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1. Introduction

Dental implants exhibit high success rates of up to 97% and above [1]. However, contributory factors related to occlusal overloading and peri-implant tissue infection may lead to implant failure [2]. Peri-implantitis is defined as an infection of the peri-implant tissues accompanied by suppuration and clinically significant progressive crestal bone loss after the adaptive phase, leading to decreased osseointegration and pocket formation [3,4]. Peri-implantitis has a reported prevalence ranging from 6.6% to 51% [5,6,7,8,9]. Various risk factors are associated with an increased risk of peri-implantitis. Prosthetic factors, including convex emergence profiles, submucosal crown margins, and excess cement in cemented implant prostheses, increase the risk of peri-implantitis [2,3]. Systemic conditions such as diabetes mellitus and osteoporosis also increase the risk of peri-implantitis [10]. Furthermore, smoking has been found to directly affect the bone surrounding the implant, thereby increasing the risk of peri-implantitis as well [11]. Biofilm removal and control with instruments such as Gracey curettes, ultrasonic scalers, and air powder abrasive devices have been employed with questionable success in the treatment of peri-implantitis since mechanical debridement also comes with its challenges, especially at the apically facing thread surfaces, as demonstrated by Steiger-Ronay et al. [12]. Antimicrobials are also ineffective if mechanical debridement is inadequately performed, as mentioned previously [13,14]. However, liquid desiccants have been reported to reduce the anaerobic bacteria load in diseased implants [15]. To date, the treatment of peri-implantitis is similar to that of periodontitis [16]. The prognosis of this condition is uncertain, and hence, determining the fundamental cause is important for preventive strategies and also targeted approaches [17].

The exact mechanism of microbial interaction in peri-implantitis is not clearly known [3]. Initial studies reported that Staphylococcus aureus plays a role in the progression of the disease [18,19]. However, the consensus on the predominance of S. aureus in peri-implantitis sites was contradicted by Belibasakis et al., as their study concluded the predominance of Treponema spp. and Synergistetes cluster A in peri-implantitis sites [19,20].

Koyanagi et al. reported a more diverse microbial profile compared to that of periodontitis [21], while other studies indicated similarity [22,23]. A microbial profile consisting of aggressive and resistant microorganisms distinct from periodontitis has also been reported previously [24]. Periodontally involved teeth act as reservoir for periopathogens which translocate to the implant sites, making chronic periodontitis an important risk factor for peri-implantitis [21,23,25,26].

Culture-dependent studies evaluating the microbiome of peri-implantitis have limited insights into the bacterial community [27,28], and more recent next-generation sequencing techniques may give us an insight into a more targeted approach to peri-implantitis treatment which, in turn, can improve the prognosis of this condition [29]. The use of next-generation sequencing allows the identification of non-culturable species as compared to conventional methods [29]. The detection of bacterial and fungal infections has been shown to be consistently accurate as compared to conventional methods [30]. In addition, next-generation sequencing has been shown to be cost-effective for identifying the disease with a given high pretest probability, as compared to culture methods [31].

This systematic review aims to summarize and critically analyze the methodology and findings of studies that have utilized next-generation sequencing techniques to elucidate the microbial profiles of peri-implantitis.

2. Results

From the initial search, 506 articles were identified after the elimination of duplicates. After performing the preliminary review of the title and abstracts, 32 articles were included for full-text screening. Based on the selection criteria, 32 studies were chosen to be included in the qualitative analysis (Figure 1). The Risk Of Bias In Non-randomized Studies–of Exposures (ROBINS-E) assessment of 32 articles is shown in Table 1. The Grading of Recommendations, Assessment, Development, and Evaluation (GRADE) approach was used (Table 2) and revealed a low certainty of evidence for the outcomes of diversity and richness as well as the abundance of taxa.

2.1. Methodology of Studies

The methodological characteristics of the studies published between 2009 and 2021 are depicted in Table 3. The total sample size of the selected studies ranged from two to one hundred and six. Fifteen studies compared the association of the periodontitis microbiome with the peri-implantitis site microbiome [21,22,25,32,35,39,41,42,45,47,48,49,51,54,57]. Twelve studies compared the microbiomes of healthy implant (HI) sites to those of peri-implantitis (PI) sites [20,33,34,40,43,44,46,51,53,55,56,58], where the healthy implant site was the control. Peri-implant mucositis (PM) was also compared to peri-implantitis in seven studies [36,37,40,47,50,52]. Smoking was investigated as a factor in microbial dysbiosis in two studies [49,50]. Furthermore, Kroger et al. [43] investigated the association between the microbial diversity and the pocket depths of implants, while Korsh et al. [38] investigated the microbiota associated with early versus late implant loss.

Oral samples collected for microbiome isolation in the 32 included studies were composed mostly of subgingival plaque samples [20,21,22,23,25,32,33,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58]. Two studies utilized supragingival plaque samples [32,53]. Sterile paper points were used to collect the subgingival plaque samples [21,22,23,25,33,35,36,37,38,39,42,43,44,46,48,49,50,51,53,54,55,57]. Eight studies utilized sterile Gracey curettes [20,32,40,41,45,47,56,58], while one study used a periodontal probe [52]. Further details on the collection method are provided in Table 3.

The DNA extraction technique, sequencing technique, targeted region, and the reference database for each study are summarized in Table 4. The microbiome profile is depicted in relation to the diversity, richness, and taxa abundance in Table 5.

Among the 32 studies reviewed, seven studies found an increase in the microbial diversity of peri-implantitis sites as compared with healthy implant sites [20,23,33,38,43,44,52]. Five studies did not report the diversity and richness of the samples collected [41,46,51,55,56,58]. Five studies reported an increase in the microbial diversity in peri-implantitis sites as compared with periodontitis sites [21,32,35,39,57]. Five studies reported a reduced microbial diversity in peri-implantitis sites compared with healthy implants in subgingival plaque [22,34,44,45,52]. Additionally, four studies reported no significant difference in diversity between healthy implants and peri-implantitis samples [23,33,37,50].

2.2. Microbial Profile

Koyanagi et al. revealed that implants with peri-implantitis had a higher abundance of Eubacterium spp. when compared to healthy implants, and this finding is also supported by Zheng et al. and Kroger et al. [21,43,52]; da Silva et al. found that healthy implants demonstrated lower proportions of Eubacterium compared to peri-implantitis sites, while Koyanagi et al. and Zheng et al. concluded that peri-implantitis sites had significantly higher proportions of Eubacterium [21,52,56]. Sanz-Martin et al. reported higher levels of Eubacterium in a healthy implant, when a diseased implant was also present in the same oral cavity [20]. Two studies found high levels of Bacteroidetes and Firmucutes in PI sites as compared to HI sites [20,46]. Three authors found higher levels of Bacteroides in diseased implants [32,33,34]. Yu et al. demonstrated that F. fastidiosum SH03 and the Fretibacterium oral taxon SH01 were linked with plaque at healthy subgingival sites [48]. This study concluded that there were no clear differences or similarities between Synergistetes communities found in diseased versus healthy sites or between periodontal/subgingival niches and peri-implant/submucosal niches [48]. Another study by Yu et al. also showed that the prevalent and abundant bacteria were Streptococcus infantis/mitis/oralis (HMT-070/HMT-071/HMT-638/HMT-677) and Fusobacterium sp. HMT-203/HMT-698 in healthy implants and diseased implants [42]. Another 18 phyla were found in low abundance, particularly the Aquificae, Chlamydiae, Gemmatimonadetes, Nitrospirae, TM6, Verrucomicrobia, and WPS2 phyla, which were present in <0.01% of the total reads for each of the four clinical site categories, with some being undetectable in one or more niches [42]. Healthy implants demonstrated higher proportions of Actinomyces, Atopobium, Gemella, Kingella and Rothia and lower levels of Campylobacter, Desulfobulbus, Dialister, Eubacterium, Filifactor, Mitsukella, Porphyromonas, and Pseudoramibacter in one study [56]. One study that underwent a pathogen-specific analysis for Archaea found that PI sites had a higher frequency of sites that were positive for Archaea [58]. Filifactor was found to be abundant in peri-implantitis sites when compared with healthy implant sites, as shown by several studies [20,35,36,40,47,55,56]. Three studies demonstrated that Parvimonas was the most abundant at peri-implantitis sites [21,55,57].

