This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Georgel, P.
Right arrow Articles by Beutler, B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Georgel, P.
Right arrow Articles by Beutler, B.

 Previous Article  |  Next Article 

Infection and Immunity, August 2005, p. 4512-4521, Vol. 73, No. 8
0019-9567/05/$08.00+0     doi:10.1128/IAI.73.8.4512-4521.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

A Toll-Like Receptor 2-Responsive Lipid Effector Pathway Protects Mammals against Skin Infections with Gram-Positive Bacteria

Philippe Georgel,1 Karine Crozat,1 Xavier Lauth,2 Evgenia Makrantonaki,3 Holger Seltmann,3 Sosathya Sovath,1 Kasper Hoebe,1 Xin Du,1 Sophie Rutschmann,1 Zhengfan Jiang,1 Timothy Bigby,1 Victor Nizet,2 Christos C. Zouboulis,3 and Bruce Beutler1*

Department of Immunology, The Scripps Research Institute, 10550 N. Torrey Pines Road, La Jolla, California 92037,1 Department of Pediatrics, University of California, San Diego, La Jolla, California 92093,2 Department of Dermatology, Charité University Medicine Berlin, Fabeckstrasse 60-62, 14195 Berlin, Germany3

Received 26 January 2005/ Returned for modification 1 March 2005/ Accepted 10 March 2005


arrow
ABSTRACT
 
flake (flk), an N-ethyl-N-nitrosourea-induced recessive germ line mutation of C57BL/6 mice, impairs the clearance of skin infections by Streptococcus pyogenes and Staphylococcus aureus, gram-positive pathogens that elicit innate immune responses by activating Toll-like receptor 2 (TLR2) (K. Takeda and S. Akira, Cell. Microbiol. 5:143-153, 2003). Positional cloning and sequencing revealed that flk is a novel allele of the stearoyl coenzyme A desaturase 1 gene (Scd1). flake homozygotes show reduced sebum production and are unable to synthesize the monounsaturated fatty acids (MUFA) palmitoleate (C16:1) and oleate (C18:1), both of which are bactericidal against gram-positive (but not gram-negative) organisms in vitro. However, intradermal MUFA administration to S. aureus-infected mice partially rescues the flake phenotype, which indicates that an additional component of the sebum may be required to improve bacterial clearance. In normal mice, transcription of Scd1—a gene with numerous NF-{kappa}B elements in its promoter—is strongly and specifically induced by TLR2 signaling. Similarly, the SCD1 gene is induced by TLR2 signaling in a human sebocyte cell line. These observations reveal the existence of a regulated, lipid-based antimicrobial effector pathway in mammals and suggest new approaches to the treatment or prevention of infections with gram-positive bacteria.


arrow
INTRODUCTION
 
Surface epithelia constitute the first line of defense against pathogens. This defense depends both on barrier function and on specific microbicidal effector molecules. For example, the mammalian skin affords physical protection partly because it is composed of tightly associated cells covered by a highly cross-linked layer of keratin and is normally impermeable to bacteria. In humans, several genetic diseases, such as mucoepithelial dysplasia or epidemolysis bullosa, which affect the cutaneous epithelial structure at different levels (23, 26), are associated with greatly increased susceptibility to infection. But the skin displays microbicidal activity even when its physical integrity is breached. It contains an arsenal of bioactive molecules, among which antimicrobial peptides (AMPs) such as defensins and cathelicidins are of critical importance to host defense against microbial invasion (reviewed in references 27 and 28).

While AMPs are the best-studied cutaneous defense molecules, other protection systems may also exist. In this regard, several lipids extracted from human skin, among which free fatty acids have been shown to be the most potent molecules, possess antistaphylococcal activity (12). In addition, monounsaturated fatty acids (MUFA) are also produced by the sebaceous glands, and some MUFA are known to be microbicidal (24). However, their contribution to antimicrobial defense has never been established in vivo, nor is their biosynthesis known to be subject to regulation by microbial stimuli. In the present report, a novel innate immunodeficiency phenotype, characterized by a reduced ability to clear an experimental skin infection with gram-positive bacteria in mice, has been traced to a mutation affecting the structure of an enzyme essential for MUFA synthesis.


arrow
MATERIALS AND METHODS
 
Mice. Germ line mutagenesis using N-ethyl-N-nitrosourea (ENU) has been described in reference 7. Animals were maintained under pathogen-free conditions in the animal care facility of the Immunology Department of The Scripps Research Institute. All mice used in the experiments were 8 to 12 weeks old. Handling of mice and experimental procedures were conducted in accordance with institutional guidelines for animal care and use.

Bacteria. Staphylococcus aureus Xen8.1 (parental strain 8325-4), Streptococcus pyogenes Xen20 (derived from serotype M49, strain 591), and Escherichia coli Xen14 (derived from EPEC WS2572) were obtained from Xenogen (Cranbury, NJ).

