Misfolded alpha-synuclein (AS) and other neurodegenerative disorder proteins display prion-like transmission of protein aggregation. Factors responsible for the initiation of AS aggregation are unknown. To evaluate the role of amyloid proteins made by the microbiota we exposed aged rats and transgenic C. elegans to E. coli producing the extracellular bacterial amyloid protein curli. Rats exposed to curli-producing bacteria displayed increased neuronal AS deposition in both gut and brain and enhanced microgliosis and astrogliosis compared to rats exposed to either mutant bacteria unable to synthesize curli, or to vehicle alone. Animals exposed to curli producing bacteria also had more expression of TLR2, IL-6 and TNF in the brain than the other two groups. There were no differences among the rat groups in survival, body weight, inflammation in the mouth, retina, kidneys or gut epithelia, and circulating cytokine levels. AS-expressing C. elegans fed on curli-producing bacteria also had enhanced AS aggregation. These results suggest that bacterial amyloid functions as a trigger to initiate AS aggregation through cross-seeding and also primes responses of the innate immune system.
The neurodegenerative disorders Parkinson’s disease (PD), Alzheimer’s disease, fronto-temporal lobar degeneration, amyotrophic lateral sclerosis and related disorders all involve the neuronal accumulation of pathogenic aggregated amyloid proteins with prion-like features1. The proteins deposited in the brain in these disorders alpha synuclein (AS), Amyloid beta (AB), tau and TDP-43 are transmissible from cell to cell, from one region of the body to another and from humans to susceptible animal hosts2. However the agent or agents responsible for the initiation of the protein misfolding is unknown. Prusiner3 and others have suggested that the initial event is stochastic, but the possibility that it is initiated by environment amyloids requires consideration4,5. The early development of constipation and anosmia and the deposition of aggregated AS in intestinal neurons up to 20 years before diagnosis in PD suggests that the initiating factor comes from the gut (including mouth, nasal passages and intestines)6. This is also suggested by the early brain pathology in PD in the dorsal motor nucleus of the vagus in the medulla, which is a region affected early in scrapie7. Furthermore, inflammatory changes are found in neurodegenerative disorders with microgliosis, astrogliosis and activation of inflammatory cytokines and lymphocytes, but without leukocyte infiltration. The factors responsible for the variable expression of this sterile inflammation are also largely unknown.
Our gut presents the greatest opportunity for exposure to foreign organisms (our microbiota). It has been known since 2002 that the bacteria and fungi make functional extracellular amyloid proteins8. Bacterial amyloid proteins are highly conserved, are involved in biofilm formation and help the bacteria with invasion, host adhesion, and resistance to destruction8,9. The best studied bacterial amyloid protein is curli made by Escherichia coli and its key element, CsgA, has been found to contain amyloidogenic peptide repeat motifs shared by yeast and human prions10 and AS11. Cross–seeding, in which one amyloidogenic protein (curli, Tau, AB or AS, yeast prions, silk protein) causes another to adopt a beta-sheet structure has been documented12. There is excellent precedent for amyloid misfolding to be initiated through gut exposure (i.e., bovine spongiform encephalopathy, serum amyloid A amyloidosis13).
The role of the immune system in neurodegeneration has now been well documented in both histopathological as well as genetic studies14. It has recently been reported that circulating neutrophils contribute to AS pathology in transgenic mice15. Nevertheless, the role of immune changes in production of disease phenotypes are not well understood. Several groups have found that many older persons with AB deposits do not have dementia16, which can be a result of lessened immune responses in some individuals17.
It has been firmly established that commensal microbiota plays a vital role in the regulation of the immune system18. This is necessary because of the massive dose of foreign antigens present in the gut, requiring the immune system to be constantly vigilant of its contents. The first step of the immune response, the innate immune system, recognizes bacterial amyloid proteins using pathways involving TLR 2/1, NLRP3, CD14, NFkB and iNOS19. This is similar to the mechanisms involved in the immune system’s recognition of AS and AB. Toll like receptor 2 is important for inflammatory processes in PD and other neurodegenerative disorders and plays an important role in enhancing AS aggregation through inhibition of autophagy20. Consequently, priming of microglia and enhancement of related immune responses to AB, AS, and other misfolded proteins produced by exposure to bacterial amyloid can thus contribute to the development of dementia16.
