Gut microbiota influences pathological angiogenesis in obesity‐driven choroidal neovascularization

Abstract Age‐related macular degeneration in its neovascular form (NV AMD) is the leading cause of vision loss among adults above the age of 60. Epidemiological data suggest that in men, overall abdominal obesity is the second most important environmental risk factor after smoking for progression to late‐stage NV AMD. To date, the mechanisms that underscore this observation remain ill‐defined. Given the impact of high‐fat diets on gut microbiota, we investigated whether commensal microbes influence the evolution of AMD. Using mouse models of NV AMD, microbiotal transplants, and other paradigms that modify the gut microbiome, we uncoupled weight gain from confounding factors and demonstrate that high‐fat diets exacerbate choroidal neovascularization (CNV) by altering gut microbiota. Gut dysbiosis leads to heightened intestinal permeability and chronic low‐grade inflammation characteristic of inflammaging with elevated production of IL‐6, IL‐1β, TNF‐α, and VEGF‐A that ultimately aggravate pathological angiogenesis.


Introduction
While AMD is the leading cause of irreversible blindness in the industrialized world (Klein & Klein, 2004;Maberley et al, 2006;Wong et al, 2014), the cellular and molecular mechanisms that precipitate disease remain incompletely understood despite significant genomewide association studies identifying susceptibility genotypes and target mechanistic pathways (Fritsche et al, 2013(Fritsche et al, , 2016Sobrin & Seddon, 2014;Black & Clark, 2016). Obesity has long been suspected as a risk factor for AMD, but increased body mass index associations with AMD were inconsistent (Zhang et al, 2016). Using 21,287 participants from the Melbourne Collaborative Cohort Study, it was recently demonstrated that each increase of 0.1 in waist/hip ratio (a measure for abdominal obesity) was associated with a 13% increase in the odds of early AMD and a 75% increase in the odds of late AMD in men, making obesity the second most important environmental risk factor for late AMD after cigarette smoking (Adams et al, 2011).
Progression of AMD is influenced by single or compounded environmental and genetic risk factors that lead to persistent low-grade inflammation and a largely innate immune response (Combadière et al, 2007;Ambati et al, 2013;Sennlaub et al, 2013). Evidence for environmental factors predisposing to AMD is supported by the fact that genetically unrelated individuals with shared long-term environmental exposure develop the disease with a concordance of 70.2% (Gottfredsdottir et al, 1999). A consequence of cohabitation and common lifestyle habits that prospectively impact disease modifiers such as systemic inflammation is microbial exchange (Song et al, 2013). Given that commensal gut microbiota exert profound influence on digestion, dietary metabolism, endotoxemia, and immune responses (Backhed et al, 2005;Turnbaugh et al, 2006;Cani et al, 2008;Cerf-Bensussan & Gaboriau-Routhiau, 2010), they are prime candidates to impact chronic low-grade inflammation (Tremaroli & Backhed, 2012). Microbiota-related low-grade inflammation is characterized by elevated pro-inflammatory gene expression and is a common consequence of an altered host-microbiota relationship caused by instigator bacteria or dietary components that influence intestinal permeability (Chassaing & Gewirtz, 2014). There is accumulating evidence that asserts the importance of intestinal permeability, a barrier aspect closely associated with the intestinal commensal microbiota as well as with the mucosal immune system, in intestinal and systemic health (Brun et al, 2007;Manco et al, 2010;Gerova et al, 2011;Neves et al, 2013;Bischoff et al, 2014). Heightened intestinal permeability can allow for an increased translocation of bacterial products such as LPS and other pathogen-associated molecular pattern molecules (PAMPs) Cerf-Bensussan & Gaboriau-Routhiau, 2010;Mehal, 2013). These PAMPs impact pro-inflammatory signaling through pattern recognition receptors (PRRs) of the innate immune system, especially the Toll-like receptors (TLRs) and Nod-like receptors (NLRs), inducing low-grade systemic inflammation (Chassaing & Gewirtz, 2014). Microglia, perivascular macrophages, a small number of dendritic cells, and RPE cells express various PRRs, including TLRs and NLRs, and may predispose for PAMPs of intestinal origin to impact ocular inflammation (Chen & Xu, 2015). In addition, bacterial products or metabolites from gut microbiota can modulate microglia maturation, morphology, and function (Erny et al, 2015) and activate retina-specific T cells that are thought to be involved in autoimmune uveitis (Horai et al, 2015).
Dysbiosis in gut microbes is particularly important for the aging population given that they modulate aging-related changes in innate immunity, sarcopenia, cognitive function, and frailty in general (O'Toole & Jeffery, 2015). Here, we sought to evaluate the contribution of intestinal flora to progression of NV AMD, particularly in the context of obesity-driven CNV.

