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Article

Amphipathic Peptide Antibiotics with Potent Activity against Multidrug-Resistant Pathogens

by
Jingru Shi
1,
Chen Chen
1,
Dejuan Wang
1,
Ziwen Tong
1,
Zhiqiang Wang
1,2,3,* and
Yuan Liu
1,2,3,4,*
1
College of Veterinary Medicine, Yangzhou University, Yangzhou 225009, China
2
Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou University, Yangzhou 225009, China
3
Joint International Research Laboratory of Agriculture and Agri-Product Safety, The Ministry of Education of China, Yangzhou University, Yangzhou 225009, China
4
Institute of Comparative Medicine, Yangzhou University, Yangzhou 225009, China
*
Authors to whom correspondence should be addressed.
Pharmaceutics 2021, 13(4), 438; https://doi.org/10.3390/pharmaceutics13040438
Submission received: 14 February 2021 / Revised: 15 March 2021 / Accepted: 20 March 2021 / Published: 24 March 2021
(This article belongs to the Special Issue New Antimicrobial Agents and Non-invasive Drug Delivery Routes: A Look into the Future)
Browse Figures
Versions Notes

Abstract

:
The emergence and prevalence of multidrug-resistant (MDR) bacteria have posed a serious threat to public health. Of particular concern are methicillin-resistant Staphylococcus aureus (MRSA) and blaNDM, mcr-1 and tet(X)-positive Gram-negative pathogens. The fact that few new antibiotics have been approved in recent years exacerbates this global crisis, thus, new alternatives are urgently needed. Antimicrobial peptides (AMPs) originated from host defense peptides with a wide range of sources and multiple functions, are less prone to achieve resistance. All these characteristics laid the foundation for AMPs to become potential antibiotic candidates. In this study, we revealed that peptide WW307 displayed potent antibacterial and bactericidal activity against MDR bacteria, including MRSA and Gram-negative bacteria carrying blaNDM-5, mcr-1 or tet(X4). In addition, WW307 exhibited great biofilm inhibition and eradication activity. Safety and stability experiments showed that WW307 had a strong resistance against various physiological conditions and displayed relatively low toxicity. Mechanistic experiments showed that WW307 resulted in membrane damage by selectively targeting bacterial membrane-specific components, including lipopolysaccharide (LPS), phosphatidylglycerol (PG), and cardiolipin (CL). Moreover, WW307 dissipated membrane potential and triggered the production of reactive oxygen species (ROS). Collectively, these results demonstrated that WW307 represents a promising candidate for combating MDR pathogens.

1. Introduction

The increasing emergence of multidrug resistance in pathogenic bacteria has posed a serious threat to public health. Of particularly concern are hard-to-treat Gram-negative bacteria [1], such as Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, and Acinetobacter baumannii, which were identified as a major cause of systemic infections in clinic [2]. In recent years, colistin is recognized as the last line of defense against multidrug-resistant (MDR) Gram-negative bacteria [3], while the emergence of mobile colistin resistance gene mcr-1 has threatened the clinical effectiveness of colistin. Moreover, tigecycline resistance mediated by tet(X) and carbapenem resistance mediated by blaNDM genes [4], and the co-harboring of blaNDM, mcr-1 and/or tet(X) genes in clinical isolates leave no choice for clinicians in the treatment of MDR pathogens associated infectious diseases. Accordingly, if the development of drug resistance is not controlled, it may cause 10 million deaths by 2050, and the economic damage could exceed $100 trillion [5]. Nevertheless, few antibiotics have been approved for clinical use in the past decades [6], there is an urgent and unmet need to identify new antibiotic candidates [7].
Antimicrobial peptides (AMPs), also known as host defense peptides, have a wide range of sources and multiple functions such as protecting host from bacterial infections [8,9]. Compared with conventional antibiotics, bacteria are not prone to develop resistance against AMPs owing to its versatile mechanisms of action varies from membrane damage to interaction with intracellular targets [10,11,12]. Therefore, AMPs have been considered as a promising treatment option to combat the increasing drug-resistant pathogens [13]. Nevertheless, majority natural AMPs have not performed high optimization for direct antibacterial activity [14,15]. By contrast, synthetic AMPs by computer-assisted de novo design or modification from the sequences of naturally occurring AMPs are more effective against bacteria [16,17,18,19]. For example, a synthetic derivative of human AMPs LL-37, termed SAAP-148, exhibited improved bactericidal activity and plasma stability in killing MDR pathogens, including biofilm-producing bacteria and persister cells [20]. In addition, the truncation of MSI-78 at the N-terminal resulted in a 14-amino-acids AMPs named MSI-1 [21], which displayed superior activity and lower toxicity than its parent AMPs. Recently, two amphipathic peptide antibiotics termed horine and verine with systemic efficiency in mice infection models were identified [22]. Meanwhile, two optimized derivatives including WW304 and WW307 were proposed, which displayed lower hemolytic activity to red blood cells (RBCs) [22]. However, the antibacterial potential of these two peptides and its synergistic effect with clinically relevant antibiotics in the fight against MDR bacteria, particularly for hard-to-treat Gram-negative bacteria carrying blaNDM, mcr, and/or tet(X) genes, remains unknown.
Herein, we systematically evaluated the antimicrobial activity of WW304 and WW307 against a panel of MDR bacteria and investigated the potential mechanisms of action. Interestingly, WW307 could efficiently kill a panel of MDR pathogenic bacteria, including methicillin-resistant Staphylococcus aureus (MRSA) and MDR Gram-negative bacteria carrying blaNDM, mcr, and/or tet(X) genes. In addition, WW307 effectively prevented biofilm formation, and eradicated established biofilms and persister cells. Moreover, WW307 retained its activity under different physiological conditions in vitro. Our further experiments uncovered that the killing activity of WW307 is related to membrane permeabilization via the interaction with bacterial-specific phospholipids, the dissipation of membrane potential and the generation of ROS.

2. Materials and Methods

2.1. Peptide Synthesis and Validation

The peptides used in this paper were synthesized by solid phase peptide synthesis (SPPS) by GL Biochem (Shanghai, China), and their accurate molecular weights were determined by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. The purity of all peptides was greater than 95%, indicating that they were accurately obtained.
The chemical structure of the peptides was mapped using Chemdraw software. Helical wheel projection and various chemical parameters such as net charge and hydrophobicity were calculated with https://www.donarmstrong.com/cgi-bin/wheel.pl (accessed on 23 March 2021).

2.2. Antibacterial Activity Tests

2.2.1. Minimum Inhibitory Concentrations (MICs) Determination

The MICs of all drugs were determined by micro-broth dilution method according to CLSI 2018 guidelines [23]. The bacterial suspension used in the experiment was appropriate 1.5 × 106 colony-forming units (CFUs) per mL and mixed with the drug solution in a sterilized 96-well microtiter plate (Corning, New York, USA), then incubated at 37 °C for 16–18 h. MIC value was defined as the minimum drug concentration without visible bacteria. Meanwhile, the density of the bacteria at 600 nm was measured, and the corresponding IC50 was calculated using log (inhibitor) vs. response variable slope (four parameters) in Graphpad Prism version 8.3.0 software (San Diego, CA, USA). To assess the role of ROS production in the antibacterial activity of WW307, increasing concentrations of N-acetylcysteine (NAC) from 0 to 5 mM were added in culture medium, followed by MICs test.

2.2.2. Mutant Prevention Concentrations (MPCs) Determination

For the MPC assay, 100 μL MRSA T144 or E. coli B2 suspensions (~1010 CFUs) were plated on Mueller-Hinton agar (MHA) plates containing increasing concentrations of WW307. Subsequently, the plates were incubated at 37 °C for 72 h. MPC was defined as the lowest peptide concentration that prevented the growth of resistant colonies [24]. For each strain, MPC was determined in at least two independent experiments.

2.2.3. Salts and Serum Stability

In order to evaluate the influence of ions and serum on the activity of AMPs, 10 mM Na+, K+, Mg2+, 10% Dulbecco’s Modified Eagle Medium (DMEM) and fetal bovine serum (FBS) were added into Mueller-Hinton broth (MHB) culture medium for subsequent MIC tests.

