Assessing the global phylum level diversity within the bacterial domain: A review
Identifieur interne : 000707 ( Pmc/Corpus ); précédent : 000706; suivant : 000708Assessing the global phylum level diversity within the bacterial domain: A review
Auteurs : Noha H. Youssef ; M. B. Couger ; Alexandra L. Mccully ; Andrés Eduardo Guerrero Criado ; Mostafa S. ElshahedSource :
- Journal of Advanced Research [ 2090-1232 ] ; 2014.
Abstract
Url:
DOI: 10.1016/j.jare.2014.10.005
PubMed: 26257925
PubMed Central: 4522544
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PMC:4522544Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Assessing the global phylum level diversity within the bacterial domain: A review</title><author><name sortKey="Youssef, Noha H" sort="Youssef, Noha H" uniqKey="Youssef N" first="Noha H." last="Youssef">Noha H. Youssef</name></author><author><name sortKey="Couger, M B" sort="Couger, M B" uniqKey="Couger M" first="M. B." last="Couger">M. B. Couger</name></author><author><name sortKey="Mccully, Alexandra L" sort="Mccully, Alexandra L" uniqKey="Mccully A" first="Alexandra L." last="Mccully">Alexandra L. Mccully</name></author><author><name sortKey="Criado, Andres Eduardo Guerrero" sort="Criado, Andres Eduardo Guerrero" uniqKey="Criado A" first="Andrés Eduardo Guerrero" last="Criado">Andrés Eduardo Guerrero Criado</name></author><author><name sortKey="Elshahed, Mostafa S" sort="Elshahed, Mostafa S" uniqKey="Elshahed M" first="Mostafa S." last="Elshahed">Mostafa S. Elshahed</name></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">26257925</idno><idno type="pmc">4522544</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4522544</idno><idno type="RBID">PMC:4522544</idno><idno type="doi">10.1016/j.jare.2014.10.005</idno><date when="2014">2014</date><idno type="wicri:Area/Pmc/Corpus">000707</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Assessing the global phylum level diversity within the bacterial domain: A review</title><author><name sortKey="Youssef, Noha H" sort="Youssef, Noha H" uniqKey="Youssef N" first="Noha H." last="Youssef">Noha H. Youssef</name></author><author><name sortKey="Couger, M B" sort="Couger, M B" uniqKey="Couger M" first="M. B." last="Couger">M. B. Couger</name></author><author><name sortKey="Mccully, Alexandra L" sort="Mccully, Alexandra L" uniqKey="Mccully A" first="Alexandra L." last="Mccully">Alexandra L. Mccully</name></author><author><name sortKey="Criado, Andres Eduardo Guerrero" sort="Criado, Andres Eduardo Guerrero" uniqKey="Criado A" first="Andrés Eduardo Guerrero" last="Criado">Andrés Eduardo Guerrero Criado</name></author><author><name sortKey="Elshahed, Mostafa S" sort="Elshahed, Mostafa S" uniqKey="Elshahed M" first="Mostafa S." last="Elshahed">Mostafa S. Elshahed</name></author></analytic><series><title level="j">Journal of Advanced Research</title><idno type="ISSN">2090-1232</idno><idno type="eISSN">2090-1224</idno><imprint><date when="2014">2014</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><title>Graphical abstract</title><fig id="f0035" position="anchor"><graphic xlink:href="fx2"></graphic></fig></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Bibel, D J" uniqKey="Bibel D">D.J. 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<front><journal-meta><journal-id journal-id-type="nlm-ta">J Adv Res</journal-id><journal-id journal-id-type="iso-abbrev">J Adv Res</journal-id><journal-title-group><journal-title>Journal of Advanced Research</journal-title></journal-title-group><issn pub-type="ppub">2090-1232</issn><issn pub-type="epub">2090-1224</issn><publisher><publisher-name>Elsevier</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">26257925</article-id><article-id pub-id-type="pmc">4522544</article-id><article-id pub-id-type="publisher-id">S2090-1232(14)00128-3</article-id><article-id pub-id-type="doi">10.1016/j.jare.2014.10.005</article-id><article-categories><subj-group subj-group-type="heading"><subject>Review</subject></subj-group></article-categories><title-group><article-title>Assessing the global phylum level diversity within the bacterial domain: A review</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Youssef</surname><given-names>Noha H.</given-names></name></contrib><contrib contrib-type="author"><name><surname>Couger</surname><given-names>M.B.</given-names></name></contrib><contrib contrib-type="author"><name><surname>McCully</surname><given-names>Alexandra L.</given-names></name></contrib><contrib contrib-type="author"><name><surname>Criado</surname><given-names>Andrés Eduardo Guerrero</given-names></name></contrib><contrib contrib-type="author"><name><surname>Elshahed</surname><given-names>Mostafa S.</given-names></name><email>Mostafa@okstate.edu</email><xref rid="cor1" ref-type="corresp">⁎</xref></contrib></contrib-group><aff id="af005">Department of Microbiology and Molecular Genetics, Oklahoma State University, Stillwater, OK, USA</aff><author-notes><corresp id="cor1"><label>⁎</label>Corresponding author. Tel.: +1 (405) 744 1192; fax: +1 (405) 744 1112. <email>Mostafa@okstate.edu</email></corresp></author-notes><pub-date pub-type="pmc-release"><day>04</day><month>11</month><year>2014</year></pub-date><pmc-comment> PMC Release delay is 0 months and 0 days and was based on .</pmc-comment>
<pub-date pub-type="ppub"><month>5</month><year>2015</year></pub-date><pub-date pub-type="epub"><day>04</day><month>11</month><year>2014</year></pub-date><volume>6</volume><issue>3</issue><fpage>269</fpage><lpage>282</lpage><history><date date-type="received"><day>21</day><month>8</month><year>2014</year></date><date date-type="rev-recd"><day>6</day><month>10</month><year>2014</year></date><date date-type="accepted"><day>23</day><month>10</month><year>2014</year></date></history><permissions><copyright-statement>© 2014 Production and hosting by Elsevier B.V. on behalf of Cairo University.</copyright-statement><copyright-year>2014</copyright-year><copyright-holder></copyright-holder><license license-type="CC BY-NC-ND" xlink:href="http://creativecommons.org/licenses/by-nc-nd/3.0/"><license-p>This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).</license-p></license></permissions><abstract abstract-type="graphical"><title>Graphical abstract</title><fig id="f0035" position="anchor"><graphic xlink:href="fx2"></graphic></fig></abstract><abstract><p>Microbial ecology is the study of microbes in the natural environment and their interactions with each other. Investigating the nature of microorganisms residing within a specific habitat is an extremely important component of microbial ecology. Such microbial diversity surveys aim to determine the identity, physiological preferences, metabolic capabilities, and genomic features of microbial taxa within a specific ecosystem. A comprehensive review of various aspects of microbial diversity (phylogenetic, functional, and genomic diversities) in the microbial (bacterial, archaeal, and microeukaryotic) world is clearly a daunting task that could not be aptly summarized in a single review. Here, we focus on one aspect of diversity (phylogenetic diversity) in one microbial domain (the Bacteria). We restrict our analysis to the highest taxonomic rank (phylum) and attempt to investigate the extent of global phylum level diversity within the Bacteria. We present a brief historical perspective on the subject and highlight how the adaptation of molecular biological and phylogenetic approaches has greatly expanded our view of global bacterial diversity. We also summarize recent progress toward the discovery of novel bacterial phyla, present evidences that the scope of phylum level diversity in nature has hardly been exhausted, and propose novel approaches that could greatly facilitate the discovery process of novel bacterial phyla within various ecosystems.