Evidence map›Paper›PMID 27941991›Full record

ArticlePLoS neglected tropical diseases2016

In vivo Distribution and Clearance of Purified Capsular Polysaccharide from Burkholderia pseudomallei in a Murine Model.

Teerapat Nualnoi, Adam Kirosingh, Sujata G Pandit, Peter Thorkildson, Paul J Brett, Mary N Burtnick, David P AuCoin

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

16 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Laboratory diagnosis of melioidosis.PLoS neglected tropical diseases · 2025
    Review
  4. Article
  5. Identification ofMicrobiology spectrum · 2024
    Article
  6. Article
  7. Review
  8. Frontiers in pharmacology · 2024
    Article
  9. Article
  10. Article
  11. Development of Immunoassays for Detection ofPathogens (Basel, Switzerland) · 2021
    Article
  12. Article
  13. The American journal of tropical medicine and hygiene · 2020
    Article
  14. Article
  15. Article
  16. Article
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 2 institutions in 1 country.

Teerapat NualnoiDepartment of Microbiology and Immunology, University of Nevada School of Medicine, Reno, Nevada, United States of America.
Adam KirosinghDepartment of Microbiology and Immunology, University of Nevada School of Medicine, Reno, Nevada, United States of America.
Sujata G PanditDepartment of Microbiology and Immunology, University of Nevada School of Medicine, Reno, Nevada, United States of America.
Peter ThorkildsonDepartment of Microbiology and Immunology, University of Nevada School of Medicine, Reno, Nevada, United States of America.
Paul J BrettDepartment of Microbiology and Immunology, University of South Alabama, Mobile, Alabama, United States of America.
Mary N BurtnickDepartment of Microbiology and Immunology, University of South Alabama, Mobile, Alabama, United States of America.
David P AuCoinDepartment of Microbiology and Immunology, University of Nevada School of Medicine, Reno, Nevada, United States of America.
University of Nevada, Reno · USUniversity of South Alabama · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Burkholderia pseudomallei is the causative agent of melioidosis, a severe infection prominent in northern Australia and Southeast Asia. The "gold standard" for melioidosis diagnosis is bacterial isolation, which takes several days to complete. The resulting delay in diagnosis leads to delayed treatments, which could result in death. In an attempt to develop better methods for early diagnosis of melioidosis, B. pseudomallei capsular polysaccharide (CPS) was identified as an important diagnostic biomarker. A rapid lateral flow immunoassay utilizing CPS-specific monoclonal antibody was developed and tested in endemic regions worldwide. However, the in vivo fate and clearance of CPS has never been thoroughly investigated. Here, we injected mice with purified CPS intravenously and determined CPS concentrations in serum, urine, and major organs at various intervals. The results indicate that CPS is predominantly eliminated through urine and no CPS accumulation occurs in the major organs. Immunoblot analysis demonstrated that intact CPS was excreted through urine. To understand how a large molecule like CPS was eliminated without degradation, a 3-dimenational structure of CPS was modeled. The predicted CPS structure has a rod-like shape with a small diameter that could allow it to flow through the glomerulus of the kidney. CPS clearance was determined using exponential decay models and the corrected Akaike Information Criterion. The results show that CPS has a relatively short serum half-life of 2.9 to 4.4 hours. Therefore, the presence of CPS in the serum and/or urine suggests active melioidosis infection and provides a marker to monitor treatment of melioidosis.

Indexed as

Administration, IntravenousAnimalsAustraliaBacterial CapsulesBurkholderia pseudomalleiDisease Models, AnimalEnzyme-Linked Immunosorbent AssayFemaleHalf-LifeImmunoblottingKidneyKineticsMelioidosisMicePolysaccharides, BacterialPolysaccharides, Bacterial

Identifiers

PMID27941991
PMCPMC5179125
OpenAlexW2563481632

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.