Evidence map›Paper›PMID 41179641›Full record

ArticleArchives of Razi Institute2025

Assessment of the Last-Resort Antibiotics against Extended Spectrum Beta-Lactamase/Carbapenemase and Biofilm Producer

Rahimi Sara, Khakpour Mohadeseh, Bakht Mehdi, Ehteram Hasan, Saghi Sarabi Hediyeh, Nikkhahi Farhad

Abstract read
In one paragraph

Article in Archives of Razi Institute, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. 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

6 authors.

Rahimi SaraMedical Microbiology Research Center, Qazvin University of Medical Sciences, Qazvin, Iran.
Khakpour MohadesehMedical Microbiology Research Center, Qazvin University of Medical Sciences, Qazvin, Iran.
Bakht MehdiMedical Microbiology Research Center, Qazvin University of Medical Sciences, Qazvin, Iran.
Ehteram HasanDepartment of pathology. Kashan University of medical sciences Kashan. Iran.
Saghi Sarabi HediyehMedical Microbiology Research Center, Qazvin University of Medical Sciences, Qazvin, Iran.
Nikkhahi FarhadMedical Microbiology Research Center, Qazvin University of Medical Sciences, Qazvin, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pneumonia caused by Klebsiella pneumoniae (K. pneumoniae) is regarded as one of the most prevalent etiologies of nosocomial infections. The objective of this study was to investigate the activity of tigecycline, azithromycin, and colistin against K. pneumoniae isolated from bronchoalveolar lavage (BAL) samples of suspected cases of ventilator-associated pneumonia (VAP) in patients with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. The present study investigates the activity of tigecycline, azithromycin, and colistin against ESBL/carbapenemase-producing K. pneumoniae. The investigation encompasses the phenotypic and genotypic screening of ESBLs, AmpC beta-lactamases, and carbapenemase enzymes. Furthermore, an evaluation was conducted to ascertain the capacity of the biofilm to form. Consequently, the presence of virulence genes was identified through the implementation of a polymerase chain reaction (PCR) method. The utilization of phenotypic detection tests resulted in the categorization of 27 (29.6%) out of 91 K. pneumoniae isolates as ESBL/carbapenemase-producing K. pneumoniae strains. Furthermore, molecular methods revealed that all 27 K. pneumoniae isolates possessed at least one of the ESBL/carbapenemase-related genes. ESBL-associated genes were detected in 91 K. pneumoniae isolates, including 19.7% blaTEM, 29.6% blaSHV, and 19.7% blaCTX-M. Carbapenemase-related genes were identified in 17.5% of the isolates, including blaOXA-48-like (15.4%) and blaNDM1 (2.1%). The investigation revealed that all 27 of the isolates demonstrated the capacity to form biofilms. In this study, the prevalence of specific genes among ESBL/carbapenemase producer K. pneumoniae isolates was investigated. The genes analyzed included entB, mrkD, fimH, Irp2, wcaG, mrkA, rmpA, iutA, and magA. The results showed that 92.59%, 92.59%, 81.48%, 88.8%, 40.74%, 11.1%, 22.22%, 18.5%, 14.81%, and 33.33% of the isolates carried entB, mrkD, fimH, Irp2, wcaG, mrkA, rmpA, iutA, and magA genes, respectively. However, the iucA gene was not detected in any of the isolates examined. Tigecycline and colistin demonstrated higher efficacy against these isolates. Multilocus sequence typing (MLST) results for four colistin-resistant isolates revealed three distinct sequence types (ST): ST3500, ST273, and two cases of ST2558. The rapid emergence and subsequent dissemination of colistin-resistant and Beta-lactamase-producing K. pneumoniae has led to a worrisome global situation. The effective antimicrobial activity of tigecycline against K. pneumoniae that produce these enzymes may be efficient in hospitalized patients in ICUs with suspected cases of VAP.

Indexed as

Anti-Bacterial Agentsbeta-LactamasesBiofilmsKlebsiella InfectionsKlebsiella pneumoniaeBacterial ProteinsColistinCOVID-19HumansIntensive Care UnitsIranMicrobial Sensitivity TestsPneumonia, Ventilator-AssociatedTigecyclineAnti-Bacterial AgentsBacterial Proteinsbeta-LactamasescarbapenemaseColistinTigecyclineCarbapenem ResistanceExtended-Spectrum Beta-lactamasesIRANK. Pneumoniae

Identifiers

PMID41179641
PMCPMC12576346

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.