</p></abstract><kwd-group><title>Keywords</title><kwd>Phylogenetic diversity</kwd><kwd>Candidate phyla</kwd><kwd>16S rRNA gene</kwd><kwd>Culture-independant diversité surveys</kwd></kwd-group></article-meta></front><body><sec id="s0005"><title>Historical background</title><p>Microbial ecology is the scientific discipline where scientists examine microbes in their environment, their impact and adaptation to their habitat and their interactions with each other. Microbial diversity surveys, which aim to identify the types of microorganisms within a specific habitat are an integral part of microbial ecology. The discovery of “animalcules” (single celled microscopic microorganisms), by Antony van Leeuwenhoek in various samples e.g. rain drops, water samples from wells and lakes, oral and stool samples from humans is, in essence, microbial diversity surveys <xref rid="b0005" ref-type="bibr">[1]</xref>. Following Leeuwenhoek’s discoveries, a relative hiatus in microbiology research ensued in the 18th and the earlier parts of the 19th century. The revival of microbiology research during the mid 19th–early 20th century was characterized by a marked shift in research philosophy. Holistic observation of microorganisms in their natural habitats was replaced with a reductionist research philosophy, with emphasis on the identification of etiological agents of microbially mediated phenomena such as fermentation and pathogenesis. Research during this era, deservedly referred to as the “golden age of microbiology” has lead to multiple seminal advances e.g. development of solid media for culturing bacteria, germ theory of disease, staining techniques, and vaccination procedures <xref rid="b0010" ref-type="bibr">[2]</xref>. However, such spectacular advances have shifted the research focus of microbiologists from an ecosystem-oriented, holistic philosophy to a reductionist, pure-culture centric focus.</p><p>The Russian/Ukrainian scientist Sergei Winogradsky, whose biography is almost as interesting as his research accomplishments, advocated a research approach that emphasizes the study of microorganisms in their natural habitats in mixed cultures or in isolates recently recovered from the ecosystem of interest. Winogradsky correctly reasoned that microorganisms in nature survive in conditions that are a far cry from the controlled, nutrient-rich conditions at which pure cultures are maintained in the laboratory. He reasoned that the behavior of a specific microorganism in its natural habitat is markedly different from its behavior in pure culture due to the differences in nutrient and resource availability between both conditions, as well as to the constant interactions with various microbial taxa coexisting within the same habitat <xref rid="b0005" ref-type="bibr">[1]</xref>. His work on environmental samples, especially soil, has clearly led to a better appreciation of the metabolic and functional diversity of microorganisms in their natural habitats.</p><p>Winogradsky’s research, and subsequent efforts by eminent microbiologists (Beijerinck, van Neal, Kluyver, and Hungate) has defined the goals of microbial ecology. These could be simplified for the non-specialist as the “who” (identity of microorganisms), “what” (their metabolic capabilities), “where” (their spatiotemporal distribution within an ecosystem as well as in a global scale), and “why” (functions in a specific ecosystem and role in geochemical cycling). The “who” is, obviously, the most basic question in microbial ecology (add references). After 340 years postanimalcules discovery and almost a century since the revival of microbial ecology by Winogradsky, one would imagine that this seemingly straightforward question has satisfactory been answered, and that the science of microbial discovery and description of new taxa would be as dead as the science of discovering new organs in the human body. This could not be any further from the truth. A global census of all microbial species on earth is now recognized as a truly impossible task <xref rid="b0015" ref-type="bibr">[3]</xref>. Even with a single sample from a highly diverse ecosystem (e.g. soil), such census still represents a daunting challenge <xref rid="b0020 b0025 b0030" ref-type="bibr">[4,5,6]</xref>.</p><p>In this review, we examine the scope of bacterial diversity within the domain Bacteria. We limit our assessment of phylogenetic diversity to the highest taxonomic rank (phylum) and attempt to address seemingly straightforward questions: How many bacterial phyla exist in nature? Have all such phyla already been described? And what approaches could be implemented to more effectively document novel, yet undescribed phylum level diversity within the Bacteria?</p></sec><sec id="s0010"><title>From the great plate count anomaly to the uncultured bacterial majority</title><sec id="s0015"><title>The great plate count anomaly and the “missing” cells</title><p>It has been observed, as early as 1932, that within freshwater samples, only an extremely small fraction of microscopically observed microbial cells is recoverable as pure cultures in microbial growth media <xref rid="b0035" ref-type="bibr">[7]</xref>. This observation (initially seen in freshwater) has since been validated in a wide array of environmental samples (e.g. marine, soils, and freshwater habitats, see <xref rid="b0040" ref-type="bibr">[8]</xref> and references within). Typically, the absolute majority (99–99.9%) of cells within an environmental sample are not recoverable in pure culture using plating or most probable number (MPN) enumeration procedure. Specific measures have been shown to slightly improve the proportion of cultured cells within select environmental samples. These include the utilization of multiple media targeting various metabolic capabilities and physiological preferences, longer incubation time <xref rid="b0045" ref-type="bibr">[9]</xref>, novel isolation contraptions <xref rid="b0050 b0055" ref-type="bibr">[10,11]</xref>, use of dilute media to mimic resource scarcity in nature and/or media mimicking natural settings <xref rid="b0060" ref-type="bibr">[12]</xref>, and the implementation of more sensitive growth detection methods <xref rid="b0055 b0065" ref-type="bibr">[11,13]</xref>. Nevertheless, even with improved methodologies, the majority of cells within highly complex habitats remain uncultured. The term “The great plate count anomaly” has been aptly coined to describe this phenomenon in 1988 <xref rid="b0040" ref-type="bibr">[8]</xref>.</p><p>A logical inquiry stemming from the recognition of this phenomenon is the identity of microorganisms escaping enrichment and isolation procedures. Do these microorganisms represent novel, hitherto unknown bacterial taxa, or do they represent close relatives of bacterial taxa available in pure culture that possess attenuated growth capabilities, multiple unidentified auxotrophies, and/or yet-unclear physiological and growth requirements? The presence of unique cellular morphologies in environmental samples that have never been recovered in pure cultures has often hinted at the putative novelty of at least a fraction of these uncultured cells <xref rid="b0070" ref-type="bibr">[14]</xref>. However, prior to the advent of molecular taxonomic approaches and their wide utilization in diversity surveys this question was mostly philosophical in nature <xref rid="b0075" ref-type="bibr">[15]</xref>.</p></sec><sec id="s0020"><title>Use of molecular phylogeny in culture-independent diversity surveys</title><p>The late American microbiologist Carl Woese pioneered the use of 16S rRNA gene as a phylogenetic marker to provide an evolutionary-based taxonomic outline for living organisms. Using comparative 16S rRNA gene sequence analysis, he proposed a three kingdom classification scheme <xref rid="b0080" ref-type="bibr">[16]</xref>, where all living creatures are grouped into three domains (Bacteria, Archaea, and Eukaryotes). His further investigation of cultured taxa within the bacterial domain has produced the first high rank taxonomic outline for Bacteria, with all known bacterial taxa grouped into 12 different phyla or divisions (<xref rid="f0005" ref-type="fig">Fig. 1</xref>) <xref rid="b0085" ref-type="bibr">[17]</xref>.