Evidence map›Paper›PMID 41826834›Full record

ArticleBMC infectious diseases2026

Targeting carbapenem-resistant and hypervirulent Klebsiella pneumoniae: in vitro evaluation of cefepime/zidebactam, aztreonam/avibactam, imipenem/relebactam, and meropenem/vaborbactam.

Yi Li, Yulian Li, Xun Jia, Huinan Mao, Dan Li, Jie Zhang

Abstract read
In one paragraph

Article in BMC infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Yi Li *School of Medicine, University of Electronic Science and Technology of China, Chengdu, Sichuan, China.
Yulian Li *Department of Laboratory Medicine, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, People's Republic of China.
Xun JiaSchool of Medicine, University of Electronic Science and Technology of China, Chengdu, Sichuan, China.
Huinan MaoCollege of Medical Technology, Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan, China.
Dan LiDepartment of Laboratory Medicine, Medical Center Hospital of Qionglai City, Chengdu, Sichuan, China. lidan229526124@163.com.
Jie ZhangDepartment of Laboratory Medicine, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, Sichuan, China. zhangjiespph@163.com.ORCID http://orcid.org/0000-0002-1654-194X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe emergence of carbapenem-resistant hypervirulent Klebsiella pneumoniae (CR-hvKp) is a growing concern because of the high mortality rates and limited treatment options. Few reports have examined the in vitro antibacterial activity of novel β-lactam/β-lactamase inhibitor drugs against CR-hvKp.

aimsThis study investigated the in vitro activity of β-lactam/β-lactamase inhibitor including cefepime/zidebactam, aztreonam/avibactam, imipenem/relabactam and meropenem/vaborbactam toward CR-hvKP isolates. Molecular epidemiological characterization of CR-hvKP strains was performed.

methodsA total of 106 non-repetitive clinical CR-hvKP strains were collected from patients at Sichuan Provincial People's Hospital between August 2018 and December 2023. A VITEK-2 compact system (bioMérieux, France) was used for the preliminary identification of strains and drug susceptibility testing, and matrix-assisted laser desorption/ionization mass spectrometry (Ci-phergen Biosystem, USA) was used to confirm the identity of all strains. CR-hvKP strains were screened using string tests and polymerase chain reaction. The E-test strip method was used to evaluate the in vitro antibacterial activity of novel antimicrobial drugs toward CR-hvKP stains. Molecular characterization of CR-hvKP strains was carried out using polymerase chain reaction amplification of resistance genes, virulence genes, housekeeping genes, and wzi genes. The virulence features of CR-hvKP strains were investigated using the Galleria mellonella infection model.

resultsThe susceptibility rates of CR-hvKP to cefepime/zidebactam and aztreonam/avibactam all exceeded 90%, with rates of 98.1% and 99.1%, respectively. CR-hvKP exhibited susceptibility rates of 57.5% and 65.1% to imipenem/relebactam and meropenem/vaborbactam, respectively. Sequencing identified ST11-KL64 as the predominant type in CR-hvKP strains. We identified three new ST subtypes, ST8115, ST8116 and ST8117. The most prevalent carbapenemase genes were bla

conclusionsCefepime/zidebactam and aztreonam/avibactam hold great promise for the treatment of CR-hvKP infections. Our findings will not only effectively address the challenge of CR-hvKP resistance, but also provide evidence to support the optimization of clinical therapeutic strategies and further promote the development and application of novel antimicrobial drugs.

Indexed as

Anti-Bacterial Agentsbeta-Lactamase InhibitorsCarbapenem-Resistant EnterobacteriaceaeKlebsiella InfectionsKlebsiella pneumoniaeAnimalsAzabicyclo CompoundsAztreonamBoronic AcidsCefepimeCyclooctanesDrug CombinationsHeterocyclic Compounds, 1-RingHumansImipenemMeropenemAnti-Bacterial AgentsavibactamAzabicyclo CompoundsAztreonambeta-Lactamase InhibitorsBoronic AcidsCefepimecefepime-zidebactamCyclooctanesDrug CombinationsHeterocyclic Compounds, 1-RingImipenemMeropenemmeropenem and vaborbactamPiperidinesrelebactamThird Generation CephalosporinszidebactamAntimicrobial resistanceCarbapenem-resistant hypervirulent Klebsiella pneumoniaeIn vitro activityMolecular epidemiologyβ-lactam/β-lactamase inhibitor (BL/BLI) combinations

Identifiers

PMID41826834
PMCPMC13101148

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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.