Evidence map›Paper›PMID 27375574›Full record

ArticleFrontiers in microbiology2016

Genomic and Metagenomic Analysis of Diversity-Generating Retroelements Associated with Treponema denticola.

Sutichot Nimkulrat, Heewook Lee, Thomas G Doak, Yuzhen Ye

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Article in Frontiers in microbiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Article
  2. Targeted hypermutation of putative antigen sensors in multicellular bacteria.Proceedings of the National Academy of Sciences of the United States of America · 2024
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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Sutichot NimkulratSchool of Informatics and Computing, Indiana University, Bloomington IN, USA.
Heewook LeeComputational Biology Department, School of Computer Science, Carnegie Mellon University, Pittsburgh PA, USA.
Thomas G DoakDepartment of Biology, Indiana University, BloomingtonIN, USA; National Center for Genome Analysis Support, Indiana University, BloomingtonIN, USA.
Yuzhen YeSchool of Informatics and Computing, Indiana University, Bloomington IN, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diversity-generating retroelements (DGRs) are genetic cassettes that can produce massive protein sequence variation in prokaryotes. Presumably DGRs confer selective advantages to their hosts (bacteria or viruses) by generating variants of target genes-typically resulting in target proteins with altered ligand-binding specificity-through a specialized error-prone reverse transcription process. The only extensively studied DGR system is from the Bordetella phage BPP-1, although DGRs are predicted to exist in other species. Using bioinformatics analysis, we discovered that the DGR system associated with the Treponema denticola species (a human oral-associated periopathogen) is dynamic (with gains/losses of the system found in the isolates) and diverse (with multiple types found in isolated genomes and the human microbiota). The T. denticola DGR is found in only nine of the 17 sequenced T. denticola strains. Analysis of the DGR-associated template regions and reverse transcriptase gene sequences revealed two types of DGR systems in T. denticola: the ATCC35405-type shared by seven isolates including ATCC35405; and the SP32-type shared by two isolates (SP32 and SP33), suggesting multiple DGR acquisitions. We detected additional variants of the T. denticola DGR systems in the human microbiomes, and found that the SP32-type DGR is more abundant than the ATCC35405-type in the healthy human oral microbiome, although the latter is found in more sequenced isolates. This is the first comprehensive study to characterize the DGRs associated with T. denticola in individual genomes as well as human microbiomes, demonstrating the importance of utilizing both individual genomes and metagenomes for characterizing the elements, and for analyzing their diversity and distribution in human populations.

Indexed as

diversity-generating retroelementshuman microbiomereverse transcriptasetemplate regionTreponema denticola

Identifiers

PMID27375574
PMCPMC4891356

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