Evidence map›Paper›PMID 41388316›Full record

ArticleVeterinary research2025

FtsZ contributes to cytoadhesion and interaction with host extracellular matrix components and plasminogen in Mycoplasma bovis.

Shanyu Jin, Shengli Chen, Huafang Hao, Shimei Lan, Xiangrui Jin, Zhangcheng Li, Xinyi Wang, Yifan Zhang, Xinmin Yan, Yuefeng Chu

Abstract read
In one paragraph

Article in Veterinary research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Shanyu Jin *State Key Laboratory for Animal Disease Control and Prevention, College of Veterinary Medicine, Lanzhou University, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, 730000, China.
Shengli Chen *State Key Laboratory for Animal Disease Control and Prevention, College of Veterinary Medicine, Lanzhou University, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, 730000, China. chenshengli@caas.cn.
Huafang HaoState Key Laboratory for Animal Disease Control and Prevention, College of Veterinary Medicine, Lanzhou University, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, 730000, China.
Shimei LanState Key Laboratory for Animal Disease Control and Prevention, College of Veterinary Medicine, Lanzhou University, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, 730000, China.
Xiangrui JinState Key Laboratory for Animal Disease Control and Prevention, College of Veterinary Medicine, Lanzhou University, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, 730000, China.
Zhangcheng LiState Key Laboratory for Animal Disease Control and Prevention, College of Veterinary Medicine, Lanzhou University, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, 730000, China.
Xinyi WangState Key Laboratory for Animal Disease Control and Prevention, College of Veterinary Medicine, Lanzhou University, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, 730000, China.
Yifan ZhangState Key Laboratory for Animal Disease Control and Prevention, College of Veterinary Medicine, Lanzhou University, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, 730000, China.
Xinmin YanState Key Laboratory for Animal Disease Control and Prevention, College of Veterinary Medicine, Lanzhou University, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, 730000, China.
Yuefeng ChuState Key Laboratory for Animal Disease Control and Prevention, College of Veterinary Medicine, Lanzhou University, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, 730000, China. chuyuefeng@caas.cn.

Funding

Chinese Academy of Agricultural Science and Technology Innovation Program CAAS-ASTIP-2021-LVRIScience and Technology Major-Project of Gansu Province 22ZD6NA001
6 · The paper itself

Abstract

Mycoplasma bovis causes serious diseases in cattle and is one of the most economically important pathogens threatening the global cattle industry. It is still a great challenge to prevent and control M. bovis infections owing to the increase in antibiotics resistance and unsatisfactorily effective commercial vaccines. FtsZ is commonly considered as a division protein in most bacteria. Owing to the limited genetic manipulation tools of M. bovis, the role of FtsZ in the pathogenicity of M. bovis remains unknown. In this study, FtsZ protein was found to be mainly distributed on the cell membrane, was highly conserved, and had good immunogenicity. FtsZ could bind to embryonic bovine lung cells (EBL) membrane extract, and this binding was inhibited by anti-FtsZ serum. In addition, FtsZ interacted with host extracellular matrix components fibronectin, laminin, vitronectin, and collagen IV in a dose-dependent manner, and promoted tissue diffusion by activating plasminogen through tissue plasminogen activator (tPA). Disruption of the ftsZ gene markedly reduced the adhesion of M. bovis to EBL cells while the complemented strain M. bovis ΔftsZ: ftsZ partly restored the adhesion ability. This is a first description that FtsZ acts as a novel adhesion protein in Mycoplasma, which interacts with host extracellular matrix components and plasminogen, and plays a vital role in adhesion and dissemination. This study expands our understanding of FtsZ significant role in the pathogenicity of M. bovis and provides a new potential vaccine and drug target against M. bovis infections.

Indexed as

Bacterial AdhesionBacterial ProteinsCattle DiseasesCytoskeletal ProteinsExtracellular MatrixMycoplasma bovisMycoplasma InfectionsPlasminogenAnimalsCattleBacterial ProteinsCytoskeletal ProteinsFtsZ protein, BacteriaPlasminogenextracellular matrixFtsZMycoplasmaMycoplasma bovisplasminogen

Identifiers

PMID41388316
PMCPMC12706882

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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.