and 1,5,9-eDLA, also displayed significant antibiofilm potential,  (1,5,, and rosmarinic acid (RA) against a resistant P. aeruginosa strain. Minimal inhibitory (MIC) and lethal concentrations (MBC) were determined, and streptomycin and ampicillin were adopted as reference compounds. (C) Antibacterial interaction against P. aeruginosa of the following compound combinations: trans,cis-NL/1,5,9-eDLA, trans,cis-NL/RA, and 1,5,9-eDLA/RA.

Immunomodulating Activity
The intensity of the inflammatory response induced by food-borne infections could be responsible for the severity of the tissue lesions; therefore, we have also tested the influence of N. rtanjensis and N. argolica subsp. argolica extracts and pure nepetalactones (cis,trans-NL and trans,cis-NL) on macrophages' activity. After 24 h of cultivation, the viability of macrophages was reduced under the influence of N. rtanjensis and N. argolica subsp. argolica leaf extracts ( Figure 5A,B) at concentrations of 500 µg mL −1 and NLs at concentrations of 100 µg mL −1 and higher ( Figure 5C,D). Therefore, extracts in concentrations of 250 µg mL −1 and NLs in concentrations of 50 µg mL −1 were used for in vitro experiments with macrophages. Both extracts and NLs exhibited no significant effect on nitrite ( Figure 5J), TNF ( Figure 5E), or IL-6 production ( Figure 5G). Additionally, the level of phagocytosis per macrophage cell remains unchanged after treatment with the analyzed extracts and NLs ( Figure 5H). Both N. rtanjensis and N. argolica subsp. argolica leaf extracts induced the elevation of proinflammatory cytokine IL-1β, while all tested compounds showed no significant effects. ROS production per cell was significantly reduced after treatment with N. rtanjensis leaf extract, while the same concentration of N. argolica subsp. argolica had no effect ( Figure 5I). Conversely, treatment with 50 µg mL −1 trans,cis-NL and cis,trans-NL increased the ROS production in macrophages.
A previous study has demonstrated the strong anti-inflammatory effect of N. argolica subsp. argolica extracts [24]. It has been shown that the extracts of N. dschuparensis, rich in NL, significantly reduce levels of proinflammatory cytokine IL-1β and cyclooxygenase 2 (COX-2) in a cerebral ischemia-reperfusion model [30]. Similarly, n-butanol extract from N. asterotricha has decreased the production of IL1-β, IL-6, TNF and ROS in J774A.1 cell line of macrophages [21]. In contrast to earlier findings, results of the present study indicate that nepetalactones are probably minor contributors to the overall immunomodulatory effects in the tested culture of macrophages and two Nepeta species.

In Conclusion
The methanol extracts of N. argolica subsp. argolica, and especially N. rtanjensis, show very promising antibacterial and antifungal potential, owing to the high content of iridoid and phenolic compounds and their additive interactions. Iridoids (trans,cis-NL, cis,trans-NL, and 1,5,9-eDLA) and dominant phenolic constituents (RA) of Nepeta species may be recommended individually or in mixtures to preserve foods and beverages as more "green/organic" alternatives for the extension of the product shelf life. Furthermore, they can be utilized to prevent and treat diseases caused by common and emerging food-borne pathogens such as L. monocytogenes, E. coli, S. aureus, P. aeruginosa, Penicillium sp. and Aspergillus spp., as well as for pathological conditions to reduce or stimulate the occurrence of proinflammatory responses. The results of the present study support the hypothesis that nepetalactone stereochemistry determines the antimicrobial activity of Nepeta species, and that iridoid glucoside 1,5,9-eDLA is an equally potent antimicrobial as nepetalactones. Taking into account their well-known health benefits for humans, iridoids of Nepeta sp. are prospective functional food additives, especially 1,5,9-eDLA, which is not volatile and is more stable in food formulations. A previous study has demonstrated the strong anti-inflammatory effect of N. arg subsp. argolica extracts [24]. It has been shown that the extracts of N. dschuparensis, ric NL, significantly reduce levels of proinflammatory cytokine IL-1β and cyclooxygena (COX-2) in a cerebral ischemia-reperfusion model [30]. Similarly, n-butanol extract f N. asterotricha has decreased the production of IL1-β, IL-6, TNF and ROS in J774A.1

Chemicals and Reagents
Solvents for HPLC/MS analyses (acetonitrile, acetic and formic acids) were of LC/MS grade, obtained from Fisher Scientific (Loughborough, UK). Methanol for plant extraction (99.8%, HPLC grade) and semi-preparative (SP) HPLC/DAD analysis was HPLC grade (AppliChem GmbH, Darmstadt, Germany). Ultra-pure deionized water was generated using the Water Purification System (New Human Power I Integrate, Human Corpora-tion, Republic of Korea). Standards of phenolics were purchased from Sigma-Aldrich (Steinheim, Germany).

