YadA, a virulence factor predominantly expressed by pathogenic Yersinia species, serves as a pivotal determinant in the pathogenesis of yersiniosis. This outer membrane protein plays multifaceted roles in bacterial adhesion, invasion, and immune evasion within the host. Its primary function lies in mediating the attachment of Yersinia bacteria to host cells, facilitating initial colonization and subsequent establishment of infection. Additionally, YadA is implicated in modulating host immune responses through various mechanisms, including interference with phagocytosis and complement-mediated killing, thereby promoting bacterial survival and dissemination within the host organism. Furthermore, YadA has been shown to interact with extracellular matrix proteins, such as collagen and fibronectin, enhancing bacterial adherence to tissues and contributing to the formation of microcolonies during infection.
Activation of YadA is intricately regulated at the transcriptional and post-translational levels, predominantly influenced by environmental cues encountered during host colonization. Transcriptional activation of the yadA gene is orchestrated by complex regulatory networks, involving both positive and negative regulators responsive to environmental signals. Notably, temperature, pH, and host cell contact have been identified as key stimuli triggering YadA expression. Moreover, post-translational modifications, including glycosylation and proteolytic processing, further modulate YadA activity and stability on the bacterial surface. Importantly, YadA activation is tightly linked to the activity of various signaling pathways within the bacterial cell, particularly those involved in stress response and adaptation to host microenvironments. Collectively, the orchestrated interplay between transcriptional regulators, environmental signals, and post-translational modifications governs the dynamic activation of YadA, culminating in its pivotal role in Yersinia pathogenesis.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Deferoxamine | 70-51-9 | sc-507390 | 5 mg | $255.00 | ||
Iron chelators can influence bacterial virulence by limiting iron availability, a critical factor for bacterial growth and virulence factor expression, potentially affecting YadA. | ||||||
TPEN | 16858-02-9 | sc-200131 | 100 mg | $130.00 | 10 | |
Zinc chelators can disrupt bacterial metal homeostasis, potentially influencing YadA expression as a stress response. | ||||||
Acetyl-L-homoserine lactone | 51524-71-1 | sc-391455 sc-391455A | 5 mg 25 mg | $65.00 $219.00 | ||
Acetyl-L-homoserine lactone disrupts bacterial communication, potentially affecting virulence factor expression, including YadA. | ||||||
Paraquat chloride | 1910-42-5 | sc-257968 | 250 mg | $168.00 | 7 | |
Compounds that increase oxidative stress in bacteria might influence YadA expression as part of a bacterial stress response. | ||||||
Ciprofloxacin | 85721-33-1 | sc-217900 | 1 g | $43.00 | 8 | |
Antibiotics stress bacteria and could influence YadA expression indirectly by affecting bacterial growth and survival. | ||||||