Therapeutic compounds targeting Lipid II for antibacterial purposes.

Resistance against commonly used antibiotics has emerged in all bacterial pathogens. In fact, there is no antibiotic currently in clinical use against which resistance has not been reported. In particular, rapidly increasing urbanization in developing nations are sites of major concern. Additionally, the widespread practice by physicians to prescribe antibiotics in cases of viral infections puts selective pressure on antibiotics that still remain effective and it will only be a matter of time before resistance develops on a large scale. The biosynthesis pathway of the bacterial cell wall is well studied and a validated target for the development of antibacterial agents. Cell wall biosynthesis involves two major processes; 1) the biosynthesis of cell wall teichoic acids and 2) the biosynthesis of peptidoglycan. Key molecules in these pathways, including enzymes and precursor molecules are attractive targets for the development of novel antibacterial agents. In this review, we will focus on the major class of natural antibacterial compounds that target the peptidoglycan precursor molecule Lipid II; namely the glycopeptides, including the novel generation of lipoglycopeptides. We will discuss their mechanism-of-action and clinical applications. Further, we will briefly discuss additional peptides that target Lipid II such as the lantibiotic nisin and defensins. We will highlight recent developments and future perspectives.

Introduction

Bacterial cell wall assembly

The cell wall of both Gram-negative and -positive bacteria comprises a peptidoglycan layer which is composed of a polymer of alternating amino sugars, N-acetylglucosamine (GlcNAc) and N-acetylmuramic acid (MurNAc). Cross-linking of the polymer chains by pentapeptides achieves mechanical strength and structural integrity of the cell.1 In addition to that it protects the cell from osmotic stress. Inhibition of peptidoglycan biosynthesis inhibits cell growth. This makes the assembly and maintenance of the peptidoglycan polymer a commonly used target for antibiotics. Figure 1 illustrates membrane events in the biosynthesis of the peptidoglycan layer.

Figure 1

Membrane bound processes in the bacterial cell wall biosynthesis cycle. Lipid II binding antibiotics are shown corresponding to the step in the cycle that they inhibit.

Note: *varying per species.2

Abbreviations: G, N-acetyl glucosamine; M, N-acetyl muramic acid; MraY, phospho-MurNAc-pentapeptide translocase; MurG, Undecaprenyldiphospho-muramoylpentapeptide beta-N-acetylglucosaminyltransferase; UMP, uridine monophosphate; UDP, uridine diphosphate.

On the cytoplasmic side of the plasma membrane first the soluble precursor UDP-MurNAc-pentapeptide is linked to the membrane carrier bactoprenol-phosphate (C55P) yielding Lipid I. In a second step GlcNac is added by the enzyme MurG to yield Lipid II.3–5 In preparation for building interpeptide bridges between individual Lipid II molecules additional amino acids are added to the pentapeptide by Fem ligases (eg Gly in case of S. aureus).2 Lipid II is then translocated along the membrane to the peripheral side by a not well understoodmechanism.Recent binding studies suggest that this process might be mediated by the flippase enzyme MurJ.6 However, other candidates including RodA and FtsW have been suggested.7,8 On the periplasmic side penicillin-binding proteins (PBPs) catalyze the incorporation of the peptidoglycan unit into the growing cell wall. Class A PBPs obtain insertion of the MurNAc-peptide-GlcNAc subunit into the nascent peptidoglycan layer (transglycosylation) before the peptidoglycan chains are linked together by the formation of peptide crossbridges through the action of both class A - and B PBPs (transpeptidation).9

The remaining complex of lipid anchor and pyrophosphate is shuttled back to the cytosolic side. It can then be reused for following Lipid II synthesis.3 The amount of Lipid II that can be synthesized is limited by the small amount of bactoprenyl phosphate that is available on the cytosolic membrane. About 2×105 molecules C55P per cell have to provide for the enduring synthesis of around 20 peptidoglycan layers in Gram-positive and 1.5 in Gram-negative bacteria.10,11 This is achieved by a high turnover rate of Lipid II which was estimated to be about 1–3 transits per second per prenyl chain.12 The dynamic process of this Lipid II cycle can therefore be regarded as a bottleneck in the bacterial cell wall synthesis. The fact that clustering and dislocating Lipid II leads to dysfunction of the cell wall synthesis suggests that any molecule that binds lipid II with high affinity is a potential antibiotic.4

Lipid II- binding antibiotics

Table 1 Overview of known antibiotic compounds that interact with Lipid II. The stage of development, and the assumed interaction with Lipid II is shown.

