Evidence map›Paper›PMID 41761076›Full record

ArticleBMC microbiology2026

Analysis of mobile genetic elements carrying mcr genes in clinical Leclercia spp. isolates.

Dayong Chen, Ting Xie, Minghui Liu, Dongsheng Zhou, Hongning Wang, Lijun Zeng, Zhe Yin

Abstract read
In one paragraph

Article in BMC microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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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

3 citing papers in PubMed.

  1. Article
  2. Identification ofAntibiotics (Basel, Switzerland) · 2026
    Article
  3. Article
4 · The record

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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

7 authors.

Dayong Chen *School of Life Science, Sichuan University, Chengdu, 610064, China.
Ting Xie *State Key Laboratory of Pathogen and Biosecurity, Academy of Military Medical Sciences, Beijing, 100071, China.
Minghui LiuState Key Laboratory of Pathogen and Biosecurity, Academy of Military Medical Sciences, Beijing, 100071, China.
Dongsheng ZhouState Key Laboratory of Pathogen and Biosecurity, Academy of Military Medical Sciences, Beijing, 100071, China.
Hongning WangSchool of Life Science, Sichuan University, Chengdu, 610064, China.
Lijun ZengDepartment of Laboratory Medicine, The Fifth Medical Center, Chinese PLA General Hospital, Beijing, 100071, China. 616do@sina.com.
Zhe YinState Key Laboratory of Pathogen and Biosecurity, Academy of Military Medical Sciences, Beijing, 100071, China. jerry9yin@163.com.

Funding

National Key Research and Development Program of China 2023YFC2605600
6 · The paper itself

Abstract

backgroundLeclercia adecarboxylata is an emerging clinical pathogen within the Enterobacteriaceae family and causes infections in immunocompromised and immunocompetent patients. It frequently exhibits resistance to a broad spectrum of β-lactams as well as to colistin, which is a last-resort antibiotic against multidrug-resistant Gram-negative bacteria. The global spread of mcr genes poses a serious public health concern. This study aimed to examine the prevalence and genetic contexts of mcr genes in clinical Leclercia spp. isolates from China.

resultsThis study identified three mobile colistin resistance genes, namely, mcr-9.1, mcr-9.2, and a novel variant mcr-11.1, among 11 clinical Leclercia isolates. Some of these isolates were assigned to two novel species: Leclercia sp. LecN1 and Leclercia sp. LecN2. mcr-11.1 showed the highest sequence similarity to mcr-9.1 and was located within two novel chromosomal integrative mobile elements (IMEs): Tn6572 and Tn6573. mcr-9.1 was carried by a chromosomally located Tn7-family/Tn6230-subfamily transposon (Tn6574) and by three IncHI2 plasmids: p707804-mcr, p1106151-mcr, and pJ807-mcr. Meanwhile, mcr-9.2 was identified in plasmid pP10164-2. These mcr genes showed diverse local genetic contexts, including mcr-11.1–wbuC–qseCB in Tn6573-family IMEs as well as IS903B–mcr-9.1–wbuC–qseCB–exeA–int–IS26 and its variants within the Tn6230-related regions of Tn6574 and IncHI2 plasmids. Tn1696-related regions carried multiple mobile genetic elements (MGEs), further facilitating the dissemination of various antibiotic resistance genes (ARGs).

conclusionsIn clinical Leclercia spp. isolates, this study identified a novel colistin resistance gene (mcr-11.1), three novel chromosomal MGEs (including Tn6572–Tn6574), as well as evidence for two new putative species. Along with four identified plasmids, these chromosomal MGEs demonstrated diverse mcr genetic contexts and suggested great potentials for the dissemination of ARGs. This study highlighted a concerning mechanism for mcr gene transfer, providing an urgent indication for ongoing resistance surveillance.

Indexed as

DNA Transposable ElementsEnterobacteriaceaeEnterobacteriaceae InfectionsInterspersed Repetitive SequencesAnti-Bacterial AgentsChinaColistinDrug Resistance, BacterialDrug Resistance, Multiple, BacterialGenes, BacterialHumansMicrobial Sensitivity TestsPlasmidsSequence Analysis, DNAAnti-Bacterial AgentsColistinDNA Transposable ElementsARGColistinLeclerciaMcr-11.1Plasmid

Identifiers

PMID41761076
PMCPMC13049778

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