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Molecular and Cellular Biology, May 2004, p. 3874-3884, Vol. 24, No. 9
0270-7306/04/$08.00+0     DOI: 10.1128/MCB.24.9.3874-3884.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Microbial Synergy via an Ethanol-Triggered Pathway

Michael G. Smith,{dagger} Shelley G. Des Etages,{dagger},{ddagger} and Michael Snyder*

Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, Connecticut 06520

Received 6 October 2003/ Returned for modification 14 January 2004/ Accepted 30 January 2004

We have discovered a microbial interaction between yeast, bacteria, and nematodes. Upon coculturing, Saccharomyces cerevisiae stimulated the growth of several species of Acinetobacter, including, A. baumannii, A. haemolyticus, A. johnsonii, and A. radioresistens, as well as several natural isolates of Acinetobacter. This enhanced growth was due to a diffusible factor that was shown to be ethanol by chemical assays and evaluation of strains lacking ADH1, ADH3, and ADH5, as all three genes are involved in ethanol production by yeast. This effect is specific to ethanol: methanol, butanol, and dimethyl sulfoxide were unable to stimulate growth to any appreciable level. Low doses of ethanol not only stimulated growth to a higher cell density but also served as a signaling molecule: in the presence of ethanol, Acinetobacter species were able to withstand the toxic effects of salt, indicating that ethanol alters cell physiology. Furthermore, ethanol-fed A. baumannii displayed increased pathogenicity when confronted with a predator, Caenorhabditis elegans. Our results are consistent with the concept that ethanol can serve as a signaling molecule which can affect bacterial physiology and survival.

* Corresponding author. Mailing address: Department of Molecular, Cellular and Developmental Biology, 266 Whitney Ave., New Haven, CT 06520. Phone and fax: (203) 432-6161. E-mail: michael.snyder{at}yale.edu.

{dagger} M.G.S. and S.G.D.E. contributed equally to this work.

{ddagger} Present address: Genomic and Proteomic Sciences, Pfizer Global Research and Development, Pfizer, Inc., Groton, Conn.

Molecular and Cellular Biology, May 2004, p. 3874-3884, Vol. 24, No. 9
0022-538X/04/$08.00+0     DOI: 10.1128/MCB.24.9.3874-3884.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.



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