Evidence map›Paper›PMID 39238028›Full record

ArticleJournal of nanobiotechnology2024

A nanoscale visual exploration of the pathogenic effects of bacterial extracellular vesicles on host cells.

Minjae Kang, Min Jeong Kim, Dokyung Jeong, Hyung-Jun Lim, Ga-Eun Go, Uidon Jeong, Eunyoung Moon, Hee-Seok Kweon, Nae-Gyu Kang, Seung Jin Hwang and 3 more

Abstract read
In one paragraph

Article in Journal of nanobiotechnology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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

4 citing papers in PubMed.

  1. Evaluation of Microbiome Therapeutic Candidates for Carbapenem-ResistantJournal of microbiology and biotechnology · 2026
    Article
  2. Article
  3. Review
  4. Article
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.

Minjae Kang *Department of Chemistry, Hanyang University, Seoul, 04763, Republic of Korea.
Min Jeong Kim *Department of Chemistry, Hanyang University, Seoul, 04763, Republic of Korea.
Dokyung JeongDepartment of Chemistry, Hanyang University, Seoul, 04763, Republic of Korea.
Hyung-Jun LimDepartment of Chemistry, Hanyang University, Seoul, 04763, Republic of Korea.
Ga-Eun GoDepartment of Chemistry, Hanyang University, Seoul, 04763, Republic of Korea.
Uidon JeongDepartment of Chemistry, Hanyang University, Seoul, 04763, Republic of Korea.
Eunyoung MoonElectron Microscopy Research Center, Korea Basic Science Institute, Cheongju, 28119, Republic of Korea.
Hee-Seok KweonElectron Microscopy Research Center, Korea Basic Science Institute, Cheongju, 28119, Republic of Korea.
Nae-Gyu KangR&D Center, LG H&H Co., Ltd, Seoul, 07795, Republic of Korea.
Seung Jin HwangR&D Center, LG H&H Co., Ltd, Seoul, 07795, Republic of Korea.
Sung Hun YounR&D Center, LG H&H Co., Ltd, Seoul, 07795, Republic of Korea.
Bo Kyoung HwangR&D Center, LG H&H Co., Ltd, Seoul, 07795, Republic of Korea.
Doory KimDepartment of Chemistry, Hanyang University, Seoul, 04763, Republic of Korea. doorykim@hanyang.ac.kr.

Funding

Korea Basic Science Institute under the R&D program C330430
6 · The paper itself

Abstract

backgroundBacterial extracellular vesicles (EVs) are pivotal mediators of intercellular communication and influence host cell biology, thereby contributing to the pathogenesis of infections. Despite their significance, the precise effects of bacterial EVs on the host cells remain poorly understood. This study aimed to elucidate ultrastructural changes in host cells upon infection with EVs derived from a pathogenic bacterium, Staphylococcus aureus (S. aureus).

resultsUsing super-resolution fluorescence microscopy and high-voltage electron microscopy, we investigated the nanoscale alterations in mitochondria, endoplasmic reticulum (ER), Golgi apparatus, lysosomes, and microtubules of skin cells infected with bacterial EVs. Our results revealed significant mitochondrial fission, loss of cristae, transformation of the ER from tubular to sheet-like structures, and fragmentation of the Golgi apparatus in cells infected with S. aureus EVs, in contrast to the negligible effects observed following S. epidermidis EV infection, probably due to the pathogenic factors in S. aureus EV, including protein A and enterotoxin. These findings indicate that bacterial EVs, particularly those from pathogenic strains, induce profound ultrastructural changes of host cells that can disrupt cellular homeostasis and contribute to infection pathogenesis.

conclusionsThis study advances the understanding of bacterial EV-host cell interactions and contributes to the development of new diagnostic and therapeutic strategies for bacterial infections.

Indexed as

Extracellular VesiclesStaphylococcus aureusEndoplasmic ReticulumGolgi ApparatusHost-Pathogen InteractionsHumansLysosomesMicroscopy, FluorescenceMicrotubulesMitochondriaStaphylococcal InfectionsStaphylococcus epidermidisBacterial EVCristae lossExtracellular vesicleSuper-resolution fluorescence microscopy

Identifiers

PMID39238028
PMCPMC11378492

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.