Rita Haller, Yiyang Cai, Nicole de Buhr, Johanna C Rieder, Dirk Schlüter, Claas Baier, Holger Rohde, Maren von Köckritz-Blickwede, Marius Vital, Volker Winstel
{"title":"传染性假中间葡萄球菌阻碍中性粒细胞胞外陷阱驱动的遏制,促进侵袭性疾病。","authors":"Rita Haller, Yiyang Cai, Nicole de Buhr, Johanna C Rieder, Dirk Schlüter, Claas Baier, Holger Rohde, Maren von Köckritz-Blickwede, Marius Vital, Volker Winstel","doi":"10.1080/22221751.2025.2482709","DOIUrl":null,"url":null,"abstract":"<p><p>Methicillin-resistant <i>Staphylococcus pseudintermedius</i> (MRSP) is an emerging zoonotic pathogen that causes a variety of clinical diseases in mammalian hosts. While it frequently causes infections in dogs and other domestic animals, accumulating evidence indicates that zoonotic spillover and cross-species transmission events favour local and invasive <i>S. pseudintermedius</i> infections in humans. However, immuno-evasive maneuvers that shape <i>S. pseudintermedius</i> pathogenicity and survival in diseased hosts remain enigmatic. Powered by multi-tech imaging and a mouse model of bloodstream infection, we illustrate that <i>S. pseudintermedius</i> adopted a virulence mechanism from predominant bacterial pathogens to surmount neutrophilic responses and neutrophil extracellular trap (NET)-mediated killing. Specifically, release of NucB, a thermostable nuclease, helps MRSP coping with the antimicrobial and pathogen-immobilizing properties of NETs and even promotes intra-neutrophil survival upon phagocytosis, thereby contributing to <i>S. pseudintermedius</i> pathogenesis and persistence within hepatic abscesses. Combined with the analysis of genetically distinct human clinical isolates, all of which display nuclease activity and features of resistance to NETosis-induced killing, our data highlight how zoonotic staphylococci overcome innate immune responses and concurrently uncover a mechanism that may exacerbate animal-borne MRSP infections in humans.</p>","PeriodicalId":11602,"journal":{"name":"Emerging Microbes & Infections","volume":" ","pages":"2482709"},"PeriodicalIF":7.5000,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12001851/pdf/","citationCount":"0","resultStr":"{\"title\":\"Transmissible <i>Staphylococcus pseudintermedius</i> thwarts neutrophil extracellular trap-driven containment to promote invasive disease.\",\"authors\":\"Rita Haller, Yiyang Cai, Nicole de Buhr, Johanna C Rieder, Dirk Schlüter, Claas Baier, Holger Rohde, Maren von Köckritz-Blickwede, Marius Vital, Volker Winstel\",\"doi\":\"10.1080/22221751.2025.2482709\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Methicillin-resistant <i>Staphylococcus pseudintermedius</i> (MRSP) is an emerging zoonotic pathogen that causes a variety of clinical diseases in mammalian hosts. 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Methicillin-resistant Staphylococcus pseudintermedius (MRSP) is an emerging zoonotic pathogen that causes a variety of clinical diseases in mammalian hosts. While it frequently causes infections in dogs and other domestic animals, accumulating evidence indicates that zoonotic spillover and cross-species transmission events favour local and invasive S. pseudintermedius infections in humans. However, immuno-evasive maneuvers that shape S. pseudintermedius pathogenicity and survival in diseased hosts remain enigmatic. Powered by multi-tech imaging and a mouse model of bloodstream infection, we illustrate that S. pseudintermedius adopted a virulence mechanism from predominant bacterial pathogens to surmount neutrophilic responses and neutrophil extracellular trap (NET)-mediated killing. Specifically, release of NucB, a thermostable nuclease, helps MRSP coping with the antimicrobial and pathogen-immobilizing properties of NETs and even promotes intra-neutrophil survival upon phagocytosis, thereby contributing to S. pseudintermedius pathogenesis and persistence within hepatic abscesses. Combined with the analysis of genetically distinct human clinical isolates, all of which display nuclease activity and features of resistance to NETosis-induced killing, our data highlight how zoonotic staphylococci overcome innate immune responses and concurrently uncover a mechanism that may exacerbate animal-borne MRSP infections in humans.
期刊介绍:
Emerging Microbes & Infections is a peer-reviewed, open-access journal dedicated to publishing research at the intersection of emerging immunology and microbiology viruses.
The journal's mission is to share information on microbes and infections, particularly those gaining significance in both biological and clinical realms due to increased pathogenic frequency. Emerging Microbes & Infections is committed to bridging the scientific gap between developed and developing countries.
This journal addresses topics of critical biological and clinical importance, including but not limited to:
- Epidemic surveillance
- Clinical manifestations
- Diagnosis and management
- Cellular and molecular pathogenesis
- Innate and acquired immune responses between emerging microbes and their hosts
- Drug discovery
- Vaccine development research
Emerging Microbes & Infections invites submissions of original research articles, review articles, letters, and commentaries, fostering a platform for the dissemination of impactful research in the field.