Deciphering the Antibacterial Mode of Action of Alpha-Mangostin on Staphylococcus epidermidis RP62A Through an Integrated Transcriptomic and Proteomic Approach

Abstract

Background: Alpha-mangostin (α-MG) is a natural xanthone reported to exhibit rapid bactericidal activity against Gram-positive bacteria, and may therefore have potential clinical application in healthcare sectors. This study sought to identify the impact of α-MG on Staphylococcus epidermidis RP62A through integrated advanced omic technologies.

Methods:S. epidermidis was challenged with sub-MIC (0.875 μg/ml) of α-MG at various time points and the differential expression pattern of genes/proteins were analyzed in the absence and presence of α-MG using RNA sequencing and LC-MS/MS experiments. Bioinformatic tools were used to categorize the biological processes, molecular functions and KEGG pathways of differentially expressed genes/proteins. qRT-PCR was employed to validate the results obtained from these analyses.

Results: Transcriptomic and proteomic profiling of α-MG treated cells indicated that genes/proteins affected by α-MG treatment were associated with diverse cellular functions. The greatest reduction in expression was observed in transcription of genes conferring cytoplasmic membrane integrity (yidC2, secA and mscL), cell division (ftsY and divlB), teichoic acid biosynthesis (tagG and dltA), fatty-acid biosynthesis (accB, accC, fabD, fabH, fabI, and fabZ), biofilm formation (icaA) and DNA replication and repair machinery (polA, polC, dnaE, and uvrA). Those with increased expression were involved in oxidative (katA and sodA) and cellular stress response (clpB, clpC, groEL, and asp23). The qRT-PCR analysis substantiated the results obtained from transcriptomic and proteomic profiling studies.

Conclusion: Combining transcriptomic and proteomic methods provided comprehensive information about the antibacterial mode of action of α-MG. The obtained results suggest that α-MG targets S. epidermidis through multifarious mechanisms, and especially prompts that loss of cytoplasmic membrane integrity leads to rapid onset of bactericidal activity.

Introduction

Staphylococcus epidermidis is one of the most important causes of nosocomial and community acquired infections (Gomes et al., 2014). It is often observed in the device related and surgical site infections, where the biofilm formation on implants and tissues further increases the treatment failure (Center for Disease Control Prevention [CDC], 2013; Danzmann et al., 2013; Gomes et al., 2014). In addition, infections associated with biofilms are persisting until the subsequent replacement or removal of implants, which causes distress to patients and lead to superfluous expenditure (Donlan and Costerton, 2002). The available antibiotic therapy can only kill planktonic cells, leaving the bacterial cells to grow within the biofilms continuously even after the termination of antibiotic therapy (Roper et al., 2000; Parra-Ruiz et al., 2012; Reiter et al., 2014). Alarmingly, the ability of biofilm to resist clearance by antibiotics increased the importance of a continuous search for novel antibacterial agents that target both planktonic and biofilm populations. Hence, new antibacterial agents are needed to combat biofilm mediated infections caused by S. epidermidis.