We have hypothesized that amyloid proteins made by our commensal partners function to trigger misfolding of amyloid proteins such as AS through cross-seeding, and cause priming of the innate immune system thereby enhancing inflammatory responses to AS4. In order to evaluate this hypothesis, we exposed aged rats and transgenic nematodes expressing human AS to bacteria producing curli. Control animals were exposed to mutant bacteria lacking the operons required for curli production. We assessed AS accumulation and aggregation and inflammation using immunocytochemistry and related techniques. Our results in both rodents and nematodes illustrate the ability of bacterial amyloid to influence important aspects of neurodegenerative processes.
Exposure to curli-producing bacteria enhances AS aggregation in rat brain and AS deposition in gut
Aged Fischer 344 rats have been described to have aggregated AS in the intestinal submucosal plexus21. We used these animals to evaluate the influence of exposure to bacteria producing amyloid proteins on AS deposition and aggregation in the gut as well as in the brain. Animals were exposed weekly via the oral route using an established method for bacterial exposure22. We found that rats exposed to wild-type bacteria producing the amyloid protein curli had enhanced AS deposition in gut ganglion cells (myenteric plexus and submucosa) (Fig. 1a, top panel). We also observed that rats exposed to wild-type bacteria producing curli had enhanced AS deposition in neurons in hippocampus (especially CA3) and striatum, as compared to rats exposed to mutant bacteria lacking the capacity to produce curli or to rats exposed only to vehicle (Fig. 1a). Deposits in neurons in the brain were proteinase K resistant, indicating the presence of aggregated AS (Fig. 2B,C). Quantitation showed that rats exposed to curli-producing bacteria had more AS deposition in the gut than the other 2 groups with an odds ratio of 2.5 (95% CI 4.4–239) demonstrating that exposed animals had a higher probability of having higher gut scores than unexposed animals (lower panel, Fig. 1a and Supplementary Figure 4). Alpha-synuclein aggregation was not related to length of exposure (2 or 3 months). AS deposits in the gut were proteinase K sensitive, suggesting the absence of AS aggregation in the gut.
Exposure to curli-producing bacteria enhances immune responses in rat brain
AS as well as the bacterial amyloid protein curli are recognized by the innate immune system with involvement of similar pathways (TLR2, CD14, NFkB, iNOS). We hypothesized that exposure to bacterial amyloid would cause priming of immune cells to create enhanced immune responses in the brain of exposed animals. Therefore we assessed markers of neuroinflammation, including microgliosis, astrogliosis and the pro-inflammatory cytokines interleukin-6 (IL-6), interleukin-1 (IL-1) tissue necrosis factor (TNF) and TLR2. We observed that microgliosis (Iba-1, allograft inflammatory factor, Fig. 1b), as well as astrogliosis (GFAP, glial fibrillary acidic protein, Fig. 2A) in the striatum, hippocampus and neocortex was significantly higher in animals exposed to curli-producing bacteria as compared to the two control groups. Interleukin-6 (IL-6) expression was also higher in the hippocampus, stratum and substantia nigra of the animals exposed to curli than in the control groups (Fig. 2D). Toll like receptor 2 (TLR2) expression was also higher in the hippocampus and striatum in animals exposed to curli-producing bacteria as compared to the other 2 groups (Fig. 2F) and TNF expression was higher in striatum and substantia nigra of animals exposed to curli-producing bacteria than that in the other 2 groups (Fig. 2G). There were no significant differences in interleukin 1 expression (Fig. 2E). The results were not related to length of exposure.
The phenotypes observed in curli-exposed rats were not related to illness, aging or cellular immune responses
In order to evaluate the possibility that the effects of exposure noted above were caused by illness induced by the bacteria we examined the relationship of the findings to body weight, evidence of inflammatory infiltrates, and survival. There were no significant differences among the 3 groups in terms of survival, body weight or cellular inflammation in oral tissues, kidneys, eyes, brain or gut (data not shown). We examined the retina in 12 eyes (4 eyes from each group) using standard histology and immunohistochemistry, as the eyes are located in proximity to oral tissues. The stratification of the retinal layers appeared similar across all eyes and groups. Frozen retinal sections (20 μm thickness) immunolabeled with GFAP (labeling astrocytes and activated Müller cells) and vimentin (labeling Müller cells) were similar across all eyes and groups (see Supplementary data).
