Migrasomes mediate the intercellular transmission of Mycoplasma hyopneumoniae

Several studies in this journal have reported that viruses can induce migrasome formation, which facilitates viral transmission and confers resistance to drug treatment [1,2,3].Mycoplasma hyopneumoniae is the etiological agent of mycoplasmal pneumonia of swine [4].Commercial vaccines can induce a humoral immune response post-immunization; however, they fail to prevent M. hyopneumoniae colonization and transmission [4,5].Previous studies indicated no correlation between humoral immunity and protective efficacy against the disease [5].Nevertheless, antiserum has been shown to inhibit M. hyopneumoniae growth in vitro [6].Furthermore, although various antimicrobials exhibit low in vitro minimal inhibitory concentrations against M. hyopneumoniae, they are ineffective at preventing infection or eradicating the bacterium from the respiratory tract [6].These findings suggest that M. hyopneumoniae employs uncharacterized mechanisms to evade clearance by antisera or antimicrobials in vivo.In this study, we aimed to clarify whether migrasomes act as vehicles to support the extracellular release and intercellular transmission of M. hyopneumoniae, thereby protecting this pathogen from neutralization by M. hyopneumoniae-specific antibodies and elimination by antimicrobials in the extracellular milieu.

Authors

Institutions

Publication Details

Journal
Journal of Infection
Published
2026-04-28
DOI
https://doi.org/10.1016/j.jinf.2026.106757
Primary Topic
Microbial infections and disease research
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Migrasomes mediate the intercellular transmission of Mycoplasma hyopneumoniae

Yilin Li, Jiacui Lai, Yue Wu, Yunchong Ma et al.
Journal of Infection
Microbial infections and disease research
article

Migrasomes mediate the intercellular transmission of Mycoplasma hyopneumoniae

Yilin Li, Jiacui Lai, Yue Wu, Yunchong Ma, Xiuwu Lian, Honglei Ding
article en

Abstract

Several studies in this journal have reported that viruses can induce migrasome formation, which facilitates viral transmission and confers resistance to drug treatment [1,2,3].Mycoplasma hyopneumoniae is the etiological agent of mycoplasmal pneumonia of swine [4].Commercial vaccines can induce a humoral immune response post-immunization; however, they fail to prevent M. hyopneumoniae colonization and transmission [4,5].Previous studies indicated no correlation between humoral immunity and protective efficacy against the disease [5].Nevertheless, antiserum has been shown to inhibit M. hyopneumoniae growth in vitro [6].Furthermore, although various antimicrobials exhibit low in vitro minimal inhibitory concentrations against M. hyopneumoniae, they are ineffective at preventing infection or eradicating the bacterium from the respiratory tract [6].These findings suggest that M. hyopneumoniae employs uncharacterized mechanisms to evade clearance by antisera or antimicrobials in vivo.In this study, we aimed to clarify whether migrasomes act as vehicles to support the extracellular release and intercellular transmission of M. hyopneumoniae, thereby protecting this pathogen from neutralization by M. hyopneumoniae-specific antibodies and elimination by antimicrobials in the extracellular milieu.

Journal of InfectionVol. 92(6)
Southwest University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Chongqing
Good health and well-being
Openalex Percentile: Top 20%
Microbial infections and disease research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.