2.2.4. Thermal, pH and Proteolytic Stability

Drugs were incubated at different temperatures (range from 40 to 121 °C) and pH (range from 2 to 12) for 1 h, then adjust back to original pH, following MIC test to evaluate their residual activity [25]. To evaluate the protease stability, pepsin, trypsin, and papain were mixed with WW307 to achieve a final concentration of 1 mM, and then incubated at 37 °C for 1 h. After incubation, the remaining protease was precipitated using acetonitrile and removed by centrifugation at 3000× g, following for MIC test.

2.2.5. LPS and Lipids Inhibition Assay

The effects of LPS and phospholipids (Sigma-Aldrich), including phosphatidylcholine (PC), phosphatidylethanolamine (PE), phosphatidylglycerol (PG), and cardiolipin (CL), on the antibacterial activity of WW307 were evaluated using the checkerboard microdilution assay [26]. Briefly, LPS from E. coli O111:B4 (0–128 μg/mL) and phospholipids (0–16 μg/mL) were 2-fold diluted into the broth, then bacteria suspension and WW307 mixture was added. Following MIC test to evaluate the activity changes of WW307.

2.3. Checkerboard Assays

The synergistic antibacterial activity of all peptides with different antibiotics were determined by micro-broth dilution using flat bottom 96-well microtiter plate (Corning, New York, USA). The mixture of bacterial solution, peptides and antibiotics were incubated at 37 °C for 16–18 h, and then the optical density (OD) at 600 nm was measured. Two biological replicates were performed for each combination and the corresponding FIC index (FICI) was calculated using the formula as follows [27]: ΣFIC = FICA + FICB; FICA = (MICA in the presence of B/MICA alone); FICB = (MICB in the presence of A/MICB alone). Synergy is defined as an FIC index of ≤0.5.

2.4. Time-Dependent Killing

MRSA T144 and E. coli B2 were cultured in 37 °C for 4–6 h, then diluted 1/1000 in MHB. In 96-well flat-bottom plates (Corning), different concentrations of WW307 (0–256 μg/mL) were added and mixed with bacterial suspension (~106 CFUs/mL), then incubated at 37 °C for 0.5, 1, 2 and 4 h, respectively. At each time point, 20 μL of the above mixture was removed and mixed with 180 μL PBS. Subsequently, ten-fold serially diluted suspensions were plated on MHA plates and incubated overnight at 37 °C. The bacterial colonies were counted and the primary CFUs/mL was calculated.

2.5. Prevention of Biofilm Formation

The ability of WW307 on the prevention of biofilm formation was assessed using crystal violet method [28]. In brief, MRSA T144 and E. coli B2 (1.5 × 106 CFUs/mL) mixed with different concentrations of WW307 were cultured in 96-well microtiter flat plate (Corning) at 37 °C. After 48 h incubation, the planktonic bacteria were removed by washing three times with sterile PBS solution. Afterward, 100 μL methanol was added and fixed for 15 min. Next, the fixed solution was sucked out for natural air drying. Dried wells were stained with 100 μL of 0.1% crystal violet for 15 min and the remaining crystal violet was rinsed with PBS for twice. Finally, 100 μL 33% acetic acid was added and cultured at 37 °C for 30 min to dissolve crystal violet. The absorbance at 570 nm was determined as a measure of biofilm mass.

2.6. Eradication of Established Mature Biofilms

Exponential phase MRSA T144 and E. coli B2 cells were diluted in 1/1,000, then mixed with 200 μL MHB and cultured in 96-well microtiter plate (Corning) at 37 °C for 48 h to promote biofilm formation [28]. After washed three times with PBS, different concentrations of WW307 were added and cultured at 37 °C. After 2 h of incubation, the wells were emptied, washed, and sonicated for 15 min to disperse biofilm cells. Next, bacteria diluted suspensions were plated on MHA plates and incubated overnight at 37 °C. Bacterial colonies were counted and the primary CFUs per mL were calculated. Finally, the remaining CFUs were used to evaluate the removal of the biofilm.

2.7. Hemolysis Analysis

The hemolytic activity on all peptides was evaluated based on previous report [28]. Briefly, fresh Sheep RBCs were washed twice with phosphate buffer (PBS), and then 8% red blood cell suspension was prepared. The increasing concentrations of AMPs and melittin were mixed with 8% red blood cell suspension, respectively, and incubated at 37 °C for 1 h. The sterilized PBS and double-distilled water (ddH2O) were used as blank and positive control, respectively. Afterwards, the supernatant was centrifuged to measure the absorption of released hemoglobin at 576 nm by an Infinite M200 Microplate reader (Tecan, Männedorf, Switzerland). The corresponding hemolysis rate was calculated.

2.8. Circular Dichroism (CD) Measurements

CD spectra of the peptides in four different solvents, including 0.01 M PBS (pH = 7.2), 50 μM LPS, 50 mM sodium dodecyl sulfate (SDS), and 50% trifluoroethanol (TFEA) [21], were measured using a J-810 spectropolarimeter (Jasco, Tokyo, Japan) at 25 °C. The wavelength recorded values were 190–300 nm, and the measurements were repeated three times.

2.9. Outer Membrane Permeabilization

Overnight MRSA T144 and E. coli B2 cells were washed and resuspended in PBS to obtain an OD600 of 0.5, followed by the addition of 0.1 μM of 1-N-phenylnaphthylamine (NPN) (Aladdin), and incubated in a constant temperature shaking table at 37 °C for 30 min in dark [29]. Subsequently, 190 µL of probe-labelled cells were incubated with 10 µL of WW307 (0 to 128 µg/mL) in a sterile 96-well black plate for 1 h. After incubation, the fluorescence intensity (λexcitation = 350 nm, λemission = 420 nm) was measured using an Infinite M200 Microplate reader (Tecan, Männedorf, Switzerland).

2.10. Membrane Permeability Assay

The fluorescent dye propidium iodide (PI) (Beyotime, Shanghai, China) was used to assess the integrity of bacterial cell membranes [30]. MRSA T144 and E. coli B2 cells were incubated with PI (0.5 μM) for 30 min in dark, and the labelled cells were treated with increasing concentrations of WW307. After 1 h incubation, the fluorescence intensity (λexcitation = 535 nm, λemission = 615 nm) was determined using an Infinite M200 Microplate reader (Tecan, Männedorf, Switzerland).

2.11. Cytoplasmic Membrane Potential

3′, 3′-dipropylthiadicarbocyanine iodide (DiSC3(5)) (Aladdin, Shanghai, China) was applied to determine the membrane potential of MRSA T144 and E. coli B2 [30]. MRSA T144 and E. coli B2 suspensions (OD600 = 0.5) were incubated with DiSC3(5) (0.5 μM) in dark for 30 min and incubated with WW307 (0–128 μg/mL) for 1 h. Then, the fluorescence intensity (λexcitation = 622 nm, λemission = 670 nm) was determined using an Infinite M200 Microplate reader (Tecan, Männedorf, Switzerland).

2.12. ROS Measurements

2′,7′-dichlorodihydrofluorescein diacetate (DCFH-DA) (Beyotime) was applied to monitor the levels of ROS in MRSA T144 and E. coli B2. DCFH-DA (10 μM) was pre-incubated with MRSA T144 and E. coli B2 cells for 30 min, then removed excess fluorescent probes that have not entered the cells by centrifugation and washing with PBS. Subsequently, the probed-cells were incubated with varying concentrations of WW307 (0–128 μg/mL) for 1 h in dark. After incubation, the fluorescence intensity (λexcitation = 488 nm, λemission = 525 nm) was immediately measured using an Infinite M200 Microplate reader (Tecan, Männedorf, Switzerland).

2.13. Statistical Analysis

All data were shown as mean ± SD. Statistical significance was determined by unpaired t test between two groups or non-parametric one-way ANOVA among multiple groups using GraphPad Prism 8 (NS, not significant; * p < 0.05, ** p < 0.01, *** p < 0.001).

3. Results

3.1. Characterizations of Peptides

As shown in Table 1, WW304 and WW307 were all cationic peptides, with net charges of +3. The purity of the two peptides were greater than 95%, indicated that the peptides were obtained accurately. The wheel diagram showed both WW304 and WW307 exhibited imperfect amphiphilic structures that possessed interrupted hydrophobic and cationic faces (Figure 1).

