- Research article
- Open Access
Comparison of microbial diversity determined with the same variable tag sequence extracted from two different PCR amplicons
- Yan He†1,
- Ben-Jie Zhou†2,
- Guan-Hua Deng1,
- Xiao-Tao Jiang1,
- Hai Zhang3 and
- Hong-Wei Zhou1Email author
© He et al.; licensee BioMed Central Ltd. 2013
- Received: 6 January 2013
- Accepted: 12 September 2013
- Published: 14 September 2013
Deep sequencing of the variable region of 16S rRNA genes has become the predominant tool for studying microbial ecology. As sequencing datasets have accumulated, meta-analysis of sequences obtained with different variable 16S rRNA gene targets and by different sequencing methods has become an intriguing prospect that remains to be evaluated experimentally.
We amplified a group of fecal samples using both V4F-V6R and V6F-V6R primer sets, excised the same V6 fragment from the two sets of Illumina sequencing data, and compared the resulting data in terms of the α-diversity, β-diversity, and community structure. Principal component analysis (PCA) comparing the microbial community structures of different datasets, including those with simulated sequencing errors, was very reliable. Procrustes analysis showed a high degree of concordance between the different datasets for both abundance-weighted and binary Jaccard distances (P < 0.05), and a meta-analysis of individual datasets resulted in similar conclusions. The Shannon’s diversity index was consistent as well, with comparable values obtained for the different datasets and for the meta-analysis of different datasets. In contrast, richness estimators (OTU and Chao) varied significantly, and the meta-analysis of richness estimators was also biased. The community structures of the two datasets were obviously different and led to significant changes in the biomarkers identified by the LEfSe statistical tool.
Our results suggest that beta-diversity analysis and Shannon’s diversity are relatively reliable for meta-analysis, while community structures and biomarkers are less consistent. These results should be useful for future meta-analyses of microbiomes from different data sources.
- Microbial diversity
- V46 hypervariable region
- V6 hypervariable region
- 16S rRNA gene
Determining 16S rRNA gene tag sequences using next generation sequencing (NGS) techniques, mainly the 454 and Illumina system platforms, has become a revolutionary tool in the field of microbiome research [1–4]. The major advantages of NGS methods are high-throughput capabilities and cost-effectiveness. Thousands of sequences per microbiome sample can be obtained easily, and hundreds to thousands of samples can be sequenced simultaneously . However, the sequencing lengths obtained by NGS are shorter than those obtained by the Sanger sequencing method, and only part of the 16S rRNA gene spanning one or more of the nine hypervariable regions can be determined . The first published study using NGS to study microbiomes determined the V6 tag of the 16S rRNA gene, and this region was short enough to be analyzed by the 454 Genome Sequencer 20 system at that time . With the improvement of NGS techniques, sequencing lengths have grown to hundreds of bases per read, with even longer tags expected in the near future . Although the short tag has proven useful for taxonomy assignment , longer tags may provide higher resolution for differentiating microbes and better taxonomy results. Until now, there has been no standard or best choice for choosing the variable regions, and researchers have historically determined diverse variable regions with varied sequencing lengths both within and across labs [3, 4, 8–10].
One of the major advantages of using DNA sequences to analyze microbiome diversity is that sequencing data obtained from different studies can be analyzed together, constituting a more cumulative approach than comparing DNA fingerprinting results . However, if and how datasets from different sequencing projects can be combined for meta-analysis has not been evaluated because few studies have sequenced and compared actual microbiome samples processed by different experimental methods. One of the most straightforward ideas is to use the same variable region for different PCR amplicons and extract sequences of that specific region from different studies for direct comparison. Theoretically, the same tag region allows for a consistent clustering of operational taxonomic units (OTUs) and taxonomy assignment; therefore, subsequent parameters, including α- and β-diversities and community structures, can be analyzed. However, experimental conditions such as primer bias and sequencing quality might affect these analyses . Until now, there have been no reports addressing this approach by amplifying real samples with different primers and extracting the same variable tag for direct comparison. In this study, we determined a total of 28 fecal microbiome samples from four individuals and amplified each sample independently with two primer sets (V4F-V6R and V6F-V6R). We analyzed the α-diversity, β-diversity, microbial community structure, and biomarkers and focused on the following two questions: First, do the results from the two datasets agree with one another? Second, can the two datasets be combined to produce reliable results? The present study provides useful information for evaluating the feasibility of meta-analysis for the study of microbiomes.
This study was approved by the Ethical Committee of Southern Medical University, and all participants provided written informed consent.