Cell culture. SZ95 sebocytes were maintained in HSG-Med (Sebomed, Berlin, Germany) supplemented with 10% heat-inactivated fetal calf serum, 5 ng/ml human epidermal growth factor, 1 mM CaCl2, 10–5 M palmitic acid, and 50 µg/ml gentamicin for 2, 4, 8, and 18 h with or without 50 ng/ml macrophage-activating lipopeptide 2 (MALP-2) or 100 ng/ml lipopolysaccharide (LPS), and the supernatants were collected for interleukin-6 (IL-6) and IL-8 evaluation by enzyme-linked immunosorbent assay. RNA was isolated from the 4- and 18-hour samples by the RNeasy Midi kit (QIAGEN, Hilden, Germany) and purified by the RNase-Free DNase set (QIAGEN) for reverse transcription-PCR (RT-PCR).

Reagents. Palmitoleic and oleic acids were purchased from Sigma. Salmonella enterica serovar Minnesota Re595 LPS was obtained from Alexis (Carlsbad, CA) and MALP-2 from EMC microcollections GmbH (Tübingen, Germany).

Skin infection. Bacterial cultures in exponential-growth phase were centrifuged, and the pellet was resuspended in 10 volumes of phosphate-buffered saline containing 10 mg/ml of inert Cytodex beads (Sigma) used as a carrier. Approximately 5 x 105 CFU of luminescent bacteria in 100 µl was injected subcutaneously into the backs of anesthetized animals. Hairs were removed by chemical depilation prior to inoculation. Luminescence was monitored daily with a charge-coupled device camera (5-min exposure of animals), and quantification was done with the IVIS program from Xenogen.

TLC. Total lipids extracted from skin biopsy specimens by chloroform-methanol were separated by silica gel thin-layer chromatography (TLC). Hexane-diethyl ether-acetic acid (70:30:1) was used as the developing solvent, and lipids were visualized under a UV lamp after being sprayed with a primuline solution (5 mg in 100 ml acetone-water [80/20]).

Semiquantitative RT-PCR. Wild-type and Tlr2–/– mutant mice were depilated and infected by subcutaneous injection of S. aureus or E. coli (5 x 105 PFU). After 24 h, the skin of the infected area was dissected and total RNA was extracted by the Trizol (Gibco) method. One microgram of RNA was used to synthesize oligo(dT)-primed cDNA (Retroscript; Ambion), which then served as a template in PCRs using primers specific for Scd1 (3'-CTCTATGGATATCGCCCCTACGACAAGAACATTC-5' in exon 5 and 3'-GAAGCTAGGAACAAGGAGGGATGTATTCAGGAGG-5' in exon 6, which allow for a distinction between genomic and cDNA amplification) or ß-actin genes. Portions (4 µl) of the PCR products were loaded onto agarose gels. Isolation of peritoneal macrophages and stimulation have been described elsewhere (7). hSCD1 and hFADS2 expression in SZ95 sebocytes was measured by semiquantitative RT-PCR using the following oligonucleotides: hSCD1f (5'-TTCAGAAACACATGCTGATCCTCATAATTCCC-3'), hSCD1r (5'-ATTAAGCACCACAGCATATCGCAAGAAAGTGG-3'), hFADS2f (5'-ACTTTGGCAATGGCTGGATTCCTACCCTC-3'), and hFADS2r (5'-ACATCGGGATCCTTGTGGAAGATGTTAGG-3'). Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) expression was used as a control.


arrow
RESULTS
 
flake: a visible phenovariant with associated immunodeficiency. In an effort to identify genes required for normal immune function, we have screened a total of 20,792 F1 and 33,202 F3 animals with ENU-induced germ line mutations for visible and immunologic phenotypes. Among these, a recessive mutation dubbed "flake" (flk) was found to cause progressive alopecia and chronic exfoliative dermatitis. These features appeared at weaning age and were more pronounced in older animals (Fig. 1). Visible disruption of epidermal integrity and sporadic spontaneous skin infections requiring antibiotic therapy prompted us to examine the integrity of the innate immune function in these mice.



View larger version (118K):
[in this window]
[in a new window]
  		FIG. 1. Visible phenotypes observed in flake mutant mice. (A) Six-week-old mouse; (B) 8-month-old mouse; (C) eye infection in an 8-month-old mouse. (D) Magnification of the mouse photograph in panel B highlights severe dermatitis.

Persistent Streptococcus pyogenes and Staphylococcus aureus skin infections in flk/flk mutant mice. The gram-positive cocci S. pyogenes and S. aureus are the leading agents of human impetigo, cellulitis, and wound infection (5, 6). Experimental full-thickness skin infection in the murine model can be reliably established by immediate subcutaneous injection with a fine-gauge needle (2, 14), overcoming the requirement for traumatic injury and the poor infectivity and reproducibility associated with epicutaneous inoculation (8).

We utilized luminescently tagged strains of Streptococcus pyogenes, Staphylococcus aureus, and Escherichia coli, each of which constitutively expressed a bacterial lux operon derived from Photorhabdus luminescens (9). The progress of each infection was monitored by external luminometry over a period of 16 days in anesthetized mice. As shown in Fig. 2A, normal C57BL/6 mice needed 8 days to completely clear a skin infection established by inoculation of 5 x 105 CFU of S. pyogenes. The flk/flk mutants showed similar kinetics of microbial clearance for the first 6 days following inoculation, but thereafter, the microbial burden in flk/flk mutants departed from control values, rising to reach a plateau that was maintained throughout the duration of the experiment. Luminescence slowly declined to reach background levels 4 weeks after inoculation in flk/flk mutants (not shown).



