Differences in the Active Endometrial Microbiota across Body Weight and Cancer in Humans and Mice.

Endometrial cancers arise from the epithelial cells lining the uterus. In 2020, endometrial cancer affected more than 417,000 women and was responsible for more than 97,000 deaths worldwide [ 1 ]. Advancing age, late-onset menopause, early menarche, chronic anovulation, unopposed estrogen therapy, tamoxifen treatment, hereditary factors such as Lynch syndrome, and nulliparity are risk factors for this malignancy [ 2 , 3 , 4 , 5 ]. Additionally, and what is perhaps of greatest concern given the increasing prevalence of obesity worldwide, is the relationship between obesity and endometrial cancer. In fact, of all malignancies, endometrial cancer has the strongest association with obesity [ 6 ]. Calle et al. also reported a 6.25-fold increased risk of uterine (endometrial) cancer-related death for morbidly obese women compared to those with a normal body mass index (BMI) [ 7 ]. Mendelian randomization studies also support obesity as a causal factor for endometrial cancer [ 8 , 9 ]. Therefore, identifying specific obesity-related factors that promote endometrial cancer development may provide an opportunity for intervention to reduce risk. The potential mechanisms linking obesity to endometrial cancer development have been discussed in detail previously [ 10 , 11 , 12 , 13 ]. Interestingly, obesity-induced imbalances in estrogen and inflammation can influence microbiota in the gut and vagina [ 14 ], and dysbiosis in these environments can promote cancer [ 14 , 15 ]. Recent studies have been interested in determining whether obesity alters microbiota in the uterus/endometrium. One study reported that microbial diversity was significantly increased in endometrial tumors of obese vs. non-obese white women [ 16 ]. Another reported that obese women had increased microbial diversity in the lower reproductive tract (cervix and vagina), but BMI was not a significant source of microbial variation within the uterus [ 17 ]. Based on these findings, further studies in this field are warranted to determine whether there is a connection between obesity and microbiota of the endometrium. The primary aim of this study was to determine whether microbiota profiles differed within the endometrium of lean vs. obese women with and without endometrial cancer. We also examined endometrial microbiota of lean and obese mice. To do this, we performed 16S rRNA transcript amplicon sequencing, which captures actively replicating bacteria of endometrial tissues from women and mice.

Women were recruited to our clinical study at the Royal Hospital for Women/Prince of Wales Private Hospital (Randwick, Sydney, Australia) from 4 April 2016 until 20 June 2018, with the inclusion criteria of: 18 years or older, postmenopausal (ceased having regular periods at least 12 months prior), body mass index (BMI) of either 30 kg/m 2 (obese), and planned hysterectomy for benign disease or endometrial cancer (diagnosis of endometrioid adenocarcinoma on currettings, any grade). A cutoff of less than 27 kg/m 2 was used for the lean groups to overcome difficulties in recruiting sufficient patients with BMI less than 25 kg/m 2 . However, the average BMI of the lean groups was below 25 kg/m 2 ( Table 1 ). Exclusion criteria were premenopausal women, BMI within the range of 27-30 kg/m 2 , recipient of an investigational new drug within prior 6 days (with an unknown action), and history of psychological illness or condition that may interfere with patient’s ability to understand the requirements of the study. No women in this study were taking antibiotics at the time of surgery or in the 3 weeks prior to surgery. The final numbers of patients (total, n = 70) in each group were as follows: (1) lean cancer ( n = 17), (2) obese cancer ( n = 23), (3) lean controls ( n = 18), and (4) obese controls ( n = 12). Consent was received from all patients prior to sample collection, and all processing and experiments were approved by the Human Research Ethics Committee (HREC) of the South Eastern Sydney Local Health District (HREC 15/339). Clinical data was recorded in a de-identified database and matching samples were stored at the Lowy Biobank UNSW, Sydney. Patient blood samples were obtained on the day of surgery following a period of fasting from food for 8 h and