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PMID: 11889090 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Characterization of an ADP-ribosyltransferase toxin (AexT) from Aeromonas salmonicida subsp. salmonicida.

Journal of bacteriology ·Vol. 184 ·No. 7 ·2002-04-00 ·Pages 1851-8

Braun M, Stuber K, Schlatter Y, Wahli T, Kuhnert P, Frey J

Abstract

An ADP-ribosylating toxin named Aeromonas salmonicida exoenzyme T (AexT) in A. salmonicida subsp. salmonicida, the etiological agent of furunculosis in fish, was characterized. Gene aexT, encoding toxin AexT, was cloned and characterized by sequence analysis. AexT shows significant sequence similarity to the ExoS and ExoT exotoxins of Pseudomonas aeruginosa and to the YopE cytotoxin of different Yersinia species. The aexT gene was detected in all of the 12 A. salmonicida subsp. salmonicida strains tested but was absent from all other Aeromonas species. Recombinant AexT produced in Escherichia coli possesses enzymatic ADP-ribosyltransferase activity. Monospecific polyclonal antibodies directed against purified recombinant AexT detected the toxin produced by A. salmonicida subsp. salmonicida and cross-reacted with ExoS and ExoT of P. aeruginosa. AexT toxin could be detected in a wild type (wt) strain of A. salmonicida subsp. salmonicida freshly isolated from a fish with furunculosis; however, its expression required contact with RTG-2 rainbow trout gonad cells. Under these conditions, the AexT protein was found to be intracellular or tightly cell associated. No AexT was found when A. salmonicida subsp. salmonicida was incubated in cell culture medium in the absence of RTG-2 cells. Upon infection with wt A. salmonicida subsp. salmonicida, the fish gonad RTG-2 cells rapidly underwent significant morphological changes. These changes were demonstrated to constitute cell rounding, which accompanied induction of production of AexT and which led to cell lysis after extended incubation. An aexT mutant which was constructed from the wt strain with an insertionally inactivated aexT gene by allelic exchange had no toxic effect on RTG-2 cells and was devoid of AexT production. Hence AexT is directly involved in the toxicity of A. salmonicida subsp. salmonicida for RTG-2 fish cells.

MeSH Terms
ADP Ribose Transferases Aeromonas/enzymology Bacterial Toxins/genetics Cloning, Molecular Genes, Bacterial/physiology Poly(ADP-ribose) Polymerases/isolation & purification,metabolism Recombinant Proteins/isolation & purification,metabolism
Chemicals
Bacterial Toxins Recombinant Proteins ADP Ribose Transferases Poly(ADP-ribose) Polymerases exoenzyme S
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Braun Martin
Institute for Veterinary Bacteriology, Center for Fish and Wildlife Health, University of Bern, CH-3012 Bern, Switzerland.
Stuber Katja
Schlatter Yvonne
Wahli Thomas
Kuhnert Peter
Frey Joachim
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Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
2002-04-00
Pages
1851-8
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC134929
Subset
IM
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