2.2.1. Phyla

The range of phyla was reported to be varied among the 25 studies. Koyanagi T et al. reported that Firmicutes (45.6%) is the most abundant phylum found in the subgingival plaque in peri-implantitis samples, followed by Bacteroidetes, Proteobacteria, Fusobacteria, Actinobacteria, TM7, Synergistetes, Spirochaetes, Tenericutes, Chloroflexi, and Deferribacteres [21]. Three studies were in concordance in concluding that Bacteroidetes is one of the genera that is found in great abundance in peri-implantitis samples [20,21,46]. The abundance of Synergistetes was reported to be higher in diseased samples in four studies in comparison to in healthy samples [20,21,23,33]. Spirochaetes was identified in diseased samples in three studies [20,21,46], with one study reporting that Spirochaetes increased significantly as peri-implantitis became more severe [20].

2.2.2. Genus

Numerous changes were reported at the genus level (Table 5), with many of them focusing on several genera which are the most abundant in the peri-implant sites. One study reported that there was a preponderance of Veillonella in diseased peri-implant mucosal tissues [45]. However, there are also studies that have suggested that Veillonella is significantly reduced in samples with an increasing peri-implantitis severity [20,53]. Veillonella was also associated with healthy implant sites in other studies [20,47,55,56]. Several authors have found that Prevotella spp. are significantly more abundant at peri-implantitis sites [23,34,36,39,53,54]. Kumar et al. and Daubert et al. found that healthy implants showed higher levels of these two microorganism species [22,45], which was also supported by Apatzidou et al., who showed their greater abundance in diseased samples [23]. Other than Veillonella and Prevotella, most studies also pointed out that Porphyromonas was commonly associated with diseased implants [20,23,51,53,56]. Several studies pointed out that Fusobacterium was present in high levels in peri-implantitis samples [21,37,41,46,55,56,57]. Five studies reported that Streptococcus was more abundant in healthy plaque samples as compared to its abundance in diseased samples [20,22,23,44,45]. Yu et al. also found that Streptococcus was found in both healthy implants and peri-implantitis sites [42]. On the contrary, Kumar et al. concluded that peri-implantitis samples demonstrated a higher level of Streptococcus [22]. A study reported that Propionibacterium, Paludibacter, Staphylococcus, Filifactor, Mogibacterium, Bradyrhizobium, and Acinetobacter are unique to peri-implant sites [47]. In addition, Actinomyces spp. has been reported to be prevalent in peri-implantitis sites [22,52,53]. However, da Silva et al. reported higher levels of Actinomyces spp. in healthy implants [56].

2.2.3. Microbiome Complex

Apart from the genera and phyla levels, Al-Ahmad et al. and Kim et al. reported that Porphyromonas gingivalis and Tannerella forsythia of the red complex are highly associated with peri-implantitis [32,46]. A study reported positive correlations with certain red and orange complex bacteria but a negatively correlation with blue complex bacteria in peri-implantitis samples [20]. Furthermore, another study reported that Bacteroidetes, Chloroflexi, Spirochaetes, Synergistetes, and TM7 positively corresponded with the pocket depths [23].

2.2.4. Peri-Implantitis with Periodontitis

Granulicatella adiacens (phylum Bacillota) was identified in two-thirds of peri-implantitis sites; these two species were also detected at periodontitis sites but not in healthy implants [57]. Shiba et al. found that the microbial composition at the genus level was diverse among the samples for each disease and between both samples from each individual, although the predominant species were similar [49]. Two studies showed that the periodontitis microbial community is more diverse than peri-implantitis sites [25,47]. Interestingly, three studies found the opposite, whereby periodontitis samples yielded lower diversities than peri-implantitis samples [21,22,57]. Aleksandrowicz et al. demonstrated that Archaea was found in diseased implants and teeth [41]. Furthermore, they were found in abundant levels at periodontitis sites when compared to peri-implantitis sites [41].

2.2.5. Peri-Implantitis with Peri-Implant Mucositis

Shi et al. reported no differences in diversity between peri-mucositis sites as compared to peri-implantitis sites, but they found an increased microbial richness in peri-mucositis sites [36]. Sousa et al. reported a decreased abundance of Bradyrhizobium in peri-mucositis sites and peri-implantitis sites [47]. One study concluded that the microbial profile associated with peri-implantitis was also present with a moderate relative abundance at peri-mucositis sites. This study also found that the Shannon index of peri-mucositis was lower than that of peri-implantitis [52]. Tsigarida et al. reported subtle differences between the peri-mucositis and peri-implantitis microbiomes, and these subtle differences were between the transition from health to disease [50]. Streptococci and Rothia were associated with peri-mucositis, while Fusobacterium and Treponema were associated with peri-implantitis, as shown by Polymeri et al. [37]

2.3. Heterogeneity of Studies

Significant heterogeneity can be identified in the methodologies of the selected studies. The ROBINS-E tool was used to assess the quality of the 32 nonrandomized cohort observational studies. The ROBINS-E tool (Table 1) showed that nine studies had some concerns, while four studies were at a high risk of bias. Table 4 illustrates the heterogenicity of the gene sequencing techniques utilized. Figure 2 illustrates the diversity reported in terms of the Shannon’s indexes reported by five studies [21,25,36,37,57]. Figure 3 illustrates the heterogeneity regarding the location (Figure 3a), database used (Figure 3b), and case definition criteria (Figure 3c) of the studies reviewed.

3. Discussion

This systematic review comprehensively reviews the current available evidence on the microbiome of peri-implantitis. Variations in the study methods, sample collection, and study design were observed. However, the review focuses on studies employing the 16S r RNA gene sequencing technique to summarize meaningful observations from the available evidence.

Ten of the studies reviewed showed that the microbial diversity of peri-implantitis is distinct and usually higher than that at healthy implant sites [14,15,17,19,24,26,28,34,38,39]. The alpha diversity considers the richness (number of taxa) and evenness (relative abundance) of species within a sample/community; the beta-diversity quantifies the identities of taxa involved between samples/communities [49]. Changes in oxygen and nutrient concentrations associated with the deepening of a pocket around an implant may be responsible for the shift in the microbial diversity [32]. Figure 2 shows the Shannon’s indexes reported by five studies, as not all studies reported indices [21,25,36,37,57]. These variations in the diversity can be explained by the heterogenicity of various factors such as the location of the study (Figure 3a), the reference database (Figure 3b), and the case criteria definition (Figure 3c). A variation in the genomic database can introduce conflicting results, as one study showed that even the use of a single database within a study can implicate systematic errors during the mapping process which subsequently affects genomic analyses [59]. In addition to that, the sample collection method and the type of sample collected are other confounding factors that may produce conflicting findings.

The studies that included in the current review originate from different countries (Figure 3a), for example, Japan [21,49,55,57], China [36,42,48,52,60], United States of America [22,25,45,50], United Kingdom [47], Germany [38,43,46,53], and The Netherlands [37]. It is significant to note that certain sections of the globe are not represented here. This may also be due to the exclusion of articles written in other languages. Hence, the current data may be significantly influenced by the diet and genetic make-up of the individuals from the representative countries [61]. The characterization of oral dysbiosis in different ethnicities and races presents significant challenges due to variations across multiple studies [62,63,64]. This is due to the highly varied diet, nutrition and lifestyle practices present over several generations in different geographical locations [65,66].

The case definition for peri-implantitis varied across the studies reviewed (Figure 3c). For example, Koyanagi et al. used a criteria of a probing depth (PD) ≥5 mm with bleeding on probing (BOP) and/or suppuration and bone loss >3 threads up to half of the implant length, while Apatzidou et al. diagnosed subjects as having peri-implantitis when there was PD ≥ 6 mm, BOP and/or suppuration, and radiographic bone loss of ≥2 mm in at least one implant surface after one year of loading [21,23]. However, it is evident that the disease severity may vary, even with the employment of the above criteria, hence making it difficult to combine or compare the results of certain studies. Standardizing the methodological quality of microbiome studies has been previously suggested as a necessary step in this direction.