clear fluids up to 2 h prior to hysterectomy. Blood samples were collected in BD vacutainers K2E (EDTA) (Cat# 367525) and sent to SEALS Pathology (Prince of Wales Hospital) for clinical chemistry testing. Endometrial tissues were collected immediately following hysterectomy by surgically opening the uterus in a sterile environment, which is thought to reduce the risk of bacterial contamination from the cervix [ 14 ]. Benign endometrial tissue was obtained from women without cancer, and benign and adjacent malignant endometrial tissue was collected from women with cancer. Intact uteri were immediately placed on ice and delivered to pathology for processing. Sections of benign or malignant endometrial tissue were collected by a pathologist under sterile conditions and immediately placed in 1 mL of Allprotect tissue reagent (Qiagen) in sterile cryovial tubes, and then stored at -80 °C until processed. All mouse experiments were carried out in accordance with relevant guidelines and regulations approved by the UNSW Animal Care and Ethics Committee (project approval #14/33A). Liver kinase B 1 (LKB1) (gene name in mice Stk11 ), floxed mice (FVB;129S6- Stk11 tm1Rdp /Nci), and Sprr2f-Cre mice (FVB-Tg(Sprr2f-cre)1Dcas/Nci) were obtained from the National Cancer Institute (USA) and maintained in pathogen-free vivaria at the University of New South Wales (Australia). Male mice ( Sprr2f-Cre; Lkb1 L /+ ) were backcrossed with pure C57BL/6J female mice (4 generations) to create mice that were >90% C57BL/6. All mice used in this study were littermate females that either lacked one copy of LKB1 in the endometrium ( Sprr2f-Cre; Lkb1 L /+ ) or were wild-type (had both copies) of the LKB1 allele ( Lkb1 + /+ ). When mice reached 6 weeks of age, they were fed either a healthy chow diet (#17 Premium Rat & Mouse-Irradiated, Gordons Specialty Feeds, NSW, Australia) or Western diet prepared in-house which contained 45% fat and 16% sucrose by kCal (based on Research Diets Inc. rodent diet D12451), as previously described [ 39 , 48 ]. Mice were housed (maximum 5/cage) at the Biological Resources Centre (UNSW) and had access to food and water ad libitum in 12-h light/dark cycles. Mice were culled on average at 73 weeks of age (~510 days old) by cervical dislocation following CO 2 asphyxiation. Tissues were collected, weighed, and fixed for histology (in 10% formalin solution) or snap-frozen in liquid nitrogen. DNA was extracted from mouse tail tips using the HotSHOT method [ 49 ]. Genomic DNA was amplified using MyTaq DNA polymerase (Bioline) with 400 nM primers. LKB1 primer sequences were PCRS5 (5′-tctaacaatgcgctcatcgtcatcct-3′), LKB36 (5′-gggcttccacctggtgccagcctgt-3′), and LKB39 (5′-gagatgggtaccaggagttggggct-3′). Cre primer sequences were NA1 (5′-ggtacacacgtcctggaatac-3′) and NA2 (5′-ttcccattctaaacaacaccctgaa-3′). PCR conditions for Cre were as follows: [94 °C (3 min), 35 cycles [94 °C (30 s), 65 °C (30 s), 72 °C (30 s)], 72 °C (3 min)] and for LKB1: [94 °C (3 min), 35 cycles [94 °C (30 s), 60 °C (30 s), 72 °C (60 s)], 72 °C (3 min)]. Samples were run on 1.5% agarose gels in TAE buffer and DNA bands were visualized with ethidium bromide on a Bio-Rad Gel Doc. Glucose tolerance tests (GTTs) were conducted on all mice at 16 weeks of age, following i.p. injection of 2 g/kg glucose solution (prepared at 333 mg/mL in sterile 0.9% saline solution). Fat mass (% of total body weight) was measured using an EchoMRI when mice were 16 weeks of age. Blood glucose levels were measured in mice at 26 weeks of age following a 17-h fast from food. Mouse uteri were inspected visually for macroscopic tumors before cutting in half (1 uterine horn each side) under sterile conditions. One half of the uterus was collected for pathology (fixed in 10% formalin solution) and the other half snap frozen for analysis of uterine microbiota. Fixed uteri were then sectioned, placed on glass slides, and stained with H&E. Slides were then analyzed by a certified pathologist in a blinded manner (Laverty Pathology, Sydney, Australia). Mouse and human endometrial tissues were powdered, and RNA was extracted using an AllPrep DNA/RNA/Protein Mini Kit (Qiagen, Cat # 80004). cDNA was synthesized from 100 ng of DNase-treated RNA using a High-Capacity cDNA reverse transcription kit (Applied Biosystems, Cat # 4368813). The V4 region of the 16S rRNA region was profiled