- Open Access
Impact of investigational microbiota therapeutic RBX2660 on the gut microbiome and resistome revealed by a placebo-controlled clinical trial
Microbiome volume 8, Article number: 125 (2020)
Intestinal microbiota restoration can be achieved by complementing a subject’s perturbed microbiota with that of a healthy donor. Recurrent Clostridioides difficile infection (rCDI) is one key application of such treatment. Another emerging application of interest is reducing antibiotic-resistant genes (ARGs) and organisms (AROs). In this study, we investigated fecal specimens from a multicenter, randomized, double-blind, placebo-controlled phase 2b study of microbiota-based investigational drug RBX2660. Patients were administered either placebo, 1 dose of RBX2660 and 1 placebo, or 2 doses of RBX2660 via enema and longitudinally tracked for changes in their microbiome and antibiotic resistome.
All patients exhibited significant recovery of gut microbiome diversity and a decrease of ARG relative abundance during the first 7 days post-treatment. However, the microbiome and resistome shifts toward average configurations from unperturbed individuals were more significant and longer-lasting in RBX2660 recipients compared to placebo. We quantified microbiome and resistome modification by RBX2660 using a novel “transplantation index” metric. We identified taxonomic and metabolic features distinguishing the baseline microbiome of non-transplanted patients and taxa specifically enriched during the process of transplantation. We elucidated the correlation between resistome and taxonomic transplantations and post-treatment dynamics of patient-specific and RBX2660-specific ARGs. Whole genome sequencing of AROs cultured from RBX2660 product and patient samples indicate ARO eradication in patients via RBX2660 administration, but also, to a lesser extent, introduction of RBX2660-derived AROs.
Through shotgun metagenomic sequencing, we elucidated the effects of RBX2660 in the microbiome and resistome. Antibiotic discontinuation alone resulted in significant recovery of gut microbial diversity and reduced ARG relative abundance, but RBX2660 administration more rapidly and completely changed the composition of patients’ microbiome, resistome, and ARO colonization by transplanting RBX2660 microbiota into the recipients. Although ARGs and AROs were transmitted through RBX2660, the resistome post-RBX2660 more closely resembled that of the administered product—a proxy for the donor—than an antibiotic perturbed state.
ClinicalTrials.gov, NCT02299570. Registered 19 November 2014
Intestinal microbiota restoration by microbiota-based therapy, such as fecal microbiota transplantation (FMT) from healthy donors to patients, has been applied as a treatment for disorders caused by intestinal dysbiosis . As the contributions of the gut microbiota to the host immune system, energy metabolism, and central nervous system have been uncovered, the range of potential applications of intestinal microbiota restoration therapy is expanding to various disorders, such as inflammatory bowel disease , functional gastrointestinal disorders , metabolic syndrome [4, 5], and neuropsychiatric disorders [6, 7]. Accordingly, studies for understanding and refining the action of intestinal microbiota restoration therapies are being actively conducted .
Clostridioides difficile infection (CDI) is one area where intestinal microbiota restoration therapy has been applied successfully. Although oral administration of antibiotics is the standard first-line therapy for CDI, antibiotics perturb the commensal gut microbiota and decrease colonization resistance against other pathogens [9, 10]. Approximately 15 to 30% of CDI patients therefore experience recurrent CDI (rCDI) resulting from either a relapse of the previous CDI or reinfection . Moreover, antibiotic therapies during CDI treatment may promote the expansion of antibiotic-resistant organisms (AROs) such as vancomycin-resistant Enterococci (VRE) [12, 13]. On the other hand, intestinal microbiota restoration has shown to be effective for CDI treatment as well as the restoration of colonization resistance against C. difficile and AROs [14, 15]. Indeed, intestinal microbiota restoration has become a commonly performed investigational therapy for rCDI with decent success rates [8, 16,17,18,19].
However, due to the transmissive nature of the treatment, microbiota restoration therapy may communicate not only desirable but also undesirable factors derived from donors. For instance, the transmission of antibiotic-resistant genes (ARGs) and AROs derived from donor samples is a potential risk of fecal transplantation [20, 21]. AROs are responsible for increasing infection cases each year, and more than 35,000 patients died as a result of ARO infections in the United States in 2017 . Recently, two cases of bacteremia caused by extended-spectrum beta-lactamase (ESBL)-producing Escherichia coli in patients after FMT from the same donor sample have been reported, resulting in the death of one of the patients . Moreover, the dissemination of ARGs and pathogenic AROs in patients hampers effective medical care of infections and results in longer hospitalization and higher medical expenditures . Still, multiple studies report efficient reduction of ARGs and decolonization of AROs through microbiota transplantation [24, 25].
