https://orcid.org/0000-0003-1412-9780
Figures
Abstract
The Gram-negative outer membrane protects bacterial cells from environmental toxins such as antibiotics. The outer membrane lipid bilayer is asymmetric; while glycerophospholipids compose the periplasmic facing leaflet, the surface layer is enriched with phosphate-containing lipopolysaccharides. The anionic phosphates that decorate the cell surface promote electrostatic interactions with cationic antimicrobial peptides such as colistin, allowing them to penetrate the bilayer, form pores, and lyse the cell. Colistin is prescribed as a last-line therapy to treat multidrug-resistant Gram-negative infections. Acinetobacter baumannii is an ESKAPE pathogen that rapidly develops resistance to antibiotics and persists for extended periods in the host or on abiotic surfaces. Survival in environmental stress such as phosphate scarcity, represents a clinically significant challenge for nosocomial pathogens. In the face of phosphate starvation, certain bacteria encode adaptive strategies, including the substitution of glycerophospholipids with phosphorus-free lipids. In bacteria, phosphatidylethanolamine, phosphatidylglycerol, and cardiolipin are conserved glycerophospholipids that can form lipid bilayers, particularly in the presence of other lipids. Here, we demonstrate that in response to phosphate limitation, conserved regulatory mechanisms induce alternative lipid production in A. baumannii. Specifically, phosphate limitation induces formation of three lipids, including amine-containing ornithine and lysine aminolipids. Mutations that inactivate aminolipid biosynthesis exhibit fitness defects relative to wild type in colistin growth and killing assays. Furthermore, we show that other Gram-negative ESKAPE pathogens accumulate aminolipids under phosphate limiting growth conditions, suggesting aminolipid biosynthesis may represent a broad strategy to overcome cationic antimicrobial peptide-mediated killing.
Author summary
Gram-negative ESKAPE pathogens, including Acinetobacter baumannii, are responsible for a dramatic increase in the morbidity and mortality of patients in healthcare settings over the past two decades. Infections are difficult to treat due to antibiotic resistance and tolerance; however, broadly conserved mechanisms that promote antibiotic treatment failure have not been extensively studied. Herein, we identify an alternative lipid biosynthesis pathway that is induced in phosphate starvation that enables Gram-negative ESKAPE pathogens, including A. baumannii, Klebsiella pneumoniae, and Enterobacter cloacae to build lipid bilayers in the absence of glycerophospholipids, which are the canonical bilayers lipid. Replacement of the anionic phosphate in the lipid headgroup with zwitterionic ornithine and lysine promote survival against colistin, a last resort antimicrobial used against Gram-negative infections. These studies suggest that ESKAPE pathogens can remodel their bilayers with phosphate free lipids to overcome colistin treatment and that aminolipid biosynthesis could be targeted to improve antimicrobial treatment.
Citation: Olea-Ozuna RJ, Campbell MJ, Quintanilla SY, Nandy S, Brodbelt JS, Boll JM (2025) Alternative lipid synthesis in response to phosphate limitation promotes antibiotic tolerance in Gram-negative ESKAPE pathogens. PLoS Pathog 21(2): e1012933. https://doi.org/10.1371/journal.ppat.1012933
Editor: Thomas Guillard, Université de Reims Champagne-Ardenne: Universite de Reims Champagne-Ardenne, FRANCE
Received: September 12, 2024; Accepted: January 24, 2025; Published: February 7, 2025
Copyright: © 2025 Olea-Ozuna et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: Data Accession #: GSE276010 in the GEO omnibus at NCBI. https://www.ncbi.nlm.nih.gov/geo/
Funding: The work was supported by funding from the National Institutes of Health (grants R35GM143053 and R01AI168159 to J.M.B and R35GM139658 to J.S.B), and the Robert A. Welch Foundation (F-1155 to J.S.B). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
The Gram-negative cell envelope consists of a symmetrical bilayer of glycerophospholipids in the inner membrane, while the outer membrane exhibits an asymmetrical composition, with glycerophospholipids in the periplasmic leaflet and lipopolysaccharide enriched in the outer leaflet [1]. The intricate organization underscores the remarkable complexity of bacterial membrane architecture, crucial for microbial survival in various environments. However, under specific stress conditions such as nutrient limitation, temperature fluctuations or exposure to antimicrobial agents, certain bacteria activate alternative lipid biosynthesis pathways or modify existing lipids to adapt and ensure cellular viability [2]. One example is aminolipids, which contain amino acid headgroups like lysine, glycine, glutamine, and serine-glycine, with ornithine being the most common [3,4]. Ornithine lipids (OLs) are phosphorus-free and found exclusively in bacteria; they are absent in archaea or eukaryotes [5]. Their basic structure comprises a 3-hydroxylated fatty acid linked by an amide bond to the α-amino group of ornithine and a second fatty acid attached by an ester bond to the 3-hydroxyl group of the first fatty acid [6]. Although OLs are found in both the inner and outer lipid bilayers of Gram-negative bacteria, they are enriched in the outer membrane [7–10]. OL biosynthesis is catalyzed by two acyltransferases, OlsB and OlsA, or by the bifunctional acyltransferase OlsF [11–13]. In some Gram-negative pathogens such as Pseudomonas aeruginosa or Vibrio cholerae, OLs are exclusively formed under phosphate limiting conditions [14,15], indicating the presence of a specific regulatory mechanism. The importance of aminolipids transcends basic physiology, especially in the context of antibiotic resistance. ESKAPE pathogens, a group of pathogens that include Acinetobacter baumannii, are notorious for their ability to overcome antibiotic treatment and cause hospital-acquired infections [16]. Aminolipid synthesis has been implicated in increased bacterial fitness under antimicrobial stress [9,17,18], potentially contributing to pathogen persistence in clinical settings. Additionally, there is a notable relationship between membrane lipid remodeling and resistance to colistin, a last-resort antibiotic that is used against multi-drug resistant Gram-negative infections [19–22]. Chemical modifications to the lipid A domain of lipopolysaccharide or enrichment of amino acid-containing glycerophospholipids have been associated with colistin resistance [23–25], highlighting the importance of understanding lipid metabolism in combating antibiotic resistance.
In this study, we demonstrate that A. baumannii produced two aminolipids in limiting phosphate growth conditions, including lysine lipids (LLs) and OLs. OL and LL synthesis is dependent on the olsB and olsA genes, and olsB expression is regulated transcriptionally by the response regulator, PhoR. Additionally, mutants deficient in aminolipid synthesis exhibit increased colistin susceptibility relative to wild type. We also found that other Gram-negative ESKAPE pathogens, including Klebsiella pneumoniae and Enterobacter cloacae, accumulate aminolipids under phosphate limited growth conditions. These findings suggest a broad survival strategy among ESKAPE pathogens that could promote survival during antibiotic treatment.