using Illumina MiSeq 2 × 250 bp chemistry as previously described [ 50 ]. Raw reads were analyzed using Mothur v1.39.1 (human) and v1.44.0 (mouse) [ 51 ] and the MiSeq standard operating procedures with some minor modifications [ 52 ]. Negative controls were buffers from the Allprep kit (RPE, RW1 and lysis buffer), two master mix solutions (without reverse transcriptase) from the cDNA reactions, and water that was used in all reactions. Operational taxonomic units (OTUs) that were detected in the negative controls were not considered if identified as a differential feature in any comparison. Read depth for 16S rRNA data from the human and mouse cohorts were 2793 and 6781 clean reads/sample after subsampling. Human patient information ( Table 1 ) was analyzed in SPSS and pairwise comparisons were performed between each group for all data points. P values were calculated using a Kruskal-Wallis H Test and were adjusted for multiple comparisons using the Bonferroni correction for multiple comparisons test. For microbiota analyses, α-diversity measures (Margalef’s species richness, Pielou’s species evenness and Shannon’s diversity index), Bray-Curtis dissimilarities, Principal Coordinate Analysis (PCoA), Analysis of Similarities (ANOSIM), and Permutational analysis of multivariate dispersions (PERMDISP) were conducted using Primer-E v6 software. Per taxon analyses were performed using LEfSe [ 53 ]. All other tests were performed in GraphPad Prism v9. Normality was tested using the Shapiro–Wilk test, and alpha diversity measures that were not normally distributed were analyzed using the Kruskal-Wallis (KW) test. Mouse data was analyzed in GraphPad Prism v9 using two-way ANOVA with Tukey’s test for multiple comparisons (alpha = 0.05).

We recruited 70 postmenopausal women undergoing hysterectomy for endometrial cancer (endometrioid adenocarcinoma) or benign pathology, either lean or obese. There were four groups: (1) lean women with endometrial cancer (lean cancer, n = 17), (2) obese women with endometrial cancer (obese cancer, n = 23), (3) lean women with benign disease (lean controls, n = 18), and (4) obese women with benign disease (obese controls, n = 12). ( Table 1 ). Patient demographics, clinicopathological data, and blood markers are displayed in Table 1 . As expected, the average BMIs for the obese groups (38.20 kg/m 2 in obese cancer and 31.95 kg/m 2 in obese controls) were significantly higher ( p < 0.05) than the lean groups (23.74 kg/m 2 for lean cancer and 23.65 kg/m 2 for lean controls) ( Table 1 ). The average ages ranged from 59–69 years across the groups, with the lean cancer group being significantly older than the lean control group on average (69 years vs. 60.5 years, p = 0.004). Most endometrial cancers were stage 1A and grade 1, and there were no significant differences in parity, gravidity, age at menarche, age at menopause, or other factors between the groups. Obese women had higher levels of blood glucose, insulin, HbA1c (hemoglobin A1c) International Federation of Clinical Chemistry (IFCC) values, HbA1c National Glycohemoglobin Standardization Program (NGSP) (%) values, C-reactive protein (CRP), and estradiol ( Table 1 ). To examine the endometrial microbiota, 16S rRNA transcript amplicon sequencing (i.e., cDNA sequencing) was performed as described in Methods and previously [ 18 ]. This method captures actively replicating bacteria and has advantages compared to sequencing DNA because it reduces potential bias from dead microbes, relic DNA, and contaminants [ 19 , 20 ], while still identifying similar taxa [ 21 ]. We also included six negative controls to reduce potential signals from contaminants. These included buffers from the Allprep kit (RPE, RW1 and lysis buffer), two master mix solutions from the cDNA reactions (without reverse transcriptase, one each for the human and mouse cohorts), and water that was used in all reactions. Results demonstrated that the number of OTUs was significantly lower in the negative control samples when compared to human and mouse endometrial samples ( Figure S1A ). Furthermore, principal coordinate (PCO) and non-metric multidimensional scaling plot (nMDS) analyses of beta diversity (microbial diversity across groups) illustrated significant differences ( p = 0.001) between controls vs. human endometrial samples ( Figure S1B,C ) and controls