In the current study, we explored the effect of a microbiota-based investigational drug RBX2660, a suspension of healthy donor microbiota [26,27,28,29], on the intestinal microbiome and resistome of recipients treated for rCDI. In an international, multicenter, randomized, and blinded phase 2b study, rCDI patients received either placebo (control group), one dose, or two doses of RBX2660 (Fig. 1), with more patients being recurrence-free after either RBX2660 regimen than placebo . Through shotgun metagenomic sequencing, we demonstrate considerable shifts of taxonomic and resistome structures common to both placebo- and RBX2660-treated patients likely from discontinuation of antibiotics, particularly during the first week after treatment. By controlling for placebo effects, we could also distinguish taxonomic and resistome changes specific to RBX2660 treatment. Furthermore, we identified discriminative features strongly correlated with microbiota transplant and demonstrated an overall decrease in AROs as well as introduction of a few AROs by RBX2660.
Study cohorts and sample collection
All donors of RBX2660 microbiota completed a comprehensive initial health and lifestyle questionnaire. Their blood and fecal samples were tested for immunodeficiency viruses, C. difficile toxin, and pathogens including AROs such as VRE and methicillin-resistant Staphylococcus aureus before enrollment into the donor program [27, 28]. Fecal specimens from a total of 66 patients and their corresponding RBX2660 products were collected during a multicenter, randomized, blinded, and placebo-controlled phase 2b study for the treatment of rCDI (Fig. 1) . Ninety-four percent of all patients (62/66) had received vancomycin, with the remainder receiving metronidazole or fidaxomicin prior to study drug (Fig. 1). Twenty-one patients received 2 doses of placebo (14 females, 9 CDI recurrence, median age 63 years), 22 patients received 1 dose of RBX2660 and 1 dose of placebo sequentially (15 females, 5 CDI recurrence, median age 63 years), and 23 patients received 2 doses of RBX2660 (15 females, 8 CDI recurrence, median age 68 years) . Each RBX2660 dose derives from a single donor, and RBX2660 dose selection was not constrained to ensure a single donor was represented in patients that received two RBX2660 doses (Supplementary Table 1). The first dose of study drug (RBX2660 or placebo) was administered 24–48 h following completion of antibiotic treatment for CDI, and the second treatment was administered 7 ± 3 days later (Fig. 1). Patients who experienced a new rCDI episode within 60 days after the first dose (9 placebo recipients, 5 single RBX2660 recipients, 8 double RBX2660 recipients) were moved to open-label treatment and received two additional doses of randomized RBX2660 (Fig. 1). Patient fecal specimens were collected at selected time points from baseline (day 0) through 365 days after the first dose. AROs from each fecal sample were isolated on selective media plates (the “Methods” section, Supplementary Table 2).
RBX2660 shifted taxonomic structures of patients’ intestinal microbiome in a dose-dependent manner
rCDI patients had significantly lower alpha diversity (Shannon diversity) than RBX2660 products before the treatment (Fig. 2a) as previously described with 16S sequencing . Following study drug administration, the alpha diversity of all rCDI patients’ microbiota increased to near-RBX2660 levels regardless of the treatment group, with the steepest increase during the first week (Fig. 2b). The largest taxonomic structural shift also occurred during the first week in all treatment groups (Fig. S1 and S2).
Bray-Curtis dissimilarities between recipient and corresponding RBX2660 product were calculated to assess the level of taxonomic transformation toward that of RBX2660. For placebo recipients, the dissimilarity was measured from a pseudo-donor (DS00) profile calculated from the average species-level taxonomic profile of all RBX2660 products in this study (Fig. 2c). The mean Bray-Curtis dissimilarity of DS00 from RBX2660 products was 0.4926, which was lower than the inter-RBX2660 Bray-Curtis distance of 0.6274. Considering the thorough inspection criteria for donors of RBX2660 products, we defined RBX2660 microbiomes as “unperturbed” gut microbiomes. Bray-Curtis dissimilarities between patients and RBX2660 demonstrate that RBX2660 administration effectively changed recipients’ microbiome structure toward unperturbed configurations at a larger magnitude and for a longer duration as compared to placebo (Kruskal-Wallis test, P = 0.043 at day 30, P = 0.028 at day 60, Fig. 2d). These microbiome shifts by RBX2660 were not sensitive to the kind of antibiotic administered prior to RBX2660 (Fig. S3).
We further compared the original Bray-Curtis dissimilarities between patients and respective RBX2660 (DR) to dissimilarities between patients and other random RBX2660 (DO). RBX2660 recipients still exhibited lower DOs than those of placebo recipients in dose-dependent manner (Fig. S4), indicating that RBX2660 shifted patients’ gut microbiomes toward an unperturbed microbiome more actively than placebo. In addition, significantly lower DRs than DOs of double-dose recipients after the RBX2660 administration demonstrated dose-dependent and specific shifts toward corresponding RBX2660 (Fig. S4). Principal coordinates analysis (PCoA) and PERMANOVA for patients and RBX2660 also indicated that placebo recipients did exhibit taxonomic structural shifts toward RBX2660, but they were not as dramatic as those of double RBX2660 dose recipients toward the first dose RBX2660 (Fig. 2e).
