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Article

Phylotypic Diversity of Bacteria Associated with Speleothems of a Silicate Cave in a Guiana Shield Tepui

by
Qi Liu
1,†,
Zichen He
1,†,
Takeshi Naganuma
1,*,
Ryosuke Nakai
2,
Luz María Rodríguez
3,4,
Rafael Carreño
3,5 and
Franco Urbani
3,6
1
Graduate School of Integrated Science for Life, Hiroshima University, 1-4-4 Kagamiyama, Higashi-Hiroshima 739-8528, Japan
2
Bioproduction Research Institute, National Institute of Advanced Industrial Science and Technology, 2-17-2-1 Tsukisamu-Higashi, Toyohira, Sapporo 062-8517, Japan
3
Venezuelan Society of Speleology, Apartado 47.334, Caracas 1041-A, Venezuela
4
Venezuelan Foundation for Seismological Research, Apartado 76.880, Caracas 1070-A, Venezuela
5
Venezuelan Institute for Scientific Research, San Antonio de los Altos, Miranda 1020-A, Venezuela
6
Department of Geology, Central University of Venezuela, Caracas 1050, Venezuela
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Microorganisms 2022, 10(7), 1395; https://doi.org/10.3390/microorganisms10071395
Submission received: 25 April 2022 / Revised: 21 June 2022 / Accepted: 7 July 2022 / Published: 11 July 2022
(This article belongs to the Special Issue Feature Collection in Environmental Microbiology Section 2021-2022)
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Abstract

:
The diversity of microorganisms associated with speleological sources has mainly been studied in limestone caves, while studies in silicate caves are still under development. Here, we profiled the microbial diversity of opal speleothems from a silicate cave in Guiana Highlands. Bulk DNAs were extracted from three speleothems of two types, i.e., one soft whitish mushroom-like speleothem and two hard blackish coral-like speleothems. The extracted DNAs were amplified for sequencing the V3–V4 region of the bacterial 16S rRNA gene by MiSeq. A total of 210,309 valid reads were obtained and clustered into 3184 phylotypes or operational taxonomic units (OTUs). The OTUs from the soft whitish speleothem were mostly affiliated with Acidobacteriota, Pseudomonadota (formerly, Proteobacteria), and Chloroflexota, with the OTUs ascribed to Nitrospirota being found specifically in this speleothem. The OTUs from the hard blackish speleothems were similar to each other and were mostly affiliated with Pseudomonadota, Acidobacteriota, and Actinomycetota (formerly, Actinobacteria). These OTU compositions were generally consistent with those reported for limestone and silicate caves. The OTUs were further used to infer metabolic features by using the PICRUSt bioinformatic tool, and membrane transport and amino acid metabolism were noticeably featured. These and other featured metabolisms may influence the pH microenvironment and, consequently, the formation, weathering, and re-deposition of silicate speleothems.

1. Introduction

Bacterial communities exist in every ecosystem on Earth, and the species compositions of the communities can be adjusted to adapt to various environmental conditions, including caves, as shown by culture-independent pyrosequencing [1]. Bacterial diversity and metabolic strategies in cave ecosystems can improve the comprehension of the biodiversity of different ecosystems around the world, as demonstrated by a metagenomic approach [2]. Although high microbial diversity in caves has been revealed by, for example, clone-by-clone sequencing [3,4], cave microbial communities are still among the least studied [5]. Cave microbial communities are affected by rock types and surface-soil richness/poorness, resulting in various geochemical and hydrochemical features of cave streams, such as pH, organic/inorganic nutrient availability, and buffering action [6,7]. On the other hand, cave microbial communities are likely involved in the formation of various geological forms, such as stalactites in limestone caves [8] and “champignons”, i.e., mushroom-like white speleothems, uniquely found in silicate caves [9]. The roles of microorganisms have been well studied but perhaps are still poorly understood [10].
Silicate caves have been discovered in 1972 in the table mountains, or tepuis, in Guiana Highlands in South America, especially in southeastern Venezuela and western Guiana [11,12,13,14,15,16,17]. Tepuis are table mountains or mesetas composed of Paleoproterozoic quartzites and sandstones, surrounded by steep cliffs [18]. In the process of exploring these isolated environments, karst structures with numerous cave systems and unique silica deposits have been found [15,19]. Due to long-term weathering and water erosion, a variety of silicate speleothems have been formed inside tepui caves. At present, three sets of the world’s largest cave systems in quartzites have been found: one of them in the most popular Roraima-tepui [11,20]; another in the Auyán-tepui, which is known for the world’s tallest waterfall, i.e., 979 m high Angel Fall or Kerepakupai Merú [21]; and the third in the Churi-tepui in the Chimantá massif, Venezuela [14]. Other complex networks of underground passages have been found but mainly with deep vertical development; in this case, it is usual to note the extreme scarcity of big speleothems.
In the Roraima-tepui cave system, the microbial involvement in the dissolution of quartz has been implied [15,22]. In another cave in the Roraima-tepui, the silicate cave microflora has been suggested to be affected by limited nitrogen and the poor buffering action of sandstones compared with surface-soil-rich carbonate caves [23]. A microbiological study performed in a cave in the Auyán-tepui showed that both quartz weathering and silica mobility were affected by chemotrophic bacterial communities [24].
This study provides the profiles of MiSeq-generated bacterial phylotypes, or operational taxonomic units (OTUs), based on partial 16S rRNA gene sequences (V3–V4 region) associated with three speleothem samples, two of which were closely similar (i.e., two speleothem types), from the silicate cave system in the Churi-tepui. The compositions and diversity of the retrieved OTUs were generally consistent with those reported for other silicate and limestone caves. The candidate metabolisms of the speleothem-associated bacteria were predicted by the PICRUSt2 bioinformatic tool [25], resulting in the metabolic implication for possible microbial involvement in silicate speleogenesis.

2. Materials and Methods

2.1. Speleothem Sample Collection

The sampling site was located in a silicate cave of table mountain “Churi-tepui” (ca. 05°15′ N, 62°00′ W) in Chimantá Massif, Gran Sabana, Bolívar State, Venezuela. Chimantá Massif is a dissected plateau with 11 table mountains or tepuis, according to the Pemón Indians’ name, 8 and 3 of which are located in the northern and southern areas, respectively. Churi-tepui belongs to the southern group, having maximum elevation of ca. 2500 m [26] or 2420 m [27] with a summit area of ca. 47.5 km2 [26]. Churi-tepui is known for a cave system that accumulates more than 20 km of passages genetically related but currently disconnected in separate caves by breakdowns [14,27]. Charles Brewer Cave is the southernmost of the system and has been mostly studied for geology, geochemistry, and hydrochemistry [15,27], and the pH values of 2.47–2.54 of the acidic cave water was reported for dripping water and “underground river” [27] (p. 38, Table 2). We sampled speleothems formed on the wall of the cave during the Japan–Venezuela Joint Expedition in October 2016.
The speleothems samples were collected at sites on the right bank of the stream between two waterfalls, which were located ca. 540 m from piedra del helicóptero at the only cave entrance by straight-line distance (Figure 1). Three speleothem samples were collected from an area of about 5 m2 in range and coded as GM1, GM2, and GM3, and their appearances can be roughly seen in Figure 2. GM1 was characterized as whitish and soft-textured (fragile), while GM2 and GM3 were blackish and hard-textured. These speleothem samples were collected by using a flame-sterilized field knife and stored in situ in pre-sterilized Whirl-Pak® plastic bags. The collected samples were then stored below 4 °C for subsequent laboratory experiments.

2.2. Crystallographic and Geochemical Analyses

Two speleothem samples, GM1 and GM2, were ground into powder using pre-autoclaved mortar and pestle for crystallographic and geochemical analyses, as well as for the DNA extraction mentioned below; GM3 was wholly expensed for DNA extraction to ensure the recovery of maximally extractable DNA. Although GM3 was not used for the analyses, it was located nearby horizontally to GM2 and resembled GM2 in its blackish appearance and hard texture. The ground powders were analyzed by: energy-dispersive X-ray spectroscopy (EDS) at 10 kV and 15 kV for soft whitish and hard blackish speleothems, respectively; and powder X-ray diffraction (PXRD) by Cu Kα radiation (1.54059 Å) for crystallographic characterization. EDS and PXRD were conducted using JED-2300T (JEOL Ltd., Tokyo, Japan) and RINT2500 (Rigaku Corp., Tokyo, Japan), respectively, at Natural Science Center for Basic Research and Development (N-BARD) of Hiroshima University. In addition, an elemental analysis on the cut surfaces of the speleothems was performed with an electron probe micro-analyzer (EPMA; JXA-iSP100; JEOL Ltd., Tokyo, Japan) at 15 kV at N-BARD. For the EPMA observation, small intact (not powdered) speleothems were embedded in epoxy resin, cut, and polished mechanically at Thin Section Workshop, Craft Plaza of Hiroshima University.