Results
Phosphate limitation induces lipid membrane composition modifications in A. baumannii
The membrane lipid composition of diverse A. baumannii isolates was analyzed, including strains ATCC 17978, ATCC 19606, and AB5075, cultivated in complex lysogeny broth (LB) medium supplemented with 32P-orthophosphoric acid. Labelled cells were collected at mid-logarithmic growth phase, lipids were extracted using the Bligh and Dyer method, and separated by hydrophobicity using two-dimensional thin-layer chromatography (TLC), as previously [20,26,27]. We also prepared lipid extracts from Escherichia coli K-12 strain W3110 for comparison, which served as a well-characterized standard [28]. TLC analysis showed conserved glycerophospholipid enrichment corresponding to known structures, including phosphatidylethanolamine (PE), phosphatidylglycerol (PG), and cardiolipin (CL) (S1A Fig). Additionally, A. baumannii strains also produced two distinct lipid species, including lyso-PE [20] and an unknown phospholipid, denoted as UPL1, that could be a CL derivative, mono-lyso CL [29]. The chemical structures of known phospholipids are shown in S1B Fig.
A. baumannii strain ATCC 17978 was cultured in minimal medium with either 1 mM (excess) or 50 μM (limiting) phosphate, conditions commonly used to distinguish between phosphate-sufficient and phosphate-limited growth [6,13–15,29,30]. Growth in 1 mM phosphate induced a lipid composition almost equivalent to growth in complex LB medium (Figs 1 and S1A). One notable change was that UPL1 was absent, and another unidentified lipid, denoted as UPL2, was formed. To explore lipid biosynthesis under phosphate-limiting conditions, membrane lipid profiles were analyzed after growth in minimal media supplemented with 50 μM (limiting) phosphate concentrations (Fig 1). Limited phosphate availability impacted relative lipid levels, suggesting decreased phosphate-containing lipid synthesis. However, unlike PE and PG glycerophospholipids, relative CL levels did not change significantly, suggesting its production may provide a strategy to maintain membrane charge stability. Concomitant production of three unknown lipids, referred to as unknown lipids 1 (U1), 2 (U2), and 3 (U3), were produced in phosphate limiting growth. Ninhydrin staining revealed that U1 and U2 contained free amines, like PE. Increased ratios of ninhydrin-stained unknown aminolipids relative to PE showed that under phosphate-limiting conditions, potential phosphate-free aminolipids were produced. The total lipid quantifications after lipids were extracted and separated on TLC is shown in S2A Fig.
Strains were grown in basal media 2 (BM2) with excess (1 mM) or limiting (50 µM) phosphate. Cells were collected, lipids were extracted using the Bligh and Dyer method and separated using 2-dimensional thin-layer chromatography. Total lipids were stained with sulfuric acid (left). Aminolipids were stained using ninhydrin (right). Specific lipids are labelled: PE, phosphatidylethanolamine; PG, phosphatidylglycerol; CL, cardiolipin; LPE, lyso-PE; U1, unknown lipid 1; U2, unknown lipid 2; UPL1, unknown phospholipid 1. Red letters denote aminolipids that provide the focus of the study.
Growth in limiting phosphate concentrations slowed growth in ATCC 17978 relative to excess phosphate (S2B Fig), and microscopic analysis revealed that cells elongated and increased their surface area when phosphate is limiting (S2C and S2D Fig), a response previously reported in other Gram-negative bacteria [31]. Additionally, while the composition of lipooligosaccharide (LOS) fractions remained consistent across limiting phosphate conditions, the relative level of LOS was decreased under phosphate limitation (S2E Fig).
Aminolipids synthesized during phosphate limitation are OLs and LLs
One dimensional TLC showed three lipids (PE, U1, and U2) stained with ninhydrin (S3A Fig). After separation of lipids based on hydrophobicity, individual bands corresponding with U1 and U2 were scraped from the TLC plates and extracted using the Bligh and Dyer method. U1 and U2 bands were analyzed by liquid chromatography-mass spectrometry (LC-MS) and structurally characterized using tandem mass spectrometry (MS/MS) (Fig 2). The elution profiles obtained for the U1 and U2 bands are displayed in Fig 2A and 2D, respectively. To determine the composition of aminolipids, a data-dependent acquisition method was used to isolate and activate the most abundant ions detected in each chromatographic peak with higher energy collisional dissociation (HCD) in negative-ionization mode. HCD of precursor m/z 621.52 found in the U1 extract resulted in the loss of the headgroup, which was observed at m/z 131.08, and corresponded to deprotonated ornithine (Fig 2B). The most abundant fragment ion (m/z 367.30) was used to identify the acyl chain connected to the headgroup as 16:0 (number of carbon atoms: double bonds). Further, the complementary ion of m/z 253.22 confirmed the identity of the fatty acid connected at the 3-hydroxyl position of the first fatty acid as 16:1. Following this analysis, lipids containing a double bond were subsequently targeted in a second LC run in the positive-ionization mode using 193 nm ultraviolet photodissociation (UVPD) for MS/MS. UVPD is an alternative fragmentation method that utilizes high-energy photons to activate and dissociate the selected lipid precursor ions, allowing localization of the double bonds within the fatty acyl chains. UVPD of precursor m/z 623.53 produced two fragment ions separated by 24 Da that originate from cleavages adjacent to the double bond. This pair of diagnostic ions localizes the double bond to the 9th position (Fig 2C). This LC-MS/MS strategy identified 49 OLs, including double bond isomers, and 10 unknown lipids in the U1 extract (S1 Table) and a total of 24 OLs and 16 unknown lipids in the U2 extract (S2 Table). HCD of the unknown lipids yielded similar fragmentation to that observed for OLs, but the fragmentation patterns were distinguished by the release of a deprotonated headgroup that corresponded to either a lysine or monomethylated ornithine headgroup (m/z 145.10) (Fig 2E). While the aminolipid head group could be either lysine or monomethylated ornithine, the absence of an ortholog for OlsG, the enzyme responsible for OL methylation [32], and the presence of olsG only in certain planctomycete genomes, strongly suggests that OL methylation is unlikely to occur in A. baumannii. Therefore, the identified lipid is denoted herein as a LL.
A. LC-MS trace of U1 lipid extract in negative-ionization mode. B. HCD (NCE 22) mass spectrum of m/z 621.52 ([M-H]−), an ornithine lipid found in the U1 extract. C. UVPD (4 pulses at 2 mJ/pulse) mass spectrum of m/z 623.53 ([M+H]+). D. LC-MS trace of U2 lipid extract in negative-ionization mode. E. HCD (NCE 22) mass spectrum of m/z 635.54 ([M-H]−), a lysine lipid found in U2 extract. F. UVPD (4 pulses at 2 mJ/pulse) mass spectrum of m/z 637.47 ([M+H]+). The selected precursor ions are labeled with asterisks in B, C, E, and F.