Serum cytokines and TLR-2
Because of our interest in systemic immune responses we evaluated serum levels of several cytokines and related molecules. Serum levels of IL-1β, IL-6, IL-10, and TNF-α were below detection levels. Serum INF-γ was detectable but there was no difference among three groups. Serum TLR2 levels were trending higher in the rats exposed to curli than the other two groups but the differences did not reach statistical significance (Supplementary Figure 3). These data do not allow us to make conclusions concerning the presence of systemic immune responses to the exposures.
AS-expressing C. elegans fed with curli-producing bacteria displayed increased AS aggregates
In order to evaluate the influence of bacterial amyloid on AS aggregation in another organism we exposed AS expressing C. elegans to wild-type E coli expressing curli and mutant E. coli lacking the ability to synthesize curli. The nematode C. elegans naturally feeds on E. coli, and protein aggregation can be studied in vivo thus representing an attractive model organism to study how bacterial exposures influences AS aggregation. We utilized a transgenic (Tg) C. elegans line expressing human AS fused with YFP (AS-YFP) in body wall muscle, allowing for visualization of aggregated AS-YFP in live animals using fluorescence microscopy23. As shown in Fig. 3a,b AS-expressing C. elegans fed with curli-producing E. coli displayed increased AS deposits compared to those fed with the mutant E. coli lacking curli production. The Congo red stained deposits coincide with those of AS-YFP, confirming that AS-YFP forms amyloidogenic aggregates recognized by Congo red (Fig. 3c). AS-aggregates accumulated in the head first and moved to the tail during adulthood. We also stained live worms with the cytosolic oxidative stress marker CellRox Red, but no difference was seen between worms exposed or not exposed to curli-producing bacteria. This suggests that enhanced AS aggregation was not due to increased oxidative stress in the cytosol. We also tested a mitochondrial oxidative stress marker MitoSox Red, but detected only weak staining in both groups. Swimming tests were also performed to evaluate locomotive activity and showed a trend toward decreased thrashing rate (~15–20%) in worms exposed to wild-type curli-producing E. coli vs. mutant E. coli lacking curli, which did not reach statistical difference (data not shown).
We have shown that exposure to bacteria producing a functional extracellular amyloid protein enhances aggregation of AS in brain neurons in aged rats and in muscle cells in nematodes. In gut neurons the exposure increased levels of AS in the submucosa. The mechanism of these effects may involve upregulation of protein expression, which is well known to enhance aggregation. These effects can also have resulted from cross-seeding, which has been reported between bacterial amyloids, including curli, and mammalian proteins24. Lee and coworkers have demonstrated that AS aggregates seed aggregation of tau25. PrPSc has been reported to seed AB aggregation and curli seeds aggregation of serum amyloid A12. However, there have been no studies on how cross-seeding by exogenous bacterial amyloid affect the propagation and aggregation of endogenous amyloid proteins in living animals.
Our finding of enhanced AS deposition without aggregation in the gut but with aggregation in the brain is of interest. Perhaps the period of exposure was too short to allow for polymerization of AS in gut neurons. It can also be that the biophysical factors involved in induction of AS aggregation and the relationship between AS expression and aggregation are different in the gut and brain (due to pH and other factors). As the bacteria were delivered orally the pathway for induction of changes in the brain can involve the autonomic nervous system, particularly the vagus and other nerves. This is the route which is believed to be responsible, at least in part, for transmission of bovine spongiform encephalopathy and related prionoses7. Recent studies have also suggested the involvement of the vagus nerve in PD26. Brain alterations can also have been induced through oral tissues and their rich innervation as well as via a hematogenous route.