3.2. Potent Antibacterial Activity of Peptide In Vitro

Next, we tested the antimicrobial activity of WW304 and WW307 against a panel of MDR bacteria, including MRSA and Gram-negative bacteria co-carrying blaNDM, mcr, and/or tet(X) genes. Results showed that WW307 displayed the best activity against all test MDR bacteria with MIC values from 1–8 μg/mL (Table 2), while WW304 only had modest activity against Gram-positive bacteria (MIC, 8 μg/mL) rather than Gram-negative bacteria (MIC, 32 or 64 μg/mL). In addition, the MPC of WW307 against MRSA T144 and E. coli B2 was 64 μg/mL. Meanwhile, we determined the IC50 values of WW304 and WW307 against all tested strains using melittin as a control. In agreement with the MIC analysis, WW307 showed the lowest IC50 values from 0.52 to 4.18 μg/mL, indicating that WW307 had superior antibacterial activity than WW304 and melittin (Figure 2). The potent broad-spectrum activity of WW307 against these MDR pathogens implied that the activity of WW307 was independent of the current existing resistance determinants. Therefore, WW307 was selected as a drug candidate for our following studies.

3.3. WW307 Is a Potent Antibiotic Adjuvant

The increasing problem of antibiotic resistance calls for new therapeutic strategies, such as antibiotic adjuvants, which offer a productive approach to combat MDR pathogens [31]. For example, cationic AMPs were found to synergize with azithromycin against MDR Gram-negative bacteria [32,33]. As such, we evaluated the adjuvant potency of WW307 in combination with different classes of antibiotic via checkerboard assay using two MDR isolates MRSA T144 [34] and E. coli B2 [35] as test strains. Consequently, we found that WW307 showed no synergistic activity against MRSA T144 when in combination with different antibiotics (Figure 3A), while WW307 potentiated the rifampicin, novobiocin and vancomycin activities against blaNDM-5 and mcr-1 co-carrying E. coli B2 (Figure 3B), with FICI of 0.14, 0.3125 and 0.375, respectively. Interestingly, WW307 had synergistic antibacterial activity with hydrophobic antibiotics such as rifampicin, novobiocin and vancomycin against E. coli B2, rather than ampicillin, kanamycin, ciprofloxacin, doxycycline, and meropenem. These results suggested that WW307 effectively synergized with Gram-positive active antibiotics against Gram-negative bacteria. Considering that the outer membrane of Gram-negative bacteria serves as a barrier for Gram-positive active antibiotics, we speculated that WW307 may serve as an outer membrane-active targeted compounds.
Considering the potential antibacterial activity and synergistic antibacterial activity of WW307, we further determined the secondary structure of WW307 in different solvents by CD analysis. As LPS is an important component of the outer membrane of Gram-negative bacteria [36], thus LPS was chosen to simulate the bacterial cell environment. The SDS with negative charge surface and TFEA were used to simulate the anionic membrane environment and hydrophobic environment of bacterial membrane, respectively [37]. As shown in Figure 4, WW307 exhibited helix and turn mixed structure in PBS. In 50 μM LPS, 50 mM SDS, and 50% TFEA, the helix ratio showed a downward trend and the proportion of random increased, while in SDS, the ratio of beta sheet increased to 80.5%. All this implied that secondary structures of WW307 would present in a hybrid form when it interacts with the bacterial membrane.

3.4. Rapid Bactericidal Efficiency of WW307 against MDR In Vitro

In consideration of the potent growth inhibitory activity of WW307 on MDR pathogens, so we next performed time- and concentration-dependent killing assays [38] to determine whether WW307 has a great bactericidal activity. As shown in Figure 5A,B, WW307 exhibited rapid killing effect on MRSA T144 and E. coli B2, and WW307 can completely eradicate MRSA T144 and E. coli B2 at 32 μg/mL and 16 μg/mL during one hour, respectively. Moreover, the bactericidal activity of WW307 exhibited an obvious time- and concentration-dependent manner. These results suggested that WW307 was a potent bactericidal antibiotic.

3.5. WW307 Exhibits Biofilm Inhibition and Eradication Activities

The production of biofilms by bacteria makes it difficult for common antibiotics to function and easy to cause chronic infections [28]. Therefore, we further evaluated the ability of WW307 on biofilms formation and eradication. As shown in Figure 5C, we observed that WW307 dose-dependently inhibited the formation of biofilms by MRSA T144 and E. coli B2 using crystal violet assay. Excitingly, a significant inhibition effect was also observed under the treatment of low level of WW307 (0.25 μg/mL, corresponding to 0.0625-fold MIC). However, the crystal violet staining method cannot characterize the effect of WW307 on metabolic activity in biofilm. The use of other methods such as 2,3,5-triphenyl-tetrazolium chloride (TTC) analysis [39] would strengthen the inhibitory ability of WW307 on biofilm formation. Furthermore, we found that established biofilms of MRSA T144 and E. coli B2 formed on a plasma-coated surface were remarkably eradicated by WW307 in a dose-dependent manner (Figure 5D).

3.6. A Desirable Stability and Safety of WW307 against Bacteria

The great stability of AMPs is a critical prerequisite for its in vivo efficacy [40]. Therefore, we assessed the residual antibacterial activity of WW307 after exposure to different temperatures and pH conditions [21]. Surprisingly, WW307 completely retained its activity after treatment under 40–121 °C or pH (2 to 12) for 1 h, indicating that WW307 possessed great thermal and pH stability (Table 3). We speculated that the great stability of WW307 may be related to the unspecific or mixed secondary structures of WW307 in solutions, which have been evidenced by CD assay. Next, we evaluated the activity of WW307 in three salt ions including Na+, K+ and Mg2+ [41]. As shown in Table 3, WW307 retained full activity against MRSA T144 and E. coli B2 in the presence of monovalent cation, while divalent cation mg2+ remarkably reduced the activity of WW307. Given that the divalent cation is usually as the stabilizer of outer membrane of Gram-negative bacteria [42], it can be speculated that the action of WW307 may be related to bacterial membrane damage. In addition, culture media containing 10% serum and DMEM were used to simulate in vivo matrix environment. The results showed that the antibacterial activity of WW307 in these two substrates reduced only two folds. Moreover, the proteolytic stability of WW307 after incubated with different proteases, including pepsin, trypsin and papain, was evaluated. No loss of antibacterial activity of WW307 in the presence of pepsin was found, whereas trypsin and papain completely abolished the activity of WW307. This may correlate with the amino acid composition of WW307, especially the high proportion of arginine at the N-terminal [43].
Safety is a key factor that prevents AMPs from entering clinical use, thus we further evaluated the hemolytic properties of WW307 with defibrillated sheep red blood cells. Consistent with previous study [22], Figure 6 showed that WW304 and WW307 had the dispensable hemolytic activity (HL50 > 128 µg/mL) on mammalian RBCs, while melittin exhibited high hemolytic activity with HL50 of 14.39 µg/mL, indicating that WW307 had higher selectivity for bacteria rather than mammalian cells.

3.7. WW307 Targets Bacteria Membrane Components and Leads to Membrane Damage

Having shown the potent antibacterial and bactericidal activities of WW307, we next sought to elucidate the potential mechanisms of action of WW307. The synergistic antibacterial activity indicated that WW307 could significantly promote the antibacterial activity of Gram-positive active antibiotics against E. coli B2, suggesting that WW307 might be a membrane-active antibiotic. Moreover, the ionic stability indicated that divalent cation Mg2+ supplementation could significantly impair the antibacterial activity of WW307 (Table 3). Considering that LPS locates in outer membrane of Gram-negative bacteria are commonly stabilized with divalent cations particularly Mg2+ [44], therefore, we further speculated that WW307 might compete with Mg2+ for binding to LPS. All these points implied that WW307 is an outer membrane destructive peptide antibiotic. In addition to the outer membrane, cytoplasmic membrane is an important barrier in both Gram-positive and Gram-negative bacteria. Accordingly, PG, CL and PE are the main constituents of the cytoplasmic membrane, while PC mainly exists in eukaryotic cells [45]. To investigate whether WW307 could target these components of bacterial membrane, varying concentrations of exogenous LPS, PG, CL, PE and PC were added in MIC analysis. The results showed that exogenous addition of LPS abolished the antibacterial activity of WW307 against MRSA T144 and E. coli B2 (Figure 7A), suggesting the close interaction of WW307 and LPS. In addition to LPS, PG and CL supplementation except for PC remarkably impaired the antibacterial activity of WW307 (Figure 7B,C), indicating a great selectivity of WW307. These results suggested that WW307 could specifically bind to bacterial membrane related components, such as LPS, PG and CL.
To further characterize membrane damage caused by WW307, a hydrophobic fluorescence probe 1-N-phenylnaphthylamine (NPN) [30] was applied to evaluate the effect of WW307 on the outer membrane permeability of E. coli B2. As a result, the fluorescence intensity showed a concentration-dependent increase, indicating that WW307 seriously disrupted the outer membrane of E. coli B2 (Figure 7D). Next, we used propidium iodide (PI) to evaluate the whole membrane permeability [46]. As shown in Figure 7E, WW307 led to a dose-dependent increase of PI fluorescence in E. coli B2, implying a remarkable damage to the bacterial membrane. Taken together, all above results suggested that WW307 was a membrane destructive antibiotic through targeting bacteria membrane related components.