Throughout human history, plants have been the inexhaustible source of novel bioactive compounds with multitude of blockbuster therapeutic drugs, which have been derived directly or indirectly from various plants (Kinghorn et al., 2011; Newman and Cragg, 2012; Veeresham, 2012; Pohlit et al., 2013; Laallam et al., 2015; Satthakarn et al., 2015; Khan et al., 2018). Among the reported plant-derived bioactive compounds, alpha-mangostin (α-MG), a natural xanthone derived from the pericarp of Garcinia mangostana has been reported for various pharmacological properties that includes antibacterial, antifungal, anti-inflammatory, anticancer, and antioxidant activity (Ibrahim et al., 2016). α-MG elicits in vitro rapid bactericidal activity against several Gram-positive pathogens (Nguyen and Marquis, 2011; Koh et al., 2013; Sivaranjani et al., 2017). As reported by Koh et al. (2013) α-MG rapidly disintegrates the cytoplasmic membrane integrity of methicillin resistant Staphylococcus aureus (MRSA), which results in loss of cytoplasmic components. The multi-step resistance selection assay from previous studies suggested that Gram-positive pathogens do not develop resistance against α-MG (Koh et al., 2013; Sivaranjani et al., 2017). Most importantly, data from our previous study confirmed that α-MG effectively inhibits the onset of biofilm formation as well as disrupts the immature and mature biofilms of S. epidermidis RP62A biofilms, though the highest concentration of vancomycin was inefficient in killing the sessile cells of S. epidermidis RP62A (Sivaranjani et al., 2017). Similarly, Nguyen et al. (2014) reported that topical application of α-MG can effectively disrupt the development and structural integrity of Streptococcus mutans biofilm, which facilitates the mechanical clearance of cariogenic biofilms. Besides, several studies have demonstrated efficient methods to synthesize α-MG derivatives that also reflects the importance of α-MG and its derivatives in biological research (Matsumoto et al., 2004; Ha et al., 2009; Xu et al., 2013; Zou et al., 2013; Fei et al., 2014; Koh et al., 2015; Li et al., 2015; Koh et al., 2016). The potential bottleneck to develop α-MG as an effective antibacterial agent is the very limited understanding of the molecular mechanism of action of α-MG. Indeed, several studies have used omics techniques to elucidate the antibacterial mode of action of plant-derived compounds (Reddy et al., 2015; Dos Santos et al., 2016). Though, the rapid antibacterial mode of action of α-MG has been already investigated through in vitro and in silico approaches (Koh et al., 2013), integrated advanced omics technologies will further augment the current knowledge on the mode of action of α-MG. In the present study, we investigated the molecular mechanism of antibacterial activity of α-MG through an integrated transcriptomic and proteomic approach.

Materials and Methods

Bacterial Strain and Chemical

Staphylococcus epidermidis RP62A (ATCC 35984) was routinely grown in Luria-Bertani (LB; HiMedia, India) and was maintained in LB with 30% glycerol at -80°C. α-MG was purchased from Sigma-Aldrich (Catalog No.: M3824) and stock solution of 1 mg/mL was prepared in methanol.

Antibacterial Assays

The minimum inhibitory concentration (MIC), minimum bactericidal concentration (MBC) and time kill kinetics assays were previously determined (Sivaranjani et al., 2017). The MIC and MBC values of α-MG were determined again to precede subsequent assays (Clinical Laboratory Standards Institute [CLSI], 2006). The spot assay was carried out to determine the antibacterial activity of α-MG on mid-log phase cultures. Different concentrations of α-MG [1.25 μg/mL (MIC), 0.875 μg/mL (0.7 MIC), 0.625 μg/mL (0.5 MIC), 0.3125 μg/mL (0.25 MIC)] were added to mid-log phase (∼2.5 × 10⁸ CFU/ml) cultures that were subsequently incubated at 37°C for 10 min. After incubation, 10 μl of serially diluted control (0.1% methanol) and α-MG treated samples were spotted on LB plates. The plates were incubated at 37°C for 18 h.

RNA-Sequencing and Data Analysis

Overnight cultures of S. epidermidis were diluted in 1:100 in LB and were grown to mid-log phase (∼2.5 × 10⁸ CFU/ml) at 37°C. Bacterial cells were treated with 0.7 MIC (0.875 μg/ml) of α-MG or 0.1% methanol (solvent control) for 10 min. After incubation, 2 volumes of RNAprotect Bacteria Reagent (Qiagen, Hilden, Germany) were added to one volume of bacterial cultures. Then, the cells were pelleted by centrifugation, resuspended in 200 μl of TE buffer containing 15 mg/ml of lysozyme and 10 μl of proteinase K and incubated at 37°C for 30 min. After incubation, zirconia beads (50 mg; 0.1 mm) were added to lyse the cells using FastPrep 24 instrument (Qbiogene, Heidelberg, Germany) and the total RNA was extracted using RNeasy Mini kit (Qiagen, Hilden, Germany). To remove genomic DNA, on-column DNA digestion was done using RNase-Free DNase set (Qiagen, Hilden, Germany). The RNA integrity was analyzed using LabChip GXII Touch HT (PerkinElmer, United States). The ribosomal RNA (rRNA) was depleted using Ribo-Zero rRNA Removal kit for Gram-positive bacteria (Illumina, San Diego, CA, United States). Sequencing library was prepared as described before with modifications (Macosko et al., 2015). The libraries were sequenced in Biomedicum Functional Genomics Unit (Helsinki, Finland). Reverse transcription of mRNA was performed using specially designed primers. Similarly to the method described in Macosko et al. (2015), all the primers shared a common sequence that served as a PCR handle. Additionally, the primers contained known 12 bp barcode (unique for each sample) and different random unique molecular identifiers (UMIs) (Macosko et al., 2015). The poly (T) regions of the oligos were replaced by random hexamers to enable the capturing of the bacterial mRNA particles. The reverse transcription, PCR amplification of the cDNA and tagmentation were performed as described by Macosko et al. (2015). Paired-end sequencing was performed on NextSeq500 sequencer (Illumina) using the sequencing primers (Macosko et al., 2015). Sequencing in 75 cycles produced 20 bp Read 1 (bases 1–12 sample barcode, bases 13–20 UMI) and 55 bp Read 2 (sequence derived from the bacterial mRNA). The raw sequencing reads were analyzed using the Dropseq Core Computational Protocol (Macosko et al., 2015). The obtained sequencing reads were aligned against the strain S. epidermidis RP62A (ATCC 35984) genome using the STAR aligner (Dobin et al., 2013). The edgeR, a Bioconductor package was used to obtain the list of differentially expressed genes (Robinson et al., 2010). The RNA sequence data has been deposited to NCBI Gene Expression Omnibus (Accession No.: GSE113302).