Sample processing and sequencing
Fecal samples were obtained from four individuals. For each individual, one sample was collected every two days for a period of two weeks. All of the samples were stored at -80°C until DNA extraction, and 200 mg of each sample was used for DNA extraction. DNA was extracted using the PowerSoil DNA kit (MoBio, USA) according to the manufacturer’s instructions. The high fidelity ExTaq cocktail (Takara, China) was used to amplify the 16S rRNA gene tags. Each DNA sample was amplified by 2 barcoded primer sets, one of which included the primers V4F 5′ GTGCCAGCMGCCGCGGTAA 3′ and V6R 5′ ACAGCCATGCANCACCT 3′, while the other included the primers V6F 5′ CNACGCGAAGAACCTTANC 3′ and V6R 5′ ACAGCCATGCANCACCT 3′. The PCR conditions included an initial denaturation step at 94°C for 2 min, 25 cycles of 94°C for 30 s, 52 ~ 59°C for 30 s and 72°C for 30 s, and a final extension at 72°C for 5 min. Each 25-μl reaction consisted of 2.5 μl of Takara 10× Ex Taq Buffer (Mg2+ free), 2 μl of dNTP Mix (2.5 mM), 1.5 μl of Mg2+ (25 mM), 0.25 μl of Takara Ex Taq DNA polymerase (2.5 units), 1 μl of template DNA, 0.5 μl of 10 μM barcode primer 967 F, 0.5 μl of 10 μM primer 1406R, and 16.75 μl of ddH2O. The two PCR products were sequenced independently in two sequencing batches at the Beijing Genomic Institute using paired-end sequencing with an Illumina HiSeq 2000 platform, and 101 bp were sequenced from each end. The sequences have been deposited in the sequence read archive (SRA) with accession number from ERS346316 to ERS346371.
Sequence processing and analysis
We wrote a Perl script to separate tags according to their barcodes with the following steps: the primer region of each tag was first identified with no mismatches allowed; tags which failed to match primers were replaced by their reverse complements, and the primer region was identified again; the barcodes (region before the primer) and target V6 region (region after the primer) were stored for each tag; tags were separated according to their barcodes, and tags without any matching samples were discarded. For quality control purposes, no mismatches were allowed in the primer or barcode regions (see above). Furthermore, we removed tags with ambiguous bases (N) and screened potential chimeras with UCHIME (de novo mode, parameters set as follows: --minchunk 20 --xn 7 –noskipgaps 2 . To unify the target region of the tags from the two primer sets, we extracted the V6 region of each tag by cutting 60 bp from the right end of the sequences from V6R primers (960 bp to 1,028 bp in E. coli). To avoid the effects of different sequencing depths, all samples were normalized to 5,000 sequences for subsequent analyses. We calculated the Good’s coverage of each sample at this depth. The formula used was , where C is the Good’s coverage, n is the number of OTUs with only one tag per sample, and N is the number of all tags in that sample. TSC was used to cluster the tags into OTUs, with the similarity threshold set to 0.97 . GAST was used to assign these sequences into taxa with the V6 database . The α-diversity indices, including Chao, Ace, Shannon and observed OTUs, were calculated using the MOTHUR . PCA was implemented using QIIME based on the Jaccard distance . LEfSe was used to determine the biomarkers with LDA = 3 . Statistical analysis was performed using SigmaPlot 12.0.
Illumina paired-end sequencing results
In total, we determined 417,821 tags with the V4F-V6R primer set (an average of 14,992 tags per sample) and 756,514 tags with the V6F-V6R primer set (an average of 27,018 tags per sample). We discarded tags with mismatches in the primer regions, which reduced the total number of tags to 306,328 for the V4F-V6R dataset (an average of 10,940 tags per sample) and to 715,634 for the V6F-V6R dataset (an average of 25,558 tags per sample). More sequences were discarded from the V4F-V6R than the V6F-V6R dataset, indicating that the sequencing quality of the V4F-V6R dataset was inferior to that of the V6F-V6R. This difference in sequencing quality affected the α-diversity estimations, which will be discussed below. Secondly, we screened the chimeras with UCHIME. Because the sequencing of 101 bp from both ends could not sequence through the whole V4 to V6 region of the 16S rRNA, we linked each pair of tags with 30 Ns to allow screening of the chimeras. After this step, we acquired 263,127 tags from the V4F-V6R primer set (an average of 9,398 tags per sample) and 714,938 tags from the V6F-V6R primer set (an average of 25,533 tags per sample). Once again, many more chimeras were found with the V4F-V6R than the V6F-V6R dataset. This result is reasonable, as the V4 to V6 region (approximately 550 bp) is much longer than the V6 region (approximately 65 bp) and spans conservative sequences in the 16S rRNA, thus being more likely to form chimeras during the process of PCR amplification . Finally, to unify the region and length of the tag, the same 60 bp sequence next to the V6R primer was extracted from both primer sets. To avoid the influence of different sequencing depths, we rarefied all samples to 5,000 tags for a consistent sequencing depth. The Good’s coverage of all samples with 5,000 tags was higher than 0.95 with 0.96 ± 0.005 (mean ± SEM) for samples from the V4F-V6R datasets and 0.98 ± 0.004 for the V6F-V6R datasets, indicating that the sequencing depth was sufficient for reliable analysis of these fecal microbial community samples. Based on these data, analyses including α-diversity (within-community diversity), β-diversity (between-communities diversity), microbial structure and biomarker determination were evaluated, as they are fundamental for microbiome research.