View larger version (42K):
[in this window]
[in a new window]
  		FIG. 2. flake mutant mice develop persistent skin infections when exposed to gram-positive bacteria. (A and B) Time course analyses of the bacterial growth in control (C57BL/6) (n = 4) and mutant (flake/flake) (n = 4) animals subcutaneously infected with S. pyogenes (A) or S. aureus (B). (Upper panels) Graphs show results of quantification by luminescence (expressed as a percentage of the luminescence in the initial inoculum) for four animals of each genotype. (Lower panels) Overlay of photographs and light detection for two representative mice for each genotype at the indicated days after inoculation. (C) Infection with E. coli.

S. pyogenes produces a small, ulcerated wound, which healed almost completely by day 8 in control mice. Ulceration was still observed in flk/flk mutant mice up to 28 days after infection, albeit without detectable luminescence in vivo. Luminescent S. pyogenes bacteria were recovered by culturing the ulcers of flk/flk mutants. Hence, even 4 weeks after experimental inoculation, flk/flk mutant mice remained persistently infected with S. pyogenes.

Infection with S. aureus (Fig. 2B) yielded results formally similar to those described above. During the initial period of observation, the bacterial burden in flk/flk mutants closely matched that in controls, but a departure in the two curves was observed on day 7 following inoculation, with gradual clearance achieved in control animals (but not in flk/flk mutants), leading to a complete recovery of the controls within 2 weeks. In contrast, luminescence remained strongly detectable in flake mice for more than 3 weeks and reached background levels later than 4 weeks after inoculation (not shown).

On the other hand, flk/flk mutants were able to clear an infection with the gram-negative bacterium Escherichia coli (Fig. 2C). Moreover, no difference between flk/flk mutants and normal controls was observed when infections with gram-positive bacteria were introduced by other routes (for example, by intravenous inoculation of Listeria monocytogenes or by intrapulmonary challenge using S. aureus [not shown]). On the basis of all the data adduced in these studies, it appears that (i) flk/flk mutants mice are impaired in their ability to sterilize skin infections with gram-positive bacteria; (ii) the phenotype does not extend to all biological compartments and, so far as we know, is limited to the skin; (iii) the single infection with a gram-negative bacterium that was examined was not affected by the mutation; and (iv) the fact that skin lesions induced by E. coli healed normally in flk/flk mice indicates that the mutation does not affect wound healing per se but rather has a selective effect on pathogen clearance.

Mapping of the flk mutation to the stearoyl CoA desaturase 1 locus. The visible phenotype imparted by flk was utilized in mapping, and concordance between visible and immunologic phenotypes was later established by examining the progeny of intercrossed F1 mice as well as other allelic variants of the locus (not shown). flk was initially mapped to chromosome 19 on 39 meioses by using a panel of 59 informative markers distributed throughout the mouse genome, in a backcross against C3H/HeN. The phenotype was fully penetrant on the mixed background, and the mutation was placed between markers D19Mit96 and D19Mit17 (Fig. 3A). Fine mapping was then performed using 12 internal chromosome-19 markers, so that on 283 meioses, the mutation was restricted to a 2.6-Mbp critical region delimited by D19Mit11 and D19Mit53 (Fig. 3B). Among the 43 genes represented within this region in the Ensembl database (Fig. 3C), we considered the stearyol coenzyme A (CoA) desaturase 1 (Scd1) gene a likely candidate, since two mutant alleles, named asebia-J and asebia-2J, have already been described for Scd1 and in both cases, mutant mice show a cutaneous phenotype described as "scaly skin" (19, 29), similar to that observed in flk homozygotes.



View larger version (35K):
[in this window]
[in a new window]
  		FIG. 3. Mapping of the flake mutation. (A) Transgenomic log likelihood ratio [Lod score (Z)] analysis shows a single peak of linkage on mouse chromosome 19. A total of 59 informative markers (horizontal axis) were included in the analysis, and 39 meioses (19 wild-type and 17 mutant animals) were genotyped at all markers. (B) Fine mapping of the distal region of chromosome 19. Analysis of a total of 283 meioses (3 representatives are shown) led to the confinement of the flake mutation between two adjacent markers 2.6 Mb apart. (C) Gene organization at the flake locus according to the Ensembl database. The Scd1 gene is circled.

The six exons of Scd1 were amplified from genomic DNA isolated from both C57BL/6 control mice and flk/flk mutants. Direct sequencing of the amplicons revealed a point mutation (C to A) in exon 5, which corresponds to position 938 in the cDNA sequence (NCBI accession number BC055453) (Fig. 4A). This ENU-induced base transversion is predicted to cause a missense mutation (T227K) within SCD1. No mutation was detected in Scd2 and Scd3 cDNAs.



View larger version (36K):
[in this window]
[in a new window]
  		FIG. 4. Molecular characterization of the flake mutation. (A) Trace file of amplified genomic DNA from homozygous flake mutant mice (top chromatogram) and normal animals (bottom chromatogram). (B) Schematic representation of the SCD1 protein and localization of the flake mutation. Vertical rectangles correspond to transmembrane domains predicted by SMART analysis.