</p><p>Building on these efforts, the American microbiologist Norman Pace has pioneered the use of 16S rRNA gene-based sequencing and analysis procedures as a tool for direct identification of microbial populations in environmental samples. This approach was originally dubbed “phylotyping” but is more commonly referred to now as “16S rRNA gene-based culture-independent diversity survey”, or simply “16S rRNA analysis” (<xref rid="f0010" ref-type="fig">Fig. 2</xref>) <xref rid="b0090" ref-type="bibr">[18]</xref>. It involves direct isolation of bulk DNA from an environmental sample followed by PCR amplification of a fragment of the 16S rRNA gene using primers targeting conserved regions within the molecule. The amplicon, representing a mix of 16S rRNA genes originating from different cells within the environmental sample of interest is then cloned and sequenced (or directly sequenced when using newer high throughput sequencing procedures, see below) <xref rid="b0075 b0095" ref-type="bibr">[15,19]</xref>. The obtained sequences are analyzed and their phylogenetic affiliation is assessed using various phylogenetic and bioinformatics procedures. This approach has the monumental advantage of being culture-independent i.e. capable of identifying microorganisms within a specific environmental samples regardless of their amenability or refractiveness to isolation <xref rid="b0090" ref-type="bibr">[18]</xref>. As such, it is well suited to address questions posed above regarding the identity and taxonomy of uncultured microorganisms routinely escaping detection in enrichment and isolation-based procedures.</p></sec><sec id="s0025"><title>The uncultured bacterial majority revealed</title><p>The 16S rRNA gene-based approach has been readily adopted in the past three decades by the absolute majority of the scientific community, and extensively utilized to study the microbial diversity in ecosystems ranging from large global habitats, e.g. oceans <xref rid="b0100 b0105 b0110 b0115 b0120 b0125 b0130 b0135 b0140 b0145 b0150 b0155 b0160 b0165 b0170 b0175 b0180 b0185 b0190 b0195 b0200" ref-type="bibr">[20–40]</xref>, and soil <xref rid="b0205 b0210 b0215 b0220 b0225 b0230 b0235 b0240 b0245 b0250 b0255 b0260 b0265 b0270 b0275 b0280 b0285 b0290 b0295 b0300" ref-type="bibr">[41–60]</xref>, to hardly accessible extreme environments such as deep sea hydrothermal vents <xref rid="b0305 b0310 b0315 b0320 b0325 b0330 b0335 b0340 b0345 b0350 b0355 b0360 b0365 b0370 b0375 b0380" ref-type="bibr">[61–76]</xref>, Antarctic lakes <xref rid="b0160 b0310 b0385 b0390 b0395 b0400 b0405 b0410" ref-type="bibr">[32,62,77–82]</xref>, and Antarctic soils <xref rid="b0165 b0310 b0415 b0420 b0425 b0430 b0435 b0440 b0445 b0450" ref-type="bibr">[33,62,83–90]</xref>. Collectively, these studies have demonstrated that the scope of phylogenetic diversity is much broader than previously implied from culture-based studies. Multiple novel microbial lineages have been identified, many of which appear to be deeply branching within the bacterial tree and unaffiliated with any of the known bacterial phyla. The discovery of these lineages necessitated coining the term candidate phylum (or candidate division) to accommodate these bacterial phyla where only 16S rRNA sequences but no isolates are available. Indeed, examination of taxonomic outlines provided by curated 16S rRNA gene databases e.g. Greengenes <xref rid="b0455" ref-type="bibr">[91]</xref> and SILVA <xref rid="b0165" ref-type="bibr">[33]</xref> suggests that, currently, the majority of currently recognized bacterial phyla are candidate phyla (<xref rid="t0005" ref-type="table">Table 1</xref>). Therefore, the application of 16S rRNA gene based diversity surveys has resulted in the discovery of multiple novel bacterial lineages at the highest taxonomic rank and have revolutionized our understanding of the scope of phylum level diversity in nature. More importantly, such analysis clearly demonstrated that a fraction of microbial cells consistently missed in enumeration and isolation approaches clearly belong to novel, hitherto unrecognized bacterial lineages.</p></sec></sec><sec id="s0030"><title>Global phylum level diversity in bacteria</title><p>These new discoveries of novel bacterial phyla and candidate phyla have added multiple new deep branches (phyla) to the bacterial trees of life, but are we done with this exercise? Has the phylum level diversity within the Bacteria been exhausted, or are there multiple, yet-undescribed novel bacterial phyla (or even domains) in nature? One would imagine that, after three decades of research, thousands of published 16S rRNA gene-based diversity surveys, 5.4 million Sanger-generated 16S rRNA gene sequences in GenBank and >1.7 billion sequences in high throughput sequencing archives e.g. SRA <xref rid="b0460" ref-type="bibr">[92]</xref>, CAMERA <xref rid="b0465" ref-type="bibr">[93]</xref>, and MG-RAST <xref rid="b0470" ref-type="bibr">[94]</xref>, and the discovery and documentation of tens of novel bacterial candidate phyla, that the global scope of diversity of bacteria on earth has been documented, at least at the highest taxonomic (phylum) level. However, based on our research experience in the last decade, the authors are now firm believers that the scope of global phylum level bacterial diversity is much greater than currently recognized in curated 16S rRNA gene databases such as Greengenes <xref rid="b0455" ref-type="bibr">[91]</xref> and SILVA <xref rid="b0165" ref-type="bibr">[33]</xref> (<xref rid="t0005" ref-type="table">Table 1</xref>). Below, we present three different reasons why we believe that this is the case, as well as procedures that could putatively facilitate the discovery of these novel phyla.</p></sec><sec id="s0035"><title>Novel bacterial phyla as constituents of the rare biosphere</title><p>Within highly diverse microbial ecosystems, several distribution models can be used to fit the frequency data, e.g. ordinary Poisson distribution, gamma-mixed Poisson, inverse Gaussian-mixed Poisson, lognormal-mixed Poisson, Pareto-mixed Poisson, and mixture of 2 exponentials-mixed Poisson <xref rid="b0290 b0475 b0480 b0485 b0490 b0495" ref-type="bibr">[58,95–99]</xref>. Regardless of the distribution pattern, the community structure in diverse habitats typically exhibits a taxon rank distribution curve with a long tail corresponding to bacterial species present in low abundance. This fraction constituting the majority of species is referred to as the “rare” biosphere <xref rid="b0100" ref-type="bibr">[20]</xref>. The reason why these lineages are present and maintained at low abundances, as well as their global distribution patterns and putative ecological roles (or lack thereof), is an active area of interest to microbial ecologists and evolutionary microbiologists.</p><p>Access to the rare members of the community has been greatly augmented by the advent of high throughput sequencing technologies and their adaptation to amplicon-based 16S rRNA gene-based diversity surveys e.g. pyrosequencing <xref rid="b0100" ref-type="bibr">[20]</xref>, and Illumina sequences <xref rid="b0500" ref-type="bibr">[100]</xref>. Such adaptation has allowed for the generation of hundreds of thousands (pyrosequencing) to millions (Illumina) of sequencing reads in a single run and hence provided unprecedented access to the rare biosphere. Collectively, these studies have documented the extremely high level of species richness within the rare biosphere. More interestingly, within such studies, a significant fraction of the obtained sequences (10–74% <xref rid="b0505 b0510 b0515 b0520 b0525" ref-type="bibr">[101–105]</xref> are considered unclassified beyond a preset sequence similarity threshold, e.g., 80%, to the closest classifiable relative in databases.