Introduction
It is well known that by the age of 5 years, primary dentition is fully established and relatively stable. The 4
th National Oral Health Survey in mainland China in 2018 [
1] revealed that in the past decade, the prevalence of dental caries in young children in China was not optimistic, and the prevalence rate showed an upward trend. The prevalence rate of dental caries in 5-year-old children was 71.9%, which was 5.8% higher than that 10 years ago. The average number of caries per child was 4.24, but the number of teeth filled due to caries was only 4.1%. Currently, the etiology of dental caries that has been accepted by most scholars is the theory of four main factors, in which bacteria play a crucial role in the initiation of dental caries.
Dental caries is defined as dysbiosis rather than a chronic infectious disease. In 1994, Marsh [
2] proposed the ecological plaque hypothesis. They found that due to changes in the oral environment, such as changes in sugar intake, diet or pH value, the relatively balanced bacterial composition in the biofilm can change remarkably, which shifts the microbiome toward cariogenic bacteria. For example, in a low pH environment, the proportion of potential cariogenic bacteria such as
Streptococcus mutans and
Lactobacilli will increase, which may break the ecological balance of the oral microbial community, leading to dental caries. This hypothesis proposes that both microorganisms and the environment are factors that induce dental caries [
3]. All found cariogenic bacteria are normal flora in the mouth, which are interdependent and maintain a dynamic balance. When the environment changes, the ecological balance of microorganisms in dental plaque, tooth surface and environment is broken, causing dental caries. Dr. Marsh proposed that dental caries can be prevented not only by targeting cariogenic bacteria but also by interfering with the process of breaking the ecological balance. Takahashi et al. [
4] proposed that the cariogenic microenvironment is a microenvironment that transitions from the dynamic stability stage to the acid production stage and finally develops to the acid resistance stage. The occurrence and development of dental caries result from an imbalance in the microbial community.
Strong evidence exists that during the development of healthy individuals, oral microbial communities change dynamically, and the oral microbiome changes physiologically. Microbial composition is specific in different age groups. In addition to Streptococcus mutans, many types of bacteria, such as Veillonellales, Actinomyces, Granulosicoccus, Leptotrichia, Thiomonas, Bifidobacterium and Prevotella, are closely related to dental caries. The imbalance of oral microbial communities may be an important mechanism of dental caries. In this study, we performed Illumina Novaseq sequencing to investigate the diversity and structure of microbial communities in saliva samples from 5-year-old children with versus without dental caries. Findings from this study will help understand the microbial etiology of dental caries in 5-year-old children and provide evidence for developing novel methods to prevent and treat dental caries.
Materials and methods
Subject selection
Patients with high caries and no caries were recruited from the same kindergarten in Yubei District of Chongqing, China. The inclusion criteria of subjects are as follows: (i) ages 54 to 66 months; (ii) no upper respiratory infections in the past fortnight; (iii) no antibiotic use in the past 2 months; (iv) no partial denture and appliance, and (v) no history of systemic diseases, oral diseases and dental treatments. Eighteen high caries (decayed, missing and filled teeth (dmft) index ≥ 6) participants and 18 no caries (dmft = 0) participants were finally selected. The definitions and diagnoses of dental caries are based on the criteria of the World Health Organization [
5]. All participants underwent a comprehensive oral examination from a specialized dentist. These participants’ parents or grandparents were sufficiently informed about the aims of the research and signed the written informed consent provided by the Ethics Committee of the Stomatological Hospital of Chongqing Medical University.
Sample collection
Before the samples of all participants were taken, sterile water was used to rinse their mouths, and they were not allowed to eat, drink or brush their teeth for 2 h. A specialized dentist collected their unstimulated saliva, placed it into 1.5-mL sterile microcentrifuge tubes, and froze it at -80 °C for further use.