The microsomal enzyme SCD1 is an iron-binding 41-kDa protein of 355 amino acids with six predicted transmembrane domains. It catalyzes {Delta}9 desaturation of long-chain unsaturated fatty acids, leading to the biosynthesis of palmitoleate (C16:1) and oleate (C18:1) as its major products. As shown in Fig. 4B, the substitution of a neutral amino acid (T) for a charged residue (K) in the mutated protein occurs within a predicted transmembrane domain and would be expected to disrupt the structural integrity of SCD1.

To test this assumption, we performed TLC to analyze the lipid composition of skin biopsy specimens from control and flk/flk mice. The latter animals exhibit a reduction in cholesterol esters (Fig. 5A), similar to that reported in the case of Scd1 knockout (KO) mice, which indicates that the flk phenotype is indeed caused by the observed allelic variant of Scd1.



View larger version (71K):
[in this window]
[in a new window]
  		FIG. 5. TLC analysis of the lipid content in wild-type and flake mutant mice. (A) TLC of lipids extracted from skin biopsy specimens of wild-type (B6) or flake (flk) mutant mice. (B) TLC of lipids purified from the skin of wild-type mice (B6 +) 1 h or 24 h after S. aureus subcutaneous infection. Lanes M, markers. Cs, cholesterol; TG, triglycerides; CE, cholesterol esters.

Palmitoleate and oleate have intrinsic antibacterial activity in vitro and in vivo. The absence of C18 and C16 fatty acid desaturase activity in Scd1flk/flk mutant mice prompted us to ask whether the lack of oleate and/or palmitoleate could account for the cutaneous immunodeficiency phenotype described above. Indeed, several reports have indicated that MUFA exhibit antimicrobial activity against gram-positive bacteria (12, 24), though there is no evidence that MUFA exert a protective effect in vivo. To test our working hypothesis, we first performed a series of in vitro experiments in which we measured the effect of each lipid on the growth of S. pyogenes, S. aureus, and E. coli.

Our results confirmed that palmitoleate and oleate each have strong bacteriostatic and bactericidal activities against S. pyogenes and S. aureus. The MICs (Table 1) of both compounds for S. pyogenes are in the micromolar range and comparable to that observed for the murine cathelicidin AMP (CRAMP). On a weight basis, the MUFA are therefore approximately 20 times as potent as cathelicidin. MUFA are also active against S. aureus, whereas CRAMP is totally inactive. On the other hand, no bacteriostatic or bactericidal activity was detected against E. coli even at millimolar MUFA concentrations (not shown), consistent with a specific effect against gram-positive bacteria.


View this table:
[in this window]
[in a new window]
  		TABLE 1. MICs and minimum bactericidal concentrations of CRAMP, oleic acid, and palmitoleic acid for S. pyogenes and S. aureus

To investigate the physiological relevance of this antimicrobial activity, we inoculated wild-type mice with S. aureus and treated the infected animals by repeated (every 2 days) subcutaneous injections of palmitoleate (100 µl of a 100 µM solution in dimethyl sulfoxide [DMSO]) or DMSO alone at the site of infection. The results of this experiment are shown in Fig. 6A and B. For both groups of mice (n = 6 animals), luminescence is expressed as a percentage of the luminescence of the initial inoculum, determined 24 h after infection. Nine days after S. aureus inoculation, palmitoleate-treated animals exhibited a 90% reduction in luminescence, compared to vehicle-treated mice. As a consequence of improved S. aureus elimination, the diameter of the ulcerative wound (measured at day 9) in lipid-treated animals was one-fourth that observed in controls (Fig. 6C). These data, which clearly illustrate the antibacterial capacities of MUFA in vitro and in vivo, also reveal that this lipid-based defense mechanism is not maximally efficacious in normal mice.



View larger version (37K):
[in this window]
[in a new window]
  		FIG. 6. Palmitoleic acid has antibacterial activity in vivo. (A) Palmitoleate (Palm) injection accelerates bacterial clearance in wild-type mice. Luminescence (expressed as a percentage of the luminescence in the initial inoculum) was measured in control (C57BL/6) mice inoculated with S. aureus (at day 0) and treated by vehicle (DMSO) or palmitoleate injections every 2 days (arrows). (B) Photographs, taken 9 days after S. aureus infection, of control (C57BL/6) mice treated by DMSO (top) or palmitoleate (bottom) injections. (C) Histogram showing the sizes of lesions measured at day 9 after infection in control (B6) mice treated with DMSO or palmitoleate. **, P < 0.01. (D) Palmitoleate treatment of S. aureus-infected flake mice. The protocol is similar to that for panel A, except that we performed 100-µl injections of a 75 mM solution of palmitoleate. (E) Photographs of infected flake mice at day 12 after DMSO (top) or palmitoleate (bottom) treatment. (F) Sizes of lesions (determined at day 12) in infected flk mutants treated with DMSO or palmitoleate. *, P < 0.05.

Under similar conditions of palmitoleate administration, flake mutants exhibited a marked reduction in bacterial growth between days 1 and 4 (also observed in wild-type mice), but S. aureus remained detectable 2 weeks after inoculation (not shown). As shown in Fig. 6D and E, a higher dose of palmitoleate (100 µl of a 75 mM solution) moderately improved bacterial clearance in flk/flk mutants and the subsequent ulcer healing (Fig. 6F). However, complete rescue of the phenotype was not achieved by this pharmacological approach (see Discussion).