3.8. WW307 Dissipates the ΔΨ Component of Bacterial Proton Motive Force

Proton motive force (PMF) is generated by bacterial transmembrane potential and is made up of two parameters: the electric potential (ΔΨ) and the transmembrane proton gradient (ΔpH). These two components work together to maintain dynamic balance of the PMF, which is critical to bacterial survival [47]. To investigate the influence of WW307 on the membrane potential of MRSA T144 and E. coli B2, 3′,3′-dipropylthiacarbocyanine iodide (DiSC3(5)) was applied for this purpose [35]. DiSC3(5) accumulates in the cytoplasmic membrane in response to the ΔΨ component of the PMF. As the disruption of ΔΨ, the probe would be released into the extracellular milieu and result in increased fluorescence. Conversely, the disruption of ΔpH would be compensated by increasing ΔΨ, resulting in enhanced DiSC3(5) uptake into the cytoplasmic membrane and therefore decreased fluorescence [48]. Our results showed that exposure of cells into varying concentrations of WW307 resulted in an immediate increase in DiSC3(5) fluorescence in a dose-dependent manner (Figure 8A,B), suggesting that WW307 selectively dissipated the ΔΨ component of the PMF. To validate this finding, we next assay the MIC changes of WW307 in different pH nutrient matrix conditions. As shown in Figure 8C,D, we observed that the antibacterial activity of WW307 decreased under acidic conditions, but increased under alkaline conditions, which is consistent with previous results that WW307 disrupted the membrane potential of MRSA T144 and E. coli B2.

3.9. WW307 Promotes the Production of ROS

The production of reactive oxygen species (ROS) has been recognized as a key factor for antibiotic-mediated killing. Given that WW307 is a potential bactericidal peptide antibiotic, we next used 2′,7′-Dichlorodihydrofluorescein diacetate (DCFH-DA) [49] to measure the ROS level in bacteria imposed by WW307. Consistently, WW307 triggered the production of ROS in a concentration-dependent manner (Figure 9A,B). To evaluate the role of ROS generation in the antibacterial activity of WW307, ROS scavenger NAC was added in the following MIC analysis. Interestingly, addition of NAC (5 mM) dramatically abolished the activity of WW307 against MRSA T144 and E. coli B2, with 4-fold increase of MIC values (Figure 9C,D). These results suggested that the production of ROS is essential for the bactericidal activity of WW307 against MDR bacterial pathogens.

4. Discussion

Recalcitrant and complicated infections in clinics caused by MDR pathogens, particularly for Gram-negative bacteria, call for novel antibacterial pipeline. Owing to the limited choice from existing antibiotic regimens in the resistance era, AMPs have attracted global attention as novel drug candidates for the treatment of infectious diseases. In this study, we investigated the antibacterial activity and mechanisms of action of two amphipathic peptides (WW304 and 307) in the fight against MDR pathogens. As a consequence, we found that WW307 exhibited potent broad-spectrum bacteriostatic and bactericidal activity for all tested pathogens, including emerging blaNDM, mcr and/or tet(X)-positive Gram-negative bacteria. Most importantly, the stability and safety evaluation indicated that WW307 retained its activity under various physiological conditions and displayed no hemolytic activity below 128 μg/mL. Nevertheless, more preclinical studies, including in vivo efficacy and toxicity evaluation in mammals, are required to further verify its effectiveness and safety.
With regard to the modes of action of WW307, we found that WW307 is a membrane-active peptide antibiotic. Consistently, most AMPs particularly for cationic AMPs exert bactericidal effects by disrupting the membrane integrity [50]. Heretofore, three classical models, including barrel-stave model, toroidal-pore model, and carpet model, were proposed to describe membrane perturbation by AMPs [51]. For example, amphibian-derived AMPs magainin 2 [52] and aurein 1.2 [53] disrupted membrane via the toroidal-pore and carpet mechanisms, respectively. In our studies, we further revealed that WW307 disrupted membrane permeability by specifically binding to bacterial membrane-specific components, including LPS, PG, and CL. Considering that these targets carry negatively charged head groups, we proposed electrostatic force between positively charged WW307 and these targets may account for its membrane interaction. Additionally, we also found that WW307 dissipated the ΔΨ component of bacterial PMF, which is essential for a variety of critical bacterial processes, such as ATP synthesis, flagellar motility, and nutrient import [47]. Recently, a novel antibiotic named halicin was identified using a deep learning approach [54]. Notably, halicin acts by dissipates the ΔpH component of PMF. These examples implied that bacterial PMF may serve as a novel antibacterial target for future antibiotic discovery and development. Furthermore, consistent with previously reported bactericidal AMPs such as WRK-12 and SLAP-S25 [55,56], ROS production was also evidenced to be important for the antibacterial activity of WW307.
In conclusion, we revealed that amphipathic peptide WW307 is a bacterial membrane-active AMP that could simultaneously disrupt the permeability of bacterial membrane, dissipate membrane potential and induce the production of ROS. These findings suggested that WW307 is a potent antibiotic candidate and shows great potential for clinical use to combat MDR pathogens.

Author Contributions

Y.L. and Z.W. conceived and designed the project; J.S., C.C., D.W. and Z.T. performed all experiments; Y.L. and J.S. analyzed the data and wrote the paper. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by the National Natural Science Foundation of China (32002331), National Key Research and Development Program of China (2018YFA0903400), Natural Science Foundation of Jiangsu Province of China (BK20190893), Agricultural Science and Technology Independent Innovation Fund of Jiangsu Province (CX(20)3091), China Postdoctoral Science Foundation (2019M651984), A Project Funded by the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD) and Lift Engineering of Young Talents of Jiangsu Association for Science and Technology.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

