Bordetella species, including Bordetella pertussis and Bordetella bronchiseptica, are responsible for causing respiratory infections in humans and animals, respectively. These bacteria employ complex signaling systems to regulate their virulence and pathogenicity. Central to Bordetella signaling is the BvgAS two-component system, which controls the transition between virulent and avirulent phases through a process known as phase variation. In the virulent phase, the BvgAS system activates the expression of key virulence factors, such as pertussis toxin, adenylate cyclase toxin, and filamentous hemagglutinin, allowing the bacteria to establish infections in the host respiratory tract. Additionally, Bordetella species use quorum sensing to coordinate behaviors like biofilm formation, further enhancing their colonization and persistence within the host. The study of Bordetella signaling pathways has provided insights into the molecular mechanisms underlying bacterial pathogenesis and has paved the way for the development of novel inhibitors that target these pathways.
The significance of Bordetella inhibitors lies in their potential to disrupt critical virulence-related processes, offering promising avenues for combating Bordetella infections. Small molecule inhibitors, as well as natural compounds, have been investigated for their ability to interfere with key aspects of Bordetella signaling. These inhibitors hold the potential to attenuate the expression of virulence factors, impair quorum sensing-mediated behaviors, inhibit biofilm formation, and ultimately reduce the severity of infections caused by Bordetella species. By targeting the signaling pathways that contribute to bacterial pathogenicity, these inhibitors may offer alternative approaches to traditional antibiotics, which may help mitigate the emergence of antibiotic-resistant strains.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Erythromycin | 114-07-8 | sc-204742 sc-204742A sc-204742B sc-204742C | 5 g 25 g 100 g 1 kg | $57.00 $245.00 $831.00 $1331.00 | 4 | |
Erythromycin is an antibiotic that inhibits protein synthesis by binding to the 50S ribosomal subunit, thereby blocking peptide bond formation. It has been used to target Bordetella pertussis, the causative agent of whooping cough. | ||||||
Azithromycin | 83905-01-5 | sc-254949 sc-254949A sc-254949B sc-254949C sc-254949D | 25 mg 50 mg 500 mg 1 g 5 g | $52.00 $103.00 $260.00 $364.00 $728.00 | 17 | |
Azithromycin is another antibiotic that works by inhibiting protein synthesis. It has been used against various Bordetella species, including B. pertussis. | ||||||
Ceftriaxone, Disodium Salt, Hemiheptahydrate | 104376-79-6 | sc-211050 sc-211050A | 1 g 5 g | $179.00 $449.00 | 1 | |
Ceftriaxone is a cephalosporin antibiotic that targets the bacterial cell wall synthesis, interfering with peptidoglycan formation. It has been used for respiratory infections caused by Bordetella bronchiseptica. | ||||||
Bithionol | 97-18-7 | sc-239383 | 25 g | $79.00 | ||
Bithionol is a compound that was identified as an inhibitor of Bordetella pertussis biofilm formation. Biofilms are structured communities of bacteria that can enhance bacterial persistence and antibiotic resistance. | ||||||
Quercetin | 117-39-5 | sc-206089 sc-206089A sc-206089E sc-206089C sc-206089D sc-206089B | 100 mg 500 mg 100 g 250 g 1 kg 25 g | $11.00 $17.00 $110.00 $250.00 $936.00 $50.00 | 33 | |
Quercetin is a natural compound found in various plants and foods. It has been studied for its potential inhibitory effects on Bordetella pertussis by disrupting bacterial attachment and biofilm formation. | ||||||
Virstatin | 88909-96-0 | sc-358715 sc-358715A | 10 mg 50 mg | $45.00 $182.00 | 2 | |
Virstatin is a synthetic compound that was identified as an inhibitor of BvgAS, a two-component regulatory system that controls the expression of key virulence factors in Bordetella pertussis. It has been shown to attenuate the virulence of B. pertussis by inhibiting the BvgAS system. | ||||||