In addition to the quality filtering results, four external standards were sequenced simultaneously with each of the two libraries for a direct comparison of the sequencing quality. The external standards were samples with only one known cloned sequence as the PCR template, and the accuracy was checked at each base position. By comparing the sequencing results of the external standards with the known sequence, we could, to some extent, evaluate the sequencing quality of the library. All external standards were also filtered to remove ambiguous bases (N) and chimeras as above. As shown in Additional file 1: Figure S1, the proportion of sequences which have 100% identity with the external standard in the V6F-V6R library was higher than that of the V4F-V6R library (0.939 vs. 0.879, t-test, P < 0.001), while the proportion of error sequences was significantly lower in the V6F-V6R than the V4F-V6R library, indicating that the sequencing quality of the former was superior to that of the latter.
Not surprisingly, the meta-analysis of species richness was significantly biased by the data source. For example, if we chose sequences from the V4F-V6R dataset for individuals A and B and sequences from the V6F-V6R dataset for individuals C and D (simulating a situation where sequences are obtained by various methods from individuals A and B in one experiment and from individuals C and D in another experiment prior to combination of the data), then A and B had much higher species richness estimates than C and D, a result which actually reflects differences in the generation of the two datasets (sequencing and PCR errors) rather than the diversity of the samples. Although we used the same HiSeq 2000 instrument for both of the datasets, the sequencing quality of the two sequencing batches was obviously different. For those datasets preserved in databases, individuals using various 454 and Illumina instruments obtained different sequencing qualities, a factor which is problematic for meta-analysis of richness estimates.
In contrast, Shannon’s diversity index showed no significant difference between the two datasets (3.77 ± 0.10 for V4F-V6R versus 4.06 ± 0.06 for V6F-V6R, P = 0.056), indicating that this index was more stable than the richness estimators and more reliable for comparison across various studies. In addition, we randomly changed the bases of these sequences to simulate sequencing errors rates of 0.1% and 1% to evaluate the effect of sequencing errors on the estimation of alpha indices. The results demonstrated that at an error rate of 0.1%, all indices including the richness estimates and Shannon index were hardly influenced (One Way ANOVA on ranks, P < 0.05, Dunn’s test for pair-wise comparisons between 0% error rate and 0.1% error rate, P > 0.05), but raising the error rate to 1% inflated the species richness estimates significantly (One Way ANOVA on ranks, P < 0.05, Dunn’s test for pair-wise comparisons between 0% error rate and 1% error rate: ACE, 546 vs. 2435, P < 0.05; Chao1, 886 vs. 3680, P < 0.05; observed species, 285 vs. 577, P < 0.05). By comparison, although the Shannon index was also inflated (5.37 vs. 5.90, P < 0.05), the extent of inflation was much smaller than that of the species richness estimators, and no significant differences were observed between the two datasets (Additional file 1: Figure S3). The explanation for this result is that Shannon diversity index depends more on highly abundant OTUs compared to species richness estimates , is consequently less sensitive to sequencing errors and was therefore able to produce similar values for both of the datasets in the present study. In support of this theory, we found in a recent study  that Shannon diversity index of freshwater and marine sediments were comparable across multiple studies.
PCA using the Jaccard distances
Subsequently, we combined all sequences from these two datasets to simulate a meta-analysis (Figure 2c, d). PCA of both binary and abundance-weighted Jaccard distances demonstrated that the pooled analysis resulted in almost the same clustering as the single dataset, and the points from the two data sources could hardly be differentiated, suggesting that meta-analysis using the Jaccard distance is relatively stable across different PCR and sequencing runs. To further understand the effect of sequencing errors on PCA, we performed procrustes analysis with the original datasets vs. datasets with simulated base error rates of 1% (Additional file 1: Figure S4). All pair-wise comparisons show that sequencing errors did not greatly affect the PCA based on the Jaccard distance, in support of our conclusions detailed above.
Microbial composition and biomarker determination
For the purposes of meta-analysis, PCA using both the binary and abundance-weighted Jaccard distance is reliable, and Shannon diversity index is also relatively stable across different studies. However, the richness estimators, especially those depending primarily on rare tags (e.g., Chao and ACE) are significantly affected by the experimental procedures unique to individual studies. The community structure, especially the relative abundance, also varies significantly between different datasets. Biomarkers between different groups are comparable between multiple experiments if the input data for the LEfSe analysis is obtained from a single experiment, but meta-analyses using combined datasets should be performed cautiously. In the present study, we only take into account primer bias and sequencing quality, and their effect on microbiota analyses from combined studies, variations in the experimental procedures of different laboratories could also affect the meta-analyses. Additional studies verifying the PCR conditions, particularly the enzyme system, DNA extraction, DNA storage effect, etc., are needed in future.
This work was supported by the National Natural Science Foundation of China (NSFC 31270152, 31322003), the COMRA project (DY125-15-R-01), the Program for New Century Excellent Talents in University (NCET-11-0921), the Guangdong Natural Science Foundation (No. S2011010004136), and the Educational Commission of Guangdong Province of China (2012KJCX0031).
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