Corrigendum: Discovery of a Novel Seminal Fluid Microbiome and Influence of Estrogen Receptor Alpha Genetic Status

Scientific Reports 6: Article number: 23027; published online: 14 March 2016; updated: 29 April 2016. In this Article, Figure 4 is a duplication of Figure 6. The correct Figure 4 appears below as Figure 1.

A second proposed mechanism for paternal transmission of information to the F 1 generation is via seminal fluid content, which could impact female reproductive tract physiology and conceptus development 3 . A third proposed possible mechanism is that the female responds to the perceived fitness of her partner by modulating her investment in his offspring [25][26][27] . In a recent review, it has been speculated that fathers may transmit information via microbiota to their partners and progeny 20 . The most likely source of such microbiota is the seminal vesicles.
Almost all mammalian males, except carnivores, possess seminal vesicles (also termed vesicular glands). These glands are simple tubular and situated below the urinary bladder and vas deferens. In humans, approximately 50-70% of the seminal fluid is produced by the seminal vesicles 28 . This fluid is slightly basic (pH < 7.2) and contains fructose, proteins, enzymes, mucus, vitamin C, flavins, phosphorylcholine, and prostaglandins. Fructose is thought to provide the primary source of metabolic energy for the spermatozoa, but this nutrient can also be utilized by microorganisms, such as fructophilic lactic acid bacteria (FLAB). Therefore, the seminal vesicles could provide a unique niche for such microorganisms to thrive 29 . The seminal vesicles also express ESR1 and 2, suggesting that their secretory activity might be affected by endogenous and environmental estrogenic hormones [30][31][32][33][34][35] . Experiments performed on mice null for ESR1 and ESR2 also implicate estrogens in regulating the function of the seminal glands [36][37][38] .
Bacteria are present in semen samples of men and can be transmitted to their female sexual partners [39][40][41][42][43][44][45][46] , but it is unclear whether these bacteria originate from colonies established in the seminal vesicles or elsewhere in the male reproductive and urinary tract systems. To address whether the seminal vesicles harbor a distinct microbiome and whether the composition of this population of microorganisms can be potentially influenced by estrogens, we collected the seminal fluid and tissue from ESR1 KO and wild-type (WT) male mice. Fecal samples from the same animals were collected to determine the extent to which the putative SFM resembled that of the large bowel.

Results
Comparison of the seminal fluid microbiome to the fecal microbiome. The first goal was to ascertain whether the seminal fluid harbored a unique microbiome. By sequencing the V4 region of the 16S rRNA gene on the Illumina MiSeq, several microbiota were identified in the seminal fluid of WT and ESR1 KO males. Collectively, they comprise a seminal fluid microbiome (SFM, Fig. 1). After identifying the presence of a SFM, we sought to determine whether the microbial community in this region differed from that present in the fecal samples of the same genotype mice. We chose this comparison as the gut or fecal microbiome is one of the best characterized to date.
When the 16S rRNA sequencing results were compared by using Greengenes Version 13_8 (which is available through QIIME, http://qiime.org/home_static/dataFiles.html ftp://greengenes.microbio.me/greengenes_release/ gg_13_5/gg_13_8_otus.tar.gz) clear distinctions were evident in the various bacterial classes when comparing fecal to seminal fluid samples (Fig. 1A). A PCoA analysis and cladogram further confirmed that the classes of bacteria inhabiting these two biological samples clustered separately ( Fig. 1B and C, p = 0.0001 by PERMANOVA). The Venn diagram revealed that of 2690 operational taxonomic units (OTUs) only 285 were common to both compartments. The seminal fluid contained 593 OTUs not found in the fecal samples (Fig. 1D).
Alpha-diversity was analyzed by plotting and comparing the Chao1 and Shannon-Weiner indices for each sample type ( Supplementary Fig. 1). Additionally, rarefaction metrics were plotted and compared between the two sample types. Taken together, these data indicate that the seminal fluid microbial community is somewhat less species-rich and less diverse than the fecal community.
