Original Article
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World J Gastroenterol. Jul 28, 2011; 17(28): 3300-3309
Published online Jul 28, 2011. doi: 10.3748/wjg.v17.i28.3300
Helicobacter pylori arginase mutant colonizes arginase II knockout mice
Songhee H Kim, Melanie L Langford, Jean-Luc Boucher, Traci L Testerman, David J McGee
Songhee H Kim, Traci L Testerman, David J McGee, Department of Microbiology and Immunology, Louisiana State University Health Sciences Center-Shreveport, Shreveport, LA 71130, United States
Melanie L Langford, University of Nebraska-Lincoln, School of Biological Sciences, Lincoln, NE 68588, United States
Jean-Luc Boucher, Laboratoire de Chimie et Biochimie Pharmacologiques et Toxicologiques, Université Paris Descartes, Paris, France
Author contributions: Kim SH, Langford ML, Testerman TL, and McGee DJ conducted experiments; Kim SH, Langford ML and McGee DJ analyzed data; McGee DJ designed experiments and prepared figures; Boucher JL provided reagents and experimental design and scientific advice on the inhibitor; McGee DJ drafted the manuscript; all authors provided editorial comments on the manuscript.
Supported by Public Health Service grant R01-CA101931 (to DJM) from the National Institutes of Health
Correspondence to: Dr. David J McGee, Department of Microbiology and Immunology MSB 2-225, Louisiana State University Health Sciences Center-Shreveport, 1501 Kings Highway, Shreveport, LA 71130, United States. dmcgee@lsuhsc.edu
Telephone: +1-318-6758138 Fax: +1-318-6755764
Received: December 23, 2010
Revised: February 19, 2011
Accepted: February 26, 2011
Published online: July 28, 2011
Abstract

AIM: To investigate the role of host and bacterial arginases in the colonization of mice by Helicobacter pylori (H. pylori).

METHODS: H. pylori produces a very powerful urease that hydrolyzes urea to carbon dioxide and ammonium, which neutralizes acid. Urease is absolutely essential to H. pylori pathogenesis; therefore, the urea substrate must be in ample supply for urease to work efficiently. The urea substrate is most likely provided by arginase activity, which hydrolyzes L-arginine to L-ornithine and urea. Previous work has demonstrated that H. pylori arginase is surprisingly not required for colonization of wild-type mice. Hence, another in vivo source of the critical urea substrate must exist. We hypothesized that the urea source was provided by host arginase II, since this enzyme is expressed in the stomach, and H. pylori has previously been shown to induce the expression of murine gastric arginase II. To test this hypothesis, wild-type and arginase (rocF) mutant H. pylori strain SS1 were inoculated into arginase II knockout mice.

RESULTS: Surprisingly, both the wild-type and rocF mutant bacteria still colonized arginase II knockout mice. Moreover, feeding arginase II knockout mice the host arginase inhibitor S-(2-boronoethyl)-L-cysteine (BEC), while inhibiting > 50% of the host arginase I activity in several tissues, did not block the ability of the rocF mutant H. pylori to colonize. In contrast, BEC poorly inhibited H. pylori arginase activity.

CONCLUSION: The in vivo source for the essential urea utilized by H. pylori urease is neither bacterial arginase nor host arginase II; instead, either residual host arginase I or agmatinase is probably responsible.

Keywords: Arginase, Helicobacter pylori, S-(2-boronoethyl)-L-cysteine, Urease, Mice