Evidence map›Paper›PMID 25098744›Full record

ArticleVirulence2014

Sialic acid involved in hypermucoviscosity phenotype of Klebsiella pneumoniae and associated with resistance to neutrophil phagocytosis.

Chen-Hsiang Lee, Chia-Chi Chang, Jien-Wei Liu, Rong-Fu Chen, Kuender D Yang

Open access · goldAbstract read
In one paragraph

Article in Virulence, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

47 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Hypermucoviscosity inJournal of bacteriology · 2026
    Review
  5. TARGETING THE CAPSULE OFbioRxiv : the preprint server for biology · 2026
    Article
  6. Decoding Host-Pathogen Dynamics inAntibiotics (Basel, Switzerland) · 2026
    Review
  7. Review
  8. Variable progressive behavior ofFrontiers in immunology · 2026
    Article
  9. Hypervirulent and Drug-ResistantInternational journal of general medicine · 2026
    Review
  10. Targeting the capsule ofFrontiers in immunology · 2026
    Article
  11. HypervirulentPharmaceuticals (Basel, Switzerland) · 2025
    Review
  12. Review
  13. Review
  14. Article
  15. Molecular analysis ofOpen veterinary journal · 2025
    Article
  16. Virulence · 2024
    Review
  17. Review
  18. Article
  19. Article
  20. Autophagy, cell death, and cytokines inEmerging microbes & infections · 2023
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 2 countries.

Chen-Hsiang LeeDivision of Infectious Diseases; Kaohsiung Chang Gung Memorial Hospital; Kaohsiung, Taiwan; Institute of Clinical Medical Sciences; Chang Gung University College of Medicine; Kaohsiung, Taiwan; Department of Medical Research; Kaohsiung Chang Gung Memorial Hospital; Kaohsiung, Taiwan.
Chia-Chi ChangDivision of Infectious Diseases; Kaohsiung Chang Gung Memorial Hospital; Kaohsiung, Taiwan.
Jien-Wei LiuDivision of Infectious Diseases; Kaohsiung Chang Gung Memorial Hospital; Kaohsiung, Taiwan.
Rong-Fu ChenDepartment of Medical Research and Development; Show Chwan Memorial Hospital; Changhua, Taiwan.
Kuender D YangInstitute of Clinical Medical Sciences; Chang Gung University College of Medicine; Kaohsiung, Taiwan; Department of Medical Research and Development; Show Chwan Memorial Hospital; Changhua, Taiwan.
Kaohsiung Chang Gung Memorial Hospital · TWChang Bing Show Chwan Memorial Hospital · TWChang Gung University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Klebsiella pneumoniae (KP) with the hypermucoviscosity (HV) phenotype has abundant capsular polysaccharides (CPS) and usually causes an invasive syndrome. Sialic acid (Sia), a component of CPS in KP strains with the HV phenotype, may be anti-phagocytic. Sia-binding immunoglobulin-like lectin-9 (Siglec-9) act as an MHC class-I receptor on neutrophils that recognizes Sia and sends a signal to dampen inflammatory response. Three clinical KP strains with KP-M1 (HV-positive; capsular serotype K1), KP-14 (HV-negative; capsular serotype non-K1/K2), and DT-X (HV-negative; capsular serotype K1) were studied. We assessed total Sia in CPS extracts using enzymatic methods and phagocytosis by neutrophils of neuraminidase-treated bacteria using flow cytometry. Neutrophil killing was evaluated in the presence and absence of antibodies against Siglec-9. The concentration of Sia was significantly higher in the CPS extract of KP-M1 (56.75 ± 6.75 μmole/10(9) cfu) than in the CPS extract of KP-14 (0.02 ± 0.01 μmole/10(9) cfu) and DT-X (a negligible value). The KP-M1 (compared with the KP-14 and DT-X) was more resistant to neutrophil phagocytosis. Both the HV phenotype and resistance to phagocytosis of KP-M1 were significantly decreased after Sia removal with neuraminidase treatment. Fluorescence microscopy with an antibody against human Siglec-9 showed attachment of KP-M1 (but were absent of KP-14 and DT-X) to the surface of neutrophils and colocalization with human Siglec-9. Engagement of Siglec-9 via Sia enhanced neutrophils killing of KP-M1 by ex vivo human neutrophils bactericidal activity assay. The result showed that Sia might be a constituent of KP-M1 CPS responsible for HV, thereby contributing to anti-phagocytic activity of this pathogen.

Indexed as

Bacterial CapsulesCells, CulturedHumansKlebsiella pneumoniaeMicrobial ViabilityN-Acetylneuraminic AcidNeutrophilsPhagocytosisN-Acetylneuraminic AcidhypermucoviscosityK. pneumoniaeneutrophilphagocytosissialic acid

Identifiers

PMID25098744
PMCPMC4139408
OpenAlexW2084847545

What OpenQuestion holds

Textmetadata
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.