Quantitative Proteomics

The mid-exponential growth phase (∼2.5 × 10⁸ CFU/ml) cultures were treated with 0.7 MIC (0.875 μg/ml) of α-MG or 0.1% methanol (solvent control) for 10 and 30 min. After incubation, α-MG treated and untreated cells were harvested by centrifugation at 3500 × g, washed with sterile PBS and resuspended in 1 ml of lysis buffer (0.1% RapiGest, 8 M urea, 100 mM ammonium bicarbonate). The cell suspension was sonicated for 10 min (Branson Sonifier 450; 30 s running, 30 s pause, pulsed mode 30%) and stored at -70°C. Prior to trypsin digestion of proteins, the protein samples were reduced with Tris (2-carboxyethyl) phosphine and alkylated with iodoacetamide. Subsequently, tryptic peptide digests were purified using C18 reversed-phase columns (Varjosalo et al., 2013) and the mass spectrometric analysis was performed in Orbitrap Elite ETD mass spectrometer (Thermo Scientific), using Xcalibur version 2.7.1 coupled with a Thermo Scientific nLCII nanoflow HPLC system. MS peak extraction and subsequent protein identification was analyzed using Proteome Discoverer software (Thermo Scientific). Calibrated peak files were searched against the S. epidermidis RP62A proteins (Uniprot) by a SEQUEST search engine. Error tolerance on the fragment and precursor ions were +0.8 Da and +15 p.p.m, respectively. For peptide identification, a stringent cut-off value (0.5% false discovery rate, FDR) was used.

Bioinformatics Tools

Gene ontology (GO) annotation and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway assignations were carried out to determine the function of differentially regulated genes, using STRING (version 10.5) with high confidence score of 0.7 (Carvalhais et al., 2014). Categories with a p-value ≤ 0.05 were set as statistically significant for gene enrichment. Differentially expressed hypothetical proteins were analyzed for putative functions using protein BLAST to search Pfam (protein families) domains in a Pfam database (version 31.0) and subcellular localization was predicted using PSORTb (Yu et al., 2010). The differentially expressed genes were also analyzed in the CELLO2GO¹ to retrieve the sub-cellular localization and functional GO annotation against Gram-positive bacteria with an E-value 0.001 (Yu et al., 2014).

Experimental Validation Using Quantitative Real-Time-PCR (qRT-PCR)

Twenty-one differentially expressed genes were selected for validation using qRT-PCR. The gene specific primers were designed using Primer3 software (version 0.4.0). The details of primers are listed in Supplementary Table 1. Total RNA was isolated as described above and cDNA was synthesized using Superscript III kit (Invitrogen Inc., United States) as per the manufacturer’s instructions. The qRT-PCR reaction was performed in 7500 Sequence Detection System (Applied Biosystems Inc., Foster, CA, United States). The mRNA expression patterns of selected genes were normalized against constitutively expressed two internal controls (16SrRNA and rplU) and quantified using 2^-ΔΔCt method. Three independent experiments were carried out in duplicate. Statistical significance was analyzed using unpaired Student t-test and considered significant at P < 0.05.

