Role of the Helicobacter pylori Sensor Kinase ArsS in Protein Trafficking and Acid Acclimation

• Published in: Journal of Bacteriology 2012-10, Vol.194 (20), p.5545-5551
• Main Authors: Marcus, Elizabeth A, Sachs, George, Wen, Yi, Feng, Jing, Scott, David R
• Format: Article
• Language: English
• Subjects: acclimation; Acids - toxicity; Bacteria; Bacterial proteins; Bacterial Proteins - metabolism; Bacteriology; Biological and medical sciences; Blotting, Western; Cell Membrane - chemistry; Enzyme kinetics; Fundamental and applied biological sciences. Psychology; Gene Deletion; Gene Expression Regulation, Bacterial; genes; Helicobacter pylori; Helicobacter pylori - chemistry; Helicobacter pylori - genetics; Helicobacter pylori - metabolism; Helicobacter pylori - physiology; Homeostasis; Kinases; membrane proteins; Microbiology; Miscellaneous; Protein Kinases - genetics; Protein Kinases - metabolism; Protein Transport; Stress, Physiological; transcription (genetics); urea; urease; Urease - analysis; Western blotting
• ISSN: 0021-9193; 1098-5530; 1067-8832
• DOI: 10.1128/JB.01263-12

Helicobacter pylori survives and grows at low pHs via acid acclimation mechanisms that enable periplasmic pH homeostasis. Important components include a cytoplasmic urease; a pH-gated urea channel, UreI; and periplasmic α-carbonic anhydrase. To allow the rapid adjustment of periplasmic pH, acid acclimation components are recruited to the inner membrane in acid. The ArsRS two-component system, in an acid-responsive manner, controls the transcription of the urease gene cluster and α-carbonic anhydrase. The aim of this study is to determine the role of ArsS in protein trafficking as a component of acid acclimation. H. pylori wild-type and ΔarsS bacteria were incubated at acidic and neutral pHs. Intact bacteria, purified membranes, and total protein were analyzed by Western blotting and urease activity measurements. The total urease activity level was decreased in the ΔarsS strain, but the acid activation of UreI was unaffected. A 30-min acid exposure increased the level and activity of urease proteins at the membrane in the wild type but not in the ΔarsS strain. The urease levels and activity of the ΔarsS strain after a 90-min acid exposure were similar to those of the wild type. ArsS, in addition to its role in urease gene transcription, is also involved in the recruitment of urease proteins to the inner membrane to augment acid acclimation during acute acid exposure. Urease membrane recruitment following prolonged acid exposure in the absence of ArsS was similar to that of the wild type, suggesting a compensatory mechanism, possibly regulated by FlgS, underscoring the importance of urease membrane recruitment and activation in periplasmic pH homeostasis.