All data in this study have been included in this manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Cochrane, S.A.; Findlay, B.; Bakhtiary, A.; Acedo, J.Z.; Rodriguez-Lopez, E.M.; Mercier, P.; Vederas, J.C. Antimicrobial lipopeptide tridecaptin A1 selectively binds to Gram-negative lipid II. Proc. Natl. Acad. Sci. USA 2016, 113, 11561–11566. [Google Scholar] [CrossRef] [Green Version]
  2. Doi, Y.; Bonomo, R.A.; Hooper, D.C.; Kaye, K.S.; Johnson, J.R.; Clancy, C.J.; Thaden, J.T.; Stryjewski, M.E.; van Duin, D. Gram-negative bacterial infections: Research priorities, accomplishments, and future directions of the antibacterial resistance leadership group. Clin. Infect. Dis. 2017, 64, S30–S35. [Google Scholar] [CrossRef] [Green Version]
  3. Li, J.; Nation, R.L.; Turnidge, J.D.; Milne, R.W.; Coulthard, K.; Rayner, C.R.; Paterson, D.L. Colistin: The re-emerging antibiotic for multidrug-resistant Gram-negative bacterial infections. Lancet Infect. Dis. 2006, 6, 589–601. [Google Scholar] [CrossRef]
  4. Ma, B.; Fang, C.; Lu, L.; Wang, M.; Xue, X.; Zhou, Y.; Li, M.; Hu, Y.; Luo, X.; Hou, Z. The antimicrobial peptide thanatin disrupts the bacterial outer membrane and inactivates the NDM-1 metallo-beta-lactamase. Nat. Commun. 2019, 10, 3517. [Google Scholar] [CrossRef] [Green Version]
  5. Mishra, B.; Lakshmaiah Narayana, J.; Lushnikova, T.; Wang, X.; Wang, G. Low cationicity is important for systemic in vivo efficacy of database-derived peptides against drug-resistant Gram-positive pathogens. Proc. Natl. Acad. Sci. USA 2019, 116, 13517–13522. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Zeng, P.; Xu, C.; Liu, C.; Liu, J.; Cheng, Q.; Gao, W.; Yang, X.; Chen, S.; Chan, K.-F.; Wong, K.-Y. De novo designed hexadecapeptides synergize glycopeptide antibiotics vancomycin and teicoplanin against pathogenic Klebsiella pneumoniae via disruption of cell permeability and potential. ACS Appl. Bio Mater. 2020, 3, 1738–1752. [Google Scholar] [CrossRef]
  7. Lazzaro, B.P.; Zasloff, M.; Rolff, J. Antimicrobial peptides: Application informed by evolution. Science 2020, 368, eaau5480. [Google Scholar] [CrossRef] [PubMed]
  8. Liu, Y.; Shi, J.; Tong, Z.; Jia, Y.; Yang, B.; Wang, Z. The revitalization of antimicrobial peptides in the resistance era. Pharmacol. Res. 2021, 163, 105276. [Google Scholar] [CrossRef] [PubMed]
  9. Bitschar, K.; Sauer, B.; Focken, J.; Dehmer, H.; Moos, S.; Konnerth, M.; Schilling, N.A.; Grond, S.; Kalbacher, H.; Kurschus, F.C.; et al. Lugdunin amplifies innate immune responses in the skin in synergy with host- and microbiota-derived factors. Nat. Commun. 2019, 10, 2730. [Google Scholar] [CrossRef]
  10. Lai, Z.; Tan, P.; Zhu, Y.; Shao, C.; Shan, A.; Li, L. Highly stabilized alpha-helical coiled coils kill gram-negative bacteria by multicomplementary mechanisms under acidic condition. ACS Appl. Mater. Interfaces 2019, 11, 22113–22128. [Google Scholar] [CrossRef] [PubMed]
  11. Kim, W.; Zou, G.; Hari, T.P.A.; Wilt, I.K.; Zhu, W.; Galle, N.; Faizi, H.A.; Hendricks, G.L.; Tori, K.; Pan, W.; et al. A selective membrane-targeting repurposed antibiotic with activity against persistent methicillin-resistant Staphylococcus aureus. Proc. Natl. Acad. Sci. USA 2019, 116, 16529–16534. [Google Scholar] [CrossRef] [Green Version]
  12. Wang, J.; Song, J.; Yang, Z.; He, S.; Yang, Y.; Feng, X.; Dou, X.; Shan, A. Antimicrobial peptides with high proteolytic resistance for combating Gram-negative bacteria. J. Med. Chem. 2019, 62, 2286–2304. [Google Scholar] [CrossRef] [PubMed]
  13. Tucker, A.T.; Leonard, S.P.; DuBois, C.D.; Knauf, G.A.; Cunningham, A.L.; Wilke, C.O.; Trent, M.S.; Davies, B.W. Discovery of next-generation antimicrobials through bacterial self-screening of surface-displayed peptide libraries. Cell 2018, 172, 618–628.e13. [Google Scholar] [CrossRef] [PubMed]
  14. Rajasekaran, G.; Kim, E.Y.; Shin, S.Y. LL-37-derived membrane-active FK-13 analogs possessing cell selectivity, anti-biofilm activity and synergy with chloramphenicol and anti-inflammatory activity. BBA-Biomembr. 2017, 1859, 722–733. [Google Scholar] [CrossRef]
  15. Liang, Y.; Zhang, X.; Yuan, Y.; Bao, Y.; Xiong, M. Role and modulation of the secondary structure of antimicrobial peptides to improve selectivity. Biomater. Sci. 2020, 8, 6858–6866. [Google Scholar] [CrossRef] [PubMed]
  16. Mishra, B.; Wang, G. Ab initio design of potent anti-MRSA peptides based on database filtering technology. J. Am. Chem. Soc. 2012, 134, 12426–12429. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  17. Tan, P.; Lai, Z.; Jian, Q.; Shao, C.; Zhu, Y.; Li, G.; Shan, A. Design of heptad repeat amphiphiles based on database filtering and structure-function relationships to combat drug-resistant fungi and biofilms. ACS Appl. Mater. Interfaces 2020, 12, 2129–2144. [Google Scholar] [CrossRef] [PubMed]
  18. Lin, S.; Wade, J.D.; Liu, S. De novo design of flavonoid-based mimetics of cationic antimicrobial peptides: Discovery, development, and applications. ACC Chem. Res. 2021, 54, 104–119. [Google Scholar] [CrossRef] [PubMed]
  19. Bhattacharjya, S.; Straus, S.K. Design, engineering and discovery of novel alpha-helical and beta-boomerang antimicrobial peptides against drug resistant bacteria. Int. J. Mol. Sci. 2020, 21, 5773. [Google Scholar] [CrossRef] [PubMed]
  20. de Breij, A.; Riool, M.; Cordfunke, R.A.; Malanovic, N.; de Boer, L.; Koning, R.I.; Ravensbergen, E.; Franken, M.; van der Heijde, T.; Boekema, B.K.; et al. The antimicrobial peptide SAAP-148 combats drug-resistant bacteria and biofilms. Sci. Transl. Med. 2018, 10, eaan4044. [Google Scholar] [CrossRef] [Green Version]
  21. Ma, L.; Xie, X.; Liu, H.; Huang, Y.; Wu, H.; Jiang, M.; Xu, P.; Ye, X.; Zhou, C. Potent antibacterial activity of MSI-1 derived from the magainin 2 peptide against drug-resistant bacteria. Theranostics 2020, 10, 1373–1390. [Google Scholar] [CrossRef]
  22. Lakshmaiah Narayana, J.; Mishra, B.; Lushnikova, T.; Wu, Q.; Chhonker, Y.S.; Zhang, Y.; Zarena, D.; Salnikov, E.S.; Dang, X.; Wang, F.; et al. Two distinct amphipathic peptide antibiotics with systemic efficacy. Proc. Natl. Acad. Sci. USA 2020, 117, 19446–19454. [Google Scholar] [CrossRef] [PubMed]
  23. Clinical and Laboratory Standards Institute. Performance Standards for Antimicrobial Susceptibility Testing; CLSI: Wayne, PA, USA, 2018. [Google Scholar]
  24. Marcusson, L.L.; Olofsson, S.K.; Komp Lindgren, P.; Cars, O.; Hughes, D. Mutant prevention concentrations of ciprofloxacin for urinary tract infection isolates of Escherichia coli. J. Antimicrob. Chemother. 2005, 55, 938–943. [Google Scholar] [CrossRef] [Green Version]
  25. Liu, Y.; Song, M.; Ding, S.; Zhu, K. Discovery of linear low-cationic peptides to target methicillin-resistant Staphylococcus aureus in vivo. ACS Infect. Dis. 2019, 5, 123–130. [Google Scholar] [CrossRef] [PubMed]
  26. Johnston, C.W.; Skinnider, M.A.; Dejong, C.A.; Rees, P.N.; Chen, G.M.; Walker, C.G.; French, S.; Brown, E.D.; Berdy, J.; Liu, D.Y.; et al. Assembly and clustering of natural antibiotics guides target identification. Nat. Chem. Biol. 2016, 12, 233–239. [Google Scholar] [CrossRef] [PubMed]