2.3. DNA Extraction, PCR Amplification, and MiSeq Sequencing

Bulk DNAs were extracted from approximately 10 g of the ground-powdered GM1, GM2, and GM3 samples with the ISOSPIN Soil DNA extraction kit (Nippon Gene Co. Ltd., Tokyo, Japan) and precipitated in 70% ethanol with precipitation facilitator Ethachinmate (Nippon Gene, Tokyo, Japan). The DNA precipitate was resuspended in sterilized ultrapure water. The concentration and purity of the extracted DNAs were checked with NanoDrop (Thermo Fisher Scientific, Waltham, MA, USA) for subsequent procedures and stored at −20 °C. PCR amplicons were generated using the Kapa HiFi HotStart ReadyMix PCR kit (Kapa Biosystems, Wilmington, MA, USA) and the bacterial V3–V4 region-specific primer pair (S-D-Bact-0341-b-S-17, 5′-CCTACGGGNGGCWGCAG-3′/S-D-Bact-0785-a-A-21, 5′-GACTACHVGGGTATCTAATCC-3′) [28]. The PCR conditions were as follows: 95 °C for 3 min with the lid being heated to 110 °C; 25 cycles of 95 °C for 30 s, 55 °C for 30 s, and 72 °C for 30 s; and a final elongation at 72 °C for 5 min. The sequence library was constructed following our previous method [29]. Pair-end 300 bp sequencing by MiSeq (Illumina, San Diego, CA, USA) was performed using a Nextera XT Index Kit (Illumina) at Department of Biomedical Science, N-BARD, Hiroshima University.

2.4. Statistical and Bioinformatic Analyses of the MiSeq-Generated V3–V4 Sequences

Raw sequence data, or raw reads, generated by MiSeq were processed with the Microbiome Taxonomic Profiling (MTP) pipeline by EzBioCloud (https://www.ezbiocloud.net/contents/16smtp) [28]. Briefly, the merging of the pair-end reads as well as PCR primer trimming were conducted using the EzBioCloud in-house pipeline; in this step, unmerged reads as well as short (<100 bp) or low-quality (averaged Q value < 25) reads were omitted. For quality-checked reads, the identical sequences were de-replicated; then, the non-redundant reads obtained were compared to EzBioCloud 16S rRNA gene sequence database PKSSU4.0, with the option of the target taxon of “bacteria”. Note that, in this curated database, the uncultured taxonomic group is tentatively given by the hierarchical name assigned to the DDBJ/ENA/GenBank sequence accession number with the following suffixes: “_s” (for species), “_g” (genus), “_f” (family), “_o” (order), “_c” (class), and “_p” (phylum). The taxonomic assignment of the reads was performed based on the following sequence similarity cut-offs: species (≥97%), genus (>97% > x ≥ 94.5%), family (> 94.5% > x ≥ 86.5%), order (>86.5% > x ≥ 82%), class (>82% > x ≥ 78.5%), and phylum (>78.5% > x ≥ 75%), where x corresponds to the sequence identity with sequences in the database. Note that these cut-offs were taken from previous studies [30,31] and are default parameters of the MTP pipeline. The reads below those cut-offs at the species or higher levels were appended with the suffix “_uc” (for unclassified). Next, all reads that could not be identified at the species level (<97% similarity) were subjected to chimera sequence detection through comparison with the EzBioCloud chimera-free reference database (https://help.ezbiocloud.net/mtp-pipeline/), and the chimera reads identified were discarded; unmatched and eukaryotic plastid reads were also excluded. The resulting final dataset was used to pick phylotypes, or operational taxonomic units (OTUs), based on the 97% similarity cut-off value. Using the EzBioCloud MTP pipeline, the rarefaction curve was computed and visualized; the alpha-diversity indices, i.e., Shannon, Simpson, and Chao1 indices, were calculated to estimate the evenness/richness of the OTUs of each speleothem.
The beta diversity showing principal component analysis (PCA) and hierarchical clustering based on the UniFrac distance matrix was also calculated to compare OTU compositions among the speleothem samples. Venn diagrams at the levels from phylum to species were also drawn. Biomarker OTUs that discriminated the speleothem microbiomes were specified by the linear discriminant analysis (LDA) [32] and LDA-Effect Size algorithm (LEfSe; http://huttenhower.sph.harvard.edu/galaxy/) [33]. The threshold on the logarithmic LDA score for discriminative features is generally set to 2 and was set to 2.5 in a rock varnish study [34]; this study set it to 4 to only focus on biomarkers with large statistical differences between samples.
Major OTUs were further projected on known human metabolic pathways available at Kyoto Encyclopedia of Genes and Genomes (KEGG; http://www.genome.jp/kegg/, accessed on 18 January 2022) [35] and Phylogenetic Investigation of Communities by Reconstruction of Unobserved States 2.0 (PICRUSt2; https://huttenhower.sph.harvard.edu/galaxy/ accessed on 18 January 2022) [36]. The above-mentioned bioinformatic analyses were also performed using the OmicStudio online tools at https://www.omicstudio.cn/tool accessed on 18 January 2022.

2.5. Sequence Data Deposition

The raw sequence data, project data, and sample data were deposited in DDBJ Sequence Read Archive (DRA013674), BioProject (PRJDB13191), and BioSample (SAMD00446319 for GM1, SAMD00446320 for GM2, and SAMD00446321 for GM3), respectively.

3. Results

3.1. Crystallographic and Geochemical Characteristics of Speleothems

The EDS spectra (Figure 3) showed that the major elements of the two speleothem samples were silicon, oxygen, and carbon, clearly indicating that the speleothems were silicate rather than carbonate. Carbon was also detected but as a minor element. The relative abundances of Si and O were different between GM1 and GM2, but the reason was unclear.
The sharp peaks in the PXRD patterns (Figure 4) corresponded to those of quartz according to Powder Diffraction File 00-046-1045 (quartz) of International Center for Diffraction Data (https://www.icdd.com). The difference in the quartz peak intensity between the two samples was due to a greater or lesser inclusion of quartz grains. The lump with a maximum at 22 degrees was the most important feature; it is typical of opal-A [37] and was observed in Venezuelan tepui cave speleothems [27] (p. 84, Figure 79A).
The EPMA images showed interesting contrasts between GM1 and GM2 (Figure 5). The elemental co-occurrence of oxygen and aluminum rather than silicon was seen in GM1, while the co-occurrence of sulfur and calcium was only seen in GM2, but they were very minor and did not affect the overall SiO2-dominant features of the speleothems.
Combining the results of the FE-SEM/EDS, PXRD, and EPMA allowed us to identify samples GM1 and GM2 as opal-A, with traces of quartz as impurities from quartz bedrock. The Al element present in sample GM1 probably belonged to pyrophyllite, a metamorphic mineral that has been extensively found in tepui bedrock. Sample GM2 also showed S and Ca, which fits with gypsum also reported for other tepui caves [27,38,39,40].

3.2. Evaluation of MiSeq-Generated V3–V4 Sequences (Reads) and OTUs

An overall total of 225,321 sequences, or reads, were generated from the three speleothem samples, 210,309 (93.3%) of which were validated for quality with an average length of 454.0 bp; 15,012 non-validated reads (6.7%) were filtered out due to low quality. For each speleothem, the number and average length of valid reads for GM1 were 87,168 (92.5% of total) and 454.5 bp; for GM2, 49,279 (99.0%) and 458.4 bp; and for GM3, 73,862 (90.8%) and 452.0 bp, respectively (Table 1).
Based on the cutoff at 97% similarity, the valid reads of GM1, GM2, and GM3 were grouped into 474, 1576, and 1134 phylotypes, or operational taxonomic units (OTUs), respectively, for a total of 3184 OTUs. The OTUs were annotated to a total of 1122 bacterial species, 516 genera, 262 families, 142 orders, 76 classes, and 30 phyla, and the hierarchical composition of each speleothem is summarized in Table 1.
The rarefaction curves for reads–OTUs relationships were drawn to calculate the coverage of retrieved OTUs over the predicted total OTUs (=the Chao1 values mentioned below). The coverages for GM1, GM2, and GM3 were 99.33%, 96.66%, and 99.10%, respectively, which showed that the sequencing depth reached in this study was sufficient to describe and characterize microbiomes in the silicate cave speleothems (Figure 6).
The distribution of OTUs among the samples was visualized using a Venn diagram (Figure 7) and the associated table (Table 2) that summarizes the numbers and names of phyla in each intersection and relative compliment (Venn diagrams at the levels from species to class are shown in Figures S1–S5). The intersection of GM1, GM2, and GM3 (GM1 ∩ GM2 ∩ GM3) had the largest numbers of phyla and reads, which showed the relative similarity of the phylum compositions among the speleothems. Eight phyla were specific to GM1 (GM1/GM2/GM3), while GM2 and GM3 had only one specific phylum.