High-fat diet modulates gut microbiota and exacerbates CNV
In light of epidemiologic data linking obesity to CNV (Seddon et al, 2003;Zhang et al, 2016), we first investigated the propensity of diets with elevated fat content to exacerbate CNV. C57BL/6J mice were raised under sterile barrier conditions and placed on a regularchow diet (RD; 16% kcal fat) or high-fat diet (HFD; 60% kcal fat), from 6 weeks of age ( Fig 1A). As expected, upon killing at 13 weeks, HFD-fed mice gained over 50% more weight than control RD-fed mice (Fig 1B and C). At 11 weeks of life, we subjected mice to a laser-induced photocoagulation model of CNV, where perforation of Bruch's membrane initiates sprouting of subretinal blood vessels from the choroid, thus mimicking NV AMD (Lambert et al, 2013). Quantification of FITC-dextran-perfused neovessels over isolectin B4 (IB4)-labeled impact area by confocal imaging 14 days after laser burn revealed a robust 60% increase in CNV in HFD-fed mice when compared to RD controls (Fig 1D and E). These experimental mouse data are in line with previously published results (Sene et al, 2013) and verify human studies (Seddon et al, 2003;Adams et al, 2011).
To tease out the contribution of gut microbes to heightened CNV in mice receiving HFD, mice were administered 0.5 g/l of the broad-spectrum, non-gut permeable  antibiotic (AB) neomycin trisulfate salt hydrate orally through their drinking water. Remarkably, HFD-fed mice treated with neomycin displayed levels of CNV akin to RD-fed control mice and thus significantly less than HFD-fed mice receiving vehicle control (Fig 1D and E). Treatment with neomycin did not impact weight gain (Fig 1B and C), hence uncoupling mouse weight from extent of CNV and strengthening the link between gut flora and pathological angiogenesis.
To ascertain that HFD and oral neomycin modify intestinal flora, we next profiled gut microbiomes. The ratio of Bacteroidetes and Firmicutes, the two dominant phyla that make up over 90% of bacterial phylogenetic types in the distal gut , is affected by diet (Turnbaugh et al, 2009;David et al, 2014). Comparison of distal gut microbiota from lean and obese individuals shows that the relative proportion of Bacteroidetes is decreased in obese individuals compared to lean individuals David et al, 2014), which is consistent with mouse studies and underscores that diet impacts intestinal flora Turnbaugh et al, 2006;Hildebrandt et al, 2009). We characterized gut microbiome composition by sequencing the hypervariable regions V2, V3, V4, V6, V7, V8, and V9 of bacterial 16S rRNA extracted from fecal pellets originating from RD-fed and HFD-fed mice receiving vehicle, as well as HFD-fed and RD-fed mice receiving neomycin (Figs 1F and EV1). Consistent with clinical data Turnbaugh et al, 2006;Wu et al, 2013), mice on HFD had shifted ratios of commensal gut microbes. Bacteroidetes/Firmicutes ratios shifted from 66%/33% of total bacteria in RD to 19%/67% in HFD. Importantly, oral neomycin restored the proportion of Bacteroidetes to~65% of total bacteria and reduced Firmicutes from~65% to < 10%. In addition, relative abundance of Proteobacteria (a microbial signature of dysbiosis in gut microbiota ) rose with HFD and further with antibiotic treatment reaching 25% of the population ( Fig 1G). Of note, HFD-fed mice host the most diverse microbiome, with a modest but important presence of Actinobacteria and Spirochaetes (0.5 and 1.5% of the total). These phyla were