Origin of Essential Oils
Essential oil (EO) of dry Nepeta rtanjensis Diklić & Milojević flowering plants, containing 72% of trans,cis-NL, and 16% of cis,trans-NL, was obtained by hydrodistillation in a Clevenger-type apparatus, as previously described by Skorić et al. [31]. The EO of Nepeta cataria L., containing 90% of cis,trans-NL, was provided by Dr. Michael Birkett from Rothamsted Research (Harpenden, UK).

Semi-Preparative HPLC/DAD Fractionation and Isolation of cis,transand trans,cis-Nepetalactone
Semi-preparative HPLC fractionation of EOs, diluted in 99.6% methanol (w:v = 1:50), was performed on an HPLC system, model HP1100 with DAD (Hewlett Packard, Santa Clara, CA, USA), connected to a Fraction collector 1200 Series (Agilent Technologies, Waldbronn, Germany). Chromatographic separation was performed using a ZORBAX SB-C18 (9.4 × 100 mm, 5 µm) column (Agilent Technologies, Waldbronn, Germany), thermostated at 40 • C. The mobile phase consisted of (A) deionized water and (B) methanol, which were applied in the following gradient elutions: 80-10% A for 30 min; 10% A during the next 10 min; 10-80% A in the next 5 min. The flow rate was set to 2.000 mL min −1 , and the detection wavelength was λ = 230 nm. The injection volume was 100 µL. Collected fractions of cis,transand trans,cis-NL (containing the desired compounds in~69% and 70% methanol, respectively) were mixed with hexane (v:v = 3:2), vigorously vortexed for 2 min, and the upper phase containing cis,transor trans,cis-NL in hexane was transferred into glass vials. Solvent was evaporated at room temperature overnight, and samples were additionally dried under the N gas flow.

GC-MS Identification of Nepetalactone Diastereoisomers in Isolated Fractions
The analysis was performed using GCMS QP2010 plus, equipped with an AOC 5000 injector (Shimadzu, Kyoto, Japan), and ZB-1 column (Phenomenex, L = 30 m, ID = 0.25 mm, df = 0.50 µm). Samples (1 µL) were injected in the split mode (1:30), with injector temperature set to 250 • C. Mass spectra were acquired in EI mode (±70 eV) in the m/z range 40-400 amu (SCAN) mode together with Single Ion Monitoring (SIM) mode, and helium (He, 99.999%) was used as a carrier gas with a flow rate of 1 mL min −1 . The column was heated linearly from 40 • C to 280 • C with a gradient of 6 • C min −1 and held at 280 • C for 5 min. Ion source temperature was set to 280 • C; interface temperature to 290 • C; SCAN 40-400 m/z; SIM 164, 166. Identification of constituents was performed by comparing their mass spectra to those from Wiley8, NIST05, and FFNSC3 libraries, using different search engines.

UHPLC-MS 2 Analysis of Isolated Fractions
Analyses were performed using a Dionex Ultimate 3000 UHPLC system (ThermoFisher Scientific, Bremen, Germany) equipped with a diode array detector (DAD) and a TSQ Quantum Access Max triple-quadrupole (QQQ) mass spectrometer (ThermoFisher Scientific, Basel, Switzerland). Chromatographic separation of NLs was performed on a Hypersil gold C18-column (50 × 2.1 mm) with 1.9 µm particle size (ThermoFisher Scientific, Fair Lawn, NJ, USA), thermostated at 40 • C. The mobile phase consisted of (A) 0.2% formic acid in water and (B) acetonitrile (MS grade, Fisher Scientific, Loughborough, UK), which were applied at the flow rate and gradient elution, as previously described by Mišić et al. [17]. Settings of the TSQ Quantum Access Max QQQ mass spectrometer were as previously described [18]. The MS data were acquired in positive ionization mode, and the collision-induced fragmentation, in a selected reaction monitoring (SRM) experiment, was performed using argon as the collision gas, with collision energy (cE) set to 30 eV.

NMR Analysis for the Structural Characterization of Isolated cis,transand trans,cis-Nepetalactone
Samples were dissolved in chloroform-d and further used in NMR analysis. The NMR spectra were recorded on a Bruker AVANC 500 NMR spectrometer equipped with a BBI 5 mm probe head at 298 K. Samples were dissolved in 99.

Preparation of Methanol Extracts
Plant material (110 g FW) was ground in liquid nitrogen (LN) and diluted in 250 mL 96% methanol. Extraction was performed overnight at 4 • C. The next day, extraction was continued in an ultrasonic bath at room temperature for 15 min. Following filtration, the sample was evaporated in a vacuum evaporator (Rotavapor RII, Buchi, Switzerland) and additionally dried under a N gas flow. Samples (4.5 g DE) were stored at 4 • C until use.

