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1.
Microbiologyopen ; 9(1): e00947, 2020 01.
Article in English | MEDLINE | ID: mdl-31595707

ABSTRACT

In gram-negative bacteria, energy-dependent active transport of iron-bound substrates across the outer membrane is achieved through the TonB systems of proteins. Three TonB systems have been identified in the human pathogen Vibrio vulnificus. The TonB1 system contains three proteins: TonB1, ExbB1, and ExbD1. Both the TonB2 and TonB3 systems have been shown to also contain a fourth protein, TtpC2 and TtpC3, respectively. Here, we report and begin to characterize two additional proteins in the TonB2 and TonB3 systems: TtpB and TtpD. Both TtpB2 and TtpD2 are absolutely required for the function of the TonB2 system in V. vulnificus. However, although both TtpB3 and TtpD3 in the TonB3 system are related to the proteins in the TonB2 system, neither are active in iron transport. All six protein components of the TonB2 system-TonB2, ExbB2, ExbD2, TtpB2, TtpC2, and TtpD2-are essential for the uptake of both endogenously produced iron-bound siderophores and exogenous siderophores produced from other organisms. Through complementation, we have shown that V. vulnificus is capable of using different TtpD2 proteins from other Vibrio species to bring in multiple siderophores. In contrast, we also demonstrate that TtpB2 must come from V. vulnificus, and not other species within the genus, to complement mutations in the TonB2 system.


Subject(s)
Bacterial Proteins/genetics , Biological Transport/genetics , Iron/metabolism , Membrane Proteins/genetics , Siderophores/genetics , Vibrio vulnificus/genetics , Amino Acid Sequence , Bacterial Proteins/metabolism , Biological Transport/physiology , Membrane Proteins/metabolism , Sequence Alignment , Siderophores/metabolism , Vibrio vulnificus/metabolism , Virulence
2.
Microbiologyopen ; 8(10): e905, 2019 10.
Article in English | MEDLINE | ID: mdl-31290613

ABSTRACT

The Gram-negative pathogen Vibrio vulnificus produces several iron-sequestration systems including a hemin uptake system in response to iron limitation as a means to acquire this essential element. Strains of this organism are capable of causing serious septicemia in humans and eels, where hemin is abundant and an advantageous source of iron. Vibrio vulnificus hemin uptake systems consist of HupA, a well studied outer membrane protein, and a recently identified HvtA protein receptor. In this study, we confirmed that the expression of the hvtA gene is iron-regulated in a fur-dependent manner. When analyzed for virulence in a hemin-overloaded murine model system, the hupA gene was more important for establishing infection than the hvtA gene. Transcriptional profiling of these genes using strains of two different biotypes, biotype 1 (human pathogen) and biotype 2 (eel pathogen), showed that the expression of the two receptors was also regulated in response to temperature. The expression of hupA was highly induced in elevated temperatures in the human pathogenic strain when tested in iron-depleted conditions. Conversely, hvtA expression was induced significantly in the eel pathogenic strain at a lower temperature, a condition where the hupA locus was relatively repressed. Our results indicate that although both hupA and hvtA are involved for optimal hemin uptake in V. vulnificus, their expression is dually regulated by the environmental cues of iron concentration and temperature. Together, these data suggest that the virulence genes hupA and hvtA are tightly regulated and strictly induced during iron limitation combined with the physiological temperature of the host organism.


Subject(s)
Bacterial Outer Membrane Proteins/metabolism , Cold Temperature , Gene Expression Regulation, Bacterial/radiation effects , Hemin/metabolism , Membrane Transport Proteins/metabolism , Vibrio vulnificus/enzymology , Virulence Factors/metabolism , Animals , Bacterial Outer Membrane Proteins/genetics , Disease Models, Animal , Gene Expression Profiling , Gene Expression Regulation, Bacterial/drug effects , Iron/metabolism , Membrane Transport Proteins/genetics , Mice , Protein Transport/drug effects , Protein Transport/radiation effects , Vibrio Infections/microbiology , Vibrio vulnificus/genetics , Vibrio vulnificus/growth & development , Vibrio vulnificus/pathogenicity , Virulence Factors/genetics
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