Evidence map›Paper›PMID 35019198›Full record

ArticleJournal of applied microbiology2022

Membrane vesicles from antibiotic-resistant Staphylococcus aureus transfer antibiotic-resistance to antibiotic-susceptible Escherichia coli.

Ae Rin Lee, Seong Bin Park, Si Won Kim, Jae Wook Jung, Jin Hong Chun, Jaesung Kim, Young Rim Kim, Jassy Mary S Lazarte, Ho Bin Jang, Kim D Thompson and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of applied microbiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

20 citing papers in PubMed, 31 citations in OpenAlex.

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  15. Loaded delta-hemolysin shapes the properties ofFrontiers in microbiology · 2023
    Article
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  18. Research Progress on Bacterial Membrane Vesicles and Antibiotic Resistance.International journal of molecular sciences · 2022
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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

13 authors at 6 institutions in 5 countries.

Ae Rin LeeLaboratory of Aquatic Animal Diseases, Research Institute of Natural Science, College of Veterinary Medicine, Gyeongsang National University, Jinju-si, Gyeongsangnam-do, Republic of Korea.
Seong Bin ParkCoastal Research Extension Center, Mississippi State University, Mississippi State, Mississippi, USA.
Si Won KimLaboratory of Aquatic Animal Diseases, Research Institute of Natural Science, College of Veterinary Medicine, Gyeongsang National University, Jinju-si, Gyeongsangnam-do, Republic of Korea.
Jae Wook JungLaboratory of Aquatic Animal Diseases, Research Institute of Natural Science, College of Veterinary Medicine, Gyeongsang National University, Jinju-si, Gyeongsangnam-do, Republic of Korea.
Jin Hong ChunLaboratory of Aquatic Animal Diseases, Research Institute of Natural Science, College of Veterinary Medicine, Gyeongsang National University, Jinju-si, Gyeongsangnam-do, Republic of Korea.
Jaesung KimLaboratory of Aquatic Animal Diseases, Research Institute of Natural Science, College of Veterinary Medicine, Gyeongsang National University, Jinju-si, Gyeongsangnam-do, Republic of Korea.
Young Rim KimLaboratory of Aquatic Animal Diseases, Research Institute of Natural Science, College of Veterinary Medicine, Gyeongsang National University, Jinju-si, Gyeongsangnam-do, Republic of Korea.
Jassy Mary S LazarteLaboratory of Aquatic Animal Diseases, Research Institute of Natural Science, College of Veterinary Medicine, Gyeongsang National University, Jinju-si, Gyeongsangnam-do, Republic of Korea.
Ho Bin JangDepartment of Microbiology, Institute for Viral Diseases, College of Medicine, Korea University, Seoul, Republic of Korea.
Kim D ThompsonMoredun Research Institute, Pentlands Science Park, Midlothian, UK.
Myunghwan JungDepartment of Microbiology, College of Medicine, Gyeongsang National University, Jinju, Republic of Korea.
Min Woo HaCollege of Pharmacy, Jeju National University, Jeju, Republic of Korea.
Tae Sung JungLaboratory of Aquatic Animal Diseases, Research Institute of Natural Science, College of Veterinary Medicine, Gyeongsang National University, Jinju-si, Gyeongsangnam-do, Republic of Korea.ORCID https://orcid.org/0000-0001-6028-0946
Gyeongsang National University · KRFlinders University · AUJeju National University · KRKorea University · KRMississippi State University · USMoredun Research Institute · GB

Funding

CRIS MIS 081710Gyeongsang National UniversityKorea Research Foundation NRF-2021R1A2B5B02002220Ministry of Food and Drug Safety 19162MFDS563USDA-ARS-SCA 58-6066-7081
6 · The paper itself

Abstract

aimBacteria naturally produce membrane vesicles (MVs), which have been shown to contribute to the spread of multi-drug resistant bacteria (MDR) by delivering antibiotic-resistant substances to antibiotic-susceptible bacteria. Here, we aim to show that MVs from Gram-positive bacteria are capable of transferring β-lactam antibiotic-resistant substances to antibiotic-sensitive Gram-negative bacteria. MATERIALS AND

methodsMVs were collected from a methicillin-resistant strain of Staphylococcus aureus (MRSA) and vesicle-mediated fusion with antimicrobial-sensitive Escherichia coli (RC85). It was performed by exposing the bacteria to the MVs to develop antimicrobial-resistant E. coli (RC85-T).

resultsThe RC85-T exhibited a higher resistance to β-lactam antibiotics compared to the parent strain. Although the secretion rates of the MVs from RC85-T and the parent strain were nearly equal, the β-lactamase activity of the MVs from RC85-T was 12-times higher than that of MVs from the parent strain, based on equivalent protein concentrations. Moreover, MVs secreted by RC85-T were able to protect β-lactam-susceptible E. coli from β-lactam antibiotic-induced growth inhibition in a dose-dependent manner.

conclusionMVs play a role in transferring substances from Gram-positive to Gram-negative bacteria, shown by the release of MVs from RC85-T that were able to protect β-lactam-susceptible bacteria from β-lactam antibiotics. SIGNIFICANCE AND IMPACT OF STUDY: MVs are involved in the emergence of antibiotic-resistant strains in a mixed bacterial culture, helping us to understand how the spread of multidrug-resistant bacteria could be reduced.

Indexed as

Anti-Bacterial AgentsMethicillin-Resistant Staphylococcus aureusDrug Resistance, Multiple, BacterialEscherichia coliMicrobial Sensitivity TestsStaphylococcus aureusAnti-Bacterial Agentsantibiotic-resistant bacteriaantibiotic-susceptible bacteriagram-negative bacteriagram-positive bacteriamembrane vesicles (MVs)vesicle-mediated transferring of antimicrobial resistance

Identifiers

PMID35019198
PMCPMC9306644
OpenAlexW4205138535

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.