LEfSe comparison (Fig. 2) of microbiota in the seminal fluid or fecal samples also emphasizes the uniqueness of the seminal fluid microbiome. The genera listed in green, most consistently describe seminal fluid. In contrast, those listed in red are the signature of fecal samples. The SFM was characterized by a preponderance of Bacilli, Proteobacteria, Actinobacteria, Fusobacteria, Flavobacteria, and Acidobacteria (P ≤ 0.05, Fig. 2). In contrast, Defferibacteres, Enericutes, Verrucomicrobia, Deltaproteobacteria, Eryspelotrichi, Closteridia, and Bacteroidetes are more consistently present in the fecal samples compared to the seminal fluid samples (P ≤ 0.05, Fig. 2). Taken together, the data strongly support the finding that the seminal fluid harbors a unique microbiome relative to that present in the fecal samples.
KEGG metabolic pathways correlating with fecal and seminal fluid microbiome differences are listed in Supplementary Data 1, and select examples are illustrated in Fig. 3. Based on the classes that differed between the fecal and SFM and KEGG correlation analyses, it is likely that the disparities in microbial composition noted above, would also contribute to a distinct metabolic milieu in seminal fluid, including changes in amino acids, carbohydrates, energy, glycan and lipid metabolites, cofactors, vitamins, and terpenoids metabolites, that could in turn impact host cell functions.
Influence of age on the seminal fluid and fecal microbiomes. As part of these studies, we screened various ages of adult WT and ESR1 KO mice (Supplementary Fig. 2A, where the fecal and seminal fluid microbiomes are organized by age of the animals). This was done to increase the likelihood of detecting a SFM, should it exist. To determine if age altered the SFM and fecal microbiome, PCoA and PERMANOVA analysis were done based on age for both microbiomes. Age did not alter the SFM composition ( Supplementary Fig. 2B, p = 0.4 by PERMANOVA). However, the fecal microbiome was altered by age ( Supplementary Fig. 2C, p = 0.01 by PERMANOVA). To determine which OTUs differed by age, metagenomeSeq 47 was performed. Thirty OTUs differed based on age. Top genera that were increased in older compared to young males include Lactobacillus, Peptostreptococcaceae, Bifidobacterium pseudolongum, Clostridiaceae, and Mollicutes (Supplementary Table 1). In contrast, Lachnospiraceae, Dehalobacterium, Bacteroides acidifaciens, Oscillospira, and another Peptococcaceae were more abundant in younger than older animals.
Influence of estrogen receptor 1 gene status on the seminal fluid microbiome. We next investigated whether ESR1 gene status had an impact on the microbiota present in the seminal fluid samples. While the majority of OTUs occurred in both the seminal fluid of WT and ESR1 KO males, each genotype also possessed genera not present in the other genotype (Fig. 4A), although these differences were insufficient to lead to statistically significant clustering of the samples, as illustrated in the PCoA analysis (Fig. 4B). To investigate the potentially subtle microbiome differences in the seminal fluid of these two genotypes, we used metagenomeSeq 47 . This analysis identified several genera that characterized the SFM of WT or ESR1 KO males (Table 1). For example, Propionibacterium acnes, was much more prevalent in the seminal fluid of WT then ESR1-/-mice, p = 0.0007. Other genera more plentiful in the seminal fluid of WT males included Acinetobacter, Corynebacterium, Streptophyta, Staphylococcus, and Neisseriaceae. In ESR1 KO mice, Turicibacter, Rhodocyclaceae, Streptococcus, and Xanthomonadaceae were much more abundant than in the seminal fluid of WT mice. These differences would also be expected to influence the metabolic environment of the fluid.
Based on the bacteria that differed, correlation analyses were performed for various KEGG metabolic and other pathways ( Fig. 5 and Supplementary Data 2). In WT males, increased abundance of P. acnes was positively correlated with an increase in the abundance in oxidative phosphorylation, several amino acids, pantohenate and CoA biosynthesis. In contrast, sporulation and energy metabolism were negatively correlated with increased abundance of P. acnes. Other genera resulting in significant positive and negative metabolic pathway correlations in the seminal fluid of WT males included Streptococcus, Anaerococcus, Lactococcus, Staphylococcus, Pseudomonas veronii, Finegoldia, Acinetobacter, Neisseriaceae, and Sphingomonas.