Even though few studies included criteria related to the systemic status of the patient, drugs taken, previous history of other oral diseases like periodontitis and the age of the patient into consideration, the varied criteria set across studies makes a meaningful comparison irrelevant. It would be greatly beneficial for future investigations into the microbiome of the oral cavity to follow a standardized protocol to facilitate comparability between studies [67].

The reviewed studies provide a deeper understanding of the microbial profile of peri-implantitis. However, the different DNA extraction kits used may have had an influence on the microbial data, for example, the Qiagen DNA MiniAmp kit, (QIAGEN, Venlo, The Netherlands) [22,25,38,42,48,50,53], GenElute Bacterial Genomic DNA kit, (Sigma-Aldrich, Munich, Germany) [43], Mora-extract kit, (AMR Inc., Tokyo, Japan) [21,57], Real-time PCR with TaqMan Probe, (Thermo Fisher Scientific, Waltham, MA, USA) [23], DNeasy Kit, (QIAGEN, Venlo, The Netherlands) [36,46], and the Masterpure purification kit, (Epicentre, Verona, Wisconsin, USA) [20,56].

Despite being considered an extension of peri-implantitis and the presence of common bacteria, peri-implant mucositis has been reported to have a distinct microbial profile in some studies [68,69]. However, a few studies were not able to provide a conclusive result on this aspect [36,37,47,50,52]. The diversity in peri-implant mucositis has been reported to be higher than at healthy implant sites [36] but lower than in peri-implantitis [52]. Moreover, the immune cell profiles of both entities seem to differ as well. Enhanced neutrophil and B-cell responses have previously been identified for peri-implantitis lesions when compared to peri-implant mucositis lesions under experimental conditions. The shift in the microbiome profile may also be explained by the increase in frequency and the number of bleeding sites subsequent to biofilm accumulation surrounding the implants [70].

The association of Veillonella sp. with healthy implant sites is well-correlated with its reduced prevalence in deeper pockets and severe disease progression [20,43,46,55]. Streptococci spp. have been identified in both diseased [21,22,53,56] and healthy sites [20,23,45]. Neisseria sp. have been associated with healthy implants and negatively correlates with the probing depth [20,40,43,44], suggesting that Neisseria sp. could have been replaced by other colonizers or may exert a protective effect. Species of the genus Neisseria are well-established primary colonizers of the dental plaque of natural teeth but are not well known for their presence in dental implants. On the contrary, three studies reported high levels of Neisseria sp. in peri-implantitis sites, which contradicts other studies [22,51,54]. Considering the common occurrence of these species in the oral cavity and the possibility of transfer from a diseased to a healthy site or vice versa leads to the lack of a clear understanding of its role in the initiation and the progression of the disease.

Numerous studies have identified Fusobacterium sp. as the dominant species in peri-implantitis [20,21,46]. Studies have also reported the presence of the genus Treponema at peri-implantitis sites of increasing severity [20,43]. However, Kumar et al. reported higher levels of the genera Treponema and Prevotella at healthy implant sites, which is the opposite to what other studies have found [22]. Peri-implantitis sites have also seen an abundance of species from the phylum Synergistetes [20,23,46]. Porphyromonas sp. have been reported at peri-implantitis sites by multiple studies [20,21,23].

A distinct microbial pattern could not be identified across all the 25 studies reviewed, possibly due to the abovementioned factors. Sahrmann et al. also found that there was an absence of a characteristic bacterial profile at peri-implantitis sites [71]. Both the current review and the review by Sahrmann et al. had a consensus that there was considerable heterogeneity in the studies reviewed [71]. The red complex is frequently identified at peri-implantitis sites, as are putative pathogens of the orange and yellow complex. Furthermore, it seems that the relative abundance of each complex changes with an increasing disease progression severity. The blue complex was also reported to be negatively correlated with peri-implantitis sites, suggesting its protective effect. The red complex was also more abundant at implant sites for subjects who smoked, which correlates well with our current understanding that smoking is a risk factor for peri-implantitis. The studies have findings that contradict one another, and this makes it difficult to obtain a characteristic microbial profile for peri-implantitis. However, it is evident that the microbiome of peri-implantitis is unique and distinct from that of periodontitis.

Carvalho et al. found that peri-implantitis lesions were associated with the presence of S. epidermidis, P. gingivalis, T. forsythia, T. denticola, F. nucleatum, and P. intermedia [72]. The review included culture-dependent studies in the analysis. On the contrary, the current systematic review only included studies that utilized next-generation sequencing due to its improved detection limit [30,73]. Additionally, Carvalho et al. reported that a definitive conclusion regarding the microbiome of peri-implantitis could not be reached due to the nature of the studies analyzed. Next-generation sequencing methods have shown that the microbiome of peri-implantitis is distinct from that of periodontitis. Non-culturable species such as Fusobacterium and the Treponema sp. HMT-257 have been detected in peri-implantitis lesions [74,75]. The current systematic review demonstrates that, even with the inclusion of only next-generation sequencing studies, a distinct and unique microbial community pattern could not be identified.

The current review is limited by the studies’ number of participants, with the highest being 139 in a study by Aleksandrowicz et al. [41]. This suggests that the results may not be generalized to the clinical setting due to the small sample size. This review is also limited by the heterogeneity presented across all studies reviewed. Hence, a characteristic microbial profile cannot be determined for future targeted therapies.

4. Materials and Methods

A systematic review of observational and case-control studies (PROSPERO) (CRD42023459266) investigating the microbiome of peri-implantitis lesions was performed on the Cochrane, Medline, and Scopus databases from inception until 1 August 2023 and reported according to the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) [76]. A focused question was formulated based on PECO (population, exposure, comparator, and outcome). The population included patients with at least one osseointegrated dental implant, the exposure was the diagnosis of peri-implantitis lesions, the comparator included healthy implants, periodontitis sites, as well as peri-implant mucositis sites, and the outcome measure was the bacterial composition obtained from samples taken from peri-implantitis sites, as assessed through next-generation sequencing. The question was as follows: Among patients with at least one osseointegrated dental implant, what would be the difference between peri-implantitis lesions, healthy implants, periodontitis, and peri-implant mucositis in terms of the bacterial composition obtained from samples as assessed via next-generation sequencing?

The search strategy involved a combination of the following key terms: peri-implantitis, inflammation, disease, infection, consequence, sequence analysis, RNA, 16S, metagenomics, metagenome, microbiota, and bacteria. The keywords were combined using the Boolean operators “AND” and “OR” in the strategic search. This systematic review followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) criteria [77].

The titles and abstracts were independently screened by two reviewers (K.C.G., R.K.M.) for eligible studies, followed by full-text reading. Data were extracted independently and in duplicate by the two reviewers (K.C.G., R.K.M.) into a data extraction form created following the Cochrane Handbook of Systematic Reviews of Interventions guidelines [76]. Observational and case-control studies investigating the microbiome of peri-implant tissues through next-generation DNA sequencing methods were included. Culture-based studies, conference papers, review articles, studies regarding peri-implantitis associated with other systematic factors (diabetes mellitus, immune disorders, etc.), and articles that examined only specific microorganisms were excluded from this systematic review. Non-English language articles and research conducted on non-human specimens were also excluded. This was followed by full-text screening for eligibility. The complete search strategy used is shown in Table 6. Table 7 depicts the inclusion and exclusion criteria for the articles.

The relevant studies were assessed with the Risk Of Bias In Non-randomized Studies-of Exposures (ROBINS-E) tool [78].