A
Schematic representation of experimental timeline where half of the mice start a high-fat diet (HFD) at 6 weeks and later half of these receive neomycin (AB) treatment from the age of 9 weeks until killing at week 13. Control mice were fed a regular-chow diet (RD). At the age of 11 weeks, mice are subjected to four laser burns per eye to perforate Bruch's membrane and recruit subretinal blood vessels from the choroid. B, C Weight gain (B) and area under the curve (C) of percentage weight gain of HFD-fed mice compared to RD-fed mice, treated with vehicle or antibiotic; n = 13 (RD), 17 (HFD), 16 (HFD+AB), 12 (RD+AB); CI 99.9%. D Compilation of compressed Z-stack confocal image of FITC-dextran-labeled CNV and single-plane confocal image of isolectin B4-stained choroidal flat mounts from RD-and HFD-fed mice, with vehicle or antibiotic treatment. E Quantification of area of FITC-dextran-labeled CNV over isolectin B4-stained laser impact area fold RD; n = 11 (RD), 16 (HFD), 11 (HFD+AB), 12 (RD+AB), with 36 (RD), 32 (HFD), 33 (HFD+AB), 34 (RD+AB) burns total; CI 99%. F, G Representative circle charts of relative abundance of bacterial phyla, class, order, and family (from central to peripheral), in gut microbiota of RD-fed mice with vehicle, HFD-fed mice with vehicle, HFD-fed mice with neomycin, and RD-fed mice with neomycin (F) and relative proportion per group of different phyla; n = 7 (RD), 8 (HFD), 6 (HFD+AB), 7 (RD+AB); Bacteroidetes; CI 99.9%, Firmicutes; CI 99%, Proteobacteria; CI 99%, Actinobacteria and Spirochaetes (G). *n.d. = not detected.
Data information: All comparisons between groups are analyzed using one-way analysis of variance (ANOVA) and Tukey's multiple comparisons test; **P < 0.01, ***P < 0.001; error bars represent mean AE SEM. Each "n" represents one mouse per experimental group; CI, confidence interval. Scale bar: 100 lm.

EMBO Molecular Medicine
Gut microbiota influences pathological angiogenesis Elisabeth MMA Andriessen et al undetectable in RD-fed mice or after receiving oral neomycin. RD mice on neomycin showed consistently higher levels of Proteobacteria at the expense of Firmicutes, confirming microbial shifts with oral neomycin. Together, these data reconcile that modulation in gut microbiota correlates with severity of CNV.
High-fat diet potentiates recruitment of microglia and macrophages during CNV Mononuclear phagocytes (MPs) such as microglia and macrophages contribute to AMD pathogenesis (Ambati et al, 2003b;Combadiere et al, 2007;Langmann, 2007) and localize to sites of neovascularization following laser-induced CNV (Combadière et al, 2007;Liu et al, 2013;Indaram et al, 2015;Luckoff et al, 2016) (Fig 2A-C). Microglia are CNS-resident macrophages that are derived from primitive macrophages in the yolk sac (Prinz et al, 2014). Upon CNS injury, they move to sites of insult and polarize to an activated state and produce pro-inflammatory cytokines (Hanisch & Kettenmann, 2007). Depending on the extent of injury, circulating monocytes may also be recruited from the bloodstream. Analysis by FACS of whole retinas and RPE-choroid-sclera complexes from mice on regular diets revealed a twofold rise in MPs (Ly6G À , F4/80 + , CD11b + ) at 3 (p3) and 7 (p7) days post-laser burn (Fig 2D and E) when compared to non-burned eyes (gating scheme in Fig EV2A). At day 14 post-burn (p14), the number of MPs returned to basal levels ( Fig 2D and E). A similar kinetic profile was observed for microglia (Ly6G À , F4/80 + , CD11b + , CX3CR1 hi CD45 lo ) (Fig 2F and G). Notably, the overall proportion of microglia within the MP population dropped in the first week following laser burn (p3 and p7), suggesting cellular infiltration from circulation ( Fig EV2B).
Importantly, a HFD potentiated these effects as the heightened CNV observed in HFD-fed mice (Fig 1D and E) was accompanied by a~twofold increase in MPs and microglia at sites of lesion when compared to control RD-fed mice ( Fig 2H-K). This increase in subretinal MPs persisted at 14 days post-burn as determined by immunofluorescent quantification of IBA-1 + cells around the laserinduced lesion (Fig 2L and M). Oral neomycin abrogated this recruitment ( Fig 2H-M), which is consistent with the observed reduction in CNV (Fig 1D and E). Hence, the intestinal microbiota of HFD-fed mice augments recruitment of microglia and other MPs that may be central to disease progression.