After confirming that A. baumannii strain ATCC 17978 produces OLs and LLs, we explored if other A. baumannii isolates form these aminolipids during phosphate limitation. One-dimensional TLC stained with ninhydrin revealed that diverse A. baumannii strains, including ATCC 17978, ATCC 19606, AB5075, AYE, and the environmental isolate, A. baylyi, were also capable of aminolipid biosynthesis in response to phosphate limitation (S3B Fig). Together, these studies suggest that Acinetobacter can form lipid bilayers with not only glycerophospholipids, but also membranes enriched with OLs and LLs when phosphate availability is limited.
Differentially regulated genes during phosphate starvation
To determine genes that regulate aminolipid biosynthesis, total RNA was isolated, rRNA was depleted, and transcripts were sequenced from A. baumannii strain ATCC 17978 after growth in minimal media supplemented with 1 mM (excess) and 50 µM (limiting) phosphate. Using a 3-fold cutoff for the weighted proportions fold change and an FDR p-value correction < 0.05, 67 upregulated genes and 109 downregulated genes were found (Fig 3A). Many down-regulated genes were involved in iron uptake, such as those coding for ferric uptake regulators (Fur) and components of the ABC transporters for iron. Additionally, genes involved in lysine degradation and amino acid metabolism were down-regulated, indicating potential changes in nitrogen metabolism under phosphate-limited conditions. Upregulated genes were associated with TAT-dependent proteins export, which could be involved in the transport of key lipids or membrane proteins, as well as phospholipases, which may play a role in membrane remodeling. Furthermore, genes related to regulation and phosphate transporters were induced, likely in response to changes in phosphate availability. A complete list of significant (P < 0.05) up- and down-regulated genes is included in S3 Table. The RNA-sequencing results were validated using qRT-PCR analysis to measure differential expression between three specific genes in excess and limiting phosphate concentrations (S4A Fig) and via phenotypic characterization of several mutants described below. Validation of the dataset suggested that phosphate limitation induces a broad transcriptional reprogramming, affecting processes such as lipid biosynthesis, membrane integrity, and nutrient uptake, which are crucial for bacterial survival under stress conditions.
A. Volcano plot of differentially regulated genes in excess and limiting phosphate. Lines indicate 3.5-fold cutoffs. B. 2D thin-layer chromatography stained with sulfuric acid showing wild type and ΔolsB strains grown in phosphate limiting (50 µM) conditions. Specific lipids are labelled: PE, phosphatidylethanolamine; PG, phosphatidylglycerol; CL, cardiolipin; OL, ornithine lipid; LL, lysine lipid; U3, unknown lipid 3; U4, unknown lipid 4. OL and LL aminolipids are labelled in red. C. Proposed ornithine lipid (OL) and lysine lipid (LL) biosynthesis pathways in A. baumannii.
One notable up-regulated gene (A1S_0889) showed a log2 fold change of 8.57 and 31% identity and 51% similarity (91% coverage) to P. aeruginosa olsB. While not induced in phosphate starvation, A. baumannii also encodes a putative olsA orthologue (A1S_2990) with 43% identity and 61% similarity (78% coverage) to P. aeruginosa olsA. OlsBA has been characterized in several bacteria and is involved in OLs biosynthesis [8,11,12,14,33]. Notably, A. baumannii olsA is located at a distinct site on the chromosome relative to olsB and is not transcriptionally regulated by phosphate concentrations.
olsB and olsA genes are required for aminolipids synthesis in A. baumannii
Differential gene expression analysis indicated changes in gene dosage in response to excess/limiting phosphate concentration. Specifically, A1S_0889 expression increased in response to phosphate limitation, whereas A1S_2990 expression did not change. To confirm that A1S_0889 was an olsB orthologue, we generated ΔolsB in A. baumannii strain ATCC 17978, by deleting codons 34 - 214. TLC analysis revealed that under phosphate limitation, aminolipids were absent in the olsB-deficient mutant and a mutant carrying only the empty vector but wild-type accumulated OLs and LLs (Fig 3B). Furthermore, olsB complementation from a non-native promoter restored OL and LL formation. Based on the lipid migration patterns in wild type, the lipids are OLs and LLs.
Additionally, we generated ΔolsB (HMPREF0010_01383) using recombineering in strain ATCC 19606 and also analyzed the olsB::tn and olsA::tn mutants from the AB5075 transposon mutant library [34], which contain insertions in the respective genes, ABUW_3039 and ABUW_0502. Lipid analysis when the mutants were cultivated under phosphate limitation showed that the wild-type strains ATCC 19606 and AB5075 produced OLs and LLs, while the olsB and olsA mutants did not (S4B and S4C Fig). The olsA::tn mutant lipid profile did not show the expected accumulation of lyso-aminolipids, consistent with findings in other Gram-negative ∆olsA mutants [30]. This suggests that lyso-aminolipids are tightly regulated and rapidly degraded within the cell. These data suggested that ornithine and lysine lipid biosynthesis in A. baumannii is dependent on OlsB and OlsA. We will also note that we observed an unknown lipid, labelled as U4 in Figs 3B and S4B that may indicate an OlsA-dependent lipid.
Together, the data supports a model suggesting that aminolipid synthesis occurs in at least two distinct steps within A. baumannii (Fig 3C), consistent with previous work in other Gram-negative bacteria [11,12]. Initially, ornithine and lysine undergo acylation in an OlsB-dependent reaction, leading to the formation of lyso-OL and lyso-LL. Subsequently, in a second step facilitated by OlsA, lyso-OL and lyso-LL are further acylated at the hydroxy position, yielding OL and LL, respectively.
Microscopic analysis and comparison of LOS fractions and levels between aminolipid-producing and aminolipid-deficient A. baumannii strains revealed no significant morphological differences (S4D and S4E Fig) or changes in LOS fractions and relative levels (S2E Fig). However, it is noteworthy that the core fraction of LOS from A. baumannii strains ATCC 19606 differs from of the ATCC 17978 or AB5075 strains. Additionally, a faint band in the core fraction was observed in the olsA::tn transposon mutant of AB5075, which was not present in the wild type strain.
Mutants deficient in aminolipids synthesis show differential growth rate under phosphate limitation
To assess growth rates under phosphate limitation, wild-type and olsB mutant strains were grown in minimal medium with limiting phosphate concentrations (S4F Fig). The optical density at 600 nm (OD600) was monitored over time. While growth of strain ATCC 17978 ΔolsB was not impacted, the growth rate in strains ATCC 19606 and AB5075 was reduced in the olsB or olsA T101 mutants, suggesting there are strain-dependent effects on aminolipid biosynthesis that impact fitness.
