Abstract
Microbial recognition is a key step in regulating the immune signaling pathways of multicellular organisms. Peptidoglycan, a component of the bacterial cell wall, exhibits immune stimulating activity in both plants and animals. Lysin motif domain (LysMD) family proteins are ancient peptidoglycan receptors that function in bacteriophage and plants. This report focuses on defining the role of LysMD-containing proteins in animals. Here, we characterize a novel transmembrane LysMD family protein. Loss-of-function mutations at the lysMD3/4 locus in Drosophila are associated with systemic innate immune activation following challenge, so we refer to this gene as immune active (ima). We show that Ima selectively binds peptidoglycan, is enriched in cell membranes, and is necessary to regulate terminal innate immune effectors through an NF-kB–dependent pathway. Hence, Ima fulfills the key criteria of a peptidoglycan pattern recognition receptor. The human Ima ortholog, hLysMD3, exhibits similar biochemical properties. Together, these findings establish LysMD3/4 as the founding member of a novel family of animal peptidoglycan recognition proteins.
Keywords: peptidoglycan, pattern recognition receptor, innate immunity, NF-kappa B, lysin motif domain, Drosophila, human
Peptidoglycan is a bacterial cell wall–derived carbohydrate and one of the most abundant polymers found in nature (1). It surrounds the cytoplasmic membrane forming a mesh-like layer (2, 3). Peptidoglycan is responsible for the rigidity and shape of bacterial cells, so disrupting either its biogenesis (e.g. antibiotics) or integrity (e.g. lysozyme) results in bacterial cell lysis. Chemically, peptidoglycan is a polymer consisting of glycan strands cross-linked via short peptide stems. The unmodified, polymerized glycan strand consists of alternating units of β-(1,4) linked GlcNAc and N-acetylmuramic acid residues. The peptide stem consists of 2 to 5 amino acid residues, which can become cross-linked to the peptide stem of an adjacent glycan strand, either directly or via an interpeptide bridge (4). Variations in the composition of both the glycan strands and the peptide bridge occur between bacterial species and growth conditions (5, 6). While peptidoglycan is produced in prokaryotes, it is not synthesized by metazoans, thus providing a unique chemical signature indicating bacterial presence.
The lysin motif domain (LysMD) was first identified as a 44 amino acid direct repeat in the bacteriophage φ29 gene 15, which encodes a lysozyme (7). Similar sequences were subsequently isolated from Streptococcus faecalis in a screen to identify autolysins involved in bacterial cell wall turnover (8). The authors noted the sequence similarity to the φ29 gene 15 lysozyme repeats previously described by Garvey et al. (7), and on this basis, they first suggested that the region could be responsible for mediating peptidoglycan binding. The structure of the LysM domain was solved for an Escherichia coli gene encoding a transglycosylase, which indicated the presence of a βααβ secondary structure with the two α helices packing onto the same side of an antiparallel β sheet (9). A potential ligand-binding site was also described on the protein surface. The possibility that LysMD-containing proteins could bind peptidoglycan was directly tested in Lactococcus lactis where three LysMD repeats in the AcmA autolysin enzyme were found to be necessary for peptidoglycan binding (10). Subsequent sequence analysis has revealed the widespread distribution of the LysMD in many organisms, with the notable exception of archaea (11, 12).
In addition to the previously defined roles in prokaryotes, LysMD-containing proteins have also emerged as one of the two main receptor types mediating the immune response in plants (13, 14). Plant LysMD-containing proteins have been shown to directly bind peptidoglycan and regulate different aspects of immune signaling (15, 16). However, since bona fide peptidoglycan-binding proteins identified in animals do not contain LysM domains (17, 18, 19), peptidoglycan recognition is thought to have evolved through convergent evolution (15). Here, we directly test the role of LysMD-containing proteins in animals. We demonstrate that a transmembrane protein containing a single LysM domain binds to peptidoglycan, is enriched in cell membranes, and functions to regulate the expression of terminal innate immune effectors in a pathogen challenge model. We conclude that LysMD-mediated peptidoglycan recognition is a conserved mechanism of immune regulation in animals.