In ESR1 KO males, several metabolic pathway alterations correlated with microbiome changes in the seminal fluid. In this group, increased abundance of P. acnes positively correlated with several amino acid metabolic pathways but negatively correlated with signal transduction mechanisms. Other genera resulting in significant positive Influence of estrogen receptor 1 gene status on the fecal microbiome. As with the seminal fluid results, the fecal samples from WT and ESR1 KO males had more OTUs in common than were unique to each genotype (Fig. 6A). However, these differences did not lead to distinct clusters for each genotype in cluster analysis, as illustrated in Fig. 6B. Analysis with metagenomeSeq 47 revealed several OTUs that differed in the fecal samples of WT compared to ESR1 KO males. The fecal samples of WT males were enriched with Ruminococcus, Dehalobacterium, Dorea, Sutterella, and Oscillospira; whereas, Parabacteroides, Coprococcus, and Clostridium were greater in the fecal samples of ESR1 KO males ( Table 2).
The fecal microbiome changes in WT and ESR1 KO were correlated with alterations in several metabolic and other pathways ( Fig. 7 and Supplementary Data 3). In WT, the genera that resulted in the most pronounced correlations included Coprococcus, Clostridiales, Bacteroidales, Bifidobacterium pseudolongum, Turicibacter, Allobaculum, Lachnospiraceae, Mogibacteriaceae, Sutterella, Oscillospira, Ruminococcaceae, Bacteroides acidifaciens and sp. Those that resulted in the greatest associations in ESR1 KO males were Clostridiales, Parabacteroides, Bacteroidales, Bifidobacterium pseudolongum, Turicibacter, Allobaculum, Lachnospiraceae, Sutterella, Oscillospira, Dehalobacterium, Ruminococcaceae, Bacteroides acidifaciens, and Clostriaceae. Discussion Speculation exists as to whether the seminal vesicles harbor a unique microbiome 20 . The current studies confirm that they do so, at least in mice. The occupants of the SFM are distinct from those residing in the fecal microbiome of these mice. This finding is not surprising as the microhabitat, including nutrient substrate availability, within the each of these biological samples differs immensely. Therefore, the microbiomes present within each of these environments have seemingly evolved over time to the specific qualities of each niche. The bacterial phyla that dominate in the seminal fluid, including Proteobacteria, Actinobacteria, Fusobacteria, and Firmicutes may be able to utilize fructose and other carbohydrates produced by the seminal fluid glands as energy sources.  66 , correlations between the PICRUSt-generated functional profile and QIIME-generated genus level bacterial abundance were calculated and plotted against genotype status for the seminal fluid samples in WT and ESR1 KO mice. Those genera that were identified by LEfSe as being different between the two biological samples are depicted. Metabolic pathway designations are delineated at the bottom of the figure. Shading intensity and size of the circles indicates the Kendall rank correlation coefficient between matrices. Orange/red indicates a positive correlation; whereas blue designates a negative correlation. Red squares surrounding the circles are indicative of a P value ≤ 0.05. As in Fig. 2, genera listed in green were indicative of seminal fluid. In contrast, those listed in red were indicative of fecal samples. Quantitative PCR or gram staining may be considered as follow-up procedures to confirm some of the OTUs identified in the SFM. Future work should also consider whether other organs of the genitourinary system, including the other accessory sex glands, are colonized by other types of bacteria.