3.3. Alpha and Beta Diversity Analyses

The Chao1, Shannon, and Simpson indices were calculated with EzBioCloud to estimate the alpha diversity (within each sample) of GM1, GM2, and GM3 (Table 3). The Chao1 index, an estimator of species richness, corresponding to the predicted OTU numbers in the rarefaction curve analysis (Figure 6), ranged from 490.40 in GM2 to 1586.63 in GM1. The Chao1 index values were almost equivalent to the number of retrieved valid OTUs, which agrees with the “high coverages” of 96.66–99.33% in the rarefaction curve analysis, as “coverage” is defined as the ratio of the number of valid reads to the Chao1 index value of the corresponding sample.
The Shannon index is an estimator of species evenness or diversity of equally abundant species. The highest Shannon index value of 5.19 was calculated for GM1, which was converted to an effective number of species (ENS) of 179.47 by e5.19 (=2.7185.19) [41], that is, the equivalent diversity with 179 equally common OTUs, corresponding to 11% of retrieved OTUs of GM1. Applying this approach to the lower Shannon index values of 3.06 for GM2 and 4.05 for GM3, ENS values as low as 21.33 and 57.40 were calculated, respectively.
The Simpson index is also an estimator of both species richness and evenness, with lower values for higher diversity. As the reciprocal of the Simpson index is regarded as a different expression of the ENS, the highest Simpson index (lowest diversity) of 0.16 for GM2 was converted to an ENS of 6.25, and the lowest Simpson index (highest diversity) of 0.02 in GM1 yielded an ENS of 50 [37].
Beta diversity, i.e., similarity/dissimilarity among samples, was represented by PCA and hierarchical cluster analysis. The PCA showed that the OTU populations of the GM1, GM2, and GM3 speleothems were distinguishable (Figure 8, left). The hierarchical cluster analysis showed a closer similarity between the GM2 and GM3 OTUs, rather than similarities with GM1 (Figure 8, right).
The LEfSe analysis identified the biomarker OTUs that affected PCA-based grouping and hierarchical clustering and discriminated the speleothem microbiomes. The cladogram generated by LEfSe showed that the discriminative biomarker OTUs were affiliated with taxa at various ranks (Figure 9). For example, OTUs affiliated with candidate phylum AD3 or “Candidatus Dormibacteraeota” (code “f” in the cladogram) were biomarkers of the GM1 microbiome.
LEfSe identified a total of 100 biomarkers with LDS scores >4 (p = 0.01183), of which 14 biomarkers had LDA scores >5, i.e., log105 or 105 (Table 4). The GM1 microbiome was characterized by the OTUs affiliated with acidobacterial class Solibacteres, while the GM2 and GM3 microbiomes were characterized by the OTUs affiliated with gammaproteobacterial genus Dyella. GM3 was also partly influenced by the OTUs affiliated with Solibacteres.

3.4. Microbiome Taxonomic Compositions

An overall total of 30 bacterial phyla were identified, of which 28, 20, and 19 phyla were found in the GM1, GM2, and GM3 speleothems, respectively (Table 1).
The dominant bacterial phyla in GM1 were Acidobacteriota (37.48% of total OTUs in GM1), Pseudomonadota (33.47%), and Chloroflexota (9.69%); in GM2 they were Pseudomonadota (73.52%), Acidobacteriota (12.37%), and Actinomycetota (10.10%); and in GM3, Pseudomonadota (44.58%), Acidobacteriota (35.09%), and Actinomycetota (9.86%) (Figure 10). The OTUs attributed to phyla Pseudomonadota and Acidobacteriota accounted for 70.95%, 85.89%, and 79.67% of the GM1, GM2, and GM3 OTUs, respectively; thus, the predominance of these phyla was revealed in the studied silicate cave speleothems.
Pseudomonadota, Acidobacteriota, and Actinomycetota represented >70% of the studied microbiomes and as high as 95.99% of the GM1 microbiome. However, the relative abundance among samples was different (Figure 10). The other phylum present in all samples was Chloroflexota, which accounted for more than 5% in the GM1 and GM3 samples. For other low-abundance phyla, the proportion of the Nitrospirota phylum detected in the GM2 sample was greater than 5%, and the proportion of Planctomycetota phylum detected in the GM3 sample was greater than 2%.

3.5. Microbial Metabolic Functions Predicted by PICRUSt2

All OTUs of each speleothem were used for the PICRUSt2 analysis to characterize the functional metabolic profile of each microbiome. At Level 2, which is a high hierarchical level of the KEGG metabolism category classification, each speleothem microbiome had the same 39 pathways (Figure 11). The “membrane transport” pathway accounted for the highest relative abundance in GM1, while “amino acid metabolism” was the highest in GM2 and GM3 and the second highest in GM1. In both pathways, GM1 showed higher relative abundances, while that of “carbohydrate metabolism” was higher in GM2 and GM3.
At KEGG Level 1 (Supplementary Figure S12), each microbiome had seven large pathways, which were “metabolism”, “genetic information processing”, “unclassified”, “environmental information processing”, “cellular processes”, “human diseases”, and “organismal systems” in the order of relative abundance. The relative abundance of the “metabolism” pathway was close to 50% in all the microbiomes.
At Level 3 (Supplementary Figure S13), each microbiome had 251 individual pathways. The “transporters” pathway had the highest proportion (4.36%) in GM1 and the second highest proportion in GM2 and GM3. The pathway categorized as “general function prediction only” had the second highest proportion (ca. 3%) in GM1 and the highest proportion (3.85%) in GM2 and GM3. Another transport pathway, “ABC transporters”, was the third most abundant in GM1 (2.83%) but was relatively low in GM2 and GM3. In contrast, GM2 and GM3 had relatively high abundances (ca. 3%) of “bacterial motility proteins”, “secretion systems”, and “two-component system”, which were higher than in GM1.

