Evidence map›Paper›PMID 36790185›Full record

ArticleAntimicrobial agents and chemotherapy2023

Genomic Insights into CRISPR-Harboring Plasmids in the Klebsiella Genus: Distribution, Backbone Structures, Antibiotic Resistance, and Virulence Determinant Profiles.

Jinzhao Long, Jiangfeng Zhang, Yanyan Xi, Jiaxue Zhao, Yuefei Jin, Haiyan Yang, Shuaiyin Chen, Guangcai Duan

Open access · greenAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

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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.

Jinzhao LongCollege of Public Health, Zhengzhou University, Zhengzhou, Henan, People's Republic of China.ORCID 0000-0002-0483-1122
Jiangfeng ZhangDepartment of Clinical Microbiology, People's Hospital of Zhengzhou University, Zhengzhou, Henan, People's Republic of China.
Yanyan XiCollege of Public Health, Zhengzhou University, Zhengzhou, Henan, People's Republic of China.
Jiaxue ZhaoCollege of Public Health, Zhengzhou University, Zhengzhou, Henan, People's Republic of China.
Yuefei JinCollege of Public Health, Zhengzhou University, Zhengzhou, Henan, People's Republic of China.ORCID 0000-0002-1523-0808
Haiyan YangCollege of Public Health, Zhengzhou University, Zhengzhou, Henan, People's Republic of China.ORCID 0000-0002-1797-304X
Shuaiyin ChenCollege of Public Health, Zhengzhou University, Zhengzhou, Henan, People's Republic of China.ORCID 0000-0001-6129-0310
Guangcai DuanCollege of Public Health, Zhengzhou University, Zhengzhou, Henan, People's Republic of China.
Zhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CRISPR systems are often encoded by many prokaryotes as adaptive defense against mobile genetic elements (MGEs), but several MGEs also recruit CRISPR components to perform additional biological functions. Type IV-A systems are identified in Klebsiella plasmids, yet the distribution, characterization, and role of these plasmids carrying CRISPR systems in the whole Klebsiella genus remain unclear. Here, we performed large-scale comparative analysis of these plasmids using publicly available plasmid genomes. CRISPR-harboring plasmids were mainly distributed in Klebsiella pneumoniae (9.09%), covering 19.23% of sequence types, but sparse in Klebsiella species outside Klebsiella pneumoniae (3.92%). Plasmid genome comparison reiterated that these plasmids often carried the cointegrates of IncFIB and IncHI1B replicons, occasionally linked to other replicons, such as IncFIA, IncFII, IncR, IncQ, and IncU. Comparative genome analysis showed that CRISPR-carrying Klebsiella plasmids shared a conserved pNDM-MAR-like conjugation module as their backbones and served as an important vector for the accretion of antibiotic resistance genes (ARGs) and even virulence genes (VGs). Moreover, compared with CRISPR-negative IncFIB/IncHIB plasmids, CRISPR-positive IncFIB/IncHIB plasmids displayed high divergences in terms of ARGs, VGs, GC content, plasmid length, and backbone structures, suggesting their divergent evolutionary paths. The network analysis revealed that CRISPR-positive plasmids yielded fierce competitions with other plasmid types, especially conjugative plasmids, thereby affecting the dynamics of plasmid transmission. Overall, our study provides valuable insights into the role of CRISPR-positive plasmids in the spread of ARGs and VGs in Klebsiella genus.

Indexed as

KlebsiellaKlebsiella InfectionsAnti-Bacterial Agentsbeta-LactamasesClustered Regularly Interspaced Short Palindromic RepeatsDrug Resistance, MicrobialGenomicsHumansKlebsiella pneumoniaePlasmidsVirulenceVirulence FactorsAnti-Bacterial Agentsbeta-LactamasesVirulence Factorsantibiotic resistanceCRISPRKlebsiellaplasmidvirulence

Identifiers

PMID36790185
PMCPMC10019312
OpenAlexW4320855866

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.