Heightened CNV in mice with dysbiosis is accompanied by increased intestinal permeability, metabolic endotoxemia, and systemic inflammation
Pattern recognition receptors (PRRs) allow the innate immune system to recognize pathogen-associated molecular patterns (PAMPs) and trigger an inflammatory reaction to fight off the microbes that produce them (Dorrestein et al, 2014). Although PAMPs circulate at low concentrations under physiologic conditions (DiBaise et al, 2012), an increase in LPS concentrations, a condition termed "metabolic endotoxemia", may provoke low-grade inflammation , insulin resistance (Cani et al, 2007), augmented cardiovascular risk (Manco et al, 2010), fatty liver disease (Brun et al, 2007), white adipose tissue inflammation (Caesar et al, 2015), and retinopathy of prematurity (ROP) (Tremblay et al, 2013). In obesity, changes in gut microbiota have been suggested to compromise barrier function of the epithelial layer of the gut, thus increasing entry of PAMPs into systemic circulation (Amar et al, 2008;Cani et al, 2008;Osborn & Olefsky, 2012).
Analysis of intestinal permeability by Evans Blue assay revealed that HFD elevated intestinal permeability by threefold when compared to controls ( Fig 3A). In our experimental paradigm, antibiotic treatment did not restore intestinal permeability of HFDfed mice as there was no significant difference between HFD-fed mice and HFD-fed mice that were treated with antibiotics ( Fig 3A).
We next determined whether the levels of circulating PAMPS were sufficient to trigger a PRR response. We therefore subjected murine macrophages that express several PRRs with a chromosomal integration of a secreted embryonic alkaline phosphatase reporter construct inducible by NF-jB and AP-1 (RAW-Blue TM cells) to serum from mice under various feeding paradigms. This reports on activation of PRRs such as Toll-like receptors (TLRs), NOD-like receptors (NLRs), RIG-I-like receptors (RLRs), and C-type lectin receptors (CLRs).
Serum from HFD-fed mice activated PRRs significantly more readily than serum from RD-fed mice as had been suggested Membrez et al, 2008;Neves et al, 2013) or HFD-fed mice receiving antibiotic treatment ( Fig 3B). The reduction in PRR response in antibiotic-treated mice may occur due to an overall reduction in the absolute number of bacteria present in the intestine.
Microbiotal transplants confirm that high-fat diet aggravates CNV through gut microbiota To ascertain that HFD-associated gut microbial communities drive increased CNV, we transplanted by oral gavage cecal microbiota harvested from the feces of RD-fed mice to HFD-fed mice (HFDxRDT). RD-fed mice transplanted with a fecal suspension of RD microbiota (RDxRDT) and HFD-fed mice transplanted with fecal A C D B Figure 3. High-fat diet augments gut permeability, metabolic endotoxemia, and systemic inflammation.
Data information: All comparisons between groups are analyzed using one-way analysis of variance (ANOVA) and Tukey's multiple comparisons test; *P < 0.05, **P < 0.01, ***P < 0.001; error bars represent mean AE SEM. Each "n" represents one mouse; CI: confidence interval. Elisabeth MMA Andriessen et al Gut microbiota influences pathological angiogenesis EMBO Molecular Medicine suspension of HFD microbiota (HFDxHFDT) served as controls ( Fig 4A). Prior to microbiotal transplantation, recipient mice were treated with ampicillin and neomycin in drinking water to deplete their original commensal microbiome. Gavage with cecal microbiota was repeated on a weekly basis to maintain a constant composition of the transplanted flora ( Fig 4B). Although mice on HFD were significantly heavier than those on RD, microbiotal transfer from RD-fed mice did not significantly alter weight gain of HFD-fed mice and thus permitted to uncouple the effects of weight gain from those of microbial transfer (Fig 4C and D).
To verify successful transplantation of diet-associated microbial phyla, we characterized fecal microbiota as above (Figs 4E and EV4A). In RDxRDT mice, Bacteroidetes were the most abundant phylum representing 75-80% of the microbiome while accounting for only 35% in HFDxHFDT mice where Firmicutes and Proteobacteria filled the balance. Transfer of RD microbiota to HFD-fed mice restored microbial proportions found in RD-fed mice (Fig 4F). In addition, improved glucose tolerance in HFDxRDT mice compared to HFDxHFDT mice attests to successful microbiotal transplants (Fig EV4B and C).
While HFDxHFDT showed a~twofold increase in CNV when compared to RDxRDT, transfer of RD microbiota to HFD-fed mice diminished CNV by~35% supporting a role for gut microbiota in pathological CNV (Fig 4G and H). In addition, our data attest to intestinal permeability being lowered through microbiotal transfer. Whereas HFDxHFDT mice show twofold higher levels of serum Evans Blue compared to RDxRDT, transfer of RD microbiota to HFD-fed mice reduced permeability to levels seen in RDxRDT mice (Fig 4I). Analysis of choroidal levels of Il6, Tnfa, and Vegfa confirmed that transfer of RD-fed fecal suspensions to HFD mice reduced overall inflammation (Fig 4J). Il1b transcripts were not affected. In concert, these results provide evidence for the influence of gut microbiota on CNV.