Table 1

Summarizes the four main classes of peptide antibiotics that target Lipid II: 1) glycopeptides, including the novel generation of lipoglycopeptides; 2) cyclic depsipeptide antibiotics; and 3) the lantibiotic group and 4) more recently, defensins

Class	Antibiotic or subclass	Stage of development	Described interaction with Lipid II	Refs
Glycopeptides	Vancomycin	Clinical use	Binds to terminal D-alanyl-D-alanine part of the pentapeptide side chain of MurNAc.	16
	Teicoplanin	Clinical use (Europe)	Similar to vancomycin (D-Ala-D-Ala domain of pentapeptide)	17
	Telavancin	Clinical use	Similar to vancomycin (D-Ala-D-Ala domain of pentapeptide)	18
	Dalbavancin	Clinical use	Similar to vancomycin (D-Ala-D-Ala domain of pentapeptide)	19
	Oritavancin	Clinical use	D-Ala-D-Ala domain of pentapeptide and additional motif at the lipid II stem peptide (crossbridge and the D-iso-glutamine in position 2)	20,21
	Mannopeptimycin	Preclinical	Unknown	22
Cyclic depsipeptide antibiotics	Katanosin B(lysobactin)	Preclinical	Complex formation with Lipid I, II and Lipid IIA (1:1)	23
	Plusbacin A3	Preclinical	Inhibition of PG chain extension by transglycosylation	24
	Ramoplanin	Phase III	Probably hydrogen bonds from the backbone NH groups of ramoplanin bind to the pyrophosphate moiety of Lipid II (2:1).	25
	Bacitracin		C55-PP	26
	Friulimicin		C55-PP	27
	Teixobactin	Preclinical	Probably hydrogen-bond interact-ions with the pyrophosphate moiety of Lipid II	28
Lantibiotics	Nisin	Preclinical	N-terminus lantinionine ring binds to pyrophosphate moiety via direct hydrogen bonding with polypeptide backbone of nisin. Also minor interactions with the first isoprene unit and the MurNAc sugar have been assumed.	29
Type A I	Subtilin	Preclinical	Similar to nisin (no structural differences in key positions)	30
(linear peptide)	Epidermin	Preclinical	Similar to nisin (no structural differences in key positions)	31
	Mutacin 1140	Preclinical	Similar to nisin (no structural differences in key positions)	32
Lantibiotics	Nukacin ISK-1	Preclinical	Based on structural similarity to mersacidin and positional significance of the amino acids in the region of ring A lipid II binding similar to mersacacidin is assumed	33
Type A II(both linear and globular)
Lacticin 481	Preclinical	Unknown	34
Lantibiotics	Mersacidin	Preclinical	Complexing the sugar phosphate group, electrostatic interactions and conformational changes are supposed to contribute to this interaction.	35
Type B(globular peptide)	Plantaricin C	Preclinical	Binding may be assigned to the same binding motif found in mersacidin but the molecular interaction differs from that between lipid II and mersacidin. An additional linking site might have been found as it contains a highly positively charged N terminus, which is missing in mersacidin.	36
Pediocin PD-1	Preclinical	Unknown	37
	Actagardine/gardimycin	Preclinical	Unknown	38
Two-component lantibiotics (synergistically acting type A I and B structures)	Lacticin 3147	Preclinical	A mersacidin like interaction between the A1 part of lacticin 3147 en lipid II is proposed.	39
Nonlantibiotic bacteriocins	Colicin M	Preclinical	Enzymatic cleavage of lipid II between the undecaprenyl and	40
			1-pyrophospho-MurNAc moiety
	Lactococcin 972	Preclinical	Unknown	41
Defensins and defensin- based compounds	Plectasin NZ2114	Preclinical	The pyrophosphate moiety forms hydrogen bonds to F2, G3 and C37 on plectasin. The D-gamma-glutamate of Lipid II forms a salt bridge with the N-terminus of plectasin and the side-chain of His18.	15
	Oryzeacin	Preclinical	Unknown
	Eurocin	Preclinical	Unknown
	Lucifensin	Preclinical	Unknown
	Gallicin	Preclinical	Unknown
	HNP-1	Preclinical	Interactions with MurNac, phosphate cage and isoprenyl units	13
	BAS0012758	Preclinical	Interactions with MurNac, phosphate cage and isoprenyl units	42
	6Jc48-1	Preclinical	Interactions with MurNac, phosphate cage and isoprenyl units	43