Based on the manufacturer’s protocol, microbial DNA was extracted from all specimens by the PowerSoil® DNA Isolation Kit. Primers 338F (5′-ACTCCTACGGGAGGCAGCAG-3′) and 806R (5′-GGACTACHVGGGTWTCTAAT-3′) were used to amplify the V3-V4 hypervariable regions of the bacterial 16S rRNA gene using PCR on the Veriti 96-Well Thermal Cycler (GeneAmp 9902, ABI, USA). Target area PCR was conducted with the following program: initial denaturation at 98 °C for 2 min, 30 cycles of denaturation at 98 °C for 30 s, annealing at 50 °C for 30 s, elongation at 72 °C for 60 s, and a final extension at 72 °C for 5 min, followed by storage at 4 °C. Target area PCR was performed in triplicate with a 30 µL mixture containing 15 µL of KOD FX Neo Buffer, 6 µL of dNTPs (2 mM each), 0.9 µL of Vn F (10 µM)/Vn R (10 μM), 0.6 µL of KOD FX Neo and 50 ng ± 20% of template DNA. Solexa PCR was conducted with the following program: initial denaturation at 98 °C for 30 s, 10 cycles of denaturation at 98 °C for 10 s, annealing at 65 °C for 30 s, elongation at 72 °C for 60 s, and a final extension at 72 °C for 5 min.
Solexa PCR was performed in triplicate with a 20-µL mixture containing 5 µL of target area PCR products, 10 µL of 2 × Q5 HF MM, and 2.5 µL of MPPI-a (2 µM)/MPPI-b (2 μM).
The final PCR products were extracted from a 1.8% agarose gel under a voltage of 120 V. Forty minutes later, overcolumn purification was performed using an OMEGA DNA purification column. The PCR products were purified, quantified, and homogenized to form a sequencing library. The built libraries were first subjected to library quality inspection, and the qualified libraries were sequenced by Illumina NovaSeq 6000 PE250.
Processing of sequencing data [6]
Primary FastQ files were divided into multiple files for processing and quality-filtered by Trimmomatic [
7]. The following standards were used for sequence combination. (i) The reads were cut off when meeting any site with an average quality score < 20 over a 50 bp sliding window. (ii) The primers were perfectly matched, allowing the mismatch of two nucleotides, and reads with ambiguous bases were not allowed. (iii) Sequences with overlap longer than 10 bp were merged based on their overlap sequence.
Using USEARCH [
8] (version 10.0), operational taxonomic units (OTUs) were clustered with a 97% similarity cut off. Additionally, chimeric sequences were recognized and deleted by UCHIME (version 8.1) [
9]. By comparing the RDP Classifier algorithm [
10] (version 2.2,
http://sourceforge.net/projects/rdpclassifier/) against the Silva [
11] 16S rRNA (Release128,
http://www.arb-silva.de) database, the taxonomy of each 16S rRNA gene sequence was analyzed based on an 80% confidence threshold.
Bioinformatics analysis was conducted using QIIME. The alpha diversity indices of Shannon, Simpson, Chao, ACE and PD_whole_tree were calculated at 97% identity by Mothur [
12] version v.1.30. Beta diversity analysis was performed by principal coordinate analysis (PCoA) based on Bray–Curtis distances at the OTU level. A hierarchical clustering analysis based on weighted UniFrac distances was also conducted [
13]. Analysis of similarities (ANOSIM) was performed using the vegan package in the R language and drawn with Python; unweighted UniFrac distances were used to compare different groups. Welch’s
t-test was used to compare the relative abundance of predominant bacteria between different groups. A Venn diagram was used to define the core microbiome at the species level using Mothur [
12]. Linear discriminant analysis of effect size (LEfSe) was conducted to define the biomarkers of the two groups. The threshold on the logarithmic LDA score for distinguishing features was set to 3 [
14]. Co-occurrence analysis among the genera was performed with Python, and co-occurrence analysis of the 80 richest genera of each group was performed at the same time. The phylogenetic investigation of communities by reconstruction of unobserved states (PICRUSt2) program was used to predict 16S rRNA-based data from high-throughput sequencing and to further analyze the composition and differential of the Kyoto Encyclopedia of Genes and Genomes (KEGG) [
15] metabolic pathway in the context of IMG microbial genome data. BugBase normalizes the OTU by the predicted 16S copy number and then predicts the microbial phenotype [
16] using the provided precomputed files. Differences were considered significant when
P < 0.05 and extremely significant when
P < 0.01. SPSS 25.0 software (SPSS Inc., Chicago, IL, USA) was used for statistical analysis. The raw data will be made available by the authors without undue reservation to any qualified researcher.