5. Conclusions

The study of the microbiome with next-generation sequencing allows more insight into the possible casual relationships between the bacteria and diseased state and not just culturable or cultivatable species. A unique and distinct microbial pattern could not be identified due to the vast heterogeneity present across all studies. The authors propose that future studies should investigate the microbial profile of peri-implantitis based on the severity of the disease to further provide insight into the progression and alteration of the microbial community within the peri-implant pocket.

A universal clinical parameter for the diagnosis of peri-implantitis should be implemented in all future studies to minimize the confounding factors. The subject pool should also be more diverse and larger to compensate for individual differences, and perhaps, a distinct microbial profile may be seen with a larger sample size. The studies reviewed also show that different groups of bacteria exist in the pockets at different stages of the diseases. This may imply that, with a complete microbial profile, an accurate estimation of the disease progression and monitoring can be performed. Furthermore, this also allows targeted drug therapies towards selective microorganisms that are strongly associated with peri-implantitis.

Author Contributions

Conceptualization, R.K.M.; methodology, R.K.M. and K.C.G.; formal analysis, R.K.M. and K.C.G.; data curation, R.K.M. and K.C.G.; writing—original draft preparation, K.C.G.; writing—review and editing, R.K.M.; supervision, R.K.M. All authors have read and agreed to the published version of the manuscript.

 Institutional Review Board Statement

Not applicable.

 Informed Consent Statement

Not applicable.

 Data Availability Statement

All data are provided with the manuscript.

 Conflicts of Interest

The authors declare no conflict of interest.

Footnotes

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Figures and Tables
View Image - Figure 1. PRISMA flowchart.Enlarge this image.

Figure 1. PRISMA flowchart.

View Image - Figure 2. Different Shannon’s indexes reported by the studies reviewed. PI—peri-implantitis, PM—peri-implant mucositis, P—periodontitis, C—comparison group [21,25,36,37,57].Enlarge this image.

Figure 2. Different Shannon’s indexes reported by the studies reviewed. PI—peri-implantitis, PM—peri-implant mucositis, P—periodontitis, C—comparison group [21,25,36,37,57].

View Image - Figure 3. (a) Location; (b) database used; (c) case definition criteria of the studies reviewed. PD: probing depth; BOP: bleeding on probing [20,21,22,23,25,32,34,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,52,53,54,55,56,57,58].Enlarge this image.

Figure 3. (a) Location; (b) database used; (c) case definition criteria of the studies reviewed. PD: probing depth; BOP: bleeding on probing [20,21,22,23,25,32,34,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,52,53,54,55,56,57,58].

View Image - Figure 3. (a) Location; (b) database used; (c) case definition criteria of the studies reviewed. PD: probing depth; BOP: bleeding on probing [20,21,22,23,25,32,34,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,52,53,54,55,56,57,58].Enlarge this image.

Figure 3. (a) Location; (b) database used; (c) case definition criteria of the studies reviewed. PD: probing depth; BOP: bleeding on probing [20,21,22,23,25,32,34,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,52,53,54,55,56,57,58].

View Image - Figure 3. (a) Location; (b) database used; (c) case definition criteria of the studies reviewed. PD: probing depth; BOP: bleeding on probing [20,21,22,23,25,32,34,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,52,53,54,55,56,57,58].Enlarge this image.

Figure 3. (a) Location; (b) database used; (c) case definition criteria of the studies reviewed. PD: probing depth; BOP: bleeding on probing [20,21,22,23,25,32,34,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,52,53,54,55,56,57,58].

The Risk Of Bias In Non-randomized Studies–of Exposures (ROBINS-E) assessment.

Author, Year Confounding Variables Measurement of the Exposure Selection of Participants Post-Exposure Interventions Missing Data Measurement of Outcome Selection of Reported Result Overall Bias
Kim et al., 2023 [32] S L S S L L L S
Song et al., 2022 [33] L L S L L L L S
Pallos et al., 2022 [34] H L L L L L L H
Barbagallo et al., 2022 [35] H S S L L L L H
Shi et al., 2021 [36] S L L L L L L L
Polymeri et al., 2021 [37] L L L L L L L L
Korsch et al., 2021 [38] L L L L L L L L
Komatsu et al., 2020 [39] S L L L L L L L
Ghensi et al., 2020 [40] S S S L L L L S
Aleksandrowicz et al., 2020 [41] S L L L L L L L
Yu et al., 2019 [42] S L L L L L L L
Kröger et al., 2018 [43] L L H L L L S H
Gao et al., 2018 [44] L L L L L L L L
Daubert et al., 2018 [45] L S L L L L L S
Al-Ahmad et al., 2018 [46] L L L L L L L L
Sousa et al., 2016 [47] L L L L L L L L
Sanz-Martin et al., 2017 [20] L L L L L L L L
Apatzidou et al., 2017 [23] S S L L L L L S
Yu et al., 2016 [48] S L L L L L L L
Shiba et al., 2016 [49] S L S L L L L S
Tsigarida et al., 2015 [50] L L L L L L L L
Jakobi et al., 2015 [51] S L S L L L L S
Zheng et al., 2014 [52] L L L L L L L L
Schaumann et al., 2014 [53] S L S L L L L S
Maruyama et al., 2014 [54] S S S L L L L S
Tamura et al., 2013 [55] L L L L L L L L
Koyanagi et al., 2013 [21] S L L L L L L L
Dabdoub et al., 2013 [25] L L L L L L L L
da Silva et al., 2013 [56] L L L L L L L L
Kumar et al., 2012 [22] H S S L L L L H
Koyanagi et al., 2010 [57] S L L L L L L L
Faveri et al., 2010 [58] L L L L L L L L

L: low risk of bias; S: some concerns; H: high risk of bias.

Grading of Recommendations, Assessment, Development, and Evaluation (GRADE) approach.

Certainty Assessment Summary of Findings
Participants(Studies)Follow-Up Risk of Bias Inconsistency Indirectness Imprecision Publication Bias Overall Certainty of Evidence Study Event Rates (%) Impact
With Conventional Methods With Next-Generation Sequencing
Outcome: Diversity and Richness
1069(32 observational studies) serious a serious b serious c not serious All plausible residual confounding would reduce the demonstrated effect Low The diversity and richness of the microbiome is heterogeneous and inconsistent across all 32 studies.
Outcome: Abundance of Taxa
1069(32 observational studies) serious a serious b serious c not serious All plausible residual confounding would suggest a spurious effect, while no effect was observed Low A heterogeneous pattern of taxa can be seen across all 32 studies reviewed.. The evidence suggests that next-generation sequencing has detected previously uncultured bacteria in diseased sites.

a. Out of the 32 studies reviewed, nine were of some concern, while four were at a high risk of bias based on the ROBINS-E assessment tool. b. Inconsistency is seen due to the heterogeneity across all 32 studies. c. Indirectness is seen due to the differences in the severity of peri-implantitis. Microbial compositions of different severities present heterogenous results.

Characteristics of the population and the results derived from the included studies.

