Evidence map›Paper›PMID 31470795›Full record

ArticleBMC genomics2019

The Komodo dragon (Varanus komodoensis) genome and identification of innate immunity genes and clusters.

Monique L van Hoek, M Dennis Prickett, Robert E Settlage, Lin Kang, Pawel Michalak, Kent A Vliet, Barney M Bishop

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.8field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 32 citations in OpenAlex.

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  11. Structure, function, and evolution ofProceedings of the National Academy of Sciences of the United States of America · 2020
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 6 institutions in 3 countries.

Monique L van HoekSchool of Systems Biology, George Mason University, Manassas, VA, 20110, USA.
M Dennis PrickettDipartimento di Scienze della Vita-Edif. C11, Università di Trieste, Via Licio Giorgieri 1, 34127, Trieste, Italy.
Robert E SettlageAdvanced Research Computing, Virginia Polytechnic Institute and State University, Blacksburg, VA, 24061, USA.
Lin KangEdward Via College of Osteopathic Medicine, Blacksburg, VA, 24060, USA.
Pawel MichalakEdward Via College of Osteopathic Medicine, Blacksburg, VA, 24060, USA.
Kent A VlietDepartment of Biology, University of Florida, Gainesville, Florida, FL, 32611, USA.
Barney M BishopDepartment of Chemistry, George Mason University, Manassas, VA, 20110, USA. bbishop1@gmu.edu.ORCID http://orcid.org/0000-0002-6626-9251
George Mason University · USEdward Via College of Osteopathic Medicine · USUniversity of Florida · USUniversity of Trieste · ITVirginia–Maryland College of Veterinary Medicine · USVirginia Tech · US

Funding

Defense Threat Reduction Agency HDTRA1-12-C-0039
6 · The paper itself

Abstract

backgroundWe report the sequencing, assembly and analysis of the genome of the Komodo dragon (Varanus komodoensis), the largest extant lizard, with a focus on antimicrobial host-defense peptides. The Komodo dragon diet includes carrion, and a complex milieu of bacteria, including potentially pathogenic strains, has been detected in the saliva of wild dragons. They appear to be unaffected, suggesting that dragons have robust defenses against infection. While little information is available regarding the molecular biology of reptile immunity, it is believed that innate immunity, which employs antimicrobial host-defense peptides including defensins and cathelicidins, plays a more prominent role in reptile immunity than it does in mammals. .

resultsHigh molecular weight genomic DNA was extracted from Komodo dragon blood cells. Subsequent sequencing and assembly of the genome from the collected DNA yielded a genome size of 1.6 Gb with 45x coverage, and the identification of 17,213 predicted genes. Through further analyses of the genome, we identified genes and gene-clusters corresponding to antimicrobial host-defense peptide genes. Multiple β-defensin-related gene clusters were identified, as well as a cluster of potential Komodo dragon ovodefensin genes located in close proximity to a cluster of Komodo dragon β-defensin genes. In addition to these defensins, multiple cathelicidin-like genes were also identified in the genome. Overall, 66 β-defensin genes, six ovodefensin genes and three cathelicidin genes were identified in the Komodo dragon genome.

conclusionsGenes with important roles in host-defense and innate immunity were identified in this newly sequenced Komodo dragon genome, suggesting that these organisms have a robust innate immune system. Specifically, multiple Komodo antimicrobial peptide genes were identified. Importantly, many of the antimicrobial peptide genes were found in gene clusters. We found that these innate immunity genes are conserved among reptiles, and the organization is similar to that seen in other avian and reptilian species. Having the genome of this important squamate will allow researchers to learn more about reptilian gene families and will be a valuable resource for researchers studying the evolution and biology of the endangered Komodo dragon.

Indexed as

AnimalsAntimicrobial Cationic Peptidesbeta-DefensinsCathelicidinsGenomeHigh-Throughput Nucleotide SequencingImmunity, InnateLizardsMultigene FamilyAntimicrobial Cationic Peptidesbeta-DefensinsCathelicidinsAntimicrobial peptideCathelicidinDefensinGene clusterInnate immunityKomodo dragonMonitor lizardVaranus komodoensis

Identifiers

PMID31470795
PMCPMC6716921
OpenAlexW2970535282

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.