vs. mouse endometrial samples ( Figure S1D,E ), indicating robust profiling of the active endometrial microbiota and minimal influence of environmental contamination. The bacterial component of the endometrial microbiota was then examined in patient samples to identify microbial signatures that may be associated with obesity and carcinogenesis. For women with cancer, we only included tumor samples to avoid duplication of that patient. Of the 70 women recruited to the study, 65 patients were included in these analyses from each of the four groups: (1) lean cancer ( n = 14), (2) obese cancer ( n = 21), (3) lean controls ( n = 18), and (4) obese controls ( n = 12). The remaining five patients had insufficient samples for these analyses. Notably, the majority (89%) of patients were Caucasian, with n = 12 Caucasian and n = 2 Asian in the lean cancer group; n = 19 Caucasian, n = 1 Asian, and n = 1 unknown in the obese cancer group; n = 16 Caucasian, n = 1 Asian, and n = 1 unknown in the lean control group; and n = 11 Caucasian, and n = 1 Asian in the obese control group. Results demonstrated that the endometrial microbiota clustered into three community types ( Figure 1 A) that were significantly different in composition (R = 0.363, p = 0.001; ANOSIM). Canonical analysis of principal coordinates had a 100% concordance (65/65) with the classification of samples into community types. In further support of the classification, the community types had significant differences in alpha diversity (microbial diversity within each sample) measures ( Figure 1 B and Figure S2 ) and significantly differentially abundant taxa ( Figure 1 C). Community type 1 (C1) had a dominance of lactic acid-producing bacteria such as Lactobacillus and Streptococcus , while community type 2 (C2) had high levels of Proteobacteria (alpha and beta) ( Figure 1 C). Community type 3 (C3) had Acinetobacter and Chryseobacterium as dominant bacteria ( Figure 1 C). Examination of beta diversity in endometrial samples from women with cancer and women without cancer (controls) demonstrated that there were no significant differences (R = 0.035, p = 0.071; ANOSIM) ( Figure 1 D). However, the ordination plot was suggestive of differential prevalence of cancer and control samples across community types ( Figure 1 D, Y = tumor samples, N = controls), and this was confirmed upon further inspection (χ 2 = 15.11, p = 0.0001; Chi-square for trend; Figure 1 E). Specifically, a significantly higher prevalence of cancer samples was identified in C2 when compared to C1 ( p = 0.007, Fisher’s exact) and C3 ( p = 0.0002, Fisher’s exact). To identify taxa enriched or depleted in cancer samples, the relative abundance of taxa in cancer samples were compared to those in controls while correcting for community type. One taxon, Lactobacillus OTU23, with 100% similarity to Lactobacillus iners , was identified to be significantly enriched in control samples [Linear discriminant analysis (LDA) score = 4.5, p = 0.0029]. To establish if obesity was associated with changes in microbiota, patients were classified according to their body mass index (BMI), and the prevalence of community types within each group was assessed. A significant increasing trend of the C2 community type was observed across BMI and cancer (χ 2 = 14.24, p = 0.0002; Chi-square for trend; Figure 1 F), suggesting obesity may play a confounding role in the context of community type prevalence. However, the relative abundance of the Lactobacillus genus was influenced by the presence of cancer and not classification according to obesity (Cancer: F(1,61) = 7.85, p = 0.0068, Obesity: F(1,61) = 0.082, p = 0.78, Interaction: F(1,61) = 0.20, p = 0.66, Figure 1 G). Differences in the microbiota between tumor samples and healthy adjacent tissue from patients with endometrial cancer were examined. The majority, 31/32, (96.9%) of paired tumor and adjacent samples classified as the same community type ( Figure 2 A), indicating a lack of substantial shifts between the two sample types within patients. In support of this, the distances between samples within patients were calculated and compared across patients in both tumor and adjacent tissue, and significantly higher distances were calculated inter-patient compared to intra-patient ( Figure 2 B). Furthermore, minimal differences in differential taxa were