C. elegans is a genetically tractable organism for elucidating the critical events mediating interactions between bacterial amyloid proteins and AS in intestinal tissues and potential propagation of AS aggregates to neurons27. The finding that AS aggregation in worms is enhanced by exposure to curli expressing bacteria can also involve a cross-seeding mechanism. Since nematodes naturally take up microorganisms as food, they allow for mechanistic studies of cross-seeding by different microbial amyloid proteins expressed by distinct strains during feeding and throughout their lifespan.
Our findings of microgliosis, astrogliosis and enhanced expression of IL-6, TLR2 and TNF in the brain following curli exposure suggest the occurrence of an enhanced local sterile inflammatory response to AS in the brain. These findings do not appear to be caused by T cell activation by bacterial amyloid, as cellular infiltrates were not found in the brain or other tissues. Activation of the immune system in both AD and PD have now been extensively established28. The importance of the immune system in AD was first proposed by Braak and colleagues6, and has been recently supported by the association of immune system genes involved in neurodegeneration (for recent review see Colonna and Wang14). It has been shown that impaired microglial proliferation slows AD in Tg mice29. Bacterial amyloid is recognized as a pathogen associated molecular pattern (PAMP) with messengers including TLR2/1, CD14, NFkB and iNOS19. These messengers of the innate immune system are also involved in its recognition of AS, AB and also curli. Recently it has been shown that TLR2 inhibition prevents AS aggregation through activation of autophagy20, suggesting that TLR2 activation through exposure to bacterial amyloid is pathogenic. Microglial TLR2 activation has also been reported to increase cellular uptake of AB and is involved in AB stimulated microglial activation30. The co-receptor molecule CD14 has also been linked to oxidative damage and dendritic degeneration following innate immune system activation31.
Priming of immune cells to respond to these bacterial or other amyloids in the gut may cause enhanced responses to neuronal amyloids in the brain. Gallo et al.32 have recently observed that bacterial amyloid binds to bacterial and eukaryotic DNA and causes amyloid polymerization, as well as enhancement of autoimmunity. The intensity of the immune system’s response to cerebral amyloid deposition is important in determining the development of dementia in AD and PD, as many older persons have been shown to have significant AB pathology without dementia and without microglial activation17.
The precise role of protein aggregation and inflammation in neurodegeneration remains unclear33. Aggregation of AS and production of toxic oligomers are pathogenic, but intracellular AS aggregation into fibrils can be protective34. Furthermore, it has been shown in studies of the molecular machinery for the production of curli, that the same protein accelerated the aggregation of one protein and inhibited the amyloid formation of another35. There is also evidence that an active immune response is neuroprotective, as suggested by the work on immunotherapy for AD. Immune responses participate in clearance of AB plaques and improved cognition in animal studies36 and microglia produce a barrier reducing the toxic effects of AB on neurotic dystrophy37. It has been proposed that the association of AD and PD with age is related to senescence of the immune system and lowered immune responses38. Thus it is conceivable that bacterial amyloids induce either a pathogenic or salutogenic effect of neurodegenerative processes in the brain39,40. Our study did not include behavioral measures and thus the effect of exposure to bacterial amyloid on the neurodegenerative phenotype resulting from the enhanced AS aggregation and immune response remains to be determined.
There is now a vast literature documenting the influence of the microbiota on metabolism, immunity, cancer, diabetes, obesity, intestinal diseases, heart disease and other conditions. Bacteria, fungi and other organisms comprising our microbiota make functional amyloid proteins. Biofilms are found in the body and up to 40% of bacterial biofilms have amyloids9. Evidence for a role for fungi in AD has recently been proposed, but the possible role for fungal amyloids has not yet been considered41. Although it is now documented that many bacteria that make amyloid proteins are components of our microbiota, the presence of these proteins in the body has not been comprehensively evaluated32. Although E coli is not a major component of our microbiota there are several other species that make amyloid proteins that are important commensal partners, including Streptococcus mutans, Staphlococcus aureus, Salmonella enterica, Mycobacterium tuberculosis and others8,42. Gene homologs encoding curli were recently determined also in four phyla: Bacteroidetes, Proteobacteria, Firmicutes, and Thermodesulfobacteria8. It is tempting to speculate that the various amyloids to which we are exposed influence misfolding of endogenous proteins with strain specificity, as has been reported for AS, AB and related proteins. That is, certain bacterial amyloids are particularly important for inducing aggregation of certain strains of a neurodegenerative disease protein, and this is reflected in distinct disease phenotypes43,44.