Results
Ima binds peptidoglycan in vitro
The Drosophila lysMD3/4 locus, immune active (ima), is predicted to encode a transmembrane protein containing a single LysM domain with homology to LysMD family proteins found in other organisms (Fig. S1A). Sequence analysis indicates that the ancestral lysMD3/4 gene underwent duplication in vertebrates, giving rise to the lysMD3 and lysMD4 genes of the lineage and that lysMD3 is the closest ima ortholog in the human genome (Fig. S1, B and C). To evaluate the function of these gene products, an in vitro affinity-binding assay was used to measure the extent to which animal LysMD-containing proteins could interact with peptidoglycan (20) (Fig. 1A). Both Ima and hLysMD3 were tested in the assay. We screened recombinant 6XHis-tagged proteins for binding to insoluble peptidoglycan and analyzed the pellet using SDS-PAGE and immunoblotting (Figs. 1A and S2, A and B). These experiments reveal that 6XHis-Ima binds insoluble peptidoglycan derived from gram-negative bacteria in vitro, but not from gram-positive bacteria (Figs. 1C and S2, C and D). Quantification showed that the extent of peptidoglycan binding is significant compared to controls (Figs. 1C and S2, C and D). Similar results were obtained for 6XHis-hLysMD3 (Figs. 1D and S2, C and D). Importantly, binding of 6XHis-Ima to peptidoglycan was both rapid and reversible (Figs. 1, E and F and S2, E and F). Furthermore, binding of 6XHis-Ima to insoluble peptidoglycan was attenuated in a dose-dependent manner through the addition of soluble competitor (Fig. 1G). We next asked if the LysM domain of Ima itself is required for peptidoglycan binding. Site-directed mutagenesis was first used to mutate a single conserved asparagine residue to alanine, within the LysM domain (Fig. 1B, asterisk). The affinity-binding assay was then used to determine the extent to which the 6XHis-ImaΔN85A mutant protein binds peptidoglycan. In contrast to 6XHis-Ima controls, 6XHis-ImaΔN85A mutants displayed a significant decrease in peptidoglycan binding (Fig. 1H). Taken together, these results demonstrate that Ima protein binds peptidoglycan derived from gram-negative bacteria in an LysMD-dependent manner.
Ima is localized to cell membranes
A biochemical fractionation assay was next used to determine the cellular compartment to which the endogenous Ima protein is localized (21, 22). Specific antiserum was first raised against Ima protein (Supporting information, experimental procedures). Next, whole fly lysates were treated with detergent to distinguish membrane from cytoplasmic subfractions, which were then analyzed using Western blotting. Our results show that Ima is detected in the cellular fraction enriched for membrane-localized marker proteins, but not in the cytosolic fraction (Figs. 2A and S3A). Similar fractionation results were obtained for the hLysMD3 protein, when it was heterologously expressed in Drosophila tissues using a ubiquitous promoter (Figs. 2B and S3B).
We next generated an in-frame GFP-tagged Ima protein (ima-GFP) expressed from the endogenous genomic locus using CRISPR/Cas9 editing technology (23, 24). The localization of Ima-GFP was first analyzed using immunoelectron microscopy, which revealed a strong signal present in the morphologically distinct Golgi apparatus of salivary gland epithelial cells, which are classically used to characterize subcellular protein localization owing to their large size (Fig. 2, C and D). Moreover, double-labeling immunofluorescence studies confirmed this initial finding and showed Ima-GFP colocalization with the Golgi-associated marker golgin-84, but not with the endosome marker Hrs (25) (Figs. 2, E–H and S4, A–D). Taken together, these studies demonstrate that Ima protein is enriched in the cellular membrane fraction and selectively colocalizes with markers of the endomembrane system.
Ima regulates innate immune signaling
To study the requirement of Ima in the response to bacterial challenge in vivo, we used CRISPR/Cas9 genome editing to delete the LysM domain from the previously uncharacterized Drosophila lysMD3/4 locus and generate the imaΔ mutation (Fig. S5, A and B). This resulted in an out-of-frame deletion in the coding region and decreased Ima protein levels (Fig. S5C). Flies homozygous for the imaΔ mutation deletion were viable and appeared morphologically normal under standard laboratory culture conditions.
We first characterized imaΔ mutants using a Drosophila challenge model of pathogen exposure. Pseudomonas entomophila (Pe) is a naturally occurring gram-negative enteric pathogen isolated from wild Drosophila (26). Exposure of WT flies to Pe through natural infection leads to a dose-dependent effect on survival (27). Therefore, to determine if imaΔ flies exhibited a phenotype in this challenge model, adult flies were exposed to Pe infection and survival was scored. Under mock conditions, no difference in survival was observed between WT and homozygous imaΔ mutant flies (Fig. 3A, dotted lines). However, these experiments revealed a marked decrease in the survival of imaΔ mutants upon Pe challenge that was robust in different genetic backgrounds and clearly observable even using low titer Pe challenge (Figs. 3A, solid lines, S6, A–C). To further confirm this phenotype, the imaΔ mutant chromosome was isogenized and then retested in the Pe challenge assay under both low and high titer Pe exposure (Supporting information, experimental procedures; Fig. S6D). Moreover, susceptibility of imaΔ mutants to Pe challenge was rescued by the presence of a WT ima transgene (Fig. 3A). Notably, the presence of a heterologously supplied WT ima transgene was also sufficient to provide protection against immune challenge in this assay, which consistently exceeded that of WT flies (Fig. 3A). Similarly, the human ima ortholog, hLysMD3, was sufficient to confer phenotypic rescue of the imaΔ mutant in the Pe challenge assay (Fig. 3B). These data indicate that LysMD-containing proteins encode conserved functions essential for host defense against a gram-negative enteric pathogen.
