{"title":"<i>MBOVJF4278_00820</i> encodes a novel cytoadhesin of <i>Mycoplasma bovis</i> binding to heparin.","authors":"Qi Wu, Zhixin Ma, Qiao Pan, Tong Liu, Jiuqing Xin, Qingyuan Xu","doi":"10.1128/iai.00606-24","DOIUrl":null,"url":null,"abstract":"<p><p><i>Mycoplasma bovis</i>, a minimal bacterium but a notorious cattle pathogen, leads to serious economic losses. This pathogen binding to host cells is emerging as a complex process involving a broad range of surface-exposed structures. For mycoplasma, adhering to host tissue is the first and crucial step of infection. It is well known that the molecules contributing to microbial cytoadhesion are important virulence factors. Here, we cloned, expressed, and purified the recombinant protein, which is encoded by <i>MBOVJF4278_00820</i>, and induced polyclonal antibodies for it in mice. The cytoadhesive properties of this surface-exposed protein were demonstrated on embryonic bovine lung (EBL) and Madin-Darby bovine kidney (MDBK) cells. Furthermore, heparin as the binding target was confirmed, and the characteristics of the interaction between this protein and heparin have also been analyzed. Our data indicate that the surface-associated <i>MBOVJF4278_00820</i>-encoded protein is a novel adhesion-related factor of <i>Mycoplasma bovis</i>.IMPORTANCEAdhesins are crucial in facilitating <i>Mycoplasma bovis</i> infection. In this study, we identified a specific <i>Mycoplasma bovis</i> adhesin that interacts with heparin on the surface of host cells. Given that heparin is ubiquitously distributed across a wide range of tissue cells, the identification of the heparin-binding adhesin is significant for elucidating how <i>Mycoplasma bovis</i> targets diverse host cells and triggers a spectrum of clinical manifestations.</p>","PeriodicalId":13541,"journal":{"name":"Infection and Immunity","volume":"93 5","pages":"e0060624"},"PeriodicalIF":2.9000,"publicationDate":"2025-05-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12070734/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Infection and Immunity","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1128/iai.00606-24","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/4/23 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Mycoplasma bovis, a minimal bacterium but a notorious cattle pathogen, leads to serious economic losses. This pathogen binding to host cells is emerging as a complex process involving a broad range of surface-exposed structures. For mycoplasma, adhering to host tissue is the first and crucial step of infection. It is well known that the molecules contributing to microbial cytoadhesion are important virulence factors. Here, we cloned, expressed, and purified the recombinant protein, which is encoded by MBOVJF4278_00820, and induced polyclonal antibodies for it in mice. The cytoadhesive properties of this surface-exposed protein were demonstrated on embryonic bovine lung (EBL) and Madin-Darby bovine kidney (MDBK) cells. Furthermore, heparin as the binding target was confirmed, and the characteristics of the interaction between this protein and heparin have also been analyzed. Our data indicate that the surface-associated MBOVJF4278_00820-encoded protein is a novel adhesion-related factor of Mycoplasma bovis.IMPORTANCEAdhesins are crucial in facilitating Mycoplasma bovis infection. In this study, we identified a specific Mycoplasma bovis adhesin that interacts with heparin on the surface of host cells. Given that heparin is ubiquitously distributed across a wide range of tissue cells, the identification of the heparin-binding adhesin is significant for elucidating how Mycoplasma bovis targets diverse host cells and triggers a spectrum of clinical manifestations.
期刊介绍:
Infection and Immunity (IAI) provides new insights into the interactions between bacterial, fungal and parasitic pathogens and their hosts. Specific areas of interest include mechanisms of molecular pathogenesis, virulence factors, cellular microbiology, experimental models of infection, host resistance or susceptibility, and the generation of innate and adaptive immune responses. IAI also welcomes studies of the microbiome relating to host-pathogen interactions.