</p><p>However, it is important to note that, while pyrosequencing-, and Illumina-based studies are excellent tools for suggesting the occurrence of novel bacterial diversities within a sample, they are very poor in accurately documenting and describing such diversity. Accurate determination of the phylogenetic affiliation of such pyrosequencing-, and Illumina-generated sequences is unfeasible, mainly due to the short-read-length output of currently available high throughput technologies, and the error rate associated with them, which preclude the direct deposition of obtained short sequences into public databases e.g. GenBank. Hopes on the development of a high throughput, long-read sequencing approach have been high, but the newer systems that offer that (e.g. PacBio SMRT) have a dreadfully high error rate (∼14% indels for PacBio SMRT sequencing) that preclude their utilization for high throughput phylogenetic studies.</p><p>Therefore, Sanger-generated near full-length 16S rRNA gene sequences remain the only viable way for the accurate description and documentation of novel bacterial lineages. In spite of the fact that an extremely large number of Sanger-generated 16S rRNA gene sequences (>5 M, as of August 2014) are currently available through the GenBank database, the absolute majority of these sequences have been obtained during the course of small-scale diversity surveys (e.g. <200 sequences generated per study). Accordingly, these studies, and consequently the entire database have an extremely poor representation of the rare biosphere within the ecosystems studied.</p><p>Two strategies have been developed as a means to obtain near full-length 16S rRNA gene sequences from the rare biosphere. The first is a brute force approach in which a large number of clones are sequenced from a single sample, and the other depends on the development of a more targeted approach to specifically access putatively novel members within the rare biosphere. Due to cost issues, relatively few studies have utilized a brute force approach for this process. For example, <xref rid="b0530" ref-type="bibr">[106]</xref> examined the bacterial diversity in grassland soil by analyzing 13,001 sequences from a single sample. This study demonstrated that rare members of the microbial community have, on average, more novelty (i.e. less sequence similarity to their closest relative in the database) compared to more abundant members of the samples. More importantly, the authors identified multiple novel lineages at various taxonomic levels, with the identification of 6 putative new phyla. Another more impressive more recent effort <xref rid="b0535" ref-type="bibr">[107]</xref> focused on analyzing ∼119,000 Sanger-generated sequences obtained from 10 equivalent sections pooled from 4 core samples of a 5 cm thick Guerrero Negro microbial mat, and resulted in the identification of 43 putatively novel phyla. Collectively, both studies, as well as other deep sequencing Sanger-based studies conducted on a smaller scale, e.g. <xref rid="b0540 b0545" ref-type="bibr">[108,109]</xref> consistently demonstrate that novel bacterial phyla are still to be encountered in the rare biosphere.</p><p>A more targeted approach to zoom in on putatively novel members of the rare biosphere has been independently developed by three different research laboratories and used to target putatively novel and rare members of the microbial community in a sulfide and sulfur-rich spring in southwestern Oklahoma (Zodletone spring) <xref rid="b0550" ref-type="bibr">[110]</xref>, freshwater microbial communities <xref rid="b0555" ref-type="bibr">[111]</xref>, and marine sponges <xref rid="b0515" ref-type="bibr">[103]</xref>. This approach (<xref rid="f0015" ref-type="fig">Fig. 3</xref>) is based on using sequences generated in high throughput sequencing surveys to identify sequences with low sequence similarity (e.g. <80%) to closest relatives in GenBank database. Primers specific to these putatively novel sequences are then designed and used in conjunction with universal bacterial primers to obtain near full length 16S rRNA amplicons which could be cloned, sequenced using Sanger sequencing, and subjected to detailed phylogenetic analysis. Using this approach, five novel bacterial phyla were identified within the rare members of the microbial community in Zodletone spring in Southwestern Oklahoma <xref rid="b0550" ref-type="bibr">[110]</xref>. Therefore, regardless of the approach utilized, it is clear that all dedicated efforts expended on identifying novelty within the rare biosphere in various ecosystems almost invariably yielded novel bacterial phyla. We hence conclude that a sustained and dedicated effort to investigate phylum level diversity in the rare biosphere in multiple complex habitats could hence have a profound effect on our understanding of the global scope of phylum level diversity within the domain Bacteria.</p></sec><sec id="s0040"><title>Novel bacterial phyla in the shadow biosphere</title><p>All 16S rRNA gene-based diversity surveys are initiated by amplification of 16S rRNA genes using primers that target conserved regions within the 16S rRNA molecule. A list of universal bacterial primers used in diversity surveys is shown in <xref rid="t0010" ref-type="table">Table 2</xref>. It has often been argued that these “universal” primers could not theoretically amplify every single microbial strain within a single complex environmental sample, and that a fraction of microbial diversity is routinely missed in PCR-based diversity studies. However, the proportion of missed diversity, or the “shadow biosphere” as a fraction of the total number of cells is currently unclear. Indeed, 16S rRNA gene sequences within genomic fragments obtained via PCR-independent techniques, e.g. cloned in fosmids <xref rid="b0560" ref-type="bibr">[112]</xref>, have mismatches to the sequences of commonly used universal 16S rRNA primers <xref rid="b0565" ref-type="bibr">[113]</xref>. Further, a detailed <italic>in silico</italic> analysis of 16S rRNA gene sequences identified in PCR-independent metagenomic survey in NCBI environmental survey repository also identified multiple 16S rRNA gene sequences that harbor mismatches to common universal bacterial 16S rRNA primers <xref rid="b0570" ref-type="bibr">[114]</xref>.</p><p>In addition, several studies provide empirical evidence that the shadow biosphere harbors a disproportionally large fraction of bacterial cells belonging to novel bacterial phyla. For example, the discovery of candidate divisions AD3, NC10, and mesophilic Thermotoga as integral constituents within soil ecosystems has long been hampered by the common mismatches exhibited in their 16S rRNA gene sequences to universal bacterial primers, resulting in their chronically common misrepresentation and outright absence in soil clone libraries <xref rid="b0575" ref-type="bibr">[115]</xref>. More importantly, recent studies from the Banfield laboratory at UC-Berkley have constituted multiple genome assemblies from metagenomic datasets derived from a variety of habitats <xref rid="b0565 b0580 b0585 b0590 b0595 b0600" ref-type="bibr">[113,116–120]</xref>. Many of these reconstituted genomes represent completely novel bacterial phyla that have never been observed before, in pure cultures, or in 16S PCR-based diversity surveys. All such novel biosphere-derived phyla exhibit multiple mismatches within their 16S rRNA gene sequences to various “universal” bacterial primers currently in use, and hence were always missed in diversity surveys. A similar situation has been encountered within the domain Archaea, where culture-independent single cell genomic analysis recovered genomes belonging to completely novel archaeal phyla with 16S rRNA gene sequences exhibiting marked mismatches, and even indels (insertions and deletions), which render them recalcitrant to amplification using current PCR primers and protocols <xref rid="b0605 b0610" ref-type="bibr">[121,122]</xref>.