Evidence map›Paper›PMID 28910350›Full record

ArticlePLoS neglected tropical diseases2017

Phylogeographic, genomic, and meropenem susceptibility analysis of Burkholderia ubonensis.

Erin P Price, Derek S Sarovich, Jessica R Webb, Carina M Hall, Sierra A Jaramillo, Jason W Sahl, Mirjam Kaestli, Mark Mayo, Glenda Harrington, Anthony L Baker and 11 more

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

12 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Colony morphotype variation inJournal of bacteriology · 2025
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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

21 authors at 6 institutions in 2 countries.

Erin P PriceGlobal and Tropical Health Division, Menzies School of Health Research, Darwin, Northern Territory, Australia.ORCID http://orcid.org/0000-0002-1079-4882
Derek S SarovichGlobal and Tropical Health Division, Menzies School of Health Research, Darwin, Northern Territory, Australia.
Jessica R WebbGlobal and Tropical Health Division, Menzies School of Health Research, Darwin, Northern Territory, Australia.
Carina M HallThe Pathogen and Microbiome Institute, Northern Arizona University, Flagstaff, Arizona, United States of America.
Sierra A JaramilloThe Pathogen and Microbiome Institute, Northern Arizona University, Flagstaff, Arizona, United States of America.
Jason W SahlThe Pathogen and Microbiome Institute, Northern Arizona University, Flagstaff, Arizona, United States of America.
Mirjam KaestliGlobal and Tropical Health Division, Menzies School of Health Research, Darwin, Northern Territory, Australia.
Mark MayoGlobal and Tropical Health Division, Menzies School of Health Research, Darwin, Northern Territory, Australia.
Glenda HarringtonGlobal and Tropical Health Division, Menzies School of Health Research, Darwin, Northern Territory, Australia.
Anthony L BakerEnvironmental and Public Health Microbiology Research Group, Microbiology and Immunology, James Cook University, Townsville, Queensland, Australia.
Lindsay C Sidak-LoftisThe Pathogen and Microbiome Institute, Northern Arizona University, Flagstaff, Arizona, United States of America.
Erik W SettlesThe Pathogen and Microbiome Institute, Northern Arizona University, Flagstaff, Arizona, United States of America.
Madeline LummisThe Pathogen and Microbiome Institute, Northern Arizona University, Flagstaff, Arizona, United States of America.
James M SchuppTranslational Genomics Research Institute, Flagstaff, Arizona, United States of America.
John D GilleceTranslational Genomics Research Institute, Flagstaff, Arizona, United States of America.
Apichai TuanyokThe Pathogen and Microbiome Institute, Northern Arizona University, Flagstaff, Arizona, United States of America.
Jeffrey WarnerEnvironmental and Public Health Microbiology Research Group, Microbiology and Immunology, James Cook University, Townsville, Queensland, Australia.
Joseph D BuschThe Pathogen and Microbiome Institute, Northern Arizona University, Flagstaff, Arizona, United States of America.
Paul KeimThe Pathogen and Microbiome Institute, Northern Arizona University, Flagstaff, Arizona, United States of America.
Bart J CurrieGlobal and Tropical Health Division, Menzies School of Health Research, Darwin, Northern Territory, Australia.
David M WagnerThe Pathogen and Microbiome Institute, Northern Arizona University, Flagstaff, Arizona, United States of America.
Northern Arizona University · USMenzies School of Health Research · AUTranslational Genomics Research Institute · USUniversity of the Sunshine Coast · AUJames Cook University · AUUniversity of Tasmania · AU

Funding

ACL HHS U01CK000480NCEZID CDC HHS U01 CK000480
6 · The paper itself

Abstract

The bacterium Burkholderia ubonensis is commonly co-isolated from environmental specimens harbouring the melioidosis pathogen, Burkholderia pseudomallei. B. ubonensis has been reported in northern Australia and Thailand but not North America, suggesting similar geographic distribution to B. pseudomallei. Unlike most other Burkholderia cepacia complex (Bcc) species, B. ubonensis is considered non-pathogenic, although its virulence potential has not been tested. Antibiotic resistance in B. ubonensis, particularly towards drugs used to treat the most severe B. pseudomallei infections, has also been poorly characterised. This study examined the population biology of B. ubonensis, and includes the first reported isolates from the Caribbean. Phylogenomic analysis of 264 B. ubonensis genomes identified distinct clades that corresponded with geographic origin, similar to B. pseudomallei. A small proportion (4%) of strains lacked the 920kb chromosome III replicon, with discordance of presence/absence amongst genetically highly related strains, demonstrating that the third chromosome of B. ubonensis, like other Bcc species, probably encodes for a nonessential pC3 megaplasmid. Multilocus sequence typing using the B. pseudomallei scheme revealed that one-third of strains lack the "housekeeping" narK locus. In comparison, all strains could be genotyped using the Bcc scheme. Several strains possessed high-level meropenem resistance (≥32 μg/mL), a concern due to potential transmission of this phenotype to B. pseudomallei. In silico analysis uncovered a high degree of heterogeneity among the lipopolysaccharide O-antigen cluster loci, with at least 35 different variants identified. Finally, we show that Asian B. ubonensis isolate RF23-BP41 is avirulent in the BALB/c mouse model via a subcutaneous route of infection. Our results provide several new insights into the biology of this understudied species.

Indexed as

Environmental MicrobiologyGenetic VariationPhylogeographyAnimalsAnti-Bacterial AgentsAustraliaBurkholderiaBurkholderia InfectionsDisease Models, AnimalGenotypeMeropenemMice, Inbred BALB CMultilocus Sequence TypingO AntigensPapua New GuineaPuerto RicoAnti-Bacterial AgentsMeropenemO AntigensThienamycins

Identifiers

PMID28910350
PMCPMC5614643
OpenAlexW2754618462

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.