Author, Year Number of Subjects Number of Implants Study Setting Duration of Implant Case Definition for Peri-Implantitis/Peri-Implant Mucositis Samples Collected Collection Method
Kim et al., 2023 [32] 109 30 H, 30 PI Korea Not stated PD ≥ 6 mmBOPRadiographic bone loss ≥3 mm Supra- and subgingival plaque Sterile Gracey curette
Song et al., 2022 [33] 14 14 H, 14 PI China Not stated PD ≥ 6 mmRadiographic bone loss ≥3 mm Subgingival plaque Sterile paper point
Pallos et al., 2022 [34] 42 21 H, 21 PI Brazil ≥2 years PD ≥ 5 mmBOP ± suppurationRadiographic bone loss ≥3 mm Unstimulated saliva Sterile plastic tube
Barbagallo et al., 2022 [35] 24 10 H, 24 PI Italy ≥1 year Increasing PD since loadingEvidence of radiographic bone lossBOP Subgingival plaque Sterile paper point
Shi et al., 2021 [36] 64 27 PM, 37 PI China ≥1 year PD ≥ 6 mmBOP/suppurationMarginal bone loss ≥3 mm Subgingival plaque Sterile paper point
Polymeri et al., 2021 [37] 41 41 PI The Netherlands ≥1 year PD ≥ 6 mmClinical inflammationRadiographic bone loss ≥3 mm Subgingival plaque Sterile paper point
Korsch et al., 2021 [38] 48 31 PI, 22 H Germany ≤3 months or ≥3 years PD ≥ 6 mmBOP and suppurationRadiographic bone loss ≥6 mm Subgingival plaque Sterile paper point
Komatsu et al., 2020 [39] 21 21 PI Japan ≥1 year PD ≥ 6 mmBOP ± suppurationRadiographic bone loss ≥3 mm Subgingival plaque Sterile paper point
Ghensi et al., 2020 [40] 72 35 H, 37 PM, 41 PI Italy ≥1 year BOPRadiographic bone loss > 2 mm Subgingival plaque Sterile Gracey curette
Aleksandrowicz et al., 2020 [41] 139 37 H, 41 PI Poland Not stated PD > 4 mmBOPSuppurationVisible three-thread loss Subgingival plaque Sterile Gracey curette
Yu et al., 2019 [42] 18 18 PI, 18 H China Not stated PD ≥ 5 mmBOP and radiographic bone loss Subgingival/submucosal plaque Sterile paper point
Kröger et al., 2018 [43] 30 45 PI Germany Not stated PD ≥ 5 mmBOPRadiographic bone loss ≥3 mm Subgingival plaque Sterile paper point
Gao et al., 2018 [44] 40 20 H, 20 PI China ≥6 months PD ≥ 4 mmBOPRadiographic bone loss ≥2 mm Subgingival plaque Sterile paper point
Daubert et al., 2018 [45] 9 5 H, 6 PI USA Not stated PD ≥ 4 mmBOP ± suppurationRadiographic bone loss > 2 mm Subgingival plaque Sterile ½ mini Gracey curette
Al-Ahmad et al., 2018 [46] 10 10 H, 10 PI Germany Not stated PD ≥ 5 mmBOP and radiographic bone loss Subgingival plaque Sterile paper point
Sousa et al., 2016 [47] 18 2 H, 2 PM, 2 PI UK Not stated PD ≥ 5 mmRadiographic bone loss of more than three threads up to half of the implant length or ≥2.5 mmBOP Subgingival plaque Sterile Gracey curette
Sanz-Martin et al., 2017 [20] 67 35 PI, 32 H Switzerland ≥1 year Radiographic bone loss ≥2 mm at the mesial/distal sideBOP Subgingival plaque Sterile Gracey curette
Apatzidou et al., 2017 [23] 10 4 H, 10 PI Greece ≥1 year PD ≥ 6 mmBOP/suppurationRadiographic bone loss ≥2 mm Subgingival plaque Sterile paper point
Yu et al., 2016 [48] 18 18 PI, 18 H China Not stated PD ≥ 5 mmBOP and radiographic bone loss ≥2 mm Subgingival plaque Sterile paper point
Shiba et al., 2016 [49] 12 12 PI, 12 P Japan 8.6 ± 7.2 PD ≥ 4 mmBOP and/or suppurationRadiographic bone loss Subgingival plaque Sterile paper point
Tsigarida et al., 2015 [50] 80 40 H, 20 PM, 20 PI USA ≥4 years Clinical inflammation (redness, swelling, BOP, suppuration)Radiographic bone loss > 2 mm Subgingival plaque Sterile paper point
Jakobi et al., 2015 [51] 18 9 H, 9 PI, 9 P Germany >6 months Presence of mobilityBOP ± suppuration Subgingival plaque Sterile paper point
Zheng et al., 2014 [52] 24 10 H, 8 PM, 6 PI China Not stated Zitzmann & Berglundh (2008) Subgingival plaque Periodontal probe
Schaumann et al., 2014 [53] 7 4.7 ± 3.6 PI Germany ≥1 year PD ≥ 4 mmBOP Radiographic bone loss Supra- and subgingival plaque Sterile paper point
Maruyama et al., 2014 [54] 20 20 PI, 20 P Japan ≥1 year PD ≥ 4 mmBOP ± suppurationPresence of radiographic bone loss Subgingival plaque Sterile paper point
Tamura et al., 2013 [55] 30 15 H, 15 PI Japan >6 months PD ≥ 4 mmBOP and suppurationRadiographic bone loss Subgingival plaque Sterile paper point
Koyanagi et al., 2013 [21] 6 6 PI Japan Not stated PD ≥ 5 mmBOP and/or suppurationRadiographic bone loss of more than three threads up to half of the implant length Subgingival plaque Sterile paper point
Dabdoub et al., 2013 [25] 81 33 H, 20 PM, 20 PI USA ≥1 year Consensus Report of the Sixth European Workshop on Periodontology Subgingival plaque Sterile paper point
da Silva et al., 2013 [56] 20 10 PI, 20 H Brazil Not stated PD ≥ 5 mmBOP and/or suppurationSaucer-shaped osseous defects of >3 mm Subgingival plaque Sterile Gracey curette
Kumar et al., 2012 [22] 40 10 H, 10 PI USA ≥1 year Classification of Periodontal Diseases (Armitage 1999)Consensus Report on Peri-Implant Diseases (Lindhe & Meyle2008) Subgingival plaque Sterile paper point
Koyanagi et al., 2010 [57] 3 3 H, 3 PI Japan 3–10 PD ≥ 5 mmBOP and/or suppurationRadiographic bone loss of more than three threads up to half of the implant length Subgingival plaque Sterile paper point
Faveri et al., 2010 [58] 50 25 H, 25 PI Brazil Not stated PD ≥ 5 mmSaucer-shaped osseous defects of >3 mmBOP and/or suppuration Subgingival plaque Sterile Gracey curette

PD: probing depth; BOP: bleeding on probing; P: periodontitis; PI: peri-implantitis; H: healthy implant; PM: peri-implant mucositis.

Summary of techniques of DNA extraction, amplification, and sequencing.