</p><p>Utilization of PCR independent metagenomic approaches as a routine procedure for assessing diversity might be possible in the future, but currently, PCR-based approaches represent the most feasible way to assess diversity. Therefore, to assess diversity within the shadow biosphere using PCR-based approaches, newer strategies are needed. One approach to potentially limit or decrease the proportion of cells missed due to primer mismatches is to utilize miniprimers (10 bp primers) instead of the standard 18–20 bp primers currently in use, and to employ engineered S-Tbr DNA polymerase instead of Taq polymerase to allow such amplification procedure <xref rid="b0570" ref-type="bibr">[114]</xref>. Theoretically, mismatches are less probable to occur in a shorter 10 bp primer when compared to a standard 18–20 bp primer. Isenbarger et al. <xref rid="b0570" ref-type="bibr">[114]</xref> used this approach to examine bacterial diversity in soil, as well as a microbial mat sample from Cabo Rojo, PR using a shorter version of the standard 27F and 1505R primers (<xref rid="t0010" ref-type="table">Table 2</xref>) [27F-10 (5′ TTCCGGTTGA) 1505R-10 (5 CCTTGTTACG)], and engineered S-Tbr DNA polymerase. The authors compared clone libraries observed using both approaches and clearly demonstrated that a higher proportion of putatively novel sequences were obtained with the miniprimer approach when compared to standard primer approach.</p><p>We further propose an additional approach based on designing multiple degenerate primers to account for mismatches to the universal 16S rRNA gene. Since base pairing is necessary to maintain 16S rRNA secondary structure, degenerate primers will be designed to theoretically maintain canonical base pairings in 16S rRNA secondary structure (<xref rid="f0015" ref-type="fig">Fig 3</xref>), i.e. any base change at one position will be compensated by a complementary base change at the pairing position (<xref rid="f0015" ref-type="fig">Fig. 3</xref>). Applications of such an exercise to two primers (27f, and 1492r) would generate a list of 21 degenerate forward, and 19 degenerate reverse primers (<xref rid="t0015" ref-type="table">Table 3</xref>). Each of these degenerate primers can theoretically be paired with the universal forward or reverse primer and used for 16S rRNA sequence amplification in a multiplexed high throughput PCR approach to identify novel sequences. Such approach has been mulled before but has never been utilized to our knowledge to identify diversity (see <xref rid="f0020" ref-type="fig">Fig. 4</xref>).</p></sec><sec id="s0045"><title>Inadequate documentation of phylum level diversity within existing databases</title><p>In addition to the failure to detect novel bacterial phyla due to their rarity in environmental samples or to their possession of mismatches to most commonly used 16S rRNA gene primers, we argue that current inadequate curation of deposited 16S rRNA gene sequences is leading to failure in recognizing novel bacterial phyla for which 16S rRNA gene sequence has already been reported. All published studies of 16S rRNA gene surveys deposit sequences obtained in a public database, most commonly GenBank database (available at <ext-link ext-link-type="uri" xlink:href="ftp://ftp.ncbi.nih.gov/blast/db/nt.%20and%20EMBL%20database" id="ir0005">ftp://ftp.ncbi.nih.gov/blast/db/nt. and EMBL database</ext-link>). Many of the studies are focused on various ecological questions and do not conduct a detailed assessment of the phylogenetic affiliation of every obtained 16S rRNA gene sequence. Therefore, 16S rRNA gene sequences representing novel phyla could be deposited unnoticed to GenBank database. Curated 16S rRNA gene databases (e.g. Greengenes <xref rid="b0455" ref-type="bibr">[91]</xref>, and SILVA <xref rid="b0165" ref-type="bibr">[33]</xref>) routinely upload recently deposited 16S rRNA gene sequences in GenBank and add such sequences to their taxonomic outlines. However, proposing novel bacterial phyla based on newly obtained sequences represent but one of the interests and responsibilities of database curators, and many novel 16S rRNA sequences that putatively represent novel bacterial phyla are simply refer to as “unclassified” in such databases.</p><p>We hypothesized that 16S rRNA sequences representing multiple novel bacterial phyla have already been obtained and deposited in public databases but has so far escaped detection and documentation due to reasons highlighted above. As a proof of principle, we queried one of such database depositories, the European Nucleotide Archive (ENA) <xref rid="b0460" ref-type="bibr">[92]</xref>, for novel 16S rRNA sequences. At the time of download (September, 2013), 3,178,046 16S rRNA gene sequences were obtained. The sequences were trimmed for length to remove all sequences shorter than 800 bp and were classified using Greengenes taxonomy and Wang method employed in Mothur. Most of the sequences (∼80%) were classified into a known phylum or candidate division with >50% bootstrap support. The remaining 20% of sequences were subjected to an extensive phylogenetic analysis using maximum likelihood approaches (implemented in RaxML <xref rid="b0615" ref-type="bibr">[123]</xref> and Mega <xref rid="b0620" ref-type="bibr">[124]</xref>). As a result, 79 different sequences were judged to represent 8 novel bacterial phyla. These 79 sequences formed eight different independent, deep branching, reproducibly monophyletic, bootstrap-supported clusters, upon applying various tree-building algorithms as well as upon varying the composition and size of the data set used for phylogenetic analysis (<xref rid="f0025" ref-type="fig">Fig. 5</xref>). Sequences representing potentially novel classes and orders belonging to known phyla were also identified (data not shown). Therefore, such analysis, conducted sequences from the relatively smaller ENA database, clearly demonstrates that novel bacterial phyla are routinely detected in diversity surveys but often escapes documentation. Similar analysis using sequences in larger databases e.g. GenBank, as well as continuous evaluation of recently deposited sequences could clearly result in the identification of additional novel phyla.</p></sec><sec sec-type="conclusions" id="s0050"><title>Conclusions</title><p>We hope to convey that, in spite of the spectacular technological advances in DNA sequences, and intense research in the area of microbial diversity, that to-date, a complete census of the phylum level diversity within the domain bacteria has not yet been realized. A similar statement could be made regarding the domain Archaea and, to some extent, the microeukaryotes. Our review summarizes progress toward such goal, and outlines potential strategies and procedures that could facilitate the discovery process. It is interesting to note that many of such novel bacterial phyla appear to have a limited distribution and often represent a minor fraction of the microbial community within a specific habitat. The reason for their retention of such cells in highly diverse habitats, and their potential role within a specific ecosystem (or lack thereof) is an issue that is currently unclear. Access to the genome of such microorganisms through single cell genomics or metagenomics, or success in obtaining representative pure cultures would be required to address such questions.