Aminolipid biosynthesis mutants are defective in colistin tolerance
Changes in lipid composition could alter the physicochemical properties of the bilayers, particularly the charge. To explore this concept, the impact of aminolipids biosynthesis on colistin tolerance was measured in A. baumannii strain ATCC 17978, where growth rate was not impacted in the olsB mutant (S4F Fig). Colistin is a cyclic peptide that directly engages with the negative membrane charge, while the hydrophobic tail forms pores, leading to bactericidal activity. Colistin is a last resort antibiotic used against multidrug resistant Gram-negative bacterial infections. Our studies indicate increased colistin susceptibility in the olsB-deficient mutant relative to the wild-type strain (Figs 4A and S5A), suggesting the antibiotic could be more effective against A. baumannii when aminolipid biosynthesis is inhibited. Under high phosphate conditions, the membrane lipid composition remains typical of standard bacterial membranes, resulting in higher relative colistin susceptibility (Fig 4C). However, in phosphate limited conditions, lipid turnover increases, leading to the replacement of phospholipids with non-phosphorylated aminolipids, which probably contributes to enhanced colistin tolerance. Overexpression of olsB in wild-type A. baumannii was sufficient to produce aminolipids during cultivation in excess phosphate (Fig 4B). Analysis demonstrated that olsB induction led to increased colistin tolerance (Figs 4C and S5B). Therefore, OlsB-dependent aminolipid biosynthesis in A. baumannii promotes colistin tolerance, a last-line antibiotic for combating multidrug-resistant Gram-negative bacteria.
Colistin-dependent killing in wild type and ΔolsB mutant strains under phosphate limitation (n = 3). Error bars indicate standard deviation. Wild type (WT) strains carrying pOlsB or empty vector were subjected to 5 mg/L colistin exposure over time. CFU/mL were calculated every 1.0 h. B. Total lipids were extracted using the Bligh and Dyer method and separated using 2D thin-layer chromatography. Lipids were stained with sulfuric acid (left). Aminolipids were stained using ninhydrin (right). Specific lipids are labelled: PE, phosphatidylethanolamine; PG, phosphatidylglycerol; CL, cardiolipin; LPE, lyso-phosphatidylethanolamine; LL, lysine lipid; OL, ornithine lipid; U3, unknown lipid 3. OL and LL are labelled in red. C. Colistin-dependent kill curves (left) and growth rate analysis (right) in wild type expressing empty vector (pEV) or pOlsB under high phosphate conditions (n = 3). Error bars indicate standard deviation.
PhoR regulates aminolipid biosynthesis in A. baumannii
Previous work established that aminolipid production generally occurs in response to phosphate limitation [6,14,15,35,36]. Consequently, we expected to find a Pho box upstream of the putative olsB gene. Using the E. coli pho box consensus sequence [37], a putative Pho box was identified that precedes the olsB gene in diverse Acinetobacter isolates, including ATCC 17978 (Fig 5A), but not preceding the olsA gene. The identified Pho box shows significant sequence similarity to the E. coli consensus (CTGTCATNNNNCTGTCAT), with conserved nucleotides present in multiple Acinetobacter strains, including A. baumannii strains ATCC 17978, 19606, AB5075, AYE, and A. baylyi. These results are consistent with our transcriptomics analysis, which also suggested olsA gene expression is not responsive to phosphate concentrations.
A. Predicted Pho box sequence alignments from A. baumannii strain 17978, 19606, AB5075, AYE, and A. baylyi olsB promoters. Black asterisks represent conserved nucleotides in the E. coli Pho box consensus (CTGTCATNNNNCTGTCAT). B. 2D thin-layer chromatography lipid analysis from A. baumannii strain ATCC 17978 wild type and mutants grown in minimal media supplemented with 50 µM (limiting) phosphate. C. 2D thin-layer chromatography lipid analysis from A. baumannii strain AB5075 wild type and the phoR Tn26 mutant in minimal media supplemented with 50 µM (limiting) phosphate. Lipids were stained with sulfuric acid. OL and LL aminolipids are labelled in red.
Phosphate sensing and diverse responses are regulated by the two-component system, PhoB/PhoR, in many bacteria [38]. When phosphate levels decrease, the sensor kinase, PhoR, becomes activated, leading to autophosphorylation. Subsequent phosphotransfer to the cognate response regulator, PhoB results in a conformational change and DNA binding [39] at target promoters to induce gene expression.
These findings imply that the PhoB/PhoR two-component system regulates OL and LL biosynthesis in A. baumannii through olsB expression. To validate this hypothesis, we generated ΔphoR (A1S_3376) in A. baumannii ATCC 17978 by deleting codons 66 to 409. Lipid analysis after growth limiting phosphate, showed that the ΔphoR mutant accumulates glycerophospholipids PE, PG, CL, and UPL2, while failing to synthesize OL, LL, and U3, unlike the wild-type strain (Fig 5B). Complementation of the phoR-deficient mutant with the PhoR allele restored OL and LL formation, while aminolipids were absent in the mutant carrying the empty vector. Expression of olsB from a non-native promotor in the ΔphoR mutant restored OL and LL biosynthesis. Additionally, we examined the lipid patterns of the phoR (ABUW_0105)-transposon mutant of A. baumannii AB5075 grown under phosphate limitation (Fig 5C). Lipidomic analysis revealed that, unlike the wild-type strain, the phoR::tn mutant predominantly accumulated phospholipids and was unable to produce OL or LLs. Together, these findings suggest that olsB expression in A. baumannii is mediated by the phoR regulatory gene.
Other Gram-negative ESKAPE pathogens form aminolipids under conditions of phosphate depletion
In addition to P. aeruginosa [14], A. baumannii is the second Gram-negative ESKAPE bacterium where the OL biosynthesis has been described using a OlsBA-dependent mechanisms. Uniquely, A. baumannii also produces LL via the same pathway. These findings prompted us to investigate if other Gram-negative ESKAPE pathogens, such as Klebsiella or Enterobacter, are also capable of aminolipid biosynthesis under phosphate limitation. TLC analysis of total lipids from K. pneumoniae, E. cloacae or P. aeruginosa after growth in minimal medium supplemented with excess phosphates showed production of the canonical membrane phospholipids PE, PG, and CL (Fig 6A). However, when cultivating P. aeruginosa in phosphate limitation (50 μM), a significant decrease in relative phospholipid levels was observed, and the synthesis of five unknown compounds and OL was induced. K. pneumoniae and E. cloacae cultivated in low phosphate concentrations (50 μM), also showed decreased levels of phospholipid production and accumulation of an unknown lipid. The unknown lipid exhibited a migration pattern and ninhydrin staining on TLC like OL, suggesting that aminolipid biosynthesis may be a conserved response to phosphate limiting growth conditions that could promote tolerance to antibiotics in Gram-negative ESKAPE pathogens.
A. 2D thin-layer chromatography of lipids extracted from wild type K. pneumoniae strain KPNIH1, E. cloacae strain ATCC 13047, and P. aeruginosa strain PAO1 grown in excess (1 mM) or limiting (50 µM) phosphate conditions. Totals lipids were stained with sulfuric acid (left). Aminolipids were stained using ninhydrin (right). Specific lipids are labelled: PE, phosphatidylethanolamine; PG, phosphatidylglycerol; CL, cardiolipin; OL, ornithine lipid; U1, U2, U3, U4, and U5; unknown compounds 1, 2, 3, 4, and 5. B. Representative MS1 spectra from shotgun analysis of aminolipids isolated from K. pneumoniae (n = 3) and E. cloacae (n = 3). The five most enriched lipids are bolded, including two ornithine lipids (OL), labelled in red.