Author, Year Method of DNA Extraction DNA Amplification and Targeted Region Sequencing Technique Reference Database
Kim et al., 2023 [32] Lucigen DNA kit, LGC Biosearch Technologies, Middleton, USA PCR amplification of the 16s rRNA gene at the V3–V4 region Illumina MiSeq Human Oral Microbiome Database
Song et al., 2022 [33] TIANamp Micro DNA Isolation Kit, TIANGEN BIOTECH, Beijing, China PCR amplification at the V3–V4 hypervariable region of 16S rRNA with the primers 338F and 806R Illumina MiSeq Human Oral Microbiome database
Pallos et al., 2022 [34] NucliSENS easyMAG, bioMérieux, Missouri, USA V4 hypervariable region of the 16S rRNA gene was amplified using F515 and R80 Ion 318™ Chip kit v2 400-base chemistry HOMD and Greengene amd NCBI 16s rRNA reference sequence
Barbagallo et al., 2022 [35] PureLink Genomic DNA kit, Thermo Fisher Scientific, USA PCR amplification of the 16s rRNA gene at V3–V4 region Illumina Miseq Human Oral Microbiome database
Shi et al., 2021 [36] DNeasy PowerSoil kit, QIAGEN, Venlo, The Netherlands PCR amplification of the 16S rRNA genes at V3–V4 region Illumina MiSeq Silva database
Polymeri et al., 2021 [37] AGOWA mag Mini DNA Isolation Kit, LGC Genomics, Teddington, United Kingdom PCR amplification of the 16S rRNA gene hypervariable region V5–V7. 454 GS-FLX + Titanium system was used for pyrosequencing Ribosomal Database Project & Human Oral Microbiome Database
Korsch et al., 2021 [38] Qiagen DNA MiniAmp Kit, QIAGEN, Venlo, The Netherlands PCR amplification of the 16s rRNA gene at V1–V2 region Illumina MiSeq Silva database
Komatsu et al., 2020 [39] Mora-extract, AMR Inc., Tokyo, Japan Not stated Illumina Miseq Human Oral Microbiome database
Ghensi et al., 2020 [40] Qiagen DNA MiniAmp kit, QIAGEN, Venlo, The Netherlands Not stated Illumina Hiseq MetaPhlAn 2 and HUMAnN2
Aleksandrowicz et al., 2020 [41] Genomic Mini kit, A&A Biotechnology, Gdańsk, Poland The 2720 Thermal Cycler was used for the amplification of archaeal and bacterial DNA. Oligonucleotide-specific primers were used to target the specific 16s rRNA gene 3130xl Genetic Analyzer GenBank
Yu et al., 2019 [42] Qiagen DNA MiniAmp kit, QIAGEN, Venlo, The Netherlands PCR amplification at the hypervariable region V3–V4 of 16s rRNA Paired-end MiSeq sequencing Human Oral Microbiome Database
Kröger et al., 2018 [43] Sigma-Aldrich GenElute Bacterial Genomic DNA Kit, Sigma-Aldrich, Munich, Germany PCR amplification of the 16s rRNA gene at V3–V4 regions Illumina MiSeq Human Oral Microbiome Database
Gao et al., 2018 [44] Not stated PCR amplification of the 16S V3–V4 regions with primers 343F and 798R Illumina Miseq Human Oral Microbiome database
Daubert et al., 2018 [45] Chelex-100, Bio-Rad, Hercules, USA PCR amplification was used to amplify prokaryotic 16S rRNA genes using universal primers (27F and 1392R). Region of amplification not stated Roche 454 Human Oral Microbiome database
Al-Ahmad et al., 2018 [46] DNeasy Blood and Tissue kit, QIAGEN, Venlo, The Netherlands PCR amplification of 16s rRNA using the universal primers 27F-YM and 1492R, region not stated Ridom TraceEdit software, version 1.1.0 GenBank
Sousa et al., 2016 [47] Not stated Amplification with PCR using the 16S rRNA gene with V5–V7 primers Illumina MiSeq Greengenes
Sanz-Martin et al., 2017 [20] Masterpure purification kit, Epicentre, Wisconsin, USA PCR amplification of the 16s rRNA gene at V3–V4 region Illumina MiSeq Ribosomal Database Project (RDP)
Apatzidou et al., 2017 [23] Proteinase K (100 mcg/mL) at 60 °C for 60 min, later boiled for 10 min Concentration measured with the Nanodrop NP-1000 spectrophotometer (Thermo Fisher Scientific, Renfrew, UK) Final concentration adjusted to 5 ng/mcL PCR amplification of the V3–V4 region of the 16s rRNA gene Illumina MiSeq Greengenes database
Yu et al., 2016 [48] Qiagen DNA MiniAmp kit, QIAGEN, Venlo, The Netherlands PCR amplification of 16s rRNA at ca. 650 bp regions corresponding to the V2–V5 region M13 forward primer Human Oral Microbiome Database
Shiba et al., 2016 [49] Not stated PCR amplification of 16s rRNA, region not stated Illumina MiSeq Human Oral Microbiome Database
Tsigarida et al., 2015 [50] Qiagen DNA MiniAmp kit, QIAGEN, Venlo, The Netherlands PCR amplification of the V1 to V3 and V7 to V9 regions The TTitanium platform was used to perform multiplexed bacterial-tag-encoded FLX amplicon pyrosequencing. Human Oral Microbiome Database
Jakobi et al., 2015 [51] Qiagen DNA MiniAmp kit, QIAGEN, Venlo, The Netherlands PCR amplification of 16s rDNA Not stated Ribosomal Database Project
Zheng et al., 2014 [52] Not stated PCR was used to amplify the V1–V3 regions of the 16s rRNA gene The 454-GS-FLX sequencing platform was used for pyrosequencing Ribosomal Database Project
Schaumann et al., 2014 [53] QIAamp DNA MiniAmp Kit, QIAGEN, Venlo, The Netherlands PCR amplification of 16s rRNA at the V1–V3 regions Pyrosequencing was performed via the GS FLX sequencer Greengenes
Maruyama et al., 2014 [54] Mora-extract, AMR Inc. Tokyo, Japan PCR amplification of the 16S V3–V4 regions with primers 806R and 515F Roche 454 Ribosomal Database Project, Human Oral Microbiome Database, and NCBI
Tamura et al., 2013 [55] Not stated PCR amplification of the 16s rRNA gene with the forward primers 16S27F and 16S341F and the reverse primers 16S1492R and 16S907R Takara Bio GenBank database
Koyanagi et al., 2013 [21] Mora-extract, AMR Inc. Tokyo, Japan PCR amplification of the 16s rRNA gene with the primers 27F and 1492R The 27F and 520R primers (BigDye Terminator Cycle Sequencing kit) were used, and 3130xl Genetic Analyzer Ribosomal Database Project-II (RDP-II)
Dabdoub et al., 2013 [25] Qiagen DNA MiniAmp kit, QIAGEN, Venlo, The Netherlands PCR amplification of the 16s rRNA gene at two regions: V1–V3 and V7–V9 Pyrotag sequencing was performed Greengenes
da Silva et al., 2013 [56] Masterpure DNA purification kit, Epicentre, Wisconsin, USA Two step PCR was performed. The first step involved two sets of forward primers in a 1:1 ratio and the reverse primer 1541R.The second step involved the same two sets of forward primers and the reverse primer 1492R. ABI Prism fluorescent bases Ribosomal Data Project (RDP) & GenBank
Kumar et al., 2012 [22] Qiagen DNA MiniAmp kit, QIAGEN, Venlo, The Netherlands PCR amplification of 16s rRNA at the V1–V3 and V7–V9 regions The Titanium platform was used to perform multiplexed bacterial-tag-encoded FLX amplicon pyrosequencing. Greengenes
Koyanagi et al., 2010 [57] Mora-extract, AMR Inc. Tokyo, Japan PCR amplification of plasmid DNA 27F and 520R primers (BigDye Terminator Cycle Sequencing kit) were used and the 3130xl Genetic Analyzer Ribosomal Database Project-II (RDP-II)
Faveri et al., 2010 [58] Proteinase K (200 mg/mL) was added to the buffer and then inactivated at 95 °C PCR amplification with the universal primer pair for Euryarchaea and the reverse primer 954rEyAr ABI Prism fluorescent bases Ribosomal Data Project (RDP) & GenBank

PCR: Polymerase chain reaction.

Microbial profiles from the retrieved studies showing the diversity and richness and the abundance of taxa.