4. Discussion

Guiana Shield tepuis present a unique geographical location, special geomorphological features, and some of the longest and deepest silicate caves in the world [20,42]. The mineralogical processes had a very long timespan to occur. The first date record from tepui silica speleothems revealed ages from 53 to 390 thousand years [43,44], so the scarcity of elements and the harsh conditions are counterweighted by the availability of longer periods for biological and mineralogical interactions. The carbon only insignificantly detected in EDS spectra of the speleothems was probably due to organic materials that are abundant in the soil of Chimanta Massif tepuis [27] (p. 42). The relative abundances of Si and O were different between the two speleothem types (Figure 3), which could be related to the hardness or softness (fragility) of the speleothems in relation to the water of crystallization and the age of speleothems. The quartz grains found in the speleothems (Figure 4) were probably impurities derived from sandstone bedrock [27] (p. 80, Figures 78–80, Table 5). The EPMA revealed the co-occurrences of Al and O in speleothem GM1 as well as Ca and S in GM2 (Figure 5), which may indicate occurrences of pyrophyllite (Al2Si4O10(OH)2) and gypsum (CaSO4), respectively, in the speleothems [27] (p. 66, Table 4; p. 85, Figure 75).
Only the results of culture-independent, MiSeq-generated V3–V4 sequences were reported in this study, although cultivation using the R2A agar plates was tried and resulted in the Sanger sequencing of 16S rRNA genes of four isolates, which were related to Bacillus and Paenibacillus spp., as shown in previous studies on limestone cave microflorae [45,46]. However, their V3–V4 sequences were not found in our dataset from Charles Brewer Cave. They might have been cultured with certain bias or as contaminants and thus were not included in this study.
This study focused on MiSeq-generated V3–V4 sequences and found a total of 30 bacterial phyla in the speleothems of a Guiana tepui silicate cave. In general, the representative phyla were mostly similar to those reported in previous studies (Table 5). Phylum Pseudomonadota accounted for the largest proportion of OTUs in this cave, followed by Acidobacteriota and Actinomycetota. Actinomycetota is generally the dominant phylum, accounting for 60% of the bacterial community of limestone caves [6]. In other calcareous cave studies, Pseudomonadota was identified as the major phylum [47,48,49,50], which is consistent with the result of this study. A study in a Venezuelan orthoquartzite cave showed the dominance of classes Actinomycetales and Alphaproteobacteria in endolithic bacterial communities close to the cave entrance [23].
Phylum Chloroflexota is a ubiquitous phylum and is often found in caves [50,51]. Bacterial communities in a Venezuelan orthoquartzite cave were dominated (82–84%) by class Ktedonobacterales of phylum Chloroflexota [23], which was the first identification of class Ktedonobacterales; we also identified the OTUs of this class, with the read number accounting for >10% of total reads.
The OTUs affiliated with phylum Nitrospirota were mainly found in GM1 (Figure 10). Nitrospirota occur in different cave systems, such as the extremely acidic Frasassi Cave in Italy [52], as well as the limestone Pajsarjeva jama Cave and Tito Busillo Cave in Spain [3]. In Oylat Cave in a Turkish marble formation, Nitrospirota was the fourth abundant phylum [53]. Species of Nitrospirota contribute to nitrogen cycling by nitrite oxidation and provide nitrogen sources to oligotrophic lava cave habitats [54].
The OTUs affiliated with photoautotrophic phylum Cyanobacteria were found in the speleothem samples. Possible routes of cyanobacterial intrusion are air flow, infiltration with the water flow, and macrobiological vectors such as spiders carrying certain microorganisms and nutrients to underground [39] (p. 34, Photo 3), while entomological resources and the influence of trogloxen fauna such as bat colonies are generally scarce in tepui caves. Silica precipitation and speleothem formation are attributed to the activities of filamentous bacteria, including cyanobacteria [24]. In this study, Cyanobacteria comprised as high as 5% of the total OTUs in three samples.
The OTU-based metabolic prediction of the speleothem microbiomes suggested the presence of chemoautotrophic bacteria, which would support the sustenance of complex microbial communities in the studied silicate cave. Natural nutrient inputs and biogeochemical microenvironments together may have a mutual influence between silica amorphization and microbiomic composition [21]. Local changes in pH and the production of metabolites that influence silica solubility can result from bacterial metabolic processes related to chemoautotrophic activities, e.g., CO2 fixation and inorganic nitrogen transformation [55,56]. In this respect, GM2 and GM3 showed high abundances of the OTUs affiliated with genus Rhizobiales (family Methylocystaceae) capable of N2 fixation. The OTUs affiliated with nitrite-oxidizing Nitrospirota, whose presence might be correlated to CO2-fixation-coupled ammonia oxidation [57], were detected in all the samples. Previous studies also indicated members of Rhizobiales and Actinomycetota to be involved in biomineralization processes and rock weathering in cave environments [58]. In this study, the amount of Rhizobiales in the three speleothem samples was as high as 19%. In addition, ammonia-oxidizing archaea, i.e., members of Thaumarchaeota, are generally dominant in the microflora of silicate caves [23] and biodegraded limestone walls (not limestone caves) [59]; therefore, archaeal OTUs should be studied with our DNA samples in future studies.
Samples GM2 and GM3 belonged to the same type of speleothems, and the microbiomic functions as predicted by PICRUSt2 showed high similarity. At KEGG Level 1, “metabolism” accounted for the highest proportion of all pathways in all the speleothem samples. Bacterial metabolisms produce corresponding metabolites, and metabolites secreted from cells can affect the near-bacteria microenvironment. At KEGG Level 2, the high proportion of the “membrane transport pathway” was consistent with the secretion of metabolites. At Level 2, “amino acid metabolism” accounted for the highest proportion, and amino acid metabolisms can change the pH of the microenvironment, which may promote the dissolution and re-precipitation of speleothems; the pH values of the studied cave waters as macroenvironments were reported as 2.52 for dripping water and 2.47–2.54 for “underground river” [27] (p. 38, Table 2). Pathways related to “carbon metabolisms” such as glycolysis/gluconeogenesis, citric acid cycle (TCA cycle), pentose phosphate pathway, and pyruvate metabolism were found at KEGG Level 3. The nitrogen metabolism, sulfur metabolism, and carbon fixation pathways were also found at Level 3. These metabolisms can produce a variety of organic and inorganic acids, thereby changing the near-bacterial microenvironment, where discrete condensation may allow elements to stay longer than in flowing or dripping water.
At present, cave microbiology belongs to a new field in biology and geology. A large part of various and numerous cave ecosystems has not been studied, and the diversity and functional potentials of cave microorganisms remain to be explored by both culture-dependent and -independent methods [60]. In our study, while understanding the diversity of bacteria in the silicate cave, we also suggested bacterial functions in rock transformation, particularly the formation/dissolution of speleothems; in addition, we aim to elucidate archaeal functions in future studies.
Table
Table 5. Comparison of representative phyla reported from silicate caves, a lava tube, limestone caves, and building walls. Sequencing methods (Seq.), target sequences, and numbers of reported phyla of domains Bacteria and Archaea. Archaeal phyla are underlined. The sequencing method of “Pyro” indicates 454 pyrosequencing. Phylum names are updated according to the latest valid names [61]. Archaeal phyla are underlined.
Table 5. Comparison of representative phyla reported from silicate caves, a lava tube, limestone caves, and building walls. Sequencing methods (Seq.), target sequences, and numbers of reported phyla of domains Bacteria and Archaea. Archaeal phyla are underlined. The sequencing method of “Pyro” indicates 454 pyrosequencing. Phylum names are updated according to the latest valid names [61]. Archaeal phyla are underlined.
Source Cave/SiteSeq.TargetPhylumReference
No.Representatives
Silicate caveMiSeqV3–V430Acidobacteriota, Pseudomonadota, Actinomycetota, Chloroflexota, NitrospirotaThis study
Silicate caveSanger16S rRNA gene9Chloroflexota, Thaumarchaeota, Acidobacteriota, Pseudomonadota, Actinomycetota[23]
Silicate caveMiSeqV4–V517Pseudomonadota, Acidobacteriota, Actinomycetota, Planctomycetota, Chloroflexota[24]
Lava tubePyroV1–V318Actinomycetota, Pseudomonadota, Nitrospirota, Acidobacteriota, Bacteroidota[54]
Limestone cavePyroV633Actinomycetota, Pseudomonadota, Acidobacteriota[1]
Limestone cavePyroMetagenome17Pseudomonadota, Actinomycetota, Planctomycetota, Thaumarchaeota, Bacillota[2]
Limestone caveSangerV36Pseudomonadota, Acidobacteriota, Actinomycetota, Planctomycetota, Bacteroidota[3]
Limestone caveSanger16S rRNA gene5Pseudomonadota, Actinomycetota, Bacteroidota, Chloroflexota[6]
Limestone caveMiSeqV3–V419Pseudomonadota, Actinomycetota, Bacillota, Acidobacteriota, Bacteroidota[8]
Limestone cavePyroV441Pseudomonadota, Bacteroidota, Actinomycetota, Bacillota, Verrucomicrobiota[44]
Limestone caveSanger16S rRNA gene6Pseudomonadota, Acidobacteriota, Actinomycetota, Planctomycetota, Bacteroidota[47]
Limestone caveSanger16S rRNA gene4Pseudomonadota, Actinomycetota, Bacteroidota, Bacillota[48]
Limestone caveSanger16S rRNA gene7Pseudomonadota, Actinomycetota, Bacteroidota, Bacillota, Nitrospirota[49]
Limestone caveMiSeqV412Pseudomonadota, Acidobacteriota, Bacillota[50]
Limestone caveSanger16S rRNA gene10Pseudomonadota, Bacteroidota, Verrucomicrobiota[52]
Limestone cavePyroV610Pseudomonadota, Actinobacterium, Acidobacterium, Bacteroidota, Verrucomicrobiota[53]
Limestone cavePyroMetagenome, V454Pseudomonadota, Thaumarchaeota, Actinomycetota, Planctimycetota, Euryarchaeota[56]
Limestone caveMiSeqV348Actinomycetota, Pseudomonadota, Acidobacteriota, Bacillota[57]
Building wallMiSeqV3–V432Actinomycetota, Cyanobacteria, Pseudomonadota, Euryarchaeota, Thaumarchaeota[59]