Our work suggests that protein misfolding and immune activation in neurodegenerative disorders are triggered through cross-seeding by exposure to exogenous microbial amyloids in the nose, mouth and gut. We need to elucidate the molecular mechanisms responsible for the observed effects of exposure to bacterial amyloid. Cross-seeding of amyloidogenic proteins by bacterial amyloids has been documented in both in vivo12 and in vitro24 (e.g, curli can cause cross-seeding of serum amyloid A12). We provide evidence for our proposed mechanism for the induction of neuroinflammation in the brain: the innate immune system utilizes TLR2 to recognize bacterial amyloid45, and we demonstrate upregulation of TLR2 in the striatum and hippocampus of animals exposed to bacteria producing curli (Fig. 2F). The scope of our study did not include the influence of enhanced AS aggregation on the function of the animals or the impact of bacterial amyloid on oxidative toxicity. The pathway by which oral and intestinal bacterial amyloid influence brain processes also remains to be documented. We also do not know which of the many bacterial amyloids are of particular importance. A metaproteomic analysis of the amyloid proteins present in the mouth and intestines has not been accomplished and will be of great interest46.
Two recent studies have also provided evidence for the potential role of intestinal bacteria in neurodegeneration. Minter and colleagues have shown that changes in the gut microbiota induced by antibiotics alter neuroinflammation and amyloid deposition in a mouse model of AD47. Harach et al. have observed that germ-free AD model mice have reduced AB pathology in the brain, compared to conventionally raised animals48. The possible contribution of bacterial amyloid to these findings has not been evaluated.
This is one of the first studies that evaluates the influence of bacterial amyloid on disease processes in living animals40. Our data suggest that amyloid proteins in the microbiota are involved in the origination and maintenance of neurodegenerative disease. Further studies on the influence of our partner organisms on the brain are certainly indicated. If the results are supported by further analysis and experimentation there are a broad range of preventive and therapeutic measures that will be of value.
Antibodies and chemicals
The protease and phosphatase inhibitor cocktails and Congo red were purchased from Sigma-Aldrich (St Louis, MO). Hypoestoxide was obtained from Immune Modulation, Inc. (Bloomington, CA). The following antibodies were used: α-synuclein (Syn-1; BD Bioscience, San Diego, CA); TNFα, glial fibrillary acidic protein (GFAP) (GA5), TH, and NeuN (Millipore, County Cork, Ireland); β-actin (Sigma-Aldrich, St Louis, MO); NF-κB p65 and phospho-NF-κB p65 (Cell Signaling, Beverly, MA); IL-1β and IL6 (Abcam, Cambridge, MA); α-synuclein (CT, Syn105) ; α-synuclein (syn211) (Life Technologies, Grand Island, NY); and Iba-1 (Wako, Richmond, VA).
Aged male Fischer 344 rats were obtained from the National Institute of Aging, NIH (M. Murthy). These rats were chosen because it has been described that their neurons in the gut develop deposits of AS with age, thus mimicking PD21. At the time of euthanasia via CO2 asphyxiation the rats were 22.5–25 months of age. All animal procedures were approved by the Institutional Animal Care and Use Committee of the University of Louisville (Protocol 12022) and were also in compliance with United States Public Health Service standards and National Institutes of Health guidelines. The University of Louisville Animal Care Facility is accredited by AAALAC International.
Bacteria preparation and exposure
A wild-type E. coli strain LSR12 and the isogenic mutant lacking both curli operons (strain C600 with deletion of the curli operons) were obtained through the generosity of M. Chapman, University of Michigan. The identity of strains has been verified using PCR with oligonucleotides priming at individual curli genes and spanning the entire curli region (oligonucleotide sequences are available upon request). We also confirmed by Congo red (CR) staining that the wild-type strain is CR-positive while curli mutant is CR-negative (data not shown). The bacteria were otherwise identical. E. coli was grown in YESCA medium (1g/l Yeast Extract, 10g/l casamimo acids) at 37 °C. TSBYE which consists of 30 grams per liter trypticase soy broth (Difco) supplemented with 2% (w/v) yeast extract, 1 mg/ml hemin (final concentration), and 5 mg/ml menadione (final concentration) (10% CO2, 10% H2, and 80% N2) at 37 °C for 48 hours.