Author, Year Groups Results
Diversity and Richness Abundance of Taxa
Kim et al., 2023 [32] Peri-implantitisPeriodontitis PI = P aPI > P b PI&P: P. gingivalis, Prevotella spp., Treponema spp., F. alocis, and F. fastidiosumPI > P: Anaerotignum lactatifermentans, Bacteroides vulgatus, Faecalibacterium prausnitzii, Olsenella uli, Parasutterella excrementihominis, Prevotella buccae, P. alactolyticus, and Slackia exigua
Song et al., 2022 [33] Peri-implantitis PI = HI bPI > HI eHI ≠ PI c (Significant difference between groups) PI: Bacteroidetes, Spirochaetes, and Synergistetes, as well as the genera of Porphyromonas,Treponema, Filifactor, Fretibacterium, Lachnospiraceae G-8, and Peptostreptococcaceae XIG-1HI: Proteobacteria, Neisseria, Streptococcus, Haemophilus, and Rothia
Pallos et al., 2022 [34] Peri-implantitis HI > PI a,eHI = PI c PI > HI: Stenotrophomonas, Enterococcus, Leuconostoc genus, Faecalibacterium prausnitzii, Haemophilus parainfluenzae, Prevotella copri, Bacteroides vulgatus, and Bacteroides stercoris
Barbagallo et al., 2022 [35] Peri-implantitisPeriodontitis PI > P aPI = P b PI: Peptostreptococcaceae, Dialister, Mongibacterium, Atopobium, and FilifactorP: Bacteroidales
Shi et al., 2021 [36] Peri-implantitisPeri-implant mucositis PI = PM (No significant difference between groups) a,b,c PI = PM: No significant difference, Bacteroidetes (45.08% in PM, 42.89% in PI), Firmicutes (21.03% in PM, 19.44% in PI), Proteobacteria (11.16% in PM, 10.41% in PI) Fusobacteria (11.12% in PM, 14.7% in PI), Spirochetes (8.38% in PM, 9.68% in PI), Porphyromonas (17.04% in PM, 16.54% in PI), Fusobacterium (9.78% in PM, 12.39% in PI), Treponema (8.37% in PM, 9.59% in PI) and Prevotella (7.43% in PM, 7.04% in PI). PI > PM: Holdemanella and CardiobacteriumPM > PI: Oribacterium, Staphylococcus, and Ramlibacter
Polymeri et al., 2021 [37] Peri-implantitisPeri-implant mucositis HI = PM = PI (No significant differences between groups) a,b,g PI: Fusobacterium nucleatum and Treponema denticolaPM: Rothia mucilaginosa and Streptococcus salivarius
Korsch et al., 2021 [38] Peri-implantitis PI > HI d PI: Fusobacterium nucleatum and Porphyromonas gingivalis HI: Streptococcus, Neisseria, Rothia and Veillonella
Komatsu et al., 2020 [39] Peri-implantitisPeriodontitis PI > P aPI = P c,g PI: Solobacterium moorei and Prevotella denticolaP: F. nucleatum, P. stomatis and Leptotrichia sp.
Ghensi et al., 2020 [40] Peri-implantitisPeri-implant mucositis PI < HI a,b PI: Treponema maltophilum, Fretibacterium fastidiosum, Pseudoramibacter alactolyticus, T. lecithinolyticum, P. gingivalis, T. forsythia, Treponema denticola, P. endodontalis, Filifactor alocis, and Desulfobulbus spp.HI: C. gingivalis, C. granulosa, C. ochracea, S. noxia, S. artemidis, Actinomyces, Capnocytophaga, Neisseria, Rothia, and Streptococcus
Aleksandrowicz et al., 2020 [41] Peri-implantitisPeriodontitis Nil PI: F nucleatum and T denticola
Yu et al., 2019 [42] Peri-implantitisPeriodontitis PI = HI (No significant difference between groups) d,f PI=HI: Streptococcus infantis/mitis/oralis (HMT-070/HMT-071/HMT-638/HMT-677) and Fusobacterium sp. HMT-203/HMT-698PI (Low abundance): Aquificae, Chlamydiae, Gemmatimonadetes, Nitrospirae, TM6, Verrucomicrobia, and WPS2 phyla
Kröger et al., 2018 [43] Peri-implantitis PI > HI g PI: Eubacteriaceae [XV], Fretibacterium sp. HMT 362, Fretibacterium fastidiosum, Peptostreptococcaceae [XI][G-6], Alloprevotella sp. HMT 473, Fastidiosipila sanguinis, Filifactor alocis, Peptostreptococcaceae [XI][G-4], Bacteriodetes [G-3] bacterium HMT 365, Treponema parvum, Clostridiales [F-1][G-1] bacterium HMT 093, and Orobacterium
Gao et al., 2018 [44] Peri-implantitis PI > HI bHI ≠ PI (Significant difference between groups) c PI: Moraxella, Micrococcus, and AcinetobacterHI: Neisseria, Haemophilus, Prevotella, Streptococcus, Porphyromonas, Clostridium, Capnocytophaga, Leptothrix, Actinomycetes, and Actinomyces
Daubert et al., 2018 [45] Peri-implantitis HI > PI a,b,c PI: Veillonella and Neisseria.
Al-Ahmad et al., 2018 [46] Peri-implantitis Not reported PI: Bacteroidetes (phylum), Fusobacterium nucleatum
Sousa et al., 2016 [47] Peri-implantitisAggressive periodontitis Peri-implant mucositis P > PI a,b,f PI: Propionibacterium, Paludibacterium, Staphylococcus, Filifactor, Mogibacterium, Bradyrhizobium, and Acinetobacter
Sanz-Martin et al., 2017 [20] Peri-implantitis PI > HI c PI: Bacteroides, Spirochetes, and Synergistetes, Tannerella forsythia, Treponema denticola, and Porphyromonas gingivalis, Filifactor alocis, Fretibacterium fastidiosum, and Treponema maltophilum HI: Proteobacteria and ActinobacteriaPI > HI: Porphyromonas (phylum Bacteroidetes), Treponema (phylum Spirochetes), Filifactor (phylum Firmicutes), Fretibacterium (phylum Synergistetes), Tannerella (phylum Bacteroidetes), T. forsythia, P. gingivalis, and T. denticola). HI > PI: Streptococcus (phylum Firmicutes), Veillonella (phylum Firmicutes), Rothia (phylum Actinobacteria), Haemophilus (phylum Proteobacteria) and Neisseria spp.
Apatzidou et al., 2017 [23] Peri-implantitis PI > HI aHI = PI (No significant difference between groups) b HI: Actinobacillus and Streptococcus PI: Prevotella, Porphyromonas, Synergistetes
Yu et al., 2016 [48] Peri-implantitisPeriodontitis PI ≠ HI (Significant difference between groups) f PI: High abundance of F. fastidiosum and Fretibacterium
Shiba et al., 2016 [49] Peri-implantitisSmokingPeriodontitis PI = P (No significant difference between groups) a,g PI ≠ P (Significant difference between groups) c PI = P: High rc-rRNA abundances Porphyromonas gingivalis, Treponema denticola, and Tannerella forsythia
Tsigarida et al., 2015 [50] Peri-implantitisSmokingPeri-implant mucositis HI = PI bHI ≠ PI (Significant difference between groups) c PI: Aggregatibacter, Capnocytophaga, Corynebacterium mucifaciens, Fretibacterium, Lachnoanaerobaculum, Lactobacillus panis, Neisseria, PrevotellaHI: Actinomyces, Alloprevotella, Capnocytophaga, Enterobacter cancerogenus, Fusobacterium gonidiaformans, Fusobacterium, Lactobacillus johnsonii, Neisseria lactamica, Porphyromonas asaccharolytica, Prevotella enoeca, Prevotella, Pseudomonas, Pseudomonas pseudoalcaligenes, SR1 [G-1], Streptococcus, Tannerella
Jakobi et al., 2015 [51] Peri-implantitisPeriodontitis Not reported PI and P: Enterococcus, Streptococcus, Porphyromonas, Fusobacterium, Prevotella, Bacillus, and FretibacteriumExclusive to PI: Neisseria and KingellaExclusive to P: Tannerella, Rothia, Parabacteroides, Parvimonas, and Filifactor HI: Enterococcus, Bacillus, Streptococcus, Fusobacterium, Prevotella, Porphyromonas, Rothia and Proteus
Zheng et al., 2014 [52] Peri-implantitisPeri-implant mucositis PM = PI (No significant differences among groups) f HI > PM fHI > PI f PI > HI a,b,g PI: Leptotrichia hofstadii, Eubacterium infirmum, Kingella denitrificans, Actinomyces cardiffensis, Eubacterium minutum, Treponema lecithinolyticum, and Gemella sanguinis, Gemella sanguinis, Eubacterium minutum, and Actinomyces cardiffensis
Schaumann et al., 2014 [53] Peri-implantitisPeriodontitis PI = P (No significant difference between groups) a PI: Porphyromonadaceae, Lachnospiraceae, and Streptococcaceae; Genera Rothia, Actinomyces, Paenibacillus, Microbacterium, Pseudoramibacter, Leptotrichia, Parascardovia, Tannerella, Granulicatella, Tessaracoccus, Clostridium, Aeromonadales, Veillonella, Capnocytophaga, Prevotella, TG5, Fusobacterium, Exiguobacterium, Enterococcus, Porphyromonas and Streptococcus.
Maruyama et al., 2014 [54] Peri-implantitisPeriodontitis PI = P a,b,c,g (no significant difference) PI: Prevotella nigrescens, Olsenella, Sphingomonas, Peptostreptococcus, and Neisseriaceae P: Peptostreptococcaceae sp. and Desulfomicrobium orale
Tamura et al., 2013 [55] Peri-implantitis Not reported PI: E nodatum, P intermedia, F nucleatum, Filifactor alocis, E brachy, Parascardovia denticolens, Parvimonas micraHI: Veillonella sp., Propionibacterium acnes, Pseudoramibacter alactolyticus, Parvimonas micra
Koyanagi et al., 2013 [21] Peri-implantitisPeriodontitis PI > P a,b PI and P: Firmicutes and Bacteroidetes, Fusobacterium spp. and Streptococcus spp.,Exclusive to PI: Parvimonas micra, Peptostreptococcus stomatis, Pseudoramibacter alactolyticus, and Solobacterium moorei PI > P sites: Dialister spp., Eubacterium spp., Porphyromonas spp., P. gingivalis. PI = P sites: T. forsythia, T. denticola
Dabdoub et al., 2013 [25] Peri-implantitisPeriodontitis P > PI a PI = P: No significant difference in the number of shared species
da Silva et al., 2013 [56] Peri-implantitis Not reported HI: Actinomyces, Atopobium, Gemella, Kingella and Rothia, Campylobacter, Desulfobulbus, Dialister, Eubacterium, Filifactor, Mitsukella, Porphyromonas and Pseudoramibacter. PI > HI: Fusobacterium nucleatum, Dialister invisus, Streptococcus sp. human oral taxon (HOT) 064, Filifactor alocis, and Mitsuokella sp. HOT 131HI > PI: Veillonella dispar, Actinomyces meyeri, and Granulicatella adiacens
Kumar et al., 2012 [22] Peri-implantitisPeriodontitis HI > PI cP > PI a PI: Actinomyces, Peptococcus, Campylobacter, nonmutans Streptococcus, Butyrivibrio, and Streptococcus mutans, B. fibrisolvens
Koyanagi et al., 2010 [57] Peri-implantitisPeriodontitis PI > P a,b PI: Chloroflexi, Tenericutes, and Synergistetes phyla Exclusive to PI: Parvimonas micra, Peptostreptococcus stomatis, Pseudoramibacter alactolyticus, Fusobacterium nucleatum, and Solobacterium moorei Detected in P: Fusobacterium nucleatum, Granulicatella adiacens
Faveri et al., 2010 [58] Peri-implantitis Not reported PI: Archaea detected at significantly higher abundance

