Evidence map›Paper›PMID 36636376›Full record

ArticleInfection and drug resistance2023

Molecular and Clinical Characteristics of Carbapenem-Resistant

Fan Hu, Meng-Lu Lin, Juan-Li Mou, Jia-Hui Feng, Kai Huang, Yao-Jia Lao, Jie Cheng, Jun Lin

Open access · goldAbstract read
In one paragraph

Article in Infection and drug resistance, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Genomic Epidemiology of NDM-1 Carbapenemase-ProducingAntibiotics (Basel, Switzerland) · 2026
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  3. Genomic characterisation and antimicrobial resistance ofFrontiers in cellular and infection microbiology · 2026
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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

8 authors at 1 institution in 1 country.

Fan Hu *Department of Gastroenterology/Hepatology, Zhongnan Hospital of Wuhan University, Wuhan, People's Republic of China.
Meng-Lu Lin *Department of Gastroenterology/Hepatology, Zhongnan Hospital of Wuhan University, Wuhan, People's Republic of China.
Juan-Li Mou *Department of Gastroenterology/Hepatology, Zhongnan Hospital of Wuhan University, Wuhan, People's Republic of China.
Jia-Hui FengDepartment of Gastroenterology/Hepatology, Zhongnan Hospital of Wuhan University, Wuhan, People's Republic of China.
Kai HuangDepartment of Gastroenterology/Hepatology, Zhongnan Hospital of Wuhan University, Wuhan, People's Republic of China.
Yao-Jia LaoDepartment of Gastroenterology/Hepatology, Zhongnan Hospital of Wuhan University, Wuhan, People's Republic of China.
Jie ChengDepartment of Gastroenterology/Hepatology, Zhongnan Hospital of Wuhan University, Wuhan, People's Republic of China.
Jun LinDepartment of Gastroenterology/Hepatology, Zhongnan Hospital of Wuhan University, Wuhan, People's Republic of China.ORCID 0000-0002-5152-6518
Wuhan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Carbapenem resistant Klebsiella pneumoniae (CRKP) is an independent risk factor for nosocomial infection which poses a serious threat to human health. How to prevent and suppress CRKP infection and explore its drug resistance mechanisms have become a huge challenge and possesses immediate significance. Methods: A total of 45 CRKP strains isolated from hospitalized patients in Zhongnan Hospital of Wuhan University were collected from August 2018-December 2020. The strain's identification and antimicrobial susceptibility tests were performed using the VITEK 2 automated identification instrument. Single molecule DNA sequencing of 45 CRKP isolates was performed by the third generation high-throughput sequencing technology. Results: The results were analyzed by multi locus sequence typing (MLST) and phylogenetic analysis. Antimicrobial susceptibility showed that 45 CRKP isolates were multi-drug resistant strains, and the resistance rates to common antibiotics were as high as 68%. Whole genome sequencing results showed that the CRKP strains carried multiple drug resistance genes and virulence factors. MLST analysis found two different sequence types (ST), of which 44 were ST11 and 1 was ST1049. Conclusion: Through whole genome sequencing (WGS), we found multiple drug-resistant genes and virulence factors, and there was obvious dominant microbiota. The source was mainly related to nosocomial infection. The ST11-KPC Klebsiella pneumoniae was the main type, which was consistent with the most common type in China. We identified several dominant microbiotas which may serve as a target in the clinical prevention and treatment of severe bacterial infections. Our finding may have a role for guiding clinical antibiotic choosing.

Indexed as

carbapenemasesKlebsiella pneumoniaeresistance genesvirulence factorwhole-genome sequencing

Identifiers

PMID36636376
PMCPMC9830055
OpenAlexW4313589330

What OpenQuestion holds

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LicenceCC BY-NC
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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.