Oral exposure of rats was performed essentially as previously described by Baker et al.49. A total of 11–13 rats per group were used per experiment. Animals were initially treated with sulfamethoxazole (MP Biomedical, Solon, OH) at a final concentration of 800 mg/ml and trimethoprim (Sigma, St. Louis, MO) at a final concentration of 400 mg/ml ad libitum for 10 days. Four days after the last antibiotic treatment, the rats were infected orally with bacteria (109 cfu) suspended in 1ml 2% carboxymethylcellulsoe (CMP; MP Biomedicsal, Solon, Oh) in sterile PBS using a 2.25 feeding needle (Popper and Sons, Inc. New Hyde Park NY). Animals were inoculated orally every week for 2 months (N = 19) or 3 months (N = 14). Animals were studied in 3 groups: Vehicle only (N = 13); exposure to wild type bacteria (curli-producing) (N = 11); and exposure to mutant bacteria (lacking curli operon) (N = 9). The vehicle control group was treated with CMC without bacteria. Rats were weighed several times each month. At the end of 2–3 months rats were sacrificed and various organs and blood were collected and banked.
Serum cytokine analyses
Blood was collected from the hearts of the aged rats treated with or without curli-producing E. coli, and control rats without any treatments (N = 7–8 per group). The blood samples were centrifuged at 4 °C (1,000 × g) for 30 min to extract the serum. The sera were stored in aliquots at −80 °C until use. ELISAs were performed according to the manufacturer’s protocol. Serums IL-1β, IL-6, IL-10, INF-γ, and TNF-α were measured by R&D Systems Quantikine ELISA kits and serum TLR-2 was determined by an ELISA kit from Antibodies-Online (Atlanta, Georgia). Data were expressed as optical density (O.D.) value at 450 nm with double wells per sample and the wavelength correction was set at 570 nm. A standard curve was created for each tested cytokine at each time to determine the concentration of the target cytokine concentration in each sample. The concentration of the positive control sample was within the linear range of the standard curve. Results presented as means ± SE, and statistical analysis was done using GraphPad Prism software. One-way analysis of variance (ANOVA) with Turkey post-hoc test was used for multiple comparisons among groups. p < 0.05 was considered statistically significant. Positive controls were tested to confirm the function of the assays.
The neuropathological studies were carried out on blinded specimens. The procedures for immunohistochemical, immunofluorescence, and neuropathological analysis have been described elsewhere50. Briefly, the right hemibrains were post-fixed in phosphate-buffered 4% paraformaldehyde at 4 °C for neuropathological analysis, blind-coded sagittal brain sections were incubated with primary antibodies at 4 °C for overnight following serial sectioning in the sagittal plane at 40 μm with a Vibratome 2000 (Leica, Deerfield, IL) for neuropathological and immunocytochemical studies. The next day, sections were incubated with either biotinylated- or FITC-conjugated secondary antibodies and detected with avidin D-HRP HRP (ABC elite, Vector Laboratories, Burlingame, CA) and with Tyramide Signal Amplification Direct system (PerkinElmer, Waltham, MA), respectively. Analysis of AS accumulation was performed using free-floating, blind-coded sections51. To determine the neuroinflammation, neurodegeneration, accumulation of α-synuclein, and NF-κB activation, we stained brain sections with Iba-1, GFAP, TNFα, IL- 1β, IL6, human α-synuclein, NF-κB, and phosphorylated NF-κB antibodies, respectively. Sections were imaged by Olympus BX41 microscope. All immunoreactivity levels were determined by optical density analysis using Image Quant 1.43 program (NIH) except the immunoreactivity of Iba-1. The cell numbers of Iba-1-positive cells were determined per field (230 μmÅ ~ 184 μm) of each animal based on cell body recognition using Image Quant 1.43 program (NIH). Immunohistochemistry was performed with antibody against full length AS, before and after proteinase K exposure. Sections were incubated overnight at 4 °C with antibodies against total a-syn (1:500, affinity purified rabbit polyclonal, Millipore)50, GFAP (mouse monoclonal, Millipore), Iba-1 (mouse monoclonal, Wako laboratories), IL6 (mouse monoclonal Cell Signaling), TLR2 (mouse monoclonal Millipore), TNFa (mouse monoclonal Cell Signaling), IL1beta (mouse monoclonal Abcam) followed by biotin-tagged anti-rabbit or anti-mouse IgG1 (1:100, Vector Laboratories, Inc., Burlingame, CA) secondary antibodies, Avidin D-HRP (1:200, ABC Elite, Vector), and visualized with diaminobenzidine. Sections were scanned with a digital Olympus bright field digital microscope (BX41).