Transcriptional activation of Scd1 occurs during gram-positive bacterial infection and is TLR2 dependent. The unsuspected in vivo antimicrobial function of MUFA prompted us to ask whether their synthesis is increased during the immune response, as is the case for other effector molecules such as CRAMP. We analyzed a 5-kb fragment of the Scd1 promoter and noted the presence of several NF-{kappa}B binding sites (Fig. 7A). We then performed semiquantitative RT-PCR experiments on skin biopsy specimens from normal or infected mice. Figure 7B shows that Scd1 mRNA accumulation is strongly induced in the skin of control (C57BL/6) mice upon S. aureus infection, whereas E. coli inoculation produces no effect. Furthermore, in mice carrying a targeted disruption of the Tlr2 gene (Tlr2–/–), the Scd1 gene is unresponsive to inoculation of gram-positive bacteria. However, Scd1 transcriptional induction might also be caused by an indirect mechanism, given the 24-h delay between infection and RNA isolation.



View larger version (44K):
[in this window]
[in a new window]
  		FIG. 7. Infection- and TLR2-dependent induction of Scd1 gene expression in mice. (A) SignalScan analysis of the Scd1 promoter. NF-{kappa}B and ISRE (interferon-stimulated regulatory element) are shown. (B) RT-PCR detection of Scd1 and ß-actin transcripts in skin biopsy specimens of uninfected control (C57BL/6) and Tlr2–/– animals (lanes 1 and 4) or after infection by S. aureus (lanes 2 and 5) or E. coli (lane 3). PCR products obtained after 30 and 40 cycles are shown. M, size standard. (C) RT-PCR detection of Scd1 and ß-actin transcripts in control (0 h) and MALP-induced peritoneal macrophages isolated from wild-type mice after 2, 4, 8, and 18 h. (D) Quantification of the Scd1/ß-actin ratio.

Macrophages, which represent an ideal system in which to study TLR signaling, also express the Scd1 gene, as reported recently (22). To determine whether isolated macrophages are capable of up-regulating Scd1 and to determine the kinetics of the response, we stimulated peritoneal macrophages isolated from wild-type mice with synthetic MALP-2 (EMC microcollections GmbH, Tübingen, Germany), a known TLR2 agonist (21). We surveyed Scd1 expression by RT-PCR on RNA samples isolated 2, 4, 8, and 18 h after stimulation. As seen in Fig. 7C and D, Scd1 expression was augmented 2 h after MALP induction and reached a fourfold increase within 18 h. This transcriptional induction of Scd1 was correlated with increased lipid synthesis in the skin of infected animals (Fig. 5B).

As previously noted, Scd1 is expressed principally in sebaceous glands, and flake mice, as well as asebia and Scd1 KO mice, exhibit atrophy of these structures (not shown). To corroborate the potential relevance of inducible Scd1 expression in human skin defense against gram-positive pathogens, we investigated the effect of MALP-2 on the immortalized human sebocyte cell line SZ95 (30). First, we noted that treatment with MALP-2, but not with LPS, induced a rapid and potent inflammatory response, manifested by increased IL-6 and IL-8 production (Fig. 8A and B). Next, we observed that SCD1 transcription is also up-regulated in this human cell line 4 h after MALP-2 stimulation (Fig. 8C and D). We extended these observations by monitoring the expression of the fatty acid desaturase 2 (FADS2) gene. FADS2 encodes a protein with enzymatic properties similar to those of SCD1 and was recently shown to be deficient in a patient affected by a severe skin condition (25) manifested by cheilosis, a hyperkeratotic rash over the arms and legs, and perineal dermatitis. In human cultured sebocytes, FADS2 is slightly but specifically induced 18 h after MALP-2 stimulation.



View larger version (25K):
[in this window]
[in a new window]
  		FIG. 8. Human sebocytes stimulated with MALP-2 show an inflammatory response and up-regulation of SCD1 and FADS2 genes. (A) IL-6 production is induced in SZ95 cells after MALP-2 treatment (50 ng/ml). LPS stimulation (100 ng/ml) shows minimal effect. (B) Quantification of IL-8 under the same conditions as those in panel A. (C) RT-PCR detection of SCD1 and FADS2 expression 4 and 18 h after LPS and MALP-2 stimulation. GAPDH expression was used as a control. (D) Quantification of the SCD1 and FADS2 signals measured in two independent experiments (± standard errors of the means) after normalization with the GAPDH signal.


arrow
DISCUSSION
 
SCD1 is an enzyme responsible for the biosynthesis of MUFA, mainly palmitoleate (C16:1) and oleate (C18:1) (15). It catalyzes {Delta}9 cis-desaturation of the carbon chain and uses palmitoyl-CoA and stearoyl-CoA as substrates. The functions of this enzyme in lipid metabolism have been intensely studied (16). Scd1–/– mice are significantly leaner than wild-type animals and are resistant to diet-induced adiposity, an effect mediated by increased expression of genes involved in fatty acid oxidation. Furthermore, compound homozygotes for hypomorphic mutations of the obese (ob) and Scd1 genes exhibit a striking attenuation of the obese phenotype (17). The observation that Scd1 is overexpressed in ob mutants indicates that at least part of the leptin's metabolic actions result from the inhibition of Scd1 (3). Two spontaneous mutant alleles of Scd1 have been described and named asebia-J (ab-J) and ab-2J (19, 29). Despite minor phenotypic differences, homozygosity for each of these alleles is associated with atrophic sebaceous glands, alopecia, and scaly skin, phenotypes which are also observed in mice carrying a targeted disruption of the gene (13).