Note: Data from references.13–15

Glycopeptides

All glycopeptides antibiotics have in common that they inhibit the cell wall synthesis by binding to the carboxyl-terminal part of the pentapeptide of lipid II. By binding to the D-Ala-D-Ala domain in growing peptidoglycan chains they disrupt transglycosylation and transpeptidation with destabilization of the cell wall and ultimately cell death.44 Vancomycin, teicoplanin and telavancin are in clinical use today and can be regarded as antibiotics of last resort for the treatment of multidrug-resistant (MDR) Gram-positive pathogens including most of the MRSA strains.44,45 Vancomycin was the first antibiotic identified as targeting Lipid II. It has continuously gained popularity after its clinical introduction in 1988. However, some clinical limitations have been observed such as poor penetration of pulmonary tissues46 and slow bactericidal activity.47,48 In addition to that, vancomycin is associated with an elevated risk of nephrotoxicity, especially when used together with aminoglycosides. Teicoplanin has essentially the same efficacy but fewer adverse effects when compared to vancomycin.49 Despite being marketed throughout Europe, teicoplanin has never been FDA approved for the US market.

Modifications to the basic heptapeptide core of the glycopeptide group have been made in the past years resulting in better pharmacokinetic and antibacterial properties in vitro.44 The (semi-)synthetic lipoglycopeptides telavancin, dalbavancin and oritavancin have an additional lipophilic fatty acyl chain which provides several advantages. By anchoring the compound to the cell membrane the binding affinity to the target site is enhanced. This mechanism also concentrates the compound at its site of action and thereby increases its potency. Lower MIC values and a longer half-life time allow for lower dosage and less frequent applications.44 Besides binding to Lipid II these compounds may provide additional antibiotic activities based on impairing vital membrane functions due to its strong amphipathic character.48,50 All three lipoglycopeptides are promising agents with activity against MDR staphylococci, enterococci and streptococci.45 Telavancin is a semisynthetic derivate of vancomycin that contains a deacylaminoethyl moeiety. Besides the already mentioned advantages obtained from the lipophilic side chain telavancin has an increased activity against MRSA and non-VanA enterococci. In comparison to vancomycin, telavancin provides a stronger binding affinity for the target binding site and better tissue penetration.48,51 Telavancin is now also available on the European market since approval by the European Medicines Agency (EMA) in 2011 for the treatment of hospital-acquired pneumonia caused by MRSA.

Despite these beneficial developments and the extended antimicrobial spectrum of the novel generation glycopeptides there is an increasing concern about dwindling activity of vancomycin and spreading bacterial resistance against glycopeptide antibiotics.52,53 Bacteria carrying the vanA-type gene cluster that encodes an epitope substitution of D-Ala-D-Lactate termini for D-Ala-D-Ala termini are able to evade the attack of glycopeptides including the generation of lipoglycopeptides.54 Although this resistance mechanism is presumed to be extremely cost extensive energetically and causes a fitness reduction in VRSA isolates, the composition of the pentapeptide of lipid II is not functionally critical. Modifications to the pentapeptide composition can therefore easily spread under the selective pressure of glycopeptide usage without any impact on cell wall synthesis.3,55 While VRSA isolates are uncommon, an increasingly growing number of clinical isolates appear with vancomycin-intermediate resistance profiles. These VISA strains cause complicated, hard-to-treat infections and are increasingly associated with poor clinical results.56 The vanA genotype, which is mediated by transposon Tn1546 is the predominant type of resistance that is reported in Europe. It is very common among enterococci which cause ~20,000 infectiond per year in the USA alone and are highly capable of horizontal gene transfer.44,57 This type of resistance is transferable to significant pathogens like MRSA due to its location on conjugative plasmids.58,59 The dissemination of glycopeptide resistance in enterococci can therefore lead to clinical isolates that are resistant to all available antibiotics.52 Five other types of vancomycin resistance (VanB, D, E and G) have been described on phenotypic and genotypic basis in enterococci. The VanA type, however is to date the only one detected in S. aureus. Glycopeptides can directly induce resistance by activating resistance pathways in susceptible isolates. Interestingly, also glycopeptide dependent growth has been described for some VanA and VanB-type enterococci. This is clinically important because long periods of vancomycin treatment can account for this phenomenon.52