Discussion
With an increasing prevalence of obesity and increasing life expectancy, the societal impact and financial burden of AMD are expected to rise dramatically in the coming years (Friedman et al, 2004;Rein et al, 2006). Polymorphisms in genes implicated in inflammation predispose to AMD (Hageman et al, 2005) with strong linkage to single nucleotide polymorphisms in CFH factors, CFHR (CFH-related factors), ARMS2, VEGFA, and TGFBR1 (Ambati et al, 2003a;Klein et al, 2005;Yu et al, 2011;Ratnapriya & Chew, 2013), yet by themselves, no single mutation can account for disease development. To date, the contribution of our "second genome" (the microbiome) has not been investigated. Our study suggests that gut microbiota influences development of neovascular lesions associated with AMD and this is particularly when obesity is a predisposing factor. We show that diets rich in fat alter the gut microbiome and in turn elevate choroidal and systemic inflammation and heighten pathological choroidal neovascularization. This effect could originate from increased intestinal permeability to PAMPs secondary to dysbiosis (Fig 5). In this regard, obesity-related changes in gut microbiota have been shown to decrease barrier function of the gut, allowing increased entry of PAMPs into systemic circulation and consequently triggering inflammation (Amar et al, 2008;Cani et al, 2008;Osborn & Olefsky, 2012). Both antibiotic treatment and microbiotal transplants from RD-fed mice lower systemic and choroidal inflammation, yet only RD-microbiotal transplants significantly lower intestinal permeability. While the microbial community of HFDxRDT mice resembles the one of RD-fed mice more closely than that of HFD-fed mice treated with antibiotics, the effects of neomycin treatment likely occur through a decrease in the absolute number of bacteria present in the gut.
Modifying microbiota can reduce systemic and local choroidal inflammation and attenuate pathological neovascularization. Of note, one of the most heavily regulated inflammatory cytokines in our experimental paradigms was IL-6. Elevated levels of IL-6 are associated with early  and late AMD (Klein et al, 2008) and are significantly related to smoking, higher body mass index, and "inflammaging", the low-grade, chronic, systemic sterile inflammation in aging, in the absence of infection (Franceschi & Campisi, 2014). Dysbiosis of gut flora may thus be an additional factor that accounts for the inconsistent responses between Data information: All comparisons between groups are analyzed using one-way analysis of variance (ANOVA) and Tukey's multiple comparisons test; *P < 0.05, **P < 0.01, ***P < 0.001; error bars represent mean AE SEM. Each "n" represents one mouse per experimental group; in (I), both eyes were used for mRNA extraction, giving two data points per mouse; CI, confidence interval. Scale bar, 100 lm. ). In addition, from an experimental perspective, our study strengthens the notion that housing and dietary considerations must be taken into account when designing animalbased studies on angiogenesis and aging. Gut microbiota is acquired shortly after birth from the surrounding environment, forming a relatively stable community that can shift composition under influence of environmental factors such as diet, exercise, and medication (Turnbaugh et al, 2009;David et al, 2014;Evans et al, 2014). Modifying gut microbiomes may thus provide minimally intrusive and cost-effective paradigms to prevent or delay exudative AMD.