In the present study, we have described flake, a visible recessive phenovariant with a highly selective innate immunodeficiency phenotype, in which there is failure to eliminate gram-positive (but not gram-negative) organisms from the skin. Using a phenotype-driven approach, we tracked the flk mutation to a missense error (T227K) that falls within the fourth of six transmembrane domains of the SCD1 protein. The replacement of a neutral by a charged residue in such a region might alternatively modify the conformation of the desaturase, which normally resides within microsomal membranes, or affect coordination of the iron atom that is necessary for enzymatic activity. Whatever the mechanism, we have demonstrated a reduction in the level of cholesterol esters (the biosynthesis of which requires MUFA) in lipid isolates from the skin of flake mutant mice, confirming that the new allele is hypofunctional.

Here we have implicated SCD1 and the products of its catalytic activity in epithelial innate immunity against gram-positive bacteria. It has been shown previously that feeding Scd1-deficient mice a MUFA-enriched diet does not alleviate the mutant phenotype, which indicates that de novo synthesis of MUFA is required for normal appearance and function of the skin. Therefore, to extend our in vitro observations, we monitored the effect of intradermal administration of palmitoleate to S. aureus-infected mice. These in vivo experiments showed that repeated subcutaneous injections of palmitoleate reduced bacterial proliferation and significantly improved the recovery of infected mice, as evidenced by reduction of the ulcerative wound. However, this beneficial effect of palmitoleic acid was less pronounced in flake mutants, despite repeated injections of higher doses of palmitoleate. The complex lipidic composition of the sebum, whose overall production is reduced in flake mutant animals, might account for this observation. It is, therefore, conceivable that antibacterial lipids (12) other than MUFA may be required for efficient clearance of the infection. Alternatively, the overactivated lipid catabolism observed in Scd1 mutants might lead to a shorter half-life of the injected lipids and could explain this discrepancy. Nevertheless, we noted that humans treated for acne problems with retinoids (which induce atrophy of the sebaceous glands) can suffer recurrent S. aureus skin infections as a side effect (10). Infections of the eye with gram-positive bacteria have also been noted in such patients (4). Indeed, we have also observed eye infections in flake mutants (Fig. 1C), as noted previously for Scd1 KO mice (13). Our data from flk/flk mice emphasize the essential role of sebaceous glands, as well as other lipid-producing organs, including perhaps the specialized meibomian glands of the eyelids, in local innate immune responses.

The mechanism by which MUFA selectively kill gram-positive bacteria remains to be determined. The length of the carbon chain and/or the level of unsaturation might be important determinants of efficacy. In addition, synergy between lipids and AMP might also be examined. flake/CRAMP double-knockout mice will prove to be useful tools with which to study this issue. Our experiments do not exclude the possibility that, in addition to their antimicrobial activity, palmitoleate and oleate might promote resistance indirectly. Modulation of signal transduction through protein modification might be one such mechanism. As reported elsewhere (11), mass spectrometry identified palmitoleate among other posttranslational modifications of the src homology domain 3 kinase Fyn, which might affect immune cell activation, as recently shown for insulin signaling in muscle cells (18).

SCD1 transcription is strongly up-regulated in mouse and human cells in a TLR2-dependent manner. Human patients with rare skin disorders such as the syndrome of ichthyosis follicularis with atrichia and photophobia (IFAP syndrome; OMIM 308205) possess atrophic sebaceous glands and coincidently suffer alopecia and recurrent skin infections reminiscent of the Flake phenotype (reviewed in reference 1). With new recognition that TLR2 and -6 are expressed in human sebocytes (C. C. Zouboulis et al., unpublished data), our results point to a prominent and unsuspected role of the sebaceous gland in the innate immune defense of the skin. Altogether, our data demonstrate the existence of an inducible lipid-based microbicidal effector pathway in the skin and establish a clear functional link between lipid metabolism and innate immunity.


arrow
ACKNOWLEDGMENTS
 
This work was supported by a grant from the NIH (U54 A154523), the Fondation Philippe (to P.G.), and the Verein zur Förderung der Dermatologie (to C.C.Z.).


arrow
FOOTNOTES
 
* Corresponding author. Mailing address: Department of Immunology, The Scripps Research Institute, 10550 N. Torrey Pines Road, La Jolla, CA 92037. Phone: (858) 784-8610. Fax: (858) 784-8444. E-mail: bruce{at}scripps.edu. Back