5. Conclusions

MiSeq V3–V4 microbiomics was performed for the first time on opal speleothems from a silicate cave. The microbiomes of the soft whitish and hard blackish speleothems were separated by differential analysis; however, dominant phyla such as Acidobacteriota, Actinomycetota, Chloroflexota, and Pseudomonadota were mostly similar to those reported for limestone caves as well as silicate caves. The occurrence of Nitrospirota was specific to the soft whitish speleothem, which may be related to the biogeochemical cycling of nitrogen. The metabolic features of the speleothem-associated microbiomes were inferred based on the V3–V4 sequences, and the inferred membrane transport and amino acid metabolism may have influences on speleological processes.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/microorganisms10071395/s1, Figure S1: Venn diagram showing the distribution of OTU-affiliated genera in GM1, GM2, and GM3 speleothems and their intersections, Figure S2: Venn diagram showing the distribution of OTU-affiliated families in GM1, GM2, and GM3 speleothems and their intersections, Figure S3: Venn diagram showing the distribution of OTU-affiliated orders in GM1, GM2, and GM3 speleothems and their intersections, Figure S4: Venn diagram showing the distribution of OTU-affiliated classes in GM1, GM2, and GM3 speleothems and their intersections, Figure S5: Venn diagram showing the distribution of OTU-affiliated phyla in GM1, GM2, and GM3 speleothems and their intersections, Figure S6: PCA plots of OTU-affiliated genera in the GM1, GM2, and GM3 speleothems, Figure S7: PCA plots of OTU-affiliated families in the GM1, GM2, and GM3 speleothems, Figure S8: PCA plots of OTU-affiliated orders in the GM1, GM2, and GM3 speleothems, Figure S9: PCA plots of OTU-affiliated classes in the GM1, GM2, and GM3 speleothems, Figure S10: PCA plots of OTU-affiliated phyla in the GM1, GM2, and GM3 speleothems, Figure S11: Expedient taxonomic names corresponding to the codes in the LEfSe cladogram (Figure 9 in the main text), Figure S12: KEGG Level 1 metabolic pathways of GM1, GM2, and GM3 speleothem microbiomes, Figure S13: KEGG Level 3 pathways of GM1, GM2, and GM3 speleothem microbiomes, Table S1: Taxonomic biomarkers having LDA scores >4 and their corresponding codes in Figure 9 and Figure S12.

Author Contributions

Q.L. performed the bioinformatic analyses and prepared the manuscript; Z.H. performed the bioinformatic analyses and edited the manuscript; T.N. planned the study, performed sample collection, and reviewed/edited the manuscript; R.N. supported the bioinformatic analyses and edited the manuscript; L.M.R., R.C. and F.U. supported the sample collection and reviewed/edited the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

Analytical parts of the study were self-funded by T.N.

Data Availability Statement

The raw sequence data, project data, and sample data are available at DDBJ Sequence Read Archive (DRA013674), BioProject (PRJDB13191), and BioSample (SAMD00446319 for GM1, SAMD00446320 for GM2, and SAMD00446321 for GM3), respectively.

Acknowledgments

The expedition was conducted as part of a television program by Japan Broadcasting Corporation, or Nippon Hoso Kyokai (NHK). This study owes a lot to the technical assistance of Venezuelan Speleological Society (SVE). Joaquín Astort Marín led the expedition. Maribel Ramos Peña, Andrés Roberto Abraham Paz, and Doménico Basile helped traversing the cave. At Hiroshima University, Makoto Maeda and Naomi Kawata conducted EDS and PXRD, respectively. Yasuhiro Shibata performed EPMA, and Hayami Ishisako prepared thin sections for the EPMA. DNA sequences were generated with Illumina MiSeq and prepared for bioinformatic analyses by Shoko Hirano and Shingo Kimura, respectively, under the supervision of Eiso Hiyama, Hiroshima University. Ayaka Ohsato participated in the preparation of DNA for MiSeq.

Conflicts of Interest

The authors declare no conflict of interest. The funder had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.