Results

Determination of α-MG Concentration for Transcriptomic and Proteomic Profiling Studies

The MIC and MBC of α-MG was found to be 1.25 and 5 μg/mL, respectively, which substantiates the results obtained from the previous study (Sivaranjani et al., 2017). Besides, Sivaranjani et al. (2017) have already reported the rapid bactericidal property of α-MG against S. epidermidis cells, where it displayed 6 log (4× MIC; 5 μg/mL) and 4 log (2× MIC; 2.5 μg/mL) reduction of viable count within 5 min of exposure time (Sivaranjani et al., 2017). Since transcriptional profiling is typically performed by the addition of antibacterial agents to mid-log phase cultures, spot assay was carried out to choose the concentration and duration of α-MG treatment. Based on the results, 0.7 MIC (0.875 μg/mL) of α-MG was chosen for 10 min and 30 min of antibacterial challenge with S. epidermidis (Supplementary Figure 1).

Global Transcriptome and Proteome Response to α-MG Treatment

Transcriptome Analysis

To uncover the antibacterial mode of action of α-MG, RNA sequencing was performed from α-MG treated (0.7 MIC, 10 min) and untreated S. epidermidis RP62A cells. A total of 2,411 genes were identified under both the conditions, which correspond to 91.84% of S. epidermidis RP62A (2,625 genes in GenBank). Of 2,411 genes, the edgeR analysis revealed differential expression of 98 genes (4.06%) with ≥1.5-fold difference in log FC (log fold change) with P < 0.001, wherein 48 (1.9%) genes were upregulated while the remaining 50 (2.07%) genes were downregulated in response to α-MG treatment. The details of differentially regulated genes, their role and the log FC are listed in Table 1. Besides, 33.6% (33/98) of differentially regulated genes were encoding uncharacterized proteins. Hence, identities of protein families and sub-cellular localization of hypothetical proteins were predicted accordingly using Pfam and PSORTb (Supplementary Table 2). In addition, 30.3% (10/33), 27.2% (9/33), 3% (1/33), and 39.3% (13/33) of the hypothetical proteins were predicted to be localized in the cytoplasmic membrane-associated, cytoplasic, extracellular and location-unknown, respectively.

The functional categorization for upregulated and downregulated genes was analyzed separately using STRING_10.5. Subsequently, GO (biological process, molecular function and cellular component) analysis for differentially regulated genes were annotated manually and the interacting network maps are shown in Figure 1A, 2A. According to GO annotation, the upregulated genes were scattered among various biological processes which included oxidation-reduction, metabolic, phosphorylation, nucleobase-containing small molecule metabolic, tricarboxylic acid (TCA) cycle and aerobic respiration processes (Figure 1B). The predominant molecular functions of upregulated genes were catalytic activity, oxidoreductase activity and other molecular functions (Figure 1C). Further, in the KEGG pathway analysis, the upregulated genes were shown to be involved in glycolysis/gluconeogenesis, TCA cycle, carbon metabolism, nitrogen metabolism, pyruvate metabolism, aminoacid biosynthesis, ABC transporters, RNA and fatty-acid degradation pathways (Figure 3A). Meanwhile, GO annotation of downregulated genes were involved in various biological processes viz., protoporphyrinogen IX biosynthetic, heme-biosynthetic, cofactor biosynthetic, sulfur compound biosynthetic and malonyl-CoA biosynthetic processes (Figure 2B). In addition, the KEGG pathway analysis indicated that the downregulated genes are involved in several metabolic pathways that include biosynthesis of secondary metabolites, fatty-acid biosynthesis, DNA replication and mismatch repair (Figure 3B). Acetyl-CoA carboxylase complex (GO.0009317) was the only significant cellular component encoded by the downregulated genes. Furthermore, the CELLO2GO, used for functional GO annotation and sub-cellular localization for proteins encoded by differentially expressed genes (Supplementary Figure 2), substantiated the results obtained from STRING_10.5 analysis. It has been reported to predict sub-cellular localization of proteins with 99.4% accuracy among Gram-positive bacteria (Yu et al., 2014). Among the proteins encoded by the 98 differentially expressed genes, 66.7, 18.9, 13.5, and 0.9% were predicted to be cytoplasmic, cytoplasmic membrane- associated, extracellular and cell wall-associated proteins, respectively.