To confirm the putative OL identity, total lipids were extracted using the Bligh and Dyer method after cells were grown in 50 μM phosphate. 1-D TLC (S6 Fig) on total lipids stained with ninhydrin showed two prevalent lipids (lane 1). The band corresponding to OLs was scraped from the plate and extracted. Extracted lipids from three replicates were run on 1-D TLC showing enrichment of the putative OL relative to PE. Negative-ionization mode MS1 shotgun analysis on the purified lipids showed five enriched lipids in each strain (Fig 6B). MS/MS analysis of the lipids present in K. pneumoniae sample revealed two ornithine lipids (m/z 595.50 and 623.53), two PE lipids (m/z 662.47 and 702.51), and a m/z consistent with phosphatidylthreonine (m/z 760.51) (S4 Table). Spectra from the E. cloacae lipid analysis included two ornithine lipids (m/z 623.54 and 595.50), PE (m/z 702.51), a m/z consistent with phosphatidylthreonine (m/z 760.51), and an unknown lipid that may be a modified OL (m/z 681.54) (S5 Table). Together the migration of the lipids via 2-D TLC and the MS analysis provide strong complementary evidence that growth in limiting phosphate results in alternative synthesis of OLs.
Discussion
Bacteria have evolved various regulatory mechanisms to sense and adapt to environmental stress. Here, we show that under phosphate-limiting conditions, A. baumannii produces ornithine and lysine lipids through regulated expression of olsB. The aminolipids alter the lipid bilayer composition to promote tolerance to colistin, an antimicrobial peptide used to treat Gram-negative bacterial infections. While subcellular localization of aminolipids in the outer membrane is unknown, localization to the surface-exposed leaflet would directly reduce the overall negative surface charge. This would reduce the electrostatic potential for cationic antimicrobial peptides such as colistin to target the cell, emphasizing changes in bilayer charge as an adaptive mechanism for A. baumannii in challenging environments. Alternatively, aminolipid accumulation in the inner leaflet of the outer membrane may alter the overall membrane dynamics, such as lipid packing and membrane fluidity, contributing to enhanced membrane stability and colistin tolerance. Broadly, cell membrane lipid modifications are vital for bacterial survival upon exposure to antimicrobial cationic peptides. For example, V. cholerae modifies lipid A with glycine or diglycine residues to resist cationic antimicrobial peptides [40]. Similarly, other Gram-negative bacteria modify their lipid A structures to resist polymyxins. For instance, P. aeruginosa and A. baumannii can add positively charged amino groups, such as ethanolamine to lipid A, reducing to overall negative charge and decreasing the binding affinity of polymyxin [20]. K. pneumoniae and Enterobacter species have been shown to add 4-amino-4-deoxy-L-arabinose (L-Ara4N) to lipid A, further neutralizing the negative charge and conferring resistance [21]. Similar strategies are employed by various bacterial species, such as P. aeruginosa, Rhizobium tropici, Staphylococcus aureus, Mycobacterium tuberculosis, and Bacillus subtilis, which modify phospholipids like PG by adding amino acids like lysine or alanine, thereby conferring polymyxins resistance [35,36,41–43].
Membrane lipid remodeling during growth under phosphate limitation is a conserved strategy across bacteria, involving the substitution of phospholipids with phosphorus-free lipids alternatives like aminolipids [44]. Interestingly, other bacteria, such as P. aeruginosa, also modify their lipid composition in response to phosphate limitation [14]. Under these conditions, P. aeruginosa incorporates OL, replacing phospholipids in the membrane. This remodeling likely ensures that the membrane remains functional and stable despite the phosphate scarcity, highlighting a similar strategy employed by various bacterial species to adapt to nutrient stress. These findings further support the idea the replacement of phospholipids with amino acid-derived lipids, such as ornithine, represents an adaptive mechanism to phosphate limitation, suggesting that this process may be widely conserved across Gram-negative bacteria. While the synthesis of these lipids is not directly induced by the presence of polymyxins, tolerance to polymyxins is an indirect consequence of lipid membrane remodeling, leading to significant changes in membrane chemical properties. The alteration could reduce the net negative charge of the membrane, thereby decreasing CAMP susceptibility.
The olsB gene is required for OL biosynthesis, but unlike other OlsB-dependent pathways, it also induces LL formation in A. baumannii, suggesting metabolic plasticity within the species. Comparing our findings with observations in other bacteria, such as the soil bacterium Rhodobacter sphaeroides, which not only produces OLs but also synthesizes glutamine lipids (GLs) [45], further highlights the metabolic diversity in aminolipid biosynthesis. Additionally, recent research has shown that marine bacteria Ruegeria pomeroyi encode two olsB paralogs, one responsible for forming OLs and the other for GLs [30]. Although these bacteria inhabit vastly different environments, the similarities suggest that the ability to use multiple substrates for aminolipid synthesis may be a common survival strategy in variable environmental conditions.
The transcriptomic analysis uncovered insights into different expression patterns of the olsB and olsA genes in response to phosphate limitation. Specifically, overexpression of the olsB gene was observed during phosphate limited growth, indicating a regulatory mechanism. However, olsA expression remained unchanged. The predicted Pho box in the promoter region of olsB suggested that the PhoB/PhoR two-component system regulates olsB under phosphate limitation conditions. The absence of a Pho box-like motif in the promotor region of olsA, in contrast to olsB, suggests that olsA is regulated by factors distinct from those controlling olsB under phosphate limiting conditions. This was confirmed by RNA sequencing (Fig 3A) and RT-PCR analysis (S4A Fig), which both showed that olsA expression remains unchanged in response to phosphate limitation, indicating that its expression is likely controlled by other regulatory mechanisms or is constitutive. Consequently, olsA is not constitutively expressed under these conditions, but rather its regulation appears to be independent of phosphate availability. The absence of a similar motif in the promoter region of olsA implies the influence of other regulatory factors on its expression, independent of phosphate availability. Furthermore, olsB overexpression with non-native promoter in A. baumannii during cultivation in excess phosphate resulted in aminolipid formation, suggesting OlsA-dependent activity occurs after OlsB has formed a lyso-aminolipid. The differential regulatory events may also suggest that OlsA utilizes other substrates. For instance, in Rhodobacter capsulatus, OlsA functions as a bifunctional enzyme, active in both OL and phosphatidic acid biosynthesis [46]. Additionally, we confirmed the role of the phoR gene as a key regulator in aminolipid biosynthesis in A. baumannii, highlighting its fine-tuned regulation in response to environmental stressors such as phosphate limitation. Interestingly, this regulatory mechanism shares similarities with species like Sinorhizobium meliloti or V. cholerae, where PhoB/PhoR also regulates OLs synthesis under phosphate limitation conditions [6,15], underscoring the evolutionary conservation of these adaptive mechanisms across different bacterial taxa.