</p></sec><sec id="s0055"><title>Conflict of interest</title><p><italic>The authors have declared no conflict of interest</italic>.</p></sec><sec id="s0060"><title>Compliance with ethics requirements</title><p><italic>This article does not contain any studies with human or animal subjects</italic>.</p></sec></body><back><ref-list><title>References</title><ref id="b0005"><label>1</label><element-citation publication-type="book" id="h0005"><person-group person-group-type="author"><name><surname>Bibel</surname><given-names>D.J.</given-names></name></person-group><chapter-title>Microbial musings</chapter-title><year>2000</year><publisher-name>Star Pub Co.</publisher-name><publisher-loc>Belmont, CA</publisher-loc></element-citation></ref><ref id="b0010"><label>2</label><element-citation publication-type="journal" id="h0010"><person-group person-group-type="author"><name><surname>Blevins</surname><given-names>S.M.</given-names></name><name><surname>Bronze</surname><given-names>M.S.</given-names></name></person-group><article-title>Robert koch and the ‘golden age’ of bacteriology</article-title><source>Int J Infect Dis</source><volume>14</volume><year>2010</year><fpage>744</fpage><lpage>751</lpage></element-citation></ref><ref id="b0015"><label>3</label><element-citation publication-type="journal" id="h0015"><person-group person-group-type="author"><name><surname>Gilbert</surname><given-names>J.A.</given-names></name><name><surname>Meyer</surname><given-names>F.</given-names></name><name><surname>Antonopoulos</surname><given-names>D.</given-names></name><name><surname>Balaji</surname><given-names>P.</given-names></name><name><surname>Brown</surname><given-names>T.</given-names></name><name><surname>Brown</surname><given-names>C.T.</given-names></name></person-group><article-title>The terabase metagenomics workshop and the vision of an earth microbiome project</article-title><source>Stand Genomic Sci</source><volume>3</volume><year>2010</year><fpage>243</fpage><lpage>248</lpage><pub-id pub-id-type="pmid">21304727</pub-id></element-citation></ref><ref id="b0020"><label>4</label><element-citation publication-type="journal" id="h0020"><person-group person-group-type="author"><name><surname>Schloss</surname><given-names>P.D.</given-names></name><name><surname>Handelsman</surname><given-names>J.</given-names></name></person-group><article-title>Towards a census of bacteria in soil</article-title><source>PLoS Comp Biol</source><volume>2</volume><year>2006</year><fpage>e92</fpage></element-citation></ref><ref id="b0025"><label>5</label><element-citation publication-type="journal" id="h0025"><person-group person-group-type="author"><name><surname>Baveye</surname><given-names>P.C.</given-names></name></person-group><article-title>To sequence or not to sequence the whole-soil metagenome?</article-title><source>Nat Rev Microbiol</source><volume>7</volume><year>2009</year><fpage>756</fpage><pub-id pub-id-type="pmid">19756015</pub-id></element-citation></ref><ref id="b0030"><label>6</label><element-citation publication-type="journal" id="h0030"><person-group person-group-type="author"><name><surname>Vogel</surname><given-names>T.M.</given-names></name><name><surname>Simonet</surname><given-names>P.</given-names></name><name><surname>Jansson</surname><given-names>J.K.</given-names></name><name><surname>Hirsch</surname><given-names>P.R.</given-names></name><name><surname>Tiedje</surname><given-names>J.M.</given-names></name><name><surname>Elsas</surname><given-names>JDv</given-names></name></person-group><article-title>Terragenome: a consortium for the sequencing of a soil metagenome</article-title><source>Nat Rev Microbiol</source><volume>7</volume><year>2009</year><fpage>252</fpage></element-citation></ref><ref id="b0035"><label>7</label><element-citation publication-type="journal" id="h0035"><person-group person-group-type="author"><name><surname>Razumov</surname><given-names>A.S.</given-names></name></person-group><article-title>The direct method of calculation of bacteria in water. 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person-group-type="author"><name><surname>Stamatakis</surname><given-names>A.</given-names></name></person-group><article-title>Raxml version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies</article-title><source>Bioinformatics</source><year>2014</year></element-citation></ref><ref id="b0620"><label>124</label><element-citation publication-type="journal" id="h0620"><person-group person-group-type="author"><name><surname>Hall</surname><given-names>B.G.</given-names></name></person-group><article-title>Building phylogenetic trees from molecular data with mega</article-title><source>Mol Biol Evol</source><volume>30</volume><issue>5</issue><year>2013</year><fpage>1229</fpage><lpage>1235</lpage><pub-id pub-id-type="pmid">23486614</pub-id></element-citation></ref><ref id="b0625"><label>125</label><element-citation publication-type="journal" id="h0625"><person-group person-group-type="author"><name><surname>Ludwig</surname><given-names>W.</given-names></name><name><surname>Strunk</surname><given-names>O.</given-names></name><name><surname>Westram</surname><given-names>R.</given-names></name><name><surname>Richter</surname><given-names>L.</given-names></name><name><surname>Meier</surname><given-names>H.</given-names></name><name><surname>Yadhukumar</surname></name></person-group><article-title>Arb: a software environment for sequence data</article-title><source>Nucleic Acids Res</source><volume>32</volume><issue>4</issue><year>2004</year><fpage>1363</fpage><lpage>1371</lpage><pub-id pub-id-type="pmid">14985472</pub-id></element-citation></ref><ref id="b0630"><label>126</label><element-citation publication-type="journal" id="h0630"><person-group person-group-type="author"><name><surname>Baker</surname><given-names>G.C.</given-names></name><name><surname>Smith</surname><given-names>J.J.</given-names></name><name><surname>Cowan</surname><given-names>D.A.</given-names></name></person-group><article-title>Review and re-analysis of domain-specific 16S primers</article-title><source>J Microbiol Meth</source><volume>55</volume><year>2003</year><fpage>541</fpage><lpage>555</lpage></element-citation></ref></ref-list><bio><graphic xlink:href="fx3"></graphic><p><bold>Noha Youssef</bold> is an Assistant Professor in the Department of Microbiology and Molecular Genetics at Oklahoma State University, Stillwater, OK, USA. She graduated with a Bachelor degree in Pharmacy from Ain Shams University, Cairo, Egypt. She obtained her PhD from the department of Botany and Microbiology at the University of Oklahoma, Norma, OK, USA. Her PHD research was in the area of petroleum microbiology and microbially enhanced oil recovery. Her post-graduate research was conducted in Dr. Elshahed laboratory, with a research focus on molecular microbial ecology and environmental genomics. Currently, research in her laboratory is focused on single cell genomics and the ecology and evolution of anaerobic fungi.</p></bio><bio><graphic xlink:href="fx4"></graphic><p><bold>Matthew Brian Couger</bold> is a doctoral student in the Microbiology and Molecular Genetics program at Oklahoma State University. He currently is serving as the Extreme Science and Engineering (XSEDE) Bioinformatics Domain Champion, a position for consulting on large-scale bioinformatics projects. His current and ongoing interest is quantitative molecular biology, molecular evolution, synthetic biology, high performance computing, and bioinformatics.</p></bio><bio><graphic xlink:href="fx5"></graphic><p><bold>Alexandra L. McCully</bold> graduated summa cum laude in 2013 from Oklahoma State University with a Bachelor of Science degree in Microbiology and Molecular Genetics. She trained as an undergraduate researcher to investigate salt adaptation strategies in halophilic microorganisms and analyze phylogenetic assignments within the domain Bacteria. Currently, she is working towards her PhD at Indiana University studying microbial metabolic interactions and biofuel production.