  27. Stokes, J.M.; MacNair, C.R.; Ilyas, B.; French, S.; Cote, J.P.; Bouwman, C.; Farha, M.A.; Sieron, A.O.; Whitfield, C.; Coombes, B.K.; et al. Pentamidine sensitizes Gram-negative pathogens to antibiotics and overcomes acquired colistin resistance. Nat. Microbiol. 2017, 2, 17028. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  28. Mwangi, J.; Yin, Y.; Wang, G.; Yang, M.; Li, Y.; Zhang, Z.; Lai, R. The antimicrobial peptide ZY4 combats multidrug-resistant Pseudomonas aeruginosa and Acinetobacter baumannii infection. Proc. Natl. Acad. Sci. USA 2019, 116, 26516–26522. [Google Scholar] [CrossRef] [Green Version]
  29. MacNair, C.R.; Tsai, C.N.; Brown, E.D. Creative targeting of the Gram-negative outer membrane in antibiotic discovery. Ann. N. Y. Acad. Sci. 2020, 1459, 69–85. [Google Scholar] [CrossRef]
  30. Liu, Y.; Jia, Y.; Yang, K.; Tong, Z.; Shi, J.; Li, R.; Xiao, X.; Ren, W.; Hardeland, R.; Reiter, R.J.; et al. Melatonin overcomes MCR-mediated colistin resistance in Gram-negative pathogens. Theranostics 2020, 10, 10697–10711. [Google Scholar] [CrossRef] [PubMed]
  31. Liu, Y.; Li, R.; Xiao, X.; Wang, Z. Antibiotic adjuvants: An alternative approach to overcome multi-drug resistant Gram-negative bacteria. Crit. Rev. Microbiol. 2019, 45, 301–314. [Google Scholar] [CrossRef] [PubMed]
  32. Lin, L.; Nonejuie, P.; Munguia, J.; Hollands, A.; Olson, J.; Dam, Q.; Kumaraswamy, M.; Rivera, H., Jr.; Corriden, R.; Rohde, M.; et al. Azithromycin synergizes with cationic antimicrobial peptides to exert bactericidal and therapeutic activity against highly multidrug-resistant gram-negative bacterial pathogens. EBioMedicine 2015, 2, 690–698. [Google Scholar] [CrossRef] [Green Version]
  33. Brochado, A.R.; Telzerow, A.; Bobonis, J.; Banzhaf, M.; Mateus, A.; Selkrig, J.; Huth, E.; Bassler, S.; Zamarreño Beas, J.; Zietek, M.; et al. Species-specific activity of antibacterial drug combinations. Nature 2018, 559, 259–263. [Google Scholar] [CrossRef]
  34. Liu, Y.; Ding, S.; Dietrich, R.; Märtlbauer, E.; Zhu, K. A biosurfactant-inspired heptapeptide with improved specificity to kill MRSA. Angew. Chem. Int. Ed. 2017, 56, 1486–1490. [Google Scholar] [CrossRef]
  35. Liu, Y.; Jia, Y.; Yang, K.; Li, R.; Xiao, X.; Zhu, K.; Wang, Z. Metformin restores tetracyclines susceptibility against multidrug resistant bacteria. Adv. Sci. 2020, 7, 1902227. [Google Scholar] [CrossRef]
  36. Maldonado, R.F.; Sá-Correia, I.; Valvano, M.A. Lipopolysaccharide modification in Gram-negative bacteria during chronic infection. FEMS Microbiol. Rev. 2016, 40, 480–493. [Google Scholar] [CrossRef] [PubMed]
  37. Yang, Z.Y.; He, S.Q.; Wang, J.J.; Yang, Y.; Zhang, L.C.; Li, Y.B.; Shan, A.S. Rational design of short peptide variants by using Kunitzin-RE, an amphibian-derived bioactivity peptide, for acquired potent broad-spectrum antimicrobial and improved therapeutic potential of commensalism coinfection of pathogens. J. Med. Chem. 2019, 62, 4586–4605. [Google Scholar] [CrossRef] [PubMed]
  38. Zheng, E.J.; Stokes, J.M.; Collins, J.J. Eradicating bacterial persisters with combinations of strongly and weakly metabolism-dependent antibiotics. Cell Chem. Biol. 2020, 27, 1544–1552.e3. [Google Scholar] [CrossRef] [PubMed]
  39. Brown, H.L.; van Vliet, A.H.M.; Betts, R.P.; Reuter, M. Tetrazolium reduction allows assessment of biofilm formation by Campylobacter jejuni in a food matrix model. J. Appl. Microbiol. 2013, 115, 1212–1221. [Google Scholar] [CrossRef]
  40. Zhu, Y.; Shao, C.; Li, G.; Lai, Z.; Tan, P.; Jian, Q.; Cheng, B.; Shan, A. Rational avoidance of protease cleavage sites and symmetrical end-tagging significantly enhances the stability and therapeutic potential of antimicrobial peptides. J. Med. Chem. 2020, 63, 9421–9435. [Google Scholar] [CrossRef]
  41. Ma, Z.; Yang, J.; Han, J.; Gao, L.; Liu, H.; Lu, Z.; Zhao, H.; Bie, X. Insights into the antimicrobial activity and cytotoxicity of engineered alpha-helical peptide amphiphiles. J. Med. Chem. 2016, 59, 10946–10962. [Google Scholar] [CrossRef] [PubMed]
  42. Vergalli, J.; Bodrenko, I.V.; Masi, M.; Moynié, L.; Acosta-Gutiérrez, S.; Naismith, J.H.; Davin-Regli, A.; Ceccarelli, M.; van den Berg, B.; Winterhalter, M.; et al. Porins and small-molecule translocation across the outer membrane of Gram-negative bacteria. Nat. Rev. Microbiol. 2020, 18, 164–176. [Google Scholar] [CrossRef] [PubMed]
  43. Olsen, J.V.; Ong, S.-E.; Mann, M. Trypsin cleaves exclusively C-terminal to arginine and lysine residues. Mol. Cell. Proteom. 2004, 3, 608–614. [Google Scholar] [CrossRef] [Green Version]
  44. Klein, G.; Kobylak, N.; Lindner, B.; Stupak, A.; Raina, S. Assembly of lipopolysaccharide in Escherichia coli requires the essential LapB heat shock protein. J. Biol. Chem. 2014, 289, 14829–14853. [Google Scholar] [CrossRef] [Green Version]
  45. Sohlenkamp, C.; Geiger, O. Bacterial membrane lipids: Diversity in structures and pathways. FEMS Microbiol. Rev. 2016, 40, 133–159. [Google Scholar] [CrossRef] [Green Version]
  46. Martin, J.K., 2nd; Sheehan, J.P.; Bratton, B.P.; Moore, G.M.; Mateus, A.; Li, S.H.; Kim, H.; Rabinowitz, J.D.; Typas, A.; Savitski, M.M.; et al. A dual-mechanism antibiotic kills gram-negative bacteria and avoids drug resistance. Cell 2020, 181, 1518–1532.e14. [Google Scholar] [CrossRef] [PubMed]
  47. Farha, M.A.; Verschoor, C.P.; Bowdish, D.; Brown, E.D. Collapsing the proton motive force to identify synergistic combinations against Staphylococcus aureus. Chem. Biol. 2013, 20, 1168–1178. [Google Scholar] [CrossRef] [Green Version]
  48. Matsuno, T.; Goto, T.; Ogami, S.; Morimoto, H.; Yamazaki, K.; Inoue, N.; Matsuyama, H.; Yoshimune, K.; Yumoto, I. Formation of proton motive force under low-aeration alkaline conditions in alkaliphilic bacteria. Front. Microbiol. 2018, 9, 2331. [Google Scholar] [CrossRef] [Green Version]
  49. Hong, Y.; Li, L.; Luan, G.; Drlica, K.; Zhao, X. Contribution of reactive oxygen species to thymineless death in Escherichia coli. Nat. Microbiol. 2017, 2, 1667–1675. [Google Scholar] [CrossRef] [PubMed]
  50. Hancock, R.E.; Sahl, H.G. Antimicrobial and host-defense peptides as new anti-infective therapeutic strategies. Nat. Biotechnol. 2006, 24, 1551–1557. [Google Scholar] [CrossRef] [PubMed]
  51. Mahlapuu, M.; Björn, C.; Ekblom, J. Antimicrobial peptides as therapeutic agents: Opportunities and challenges. Crit. Rev. Biotechnol. 2020, 40, 978–992. [Google Scholar] [CrossRef] [PubMed]
  52. Mescola, A.; Marín-Medina, N.; Ragazzini, G.; Accolla, M.; Alessandrini, A. Magainin-H2 effects on the permeabilization and mechanical properties of giant unilamellar vesicles. J. Colloid Interface Sci. 2019, 553, 247–258. [Google Scholar] [CrossRef]
  53. Shahmiri, M.; Cornell, B.; Mechler, A. Phenylalanine residues act as membrane anchors in the antimicrobial action of Aurein 1.2. Biointerphases 2017, 12, 05G605. [Google Scholar] [CrossRef] [PubMed]
  54. Stokes, J.M.; Yang, K.; Swanson, K.; Jin, W.; Cubillos-Ruiz, A.; Donghia, N.M.; MacNair, C.R.; French, S.; Carfrae, L.A.; Bloom-Ackerman, Z.; et al. A deep learning approach to antibiotic discovery. Cell 2020, 180, 688–702. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  55. Liu, Y.; Shi, J.; Tong, Z.; Jia, Y.; Yang, K.; Wang, Z. Potent broad-spectrum antibacterial activity of amphiphilic peptides against multidrug-resistant bacteria. Microorganisms 2020, 8, 1398. [Google Scholar] [CrossRef] [PubMed]