Dalbavancin is a semisynthetic derivate of teicoplanin-like antibiotic A-40,926. The acetylglucosamine group of teicoplanin has been removed in order to achieve improved efficacy against VanA enterococci, unfortunately without success.48,60 Oritavancin is the only glycopeotide that is effective against the vanA type isolates because of its ability of binding Lipid II in species with the substitute D-Ala-D-Lac that causes resistance against the other glycopeptide antibiotics. This ability can be explained by binding sites at the Lipid II stem peptide.21 Additional interactions have been described, including the pentaglycine crossbridge or the D-isoglutamine in position 2 of the Lipid II stem peptide of S. aureus and the D-aspartate/D-asparagine cross-bridge in Enterococcus faecium.21,61 However, in vitro induction of moderate level resistance to oritavancin has been observed in Enterococci isolates that express the VanA or VanB phenotypes.62

Clinical trials on (lipo-) glycopeptide antibiotics

For decades vancomycin has been the first line treatment of infections with MRSA including skin and soft-tissue infections, bacterial pneumonia and infectious endocarditis. However, since vancomycin was approved around thirty years ago (and teicoplanin in the European Union), three novel semisynthetic antibiotics targeting Lipid II have been developed that build up the generation of lipoglycopeptides: telavancin, oritavancin and dalbavancin. As described earlier the molecules of lipoglycopeptides differ from that of vancomycin by the presence of a lipophilic fatty acyl side chain that improves target binding, potency and pharmacokinetic properties.63–65