identified between tumor and adjacent tissue ( Figure 2 C), and no taxa were identified when correction for community type was applied. Next, we sought to investigate whether obesity alters uterine microbiota in mice. Liver kinase B1 ( LKB1 ) is a tumor suppressor in endometrial cancer [ 22 , 23 ] with expression lost in 20–50% of sporadic endometrial cancer cases [ 24 , 25 ]. Researchers previously reported that Cre-induced knockout of both LKB1 (mouse gene Stk11 ) alleles in the endometrium of mice ( Sprr2f-Cre; Lkb1 L/L ) promotes the development of highly invasive adenocarcinomas in 100% of mice [ 23 ]. In contrast, mice that lacked one copy of LKB1 in the endometrium ( Sprr2f-Cre; Lkb1 L /+ ) were weakly susceptible to endometrial cancer, with one out of 12 mice developing a focal endometrial tumor at ~600 days old [ 23 ]. We backcrossed the LKB1 floxed and Sprr2f-Cre mice onto a C57BL/6J background to minimize strain-specific effects of the mixed FVB and 129 backgrounds of the initial founder mice. The C57BL/6 strain was chosen because it is more susceptible to diet-induced obesity [ 26 , 27 ]. Importantly, the cancer phenotype observed in Sprr2f-Cre; Lkb1 L/L female mice on the FVB;129 mixed background was maintained in C57BL/6J female mice ( Figure S3A–C ). Mice that lacked one copy of LKB1 in the endometrium ( Sprr2f-Cre; Lkb1 L /+ ) were used determine whether obesity promotes endometrial cancer in this model, and to examine the relationship between obesity and uterine microbiota in mice. Female Sprr2f-Cre; Lkb1 L /+ mice fed Western diets were compared to mice of the same genotype fed chow diets ( Figure 3 A). We also included a small number ( n = 4) of wild-type littermates (that had both copies of the LKB1 allele in the endometrium, Lkb1 + /+ ) as additional controls ( Figure 3 A). Mice were weaned at 3 weeks of age and fed a chow diet until 6 weeks of age. Mice then either continued a chow diet or began a Western diet until they were ~73 weeks old (average age of 510 days old) ( Figure 3 A). This time point was chosen because we wanted the mice to be at early reproductive senescence (as per our human cohort). We estimated that 510-day-old mice would be ~58 in human years [ 28 ], which is ~6 years after the average age of menopause in humans. Metabolic analyses confirmed that all mice (both genotypes) fed a Western diet had poorer glucose clearance after a glucose bolus challenge ( Figure 3 B,C), higher fasting blood glucose ( Figure 3 D), higher body fat mass ( Figure 3 E), and higher body weight ( Figure 3 F), liver weight ( Figure 3 G), gonadal fat weight ( Figure 3 H), subcutaneous fat weight ( Figure 3 I), and brown fat weight ( Figure 3 J) compared to mice fed the chow diet. Therefore, Western diet feeding resulted in the expected effects of obesity and obesity-related metabolic impairment. However, histological analyses found no change in uterine pathology, with similar percentages of mice having normal histology, hyperplasia, and atypical hyperplasia between the chow vs. Western diet groups for both genotypes (Chi-square = 0.95, p = 0.62, Table 2 ). Approximately half of all mice (31/61) had atypical hyperplasia but only two mice (one each from the chow and Western diet groups) had cancer (grade 1/stage 1A endometrial adenocarcinoma). Therefore, obesity did not promote endometrial cancer development or hyperplasia/atypical hyperplasia in C57BL/6J mice, regardless of genotype. The actively replicating bacterial component of the endometrial microbiota was then profiled in lean and obese mice (of both genotypes) using 16S rRNA transcript amplicon sequencing. Uterine microbiota of mice clustered into three community types (C1-3, Figure 4 A) that were significantly different in composition (R = 0.419, p = 0.001; ANOSIM). The community types were different in their alpha diversity measures, driven by species evenness ( Figure 4 B and Figure S4A,B ). Analysis of taxa that were differentially abundant across the community types identified C1 to be enriched with Lactobacillus and Pseudomonas , C2 with Deinococcus, and C3 with Acinetobacter , Sphingomonas , Brevundimonas, and Massilia ( Figure 4 C). Canonical analysis of principal coordinates had a high concordance with the classification of samples into community types (96.7%, 59/61 samples). To assess if these community types were