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The truncated major pilin subunit SBP2’ contributes to Streptococcus suis meningitis by interacting with host plasminogen
Journal article   Open access   Peer reviewed

The truncated major pilin subunit SBP2’ contributes to Streptococcus suis meningitis by interacting with host plasminogen

Genglin Guo, Pei Li, Yu Zhou, Quan Li, Yanfei Yu, Jiahui An and Wei Zhang
Applied and environmental microbiology, e0126726
10 Aug 2026
DOI: https://doi.org/10.1128/aem.01267-26
PMID: 42573261
Featured in Collection :   Drexel's Newest Publications
url
https://doi.org/10.1128/aem.01267-26View
Published, Version of Record (VoR) Open

Abstract

Bacterial Genetics Bacterial Meningitis Bacterial Pathogenesis Bacterial Taxonomy Central Nervous System Infections Clinical Microbiology and Infectious Diseases Host Cell Invasion Microbial Pathogenesis and Immunology Microbial Physiology and Genetics Model Organisms Pathogen-Specific Genetics (E.g., Staphylococcal, Rickettsial, Meningococcal) Pathogen-Specific Immunity Streptococcal Invasion Streptococcal Pathogenesis Streptococcus Streptococcus Species Bacteriology Environmental Microbiology
Meningitis is one of the most striking manifestations of Streptococcus suis infection. Although multiple virulence-associated factors have been identified, the mechanisms underlying meningitis development remain incompletely understood. In S. suis, a srtBCD pilus gene cluster has been identified; our previous study suggested its association with bacterial virulence. In this study, we investigated the role of the srtBCD cluster in S. suis pathogenesis and confirmed that SBP2’ was specifically localized on the bacterial surface and was found to be essential for full virulence in a murine infection model, whereas deletion of other minor subunits had minimal impact. Using brain microvascular endothelial cells (BMECs), microglia, and a BALB/c mouse model, we examined how SBP2’ promotes the development of S. suis meningitis. Our results show that SBP2’ enhances bacterial colonization of BMECs and recruits host plasminogen, facilitating extracellular matrix (ECM) degradation, and thereby promoting bacterial invasion. In addition, SBP2’ enables S. suis to evade microglial phagocytosis and improves its intracellular survival. Importantly, a monoclonal antibody targeting SBP2’ conferred significant immunoprotection in mice. Together, these findings identify SBP2’ as an important virulence factor and plasminogen-binding receptor that facilitates S. suis traversal of the blood-brain barrier.IMPORTANCEStreptococcus suis is an important zoonotic bacterial pathogen that could lead to severe damage in the central nervous system, but the mechanism underlying the breakthrough of the blood-brain barrier is still unclear. Pili are commonly considered virulence factors and subunit vaccine candidates, but no pilus structure could be observed on the surface of S. suis serotype 2. In this study, we found that the srtBCD pilus cluster, which was considered a pseudogene because of the truncation of the major pilus subunit, could be expressed, and the truncated major pilus subunit could be detected on the cell surface and be involved in the pathogenesis of S. suis serotype 2. Notably, monoclonal antibodies targeting SBP2’ provide immunoprotection in mice, reducing bacterial loads and brain damage. These findings identify SBP2’ as a key virulence factor and therapeutic target, offering insights into S. suis meningitis mechanisms.

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