When comparing groups based on rCDI treatment success, treatment-failure patients (who experienced a new rCDI episode within 60 days post-treatment) and treatment-success patients did not exhibit significant differences (Fig. S5a–c). This is likely due to limited number of treatment-failure samples after baseline, as patients were omitted from the current blinded study for the standard-of-care treatment at failure determination. Thus, we performed general linear model-based multivariate statistical analyses of patients’ baseline metagenomes using MaAsLin2  to identify baseline features correlated to rCDI prevention success or failure. Klebsiella pneumoniae was the only species whose relative abundance was significantly associated with treatment failure in all patients (Fig. S5d). When patients were grouped by RBX2660 dose, the model identified K. pneumoniae as the only potential failure-associated feature again from placebo recipients (Fig. S5e) but did not from RBX2660 recipients.
RBX2660 transplanted taxonomic structures to patients
To quantify and compare patients’ levels of change in microbiome composition, we calculated a transplantation index quantifying the extent of microbiome convergence toward corresponding RBX2660 product. This index was defined as the change in Bray-Curtis distances between baseline (DistanceBL) and selected time point (DistanceT), scaled by the distance from RBX2660 at baseline: (DistanceBL − DistanceT)/DistanceBL. DS00 was used for placebo recipients, who were then used to determine taxonomic transplantation success. To validate the transplantation index as a metric for quantifying microbiome shifts by RBX2660, we also calculated pseudo transplantation indices using dissimilarities between patients and random, non-corresponding RBX2660 products and compared them with the original transplantation indices. The dose-dependent increase in pseudo indices (Fig. S6) is additional evidence that RBX2660 shifted patients’ intestinal microbiome toward the unperturbed microbiome of RBX2660. Some of the pseudo indices were lower than zero, indicating that the transplantation index well reflects individual directionality of recipient’s microbiome shift toward respective RBX2660 (Fig. S6). Statistically significant differences between the original and pseudo transplantation indices of double-dose recipients, but not single dose (Fig. S6), connoted that double-dose administration allows more RBX2660-specific microbiome shift than single dose.
RBX2660 recipients were categorized as transplanted or non-transplanted based on whether their transplantation index was higher (transplanted) or lower (non-transplanted) than the maximum value of the placebo group (Fig. 3a). The transplantation ratio trended higher in double-dose recipients versus single-dose recipients; this categorization showed 33.3% and 70.6% transplantation for single- and double-dose recipients, respectively, by day 7 (Chi-square test, P = 0.02752), and 29.4% and 58.3% by day 60 (Chi-square test, P = 0.1212). Non-transplanted patients at day 7 maintained non-transplanted status until day 60, regardless of dose. On the other hand, 1 single-dose recipient (R1-21) and 3 double-dose recipients (R2-01, R2-03, and R2-14) failed to maintain their transplanted state at day 7 until day 60 and eventually reverted to below the transplantation threshold. Veillonella atypica was the only baseline taxonomic feature determined by linear discriminant analysis effect size (LEfSe)  that distinguished patients with successful microbiome transplantation by day 60 from non-transplanted patients in both single and double RBX2660 treatment arms (Fig. 3b).
Although double RBX2660 dosage led to more effective transplantation of RBX2660 microbiome structure, there were 4 double-dose recipients (R2-01, R2-02, R2-03, R2-14) who showed lower transplantation indices than placebo recipients at day 60 (Fig. 3a and S7a). All of the 4 patients received vancomycin prior to RBX2660 administration (Fig. 1). We determined 18 taxa (Fig. 3c) and 21 functions (Fig. S7b) as features specifically explaining the baseline microbiome of these 4 patients by comparing with other double-dose recipients that showed durable taxonomic transplantation by day 60 using LEfSe . Of these, 4 taxonomic features were fungi, which are intrinsically vancomycin insensitive, and 7 functional features of eukaryote-specific metabolic pathways (Fig. 3c and S6b). We further investigated the predicted vancomycin insensitivity of other taxonomic features and found 8 additional intrinsically vancomycin-resistant bacteria including Pediococcus strains [32,33,34] and Lactobacillus and Leuconostoc strains [35,36,37] as well as gram-negative and fungal strains. Enterococcus casseliflavus, which has low level resistance to vancomycin, was also identified . Four taxa (Clostridium glycolicum , Gemella haemolysans , E. faecalis , and C. difficile ) are predicted to be vancomycin susceptible. Compared to the transplanted patients, the 4 non-transplanted patients did not exhibit any other distinctive taxonomic characteristics in terms of alpha diversity and composition of Bacteroidetes, Firmicutes, and Proteobacteria phyla (Fig. S7c–g).
Beyond baseline features, we further investigated which taxa were enriched during the process of transplantation. Through a two-part zero-inflated beta regression model with random effects (ZIBR) test , we investigated a subset of 12 patients (R1-02, R1-03, R1-09, R1-14, R1-21, R2-05, R2-06, R2-10, R2-11, R2-12, R2-13, and R2-20) matched for 4 different time points: baseline, day 7, 30, and 60. ZIBR models a taxon’s presence and absence (logistic component) as well as its non-zero abundance (Beta component), while incorporating patient and time as random variables (random intercepts). Only two genera, Barnesiella and Coprobacillus, are significantly correlated with the taxonomic transplantation. Barnesiella is significantly overrepresented in the transplanted patients as early on as day 7, while Coprobacillus is overrepresented in non-transplanted patients at days 30 and 60 (Fig. 3d). At the species level, ZIBR models identified Barnesiella intestinihominis, Coprobacillus (unclassified), Bacteroides ovatus, Bacteroides uniformis, Ruminococcus obeum, and Akkermansia muciniphila (Fig. 3e, A. muciniphila was omitted because its time point comparisons were not statistically significant in the actual data). Barnesiella intestinihominis and unclassified Coprobacillus species followed near-identical patterns from the genus-level analysis due to single species being identified from each genus.