Comparison of genera upregulated in the seminal fluid of ESR1 KO or WT males revealed genotypic differences. There were several genera in common with prior studies [39][40][41][42][43][44][45][46] with semen from men including Peptoniphilus (greater in ESR1 KO), Anaerococcus (greater in WT), Finegoldia (greater in WT), Staphylococcus (greater in WT), Streptococcus (greater in ESR1 KO), Corynebacterium (greater in ESR1 KO), and Lactobacillus (greater in WT). Based on our current findings, it suggests that genetic background, at least in mice, can influence bacterial colonies in the SFM. One genera discovered in the SFM that was not identified in these earlier reports is P. acnes, which is the causative agent in men and inoculated rodents for chronic prostatitis that can culminate in prostate cancer 48,49 . Considering these data, seminal fluid may serve as a storage pool for P. acnes, whereupon it may incite infection or cancer only after reaching the prostate gland. As Table 1 illustrates, P. acnes is more plentiful in WT compared to ESR1 KO males. WT and ESR1 KO mice typically do not develop prostate cancer. However, when they are bred with TRansgenic Adenocarcinoma of Mouse Prostate (TRAMP) mice, differences emerge in prostate cancer incidence 50 . ESR1 KO/TRAMP mice were less likely to develop aggressive prostate cancer compared to WT/TRAMP mice (5% vs. 19% incidence rate). Notably, current findings suggest that the decreased incidence of prostate cancer in ESR1 KO mice 50 might be due to the lower amounts of P. acnes present in their seminal fluid. The Slusarz et al. 50 study also revealed that ESR2 KO/TRAMP mice had the highest incidence (41%) of prostate cancer. The ESR2 gene was originally identified in the prostate gland 51 . We are in the process of characterizing the SFM in ESR2 KO mice. The prediction is that this group will even have greater abundance of P. acnes compared to control mice.
The microbiome alterations in the seminal fluid may also induce changes in virulence factors and the metabolic milieu in these secretions. As shown in Fig. 5, P. acnes, Streptophyta spp, Corynebacterium spp, Pseudomonas veronii, and Acinetobacter spp in WT males and P. acnes, H. parainfluenzae, Acinetobacter spp, and Sphingomonas are positively associated with significant amounts of metabolic pathway changes in the seminal fluid. Thus, some of the previously identified diet-induced metabolite changes in the seminal fluid may represent a combination of bacterial and host metabolites 3 . The former may influence male reproductive function and overall health (including risk for prostate cancer in the case of P. acnes). The genome of P. acnes encodes all of the essential components of oxidative phosphorylation 52 . In WT males, increased abundance of this bacterium is associated with greater oxidative phosphorylation metabolic pathways, which may increase the amount of reactive oxygen species, damaging free radicals, and increase the risk for diseases, including prostate cancer. Additionally, transfer of the microbiome to a reproductive partner could influence her reproduction/health, as well as that of the resulting offspring, and even more distant descendants. Therefore, a better understanding of the SFM and how it might be influenced by intrinsic and extrinsic factors is essential.
The microbiomes in fecal samples from WT and ESR1 KO were analyzed in these studies primarily to determine how they compared to the SFM. However, our findings may also partially explain some of the prior phenotypic studies with these animals. For instance, ESR1 KO mice demonstrate obesity, adipocyte hyperplasia and hypertrophy, insulin resistance, and impaired glucose tolerance 53 . At the time, these and other phenotypic disruptions identified in this transgenic mouse model were presumed to be mediated by direct ablation of the ESR1 gene. However, gut dysbiosis can result in metabolic, neurological, and other disease states [54][55][56][57][58] . For instance, two Lachnospiraceae were increased in the fecal samples of ESR1 KO males (Table 2), and gut colonization by this bacterial family is associated with increased body weight and hyperglycemia in germ-free ob/ob mice 59 . Christensenellaceae is another bacterium augmented in the stool of this group. Increased abundance of this . While the Venn diagram comparison reveals that there are differences in the SFM between WT and ESR1 KO animals, they did not result in distinct clustering between these two genotypes. Consequently, metagenomeSeq 47 was used to determine which OTUs differed between WT and ESR1 KO males (Table 1).
bacterial family positively correlates with body weight and food intake 60 . Administration of an obesogenic diet to mice is associated with an increase in Rikenellaceae 61 ,which was significantly greater in ESR1 KO males. Thus, ESR1 KO mice demonstrate genera in their fecal microbiome previously associated with obesity. As with other studies in this area, cause and effect are not certain. For instance, do the gut microbial changes and their products, virulence factors and metabolites underpin the metabolic disruptions, as has been suggested 54,55,58 ? Alternatively, do the metabolic disturbances change the nutrient availability and thereby induce shifts in the gut microbiota?