FIGURE 1

FIGURE 2

FIGURE 3

Proteome Analysis

Proteomic profiling was employed to gain additional insights on the different cellular responses upon α-MG treatment. A total of 589 proteins were identified from all conditions, which corresponds to 23.51% of the predicted proteome (2505 proteins in UniProtKB database) of S. epidermidis RP62A. Prior to further analyses, Venn diagram (Supplementary Figure 3) was constructed to summarize the differences and similarities between proteins expressed in each conditions. It demonstrated that 492 proteins were expressed under all the conditions. Changes in proteome level were studied by comparing control cells with α-MG treated (0.7 MIC) cells at two different time points (10 and 30 min). Over all, differential expression (≥1.5-fold up- or down-regulation, p ≤ 0.05) of 89 proteins in response to α-MG treatment was observed: 34 proteins at 10 min (2 upregulated and 32 downregulated) and 70 proteins at 30 min (38 upregulated and 32 downregulated) (Table 2). However, only fifteen differentially expressed proteins (1 up- and 14 down-regulated) were found at both the time points. Of 89 proteins, 24 proteins were uncharacterized protein. The details of protein families and sub-cellular localization of uncharacterized proteins are listed in Supplementary Table 3. It was observed that most of the hypothetical proteins were localized in cytoplasmic membrane and cytoplasm (Supplementary Table 3). According to GO annotation, the upregulated and downregulated proteins are involved in various biological process and molecular function (Figure 4). The protein-protein interaction maps of upregulated and downregulated proteins are shown in Supplementary Figure 4. The KEGG pathway analysis predicted that the most strongly upregulated proteins are ribosomal proteins, and the most strongly downregulated proteins are involved in various metabolic pathways that include nucleotide excision repair, ABC transporters and phosphotransferase system (Figure 5). Besides, the GO annotation analysis of differentially regulated proteins using CELLO2GO is depicted in the Supplementary Figure 5. Among 89 differentially regulated proteins, 71, 15, and 11% were predicted to be cytoplasmic, membrane-associated, and extracellular proteins, respectively.

FIGURE 4

FIGURE 5

Validation of RNA-Sequencing and LC-MS/MS Data by qRT-PCR

The transcriptomic and proteomic results were further validated using qRT-PCR. qRT-PCR was performed with RNA isolated from bacteria under the similar experimental conditions used for the RNA-sequencing and LC-MS/MS analysis experiments. A total of 21 genes were selected randomly based on the functional categorization and KEGG pathway analysis. The obtained results were consistent with the transcriptomic and proteomic data (Figure 6), which not only validated the expression profiles of the selected genes, but also substantiated the reliability and accuracy of our transcriptome and proteome analyses. Based on the integrated transcriptome and proteome analyses and further validation through qRT-PCR, it was speculated that α-MG targets S. epidermidis through multifarious pathways viz., by principally targeting the cytoplasmic membrane integrity and by subsequently affecting fatty acid biosynthesis, DNA replication, DNA repair machinery, oxidative and cellular stress responses.

FIGURE 6

Discussion

The combination of transcriptome and proteome analyses demonstrated a panoramic view of the antibacterial mechanism of α-MG on S. epidermidis. Koh et al. (2013) reported that the rapid bactericidal action of α-MG is comparable with cell membrane lytic cationic antimicrobial peptides (CAMPs). The presence of carbonyl and hydroxyl groups might confer the negative charge to α-MG (Ahmad et al., 2013). Unlike conventional antibiotics that interact with specific targets, many CAMPs bind to anionic bacterial surface and perturb the cyotplasmic membrane (Hancock, 2001). In addition, α-MG is known to interact with transmembrane precursor proteins via hydrogen bonding (Wang et al., 2012). In parallel with this report, α-MG strongly downregulated the yidC2 gene (Table 1), which is involved in the integration of nascent membrane protein with dependent from or independent from the Sec-translocase (van der Laan et al., 2003). The proper membrane biogenesis depends on YidC, wherein it acts as a protein insertase, facilitates protein folding, ensues proper topology and an assembly factor for transmembrane proteins (Wang and Dalbey, 2011). The downregulated gene yidC2 (encoding a membrane protein insertase) was found to interact with the Sec pathway proteins such as SecA, SecY and FtsY, and the cell division protein FtsQ (encoded by divlB). The data from qRT-PCR revealed that secA, ftsY and divlB were downregulated upon α-MG treatment (Figure 6). Though data on the Sec system of Staphylococcus spp. is scarce, secA has been shown to be essential for cell viability (Ji et al., 2001; Jin et al., 2015). The small analogs of Rose Bengal inhibited the secA1 and secA2 of S. aureus thereby reducing the toxin secretion and bypassing the negative effect of efflux pumps (Ji et al., 2001). In addition, MscL (large conductance mechanosensitive channel protein) plays a vital role in protecting cells from osmotic downshock (Booth and Louis, 1999), which was downregulated upon α-MG treatment (Table 1). Facey et al. (2007) suggested that signal recognition particle (SRP) plays an important role in targeting of MscL protein to the cytoplasmic membrane and hence, the deletion of SRP receptor FtsY had a significant effect on the insertion of MscL. Moreover, the depletion of YidC2 inhibits the translocation of protein across the membrane. This confirms that downregulation of YidC2 and FtsY expression could inhibit the insertion of membrane protein MscL. Hence, the downregulation of these very important cytoplasmic membrane associated genes/proteins further corroborate that α-MG elicits bacterial killing by affecting the integrity of cytoplasmic membrane.