Resistome regression significantly correlated with transplantation index
Prior to treatment, rCDI patients showed a similar resistome alpha diversity (Wilcoxon signed-rank test, P = 0.18, Fig. 4a) when ARGs were grouped into ARG families based on the organizational structure in CARD . However, the relative abundance of total ARGs was significantly higher in the patients than RBX2660 (Wilcoxon signed-rank test, P < 0.0001, Fig. 4b). It decreased over time in all treatment arms including the placebo group (Fig. 4c). Patients’ resistome composition was distinct from RBX2660 products, but the antibiotic treatment prior to study drug administration did not lead to noticeable difference in resistome (Fig. S8a–c). Specifically, major facilitator superfamily (MFS) and resistance-nodulation-cell division (RND) efflux pumps were the major ARG families present in rCDI patients before the treatment, whereas CfxA beta-lactamase, tetracycline-resistant ribosomal protection proteins, and Erm 23S rRNA methyltransferases were representative of the RBX2660 resistome (Fig. Se).
We tracked individual changes in resistome composition of each patient for 60 days using t-distributed stochastic neighbor embedding (t-SNE) analysis  and resistome transplantation indices defined analogously to the microbiome transplantation index. rCDI patients showed distinctive resistome compositions as compared to those of RBX2660 prior to the treatment, but over time their resistome compositions converged to become similar to RBX2660 (Fig. 4d). The speed of resistome transformation toward RBX2660-like structures varied by patient. The convergence toward RBX2660 resistome structure showed strong correlation to the taxonomic transplantation irrespective of treatment arm (R2 = 0.406, P < 0.0001, Fig. 4e). RBX2660 administration led to higher taxonomic and resistome transplantation indices than the placebo (Fig. 4e).
To identify features distinguishing patient and RBX2660 resistomes, we used a random forest classifier (Fig. S9a–b). Of the top 10 features of importance, 7 ARGs, namely MFS efflux pump, RND efflux pump, OXY β-lactamase, Pmr phosphoethanolamine transferase, undecaprenyl pyrophosphate related proteins, ATP-binding cassette (ABC) efflux pump, small multidrug resistance (SMR) efflux pump, and tetracycline-resistant ribosomal protein, were specific to patients’ baseline resistomes. Class A β-lactamases (CfxA and CblA) and a tetracycline-resistance protein, which are frequently identified in healthy populations or donor stools in FMT trials [20, 46,47,48,49], were classified as RBX2660-specific ARGs (Fig. 5a). Relative abundances of all selected ARGs were significantly altered in recipients one week after study drug administration (Fig. 5b–k). The regression of patient-origin ARGs occurred in all patients without statistically significant differences among placebo and RBX2660 recipients (Fig. 5b–h and S9c–i). Administration of RBX2660 increased relative abundances of RBX2660-origin β-lactamases in a dose-dependent manner (Fig. 5i, j), while the relative abundance of tetracycline-resistant ribosomal protection protein increased in all patients irrespective of treatment (Fig. 5k).
RBX2660 effectively cleared AROs compared to placebo but introduced new AROs
We identified both persisting and newly introduced AROs based on whole genome sequence analyses of isolates from both blind and open-label treatment patients. ARO isolates were Escherichia coli (n = 104), vancomycin-resistant Enterococcus (VRE) (n = 25), and other species (n = 135). The majority of RBX2660-derived AROs were E. coli (Fig. 6). We selected E. coli and VRE, the plurality of screened AROs, for further analyses based on availability of donor-recipient matched pairs and longitudinal samples. Pairwise average nucleotide identity (ANI) was above 97% for all E. coli isolates (Fig. S10), with more than 99.43% identity for all VRE (Fig. S11). Core genome phylogeny indicated the E. coli were mostly of the B2 and D phylogroups. Isolates not only clustered together based on the patient of origin, but also with their corresponding RBX2660 (Fig. S10).
In general, RBX2660 recipients demonstrated faster clearance of AROs as compared to placebo recipients (Fig. 6). Simultaneously, new AROs from RBX2660, mostly E. coli, were introduced to corresponding patients. Calculation of single nucleotide polymorphism (SNP) distances (the “ARO tracking and SNP calling” section) revealed many of these AROs were likely clonal, with a median of 6 SNPs for all pairwise distances indicating near-identical genomes (Supplementary Table 3). We sorted post-treatment ARO E. coli into RBX2660-origin or patient-origin strains and determined clonal persistence following RBX2660 intervention. The introduced AROs were found in patients longitudinally for up to 1 year post-treatment (Fig. 6). In some cases, we observed clonal persistence of patient AROs (e.g., patients R1-05 and R2-18), while in some we observed strain replacement by RBX2660-derived AROs (e.g., patient R2-16). Interestingly, patients receiving the same RBX2660 product did not display identical trends. Patient R2-21 received the same RBX2660 product as R2-18 yet only R2-21 engrafted the RBX2660 ARO (Fig. 6). Persisting AROs derived from patients R1-05 and R2-18 showed higher phenotypic resistance than their corresponding RBX2660-derived AROs, which failed to engraft. On the other hand, patient R2-21 lacked baseline AROs and perhaps provided a “clean slate” for the ARO engraftment.
