Article
Bordetella Bsp22 forms a filamentous type III secretion system tip complex and is immunoprotective in vitro and in vivo.
Department of Microbiology, Immunology and Molecular Genetics, David Geffen School of Medicine, University of California, Los Angeles, CA 90095, USA.
Molecular Microbiology (impact factor:
5.01).
12/2008;
71(2):492-504.
DOI:10.1111/j.1365-2958.2008.06543.x
pp.492-504
Source: PubMed
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Citations (0)
- Cited In (2)
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Article: Iron starvation regulates the type III secretion system in Bordetella bronchiseptica.
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ABSTRACT: The type III secretion system (T3SS) plays a key role in the exertion of full virulence by Bordetella bronchiseptica. However, little is known about the environmental stimuli that induce expression of T3SS genes. Here, it is reported that iron starvation is a signal for T3SS gene expression in B. bronchiseptica. It was found that, when B. bronchiseptica is cultured under iron-depleted conditions, secretion of type III secreted proteins is greater than that in bacteria grown under iron-replete conditions. Furthermore, it was confirmed that induction of T3SS-dependent host cell cytotoxicity and hemolytic activity is greatly enhanced by infection with iron-depleted Bordetella. In contrast, production of filamentous hemagglutinin is reduced in iron-depleted Bordetella. Thus, B. bronchiseptica controls the expression of virulence genes in response to iron starvation.Microbiology and Immunology 02/2012; 56(6):356-62. · 1.30 Impact Factor -
Article: Differential expression of type III effector BteA protein due to IS481 insertion in Bordetella pertussis.
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ABSTRACT: Bordetella pertussis is the primary etiologic agent of the disease pertussis. Universal immunization programs have contributed to a significant reduction in morbidity and mortality of pertussis; however, incidence of the disease, especially in adolescents and adults, has increased in several countries despite high vaccination coverage. During the last three decades, strains of Bordetella pertussis in circulation have shifted from the vaccine-type to the nonvaccine-type in many countries. A comparative proteomic analysis of the strains was performed to identify protein(s) involved in the type shift. Proteomic analysis identified one differentially expressed protein in the B. pertussis strains: the type III cytotoxic effector protein BteA, which is responsible for host cell death in Bordetella bronchiseptica infections. Immunoblot analysis confirmed the prominent expression of BteA protein in the nonvaccine-type strains but not in the vaccine-type strains. Sequence analysis of the vaccine-type strains revealed an IS481 insertion in the 5' untranslated region of bteA, -136 bp upstream of the bteA start codon. A high level of bteA transcripts from the IS481 promoter was detected in the vaccine-type strains, indicating that the transcript might be an untranslatable form. Furthermore, BteA mutant studies demonstrated that BteA expression in the vaccine-type strains is down-regulated by the IS481 insertion. The cytotoxic effector BteA protein is expressed at higher levels in B. pertussis nonvaccine-type strains than in vaccine-type strains. This type-dependent expression is due to an insertion of IS481 in B. pertussis clinical strains, suggesting that augmented expression of BteA protein might play a key role in the type shift of B. pertussis.PLoS ONE 01/2011; 6(3):e17797. · 4.09 Impact Factor
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Keywords
abundantly secreted substrate
Bacterial two-hybrid analysis
bind BopD
Bordetella bronchiseptica tip complex
Bordetella species
Bordetella T3SS
Bordetella T3SS apparatus
Bordetella translocation pore
cell-surface exposure
cross-linking analysis
eukaryotic cells
immunoprotective properties
maximum likelihood phylogenetic analysis
next-generation subunit vaccines
pore-forming translocation apparatus
protective effects
secreted proteins
T3SS tip complex proteins
transmission electron microscopy
variable length flexible filaments