Finally, the presence of olsB and olsA orthologues in A. baumannii raises questions about the diversity of aminolipid biosynthesis pathways among pathogens. Interestingly, bacteria such as Klebsiella and Enterobacter lack these orthologs, suggesting distinct biosynthesis pathways compared to A. baumannii. This absence prompts further investigation into alternative pathways or genes involved in aminolipid synthesis and their implications for antibiotics resistance and environmental adaptation.
Conclusion
The study highlights the impact of phosphate limitation on lipid membrane composition in A. baumannii, resulting in the synthesis of OLs and LLs through regulated olsB gene expression. Aminolipids can promote tolerance to colistin, an important last-line antimicrobial. These results also underscore the role for phoR gene in regulating aminolipid synthesis in A. baumannii and show that other Gram-negative ESKAPE pathogens produce aminolipids under phosphate-depleted conditions. Aminolipid biosynthesis is a common adaptive response to phosphate limitation, which could promote pathogen survival both in hospital environment and within the host.
Materials and methods
Bacterial strains and growth
All strains and plasmids used in this study are listed in S6 Table. E. coli, Acinetobacter strains, K. pneumoniae, E. cloacae or P. aeruginosa were initially cultured from frozen stocks on Luria-Bertani (LB Miller) agar at 37 °C. Isolated colonies were used to inoculate LB Miller broth or minimal medium (Tris minimal succinate [TMS]) [47]; supplemented with different phosphate concentrations at 37 °C. The minimal medium included: Na-succinate 20 mM, NaCl 200 mg/mL, NH4Cl 450 mg/mL, CaCl2 200 mg/mL, KCl 200 mg/mL, MgCl2 450 mg/mL, FeCl2 10 mg/L, and MnCl2 10 mg/L, with 10 mM 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid (HEPES) buffer used at pH 7.2. Na2HPO4 was then added to achieve a final concentration of 1 mM (excess) or 50 μM (limiting). All components were dissolved in deionized water and sterilized by filtration through 0.22 μm pore-size filters and dissolved in deionized H2O. To generate growth curves, overnight cultures of A. baumannii strains were diluted to an OD600 of ~0.05 in 5 mL of medium, then incubated in glass test tubes at 37 °C for 24 hours. Growth curve data were analyzed and plotted using GraphPad Prism software.
A. baumannii strain ATCC 17978 has been shown to be a mixture of two variants [48]. Colony PCR using primers specific to the cardiolipin synthase gene (clsC2) resulted in a PCR product, indicating this study was specific to only the A. baumannii 17978 UN variant. A. baumannii strains AB5075 and ATCC 19606 have been shown to produce colonies with two opacity phenotypes that are phase variable [49]. Microscopic examination showed a majority of opaque forms in strains AB5075 and ATCC 19606 with only 2–3 translucent colonies out of > 200 colonies found on each plate (n = 3 for each strain). The strain ATCC 19606 ΔolsB and strain AB5075 olsB::tn and olsA::tn mutants were also examined, but only included opaque variants.
Construction of mutant and complementation A. baumannii strains
The primers utilized in this study are listed in S7 Table. Genetic mutants of A. baumannii were generated following established protocols [50–53]. Briefly, A. baumannii carrying the pMMB67EHTetR plasmid containing the RECAb coding sequences was diluted from an overnight culture into LB Miller broth containing 10 µg/mL of tetracycline at an OD600 of ~0.05 and incubated for 45 minutes. RECAb expression was induced by adding 2 mM IPTG, and cells were cultured at 37 °C until they reached mid-log growth phase (OD600 of ~0.4). After washing the cells three times in ice-cold 10% glycerol, 1010 cells were electroporated in a 2-mm cuvette at 1.8 mV with 5 µg of a recombineering linear PCR product. Subsequently, the cells were cultured for 4 hours in 4 mL of LB Miller broth with 2 mM IPTG and then plated on LB agar supplemented with 20 µg/mL of kanamycin. Mutations were validated using PCR.
To cure isolated mutants of the pMMB67EHTetR::RECAb plasmid after mutant isolation, strains were streaked for isolated colonies on LB Miller agar supplemented with 2 mM NiCl2 to select cells that had lost the tetracycline cassette [51–54]. Cured insertion mutants were then electroporated with pMMB67EHTetR carrying the FLP recombinase. Cells were recovered for 1 hour in 5 mL of LB Miller broth and plated on LB agar containing 10 µg/mL of tetracycline and 2 mM IPTG to induce expression of the FLP recombinase. Excision of the kanamycin cassette was confirmed by PCR.
To complement the A. baumannii ATCC 17978 mutants, the coding sequence from A1S_0889 (olsB) was cloned into the KpnI/SalI sites, while the coding sequence from A1S_3376 (phoR) was cloned into the KpnI/BamHI sites in pMMB67EHKanR. Plasmids were expressed in the respective mutants, and all strains were grown in 30 µg/mL of kanamycin and 1 mM IPTG for expression.
Analysis of total lipids and aminolipids
Overnight cultures were used to inoculate 10 mL minimal medium 1 mM phosphate, or 20 mL minimal medium 50 µM phosphate to achieve an OD600 of ~0.05, and then incubated for 24 hours at 37 °C. After the incubation period, cells were collected by centrifugation. Lipids were extracted using the Bligh and Dyer (1959) method [55]. The chloroform phase was separated into the individual components on high-performance TLC silica gel plates. For one-dimensional TLC analysis, the plates were developed with chloroform-methanol-water (130:50:8 v/v) mixture. For two-dimensional TLC analysis, a chloroform-methanol-water (140:60:10 v/v) mixture was used in the first dimension and chloroform-methanol-acetic acid (130:50:20 v/v) mixture was used in the second dimension. Lipids on TLC were visualized by treating the plates with 10% sulfuric acid in ethanol at 150 °C (total lipids) or 0.2% ninhydrin in acetone at 100 °C (aminolipids). Lipid quantifications were done using ImageJ software to detect spots above background. Each experiment was independently replicated three times, one representative data set was reported in the quantification, and one representative image was included.
Analysis of 32P-labeled phospholipids
Overnight cultures were diluted to an OD600 of ~0.05 in 10 mL LB Miller broth supplemented with 5 µCi/mL 32P ortho-phosphoric acid (PerkinElmer) and grown until reaching an OD600 of ~0.6. After harvesting the cells, lipid extraction was performed using Bligh and Dyer method [55], followed by analysis using TLC as previously described. Subsequently, the TLC plates were dried, exposed to a phosphorimaging screen, and scanned using an Amersham Typhoon laser scanner.