Isolate ARGs did not indicate a changing resistance profile for these ARO lineages over time. For instance, E. coli isolates exhibited an average of 60 predicted ARGs, and these numbers remained stable throughout the time frame of this investigation (Supplementary Table 4). The 15 RBX2660-origin AROs which were engrafted to corresponding recipients harbored beta-lactamase genes such as AmpC (12 AROs), TEM-1 (8), CARB (3, one each of CARB-17, 19, and 20), or CTX-M-14 (1) (Supplementary Table 4). Antibiotic susceptibility testing (AST) corroborated these findings on the phenotypic level with all introduced AROs being resistant to ciprofloxacin and levofloxacin, and 60% (9/15) resistant to ampicillin (Fig. S12). Approximately half were resistant or intermediate to trimethoprim-sulfamethoxazole (7) and doxycycline (7), and a few were resistant to ampicillin-sulbactam (3) and cefazolin (4), while all were susceptible to cefotetan, ceftazidime, meropenem, imipenem, piperacillin-tazobactam, ceftazidime-avibactam, amikacin, aztreonam, tigecycline, and nitrofurantoin (Supplementary Table 2). The introduced AROs were Enterobacteriaceae and resistant to a median of 4 antibiotics, which was less than that of the patient-origin Enterobacteriaceae AROs (median resistance to 7 antibiotics, Supplementary Table 2). The most resistant isolate introduced from RBX2660 was an E. coli strain which was engrafted into patient R1-09. It was retrieved at 5 subsequent time points (final fecal sample collected at 12 months, all < 20 SNPs, Fig. 6, Supplementary Table 2). This isolate, DI11, was resistant to ceftriaxone and cefepime and classified as an ESBL-producing E. coli (Supplementary Table 2). We further validated ESBL production of DI11 and the corresponding patient isolates using double-disk diffusion tests (Supplementary Table 6).
We investigated factors underlying changes in the microbiome derived from RBX2660 in a randomized, double-blind, placebo-controlled clinical trial . Consistent with a previous evaluation  but in higher resolution using shotgun metagenomic sequencing, we demonstrated RBX2660 dose-dependent changes in the microbiome. Still, all patients initially increased alpha diversity and shifted taxonomic structure regardless of treatment, which could be accredited to the natural trajectory of recovery after antibiotic discontinuation [10, 50]. We hypothesized that it would be possible to distinguish RBX2660-derived effects from the microbiome recovery after antibiotic discontinuation by assessing both extent and direction of microbiome shifts of placebo recipients as thresholds. To test the hypothesis, we developed a simple yet novel metric, the transplantation index. The transplantation index accounts for long-term changes in the microbiome toward corresponding RBX2660 while controlling for individual variation in baseline composition. With the highest transplantation index among placebo recipients as threshold, we demonstrated that RBX2660 recipients exhibited stronger and longer-lasting microbiome changes toward corresponding RBX2660 than placebo recipients.
In an effort to predict transplantation success, we identified baseline taxonomic features that had strong correlations with taxonomic non-transplantation. Species with intrinsic vancomycin resistance were discriminative baseline features of the 4 patients who failed to acquire or maintain transplantation by double RBX2660 administration by day 60 (R2-01, R2-02, R2-03, and R2-14). Previously reported microbiome signatures of vancomycin administration including lower diversity, lower Firmicutes, and higher Proteobacteria levels [10, 51, 52] could not distinguish the 4 non-transplanted patients from transplanted patients. The specific enrichment of intrinsically vancomycin-resistant species therefore could be an indicator of more severe microbiome disturbance by vancomycin. Interestingly, the baseline relative abundance of V. atypica was significantly and positively correlated with durable taxonomic transplantation of RBX2660 microbiome in both the single- and double-dose arms. V. atypica has long been known as an oral bacteria that communicates and develops oral plaque biofilm with lactic acid bacteria [53, 54], but a recent study has highlighted its capacity to build metabolomic networks via a peculiar metabolic function—converting lactate to propionate—in the host gut . Further studies combining both metagenomic and metabolomic analyses are required to uncover the mechanism underlying the positive role of V. atypica in durable microbiota transplantation. Relative abundances of Barnesiella and Coprobacillus genera are significantly correlated with taxonomic transplantation status. Barnesiella, which exhibited positive correlation with taxonomic transplantation, also has been linked to clearance of VRE colonization in mice . Two Bacteroides species, B. ovatus and B. uniformis, were overrepresented in transplanted patients, reflecting the previous report on their correlation with the unperturbed gut microbiome [57, 58].