Telavancin, the first developed and approved lipoglycopeptide antibiotic has been evaluated in six randomised controlled trials which will be briefly discussed. The FAST and FAST 2 Study (published in 2005 and 2006) compared clinical outcomes of complicated Gram-positive skin and skin structure infections (cSSTI) treated with either telavancin (FAST: 7.5 mg/kg, FAST 2: 10 mg/kg once daily) or the standard treatment that comprised of vancomycin (1 g twice daily) or ß-lactam antibiotics (nafcillin, oxacillin or cloxacillin in a standard dose). This phase II trials included respectively 167 and 195 patients and showed equal clinical cure rates in both treatment arms (FAST: 80% vs 77%; FAST 2: 96% vs 90% for telavancin vs standard treatment). In the subgroup of patients with MRSA infections (n=48) telavancin was superior to the standard treatment within the FAST trial with cure rates of 82% versus 69% for the standard treatment.66 However, this difference was not statistically significant (p=1.0) and this finding could not be reproduced within the second trial (FAST 2) where cure rates of MRSA infections did not significantly differ in both arms (96% vs 90%). It is important to note, that the amount of patients in the standard treatment arms receiving vancomycin was higher in the FAST 2 Study (93%) compared to the FAST 1 study (75%) which might have contributed to different results.67 The studies also assessed microbiologic eradication rates of MSSA and MRSA after treatment. In contrast to the FAST trial where treatments were equivalent in this aspect, the second trial revealed higher eradication rates in the telavancin group (92% vs 78%, p=0.07) and in the subgroup with proven MRSA infections (92% vs 68%, p=0.04).67 This finding might be due to the use of higher telavancin doses (10 mg/kg) in comparison to the FAST trial. As expected from in vitro studies telavancin had lower minimal inhibitory concentrations (MIC’s) for clinical isolates of S. aureus including MRSA (MIC90≤0.25 vs 1 µg/mL for vancomycin).66–70 In 2008, the results of two methodologic identical randomised controlled phase III trials (ATLAS 1 and 2) were published that confirmed non-inferiority of televancin (10 mg/kg once daily) to vancomycin (1 g twice daily) for the treatment of cSSTI (more recently redefined as acute bacterial skin and skin structure infections, ABSSSI). Of 1867 enrolled patients, 1693 were evaluable for the test of cure outcome. Overall, no differences between both treatments were found concerning clinical cure rates, microbiological eradication and general safety.71 Telavancin was subsequently approved by the FDA (2009) and EMA (2011) for the treatment of cSSTI/ABSSSI. Telavancin has also been assessed for other types of infections. In 2011, data from the ATTAIN studies that included 1503 patients showed non-inferiority of telavancin for the treatment of hospital-acquired pneumonia caused by Gram-positive pathogens including MRSA. This led to an extended approval for this indication in the EU.72 In 2014, the ASSURE study evaluated telavancin for treating uncomplicated S. aureus bloodstream infections including catheter associated S. aureus bacteraemia. The phase II study compared clinical outcomes of treatment with telavancin versus vancomycin. Unfortunately, only 17 out of 60 included patients were clinically evaluable. However, in this proportion clinical cure rates of telavancin were similar to that of vancomycin indicating a potential use of telavancin in gram-positive bloodstream infections.73 The results of the FAST, ATLAS and ATTAIN trials were summarized in a meta-analysis published in 2012 which evaluated the general efficacy and safety of telavancin. Pooled data showed equal clinical cure rates of telavancin in comparison to vancomycin. Microbiologic eradication rates favoured telavancin (90% vs 84%; OR 1.71; 95% CI: 1.08–2.70), but the risk of an increase in serum creatinine slightly favoured vancomycin (OR 2.22; 95% CI 1.38–3.57). The authors therefore concluded that the risk of nephrotoxicity should be taken into account for treatment decisions.74 Safety outcomes of telavancin versus vancomycin were also compared in a post hoc analysis of data from the ATTAIN studies after exclusion of patients with pre-existing acute renal failure and severe renal failure defined as glomerular filtration rate <30 mL/min. In contrast to the previous meta-analysis this study showed no significant differences in renal adverse events among patients treated with either telavancin or vancomycin.75 In summary, telavancin has proven non-inferiority to vancomycin for the treatment of Gram-positive ABSSSI and seems to be a rational alternative for infections with pathogens that are intermediate susceptible for vancomycin or in case of vancomycin intolerance. Although there is some evidence for nephrotoxicity of telavancin, dosing does not need to be guided by serum concentrations which forms a practical advantage to vancomycin.63,64,76

The lipoglycopeptide oritavancin has a prolonged terminal half-life of 245 hrs due to a slow elimination rate.63 This makes it favourable for single or infrequent dosing. In 2011, the SIMPLIFI trial compared clinical response rates at treatment days 21–29 of patients with ABSSSI treated with oritavancin administered either daily (200 mg for 3 to 7 days), in one single dose (1200 mg), or in an infrequent dose (800 mg, and possibly additional 400 mg on day 5). Surprisingly, the test of cure rates in the clinically evaluable population (n=228) were equal in all study groups (72.4%, 81.5% and 77.5%, respectively). Furthermore, similar safety profiles were found in all administration patterns.77 This phase II study was followed by two phase III trials (SOLO I and SOLO II) published in 2014 and 2015, that demonstrated non-inferiority of a single administration of 1200 mg of oritavancin to a 7 to 10 day treatment with vancomycin (1 g twice daily) for treating Gram-positive ABSSSI. There was no significant difference in the primary composite endpoint demonstrating an early treatment response (cessation of spreading or reduction in lesion size, absence of fever and no use of a rescue antibiotic). Cure rates were 79.6% versus 82.9% (SOLO I) and 82.7% versus 80.5% (SOLO II) in the oritavancin and vancomycin treated group, respectively.78–80 Oritavancin was subsequently approved by the authorities in 2014 (FDA) and 2015 (EMA). The lipoglycopeptides telavancin and oritavancin have in common that they provide an additional mechanism of bacterial killing by disrupting the integrity of the bacterial cell membrane. This dual mode of action may contribute to the sustained activity of those agents against vancomycin intermediate susceptible and resistant S. aureus. While both antibiotics provide activity against enterococci carrying the vanB-type resistance gene only oritavancin is active against vancomycin resistant species due to vanA as previously described.64 The pharmacokinetic profile of oritavancin allows for a single dose treatment which makes it an excellent option for outpatient treatment and reducing prolonged hospital stays.