References

  1. Ortiz, M.; Neilson, J.W.; Nelson, W.M.; Legatzki, A.; Byrne, A.; Yu, Y.; Wing, R.A.; Soderlund, C.A.; Pryor, B.M.; Pierson, L.S., III; et al. Profiling bacterial diversity and taxonomic composition on speleothem surfaces in Kartchner Caverns, AZ. Microb. Ecol. 2013, 65, 371–383. [Google Scholar] [CrossRef] [PubMed]
  2. Ortiz, M.; Legatzki, A.; Neilson, J.W.; Fryslie, B.; Nelson, W.M.; Wing, R.A.; Soderlund, C.A.; Pryor, B.M.; Maier, R.M. Making a living while starving in the dark: Metagenomic insights into the energy dynamics of a carbonate cave. ISME J. 2014, 8, 478–491. [Google Scholar] [CrossRef] [PubMed]
  3. Schabereiter-Gurtner, C.; Saiz-Jimenez, C.; Piñar, G.; Lubitz, W.; Rölleke, S. Phylogenetic 16S rRNA analysis reveals the presence of complex and partly unknown bacterial communities in Tito Bustillo cave, Spain, and on its Palaeolithic paintings. Environ. Microbiol. 2002, 4, 392–400. [Google Scholar] [CrossRef]
  4. Pašić, L.; Kovče, B.; Sket, B.; Herzog-Velikonja, B. Diversity of microbial communities colonizing the walls of a Karstic cave in Slovenia. FEMS Microbiol. Ecol. 2009, 71, 50–60. [Google Scholar] [CrossRef] [Green Version]
  5. Riquelme, C.; Marshall Hathaway, J.J.; Enes Dapkevicius, M.d.L.N.; Miller, A.Z.; Kooser, A.; Northup, D.E.; Jurado, V.; Fernandez, O.; Saiz-Jimenez, C.; Cheeptham, N. Actinobacterial diversity in volcanic caves and associated geomicrobiological interactions. Front. Microbiol. 2015, 6, 1342. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Barton, H.A.; Taylor, N.M.; Kreate, M.P.; Springer, A.C.; Oehrle, S.A.; Bertog, J.L. The impact of host rock geochemistry on bacterial community structure in oligotrophic cave environments. Int. J. Speleol. 2007, 36, 93–104. Available online: https://digitalcommons.usf.edu/kip_articles/2632 (accessed on 9 July 2022). [CrossRef] [Green Version]
  7. Adetutu, E.M.; Thorpe, K.; Bourne, S.; Cao, X.S.; Shahsavari, E.; Kirby, G.; Ball, A.S. Phylogenetic diversity of fungal communities in areas accessible and not accessible to tourists in Naracoorte Caves. Mycologia 2011, 103, 959–968. [Google Scholar] [CrossRef] [Green Version]
  8. Michail, G.; Karapetsi, L.; Madesis, P.; Reizopoulou, A.; Vagelas, I. Metataxonomic analysis of bacteria entrapped in a stalactite’s core and their possible environmental origins. Microorganisms 2021, 9, 2411. [Google Scholar] [CrossRef]
  9. Lundberg, J.; Brewer-Carías, C.; McFarlane, D.A. On biospeleothems from a Venezuelan tepui cave: U-Th dating, growth rates, and morphology. Int. J. Speleol. 2018, 47, 361–378. [Google Scholar] [CrossRef]
  10. Forti, P. Biogenic speleothems: An overview. Int. J. Speleol. 2001, 30, 39–56. [Google Scholar] [CrossRef]
  11. Šmída, B.; Audy, M.; Vlček, L. Expedícia Roraima, Venezuela, január 2003—Cueva Ojos de Cristal (Kryštálové oči). Slov. Speleol. Spoločnosť 2003, 34, 1–192. [Google Scholar]
  12. Aubrecht, R.; Brewer-Carías, C.; Šmída, B.; Audy, M.; Kováčik, Ľ. Anatomy of biologically mediated opal speleothems in the world’s largest sandstone cave: Cueva Charles Brewer, Chimantá Plateau, Venezuela. Sediment. Geol. 2008, 203, 181–195. [Google Scholar] [CrossRef]
  13. Piccini, L.; Mecchia, M. Solution weathering rate and origin of karst landforms and caves in the quartzite of Auyan-tepui (Gran Sabana, Venezuela). Geomorphology 2009, 106, 15–25. [Google Scholar] [CrossRef]
  14. Šmída, B.; Brewer-Carías, C.; Audy, M.; Mayoral, F.; Bakšić, D.; Vlček, L.; Stanković, J. Churi-tepui cave system: Inside the second largest quarzite cave in the world. Natl. Speleol. Soc. News 2010, 68, 16–23. [Google Scholar]
  15. Aubrecht, R.; Lánczos, T.; Gregor, M.; Schlögl, J.; Šmída, B.; Liščák, P.; Brewer-Carías, C.; Vlček, L. Sandstone caves on Venezuelan tepuis: Return to pseudokarst? Geomorphology 2011, 132, 351–365. [Google Scholar] [CrossRef]
  16. Mecchia, M.; Sauro, F.; Piccini, L.; De Waele, J.; Sanna, L.; Tisato, N.; Lira, J.; Vergara, F. Geochemistry of surface and subsurface waters in quartz-sandstones: Significance for the geomorphic evolution of tepui table mountains (Gran Sabana, Venezuela). J. Hydrol. 2014, 511, 117–138. [Google Scholar] [CrossRef]
  17. Urbani, F.; Carreño, R. Cuevas en cuarcitas proterozoicas de la Guayana Venezolana (1971–2021): Medio siglo de exploraciones y estudios geoespeleológicos. In Memorias II Congreso Colombiano de Espeleología; Bohórquez, G.E.V., Ed.; Asociación Espeleológica Colombiana: Bogotá, Columbia, 2021; pp. 203–209. [Google Scholar]
  18. Suárez, P.; Gutiérrez, A.V.; Salazar, V.; Puche, M.L.; Serrano, Y.; Martínez, S.; González, G.; Fernández-Delgado, M. Virulence properties and antimicrobial resistance of Pseudomonas aeruginosa isolated from cave waters at Roraima Tepui, Guayana Highlands. Lett. Appl. Microbiol. 2020, 70, 372–379. [Google Scholar] [CrossRef]
  19. Galán, C. Disolución y génesis del karst en rocas cabonáticas y rocas silíceas: Un estudio comparativo. Munibe 1991, 43, 43–72. [Google Scholar]
  20. Galán, C.; Herrera, F.; Carreño, R.; Pérez, M. Roraima Sur System, Venezuela: 10.8 km, world’s longest quartzite cave. Bol. Soc. Venez. Espeleol. 2004, 38, 53–60. [Google Scholar]
  21. Sauro, F. Structural and lithological guidance on speleogenesis in quartz–sandstone: Evidence of the arenisation process. Geomorphology 2014, 226, 106–123. [Google Scholar] [CrossRef]
  22. Kunicka-Goldfinger, W. Preliminary observations on the microbiology of karst caves of the Sarisariñama plateau in Venezuela. Bol. Soc. Venez. Espeleol. 1982, 19, 133–136. [Google Scholar]
  23. Barton, H.A.; Giarrizzo, J.G.; Suarez, P.; Robertson, C.E.; Broering, M.J.; Banks, E.D.; Parag, A.; Vaishampayan, P.A.; Kasthisuri Venkateswaran, K. Microbial diversity in a Venezuelan orthoquartzite cave is dominated by the Chloroflexi (Class Ktedonobacterales) and Thaumarchaeota Group I.1c. Front. Microbiol. 2014, 5, 615. [Google Scholar] [CrossRef] [Green Version]
  24. Sauro, F.; Cappelletti, M.; Ghezzi, D.; Columbu, A.; Hong, P.-Y.; Zowawi, H.M.; Carbone, C.; Piccini, L.; Vergara, F.; Zannoni, D.; et al. Microbial diversity and biosignatures of amorphous silica deposits in orthoquartzite caves. Sci. Rep. 2018, 8, 17569. [Google Scholar] [CrossRef]
  25. Douglas, G.M.; Maffei, V.J.; Zaneveld, J.R.; Yurgel, S.N.; Brown, J.R.; Taylor, C.M.; Huttenhower, C.; Langille, M.G.I. PICRUSt2 for prediction of metagenome functions. Nat. Biotechnol. 2020, 38, 685–688. [Google Scholar] [CrossRef] [PubMed]
  26. Huber, O. Geographical and physical features. In Flora of the Venezuelan Guayana. Vol. 1. Introduction; Steyermark, J.A., Berry, P.E., Holst, B.K., Eds.; Missouri Botanical Garden and Timber Press: Portland, OR, USA, 1995; pp. 1–61. [Google Scholar]
  27. Aubrecht, R.; Barrio-Amorós, C.L.; Breure, A.S.H.; Brewer-Carías, C.; Derka, T.; Fuentes-Ramos, O.A.; Gregor, M.; Kodada, J.; Kováčik, Ľ.; Lánczos, T.; et al. Venezuelan Tepuis: Their Caves and Biota; Acta Geologica Slovaca Monograph; Comenius University: Bratislava, Slovakia, 2012; 167p. [Google Scholar]
  28. Klindworth, A.; Pruesse, E.; Schweer, T.; Peplies, J.; Quast, C.; Horn, M.; Glöckner, F.O. Evaluation of general 16S ribosomal RNA gene PCR primers for classical and next-generation sequencing-based diversity studies. Nucleic Acids Res. 2013, 41, e1. [Google Scholar] [CrossRef] [PubMed]
  29. Faluaburu, M.S.; Nakai, R.; Imura, S.; Naganuma, T. Phylotypic characterization of mycobionts and photobionts of rock tripe lichen in East Antarctica. Microorganisms 2019, 7, 203. [Google Scholar] [CrossRef] [Green Version]
  30. Yoon, S.H.; Ha, S.M.; Kwon, S.; Lim, J.; Kim, Y.; Seo, H.; Chun, J. Introducing EzBioCloud: A taxonomically united database of 16S rRNA gene sequences and whole-genome assemblies. Int. J. Syst. Evol. Microbiol. 2017, 67, 1613–1617. [Google Scholar] [CrossRef] [PubMed]
  31. Yarza, P.; Yilmaz, P.; Pruesse, E.; Glöckner, F.O.; Ludwig, W.; Schleifer, K.H.; Whitman, W.B.; Euzéby, J.; Amann, R.; Rosselló-Móra, R. Uniting the classification of cultured and uncultured bacteria and archaea using 16S rRNA gene sequences. Nat. Rev. Microbiol. 2014, 12, 635–645. [Google Scholar] [CrossRef]
  32. Fisher, R.A. The use of multiple measurements in taxonomic problems. Ann. Eugenic. 1936, 7, 179–188. [Google Scholar] [CrossRef]
  33. Segata, N.; Izard, J.; Waldron, L.; Gevers, D.; Miropolsky, L.; Garrett, W.S.; Huttenhower, C. Metagenomic biomarker discovery and explanation. Genome Biol. 2011, 12, R60. [Google Scholar] [CrossRef] [Green Version]