Animals
All animal procedures were validated by the Animal Care Committee of the University of Montreal and Hôpital Maisonneuve-Rosemont in accordance with the guidelines established by the Canadian Council on Animal Care. Briefly, 6-week-old male C57BL/6 WT mice, purchased from The Jackson Laboratory, raised under sterile barrier conditions and housed under a 12-h light cycle with water and food ad libitum were placed on either a regular-chow diet (RD) (16% kcal fat, 63% kcal carbohydrate, 21% kcal protein) or a high-fat diet (HFD) (60% kcal Figure 5. High-fat diet-induced dysbiosis increases intestinal permeability, metabolic endotoxemia, and systemic and local inflammation and ultimately contributes to CNV. The ratio of Bacteroidetes and Firmicutes, the two dominant phyla in intestinal flora, decreases significantly in high-fat diet (HFD)-fed mice compared to regular-chow diet (RD)-fed mice, with a relative increase in Firmicutes in HFD-fed mice and decrease in Bacteroidetes. This dysbiosis is accompanied by heightened intestinal permeability, which allows increased translocation of pathogen-associated molecular patterns (PAMPs) (endotoxemia). Recognition of these microbe-specific molecules by pattern recognition receptors (PRRs) present on innate immune cells triggers synthesis and excretion of cytokines causing chronic systemic low-grade inflammation. Ultimately, this exacerbates CNV. fat, 26% kcal carbohydrate, 14% kcal protein) for 7 weeks and weighed weekly to register weight gain. At the age of 9 weeks, half of the RD and half of the HFD mice received antibiotic treatment with 0.5 g/l neomycin trisulfate salt hydrate in their drinking water, resulting in four different experimental groups: Control (RD), Antibiotics (RD+AB), High-Fat (HFD), and High-Fat + Antibiotics (HFD+AB). Neomycin is not absorbed from the gut ; therefore, the antibiotic treatment was isolated to the GI tract and had no direct systemic effect. At the age of 13 weeks, fecal pellets and blood were collected before sedation with isoflurane gas and cervical dislocation. Eyes were enucleated, dissected, and stored at À80°C for mRNA extraction.

Laser-induced CNV
At the age of 11 weeks, mice were anesthetized with 10 ll/g body weight of a 10% ketamine and 4% xylazine solution, and their Bruch's membrane was ruptured using an argon laser as described previously (Lambert et al, 2013). Two weeks after CNV induction, the mice were perfused with 0.5 ml of 15 mg/ml of fluorescein isothiocyanate (FITC)-dextran (average mol wt 20,000) and killed. Eyes were enucleated and processed for analysis by immunohistochemistry. The sclera-choroid-RPE cell complex was mounted onto a slide, and the burns and macrophages were photographed with an Olympus FV1000 microscope. The neovascularization was captured in a Z-stack, and the lesion caused by the laser impact was captured in a single-plane image. The Z-stacks were compressed into one image, and the FITC-dextran-labeled neovascular area and the area of the lesion were measured per lesion in ImageJ.

Immunohistochemistry
Eyes were fixed for 30 min in 4% PFA at room temperature, before dissection of the sclera-choroid-RPE cell complex. After a secondary fixation of 15 min in 4% PFA at room temperature, the choroids were stained with rhodamine-labeled Griffonia (Bandeiraea) Simplicifolia Lectin I (Vector Laboratories Inc.) in 1 mM CaCl 2 in PBS and IBA-1 (rabbit polyclonal; Wako).