PI: Peri-implantitis; HI: healthy implants; P: periodontitis; PM: peri-mucositis. a: Shannon’s index; b: Chao1 index; c: Principal Coordinate Analysis (PCoA); d: permutational multivariate analysis of variance (PERMANOVA); e: InvSimpson’s index; f: weighted Unifrac distance analysis; g: number of operational taxonomic units (OTUs).

Search strategies employed.

Database Search Terms
Medline (Peri-implantiti$ OR Peri adj2 Implantiti$ OR Peri-implant$ adj2 inflam$ OR Peri-implant$ adj2 infect$ OR Peri-implant$ adj2 disease$ OR exp Peri-Implantitis/or exp Dental Implants/or exp Dental Implantation, Endosseous/OR peri-implant adj2 mucositi$ OR peri adj2 implant adj2 mucositi$ OR periimplant adj2 mucositi$ OR periimplant$ adj2 mucos$) AND (exp sequence analysis/or exp sequence analysis, dna/or exp sequence analysis, rna/or exp rna-seq/OR exp RNA, Ribosomal, 16S/OR exp Microbiota/OR exp Bacteria/)
Cochrane (peri-implantiti* OR periimplantiti* OR (Peri-Implantitis):ti,ab,kw OR Peri-implant* NEAR/2 inflam* OR Peri-implant* NEAR/2 infect* OR peri-implant muco*sitis OR peri-implant NEAR/2 disease* OR peri-implant infect* OR MeSH descriptor: [Peri-Implantitis] explode all trees OR periimplant* NEAR/2 mucos*) AND (dental implant* OR dental implant, endosseous OR endosseous dental implant*) AND (MeSH descriptor: [Sequence Analysis, DNA] explode all trees OR MeSH descriptor: [Sequence Analysis] explode all trees OR MeSH descriptor: [Sequence Analysis, RNA] explode all trees OR MeSH descriptor: [RNA-Seq] explode all trees OR MeSH descriptor: [RNA, Ribosomal, 16S] explode all trees OR MeSH descriptor: [Microbiota] explode all trees OR MeSH descriptor: [Bacteria] explode all trees)
Scopus (peri-implant* OR peri W/2 implant* OR peri-implant* W/2 inflam* OR peri-implant* W/2 infect* OR peri-implant* W/2 disease* OR peri-implant W/2 mucositi* OR peri W/2 implant W/2 mucositi* OR periimplant W/2 mucositi* OR periimplant* W/2 mucos*) AND (dental AND implants OR dental AND implantation AND endosseous) AND ((sequence AND analysis) OR (sequence AND analysis AND dna) OR (sequence AND analysis AND rna) OR rna-seq OR (rna AND ribosomal AND 16s)) AND (microbiota OR bacteria)

ti: Title; ab: Abstract; kw: Keywords; exp: Explode.

Inclusion and exclusion criteria used for the studies screened.

Inclusion Criteria Exclusion Criteria
Observational and case-control studies investigating the microbiome of peri-implant tissues through next-generation DNA sequencing methods.Human studies in English Culture-based studies, conference papers, review articles, studies regarding peri-implantitis associated with other systematic factors (diabetes mellitus, immune disorders, etc.) Articles that examined only specific microorganisms. Non-English language articles and research conducted on non-human specimens.

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Abstract

(1) Introduction: Current evidence shows that mechanical debridement augmented with systemic and topical antibiotics may be beneficial for the treatment of peri-implantitis. The microbial profile of peri-implantitis plays a key role in identifying the most suitable antibiotics to be used for the treatment and prevention of peri-implantitis. This systematic review aimed to summarize and critically analyze the methodology and findings of studies which have utilized sequencing techniques to elucidate the microbial profiles of peri-implantitis. (2) Results: Fusobacterium, Treponema, and Porphyromonas sp. are associated with peri-implantitis. Veillonella sp. are associated with healthy implant sites and exhibit a reduced prevalence in deeper pockets and with greater severity of disease progression. Streptococcus sp. have been identified both in diseased and healthy sites. Neisseria sp. have been associated with healthy implants and negatively correlate with the probing depth. Methanogens and AAGPRs were also detected in peri-implantitis sites. (3) Methods: The study was registered with the International Prospective Register of Systematic Reviews (PROSPERO) (CRD42023459266). The PRISMA criteria were used to select articles retrieved from a systematic search of the Scopus, Cochrane, and Medline databases until 1 August 2023. Title and abstract screening was followed by a full-text review of the included articles. Thirty-two articles were included in the final qualitative analysis. (4) Conclusions: A distinct microbial profile could not be identified from studies employing sequencing techniques to identify the microbiome. Further studies are needed with more standardization to allow a comparison of findings. A universal clinical parameter for the diagnosis of peri-implantitis should be implemented in all future studies to minimize confounding factors. The subject pool should also be more diverse and larger to compensate for individual differences, and perhaps a distinct microbial profile can be seen with a larger sample size.

Details

Title
The Microbiome of Peri-Implantitis: A Systematic Review of Next-Generation Sequencing Studies
Author
Koay Chun Giok 1 ; Rohit Kunnath Menon 2   VIAFID ORCID Logo 

1  School of Dentistry, International Medical University, Kuala Lumpur 57000, Malaysia; [email protected] 
2  College of Dentistry, Ajman University, Ajman 346, United Arab Emirates 
First page
1610
Publication year
2023
Publication date
2023
Publisher
MDPI AG
e-ISSN
20796382
Source type
Scholarly Journal
Language of publication
English
DOI
https://doi.org/10.3390/antibiotics12111610
ProQuest document ID
2892949423
Copyright
© 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.