α-MG induced the expression level of certain heat-shock proteins (ClpB, ClpC, and GroEL) that ultimately rescue the cells from the lethal effect of α-MG (Table 1 and Figure 6). In parallel with our observation, the enhanced expression of the groES and groEL genes was observed upon oxacillin treatment, suggesting that upregulation of these heat-shock protein encoding genes is an integral part of cell wall active-antibiotic stress response (Singh et al., 2001). Under stress conditions, the chaperons and heat-shock proteins are capable of reactivating and refolding denatured proteins. Acyldepsipeptides, a new class of antibiotics, activate ClpP to degrade the cell division protein FtsZ, thereby arresting cell division (Sass et al., 2011). In line with this report, it was hypothesized that α-MG decrease the expression level of cell division related proteins (FtsY and DivlB) by increasing the Clp protease activity. Further, α-MG treatment increased the expression level of asp23 encoding the alkaline shock protein (Table 1 and Figure 6). In S. aureus, the transcription of asp23 is used as a marker for the activity of alternative sigma factor Sigma^B, which responds to various stress conditions by rapidly increasing its activity (Bischoff et al., 2001; Senn et al., 2005; Cebrian et al., 2009). Further, increased expression levels of the oxidative stress response genes, katA and sodA (encoding catalase and superoxide dismutase, respectively) were observed on α-MG treatment (Table 1 and Figure 6).

In addition to cytoplasmic membrane perturbation, α-MG seems to target very basic metabolic processes in order to kill the bacteria. Enzymes responsible for DNA replication play an indispensable role in cell growth and are therefore appropriate targets for antimicrobial agents. DNA polymerase I is encoded by the gene polA and two other important DNA replication specific enzymes, DNA polymerase III C and DNA polymerase III E are encoded by polC and dnaE. Both polC and dnaE are essential for chromosomal DNA replication in Gram-positive bacteria (Dervyn et al., 2001; Inoue et al., 2001). As reported by Inoue et al. (2001), inactivation of either polC or dnaE has a bactericidal effect on S. aureus. In addition, the downregulated genes uvrA and mfd have been shown to be involved in nucleotide excision repair machinery. UvrA detects the damaged DNA and the transcription repair coupling factor mfd attract the DNA-excision repair machinery to the damaged DNA (Ambur et al., 2009). Our transcriptomic and proteomic data shows the downregulation of polA, polC, dnaE, uvrA, and mfd genes upon α-MG treatment (Table 2 and Figure 6). Besides, the transcriptomic data shows the downregulation of the accB gene encoding a protein that interacts with AccC, AccB, AccA, AccD, FabF, FabG, FabH, FabI, and FabZ proteins (Table 1). These proteins are involved in fatty acid biosynthetic pathway (FASII), in which AccB is involved in the first committed step of FASII, catalyzing the formation of malonyl-CoA from acetyl-CoA. The qRT-PCR analysis also demonstrated the downregulation of all the selected genes involved in FASII pathway (Figure 6). In line with our report, platensimycin and platencin were shown to inhibit key FASII enzymes such as FabB/F and/or FabH against S. aureus, Streptococcus pneumonia, Enterococcus faecalis and Enterococcus faecium, which resulted in bacterial growth inhibition (Wang et al., 2006, 2007; Wright and Reynolds, 2007). In general, it is hypothesized that α-MG subsided the DNA replication, DNA repair machinery and fatty acid biosynthesis pathway which might further augment the bactericidal property of α-MG against S. epidermidis.