Natural infection by Pe impacts host viability through effects on the gut epithelial barrier (26). Given that ima is necessary to protect against Pe challenge and that Ima protein is also present in gut enterocytes (Fig. 3D), we next tested if expression of a heterologously supplied WT ima transgene under the control of a gut-specific promoter was sufficient to rescue survival. Consistent with its endogenous distribution, expression of ima in gut enterocytes is sufficient to completely rescue lethality of the imaΔ mutant following Pe challenge (Fig. 3E), although not to the same extent as ubiquitous expression suggesting function in other tissues, as well. Thus, ima functions in gut epithelial cells to protect against natural enteric infection by the gram-negative Pe pathogen.
Antimicrobial peptides (AMPs) are key terminal effectors of the humoral innate immune response that are transcribed in response to bacterial challenge (28). Therefore, to extend this characterization of the ima loss-of-function phenotype, we used qPCR to directly measure transcription levels using a panel of innate immune system target genes. In each case, loss of ima resulted in dysregulation of AMP expression in whole adult flies 24 h following Pe exposure (Fig. 3C). Dysregulation of AMP expression was also observed in isolated gut tissue samples derived from imaΔ mutants (Fig. 3F). Taken together, these studies demonstrate that ima is necessary to negatively regulate systemic and local AMP expression in response to enteric infection by the gram-negative Pe pathogen.
The host immune response to gram-negative pathogens is mediated by the immune deficiency (Imd) signaling pathway, which can result in death when misregulated (28). In this pathway, peptidoglycan is sensed by the peptidoglycan recognition proteins PGRP-LC and PGRP-LE, and transcriptional responses are mediated by the Relish/NF-kB transcription factor. Therefore, if the response of ima mutants to Pe results from Imd pathway hyperactivation as suggested by immune target gene expression, then ima mutant phenotypes should be genetically suppressed by simultaneously altering the Imd signaling pathway. To test this prediction directly, the imaΔ survival phenotype was first analyzed in animals also lacking one copy of established Imd signaling components. This manipulation significantly rescued the survival of imaΔ mutants in response to Pe challenge (Fig. 4A). Similarly, the activation of target gene expression seen in imaΔ mutants was also suppressed following reduction of Imd pathway members (Fig. 4B). Finally, nuclear location of the Relish/NF-kB transcription factor, a marker of Imd pathway activation, was found to be elevated in imaΔ mutants (Fig. 4C). Taken together, these findings support the conclusion that Ima normally protects the host against enteric gram-negative challenge by inhibiting Imd pathway activation and thus moderating the tissue damaging effects of AMP misregulation.
Discussion
The ancient LysMD-containing receptor family is conserved throughout evolution including in humans. LysMD-mediated recognition has been linked to host/pathogen signaling interactions in prokaryotic viruses, prokaryotes, and plants, suggesting that LysMDs are prototypical pattern recognition receptors. Yet, a role for LysMD-containing proteins in animal peptidoglycan sensing has not been directly tested. In this study, we hypothesized that LysMD-containing proteins function as peptidoglycan recognition proteins to regulate immunity in animals. We tested three key predictions of this assertion and demonstrate that Ima, Drosophila LysMD3/4, and its human homolog, hLysMD3, bind peptidoglycan, localize to cell membranes, and promote survival and immune signaling in a pathogen challenge model. Hence, we conclude that LysMD-mediated peptidoglycan recognition is conserved and provides immunity in animals.
There is precedent for peptidoglycan pattern recognition receptors to localize to different subcellular compartments, including the cytoplasm and cell surface. Our results indicate that LysMD receptors such as Ima are among the former class of proteins. Ima interacts genetically with the canonical Imd immune signaling pathway to negatively regulate innate immune signaling through Rel/NF-kB and downstream AMP target genes. Taking the biochemical, localization, and genetic data together suggests several models of Ima function consistent with these findings that may not be mutually exclusive: First, Ima could function as a bona fide inhibitory immune receptor to directly regulate host immune responses through a novel pathway. While signal transduction in the Drosophila immune system is well described, it is worth noting that a large number of immune responsive genes are regulated independently of the canonical immune signaling pathways (29). Nevertheless, beyond the LysM domain, no additional regions of homology were detected in the ima coding region. Second, Ima could function as part of an inhibitory coreceptor complex with previously identified proteins, such as the PGRP family receptors. Such signaling complexes could function to either directly regulate immune activation or act indirectly by influencing the localization, multimerization, or availability of essential immune signaling components. Finally, Ima may function as a competitive agonist (or molecular “sponge”) that does not directly utilize downstream immune effectors but rather functions to buffer levels of free peptidoglycan by sequestering it from interactions with other peptidoglycan sensing systems. According to this model, Ima would protect against lethal tissue damage that would otherwise result from inappropriate innate immune activation. Therefore, it will be important that future studies identify interacting proteins directly associated with LysMD family proteins in animal models.