  56. Song, M.; Liu, Y.; Huang, X.; Ding, S.; Wang, Y.; Shen, J.; Zhu, K. A broad-spectrum antibiotic adjuvant reverses multidrug-resistant Gram-negative pathogens. Nat. Microbiol. 2020, 5, 1040–1050. [Google Scholar] [CrossRef]
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Figure 1. Design and characterization of two amphipathic Antimicrobial peptides (AMPs). (A) Chemical structures of two active AMPs (WW304 and WW307). (B) Helical wheel projections of WW304 and WW307. The hydrophilic residues as circles, hydrophobic residues as diamonds, and potentially positively charged as pentagons. Hydrophobicity is color coded as well: the most hydrophobic residue is green, and the amount of green is decreasing proportionally to the hydrophobicity, with zero hydrophobicity coded as yellow.
Figure 1. Design and characterization of two amphipathic Antimicrobial peptides (AMPs). (A) Chemical structures of two active AMPs (WW304 and WW307). (B) Helical wheel projections of WW304 and WW307. The hydrophilic residues as circles, hydrophobic residues as diamonds, and potentially positively charged as pentagons. Hydrophobicity is color coded as well: the most hydrophobic residue is green, and the amount of green is decreasing proportionally to the hydrophobicity, with zero hydrophobicity coded as yellow.
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Figure 2. Half-maximal inhibitory concentrations (IC50) assay of WW304, WW307, and melitten against 10 tested MDR pathogens. Dose response curves (A–C) and IC50 values (D) of WW304, WW307, and melitten on tested pathogens.
Figure 2. Half-maximal inhibitory concentrations (IC50) assay of WW304, WW307, and melitten against 10 tested MDR pathogens. Dose response curves (A–C) and IC50 values (D) of WW304, WW307, and melitten on tested pathogens.
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Figure 3. Checkerboard broth microdilution assays between WW307 with different classes of antibiotics against methicillin-resistant Staphylococcus (MRSA) T144 and E. coli B2. (A) Synergistic antibacterial activity of WW307 with four antibiotics against MRSA T144. (B) Synergistic antibacterial activity of WW307 with eight antibiotics against E. coli B2. Bacterial cells and drugs were cultured at 37 °C for 16–18 h, then the density of cells at 600 nm was measured, the darker color means the higher density of bacteria. Data represent the mean of two biological replicates.
Figure 3. Checkerboard broth microdilution assays between WW307 with different classes of antibiotics against methicillin-resistant Staphylococcus (MRSA) T144 and E. coli B2. (A) Synergistic antibacterial activity of WW307 with four antibiotics against MRSA T144. (B) Synergistic antibacterial activity of WW307 with eight antibiotics against E. coli B2. Bacterial cells and drugs were cultured at 37 °C for 16–18 h, then the density of cells at 600 nm was measured, the darker color means the higher density of bacteria. Data represent the mean of two biological replicates.
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Figure 4. Circular dichroism (CD) spectra of WW307 in various solutions. PBS (10 mM, pH = 7.4), lipopolysaccharide (LPS) (50 μM), sodium dodecyl sulfate (SDS) (50 mM), and 50% TFEA were used. The values from three scans were averaged per sample, and the peptide concentrations were fixed at 100 μg/mL.
Figure 4. Circular dichroism (CD) spectra of WW307 in various solutions. PBS (10 mM, pH = 7.4), lipopolysaccharide (LPS) (50 μM), sodium dodecyl sulfate (SDS) (50 mM), and 50% TFEA were used. The values from three scans were averaged per sample, and the peptide concentrations were fixed at 100 μg/mL.
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Figure 5. Bactericidal ability and anti-biofilm activity of WW307. (A,B) The time- and concentration-killing curves of WW307 against MRSA T144 and E. coli B2. The mixture of varying concentrations of WW307 (0–256 μg/mL) and bacterial solution was incubated at 37 °C for 0.5, 1, 2, and 4 h, respectively. Afterwards, ten-fold serially suspensions were plated on MHA plates and incubated overnight, and the corresponding CFUs were counted and calculated. (C) Inhibitory effects of WW307 on MRSA T144 and E. coli B2 biofilm formation. Bacterial cells were cultured in 96-well plates at 37 °C with or without WW307 (0–4 μg/mL). After 48 h incubation, the biofilm mass was determined using crystal violet method. (D) Eradication abilities of WW307 against mature biofilm by MRSA T144 and E. coli B2. Bacterial suspensions were cultured at 37 °C for 48 h. Then, WW307 from 0 to 128 μg/mL was added and incubated at 37 °C for 2 h. Eradication effect of WW307 on biofilm was evaluated by determining the remaining CFUs. All data from at least three biological replicates were presented as mean ± SD, and the statistical significance was determined by unpaired t test (C) or non-parametric one-way ANOVA (D) (* p < 0.05, ** p < 0.01. *** p < 0.001, **** p < 0.0001).
Figure 5. Bactericidal ability and anti-biofilm activity of WW307. (A,B) The time- and concentration-killing curves of WW307 against MRSA T144 and E. coli B2. The mixture of varying concentrations of WW307 (0–256 μg/mL) and bacterial solution was incubated at 37 °C for 0.5, 1, 2, and 4 h, respectively. Afterwards, ten-fold serially suspensions were plated on MHA plates and incubated overnight, and the corresponding CFUs were counted and calculated. (C) Inhibitory effects of WW307 on MRSA T144 and E. coli B2 biofilm formation. Bacterial cells were cultured in 96-well plates at 37 °C with or without WW307 (0–4 μg/mL). After 48 h incubation, the biofilm mass was determined using crystal violet method. (D) Eradication abilities of WW307 against mature biofilm by MRSA T144 and E. coli B2. Bacterial suspensions were cultured at 37 °C for 48 h. Then, WW307 from 0 to 128 μg/mL was added and incubated at 37 °C for 2 h. Eradication effect of WW307 on biofilm was evaluated by determining the remaining CFUs. All data from at least three biological replicates were presented as mean ± SD, and the statistical significance was determined by unpaired t test (C) or non-parametric one-way ANOVA (D) (* p < 0.05, ** p < 0.01. *** p < 0.001, **** p < 0.0001).
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Figure 6. Hemolytic activity of peptides against mammalian red blood cells (RBCs). HL50 is the peptide concentration that causes 50% hemolysis. Sterilized PBS and ddH2O were used as a negative control and positive control, respectively.
Figure 6. Hemolytic activity of peptides against mammalian red blood cells (RBCs). HL50 is the peptide concentration that causes 50% hemolysis. Sterilized PBS and ddH2O were used as a negative control and positive control, respectively.
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Figure 7. WW307 disrupts bacterial membrane permeability by specifically targeting lipopolysaccharide (LPS) and various phospholipids. (A) Exogenous addition of LPS deriving from E. coli O111:B4 impaired the antibacterial activity of WW307 against MRSA T144 and E. coli B2 in a dose-dependent manner. (B,C) Increased MICs of WW307 against MRSA T144 and E. coli B2 in the presence of PG, CL and PE. The 96-well plates were incubated at 37 °C for 16-18 h for MIC analysis. (D,E) WW307 disrupted the outer membrane and whole cell membrane permeability of E. coli B2, which were assessed by fluorescence probes 1-N-phenylnaphthylamine (NPN, excitation 350 nm and emission 420 nm) and propidium iodide (PI, excitation 535 nm and emission 615), respectively. Bacterial cells were incubated with fluorescent probes at 37 °C for 30 min in dark, then different concentrations of WW307 (0–128 μg/mL) was added and incubated at 37 °C for 1 h. All data were presented as mean ± SD, and the statistical significance was determined by non-parametric one-way ANOVA (NS, not significant; *** p < 0.001, **** p < 0.0001).