Furthermore, our transcriptomic and proteomic data shows the downregulation of tagG (encoding the teichoic acid ABC transporter protein) known to be involved in teichoic acids biosynthesis pathway (Tables 1, 2). The cell wall of gram-positive bacteria is mainly composed of peptidoglycan and Teichoic acids, both of which are important for maintaining the shape and structural integrity of the bacterial cell. Teichoic acids are anomeric polyglycerophosphate chains, which are exported via TagGH, a two component ABC transporter and then, either coupled with peptidoglycan (wall teichoic acids) or anchored from the cytoplasmic membrane (lipoteichoic acids). However, the D-alanylation modification regulates the interactions between bacterial cell membrane and CAMPs. For instance, increased D-alanylation of TAs provides resistance to CAMPs, possibly by increasing positive surface charge density. Our transcriptomic data suggested that the expression of dltA was clearly downregulated upon α-MG treatment (Table 1). The D-alanylation of TAs is directed by the dlt operon, where DltA begins the biosynthetic pathway by activating the D-alanine from aminoacyl adenylate. May et al. (2005) reported the analog of D-Ala aminoacyl adenylate as the inhibitor of DltA, that enhanced the susceptibility of Bacillus subtilis against cationic antibiotic vancomycin. In line with this report, our previous study signifies that the continuous exposure of α-MG does not induce resistance in planktonic as well as biofilm cells of S. epidermidis. This is possibly due to the downregulation of dltA which in turn averts positive surface charge density on bacterial membrane and facilitates the interaction between α-MG and bacterial cell membrane. Moreover, dltA mutant strain of S. aureus is unable to form biofilm on glass or polystyrene, which has been attributed by the inhibition of initial adherence and not accumulation, as the levels of polysaccharide intercellular adhesin (PIA) were unaltered (Gross et al., 2001). S. epidermidis and S. aureus have shown to possess icaABCD operon, wherein icaA encodes for N-acetylglucosaminyltransferase, an enzyme which is important for synthesis of PIA. The proteomic and qRT-PCR analyses showed downregulation of icaA which goes in parallel with our previous report (Sivaranjani et al., 2017), in which a less pronounced biofilm inhibition was observed at sub-MIC of α-MG. Of note, the mode of action of α-MG appears to involve compromising the cytoplasmic membrane integrity of Gram-positive bacteria. The cytoplasmic membrane perturbing ability of α-MG may also add credits in restricting the acquisition of bacterial resistance, as there is evidence suggesting that bacteria do not easily acquire resistance against membrane active antibacterial agents (Przybylski et al., 1998; Ooi et al., 2009).

Conclusion

Based on the integrated high throughput transcriptomic and proteomic analyses, the antibacterial mode of action of α-MG was identified to be more complex that targets multiple metabolic pathways. It was speculated that the principal target of α-MG seems to be cytoplasmic membrane which further orchestrate the downregulation of genes important for various metabolic pathways. α-MG downregulated the genes involved in FASII pathway, cell division, DNA replication, homologous recombination, mismatch repair, resistance development, biofilm, oxidative stress and cellular stress response, which are believed to be secondary targets of α-MG (Figure 7). As α-MG targets several metabolic pathways, resistance development by the bacterium will be minimal and thus α-MG may be further exploited for clinical trials. To our knowledge, this is one of the very first reports that potentiate the antibacterial activity of α-MG through an integrated transcriptomic and proteomic approach.

FIGURE 7

In addition, as α-MG targets multifarious pathway, further in depth analysis viz., mutational and in vivo studies on each pathway can be evaluated to identify the primary and secondary targets of α-MG. This will pave the way to develop α-MG as one of the vital drug candidates to treat the infections caused by S. epidermidis. Further, combination of any known bioactive compounds or with effective antibiotics not only increases the activity of known bioactive compounds but also can possibly assist the clinical development of these bioactive compounds. Further, combinatorial therapy avoids the resistant development by the bacterial pathogens as it involves the usage of lower/shorter dosing regimens. Hence, combination of α-MG with other well-known phytochemicals or conventional antibiotics can be carried out to evaluate the bactericidal property on mature biofilms.

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