Shotgun mass spectrometry
Dried lipid content from Bligh and Dyer extracted TLC bands of E. cloacae WT and K. pneumoniae WT biological replicates were solubilized in chloroform and resuspended in methanol: isopropanol (1:1) at a concentration of 200 µM. Shotgun analysis was performed in negative-ionization mode on a Thermo Scientific Orbitrap Fusion Lumos Tribrid mass spectrometer. Nanoelectrospray ionization was performed using Pd/Au-coated pulled-tip glass capillaries (20 nm i.d.) at a spray voltage of −1000 V and a capillary temperature of 275 °C. Spectra were acquired at a resolution of 50,000 at m/z 200, an AGC target between 5E4 and 1E5, and an RF lens of 60%. All MS1 and MS/MS spectra were an average of 50 scans. The top 5 most abundant species were subjected to higher energy collisional dissociation (HCD) for identification. MS/MS spectra were obtained with an isolation width of 1 m/z and a normalized collision energy (NCE) ranging from 22–26%.
Liquid chromatography
Lipids isolated from Acinetobacter baumannii were separated using reversed-phase liquid chromatography (LC) on an Acquity UPLC CSH C18 column (pore size 130 Å, 1.7 μm particle size, 2.1 mm × 100 mm, Waters) integrated with a Dionex Ultimate 3000 UHPLC system (Thermo Fisher Scientific). Mobile phase A and B were comprised of methanol: water: acetonitrile (3:4:3) and isopropanol: water: acetonitrile (90:2.5:7.5), respectively, each containing 10 mM ammonium formate. Dried lipid content from TLC bands was extracted via a Bligh and Dyer protocol and resuspended in 50:50 mobile phase (A: B) at a concentration of 100 ng/µL. A 9 µL injection volume was used, and the column compartment was maintained at a temperature of 50 °C. Aminolipids were separated at a flow rate of 0.275 mL/min with the following gradient: hold at 10% B (0–1 min), 10–45% B (1–5 min), 45–70% B (5–23 min), 70–95% B (23–24 min), hold at 95% B (24–29 min), 95–10% B (29–29.5), and hold at 10% B (29.5–35 min).
Untargeted LC-MS with HCD and targeted LC-MS with UVPD experiments
An untargeted negative-ionization mode LC-MS with HCD method was utilized to screen Acinetobacter baumannii lipid extracts on a Thermo Scientific Orbitrap Fusion Lumos Tribrid mass spectrometer via heated electrospray ionization. Various source parameters included a spray voltage of -3800 V, sheath gas setting of 5, aux gas setting of 10, and capillary temperature of 300 °C. MS1 data was collected at a resolution of 30,000 at m/z 200 in the Orbitrap analyzer with a scan range of m/z 500–1000, RF lens of 80%, and an AGC target of 5E5. A data-dependent acquisition method was used where the top 5 most abundant ions above an intensity threshold of 5E4 were selected for MS/MS analysis with HCD. Species were isolated using a 1 m/z window and subjected to a collision energy corresponding to NCE of 22%. MS/MS spectra were acquired at a resolution of 30,000 at m/z 200 in the Orbitrap analyzer, AGC target of 1E5, maximum injection time of 250 ms, and 2 microscans/scan.
A targeted positive-ionization mode LC-MS/MS method was performed on a Thermo Scientific Orbitrap Eclipse Tribrid mass spectrometer equipped with an ArF excimer laser (Coherent, Inc.) for 193 nm ultraviolet photodissociation (UVPD). The heated electrospray ionization source was operated at + 3800 V, and the source parameters described in the untargeted experiments were implemented. MS/MS scans with UVPD were acquired in a data-dependent manner, with 5 scans collected between each MS1 master scan, and with an intensity threshold set at 5E4. A targeted mass filter was employed that included the m/z values and start/end retention times for unsaturated aminolipids identified from the negative-ionization mode LC-MS with HCD run (with a 15-ppm error tolerance). Aminolipids were isolated with a 1 m/z window and activated with 4 laser pulses at 2 mJ/pulse for double bond localization. MS/MS spectra were acquired at a resolution of 30,000 at m/z 200 in the Orbitrap analyzer, q-value of 0.1, AGC target of 5E5, maximum injection time of 500 ms, and 5 microscans/scan. Data was manually interpreted using Thermo Xcaliber Qual Browser and ChemDraw. Precursor and fragment ions were assigned within 10 and 15 ppm mass error, respectively.
RNA sequencing
Transcriptome sequencing analysis was performed as described previously, with modification [53]. Briefly, total RNA was extracted from A. baumannii ATCC 17978 cultures grown in minimal medium supplemented with either excess (1 mM) or limiting (50 μM) phosphate at OD600 of ~0.5 in triplicate, utilizing the Direct-Zol RNA miniprep kit (Zymo Research). Genomic DNA contamination was eliminated using the Turbo DNA-free DNA removal kit (Invitrogen). DNAase-treated RNA samples were then forwarded to SeqCenter for sequencing on the Illumina NextSeq 550 sequencing. Subsequently, the CLC Genomic Workbench software (Qiagen) was employed to map the obtained sequencing data to the A. baumannii ATCC 17978 genome annotations and determine the read per kilobase per million (RPKM) expression values and determine the weighted-proportions fold changes in expression values between excess or limitation phosphate conditions. Data were analyzed and plotted using GraphPad Prism software. Data Accession #: GSE276010.
Quantitative RT-PCR
Relative-abundance quantitative PCR (qPCR) was performed as previously described [20,21,53]. In brief, total RNA was extracted from bacterial cultures using the Direct-Zol RNA Miniprep Kit (Zymo Research), followed by DNase digestion to remove any genomic DNA. The RNA was then reverse transcribed into cDNA using the Invitrogen SuperScript III Reverse Transcriptase (Thermo Fisher), with a final RNA concentration of 5 ng/µl. One microliter of the resulting cDNA was used as a template in a 10-µl quantitative RT-PCR (qRT-PCR) reaction, conducted with Power SYBR Green Master Mix (Applied Biosystems). qRT-PCR was carried out on a QuantStudio 3 Real-Time PCR System (Thermo Fisher Scientific). Relative expression levels were calculated using the ΔΔCt method [56], with normalization of gene targets to the rpoA signal.
Microscopy and image analysis
Cells were grown as stated above and fixed with paraformaldehyde (PFA) and mounted on 1.5% agarose in 1X phosphate-buffered saline (PBS). Imaging was performed using a Nikon Eclipse Ti-2 wide-field epifluorescence microscope equipped with a Photometrics Prime 95B camera and a Plan Apo 100x, 1.45 numerical aperture objective lens. Images were captured using NIS Elements software. Image analysis was conducted using the microbeJ plugin of ImageJ software.