Editor: F. C. Fang


arrow
REFERENCES
 
    1
  1. Alfadley, A., H. K. Al, and A. K. Al. 2003. Ichthyosis follicularis: a case report and review of the literature. Pediatr. Dermatol. 20:48-51.[CrossRef][Medline]
    2. 2
  2. Bunce, C., L. Wheeler, G. Reed, J. Musser, and N. Barg. 1992. Murine model of cutaneous infection with gram-positive cocci. Infect. Immun. 60:2636-2640.[Abstract/Free Full Text]
    3. 3
  3. Cohen, P., M. Miyazaki, N. D. Socci, A. Hagge-Greenberg, W. Liedtke, A. A. Soukas, R. Sharma, L. C. Hudgins, J. M. Ntambi, and J. M. Friedman. 2002. Role for stearoyl-CoA desaturase-1 in leptin-mediated weight loss. Science 297:240-243.[Abstract/Free Full Text]
    4. 4
  4. Egger, S. F., V. Huber-Spitzy, K. Bohler, and C. Scholda. 1995. Isotretinoin administration in treatment of acne vulgaris. A prospective study of the kind and extent of ocular complications. Ophthalmologe 92:17-20. (In German.)[Medline]
    5. 5
  5. Guay, D. R. 2003. Treatment of bacterial skin and skin structure infections. Expert Opin. Pharmacother. 4:1259-1275.[CrossRef][Medline]
    6. 6
  6. Hedrick, J. 2003. Acute bacterial skin infections in pediatric medicine: current issues in presentation and treatment. Paediatr. Drugs 5(Suppl. 1):35-46.
    7. 7
  7. Hoebe, K., X. Du, J. Goode, N. Mann, and B. Beutler. 2003. Lps2: a new locus required for responses to lipopolysaccharide, revealed by germline mutagenesis and phenotypic screening. J. Endotoxin Res. 9:250-255.[CrossRef]
    8. 8
  8. Kraft, W. G., P. T. Johnson, B. C. David, and D. R. Morgan. 1986. Cutaneous infection in normal and immunocompromised mice. Infect. Immun. 52:707-713.[Abstract/Free Full Text]
    9. 9
  9. Kuklin, N. A., G. D. Pancari, T. W. Tobery, L. Cope, J. Jackson, C. Gill, K. Overbye, K. P. Francis, J. Yu, D. Montgomery, A. S. Anderson, W. McClements, and K. U. Jansen. 2003. Real-time monitoring of bacterial infection in vivo: development of bioluminescent staphylococcal foreign-body and deep-thigh-wound mouse infection models. Antimicrob. Agents Chemother. 47:2740-2748.[Abstract/Free Full Text]
    10. 10
  10. Leyden, J. J., K. J. McGinley, and A. N. Foglia. 1986. Qualitative and quantitative changes in cutaneous bacteria associated with systemic isotretinoin therapy for acne conglobata. J. Investig. Dermatol. 86:390-393.[CrossRef][Medline]
    11. 11
  11. Liang, X., Y. Lu, M. Wilkes, T. A. Neubert, and M. D. Resh. 2004. The N-terminal SH4 region of the Src family kinase Fyn is modified by methylation and heterogeneous fatty acylation: role in membrane targeting, cell adhesion, and spreading. J. Biol. Chem. 279:8133-8139.[Abstract/Free Full Text]
    12. 12
  12. Miller, S. J., R. Aly, H. R. Shinefeld, and P. M. Elias. 1988. In vitro and in vivo antistaphylococcal activity of human stratum corneum lipids. Arch. Dermatol. 124:209-215.[Abstract/Free Full Text]
    13. 13
  13. Miyazaki, M., W. C. Man, and J. M. Ntambi. 2001. Targeted disruption of stearoyl-CoA desaturase1 gene in mice causes atrophy of sebaceous and meibomian glands and depletion of wax esters in the eyelid. J. Nutr. 131:2260-2268.[Abstract/Free Full Text]
    14. 14
  14. Nizet, V., T. Ohtake, X. Lauth, J. Trowbridge, J. Rudisill, R. A. Dorschner, V. Pestonjamasp, J. Piraino, K. Huttner, and R. L. Gallo. 2001. Innate antimicrobial peptide protects the skin from invasive bacterial infection. Nature 414:454-457.[CrossRef][Medline]
    15. 15
  15. Ntambi, J. M. 1995. The regulation of stearoyl-CoA desaturase (SCD). Prog. Lipid Res. 34:139-150.[CrossRef][Medline]
    16. 16
  16. Ntambi, J. M., and M. Miyazaki. 2004. Regulation of stearoyl-CoA desaturases and role in metabolism. Prog. Lipid Res. 43:91-104.[CrossRef][Medline]
    17. 17
  17. Ntambi, J. M., M. Miyazaki, J. P. Stoehr, H. Lan, C. M. Kendziorski, B. S. Yandell, Y. Song, P. Cohen, J. M. Friedman, and A. D. Attie. 2002. Loss of stearoyl-CoA desaturase-1 function protects mice against adiposity. Proc. Natl. Acad. Sci. USA 99:11482-11486.[Abstract/Free Full Text]
    18. 18
  18. Rahman, S. M., A. Dobrzyn, P. Dobrzyn, S. H. Lee, M. Miyazaki, and J. M. Ntambi. 2003. Stearoyl-CoA desaturase 1 deficiency elevates insulin-signaling components and down-regulates protein-tyrosine phosphatase 1B in muscle. Proc. Natl. Acad. Sci. USA 100:11110-11115.[Abstract/Free Full Text]
    19. 19
  19. Sundberg, J. P., D. Boggess, B. A. Sundberg, K. Eilertsen, S. Parimoo, M. Filippi, and K. Stenn. 2000. Asebia-2J (Scd1ab2J): a new allele and a model for scarring alopecia. Am. J. Pathol. 156:2067-2075.[Abstract/Free Full Text]
    20. 20
  20. Takeda, K., and S. Akira. 2003. Toll receptors and pathogen resistance. Cell. Microbiol. 5:143-153.[CrossRef][Medline]
    21. 21
  21. Takeuchi, O., A. Kaufmann, K. Grote, T. Kawai, K. Hoshino, M. Morr, P. F. Muhlradt, and S. Akira. 2000. Preferentially the R-stereoisomer of the mycoplasmal lipopeptide macrophage-activating lipopeptide-2 activates immune cells through a toll-like receptor 2- and MyD88-dependent signaling pathway. J. Immunol. 164:554-557.[Abstract/Free Full Text]
    22. 22
  22. Uryu, S., S. Tokuhiro, and T. Oda. 2003. ß-Amyloid-specific upregulation of stearoyl coenzyme A desaturase-1 in macrophages. Biochem. Biophys. Res. Commun. 303:302-305.[CrossRef][Medline]
    23. 23
  23. Vidal, F., D. Aberdam, C. Miquel, A. M. Christiano, L. Pulkkinen, J. Uitto, J. P. Ortonne, and G. Meneguzzi. 1995. Integrin beta 4 mutations associated with junctional epidermolysis bullosa with pyloric atresia. Nat. Genet. 10:229-234.[CrossRef][Medline]
    24. 24
  24. Wille, J. J., and A. Kydonieus. 2003. Palmitoleic acid isomer (C16:1{Delta}6) in human skin sebum is effective against gram-positive bacteria. Skin Pharmacol. Appl. Skin Physiol. 16:176-187.[CrossRef][Medline]
    25. 25
  25. Williard, D. E., J. O. Nwankwo, T. L. Kaduce, S. D. Harmon, M. Irons, H. W. Moser, G. V. Raymond, and A. A. Spector. 2001. Identification of a fatty acid {Delta}6-desaturase deficiency in human skin fibroblasts. J. Lipid Res. 42:501-508.[Abstract/Free Full Text]
    26. 26
  26. Witkop, C. J., Jr., J. G. White, R. A. King, M. V. Dahl, W. G. Young, and J. J. Sauk, Jr. 1979. Hereditary mucoepithelial dysplasia: a disease apparently of desmosome and gap junction formation. Am. J. Hum. Genet. 31:414-427.[Medline]
    27. 27
  27. Zasloff, M. 2002. Antimicrobial peptides of multicellular organisms. Nature 415:389-395.[CrossRef][Medline]
    28. 28
  28. Zasloff, M. 2002. Antimicrobial peptides in health and disease. N. Engl. J. Med. 347:1199-1200.[Free Full Text]
    29. 29
  29. Zheng, Y., K. J. Eilertsen, L. Ge, L. Zhang, J. P. Sundberg, S. M. Prouty, K. S. Stenn, and S. Parimoo. 1999. Scd1 is expressed in sebaceous glands and is disrupted in the asebia mouse. Nat. Genet. 23:268-270.[CrossRef][Medline]
    30. 30
  30. Zouboulis, C. C., H. Seltmann, H. Neitzel, and C. E. Orfanos. 1999. Establishment and characterization of an immortalized human sebaceous gland cell line (SZ95). J. Investig. Dermatol. 113:1011-1020.[CrossRef][Medline]

