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Study on identification and biological function of small RNAs in Klebsiella pneumoniae

Identification and Functional Study of Klebsiella pneumoniae Small RNAs

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600129417
Enrollment
Unknown
Registered
2026-08-04
Start date
2026-08-10
Completion date
Unknown
Last updated
2026-08-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infections caused by Klebsiella pneumoniae, including pneumonia, bacteremia, liver abscess, urinary tract infection

Interventions

ESBL-producing multidrug-resistant group:None
Carbapenem-resistant Klebsiella pneumoniae (CRKP) group:None
Hypervirulent Klebsiella pneumoniae (hvKP) group:None

Sponsors

The First Affiliated Hospital of the Baotou Medical College of Inner Mongolia University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Strains are identified as Klebsiella pneumoniae by VITEK mass spectrometry or 16S rRNA sequencing; 2. Clear origin: clinical isolates (specimens from pulmonary infection, bloodstream infection, liver abscess and urinary tract) or standard reference strains (ATCC 700603, hvKP ATCC BAA-2146, carbapenem-resistant CRKP strains); 3. After resuscitation, strains exhibit favorable growth on plates without microbial contamination and show stable subculture performance; 4. Clinical isolates are accompanied by complete medical record information, including infection site, antibiotic medication history, antimicrobial susceptibility results and patients' underlying diseases, which supports grouping (cKP/hvKP/CRKP); 5. Strains can be stably cryopreserved and repeatedly passaged, without spontaneous degradation or plasmid loss.

Exclusion criteria

Exclusion criteria: 1. Strains identified as other Klebsiella species by mass spectrometry or gene sequencing (including Klebsiella oxytoca, Klebsiella rhinoscleromatis, etc.); 2. Mixed contaminating bacteria observed via plate microscopy; 1.single colonies cannot be obtained after repeated purification; 3. Strains exhibit degeneration, retarded growth and spontaneous autolysis after multiple passages, which prevents RNA extraction and phenotypic experiments; 4. Clinical isolates without complete medical records or antimicrobial susceptibility data, making grouping analysis unavailable; 5. Strains carry lethal defects and display abnormal cell division, failing to support the construction of gene knockout/overexpression strains; 6. Strains degraded due to improper preservation and repeated freeze-thaw cycles, resulting in poor RNA integrity (RIN < 6.0).

Design outcomes

Primary

MeasureTime frame
Relative mRNA expression of target gene;

Secondary

MeasureTime frame
Age; MIC; Site of infection;

Countries

China

Contacts

Public ContactLiu Ying

The First Affiliated Hospital of the Baotou Medical College of Inner Mongolia University of Science and Technology

66233102@qq.com+86 472 2178348

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 25, 2026