We also hypothesized that microbiome features of patients are also associated with the prevention of CDI recurrence during the RBX2660 clinical trial. General linear model-based multivariate statistical analyses identified K. pneumoniae as a species associated with treatment failure from all patients or only placebo recipients but did not from RBX2660 recipients. Baseline K. pneumoniae might indeed be a rCDI-associated feature, such as a biomarker of the imbalanced microbiome  that underlies CDI, but not correlate with the outcomes of RBX2660 recipients whose microbiomes were affected by RBX2660. Together with the higher efficacy for RBX2660 on the rCDI prevention than placebo , the model outputs suggest that RBX2660 transplantation restored the disturbed intestinal microbiota to outcompete C. difficile. We reckoned that both dose levels provide enough unperturbed microbiota to exceed a minimum threshold to achieve clinical efficacy, and the second dose provides additional microbiota from which the taxonomic transplantation may arise. Despite their apparent difference between transplantation indices of single- and double-dose recipients, the two treatment arms showed equivalent clinical efficacy . Likewise, although early-stage transplantation by day 7 appeared to be an important factor determining durable transplant by day 60, it did not always secure successful prevention of rCDI and vice versa.
The differences between rCDI patients and RBX2660 in both ARG relative abundance and resistome architecture became narrowed in all the three treatment arms over time. These outcomes suggest that antibiotic discontinuation could be the driver of the changes in resistome during this clinical trial. Despite the natural recovery after antibiotic discontinuation, we hypothesized that transplantation of RBX2660 microbiota shaped patient resistome. RBX2660 indeed simultaneously introduced and eradicated both ARGs and AROs in patients during the process of transplantation. Previous studies have also demonstrated the efficacy of FMT for eradicating AROs , but to our knowledge this is the first to comprehensively track clonality for both RBX2660- and patient-derived ARO isolates. Most introduced AROs were antibiotic-resistant E. coli that are commonly present in a healthy population [61, 62].
We identified one ESBL-producing E. coli strain from a RBX2660 product carrying AmpC and CTX-M-14, whose RBX2660 product was administered to one patient, R1-09. The patient was a single-dose recipient, with recorded treatment success (i.e., no recurrence of CDI and absence of diarrhea for 8 weeks post-treatment) and no known clinical disease resulted from the trial. ESBL-producing E. coli are not inherently more virulent than other strains but can pose a therapeutic challenge if infection occurs . Of note, this trial enrolled patients from December 2014 to November 2015, prior to recognition of ESBL as an important aspect of donor screening. At that time, donor stools were screened for carbapenem-resistant Enterobacteriaceae (CRE) but not ESBL, whereas Rebiotix now screens all donor stools for both CRE and ESBL. Moreover, to date, there have been no adverse infection events due to bacterial transmission from RBX2660 in any clinical trials. In light of a recent death caused by ESBL-producing E. coli bacteremia in an immunocompromised patient after FMT , our findings highlight the importance of a controlled and regulated donor screening program as well as mandatory, monitored safety reporting. Likewise, our findings prompt a general consideration of risk factors for infections from intestinal microorganisms in any life biotherapeutic investigational product.
We thoroughly examined the impact of RBX2660 on the taxonomic structure, resistome, and ARO colonization of recipients during a randomized and placebo-controlled clinical trial. This study is based on samples from a completed placebo-controlled clinical trial of intestinal microbiota restoration, which enabled us to determine microbiome effects of the microbiota-based drug. Using the transplantation index, the current study demonstrated that RBX2660 administration transplanted its microbiota in the recipients in a dose-dependent manner. V. atypica- and intrinsic vancomycin-resistant species were discriminative features of patients showing long-lasting microbiota transplantation and resisting microbiota transplantation, respectively. While antibiotic discontinuation alone significantly reduced patient-origin ARGs, RBX2660 administration led to more dynamic transformations of the resistome. RBX2660 simultaneously introduced RBX2660-origin ARGs in a dose-dependent manner. RBX2660 more efficiently decolonized AROs than placebo but simultaneously introduced new AROs. Genomic outcomes of intestinal microbiota restoration with RBX2660 in the current study show both latent limitations of microbiota transplantation as well as its potential benefits and highlight the importance of the design and quality control of microbiota-based drugs.
Study cohort, drug, and specimen
Subjects were recruited from among 17 centers in the USA and Canada from 10 December 2014 through 13 November 2015. Subjects were adults with recurrent CDI who have had either (i) at least two recurrences after a primary episode (total three CDI episodes) and had completed at least two rounds of oral antibiotic therapy or (ii) had at least two episodes of severe CDI resulting in hospitalization. They were randomly assigned to one of three treatment groups: placebo, single, or double doses of RBX2660. All treatments were blinded and delivered by enema . The second dose was administered approximately 7 days after the first dose. For patients that received two RBX2660 doses, donor selection was random and not constrained to provide a single representative donor per patient.