  34. Esposito, A.; Borruso, L.; Rattray, J.E.; Brusetti, L.; Ahmed, E. Taxonomic and functional insights into rock varnish microbiome using shotgun metagenomics. FEMS Microbiol. Ecol. 2019, 95, fiz180. [Google Scholar] [CrossRef] [PubMed]
  35. Kanehisa, M.; Goto, S.; Sato, Y.; Kawashima, M.; Furumichi, M.; Tanabe, M. Data, information, knowledge and principle: Back to metabolism in KEGG. Nucleic Acids Res. 2014, 42, D199–D205. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  36. Afgan, E.; Baker, D.; Batut, B.; van den Beek, M.; Bouvier, D.; Cech, M.; Chilton, J.; Clements, D.; Coraor, N.; Grüning, B.A.; et al. The Galaxy platform for accessible, reproducible and collaborative biomedical analyses: 2018 update. Nucleic Acids Res. 2018, 46, W537–W544. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  37. Liesegang, M.; Milke, R. Australian sedimentary opal-A and its associated minerals: Implications for natural silica sphere formation. Am. Mineral. 2014, 99, 1488–1499. [Google Scholar] [CrossRef]
  38. Urbani, F. Venezuelan cave minerals. Bol. Soc. Venezolana Espeleol. 1996, 30, 1–13. [Google Scholar]
  39. Carreño, R.; Urbani, F. Observaciones sobre las espeleotemas del Sistema Roraima Sur. Bol. Soc. Venez. Espeleol. 2005, 38, 28–33. [Google Scholar]
  40. Sauro, F.; Tisato, N.; Waele, J.; Bernasconi, S.M.; Bontognali, T.R.R.; Galli, E.; Sheldon, N. Source and genesis of sulphate and phosphate–sulphate minerals in a quartz-sandstone cave environment. Sedimentology 2014, 61, 1433–1451. [Google Scholar] [CrossRef]
  41. Jost, L. Entropy and diversity. Oikos 2006, 113, 363–375. [Google Scholar] [CrossRef]
  42. Urbani, F. Notas sobre el origen de las cavidades en rocas cuarcíferas precámbricas del grupo Roraima, Venezuela. Interciencia 1986, 11, 298–300. [Google Scholar]
  43. González, L.; Gómez, R. High resolution speleothem paleoclimatology of northern Venezuela: A progress report. Bol. Soc. Venez. Espeleol. 2002, 36, 51–53. [Google Scholar]
  44. Lundberg, J.; Brewer-Carías, C.; McFarlane, D.A. Preliminary results from U-Th dating of glacial-interglacial deposition cycles in a silica speleothem from Venezuela. Quat. Res. 2010, 74, 113–120. [Google Scholar] [CrossRef]
  45. Yasir, M. Analysis of bacterial communities and characterization of antimicrobial strains from cave microbiota. Braz. J. Microbiol. 2018, 49, 248–257. [Google Scholar] [CrossRef] [PubMed]
  46. Brar, A.M.; Bergmann, D. Culture-based analysis of ‘Cave Silver’ biofilms on Rocks in the former Homestake mine in South Dakota, USA. Int. J. Speleol. 2019, 48, 145–154. [Google Scholar] [CrossRef] [Green Version]
  47. Schabereiter-Gurtner, C.; Saiz-Jimenez, C.; Pinar, G.; Lubitz, W.; Rolleke, S. Altamira cave Paleolithic paintings harbor partly unknown bacterial communities. FEMS Microbiol. Lett. 2002, 211, 7–11. [Google Scholar] [CrossRef] [Green Version]
  48. Barton, H.A.; Taylor, M.R.; Pace, N.R. Molecular phylogenetic analysis of a bacterial community in an oligotrophic cave environment. Geomicrobiol. J. 2004, 21, 11–20. [Google Scholar] [CrossRef]
  49. Schabereiter-Gurtner, C.; Saiz-Jimenez, C.; Piñar, G.; Lubitz, W.; Rölleke, S. Phylogenetic diversity of bacteria associated with Paleolithic paintings and surrounding rock walls in two Spanish caves (Llonín and La Garma). FEMS Microbiol. Ecol. 2004, 47, 235–247. [Google Scholar] [CrossRef]
  50. Zhu, H.-Z.; Zhang, Z.-F.; Zhou, N.; Jiang, C.-Y.; Wang, B.-J.; Cai, L.; Liu, S.-J. Diversity, distribution and co-occurrence patterns of bacterial communities in a karst cave system. Front. Microbiol. 2019, 10, 1726. [Google Scholar] [CrossRef] [Green Version]
  51. Hershey, O.S.; Barton, H.A. The microbial diversity of caves: Analysis and synthesis. In Cave Ecology; Ecological, Studies; Moldovan, O., Kováč, Ľ., Halse, S., Eds.; Springer: New York, NY, USA, 2018; Volume 235, pp. 69–90. [Google Scholar] [CrossRef]
  52. Macalady, J.L.; Lyon, E.H.; Koffman, B.; Albertson, L.K.; Meyer, K.; Galdenzi, S.; Mariani, S. Dominant microbial populations in limestone-corroding stream biofilms, Frasassi cave system, Italy. Appl. Environ. Microbiol. 2006, 72, 5596–5609. [Google Scholar] [CrossRef] [Green Version]
  53. Gulecal-Pektas, Y. Bacterial diversity and composition in Oylat Cave (Turkey) with combined Sanger/pyrosequencing approach. Pol. J. Microbiol. 2016, 65, 69–75. [Google Scholar] [CrossRef] [Green Version]
  54. Lavoie, K.H.; Winter, A.S.; Read, K.J.; Hughes, E.M.; Spilde, M.N.; Northup, D.E. Comparison of bacterial communities from lava cave microbial mats to overlying surface soils from Lava Beds National Monument, USA. PLoS ONE 2017, 12, e0169339. [Google Scholar] [CrossRef]
  55. Desai, M.S.; Assig, K.; Dattagupta, S. Nitrogen fixation in distinct microbial niches within a chemoautotrophy-driven cave ecosystem. ISME J. 2013, 7, 2411–2423. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  56. Tetu, S.G.; Breakwell, K.; Elbourne, L.D.H.; Holmes, A.J.; Gillings, M.R.; Paulsen, I.T. Life in the dark: Metagenomic evidence that a microbial slime community is driven by inorganic nitrogen metabolism. ISME J. 2013, 7, 1227–1236. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  57. De Mandal, S.; Chatterjee, R.; Kumar, N.S. Dominant bacterial phyla in caves and their predicted functional roles in C and N cycle. BMC Microbiol. 2017, 17, 90. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  58. Riquelme, C.; Dapkevicius, M.D.E.; Miller, A.Z.; Charlop-Powers, Z.; Brady, S.; Mason, C.; Cheeptham, N. Biotechnological potential of Actinobacteria from Canadian and Azorean volcanic caves. Appl. Microbiol. Biotechnol. 2017, 101, 843–857. [Google Scholar] [CrossRef] [Green Version]
  59. Coelho, C.; Mesquita, N.; Costa, I.; Soares, F.; Trovão, J.; Freitas, H.; Portugal, A.; Tiago, I. Bacterial and archaeal structural diversity in several biodeterioration patterns on the limestone walls of the Old Cathedral of Coimbra. Microorganisms 2021, 9, 709. [Google Scholar] [CrossRef] [PubMed]
  60. Kosznik-Kwaśnicka, K.; Golec, P.; Jaroszewicz, W.; Lubomska, D.; Piechowicz, L. Into the unknown: Microbial communities in caves, their role, and potential use. Microorganisms 2022, 10, 222. [Google Scholar] [CrossRef] [PubMed]
  61. Oren, A.; Garrity, G.M. Valid publication of the names of forty-two phyla of prokaryotes. Int. J. Syst. Evol. Microbiol. 2021, 71, 005056. [Google Scholar] [CrossRef]
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Figure 1. Site of sample collection in Cueva Charles Brewer (Charles Brewer Cave), Churi tepui. The cave map was modified from [9,12].
Figure 1. Site of sample collection in Cueva Charles Brewer (Charles Brewer Cave), Churi tepui. The cave map was modified from [9,12].
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Figure 2. Morphological appearances of the speleothem samples. GM1: speleothem shows a morphology similar to “champignons”. GM2 and GM3: speleothems show coral-like morphology. The lengths of the knife blade and handle in the left and middle photos were 9 cm and 12 cm, respectively.
Figure 2. Morphological appearances of the speleothem samples. GM1: speleothem shows a morphology similar to “champignons”. GM2 and GM3: speleothems show coral-like morphology. The lengths of the knife blade and handle in the left and middle photos were 9 cm and 12 cm, respectively.
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Figure 3. EDS spectra of two speleothem types, GM1 (upper) and GM2 (lower).
Figure 3. EDS spectra of two speleothem types, GM1 (upper) and GM2 (lower).
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Figure 4. PXRD patterns of two speleothem types, GM1 (upper) and GM2 (lower), with the database pattern of quartz, SiO2 (lowermost).
Figure 4. PXRD patterns of two speleothem types, GM1 (upper) and GM2 (lower), with the database pattern of quartz, SiO2 (lowermost).
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Figure 5. EPMA images of cross-sections of two speleothems, GM1 (left) and GM2 (right). Warm and cool colors indicate high and low relative abundances, respectively; black areas reveal the absence or less-than-detectable presence of elements.
Figure 5. EPMA images of cross-sections of two speleothems, GM1 (left) and GM2 (right). Warm and cool colors indicate high and low relative abundances, respectively; black areas reveal the absence or less-than-detectable presence of elements.