</p></bio><bio><graphic xlink:href="fx6"></graphic><p><bold>Andres Eduardo Guerrero</bold> Criado has studied in Venezuela, the United States, and Spain. Currently as an undergraduate of Microbiology, Cell and Molecular Biology and Genetics/Biochemistry at Oklahoma State University he is involved in research in bioinformatics, phylogeny, microbial ecology and protein structure elucidation under Dr. Noha Youssef. In addition, at Washington University in St. Louis Medical School he collaborated with Dr. Jean Schaffer and her Diabetic Cardiovascular Disease Center studying the role of RNASET2 in oxidative stress. The duality of these programs offers the perfect combination of research and practice to pursue a degree in Medical Research.</p></bio><bio><graphic xlink:href="fx7"></graphic><p><bold>Mostafa Elshahed</bold> graduated from Cairo University faculty of Pharmacy in 1993. He obtained his Ph.D. from the University of Oklahoma in 2001. His PhD studies focused on elucidating the pathways for benzoate degradation under anaerobic conditions. His post-doctoral studies, also at the university of Oklahoma focused on the microbial ecology of terrestrial sulfidic springs. Dr. Elshahed joined Oklahoma State University as an Assistant Professor in 2007 and was promoted to an associate professor in 2011. Currently Dr. Elshahed has multiple research interests including Environmental genomics, petroleum microbiology, and the biology and metabolism of the anaerobic fungi.</p></bio><ack id="ak005"><title>Acknowledgments</title><p>Funding in our laboratory to support work on bacterial diversity and environmental genomics is supported by the <funding-source id="gp005">National Science Foundation Microbial Observatories Program</funding-source> (Grant EF0801858).</p></ack><fn-group><fn id="d32e975"><p>Peer review under responsibility of Cairo University.</p><p><fig id="f0030"><graphic xlink:href="fx1"></graphic></fig></p></fn></fn-group></back><floats-group><fig id="f0005"><label>Fig. 1</label><caption><p>Phylogenetic tree depicting the twelve “original” bacterial phyla proposed by Carl Woese in his seminal review on bacterial evolution. Adapted from Ref. <xref rid="b0045" ref-type="bibr">[9]</xref>. These phyla are Thermotogae, Chloroflexi (Green non-sulfur Bacteria), Deinococcus, Spirochaetes, Chlorobia (Green sulfur bacteria), Bacteroidetes, Planctomycetes, Chlamydia, Cyanobacteria, Gram-positive Bacteria (comprising the high GC Actinobacteria, and the low GC Firmicutes), Proteobacteria (Purple bacteria).</p></caption><graphic xlink:href="gr1"></graphic></fig><fig id="f0010"><label>Fig. 2</label><caption><p>Flowchart depicting the “16S rRNA analysis” protocol. The protocol starts by DNA extraction, followed by amplifying the small subunit rRNA gene using universal or domain-specific primers. PCR products are then cloned and sequenced. Obtained small subunit rRNA gene sequences are then analyzed, binned into operational taxonomic units (OTUs), and used for phylogenetic inferences.</p></caption><graphic xlink:href="gr2"></graphic></fig><fig id="f0015"><label>Fig. 3</label><caption><p>Flowchart depicting a targeted approach developed for the identification of novel bacterial phyla within the rare biosphere. The approach combines the sequence read length and accuracy of the Sanger sequencing approach with the high throughput capability of next generation (Pyrosequencing or Illumina) sequencing approaches. Pyrosequencing or Illumina sequencing output are first used to identify potentially novel members within rare members of the community. The short sequences are then used to design custom primers. The newly designed primers are then used in conjunction with a forward, or reverse bacterial primer for amplification of near-complete 16S rRNA gene sequences. Obtained PCR products are cloned and Sanger-sequenced, and the sequences obtained are used for detailed phylogenetic inferences.</p></caption><graphic xlink:href="gr3"></graphic></fig><fig id="f0020"><label>Fig. 4</label><caption><p>Secondary structure of regions (A) 8–27, and (B) 1492–1510 of the 16S rRNA molecule. Canonical base pairing (shown as lines) is targeted for designing degenerate primers such that a change in one base is associated with a complementary change in the pairing position. Noncanonical base pairings (A-A, C-C, G-G, C-A, U-G, G-A, U-U), and wobble base pairing (G-U), often a consequence of canonical pairings, are theoretically less necessary for maintaining ribosomal integrity, and so are not targeted for primer design. The sequences of all possible degenerate 27F and 1492R primers are shown in <xref rid="t0015" ref-type="table">Table 3</xref>.</p></caption><graphic xlink:href="gr4"></graphic></fig><fig id="f0025"><label>Fig. 5</label><caption><p>Maximum likelihood dendogram based on the 16S rRNA gene sequences affiliated with representatives of the putatively novel phyla (PNP1-PNP8). Bootstrap values (in percentages) are based on 1000 replicates and are shown for branches with more than 50% bootstrap support. Sequences obtained from the ENA database (<italic>n</italic> = 3,178,046) were classified in MOTHUR using classify.seqs command with the Greengenes taxonomy outline and Wang method. Sequences that failed to classify into a known phylum with at least 50% bootstrap support (<italic>n</italic> = 664,621) were considered potentially novel and were subjected to extensive phylogenetic analysis using a combination of Mega <xref rid="b0620" ref-type="bibr">[124]</xref>, RaxML <xref rid="b0615" ref-type="bibr">[123]</xref>, and Arb <xref rid="b0625" ref-type="bibr">[125]</xref>. Seventy-nine sequences formed 8 independent, deep-branching, reproducibly monophyletic, bootstrap-supported clusters, upon applying various tree-building algorithms as well as upon varying the composition and size of the data set used for phylogenetic analysis. Representatives of these 8 novel phyla are shown in the tree along with their source.</p></caption><graphic xlink:href="gr5"></graphic></fig><table-wrap id="t0005" position="float"><label>Table 1</label><caption><p>Bacteria phyla names according to Greengenes <xref rid="b0455" ref-type="bibr">[91]</xref> and SILVA <xref rid="b0165" ref-type="bibr">[33]</xref> databases (August 2014).<xref rid="tblfn1" ref-type="table-fn">a</xref></p></caption><table frame="hsides" rules="groups"><thead><tr><th>Greengenes</th><th>SILVA</th></tr></thead><tbody><tr><td>AC1</td><td></td></tr><tr><td><italic>Acidobacteria</italic></td><td><italic>Acidobacteria</italic></td></tr><tr><td><bold>Actinobacteria</bold></td><td><bold>Actinobacteria</bold></td></tr><tr><td>AD3</td><td></td></tr><tr><td>AncK6</td><td></td></tr><tr><td></td><td>aquifer1</td></tr><tr><td></td><td>aquifer2</td></tr><tr><td><italic>Aquificae</italic></td><td><italic>Aquificae</italic></td></tr><tr><td><italic>Armatimonadetes</italic></td><td><italic>Armatimonadetes</italic></td></tr><tr><td><bold>Bacteroidetes</bold></td><td><bold>Bacteroidetes</bold></td></tr><tr><td></td><td>BD1-5</td></tr><tr><td>BHI80-139</td><td>BHI80-139</td></tr><tr><td>BRC1</td><td>BRC1</td></tr><tr><td><italic>Caldiserica</italic></td><td><italic>Caldiserica</italic></td></tr><tr><td><italic>Caldithrix</italic></td><td></td></tr><tr><td>CD12</td><td></td></tr><tr><td><bold>Chlamydiae</bold></td><td><bold>Chlamydiae</bold></td></tr><tr><td><bold>Chlorobi</bold></td><td><bold>Chlorobi</bold></td></tr><tr><td><bold>Chloroflexi</bold></td><td><bold>Chloroflexi</bold></td></tr><tr><td><italic>Chrysiogenetes</italic></td><td><italic>Chrysiogenetes</italic></td></tr><tr><td></td><td>CKC4</td></tr><tr><td><bold>Cyanobacteria</bold></td><td><bold>Cyanobacteria</bold