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Expansion of nickel binding- and histidine-rich proteins during gastric adaptation of Helicobacter species

Fischer, F. (författare)
Vorontsov, Egor, 1988 (författare)
Gothenburg University,Göteborgs universitet,Core Facilities, Proteomics,Core Facilities, Proteomics
Turlin, E. (författare)
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Malosse, C. (författare)
Garcia, C. (författare)
Tabb, D. L. (författare)
Chamot-Rooke, J. (författare)
Percudani, R. (författare)
Vinella, D. (författare)
De Reuse, H. (författare)
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 (creator_code:org_t)
2022-08-24
2022
Engelska.
Ingår i: Metallomics. - : Oxford University Press (OUP). - 1756-5901 .- 1756-591X. ; 14:9
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Acquisition and homeostasis of essential metals during host colonization by bacterial pathogens rely on metal uptake, trafficking, and storage proteins. How these factors have evolved within bacterial pathogens is poorly defined. Urease, a nickel enzyme, is essential for Helicobacter pylori to colonize the acidic stomach. Our previous data suggest that acquisition of nickel transporters and a histidine-rich protein (HRP) involved in nickel storage in H. pylori and gastric Helicobacter spp. have been essential evolutionary events for gastric colonization. Using bioinformatics, proteomics, and phylogenetics, we extended this analysis to determine how evolution has framed the repertoire of HRPs among 39 Epsilonproteobacteria; 18 gastric and 11 non-gastric enterohepatic (EH) Helicobacter spp., as well as 10 other Epsilonproteobacteria. We identified a total of 213 HRPs distributed in 22 protein families named orthologous groups (OGs) with His-rich domains, including 15 newly described OGs. Gastric Helicobacter spp. are enriched in HRPs (7.7 +/- 1.9 HRPs/strain) as compared to EH Helicobacter spp. (1.9 +/- 1.0 HRPs/strain) with a particular prevalence of HRPs with C-terminal histidine-rich domains in gastric species. The expression and nickel-binding capacity of several HRPs was validated in five gastric Helicobacter spp. We established the evolutionary history of new HRP families, such as the periplasmic HP0721-like proteins and the HugZ-type heme oxygenases. The expansion of histidine-rich extensions in gastric Helicobacter spp. proteins is intriguing but can tentatively be associated with the presence of the urease nickel enzyme. We conclude that this HRP expansion is associated with unique properties of organisms that rely on large intracellular nickel amounts for their survival.

Ämnesord

NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)

Nyckelord

Histidine-rich proteins
metal binding proteins
phylogenetics
Helicobacter pylori
nickel
urease
crystal-structure
escherichia-coli
genome sequence
heme oxygenase
pylori
cloning
cobalt
family
gene
identification
Biochemistry & Molecular Biology

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