The selection and screening of donors for RBX2660 were performed as previously described [27, 28]. The placebo composed of normal saline and formulation solution including cryoprotectant in the same proportions used for the RBX2660 preparation. RBX2660 and placebo were stored frozen after preparation until administration. They were thawed for 24 h in a refrigerator and administered within 48 h after thawing. AROs were isolated from patient fecal samples and RBX2660 products on selective agar media plates, chromID VRE (bioMerieux, Marcy-l’Etoile, France), MacConkey with Cefotaxime (Hardy Diagnostics, Santa Maria, CA), MacConkey with Ciprofloxacin, (Hardy Diagnostics), and HardyCHROMTM ESBL (Hardy Diagnostics), at 35°C in air. The remaining fecal samples were stored frozen at − 80 °C until metagenomic DNA extraction. Isolate colonies were sub-cultured to trypticase soy agar with 5% sheep blood (Becton Dickinson, Franklin Lakes, NJ) and identified using VITEK MS matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) system [64, 65]. Each isolate was frozen in tryptic soy broth with glycerol at − 80°C.
Antibiotic susceptibility testing
Antibiotic susceptibility testing was performed through Kirby Bauer disk diffusion, and the resulting zone sizes were interpreted according to the M100 document from the Clinical and Laboratory Standards Institute .
DNA extraction and sequencing
Metagenomic DNA was extracted from approximately 100 mg of fecal samples using DNeasy PowerSoil Kit (Qiagen) following the manufacturer’s protocol excepting the lysis step: fecal samples were lysed by 2 rounds of bead beating for 2 min (total 4 min) at 2500 oscillations/min using a Mini-Beadbeater-24 (Biospec Products). Samples were chilled on ice for 2 min between the two bead beating rounds. Extracted DNA was quantified using a Qubit fluorometer dsDNA HS Assay (Invitrogen) and stored at − 20 °C until the library preparation. Metagenomic DNA was diluted to 0.5 ng/μL before preparing the sequencing library. Libraries were prepared using the Nextera DNA Library Prep Kit (Illumina) as previously described . The libraries then were purified through the Agencourt AMPure XP system (Beckman Coulter) and quantified by Quant-iT PicoGreen dsDNA Assay Kit (Invitrogen) before sequencing. Approximately 70 library samples were pooled in an equimolar manner at the final concentration of 5 nM for each sequencing lane. Prepared pools were submitted for 2 × 150 bp paired-end sequencing on an Illumina NextSeq High-Output platform at the Center for Genome Sciences and Systems Biology at Washington University in St. Louis with a target sequencing depth of approximately 5.5 million reads per sample.
Isolate genomic DNA was extracted using QIAmp BiOstic Bacteremia DNA Kit (Qiagen). Libraries for whole genome sequencing of isolates were prepared from diluted genomic DNA (0.5 ng/μL) as described above. About 180 libraries were pooled together in an equimolar manner at the final concentration of 5 nM for each sequencing lane. Prepared pools were submitted for 2 × 150 bp paired-end sequencing on an Illumina NextSeq High-Output platform at the Center for Genome Sciences and Systems Biology at Washington University in St. Louis with a target sequencing depth of approximately 2 million reads per sample.
Data processing and genome assembly
Sequence reads were binned by index sequence. Adapter and index sequences were trimmed using Trimmomatic v.0.38  using the following parameters: java -Xms2048m -Xmx2048m -jar trimmomatic-0.38.jar PE -phred33 ILLUMINACLIP: NexteraPE-PE.fa:2:30:10:1:true SLIDINGWINDOW:4:15 LEADING:10 TRAILING:10 MINLEN:60. Human sequence contamination was eliminated using Deconseq , and the qualities of resulting reads were verified by FastQC (https://github.com/s-andrews/FastQC).
Isolate genomes were assembled, assessed, and annotated using SPAdes , QUAST , and Prokka , respectively. Average nucleotide identity between E. coli and VRE isolate pairs were calculated using dnadiff . Within-species pan genomes and core genome alignments were obtained with Roary  with default parameters, using 24 and 4 NCBI reference strains (Supplementary Table 5) for E. coli and VRE, respectively, with additional Escherichia fergusonii and general Enterobacter faecalis as outgroups. Alignments were converted via FastTree  and visualized on iTOL v4 .
Microbiome taxonomic composition was predicted by MetaPhlAn v2.0  and controlled for relative abundance. Genus-level composition plots were obtained by grouping together genus present in less than 50% of samples as “Other.” DS00 pseudo-donor microbiome was obtained by averaging the species-level taxonomic profiles of all RBX2660 microbiomes. Bray-Curtis distances were calculated using the vegan package  and visualized as PCoA plots via the ape package  in R 3.5.3. LEfSe  identified baseline taxonomic and metabolic features distinguishing transplanted and non-transplanted patients (alpha value for the factorial Kruskal-Wallis test = 0.05, threshold on the logarithmic LDA score = 2). HUMAnN2  was employed for metabolic pathway prediction. Longitudinal changes distinguishing transplanted and non-transplanted patients were identified using the ZIBR  package in R. Taxa were filtered for non-zero presence in at least 40% samples, and > 0.01 relative abundance in the 90th percentile. Each taxon’s relative abundance was modeled as both the logistic (X) and beta (Z) components (alpha value for Benjamini-Hochberg-adjusted P = 0.05) with transplantation outcome as a fixed effect. Baseline features distinguishing patients with and without rCDI were detected using MaAsLin2. MaAsLin2 is a general linear model-based association detector for microbiome associations with metadata, in this case associations with treatment outcome (success or failure). Taxa were filtered with a minimum prevalence of 0.1 and a minimum relative abundance of 0.0001. Five different models were fitted: one for all patients (total n = 63), one for each treatment arm separately (placebo, n = 21; single dose, n = 22; double dose, n = 21), as well as one for RBX2660 recipients (n = 43) (alpha value for Benjamini-Hochberg-adjusted P = 0.05).