Experimental procedures
In vitro–binding assay
Peptidoglycan-binding assays were performed with modifications as previously described (20). Binding reactions with recombinant Ima and hLysM3 proteins were established as follows: 50 μg of ultrapure insoluble E. coli K12 peptidoglycan (Invivogen) was mixed in a low protein binding microcentrifuge tube with 1 μg of His-tagged protein in 300 μl volume of 0.1 M phosphate buffer pH 7.0 and incubated overnight at 4 °C.
Biochemical fractionation
Membrane fractionation assays were performed with modification as previously described (21, 22). Ten female flies were frozen and then homogenized 1 min using a rotary Teflon pestle.
Microscopy
Tissue samples were processed for immunoelectron microscopy by fixing in 4% formaldehyde in PBS. Negative controls excluded primary antibodies. Whole mount samples for immunostaining was performed using standard methodology. Antisera: mouse anti-p120 Golgi (1:100 Calbiochem); rabbit anti-Relish 130-10080 (1:300, RayBiotech); chicken anti-GFP (1:10,000, Abcam); mouse anti-golgin-84 (1:100, Developmental Studies Hybridoma Bank (DSHB) clone 12-1); guinea pig anti-GMAP (1:2000, DSHB); mouse anti-Hrs (1:100, DSHB clone 27-4); Alexa Fluor–conjugated secondary antibodies (1:2000, Molecular Probes). Whole mount samples were analyzed on a Leica DM5000 compound or Leica TCS SP5 confocal microscope. Images were processed for brightness and contrast in Photoshop CS (Adobe). Fluorescence signal quantitation was performed using ImageJ, and colocalization analysis performed using the JACoP plugin for ImageJ.
Fly strains
w1118 (BL#3605, control); isogenized w1118 (BL#5905, w1118iso, control); w1118; imaΔ/CyO, actin-GFP (this study); y1, w1118; imaΔ/CyO, actin-GFP (this study); w1118; imaΔiso/CyO, actin-GFP (this study); w1118; ima::GFP/CyO (this study); w1118; UAS-ima (this study); w1118; UAS-hLysMD3 (this study); w1118; da-gal4; Myo1A-gal4; w, RelishE20 (loss-of-function mutation in translational start codon); w; PGRP-LCΔ5; w; PGRP-LC1; w; PGRP-LE112. Additional information, http://flybase.org.
Microbial exposure
Natural infections were performed as previously described by exposing adult flies to either P. entomophila or Erwinia carotovora carotovora 15 (E.cc15) (27). Flies were transferred to standard fly food vials covered with Whatman filter paper and supplemented with 0.2 ml of Pe suspension in 5% sucrose or 5% sucrose alone. Following a 24 h exposure, flies were transferred to standard media and their survival was subsequently monitored.
Quantitative reverse transcription PCR
Tissue was collected from whole adult bodies (n = 10 females per treatment per trial) or from 15 adult guts. RpL32 was used as a standard unaffected by Pe treatment (27). Transcript levels relative to rpl32 were calculated using the 2−ΔCT method and were normalized to mock-treated WT levels.
Data availability
All data described in this study are contained within the main manuscript and supporting information.
Supporting information
This article contains supporting information.
Conflict of interest
The authors declare that they have no conflicts of interest with the contents of this article.
Acknowledgments
We thank Bloomington Drosophila Stock Center, Developmental Studies Hybridoma Bank, and Washington University Center for Cellular Imaging for resources that facilitated this study.
Author contributions
M. S., J. W., J. G., R. B.-E., C. C. Y., and C. A. M., conceptualization; M. S., J. W., J. G., R. B.-E., and C. A. M. investigation; M. S., J. W., J. G., and R. B.-E. formal analysis; M. S. and C. A. M., writing–original draft.
Funding and additional information
This research was supported by the National Institute of Health (R01 DK 108990, R01 DK117335 to C. A. M). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
Reviewed by members of the JBC Editorial Board. Edited by Clare E. Bryant
Supporting information
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Supplementary Materials
Data Availability Statement
All data described in this study are contained within the main manuscript and supporting information.