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Journal of Clinical Microbiology, May 1998, p. 1232-1235, Vol. 36, No. 5
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.

Growth and Survival of Helicobacter pylori in Defined Medium and Susceptibility to Brij 78

N. Albertson, I. Wenngren, and J.-E. Sjöström*

Department of Cell Biology and Biochemistry, Preclinical Research and Development, Astra Hässle AB, Mölndal, Sweden

Received 30 September 1997/Returned for modification 19 December 1997/Accepted 11 February 1998

The gastrointestinal pathogen Helicobacter pylori requires supplementation with either fetal calf serum (FCS), bovine serum albumin (BSA), or (2,6-dimethyl)-beta -cyclodextrin (CD) for growth in a complex or defined medium. Because the availability of medium in which all components were chemically defined would facilitate metabolic studies of H. pylori, growth of the type strain, ATCC 43504, was compared in a defined medium with different growth additives. The dependency of H. pylori growth on FCS or BSA in a defined medium could partially be replaced by dependency on CD and cholesterol when the last two components were both added to the defined medium. Growth and cell yield were not affected by the addition of glucose, but the culture viability (numbers of CFU per milliliter was extended. Because therapeutic antifoams are used to relieve gastrointestinal symptoms we studied whether the unique susceptibility of H. pylori to the emulsifier polyoxyethylene-20-stearylether (Brij 78) was growth dependent or medium specific. The bactericidal activity exerted in buffer at pH 5 was independent of the preculture medium, and a 5-h exposure of the bacteria to 1.28 to 2.56 µg of Brij 78 per ml reduced the numbers of viable bacteria by >5 log10. The MICs (0.16 to 0.32 µg/ml) were lower than the corresponding minimal bactericidal concentrations in different growth media and were affected by FCS or BSA. In conclusion, CD plus cholesterol promotes the growth of H. pylori in a serum-free defined medium in which glucose enhances cell viability. The antibacterial activity exerted by Brij 78 is neither growth dependent nor medium specific.


* Corresponding author. Mailing address: Department of Cell Biology and Biochemistry, Astra Hässle AB, S 43183 Mölndal, Sweden. Phone: 46 31 776 1000. Fax: 46 31 776 3761. E-mail: jan-eric.sjostrom{at}hassle.se.astra.com.


Journal of Clinical Microbiology, May 1998, p. 1232-1235, Vol. 36, No. 5
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.



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