Similar to oritavancin, dalbavancin has an extensive terminal elimination rate (187 hrs) which allows for infrequent dosing intervals. Dalbavancin was firstly evaluated in a phase II proof-of-concept study including 62 patients with ABSSSI receiving either a two dose regimen of dalbavancin (1000 mg at day 1 and 500 mg at day 8), a single dose (1100 mg) or a prospectively defined standard of care treatment. Clinical success rates (defined as cure or improvement) at the follow-up visit were 94.1% among patients treated with two doses of dalbavancin, 61.5% in the one dose only group and 76.2% among patients treated with the standard-of-care.81 The two-dose regimen was subsequently integrated into phase III clinical trials. Two identically designed non-inferiority trials (DISCOVER 1 and 2) compared treatment outcomes of ABSSSI with two doses of dalbavancin (1000 mg +500 mg at day 8) and vancomycin (1 g or 15 mg/kg twice daily) with an option to switch to oral linezolid after day 3 in the vancomycin treated group. A combined analysis of this double-blind randomized controlled phase III trials including 1312 patients from 2014 showed equal results for both arms concerning early clinical responses (primary endpoint, similar to the SOLO trials) and clinical cure rates (secondary endpoint). According to the pooled analysis 79.7% of the dalbavancin group and 97.8% of the control group showed an early clinical response. Clinical cure rates were 90.6% in the dalbavancin group versus 93.8% in the control group.82 The approved two-dose regimen of dalbavancin was challenged in a separate randomized clinical trial comparing efficacies against a single dose of 1500 mg in 698 patients with ABSSSI. The primary endpoint, a 20% reduction in lesion size or more at 48 to 72 hrs was achieved among 81.4% and 48.2% of the single-dose and two-dose treated group, respectively. Clinical outcomes of evaluable patients, including patients with MRSA-positive baseline cultures and adverse events were also similar in both groups.83 These data resulted in an extended approval, including a single-dose treatment of 1500 mg of dalbavancin for the management of ABSSSI. Dalbavancin was furthermore evaluated in phase II randomized controlled trial including 75 patients with catheter associated bloodstream infections caused by S. aureus or coagulase-negative staphylococci (CNS). The primary combined endpoint was a clinically and microbiological treatment response. This was achieved among 87% of patients treated with the two dose regimen of dalbavancin versus 50% among patients treated with vancomycin twice daily for 14 days.84 Hence, dalbavancin might be a good alternative for treating catheter-associated blood stream infections with susceptible organisms. Data from phase I trials assessing pharmacokinetics and distribution of dalbavancin (two-dose regimen) into bone and articular tissues do also suggest that it might be an effective treatment for osteomyelitis because of a long acting tissue exposure, exceeding the MIC of S. aureus for a period of 8 weeks.85 Like oritavancin, dalbavancin is therefore an excellent candidate for use in outpatients that needs a long lasting antimicrobial therapy as in endocarditis and osteomyelitis. However, at this point the only approved indication is the treatment of ABSSSI.

Cyclic depsipeptide antibiotics

This structural diverse group consists of nonribosomal antibiotic peptides (NRPs) that are derived from natural bacterial products, mainly produced by soil bacteria. Structurally, depsipeptides contain one or more ester bonds along with the amide bonds. They have distinct binding motives on Lipid II that include the pyrophosphate-sugar moiety, but not the stem peptide which is targeted by all (lipo-) glycopeptide antibiotics. As development of resistance to glycopeptides is basically caused by changes in the stem peptide, depsipeptides can be considered interesting candidates for further drug development.