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Figure 6. Rarefaction curves based on the numbers of reads and OTUs for the GM1, GM2 and GM3 speleothems.
Figure 6. Rarefaction curves based on the numbers of reads and OTUs for the GM1, GM2 and GM3 speleothems.
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Figure 7. Venn diagram showing the distribution of OTU-affiliated phyla in GM1, GM2, and GM3 speleothems and their intersections. Names of phyla in each intersection and relative compliment are shown in Table 2. Venn diagrams for species, genera, families, orders, and classes are shown in Supplementary Figures S1–S5.
Figure 7. Venn diagram showing the distribution of OTU-affiliated phyla in GM1, GM2, and GM3 speleothems and their intersections. Names of phyla in each intersection and relative compliment are shown in Table 2. Venn diagrams for species, genera, families, orders, and classes are shown in Supplementary Figures S1–S5.
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Figure 8. PCA-based grouping (left) and hierarchical clustering dendrogram (right) of OTU-affiliated species in GM1, GM2, and GM3 speleothems. PCA and dendrogram for genera, families, orders, classes, and phyla are shown in Supplementary Figures S6–S10.
Figure 8. PCA-based grouping (left) and hierarchical clustering dendrogram (right) of OTU-affiliated species in GM1, GM2, and GM3 speleothems. PCA and dendrogram for genera, families, orders, classes, and phyla are shown in Supplementary Figures S6–S10.
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Figure 9. LEfSe cladogram showing taxonomic biomarkers for speleothems GM1, GM2, and GM3. The innermost node corresponds to the Bacteria domain, followed by the concentrically arranged nodes of class, order, family, genus, and species. Red, green, and blue nodes/shades indicate taxa that are significantly higher in relative abundance. The diameter of each node is proportional to the abundance of the taxon. Codes in the cladogram with corresponding taxonomic ranks/names are listed in Supplementary Figure S11.
Figure 9. LEfSe cladogram showing taxonomic biomarkers for speleothems GM1, GM2, and GM3. The innermost node corresponds to the Bacteria domain, followed by the concentrically arranged nodes of class, order, family, genus, and species. Red, green, and blue nodes/shades indicate taxa that are significantly higher in relative abundance. The diameter of each node is proportional to the abundance of the taxon. Codes in the cladogram with corresponding taxonomic ranks/names are listed in Supplementary Figure S11.
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Figure 10. Taxonomic compositions of OTUs from the GM1, GM2, and GM3 speleothems. Nine bacterial phyla and two phylum-level lineages (AD3 and OMAN) were observed with >1% sequence abundance in at least one sample in the MiSeq read data.
Figure 10. Taxonomic compositions of OTUs from the GM1, GM2, and GM3 speleothems. Nine bacterial phyla and two phylum-level lineages (AD3 and OMAN) were observed with >1% sequence abundance in at least one sample in the MiSeq read data.
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Figure 11. KEGG Level 2 metabolic pathways of GM1 (red), GM2 (green), and GM3 (blue) speleothem microbiomes. Pathway categories are shown in the order of relative abundances in GM1.
Figure 11. KEGG Level 2 metabolic pathways of GM1 (red), GM2 (green), and GM3 (blue) speleothem microbiomes. Pathway categories are shown in the order of relative abundances in GM1.
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Table
Table 1. Numbers of MiSeq-generated reads, derived OTUs, and annotated taxa in each speleothem sample and the corresponding overall total numbers. Note that the overall total taxa numbers are smaller than simple sums of those for GM1, GM2, and GM3 due to overlaps among samples.
Table 1. Numbers of MiSeq-generated reads, derived OTUs, and annotated taxa in each speleothem sample and the corresponding overall total numbers. Note that the overall total taxa numbers are smaller than simple sums of those for GM1, GM2, and GM3 due to overlaps among samples.
SampleRaw ReadValid ReadPhylotype
(OTU)		SpeciesGenusFamilyOrderClassPhylum
GM194,20587,16815765743261891156728
GM249,76349,27947429816690613720
GM381,35373,8621134365239137834819
Overall225,321210,309318411225162621427630
Table
Table 2. Names of phyla in relative compliments and intersections of the Venn diagram (Figure 7). Valid names and candidatus taxa are shown in italic (oblique) and roman (upright) styles, respectively, in the order of read abundance.
Table 2. Names of phyla in relative compliments and intersections of the Venn diagram (Figure 7). Valid names and candidatus taxa are shown in italic (oblique) and roman (upright) styles, respectively, in the order of read abundance.
SpeleothemPhylum
GM1GM2GM3No.Name
● 8Parcubacteria_OD1, Latescibacteria_WS3, Omnitrophica_OP3, Kazan, Spirochaetota, Peregrinibacteria, Aminicenantes_OP8, DQ499300_p
● 1Deinococcota
●1DQ833500_p
●● 2Nitrospirota, Saccharibacteria_TM7
● ●1Gemmatimonadota
●●0
●●●17Pseudomonadota, Acidobacteriota, Actinomycetota, Chloroflexota, Cyanobacteria, Planctomycetota, AD3, Elusimicrobiota, OMAN, Chlamydiota, Bacteroidota, Chlorobiota, Verrucomicrobiota, Armatimonadota, TM6, Bacillota, Microgenomates_OP11
28201930
Table
Table 3. Alpha diversity indices, i.e., Chao1, Shannon, and Simpson indices, for the OTUs for the GM1, GM2, and GM3 speleothems. Effective number of species (ENS) values were calculated from the Shannon and Simpson indices, showing the same tendency of the highest value in GM1 and the lowest value in GM2.
Table 3. Alpha diversity indices, i.e., Chao1, Shannon, and Simpson indices, for the OTUs for the GM1, GM2, and GM3 speleothems. Effective number of species (ENS) values were calculated from the Shannon and Simpson indices, showing the same tendency of the highest value in GM1 and the lowest value in GM2.
SampleValid ReadOTUChao1Shannon
(ENS)		Simpson
(ENS)
GM187,16815761586.635.19
(179.47)		0.02
(50)
GM249,279474490.403.06
(21.33)		0.16
(6.25)
GM373,86211341144.314.05
(57.40)		0.07
(14.29)
Table
Table 4. Taxonomic biomarkers having LDA scores >5 and their corresponding codes in Figure 9 and Figure S12. All biomarkers with LDA scores >4 are shown in Supplementary Table S1.
Table 4. Taxonomic biomarkers having LDA scores >5 and their corresponding codes in Figure 9 and Figure S12. All biomarkers with LDA scores >4 are shown in Supplementary Table S1.
Code in
Figure 9 and Figure S12		Rank of BiomarkerLDA
Score
PhylumClassOrderFamilyGenusSpecies
GM1pAcidobacteriotaSolibacteresPAC000121_oPAC000121_f 5.224
qAcidobacteriotaSolibacteresPAC000121_o 5.222
yAcidobacteriota 5.161
xAcidobacteriotaSolibacteres 5.154
GM2h0PseudomonadotaGammaproteobacteriaXanthomonadalesXanthomonadaceae 5.502
h1PseudomonadotaGammaproteobacteriaXanthomonadales 5.499
g6PseudomonadotaGammaproteobacteriaXanthomonadalesXanthomonadaceaeDyella 5.451
h2PseudomonadotaGammaproteobacteria 5.360
g4PseudomonadotaGammaproteobacteriaXanthomonadalesXanthomonadaceaeDyellaD. kyungheensis5.283
h3Pseudomonadota 5.276
GM3g5PseudomonadotaGammaproteobacteriaXanthomonadalesXanthomonadaceaeDyellaD. terrae5.077
vAcidobacteriotaSolibacteresSolibacteralesPAC002115_f 5.036
uAcidobacteriotaSolibacteresSolibacteralesPAC002115_fPAC002115_g 5.021
wAcidobacteriotaSolibacteresSolibacterales 5.011
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Liu, Q.; He, Z.; Naganuma, T.; Nakai, R.; Rodríguez, L.M.; Carreño, R.; Urbani, F. Phylotypic Diversity of Bacteria Associated with Speleothems of a Silicate Cave in a Guiana Shield Tepui. Microorganisms 2022, 10, 1395. https://doi.org/10.3390/microorganisms10071395

AMA Style

Liu Q, He Z, Naganuma T, Nakai R, Rodríguez LM, Carreño R, Urbani F. Phylotypic Diversity of Bacteria Associated with Speleothems of a Silicate Cave in a Guiana Shield Tepui. Microorganisms. 2022; 10(7):1395. https://doi.org/10.3390/microorganisms10071395

Chicago/Turabian Style

Liu, Qi, Zichen He, Takeshi Naganuma, Ryosuke Nakai, Luz María Rodríguez, Rafael Carreño, and Franco Urbani. 2022. "Phylotypic Diversity of Bacteria Associated with Speleothems of a Silicate Cave in a Guiana Shield Tepui" Microorganisms 10, no. 7: 1395. https://doi.org/10.3390/microorganisms10071395

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