LOS staining and analysis
All cultures were grown in test tubes containing 5 mL of minimal medium with either excess (1 mM) or limiting (50 μM) phosphate at 37 °C in a shaker overnight. For the complementation strains, 30 µg/mL kanamycin and 1 mM IPTG were added. The OD600 of the overnight cultures was measured and normalized to OD600 of ~1. The cells were then centrifuged at 15,000 rpm for 5 minutes. Each pellet was resuspended in 100 μl of 1X Sample Buffer (4X LDS Sample Buffer, 4% β-mercaptoethanol, and water) and boiled in water for 10 minutes. After cooling, proteinase K was added to each sample and mixed. The samples were then incubated in a 55 °C water bath overnight. The following day, the samples were boiled in water for 5 minutes and SDS-PAGE was performed. The gel was then fixed and treated according to the protocol in the Pro-Q Emerald 300 Lipopolysaccharide Gel Stain Kit by Thermo Fisher Scientific (P20495).
Colistin susceptibility assays
Overnight cultures were diluted to OD600 ~0.150 in minimal medium supplemented with either excess (1 mM) or limiting (50 μM) phosphate containing 5 mg/L colistin. Each culture, comprising 15 mL, was incubated in 125 mL Erlenmeyer flasks at 37 °C with agitation at 250 rpm. Survivors were analyzed at specific time points by serial dilution plating on LB agar.
Supporting informations
S1 Fig. Escherichia coli (Ec) and Acinetobacter baumannii (Ab) lipid composition after growth in complex media.
A. Strains were grown in complex media (LB broth) in the presence of 32P-orthopohosphoric acid until mid-logarithmic growth phase. Cells were collected and total lipids were extracted using the Bligh and Dyer method and separated using 2-dimensional thin-layer chromatography. Labelled lipids include anionic cardiolipin (CL) and phosphatidylglycerol (PG), aminolipids phosphatidylethanolamine (PE) and lyso-PE (LPE), and unknown phospholipid 1 (UPL1). B. PG, PE, CL and LPE chemical structures. Head groups are red, the glycerol backbone is blue, and fatty acids are black.
https://doi.org/10.1371/journal.ppat.1012933.s001
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S2 Fig. Effect of phosphate availability on growth, cell morphology, and LOS production.
A. Quantification of total lipid in TLC Fig 1 grown in excess or limiting phosphate concentrations. Lipids are graphed as a percentage of the total. Significance testing conducted using Student t test with two-tailed distribution assuming equal variance. Lines indicate standard deviation. *P < 0.05; ns is not significant. B. A. baumannii ATCC 17978 was cultured in minimal medium containing either excess (1 mM) or limiting (50 µM) phosphate for 24 hours. C. Phase-contrast images of A. baumannii grown under these conditions, captured during the exponential phase. Scalebar is 10 µm. D. Cell length and area were quantified for each population (n ≥ 150) using ImageJ software. Each point represents an individual cell. The experiment was repeated twice, and one representative dataset was reported. Significance testing conducted using Student t test with two-tailed distribution assuming equal variance. ***P < 0.001, ****P < 0.0001. E. Proteinase K-treated whole-cell lysate from wild-type A. baumannii strains ATCC 17978, ATCC 19606, and AB5075, as well as from aminolipid-deficient mutants grown under excess (1mM) or limiting (50 µM) phosphate conditions. The LOS samples were separated using SDS-PAGE and stained using Pro-Q Emerald 300.
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S3 Fig. Thin-layer chromatography of Acinetobacter aminolipids.
A. To produce A. baumannii lipid samples for MS analysis, total lipids were separated using thin-layer chromatography and scraped from the plate, extracted using the Bligh and Dyer method, and run alongside lipid controls. Extractions resulted in isolation of U1 & U2, U1, or U2. Lipids were stained with ninhydrin to visualize aminolipids. Specific lipids are labelled: PE, phosphatidylethanolamine; U1, unknown lipid 1; U2, unknown lipid 2. B. Cells were grown in minimal medium supplemented with excess (1mM) or limiting (50 µM) phosphate conditions from indicated Acinetobacter strains. Total lipids were extracted from cells grown in media with limiting phosphate concentrations. Total lipids were spotted on thin-layer chromatography and separated based on hydrophobicity. Plates were stained with ninhydrin to visualize aminolipids. Specific lipids are labelled: PE, phosphatidylethanolamine; OL, ornithine lipid; LL, lysine lipid.
https://doi.org/10.1371/journal.ppat.1012933.s003
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S4 Fig. olsB and olsA are required for ornithine and lysine lipid biosynthesis in A. baumannii.
A. Relative-abundance quantitative PCR (qPCR) of genes after A. baumannii growth in excess or limiting phosphate concentrations (n = 3). Lines indicate standard deviation. Significance testing was conducted using Student t test with two-tailed distribution assuming equal variance. *P < 0.05; ns = not significant. B. 2D thin-layer chromatography lipid analysis in ATCC 19606 wild type and the ΔolsB mutant strain after growth in limiting (50 µM) phosphate concentrations. Lipids were stained with sulfuric acid. C. Analysis in AB5075 wild type and transposon (Tn101) mutant strains after growth in limiting (50 µM) phosphate concentrations. Specific lipids are labelled: PE, phosphatidylethanolamine; PG, phosphatidylglycerol; CL, cardiolipin; OL, ornithine lipid; LL, lysine lipid. OL and LL aminolipids are labelled in red. D. Phase-contrast images of A. baumannii strain ATCC 17978 grown under phosphate limiting conditions, captured during exponential phase growth. Scalebar is 10 µm. E. Cell length and area of strain ATCC 17978 were quantified for each population (n ≥ 150) using ImageJ software. Each point represents an individual cell. Significance testing was conducted using Student t test with two-tailed distribution assuming equal variance. ns = not significant. F. Optical density (OD600) measurements of A. baumannii strains grown in 50 µM phosphate over 24 h.
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S5 Fig. Aminolipid formation promotes A. baumannii tolerance to colistin.
Growth (OD600) of A. baumannii ATCC 17978 strains was measured at 37 °C in minimal medium with limiting phosphate (A) or excess phosphate (B), and in the presence of colistin at concentrations of 1, 2.5, or 5 mg/L.
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S6 Fig. Thin-layer chromatography of E. cloacae and K. pneumoniae aminolipids.
To produce E. cloacae and K. pneumoniae samples for MS analysis, total lipids were extracted from cells grown in media with limiting phosphate concentrations. Total lipids were separated using thin-layer chromatography and scraped from the plate, extracted using the Bligh and Dyer method, and run alongside lipid controls. Lipids were stained with ninhydrin to visualize aminolipids. Specific lipids are labelled: PE, phosphatidylethanolamine; OL; ornithine lipid (predicted).
https://doi.org/10.1371/journal.ppat.1012933.s006
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S1 Table. Identity of aminolipids in unknown lipid 1 biological replicates.
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S2 Table. Identity of aminolipids in unknown lipid 2 (U2) biological replicates.
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S3 Table. Differentially regulated genes in excess and limiting phosphate.
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S4 Table. Lipids present in the top five most abundant species from K. pneumoniae biological replicates.
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S5 Table. Lipids present in the top five most abundant species from E. cloacae biological replicates.
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S6 Table. Strains and plasmids used in this study.
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