Ramoplanin and its analogues (A1-A3) were first discovered in 1984 by an industrial drug screening programme as product of spore forming soil bacteria belonging to the genus of Actinoplanes sp.86 This macrocyclic depsipeptide inhibits the extracellular transglycosylation by binding to Lipid II. Efforts to identify the exact structure of the ramoplanin-Lipid II complex were not successful due to ligand-induced polymerization of the antibiotic-Lipid II complex, resulting in insoluble fibrils without antimicrobial activity.87 However, early studies could show that binding does not depend on the presence of the D-Ala-D-Ala domain and rather involve the pyrophosphate moiety of Lipid II.25 In analogy with lipoglycopeptides, ramoplanins are proposed to exert additional antibacterial effects by interfering with cell membrane integrity.88 Like vancomycin, ramoplanin is not absorbed when administered orally and might be an interesting alternative for vancomycin in treating gastrointestinal infections with Clostridium difficile or intestinal colonization with VRE.89 The latter was demonstrated in one clinical trial with 68 patients receiving ramoplanin (100 mg or 400 mg) or a placebo but the suppression of VRE did not show sustainable effect.90

Katanosin B, which is structurally identical to lysobactin, forms 1:1 complexes with several cell wall precursors including Lipid II.23 Although this agent was first discovered in 1987, the exact binding site has not been described to date. One study from 1988 demonstrated favourable in vitro activity against a wide range of bacteria. However, in vivo studies indicated a relatively high toxicity in mice.91 Efforts to further develop this compound have since been limited in the past years. The cyclic depsipeptides plusbacin A3, bacitracin and friulimicin are also suspected to exert their antibacterial effects by binding to Lipid II or its intermediates, but reported evidence for molecular interactions with Lipid II is limited.92–94

Teixoplanin is novel antibiotic of the cyclic depsipeptide group that has recently been discovered in a screen of uncultured soil bacteria. Binding to Lipid II is most probably mediated by hydrogen-bonds in the pyrophosphate sugar region.95 Teixoplanin is active against a wide range of Gram-positive pathogens, including MRSA and VRE. Like ramoplanin, teixoplanin is also highly active against C. difficile but with an even lower minimum inhibitory concentration (MIC) of 0.005 µg mL.−1

Lantibiotics

Lantibiotics are a large family of peptides that are produced by certain strains of bacilli to kill other bacteria. They block the cell wall synthesis by clustering the Lipid II molecules into patches and therefore relocate it within the membrane.96 Nisin, a type A lantibiotic, has been extensively studied and serves as the paradigm for this family of anti-microbial peptides. Nisin was discovered almost a century ago and initially recognized for its use in the food industry as a preservative before its recognition as an antimicrobial.97–99 Characteristic of lantibiotics, nisin contains lanthionine rings formed by thioether and dehydrated serine and threonine amino acid residues.100,101 Nisin was shown to cluster Lipid II at a 1:2 ratio within the cytoplasmic membrane, but outside the region where it is normally active.11,102 Following its primary interaction with Lipid II, additional nisin molecules are recruited in a larger complex that is capable of membrane perturbation by forming pores in lipid layers.103 The pore is thought to consist of 8 molecules nisin and 4 molecules of lipid II and during the killing these complexes have been shown form even larger clusters.11,104 Together with observations such as the propensity of Lipid II to enhance the pore forming capacity of nisin in lipid layers, an actual model of this interaction suggests that Lipid II acts as a scaffold for the peptide to dock at the membrane surface prior to insertion and pore formation.1,4,29,101,105 Interestingly, resistance to the antibacterial action of nisin was found not to be determined by the level of Lipid II per se, suggesting additional mechanisms-of-action for this peptide.106

Defensins and defensin- based compounds

Antimicrobial peptides such as defensins were believed to kill microorganisms by permeabilizing the cell membranes. Due to their cationic nature, they preferentially target bacterial membranes which contain large amounts of negatively charged phospholipids, whereas the mammalian cell membrane is composed of neutral, zwitterionic phospholipids exclusively. Various models for the selective activity of antimicrobial peptides towards microorganisms have been proposed.107 These include the formation of solvent-permeable pore structures, covering the membrane like detergents or possible inhibition of metabolic processes of microorganisms through intracellular targeting.107 These models agree on the importance of electrostatic interactions in initiating membrane association of cationic peptides.