Infection and Immunity, August 2005, p. 4512-4521, Vol. 73, No. 8
0019-9567/05/$08.00+0     doi:10.1128/IAI.73.8.4512-4521.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.



This article has been cited by other articles:

  • Do, T. Q., Moshkani, S., Castillo, P., Anunta, S., Pogosyan, A., Cheung, A., Marbois, B., Faull, K. F., Ernst, W., Chiang, S. M., Fujii, G., Clarke, C. F., Foster, K., Porter, E. (2008). Lipids Including Cholesteryl Linoleate and Cholesteryl Arachidonate Contribute to the Inherent Antibacterial Activity of Human Nasal Fluid. J. Immunol. 181: 4177-4187 [Abstract] [Full Text]  
  • Smith, K. R., Thiboutot, D. M. (2008). Thematic review series: Skin Lipids. Sebaceous gland lipids: friend or foe?. J. Lipid Res. 49: 271-281 [Abstract] [Full Text]  
  • MacDonald, M. L. E., Singaraja, R. R., Bissada, N., Ruddle, P., Watts, R., Karasinska, J. M., Gibson, W. T., Fievet, C., Vance, J. E., Staels, B., Hayden, M. R. (2008). Absence of stearoyl-CoA desaturase-1 ameliorates features of the metabolic syndrome in LDLR-deficient mice. J. Lipid Res. 49: 217-229 [Abstract] [Full Text]  
  • Yu, F.-S. X., Hazlett, L. D. (2006). Toll-like Receptors and the Eye.. IOVS 47: 1255-1263 [Full Text]  

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Georgel, P.
Right arrow Articles by Beutler, B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Georgel, P.
Right arrow Articles by Beutler, B.

Copyright © 2009 by the American Society for Microbiology.   For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»