Caenorhabditis elegans studies
Standard conditions were used for C. elegans propagation on NGM (nematode growth medium) plates seeded with E. coli OP50-1 at 20 °C. Transgenic (Tg) C. elegans line expressing human AS fused with YFP (AS-YFP) (strain NL5901, Punc-54::AS::YFP) in body wall muscle23 was obtained from the Caenorhabditis Genetics Center (CGC). The use of these animals allowed for visualization of aggregated AS-YFP in live animals using fluorescence microscopy. Tg AS-YFP nematodes were age-synchronized by hypochlorite bleaching, hatched overnight and were subsequently cultured on NGM plates seeded with E. coli OP50-1 until larval stage L4 (adult day 0). They were then fed for three days solely on fresh NGM plates seeded with either curli-producing E. coli or mutant E. coli unable to produce curli (non-curli mutant). Fluorescence microscopy was performed on immobilized live animals to visualize AS-YFP using an eVOS microscope (Life Technologies) and imaging was acquired under identical conditions for nematodes fed with either wild-type or mutant bacteria. The experiments were repeated three times, each with 10 worms for each treatment group. As characterized previously23, AS aggregates are recognized as fluorescent foci of inclusions containing AS-YFP within muscle cells in this C. elegans model.
Congo red staining of worms was performed using the procedures modified from that described previously52. Worms were fixed by incubation in 4% paraformaldehyde in Dulbecco’s phosphate buffered saline for 15 h at 4 °C, and were permealized at 37 °C for 15 h in a solution of 1% Triton X-100, 5% beta-mercaptoethanol, 125 mM Tris-HCl, pH 7.5. Worms were then mounted on glass slide and stained with 0.5 mg/ml Congo red in 50% ethanol for 1 min. Destaining was immediately carried out using several rinses of 50% ethanol until solution became colorless, and then one rinse each with 75% ethanol, 50% ethanol, and water. A drop of Fluoromount was applied and stained worms were visualized for red fluorescence using a Leica fluorescence microscope.
GraphPad Prism (GraphPad Software, San Diego, CA) was used for statistical analysis. All data are presented as means ± s.e.m and were analyzed for statistical significance by using either unpaired t test or two-way ANOVA (general linear model) followed by Bonferroni’s multiple comparison post-test. Ordinal logistic regression was used to compare the OR for gut AS deposition53. The statistical software package R was also used. One-way ANOVA poshoc Dunnet p < 0.05 was used when comparing to control.
How to cite this article: Chen, S. G. et al. Exposure to the Functional Bacterial Amyloid Protein Curli Enhances Alpha-Synuclein Aggregation in Aged Fischer 344 Rats and Caenorhabditis elegans. Sci. Rep. 6, 34477; doi: 10.1038/srep34477 (2016).
This work was supported in part by funding from the Michael J. Fox Foundation (New York, NY), the University of Louisville, Dr. W. Cowan and Mrs. S. Ford Grissom. The authors are grateful to M. Chapman (University of Michigan) for the contribution of materials. The authors are also grateful to H. Kaplan for evaluation of ocular tissues, P. O’Toole for helpful discussions and S. Nandi for technical assistance.
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