></td></tr><tr><td><italic>Deferribacteres</italic></td><td><italic>Deferribacteres</italic></td></tr><tr><td><bold>Thermi</bold></td><td><bold>Deinococcus-Thermus</bold></td></tr><tr><td><italic>Dictyoglomi</italic></td><td><italic>Dictyoglomi</italic></td></tr><tr><td><italic>Elusimicrobia</italic></td><td><italic>Elusimicrobia</italic></td></tr><tr><td>EM3</td><td></td></tr><tr><td>EM19</td><td></td></tr><tr><td>FBP</td><td></td></tr><tr><td>FCPU426</td><td></td></tr><tr><td><italic>Fibrobacteres</italic></td><td><italic>Fibrobacteres</italic></td></tr><tr><td><bold>Firmicutes</bold></td><td><bold>Firmicutes</bold></td></tr><tr><td><italic>Fusobacteria</italic></td><td><italic>Fusobacteria</italic></td></tr><tr><td></td><td>GAL08</td></tr><tr><td>GAL15</td><td></td></tr><tr><td><italic>Gemmatimonadetes</italic></td><td><italic>Gemmatimonadetes</italic></td></tr><tr><td>GN01</td><td></td></tr><tr><td>GN02</td><td></td></tr><tr><td>GN04</td><td></td></tr><tr><td>GOUTA4</td><td>GOUTA4</td></tr><tr><td>H-178</td><td></td></tr><tr><td>Hyd24-12</td><td>Hyd24-12</td></tr><tr><td>Kazan-3B-28</td><td></td></tr><tr><td></td><td>KB1</td></tr><tr><td>KSB3</td><td></td></tr><tr><td>LCP-89</td><td></td></tr><tr><td></td><td>JL-ETNP-Z39</td></tr><tr><td></td><td>JS1</td></tr><tr><td>LD1</td><td>LD1-PA38</td></tr><tr><td><italic>Lentisphaerae</italic></td><td><italic>Lentisphaerae</italic></td></tr><tr><td>MAT-CR-M4-B07</td><td></td></tr><tr><td>MVP-21</td><td></td></tr><tr><td>MVS-104</td><td></td></tr><tr><td>NC10</td><td></td></tr><tr><td><italic>Nitrospirae</italic></td><td><italic>Nitrospirae</italic></td></tr><tr><td>NKB19</td><td></td></tr><tr><td>NPL-UPA2</td><td>NPL-UPA2</td></tr><tr><td>OC31</td><td>OC31</td></tr><tr><td>OctSpA1-106</td><td></td></tr><tr><td>OD1</td><td>OD1</td></tr><tr><td>OP1</td><td></td></tr><tr><td>OP3</td><td>OP3</td></tr><tr><td>OP8</td><td>OP8</td></tr><tr><td>OP9</td><td>OP9</td></tr><tr><td>OP11</td><td>OP11</td></tr><tr><td>PAUC34f</td><td></td></tr><tr><td><bold>Planctomycetes</bold></td><td><bold>Planctomycetes</bold></td></tr><tr><td>Poribacteria</td><td></td></tr><tr><td><bold>Proteobacteria</bold></td><td><bold>Proteobacteria</bold></td></tr><tr><td></td><td>RsaHF231</td></tr><tr><td></td><td>S2R-29</td></tr><tr><td>SAR406</td><td></td></tr><tr><td>SBR1093</td><td></td></tr><tr><td></td><td>SBYG-2791</td></tr><tr><td>SC4</td><td></td></tr><tr><td></td><td>SHA-109</td></tr><tr><td></td><td>SM2F11</td></tr><tr><td><bold>Spirochaetes</bold></td><td><bold>Spirochaetae</bold></td></tr><tr><td>SR1</td><td>SR1</td></tr><tr><td><italic>Synergistetes</italic></td><td><italic>Synergistetes</italic></td></tr><tr><td>TA06</td><td>TA06</td></tr><tr><td><italic>Tenericutes</italic></td><td><italic>Tenericutes</italic></td></tr><tr><td></td><td><italic>Thermodesulfobacteria</italic></td></tr><tr><td><bold>Thermotogae</bold></td><td><bold>Thermotogae</bold></td></tr><tr><td>TM6</td><td>TM6</td></tr><tr><td>TM7</td><td>TM7</td></tr><tr><td>TPD-58</td><td></td></tr><tr><td><italic>Verrucomicrobia</italic></td><td><italic>Verrucomicrobia</italic></td></tr><tr><td>VHS-B3-43</td><td></td></tr><tr><td></td><td>WCHB1-60</td></tr><tr><td></td><td>WD272</td></tr><tr><td>WPS-2</td><td></td></tr><tr><td>WS1</td><td></td></tr><tr><td>WS2</td><td></td></tr><tr><td>WS3</td><td>WS3</td></tr><tr><td>WS4</td><td></td></tr><tr><td>WS5</td><td></td></tr><tr><td>WS6</td><td>WS6</td></tr><tr><td>WWE1</td><td></td></tr><tr><td>ZB3</td><td></td></tr></tbody></table><table-wrap-foot><fn id="tblfn1"><label>a</label><p>Phyla shown in Boldface are those already known with cultured representatives prior to the advent of 16S rRNA gene diversity surveys. Phyla in italics are those with cultured representatives originally identified using 16S rRNA sequencing as uncultured bacterial phyla, with representative isolates subsequently obtained. The rest of the phyla currently have no cultured representatives.</p></fn></table-wrap-foot></table-wrap><table-wrap id="t0010" position="float"><label>Table 2</label><caption><p>Common 16S rRNA bacterial primers used for culture-independent analysis.<xref rid="tblfn2" ref-type="table-fn">a</xref></p></caption><table frame="hsides" rules="groups"><thead><tr><th>Primer name</th><th>Primer sequence<xref rid="tblfn3" ref-type="table-fn">b</xref></th></tr></thead><tbody><tr><td>8F</td><td>AGAGTTTGATCCTGGCTCAG</td></tr><tr><td>27F</td><td>AGAGTTTGATCMTGGCTCAG</td></tr><tr><td>338R</td><td>GCCTTGCCAGCCCGCTCAG</td></tr><tr><td>338F</td><td>ACTCCTACGGGAGGCWGCAGC</td></tr><tr><td>518R</td><td>GTATTACCGCGGCTGCTGG</td></tr><tr><td>530F</td><td>ACGCTTGCACCCTCCGTATT</td></tr><tr><td>805R</td><td>GGATTAGATACCCTGGTAGTC</td></tr><tr><td>967F</td><td>CAACGCGAAGAACCTTACC</td></tr><tr><td>1238R</td><td>GTAGCRCGTGTGTMGCCC</td></tr><tr><td>1100F</td><td>YAACGAGCGCAACCC</td></tr><tr><td>1492R</td><td>CGGTTACCTTGTTACGACTT</td></tr></tbody></table><table-wrap-foot><fn id="tblfn2"><label>a</label><p>F indicates a forward primer and R indicates a reverse primer. Number in the primer name indicates the starting position of the primer sequence within the <italic>E. coli</italic> 16S rRNA gene sequence.</p></fn></table-wrap-foot><table-wrap-foot><fn id="tblfn3"><label>b</label><p>Data from references <xref rid="b0285 b0630" ref-type="bibr">[57,126]</xref>.</p></fn></table-wrap-foot></table-wrap><table-wrap id="t0015" position="float"><label>Table 3</label><caption><p>List of degenerate primers for 27F and 1492R designed as specified in the text. The sequences of the non-degenerate 27F and 1492R are given in the table heading.</p></caption><table frame="hsides" rules="groups"><tbody><tr><td>AGAGUUUGAUCAUGGCUCAG</td><td>AAGUCGUAACAAGGUAACC</td></tr><tr><td><bold>B</bold>GAGUUUGAUCAUGGCUCAG</td><td><bold>G</bold>AGUCGUAACAAGGUAACC</td></tr><tr><td>A<bold>H</bold>AGUUUGAUCAUGGCU<bold>D</bold>AG</td><td>A<bold>G</bold>GUCGUAACAAGGUAACC</td></tr><tr><td>AG<bold>B</bold>GUUUGAUCAUGGC<bold>V</bold>CAG</td><td>AA<bold>H</bold>UCGUAACAAGGUAACC</td></tr><tr><td>AGA<bold>H</bold>UUUGAUCAUGH<bold>D</bold>UCAG</td><td>AAG<bold>C</bold>CGUAACAAGGUAACC</td></tr><tr><td>AGAG<bold>G</bold>UUGAUCAUG<bold>H</bold>CUCAG</td><td>AAGU<bold>D</bold>GUAACAAGGUAACC</td></tr><tr><td>AGAG<bold>A</bold>UUGAUCAUG<bold>H</bold>CUCAG</td><td>AAGUC<bold>H</bold>UAACAAGGUAACC</td></tr><tr><td>AGAG<bold>C</bold>UUGAUCAUG<bold>H</bold>CUCAG</td><td>AAGUCG<bold>C</bold>AACAAGGUAACC</td></tr><tr><td>AGAGU<bold>G</bold>UGAUCAUG<bold>H</bold>CUCAG</td><td>AAGUCGU<bold>G</bold>ACAAGGUAACC</td></tr><tr><td>AGAGU<bold>A</bold>UGAUCAUG<bold>H</bold>CUCAG</td><td>AAGUCGUA<bold>B</bold>CAAGGUAACC</td></tr><tr><td>AGAGU<bold>C</bold>UGAUCAUG<bold>H</bold>CUCAG</td><td>AAGUCGUAA<bold>D</bold>AAGGUAACC</td></tr><tr><td>AGAGUU<bold>C</bold>GAUCAUGGCUCAG</td><td>AAGUCGUAAC<bold>G</bold>AGGUAACC</td></tr><tr><td>AGAGUUU<bold>A</bold>AUCAUGGCUCAG</td><td>AAGUCGUAACA<bold>G</bold>GGUAACC</td></tr><tr><td>AGAGUUUG<bold>G</bold>UCAUGGCUCAG</td><td>AAGUCGUAACAA<bold>A</bold>GUAACC</td></tr><tr><td>AGAGUUUGA<bold>V</bold>CAUGGCUCAG</td><td>AAGUCGUAACAAG<bold>A</bold>UAACC</td></tr><tr><td>AGAGUUUGAU<bold>D</bold>AUGGCUCAG</td><td>AAGUCGUAACAAGG<bold>V</bold>AACC</td></tr><tr><td>AGAGUUUGAUC<bold>B</bold>UGGCUCAG</td><td>AAGUCGUAACAAGGU<bold>B</bold>ACC</td></tr><tr><td>AGAGUUUGAUCA<bold>C</bold>GGCUCAG</td><td>AAGUCGUAACAAGGUA<bold>B</bold>CC</td></tr><tr><td>AGAGUUUGAUCAU<bold>U</bold>GCUCAG</td><td>AAGUCGUAACAAGGUAA<bold>D</bold>C</td></tr><tr><td>AGAGUUUGAUCAUG<bold>U</bold>CUCAG</td><td>AAGUCGUAACAAGGUAAC<bold>D</bold></td></tr><tr><td>AGAGUUUGAUCAUGGCUC<bold>G</bold>G</td><td></td></tr><tr><td>AGAGUUUGAUCAUGGCUCA<bold>H</bold></td><td></td></tr></tbody></table></table-wrap></floats-group></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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