Discussion
Bacteria in dental biofilms are considered to be essential in the occurrence and development of dental caries [
2,
17]. To comprehensively study the oral microbiome and understand its etiology, high-throughput technology is an effective method to study the composition and structure of microbial communities related to health and disease.
Previous studies have helped us to increase our understanding of microbial compositions at different ages. Some researchers found that
Firmicutes was lower and
Proteobacteria was higher in children than in adolescents and adults, while the conclusions were completely opposite in adolescents and adults [
18]. According to a previous study [
19], it is generally believed that microorganisms attached to the surface of teeth and mucous membranes continue to flow into saliva, making it the repository of oral microbial communities and a "fingerprint" of all oral microbiota. Findings of this study in which saliva samples were used will help us to comprehensively understand the microbial communities associated with early childhood dental caries.
Previous studies have reported that when dental caries occurs, the alpha diversity of microbial communities in the mouth will decrease [
20,
21]. In contrast, the alpha diversity of microbial communities measured in this study demonstrated that the diversity and abundance of microbial communities were similar between the high caries and no caries groups. This is also supported by the results of a previous study [
22]. It is speculated that the reason for the inconsistent results between different studies may be attributed to a certain extent to the choice of subjects. The subjects in this study have high homogeneity. All subjects lived in the same area and had similar diets and lifestyles. Although their salivary microbial communities have certain differences in species composition, their microbial diversities are highly similar.
The detected OTUs were distributed among 16 phyla, 26 classes, 56 orders, 93 families, 173 genera, and 218 species. Phyla mainly included
Firmicutes, Bacteroides, Proteobacteria, Actinobacteria, Fusobacteria,
Patescibacteria, Epsilonbacteraeota, Cyanobacteria, Acidobacteria and
Spirochaetes. These results are similar to previous findings [
23,
24]. This indicates that the microbial community structure in the mouth is relatively stable. It can be seen from the community bar graph that the microbial community structure in the high caries group was similar to that in the no caries group. This indicates that the disease state may not have a remarkable impact on bacterial composition.
At the genus level, the most popular bacteria in the two groups were basically the same, but the relative abundances were different.
Prevotella is often detected in the study of caries-related microorganisms in children, and
Prevotella is considered to be used as a marker to detect caries in young children [
25].
Prevotella is a gram-negative bacterium of the
Bacteroidetes phylum that has been considered a potential periodontal pathogen for a long time. Its role in dental caries has been recognized in a recent study [
26]. However, in this study,
Prevotella was higher in the no caries group than in the high caries group. This finding supports the "ecological plaque hypothesis", which states that dental caries is the result of the destruction of the steady state of resident microorganisms rather than the activity of specific microorganisms [
27].
LEfSe shows different groups of potential biomarkers. Among these remarkably different genera,
Propionibacterium showed higher abundance in the high caries group than in the no caries group. Xiao et al. [
28] isolated
Propionibacterium from human caries. They found that the main terminal metabolites of
Propionibacterium are a large amount of propionic acid and acetic acid, as well as an appropriate amount of succinic acid.
Streptococcus mutans is a type of
Streptococcus that is recognized as one of the main cariogenic bacteria; however, in this study, no differences in
Streptococcus mutans were found between the high caries and no caries groups. Agnello et al. [
29] found that the oral microbial communities in Aboriginal children with severe early childhood caries were remarkably different from those in children with no caries. In addition, they detected extremely abundant
Streptococcus mutans in the microbial plaque of children with severe early childhood caries. However, due to different population characteristics and analysis methods, some scholars also found that the relative abundance of
Streptococcus in the microbial plaque decreased when caries occurred [
18]. In many healthy subjects, the content of
Streptococcus mutans was higher than that detected in patients with white spot lesions and dentin caries lesions [
21,
30]. A high abundance of
Streptococcus mutans does not always exist in the microbial plaque of patients with different degrees of caries [
31]. The percentage of high abundance of
Streptococcus mutans in the microbial community is not linearly correlated with the progress of caries from healthy teeth to deep caries [
21]. Therefore, some scholars believe that the level of
Streptococcus mutans is not significantly correlated with the severity of caries [
32]. Epidemiological and caries risk assessment data also show that in recent decades, the use of caries preventive methods taking
Streptococcus mutans as the main target has had little effect.
