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Omics Analysis of Blood-Responsive Regulon in Bordetella pertussis Identifies a Novel Essential T3SS Substrate
J. Drzmisek, D. Stipl, D. Petrackova, B. Vecerek, A. Dienstbier
Jazyk angličtina Země Švýcarsko
Typ dokumentu časopisecké články
Grantová podpora
19-12338S
Grantová Agentura České Republiky
CZ.02.2.69/0.0/0.0/17_050/0008376
Europeam Social Fund
NLK
Free Medical Journals
od 2000
Freely Accessible Science Journals
od 2000
PubMed Central
od 2007
Europe PubMed Central
od 2007
ProQuest Central
od 2000-03-01
Open Access Digital Library
od 2000-01-01
Open Access Digital Library
od 2007-01-01
Health & Medicine (ProQuest)
od 2000-03-01
ROAD: Directory of Open Access Scholarly Resources
od 2000
PubMed
33450976
DOI
10.3390/ijms22020736
Knihovny.cz E-zdroje
- MeSH
- anotace sekvence MeSH
- bakteriální proteiny metabolismus MeSH
- Bordetella pertussis fyziologie MeSH
- chromatografie kapalinová MeSH
- faktory virulence MeSH
- genomika * metody MeSH
- lidé MeSH
- proteomika * metody MeSH
- regulace genové exprese u bakterií MeSH
- sekreční systém typu III genetika metabolismus MeSH
- stanovení celkové genové exprese MeSH
- tandemová hmotnostní spektrometrie MeSH
- transkriptom MeSH
- virulence MeSH
- výpočetní biologie metody MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
Bacterial pathogens sense specific cues associated with different host niches and integrate these signals to appropriately adjust the global gene expression. Bordetella pertussis is a Gram-negative, strictly human pathogen of the respiratory tract and the etiological agent of whooping cough (pertussis). Though B. pertussis does not cause invasive infections, previous results indicated that this reemerging pathogen responds to blood exposure. Here, omics RNA-seq and LC-MS/MS techniques were applied to determine the blood-responsive regulon of B. pertussis. These analyses revealed that direct contact with blood rewired global gene expression profiles in B. pertussis as the expression of almost 20% of all genes was significantly modulated. However, upon loss of contact with blood, the majority of blood-specific effects vanished, with the exception of several genes encoding the T3SS-secreted substrates. For the first time, the T3SS regulator BtrA was identified in culture supernatants of B. pertussis. Furthermore, proteomic analysis identified BP2259 protein as a novel secreted T3SS substrate, which is required for T3SS functionality. Collectively, presented data indicate that contact with blood represents an important cue for B. pertussis cells.
Citace poskytuje Crossref.org
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