associated with pathological outcomes, microbiota composition was assessed against the four outcomes (normal, hyperplasia, atypical hyperplasia, and adenocarcinoma) ( Figure 4 D), and a significant relationship was observed (R = 0.136, p = 0.013; ANOSIM). Pairwise analysis revealed that this relationship was driven by differences between normal and hyperplastic tissues in addition to normal and atypical hyperplastic tissues ( Figure 4 E). The prevalence of each pathological outcome within each community type was then assessed, which suggested an increasing prevalence of disease from C1 to C3 ( Figure 4 F). The prevalence of normal vs. disease (hyperplasia, atypical hyperplasia, and adenocarcinoma) was compared across community types which displayed a trend towards a difference (χ 2 = 3.65, p = 0.056; Chi-square for trend), which was due to differences between C1 and C3 ( p = 0.012, Fisher’s Exact). The community types in the mouse uteri were not due to differences in diet or body weight at endpoint ( Figure S4C,D ).

Obesity is a major risk factor for endometrial cancer, particularly endometrioid adenocarcinomas that account for most endometrial cancer cases [ 29 ]. Although this cancer type typically favors a good prognosis, there remains an increased risk of cancer-related death, particularly among morbidly obese women [ 7 ], and risks associated with surgery [ 30 ]. As such, identifying obesity-related factors that may promote cancer development in obese women is an important step forward in developing strategies to reduce cancer risk. This study found obesity and cancer were associated with the prevalence of microbial community types in the human endometrium. Previous studies have also indicated that obesity may be associated with microbiota changes in the endometrium. One study (published conference abstract) noted a potential trend ( p = 0.07) towards a difference in uterine microbial composition between obese and non-obese (BMI < 30 kg/m 2 ) Caucasian women with endometrial cancer [ 31 ]. The same group recently reported that microbial diversity was significantly increased in endometrial tumors of obese vs. non-obese white women [ 16 ]. Furthermore, the abundance of Firmicutes was significantly higher, while the abundance of OD1 was significantly lower, in endometrial tumors of non-obese vs. obese white women [ 16 ]. Another study by Walsh et al. found that obese women had increased microbial diversity in the lower reproductive tract (cervix and vagina), but BMI was not a significant source of microbial variation within the uterus [ 17 ]. Therefore, obesity could be playing some role in shaping the microbiota of the endometrium. However, in our mouse model, we found that diet-induced obesity was not associated with microbial community types within the endometrium. Therefore, further studies in humans are required to determine whether obesity-related microbiota changes influence cancer development in the endometrium. Lactobacillus are thought to play a protective role in the female reproductive tract. In the lower reproductive tract, a dominance of Lactobacillus species, including L. crispatus , L. gasseri , and L. jensenii, may protect against pathogens because they produce lactic acid (via metabolism of glycogen byproducts) and bacteriocins, and prevent pathogen adhesion to the vaginal epithelium via competitive exclusion [ 14 ]. Dysbiosis of vaginal microbiota, whereby Lactobacillus are depleted, and diverse anaerobes dominate, is associated with increased risk of preterm birth, sexually transmitted infections, miscarriages, and gynecological cancers, including cervical cancer [ 14 , 32 ]. Lactobacillus presence in the uterus may also be a marker of reproductive health, as reviewed [ 33 , 34 ]. In our study we found that women with cancer had significantly lower levels of Lactobacillus in the endometrium compared with women without cancer (controls). Therefore, higher amounts of Lactobacillus in the uterus may be associated with lower cancer risk. However, it is important to note that we also identified other bacteria enriched in the C1 community type alongside Lactobacillus , including Streptococcus , Pseudomonas , Paracoccus , and Escherichia . The other two community types were enriched with Sphingomonas , Methylobacterium , and Brevundimonas (C2); and Acinetobacter and Chryseobacterium (C3). Interestingly, the C3 community type enriched with Acinetobacter had the most control samples, i.e., the lowest cancer samples, suggesting that Acinetobacter may be associated with a normal (or at least benign) endometrium. In support of this, a study by Winters et al. reported that the endometria of women with a median age of 45 (who underwent hysterectomy for fibroids) were dominated by Acinetobacter and not Lactobacillus , with a single Acinetobacter OTU having over 60% relative abundance in the endometrium [ 35 ]. Another study by Chen et al. reported that the uteri of women of reproductive age were dominated by Lactobacillus (30.6%), Pseudomonas (9.09%), and Acinetobacter (9.07%) [ 36 ]. Therefore, our study results complement the findings of others in this field. However, more research is required to understand the roles of Lactobacillus and Acinetobacter in uterine health, and whether their abundance is impacted by factors like menopause and cancer. Our human data revealed that one taxon, similar to Lactobacillus iners , was significantly enriched in the endometria of women without cancer vs. women with cancer. Our results support a study by Walsh et al., which reported that two taxa similar to L. iners were depleted in endometrial cancer tissues compared to benign tissues [ 17 ]. However, Winters et al. reported that L. iners was rarely detected in endometria of women with an average age of 45 years [ 35 ]. These studies further highlight the controversies surrounding the role of L. iners in the female reproductive tract [ 37 , 38 ]. Of the four most common vaginal Lactobacillus species, only L. iners is unable to synthesize D-lactic acid (due to the absence of the gene-encoding D-lactate dehydrogenase) and instead produces L-lactic acid [ 32 ]. L-lactic acid is thought to be less protective against vaginal dysbiosis and infections than D-lactic acid [ 39 ]. Furthermore, L. iners is unable to produce hydrogen peroxide which, through hydroxyl free radical production, inhibits catalase-negative anaerobic bacteria [ 32 ]. A dominance of L. iners in the cervix was associated with obesity in premenopausal Korean women [ 40 ]. However, this study defined obesity as a BMI of ≥25 kg/m 2 , and the association between L. iners and obesity was not observed in postmenopausal women. Nevertheless, L. iners is a normal inhabitant of the female reproductive tract [ 41 ] and is thought to be a transitional species that colonizes the vagina following disruption [ 37 ]. Other studies suggest that L. iners is not pathogenic, and in fact may be important for host defense and restoring the vaginal microbiota via production of anti-inflammatory and antimicrobial molecules [ 37 ]. It is therefore unclear whether L. iners plays differing roles in the epithelium of the lower vs. upper female reproductive tract. Many human pathogens are from the Proteobacteria phylum, including Helicobacter pylori , which is a risk factor for non-cardia gastric cancer. Proteobacteria are Gram-negative bacteria with lipopolysaccharide (LPS) in the outer membrane, and LPS is an endotoxin that induces a strong inflammatory response [ 42 ]. In our study, Proteobacteria including Sphingomonas , Brevundimonas, and Methylobacterium (in humans) and Sphingomonas , Brevundimonas, Acinetobacter , and Massilia (in mice) were associated with uterine pathologies. Other studies support a role for Proteobacteria in reproductive failure and endometriosis, in addition to endometrial and ovarian cancers [ 33 , 43 , 44 , 45 ]. Proteobacteria was the most abundant phyla, with an enrichment of Sphingomonas , Methylobacterium, and Acinetobacter genera in ovarian cancer tissues compared to normal distal fallopian tubes [ 46 ]. Whether these bacteria contribute to an inflammatory microenvironment within the uterus and cancer development remains to be determined. Analysis of the microbiota in mouse endometrial samples revealed three distinct community types. However, these were not associated with Western diet or mouse body weights. Therefore, obesity was not associated with endometrial microbial community types in mice. The differences we observed between the mouse and human data could be attributed to several factors. In particular, the conditions driving obesity in mice were better controlled, e.g., mice of the same strain were fed the same diets (chow or Western diet) for a similar period, whereas in humans, the onset of obesity could occur at different times and be impacted by different diets and a sedentary lifestyle. However, like in humans, an enrichment of Lactobacillus genera was associated with lower prevalence of disease (normal uterine histology), while Proteobacteria genera were associated with uterine pathologies in mice. Interestingly, Sphingomonas and Brevundimonas were both enriched in human (C2) and mouse (C3) community types and were associated with the presence of cancer and uterine pathologies (hyperplasia/atypical hyperplasia). Therefore, these bacteria may be associated with uterine pathologies across mammalian species. However, it is important to note that the OTUs within those genera (driving the community types in humans and mice) had sequence similarities to distinct species i.e., it is likely these were different species. Evaluation of uterine microbiota could have been at risk of contamination due to sampling technique, e.g., collection via the cervicovaginal canal, or external contaminants during processing [ 35 , 47 ]. We reduced the potential risk of contamination by collecting endometrial tissue immediately following hysterectomy (under sterile conditions), including controls in our sequencing to exclude potential contamination from kit reagents (also referred to as the “kitome” [ 35 ]), and profiling viable bacteria by sequencing cDNA from DNase-treated RNA. This method, compared with sequencing DNA, captures actively replicating bacteria and reduces potential bias from dead microbes, relic DNA, and contaminants, and is well suited to samples with a lower abundance of microbes [ 19 , 20 ]. Indeed, several studies have indicated there are approximately 10,000-fold fewer bacteria in the upper female reproductive tract compared to the lower reproductive tract [ 14 , 35 ]. To our knowledge, ours is the first to study to investigate the “active” microbiota of the endometrium. Furthermore, our study complements that of others in this field to gain a broader understanding of microbiota in the endometrium. A previous study reported that microbial diversity was the same in the mid-endometrium vs. the whole endometrium within patients [ 35 ]. However, no study has yet compared the microbiota of endometrial tumor tissue vs. adjacent non-tumor tissue. Our study found microbiota profiles were similar between matched tumor vs. non-tumor endometrial tissue within patients. These results suggest that the presence of the tumor itself does not impact the local microbiota, and that changes to endometrial microbiota community types (that are observed between patients with and without cancer) may occur prior to tumorigenesis. However, further studies are required to determine whether dysbiosis of the uterus/endometrium causes cancer development in this environment. A limitation of our study was that our controls were from patients with benign conditions and thus, samples were not necessarily from a normal endometrium. Furthermore, while we report that no patients were taking antibiotics in the 3 weeks prior or at the time of surgery, we did not have information on antibiotic intake prior to that. Nevertheless, other studies in this field have excluded patients who had taken antibiotics within 2 weeks of surgery [ 43 ] or 10 days prior to surgery [ 35 ].

This study found that obesity and cancer were associated with the prevalence of microbial community types in the human endometrium, but Western diet-induced obesity was not associated with microbial community types in the mouse endometrium. The presence of endometrial cancer (but not obesity) in women was associated with decreased abundance of the Lactobacillus genus in the endometrium. Furthermore, Lactobacillus OTU23 (100% similarity to Lactobacillus iners ) was enriched in endometrial samples from women without endometrial cancer. In mice, an enrichment of Lactobacillus was associated with lower prevalence of disease (normal uterine histology). These results suggest that obesity and cancer may influence microbiota community types in the endometrium (at least in humans) and Lactobacillus may be protective in the endometrium, like in the lower female reproductive tract. This study therefore supports further research into the role of microbiota in endometrial cancer development.