HRMS Analysis of N. rtanjensis Methanol Extract
Dry methanol extract of N. rtanjensis was diluted in 96% methanol (1:1 = w:v) in an ultrasonic bath at 100 Hz and 25 • C, and filtered through 13 mm (pore size 0.22 µm) filters (ANPEL Laboratory Technologies (Shanghai) Inc., Shanghai, China). The sample was chromatographically separated on a Waters Acquity UPLC Q-TOF system using an Acquity UPLC ® BEH C18 column (particle size 1.7 µm, dimensions 2.1 × 100 mm). The mobile phase consisted of 0.1% formic acid in water (A) and 0.1% formic acid in acetonitrile (B). The mobile phase was eluted with a flow rate of 0.3 mL min −1 , and the elution gradient was as follows: 0-1 min 5% B, 1-12 min 5-95% B, 12-12.2 min 95-5% B, 12.2-15 min 5% B. The LC system was connected to the mass spectrometer with an electrospray ionization (ESI) source operating in negative ionization mode, with the following operating conditions: mass range of 50 Da to 1200 Da, low collision energy (cE) of 10 keV, high cE at 20 keV, target column temperature of 45 • C, target sample temperature of 15 • C, resolution of 20,000, source desolvation temperature of 350 • C, source temperature of 120 • C, capillary voltage of 2.50 kV, cone gas flow of 50.0 l h −1 , desolvation gas flow of 750.0 l h −1 , nebulizer gas flow of 6.5 bar, trap gas flow of 2.00 mL min −1 , and IMS gas flow of 90.00 mL min −1 .

Preparation of Methanol Extracts
Above-ground parts of N. rtanjensis and N. argolica subsp. argolica cultured in vitro were harvested, weighed, and ground in LN. The material was extracted with 99.8% methanol (w:v = 1:10) by vortexing for 1 min and in an ultrasonic bath for 15 min. After centrifugation for 20 min at 10,000× g, the supernatants were filtered through 0.2 µm cellulose filters (Agilent Technologies, Santa Clara, CA, USA), and stored at 4 • C until use.

Identification of Phytochemicals in Methanol Extracts Using UHPLC-LTQ OrbiTrap XL
UHPLC separation was carried out on an Accela 600 system coupled to the LTQ Orbi-Trap XL mass spectrometer (ThermoFisher Scientific, Bremen, Germany). The analytical column used for separation was a Syncronis C18 column (100 × 2.1 mm, 1.7 µm) heated to 40 • C. The mobile phase was composed of (A) 0.1% formic acid (MS grade, Sigma-Aldrich, Steinheim, Germany) and (B) acetonitrile (MS grade, Merck, Darmstadt, Germany) with 0.1% formic acid. The flow rate was set to 0.175 mL min −1 and the gradient elution program was previously described by Banjanac et al. [32]. MS parameters of the ion source and the other MS settings were as previously described in Banjanac et al. [32].

UHPLC/qqqMS 2 Quantification of Major Iridoids in Methanol Extracts
Quantification of iridoids in N. rtanjensis samples was performed using the UH-PLC/qqqMS2 instrument settings described in Section 3.2.4. The MS data were acquired simultaneously in positive (cis,trans-and trans,cis-NL) and negative mode (1,5, in selected reaction monitoring (SRM) mass spectrometric scanning mode, with collisioninduced fragmentations performed using argon as the collision gas, and collision energy (cE) set to 30 eV. An SRM experiment for quantitative analysis was performed using two diagnostic MS 2 fragments for each compound. Quantifications of cis,trans-NL, trans,cis-NL, and 1,5,9-eDLA acid were performed using calibration curves of isolated standards, and the total amount of compounds in samples was expressed as µg 100 mg −1 dry extract.

UHPLC/qqqMS 2 Quantification of Major Phenolics in Methanol Extracts
Phenolics in the methanol extract of N. rtanjensis were chromatographically separated on a Syncronis C18 column (100 × 2.1 mm) with 1.7 µm particle size (ThermoFisher Scientific, USA), thermostated at 40 • C. The mobile phase consisted of (A) 0.1% acetic acid in water and (B) acetonitrile (MS grade, FisherScientific, UK), which were applied in the following gradient elutions: 5% B in the first minute, 5-95% B from 1.0 to 16.0 min, from 95% to 5% B for 16.0-16.2 min, and 5% B until the 20th min. The flow rate was set to 0.3 mL min −1 , and the injection volume was 5 µL. Settings of the TSQ Quantum Access Max QQQ mass spectrometer for the time-selected reaction monitoring (tSRM) experiment were as previously described inČolić et al. [33]. Xcalibur software (version 2.2) was used for instrument control, data acquisition, and analysis. The total amount of compounds in samples was calculated based on the calibration curve of pure compounds and expressed as µg 100 mg −1 dry extract.

