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Infection and Immunity, August 1999, p. 4008-4013, Vol. 67, No. 8
Departamento de Microbiología,
Received 29 March 1999/Returned for modification 20 April
1999/Accepted 13 May 1999
Two different representative recombinant clones encoding
Aeromonas hydrophila lipases were found upon screening on
tributyrin (phospholipase A1) and egg yolk agar
(lecithinase-phospholipase C) plates of a cosmid-based genomic
library of Aeromonas hydrophila AH-3 (serogroup O34)
introduced into Escherichia coli DH5
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Cloning, Sequencing, and Role in Virulence of Two
Phospholipases (A1 and C) from Mesophilic Aeromonas sp.
Serogroup O:34
. Subcloning, nucleotide sequencing, and in vitro-coupled transcription-translation experiments showed that the phospholipase A1 (pla) and C
(plc) genes code for an 83-kDa putative lipoprotein and a
65-kDa protein, respectively. Defined insertion mutants of
A. hydrophila AH-3 defective in either pla or
plc genes were defective in phospholipase A1
and C activities, respectively. Lecithinase (phospholipase C) was shown
to be cytotoxic but nonhemolytic or poorly hemolytic. A. hydrophila AH-3 plc mutants showed a more than
10-fold increase in their 50% lethal dose on fish and mice, and
complementation of the plc single gene on these mutants
abolished this effect, suggesting that Plc protein is a virulence
factor in the mesophilic Aeromonas sp. serogroup O:34
infection process.
*
Corresponding author. Mailing address: Departamento de
Microbiología, Facultad de Biología, Universidad de
Barcelona, Diagonal 645, 08071 Barcelona, Spain. Phone:
34-93-4021486. Fax: 34-93-4110592. E-mail:
juant{at}bio.ub.es.
Infection and Immunity, August 1999, p. 4008-4013, Vol. 67, No. 8
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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