Evidence map›Paper›PMID 35352958›Full record

ArticleMicrobiology spectrum2022

Genetic Diversity and Pathogenic Features in Klebsiella pneumoniae Isolates from Patients with Pyogenic Liver Abscess and Pneumonia.

Lin Gan, Chao Yan, Jinghua Cui, Guanhua Xue, Hanyu Fu, Bing Du, Hanqing Zhao, Junxia Feng, Yanling Feng, Zheng Fan and 13 more

Open access · goldAbstract read
In one paragraph

Article in Microbiology spectrum, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Pooled it
  2. Protective Effect ofMicroorganisms · 2026
    Article
  3. Review
  4. Pathogenic diversity ofFrontiers in microbiology · 2026
    Article
  5. Modulation of NK Cell Properties by ESKAPE Group Bacteria.International journal of molecular sciences · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Rapid detection ofFrontiers in cellular and infection microbiology · 2022
    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

23 authors at 3 institutions in 1 country.

Lin GanDepartment of Bacteriology, Capital Institute of Pediatricsgrid.418633.b, Beijing, China.
Chao YanDepartment of Bacteriology, Capital Institute of Pediatricsgrid.418633.b, Beijing, China.
Jinghua CuiDepartment of Bacteriology, Capital Institute of Pediatricsgrid.418633.b, Beijing, China.
Guanhua XueDepartment of Bacteriology, Capital Institute of Pediatricsgrid.418633.b, Beijing, China.
Hanyu FuDepartment of Bacteriology, Capital Institute of Pediatricsgrid.418633.b, Beijing, China.
Bing DuDepartment of Bacteriology, Capital Institute of Pediatricsgrid.418633.b, Beijing, China.
Hanqing ZhaoDepartment of Bacteriology, Capital Institute of Pediatricsgrid.418633.b, Beijing, China.
Junxia FengDepartment of Bacteriology, Capital Institute of Pediatricsgrid.418633.b, Beijing, China.
Yanling FengDepartment of Bacteriology, Capital Institute of Pediatricsgrid.418633.b, Beijing, China.
Zheng FanDepartment of Bacteriology, Capital Institute of Pediatricsgrid.418633.b, Beijing, China.
Pan MaoState Key Laboratory of Infectious Disease Prevention and Control, National Institute for Communicable Disease Control and Prevention, Collaborative Innovation Center for Disease Control and Prevention, Beijing, China Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention, Beijing, China.
Tongtong FuDepartment of Bacteriology, Capital Institute of Pediatricsgrid.418633.b, Beijing, China.
Ziying XuDepartment of Bacteriology, Capital Institute of Pediatricsgrid.418633.b, Beijing, China.
Shuheng DuDepartment of Bacteriology, Capital Institute of Pediatricsgrid.418633.b, Beijing, China.
Shiyu LiuDepartment of Bacteriology, Capital Institute of Pediatricsgrid.418633.b, Beijing, China.
Rui ZhangDepartment of Bacteriology, Capital Institute of Pediatricsgrid.418633.b, Beijing, China.
Qun ZhangDepartment of Bacteriology, Capital Institute of Pediatricsgrid.418633.b, Beijing, China.
Nannan LiDepartment of Bacteriology, Capital Institute of Pediatricsgrid.418633.b, Beijing, China.
Xiaohu CuiDepartment of Bacteriology, Capital Institute of Pediatricsgrid.418633.b, Beijing, China.
Xiaoran LiDepartment of Bacteriology, Capital Institute of Pediatricsgrid.418633.b, Beijing, China.
Yao ZhouDepartment of Bacteriology, Capital Institute of Pediatricsgrid.418633.b, Beijing, China.
Lei HuangTreatment and Research Center for Infectious Diseases, The Fifth Medical Center of PLA General Hospital, Beijing, China.
Jing YuanDepartment of Bacteriology, Capital Institute of Pediatricsgrid.418633.b, Beijing, China.ORCID 0000-0002-6939-9676
Capital Institute of Pediatrics · CNChinese PLA General Hospital · CNNational Institute for Communicable Disease Control and Prevention · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

While Klebsiella pneumoniae is a common cause of nosocomial and community-acquired infections, including pneumonia and pyogenic liver abscess, little is known about the population structure of this bacterium. In this study, we investigated the prevalence and molecular characteristics of K. pneumoniae isolates from carriers, pyogenic liver abscess patients, and pneumonia patients, and genomic and phenotypic assays were used to determine the differences among the isolates. A total of 232 K. pneumoniae isolates were subtyped into 74 sequence types (STs). The isolates from different sources had their own STs, and the predominant subtypes in liver abscess and pneumonia patients were ST23 and ST11, respectively. Pangenome analysis also distinguished three phylogroups that were consistent with the isolate sources. The isolates collected from liver abscess patients carried significantly more virulence factors, and those from pneumonia patients harbored significantly more resistance genes and replicons. Almost all isolate STs (93/97 [95.88%]) from liver abscesses strongly correlated with the virulence factor salmochelin, while most pneumonia isolate STs (52/53 [98.11%]) from pneumonia did not correlate with salmochelin. The isolates collected from liver abscesses showed higher virulence in the cytotoxicity and mouse models. These data provide genomic support for the proposal that isolates collected from carriers, liver abscess patients, and pneumonia patients have distinct genomic features. Isolates from the different sources are largely nonoverlapping, suggesting that different patients may be infected via different sources. Further studies on the pathogenic mechanisms of salmochelin and other virulence factors will be required.

Indexed as

Community-Acquired InfectionsCross InfectionKlebsiella InfectionsLiver Abscess, PyogenicPneumoniaAnimalsGenetic VariationHumansKlebsiella pneumoniaeMiceVirulence FactorsVirulence Factorsantibiotic resistanceKlebsiella pneumoniaepneumoniapyogenic liver abscessvirulence

Identifiers

PMID35352958
PMCPMC9045331
OpenAlexW4220978829

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.