Network analysis showed the potential correlation of oral microbiota with dental caries. Different groups show different bacterial interactions. The relationship between oral microbial communities in the no caries group was more complex than that in the high caries group. This finding indicates that some microbial relationships may be destroyed, leading to ecological imbalance and resulting in the development of caries. This is consistent with the finding from a previous study [
33].
In this study, we analyzed the function of the salivary microbial community in 5-year-old children from Chongqing, China. We found that when the function of the salivary microbial community was class 3, Mineral absorption gene clusters were concentrated in saliva of children without caries. The possible reason is that the occurrence of dental caries is related to tooth mineralization. The microorganisms in the saliva of children without caries can promote the active absorption of minerals, resist the damage of acid to tooth enamel and the loss of minerals, thus preventing the occurrence of caries. Wang et al. [
34] found that the functional difference between children with high caries and no caries was mainly reflected in carbohydrate metabolism. Liu et al. [
35] studied the microbial function in deep dentinal carious lesions and found that carbohydrate metabolism and amino acid metabolism drive the occurrence of caries. However, no differences in carbohydrate and amino acid metabolism were found in this study. These findings suggest that in addition to further investigating the products of functional genes of carbohydrate and amino acid metabolism and analyzing the role of carbohydrates in oral flora metabolism, other metabolic pathways, such as mineral absorption, can provide a new entry point for etiology research, prevention and risk assessment of dental caries.
BugBase analysis showed that there was a phenotypic difference in Facultatively_Anaerobic between the high caries and no caries groups. The obtained results also showed that at the genus level,
Streptococcus was the main factor that caused the increase in Facultatively_Anaerobic in the high caries group. Previous studies have fully revealed the role of
Streptococcus in the occurrence and development of dental caries [
36,
37]. However, there was no significant difference in the content of
Streptococcus between the high caries and no caries groups. This finding was also supported by the results of other relevant studies [
38‐
40]. It is speculated that this result occurs possibly because
Streptococcus contains many bacterial species, such as
Streptococcus mutans,
Streptococcus sanguinis,
Streptococcus oralis,
Streptococcus sobrinus, and
Streptococcus mitis. These bacterial species play different roles in the occurrence of caries; thus, the relative contents may have different trends in the occurrence and development of dental caries, resulting in the stability of the overall content of
Streptococcus. The mouth, as part of the digestive system, is located at the beginning of the whole system, and it is in direct contact with the external environment. Therefore, the overall composition of oral microbial communities shows a high degree of dynamics [
41]. Temperature, pH, salinity, redox potential, and the acquisition of oxygen or nutrients also have a certain impact on microbes. Under normal conditions, the microbial community present in the mouth can resist the invasion and colonization by alien species; thus, it can regulate local and systemic health. On the other hand, the imbalance of the microbial community may lead to oral diseases such as common dental caries and periodontal disease [
42,
43]. According to the "ecological plaque hypothesis", dental caries results from the disruption of the normal microbial community balance due to changes in the oral environment [
3]. The results of this study once again show that the microbial changes involved in dental caries are more complex than expected. The occurrence of dental caries is not caused by a specific bacterium, but the structure of microbial communities among all microorganisms in the mouth has changed [
3]. The eruption of permanent teeth and the increase in age will affect oral microorganisms [
30,
44]; therefore, the study of the oral microbiome should be based on age. To exclude the influence of age, in this study, we selected only 5-year-old children as subjects. To try to control the effect of the external environment on saliva samples, we only selected saliva samples of children living in the same area. We investigated the microbial communities in saliva samples from 5-year-old children with versus without dental caries and provided evidence for the diagnosis and prevention of dental caries in 5-year-old children from the perspective of microbiology. However, the sample size is slightly small. Moreover, saliva samples are affected by various factors, such as environmental factors and dietary factors, resulting in inconsistencies between the results of this study and other research results. Therefore, it is necessary to increase the sample size to further discuss and validate the results of this study.
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