Disruption of the functional integrity of the bacterial membrane is a common mode of action of many antibacterial compounds and was believed to be the primary mode of bacterial killing by defensins. An early study reported on the bactericidal activity of Human Neutrophil Peptides (HNP-1–3) against E. coli, suggesting a sequential permeabilization of the outer and inner membranes.108 However, we and others reported that linear, unstructured defensins retained their antibacterial activity in a strain-selective manner.109,110 Further we showed that certain defensins were shown to preferentially kill Gram-positive bacteria, whereas other defensins that carry more positive charge kill Gram-negative strains more effectively.111,112 Based on these observations, we were among the first to report on the functional interaction between Lipid II and Human Neutrophil Peptide 1 (HNP-1), a member of a major family of natural antimicrobial peptides called defensins that protect the host’s epithelial surfaces against microbial invasion.13,113 Several studies on defensins from other species, including fungi,15 invertebrates14 and humans114 have firmly established Lipid II as a target for this class of natural antimicrobial peptides. In their landmark report, Schneider et al reported on the Lipid II-binding fungal defensin plectasin. In this study, interactions between plectasin and the solvent-exposed pyrophosphate region of Lipid II were described.15 These interactions involved residues Phe2, Gly3, Cys4 and Cys37 as well as the N-terminus and His18 side-chain of this defensin. Human defensin peptides themselves are unlikely to be developed into therapeutics because of their well-described functional versatility.115–119 A derivative of the fungal defensin plectasin, termed NZ2114, has shown most promise to date, with in vivo efficacy in infectious models as well as applications to combat biofilm formation.120–122 Similar to the plectasin study, we identified C-terminal hydrophobic residues Ile20 and Leu25 of Human Neutrophil Peptide-1 to be mainly involved in Lipid II binding. However, since HNP-1 and other defensins show little promise as therapeutics, we identified small molecules that bind to Lipid II via a unique mechanism. Using functional and structural approaches, these small molecules bind to three distinct sites of the Lipid II molecule and are excellent lead candidates for the development of next-generation drugs for this target.13,42,43,123,124

Future perspective

The discovery of the glycopeptide vancomycin and development of its next-generation derivatives has been an important milestone in the treatment of multi-drug resistant Gram-positive infections. Currently, vancomycin still serves as a first-line treatment for many infections caused by Gram-positive pathogens including methicillin-resistant S. aureus (MRSA), coagulase-negative Staphylococci (CNS) and Enterococci. In general, the clinical use of vancomycin has important drawbacks that might increase the use of next-generation glycopeptides in the future. Besides its infamous nephrotoxicity, the IV-only route of administration every 12 hrs and the need for a trough concentration-guided dosing are unpractical. Especially in cases of complex infections that require prolonged treatments like osteomyelitis or endocarditis this fact forms a relevant disadvantage that hinders early release from hospital and treatments in an out-patient setting. The novel class of lipoglycopeptides showed non-inferiority in clinical studies and can solve some of these problems. However, an oral alternative with a favorable safety profile is urgently needed. In addition to the practical issues with the available glycopeptides, it will only be a matter of time before resistance against this class of antibacterials will reach a breaking point.125 Though still low, resistance to vancomycin in staphylococci is increasing and a number of vancomycin insensitive strains have been described.56 Vancomycin resistance is a particular acute issue for vancomycin-resistant and multi-drug resistant (MDR) Enterococci.126 In case of MDR Enterococci, resistance to alternatives of vancomycin such as oxazolidinone-linezolid, daptomycin, tigecycline and the last resort formulation quinupristin/dalfopristin, can lead to serious limitations for available treatments options.127,128 As all compounds of the (lipo-)glycopeptide group basically share a similar mode of action, a high degree of cross-resistance can be expected. Still, Lipid II and the peptidoglycan synthesis remain attractive and underexplored targets for antibiotic drug discovery when focusing on compounds with a distinct mode of interaction to that of already approved compounds. In this light, small molecules that interfere with peptidoglycan synthesis129 or that bind to Lipid II directly,42,43,123 hold promise for the development of novel classes of orally available drugs.