Microbiome sequencing
DNA was extracted from fecal pellets with the Qiagen QIAamp Fast Stool Mini Kit according to the manufacturer's instructions with several small modifications; briefly, 2-3 fecal pellets were homogenized in 500 ll InhibitEX Buffer using a disposable homogenizing pestle and vortex. The suspension was heated for 5 min at 70°C before stool particles were pelleted by 1-min centrifugation at 20,000 g. The supernatant was thoroughly mixed with 20 ll proteinase K before 500 ll Buffer AL was added and the mix was incubated at 70°C for 10 min. After the addition of 500 ll of 100% ethanol, the lysate was applied to the QIAamp spin column and centrifuged for 1 min at 20,000 g. The filtrate was discarded before 500 ll Buffer AW1 was added to the spin column and centrifuged for 1 min at 20,000 g. This step was repeated with 500 ll Buffer AW2. The spin column was dried by centrifugation for 3 min at 20,000 g in a clean 2-ml collection tube. The DNA was eluted in 200 ll of Buffer ATE, directly pipetted on the QIAamp membrane, and collected in a clean Eppendorf tube.
After DNA extraction from the fecal pellets, the Thermo Fisher Ion 16S TM Metagenomics Kit was used to amplify the hypervariable regions V2, V3, V4, V6, V7, V8, and V9 of bacterial 16S rRNA. The amplified fragments were then bar-coded, sequenced on the Ion PGM sequencer system, and analyzed with the Ion Reporter Software.

Intestinal permeability assay
Mice were injected by oral gavage with 1 ml of 50 mg/ml Evans Blue divided over five injections, 30 min apart. After 24 h, 120 ll of blood was collected from the submandibular vein. Serum was analyzed for Evans Blue concentration with a spectrophotometer at an optical density of 620-740 nm and quantified with the help of a standard dilution curve.

RAW-blue assay
Blood was collected through cardiac puncture, and serum was stored at À80°C until use in the RAW-Blue assay. PAMPs were assayed with RAW-Blue TM cells (InvivoGen, San Diego, CA) through detection of NF-jB/AP-1 activation following activation of TLRs (with the exception of TLR5), NOD1/2, and dectin-1 using a modified version of the manufacturer's protocol. RAW-Blue TM cells were grown in growth medium (DMEM, 4.5 g/l glucose, 2 mM L-glutamine, 10% fetal bovine serum (FBS), 100 lg/ml Zeocin TM (InvivoGen, San Diego, CA)). The assay was performed when the cells were in passage 10-15 by plating 10 5 cells in 96-well plates containing basal DMEM. After 6 h of starvation 30 ll of mouse serum, 30 ll of FBS(Àcontrol) or 30 ll of FBS+LPS (+ control) was added per well and cells were incubated for 21 h at 37°C under an atmosphere of 5% CO 2 /95% air. SEAP levels were determined using a spectrophotometer at 620-655 nm after a 1-to 3-h incubation at 37°C of 20 ll of induced RAW-Blue TM cell supernatant with 180 ll QUANTI-Blue TM (InvivoGen, San Diego, CA).

Cytokine assessment
Serum cytokine assays were performed using a Bio-plex Mouse Cytokine 6-plex panel (1 × 96-well) (Bio-Rad) according to the manufacturer's instructions. The Bio-Plex cytokine assay is a multiplex bead-based assay involving matrices that is designed to quantitate multiple cytokines as follows. The wells of a 96-well plate were pre-wet with 100 ll of Bio-Plex assay buffer. 50 ll of vortexed multiplex bead working solution was pipetted into each well and immediately removed. Wells were washed twice with the Bio-Plex wash buffer before 25 ll of vortexed Bio-Plex Detention Antibody working solution was added to each well and incubated for 30 min. After a triple wash with the Bio-Plex wash buffer, 50 ll of vortexed 1× streptavidin-PE was added to each well and incubated for 30 min. After three washes, the beads in each well were resuspended with 125 ll of Bio-Plex assay buffer and vortexed for 30 s, and the plate was immediately read on the Bio-Plex system. Cytokine concentrations were calculated from the standard curve by the use of Bio-Plex manager software. Samples were run in duplicate.