Figure 7. WW307 disrupts bacterial membrane permeability by specifically targeting lipopolysaccharide (LPS) and various phospholipids. (A) Exogenous addition of LPS deriving from E. coli O111:B4 impaired the antibacterial activity of WW307 against MRSA T144 and E. coli B2 in a dose-dependent manner. (B,C) Increased MICs of WW307 against MRSA T144 and E. coli B2 in the presence of PG, CL and PE. The 96-well plates were incubated at 37 °C for 16-18 h for MIC analysis. (D,E) WW307 disrupted the outer membrane and whole cell membrane permeability of E. coli B2, which were assessed by fluorescence probes 1-N-phenylnaphthylamine (NPN, excitation 350 nm and emission 420 nm) and propidium iodide (PI, excitation 535 nm and emission 615), respectively. Bacterial cells were incubated with fluorescent probes at 37 °C for 30 min in dark, then different concentrations of WW307 (0–128 μg/mL) was added and incubated at 37 °C for 1 h. All data were presented as mean ± SD, and the statistical significance was determined by non-parametric one-way ANOVA (NS, not significant; *** p < 0.001, **** p < 0.0001).
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Figure 8. WW307 dissipates the ΔΨ component of the proton motive force (PMF). (A,B) WW307 dissipated the membrane potential of MRSA T144 and E. coli B2, determined by monitoring the fluorescence intensity of 3,3’-dipropylthiadicarbocyanine iodide (DiSC3(5), excitation at 622 nm and emission at 670 nm). DiSC3(5)-labeled cells were incubated with WW307 at 37 °C for 1 h prior to fluorescence intensity determination. (C,D) The shift to alkaline environment enhanced the antibacterial activity of WW307 against MRSA T144 and E. coli B2. In A and B, all data were expressed as mean ± SD, and the statistical significance was determined by non-parametric one-way ANOVA (NS, not significant; ** p < 0.01, **** p < 0.0001).
Figure 8. WW307 dissipates the ΔΨ component of the proton motive force (PMF). (A,B) WW307 dissipated the membrane potential of MRSA T144 and E. coli B2, determined by monitoring the fluorescence intensity of 3,3’-dipropylthiadicarbocyanine iodide (DiSC3(5), excitation at 622 nm and emission at 670 nm). DiSC3(5)-labeled cells were incubated with WW307 at 37 °C for 1 h prior to fluorescence intensity determination. (C,D) The shift to alkaline environment enhanced the antibacterial activity of WW307 against MRSA T144 and E. coli B2. In A and B, all data were expressed as mean ± SD, and the statistical significance was determined by non-parametric one-way ANOVA (NS, not significant; ** p < 0.01, **** p < 0.0001).
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Figure 9. WW307 triggers the production of ROS in MRSA T144 and E. coli B2. The production of ROS of MRSA T144 (A) and E. coli B2 (B) was determined by 2’,7’-dichlorodihydrofluorescein diacetate (DCFH-DA, excitation at 488 nm and emission at 525 nm). Before fluorescence assay, probe-labelled cells were incubated with WW307 at 37 °C for 1 h. (C,D) N-acetylcysteine (NAC) supplementation abolished the antibacterial activity of WW307 against MRSA T144 and E. coli B2. In A and B, all data were presented as mean ± SD, and the statistical significance was determined by non-parametric one-way ANOVA (NS, not significant; * p < 0.05, ** p < 0.01, **** p < 0.0001).
Figure 9. WW307 triggers the production of ROS in MRSA T144 and E. coli B2. The production of ROS of MRSA T144 (A) and E. coli B2 (B) was determined by 2’,7’-dichlorodihydrofluorescein diacetate (DCFH-DA, excitation at 488 nm and emission at 525 nm). Before fluorescence assay, probe-labelled cells were incubated with WW307 at 37 °C for 1 h. (C,D) N-acetylcysteine (NAC) supplementation abolished the antibacterial activity of WW307 against MRSA T144 and E. coli B2. In A and B, all data were presented as mean ± SD, and the statistical significance was determined by non-parametric one-way ANOVA (NS, not significant; * p < 0.05, ** p < 0.01, **** p < 0.0001).
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Table
Table 1. Key physicochemical parameters of amphipathic peptides.
Table 1. Key physicochemical parameters of amphipathic peptides.
NameSequence (N → C)FormulaMWNet ChargepI #Purity (%)
WW291WWWLRKIW-NH2C68H89N17O81272.58+211.0096.57%
WW304WWWLRRRW-NH2C68H90N22O81343.62+312.3095.33%
WW295RKIWWWWL-NH2C68H89N17O81272.58+211.0095.49%
WW307RRRWWWWV-NH2C67H88N22O81329.59+312.3095.79%
# The pI values of derivatives were determined by ExPASy (http://web.expasy.org/compute_pi/, accessed on 15 March 2021).
Table
Table 2. Antimicrobial activity of amphiphilic peptides against a panel of MDR pathogenic bacteria (MIC, μg/mL).
Table 2. Antimicrobial activity of amphiphilic peptides against a panel of MDR pathogenic bacteria (MIC, μg/mL).
Organisms and PhenotypesWW304WW307MelittinMEMCOLTIG
S. aureus G16 (RIFR)81221<0.0625
MRSA T1448441160.25
E. coli B2 (mcr-1 + blaNDM-5)64483282
E. coli C3 (blaNDM-1)64488<0.1252
E. coli G6 (blaNDM-5)6484640.52
E. coli G92 (mcr-1)6444<0.12544
E. coli CP131 (mcr-3)3244<0.12542
E. coli 1F28 (tet(X4))32440.250.12516
A. baumannii C222 (tet(X6))6448<0.125<0.12564
P. cibarius HNCF44W (blaNDM-1 + tet(X6))6424>16>25664
RIFR, rifampicin-resistant; MRSA, methicillin-resistant Staphylococcus aureus. MEM, meropenem; COL, colistin; TIG, tigecycline.
Table
Table 3. Thermal, pH, salts and protease stability of WW307 against MRSA T144 and E. coli B2 (MIC, μg/mL).
Table 3. Thermal, pH, salts and protease stability of WW307 against MRSA T144 and E. coli B2 (MIC, μg/mL).
TreatmentsWW307
MRSA T144E. coli B2
Control44
Temperature
40 °C44
60 °C44
80 °C44
100 °C44
121 °C44
pH
244
444
644
844
1044
1248
Salt ions (10 mM)
Na+44
K+44
Mg2+1616
Protease (1 mg/mL)
Pepsin44
Trypsin>128>128
Papain>128>128
Serum (10%)88
DMEM (10%)88
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Shi, J.; Chen, C.; Wang, D.; Tong, Z.; Wang, Z.; Liu, Y. Amphipathic Peptide Antibiotics with Potent Activity against Multidrug-Resistant Pathogens. Pharmaceutics 2021, 13, 438. https://doi.org/10.3390/pharmaceutics13040438

AMA Style

Shi J, Chen C, Wang D, Tong Z, Wang Z, Liu Y. Amphipathic Peptide Antibiotics with Potent Activity against Multidrug-Resistant Pathogens. Pharmaceutics. 2021; 13(4):438. https://doi.org/10.3390/pharmaceutics13040438

Chicago/Turabian Style

Shi, Jingru, Chen Chen, Dejuan Wang, Ziwen Tong, Zhiqiang Wang, and Yuan Liu. 2021. "Amphipathic Peptide Antibiotics with Potent Activity against Multidrug-Resistant Pathogens" Pharmaceutics 13, no. 4: 438. https://doi.org/10.3390/pharmaceutics13040438

APA Style

Shi, J., Chen, C., Wang, D., Tong, Z., Wang, Z., & Liu, Y. (2021). Amphipathic Peptide Antibiotics with Potent Activity against Multidrug-Resistant Pathogens. Pharmaceutics, 13(4), 438. https://doi.org/10.3390/pharmaceutics13040438

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