Identifying Group-Specific Sequences for Microbial Communities Using Long k-mer Sequence Signatures
Identifieur interne : 001E37 ( Ncbi/Curation ); précédent : 001E36; suivant : 001E38Identifying Group-Specific Sequences for Microbial Communities Using Long k-mer Sequence Signatures
Auteurs : Ying Wang [République populaire de Chine] ; Lei Fu [République populaire de Chine] ; Jie Ren [États-Unis] ; Zhaoxia Yu [États-Unis] ; Ting Chen [États-Unis, République populaire de Chine] ; Fengzhu Sun [États-Unis, République populaire de Chine]Source :
- Frontiers in Microbiology [ 1664-302X ] ; 2018.
Abstract
Comparing metagenomic samples is crucial for understanding microbial communities. For different groups of microbial communities, such as human gut metagenomic samples from patients with a certain disease and healthy controls, identifying
Url:
DOI: 10.3389/fmicb.2018.00872
PubMed: 29774017
PubMed Central: 5943621
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Identifying <italic>Group-Specific</italic>
Sequences for Microbial Communities Using Long <italic>k</italic>
-mer Sequence Signatures</title>
<author><name sortKey="Wang, Ying" sort="Wang, Ying" uniqKey="Wang Y" first="Ying" last="Wang">Ying Wang</name>
<affiliation wicri:level="1"><nlm:aff id="aff1"><institution>Department of Automation, Xiamen University</institution>
,<addr-line>Xiamen</addr-line>
,<country>China</country>
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<country xml:lang="fr">République populaire de Chine</country>
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<author><name sortKey="Fu, Lei" sort="Fu, Lei" uniqKey="Fu L" first="Lei" last="Fu">Lei Fu</name>
<affiliation wicri:level="1"><nlm:aff id="aff1"><institution>Department of Automation, Xiamen University</institution>
,<addr-line>Xiamen</addr-line>
,<country>China</country>
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<country xml:lang="fr">République populaire de Chine</country>
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<author><name sortKey="Ren, Jie" sort="Ren, Jie" uniqKey="Ren J" first="Jie" last="Ren">Jie Ren</name>
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,<addr-line>CA</addr-line>
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<author><name sortKey="Yu, Zhaoxia" sort="Yu, Zhaoxia" uniqKey="Yu Z" first="Zhaoxia" last="Yu">Zhaoxia Yu</name>
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,<addr-line>Irvine, CA</addr-line>
,<country>United States</country>
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<country xml:lang="fr">République populaire de Chine</country>
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<author><name sortKey="Sun, Fengzhu" sort="Sun, Fengzhu" uniqKey="Sun F" first="Fengzhu" last="Sun">Fengzhu Sun</name>
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,<addr-line>CA</addr-line>
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<series><title level="j">Frontiers in Microbiology</title>
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<front><div type="abstract" xml:lang="en"><p>Comparing metagenomic samples is crucial for understanding microbial communities. For different groups of microbial communities, such as human gut metagenomic samples from patients with a certain disease and healthy controls, identifying <italic>group-specific</italic>
sequences offers essential information for potential biomarker discovery. A sequence that is present, or rich, in one group, but absent, or scarce, in another group is considered “<italic>group-specific</italic>
” in our study. Our main purpose is to discover <italic>group-specific</italic>
sequence regions between control and case groups as disease-associated markers. We developed a long <italic>k</italic>
-mer (<italic>k</italic>
≥ 30 bps)-based computational pipeline to detect <italic>group-specific</italic>
sequences at strain resolution free from reference sequences, sequence alignments, and metagenome-wide <italic>de novo</italic>
assembly. We called our method MetaGO: <italic>Group-specific</italic>
oligonucleotide analysis for metagenomic samples. An open-source pipeline on <italic>Apache Spark</italic>
was developed with parallel computing. We applied MetaGO to one simulated and three real metagenomic datasets to evaluate the discriminative capability of identified <italic>group-specific</italic>
markers. In the simulated dataset, 99.11% of <italic>group-specific</italic>
logical <italic>40</italic>
-mers covered 98.89% <italic>disease-specific</italic>
regions from the disease-associated strain. In addition, 97.90% of <italic>group-specific</italic>
numerical <italic>40</italic>
-mers covered 99.61 and 96.39% of differentially abundant genome and regions between two groups, respectively. For a large-scale metagenomic liver cirrhosis (LC)-associated dataset, we identified 37,647 <italic>group-specific 40-</italic>
mer features. Any one of the features can predict disease status of the training samples with the average of sensitivity and specificity higher than 0.8. The random forests classification using the top 10 <italic>group-specific</italic>
features yielded a higher AUC (from ∼0.8 to ∼0.9) than that of previous studies. All <italic>group-specific 40-</italic>
mers were present in LC patients, but not healthy controls. All the assembled 11 <italic>LC-specific</italic>
sequences can be mapped to two strains of <italic>Veillonella parvula</italic>
: UTDB1-3 and DSM2008. The experiments on the other two real datasets related to Inflammatory Bowel Disease and Type 2 Diabetes in Women consistently demonstrated that MetaGO achieved better prediction accuracy with fewer features compared to previous studies. The experiments showed that MetaGO is a powerful tool for identifying <italic>group-specific k</italic>
-mers, which would be clinically applicable for disease prediction. MetaGO is available at <ext-link ext-link-type="uri" xlink:href="https://github.com/VVsmileyx/MetaGO">https://github.com/VVsmileyx/MetaGO</ext-link>
.</p>
</div>
</front>
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