Resistome identification and random forest classifier
ARGs in the microbiome were identified using ShortBRED  with CARD . Isolate ARGs were identified with RGI and CARD [44, 82]. The resulting genes were manually curated into more general ARG families (n = 64). A subset of 70% of available resistomes were then used to train a random forest classifier distinguishing patient baseline and RBX2660 resistomes (training set n = 103), which was then tested on the remaining samples (test set n = 45). The random forest classifier was built with the package scikit-learn (https://scikit-learn.org/stable/index.html) on Python 3.7.3, with trees averaging 12 nodes and a maximum depth of 4.
ARO tracking and SNP calling
SNPs were called using Bowtie2 , SAMtools, and BCFtools , with the first isolate from the patient or corresponding RBX2660 product used as the reference genome. Reads from subsequent isolates of the same species were aligned against the reference with Bowtie2 (-X 2000 --no-mixed --very-sensitive --n-ceil 0,0.01). BAM files were obtained and sorted with SAMtools (view and sort), which were then converted to pileup files (mpileup). BCFtools view generated VCF files, and variants were called, with the following criteria: minimum coverage of 10 reads per SNP, major allele frequency above 95%, and FQ-score of − 85 or less. Indels were excluded. VCF files for each patient were compiled with BCFtools merge, after which SNPs were parsed and counted using custom python and R scripts.
Availability of data and materials
Fecal microbiota transplantation
C. difficile infection
Recurrent C. difficile infection
Single nucleotide polymorphism
Average nucleotide identity
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The authors thank Robert Thänert, Alaric D’Souza, Manish Boolchandani, Amy Langdon, and Drew Schwartz for providing significant intellectual support. Additionally, we would also like to thank the staff at the Edison Family Center for Genome Sciences and Systems Biology at Washington University School of Medicine: Bonnie Dee and Keith Page for administrative support, Jessica Hoisington-Lopez for managing the high-throughput sequencing core, and Eric Martin and Brian Koebbe for computational support.
This work was supported by awards to the authors from the Centers for Disease Control and Prevention Epicenter Prevention Program Grant (5U54CK000162)
Ethics approval and consent to participate
Participants of the Rebiotix Phase 2b study were enrolled at 21 centers in the USA and Canada from 10 December 2014 through 13 November 2015. The study protocol received institutional review board approval at each center. All participants provided written informed consent .
Consent for publication
Rebiotix provided access to study specimens and data, and reviewed the manuscript prior to submission, but was not involved in this study’s design, specimen processing, data analysis, or interpretation. Erik R. Dubberke is a consultant for Sanofi, Pfizer, Synthetic Biologics, BioK+, and Rebiotix, and has a grant from Pfizer.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Taxonomic overview of patient stool samples at the genus level. Figure S2. Taxonomic shift by treatments (related Fig. 2). Figure S3. The effect of antibiotics prior to study drug on taxonomic shift by RBX2660 (related Fig. 2 and 3). Figure S4. Bray-Curtis dissimilarities between patients and respective RBX2660 (DR) or other random RBX2660 (DO). Figure S5. Changes in the Bray-Curtis dissimilarities between a patient and corresponding donor. Figure S6. Transplantation indices (TIs) and pseudo transplantation indices (pTIs). Figure S7. Additional discriminative features of the obstinate patients (related Fig. 3). Figure S8. Comparison of resistome compositions. Figure S9. Random forest classifier successfully distinguished between donor and patient baseline resistomes (related Fig. 5). Figure S10. Average nucleotide identity (ANI) and core genome phylogeny of E. coli isolates. Figure S11. Average nucleotide identity (ANI) and core genome phylogeny of VRE isolates. Figure S12. Antibiotic susceptibility testing (AST).
Supplementary Table 1 Patient drug identifiers.
Supplementary Table 2 AST results.
Supplementary Table 3 SNP distances.
Supplementary Table 4 ARG data.
Supplementary Table 5 NCBI references.
Supplementary Table 6 Double disk test.
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Kwak, S., Choi, J., Hink, T. et al. Impact of investigational microbiota therapeutic RBX2660 on the gut microbiome and resistome revealed by a placebo-controlled clinical trial. Microbiome 8, 125 (2020). https://doi.org/10.1186/s40168-020-00907-9
- Microbiota-based therapy
- Clostridioides difficile infection
- Antibiotic-resistant organisms