While the SFM did not change throughout adulthood in WT or ESR1 KO animals, the fecal microbiome showed differences with increasing age. Other studies with even older rodent models have shown that age can affect the gut microbiome 62,63 . Langille et al. 63 reported that the top overexpressed OTU in the gut microbiome of older mice was Rikenellaceae. In the current studies, this bacterial family was also significantly increased in older compared to young adult animals (Supplementary Table 1). Bacterial shifts in the gut microbiome may occur with age due to alterations in host metabolites, hormones, gastrointestinal structure and physiology, or other intrinsic properties. Conversely, the environment and nutrient composition within the seminal fluid may remain more stable with age, and thus, less prone to bacterial fluctuations.
In conclusion, we have made the novel discovery that the seminal vesicles harbor a unique microbiome. The microbial composition of the SFM can be affected by whether mice possess functional Esr1 genes. Microbiome shifts in the SFM and the potential changes in the abundance of concomitant metabolic pathways may impact male reproduction and health, his female reproductive partners, offspring, and future descendants. Thus, understanding the SFM and how the resident populations may be influenced by genetic background and environmental factors may spawn future research in biomedical sciences. Increased abundance of P. acnes and associated metabolic pathways in the seminal fluid of WT animals might render them at greater risk for prostate cancer under certain genetic and environmental conditions. Lastly, dysbiosis in the fecal microbiome of ESR1 KO mice might induce systemic effects. Collection of fecal and seminal fluid samples. Prior to euthanasia, each animal was placed one per cage without any bedding. Adult males ranging in age from 3 to 13 months of age were used for these studies. Four to five fecal boli were collected from each animal. We collected the fecal samples ex vivo to replicate the approach used in similar studies 65,66 and to ensure that the bacterial composition was reflective of the entire gastrointestinal system, including the rectum and anus. The animals were then intra-peritoneally injected with ~0.8 to 0.9 ml of 1.2% concentration of avertin (Sigma-Aldrich, Saint Louis, Missouri). After they were anesthetized, as evidenced by lack of corneal and leg withdrawal reflexes, the fur from the abdominal region extending from the xiphoid process to the pelvic region was shaved with a Wahl Clipper Corp, model 9962 (Wahl, Shelton, CT). The animals were then surgically scrubbed with a combination of 75% BD alcohol swabs (Becton, Dickinson and Company; Franklin Lakes, NJ) and betadine (Equate, Bentonville, Arkansas). The surgically prepped males were placed in   Bioinformatics and amplicon analysis. Paired-end Illumina MiSeq DNA reads were joined using FLASH 70 . Usearch7 71 was used to clean contigs and remove those with E > 0.5, as explained here: http://drive5. com/usearch/manual/exp_errs.html. Contigs were clustered to 97% identity against DNA sequences in the Greengenes database 72 , version 13_5, using the QIIME 73 , version 1.8, script pick_closed_reference_otus.py, which obviates chimera and PCR error detection. For alpha-diversity, Chao1 (species richness) and Shannon (species diversity) values were calculated and plotted using the phlyoSeq R package 74 . Rarefaction metrics were calculated using the alpha_rarefaction.py script in the Qiime package 73 and plotted using Microsoft Excel ( Supplementary Fig. 1). Measurements of beta-diversity were facilitated by the QIIME script beta_diversity_through_plots.py and visualized using Principal Coordinate Analysis, PCoA, as implemented in QIIME 73 . LEfSe 75 was used to identify genera most consistently different between sample types. LEfSe results were visualized using taxonomy bar-chart and cladogram plots, as implemented on the LEfSe website, http://huttenhower.sph.harvard.edu/galaxy/. PCoA was used to determine whether age of WT and ESR1 KO mice affected the seminal fluid and fecal microbiome samples, where two age-ranges where compared: <220 and >220 days of age. For the fecal microbiome, metage-nomeSeq 47 , version 1.10.0 was used to identify the OTUs in WT and ESR1 KO that varied based on these two age groups. To identify genera associated with the WT and ESR1 KO genotypes within fecal and seminal sample types, we used metagenomeSeq 47