Real-time PCR analysis
After enucleation eyes were dissected to isolate retinas and sclerachoroid-RPE cell complex. RNA was isolated using TRIzol and digested with DNase I to prevent amplification of genomic DNA contaminants. M-MLV reverse transcriptase (Life Technologies) was used for the reversed transcription, and SYBR Green (Bio-Rad) to determine gene expression in an ABI Biosystems Real-Time PCR machine with b-actin (Actb) as a reference gene. We used the following primers: Mouse Actb

Microbiota transplant
A litter of six C57BL/6 WT mice was divided over three cages, representing three experimental groups: regular-chow diet-fed mice receiving a transplant from regular-chow diet-fed mice (RDxRDT), high-fat diet-fed mice receiving a transplant from high-fat diet-fed mice (HFDxHFDT), and high-fat-fed mice receiving a transplant from regular-chow diet-fed mice (HFDxRDT). At the age of 6 weeks, two cages were started on HFD, while the other cage remained on a regular-chow diet. Mice received antibiotics (ampicillin 1.0 g/l + neomycin 0.5 g/l) in their drinking water for 5 days, to deplete the original gut microbiota, as described before (Ellekilde et al, 2014). Two days after discontinuing the antibiotics, they received their first microbiota transplant, from mice on either a regular-chow diet or a high-fat diet.
Feces were collected from 20 different donor mice, either on RD or on HFD for at least 5 weeks. The fecal pallets were collected in 2.5 ml of sterile PBS with 0.05% cysteine HCL, homogenized, and centrifuged at 200 g for 5 min. 200 ll of the supernatant was introduced orally to the mice with the help of flexible gavage needles. This was repeated with fresh fecal samples every 7 days for the duration of the experiment. At the age of 11 weeks, mice were subjected to four laser burns per eye. Mice were weighed weekly and feces were collected for analysis by 16S sequencing. Mice are coprophagic, and hence, care is taken to isolate individuals with given gut microbiota modifying protocols.

Statistical analysis
Results are presented as mean AE SEM. GraphPad Prism version 6.00 (GraphPad Software, San Diego, CA; www.graphpad.com) was used to analyze the statistical significance of differences by one-way ANOVA and Tukey's multiple comparisons test or a two-tailed Student's t-test, where appropriate. Data with P < 0.05 were considered statistically different: *P < 0.05, **P < 0.01, and ***P < 0.001.
Expanded View for this article is available online. Acknowledgements E.A. holds scholarships from the Réseau en Recherche en Santé de la Vision and the Faculté des Études Supérieures de l'UdM. P.S. holds The The paper explained Problem Age-related macular degeneration in its neovascular form (NV AMD) is the leading cause of vision loss among adults above the age of 60. Epidemiological data suggest that in men, overall abdominal obesity is the second most important environmental risk factor after smoking for progression to late-stage NV AMD. To date, the mechanisms that underscore this observation remain ill-defined. Given the impact of high-fat diets on gut microbiota, we investigated whether commensal microbes influence the evolution of AMD.

Results
Using mouse models of NV AMD, microbiotal transplants and other paradigms that modify the gut microbiome, we uncoupled weight gain from confounding factors and demonstrate that high-fat diets exacerbate choroidal neovascularization (CNV) by altering gut microbiota. Gut dysbiosis leads to heightened intestinal permeability and chronic low-grade inflammation with elevated production of IL-6, IL-1b, TNF-a and VEGF-A that ultimately exacerbate pathological angiogenesis.

Impact
With an increasing prevalence of obesity and increasing life expectancy, the societal impact and financial burden of AMD are expected to rise dramatically in the coming years. Our study suggests that gut microbiota influences development of neovascular lesions associated with AMD, particularly when obesity is a predisposing factor. Modifying microbiota can reduce systemic and local choroidal inflammation and attenuate pathological neovascularization and may thus provide minimally intrusive and cost-effective paradigms to prevent or delay exudative AMD.