Microdilution Method
Antimicrobial activity was analyzed by adopting the modified microdilution technique as previously described by Soković et al. [35].
Determination of minimum inhibitory concentrations (MICs), and the minimum bactericidal concentrations (MBCs) and fungicidal concentrations (MFCs) were performed by a serial dilution technique using 96-well microtiter plates. The compounds investigated were dissolved in 5% DMSO in concentration 2 mg mL −1 , and for the extracts 10 mg mL −1 , and added in broth medium with inoculum.

Antibiofilm Activity
The method was performed as described in Sirakanyan et al. [36]. Briefly, P. aeruginosa resistant strain was incubated with MIC and subMIC (0.5 MIC) concentrations of tested compounds or methanol extracts in Tryptic soy broth (TSB) enriched with 2% glucose at 37 • C. After 24 h, each well was washed twice with sterile PBS (phosphate-buffered saline, pH 7.4) and fixed with methanol for 10 min. After the removal of methanol, the plate was air-dried. Biofilm was stained with 0.1% crystal violet (Bio-Merieux, France) for 30 min. Wells were washed with water, air-dried, and 100 µL of 96% ethanol (Zorka, Serbia) was added. The absorbance was read at 620 nm on a Multiskan™ FC Microplate Photometer, Thermo Scientific ™. The percentage of inhibition of biofilm formation was calculated according to the following formula: [(A 620 control-A 620 sample)/A 620 control] × 100.
3.6. Immunomodulating Activity of Two Nepeta Species Methanol Extracts and Isolated Nepetalactones 3.6.1. Cells and Cell Cultures Resident peritoneal cells were isolated from Dark Agouti rats that were maintained in the animal facility of the IBISS-UB. The experimental procedures were approved by the local Ethics Committee (IBISS-UB, No (02-09/16)). Macrophages were isolated as previously described [38]. Following isolation, macrophages were stimulated with 10 ng mL −1 lipopolysaccharide (LPS, Sigma-Aldrich) and treated with extracts and NLs (cis,trans-NL and trans,cis-NL).

Cell Viability Assays
A Crystal Violet (CV) test was used to determine the number of living, adherent macrophages. At the end of the treatment, supernatants were removed; cells were washed with PBS and fixed with methanol. The cells were stained with 0.1% CV solution. After staining, plates were washed with water and dye was dissolved in 33% acetic acid solution. The absorbance of the solution was measured in triplicates by an automated microplate reader (LKB 5060-006, LKB, Vienna, Austria) at 540 nm. The intensity of the dye corresponded to the viability of the cells.

ELISA Test for Determination of Cytokines
Cytokine concentration in cell culture supernatants was determined using the sandwich ELISA assay. For this purpose, 96-well MaxiSorp microtiter plates (Nunc, Roskilde, Denmark) and commercial antibody pairs were used to measure the concentrations of the respective cytokines: IL-1β, IL-6, TNF (eBioscience). The process was performed according to the protocols provided by the manufacturer. The lower limit of detection was 30 pg mL −1 , while the upper limit of detection was 10 ng mL −1 for all of the ELISA tests performed. The concentrations of cytokines (ng mL −1 ) were determined using the standard curves made with appropriate concentrations of the recombinant cytokines.

Detection of Phagocytosis
The level of phagocytosis in macrophages was determined by flow cytofluorimetry. Fluorescently labeled latex beads (1 µm, yellow green, Sigma-Aldrich) were preopsonized in PBS with 50% FCS, 1 h at 37 • C. A preopsonized bead solution was added over macrophages (1 × 105/well) and incubated at 37 • C for an additional hour. Following this, the solution was removed, the cells were washed twice with PBS, stripped off, and analyzed by flow cytofluorimetry. The results are presented as the mean fluorescence intensity (mfi) of the population.

Detection of ROS and NO Production
ROS generation was assessed by dihydrorhodamine 123 (DHR, SigmaAldrich, Steinheim, Germany) staining. The cells were pretreated with extracts and nepetalactones for 24 h, then incubated in the presence of 1 µM DHR for 30 min, stimulated with LPS for an additional 90 min, and analyzed by flow cytofluorimetry. The results are presented as mean fluorescence intensity (mfi) of the population. The production of NO in the supernatants of treated macrophages was determined by a Griess reaction based on nitrite accumulation. Briefly, triplicate aliquots of cell-free supernatants were mixed with an equal volume of Griess reagent (1:1 mixture of 0.1% naphthylethylenediaminedihydrochloride and 1% sulphanilamide in 5% H 3 PO 4 ). The absorbance of the solutions was measured by microplate reader at 540 nm, and the nitrite concentration was calculated based on the standard curve for NaNO 2 .