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Infection and Immunity, October 2001, p. 6084-6090, Vol. 69, No. 10
Molecular Genetics Laboratory, International
Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka-1212,
Bangladesh,1 and Department of
Microbiology and Molecular Genetics, Harvard Medical School,
Boston, Massachusetts 021152
Received 7 March 2001/Returned for modification 1 June
2001/Accepted 25 June 2001
Toxigenic Vibrio cholerae strains are lysogens of
CTX
0019-9567/01/$04.00+0 DOI: 10.1128/IAI.69.10.6084-6090.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Diminished Diarrheal Response to Vibrio cholerae
Strains Carrying the Replicative Form of the CTX
Genome
instead of CTX
Lysogens in Adult Rabbits
, a filamentous bacteriophage which encodes cholera toxin (CT).
Following infection of recipient V. cholerae cells by
CTX
, the phage genome either integrates into the host chromosome at
a specific attachment site (attRS) or exists as a
replicative-form (RF) plasmid. We infected naturally occurring
attRS-negative nontoxigenic V. cholerae or attenuated (CTX
attRS negative)
derivatives of wild-type toxigenic strains with CTX
and examined the
diarrheagenic potential of the strains carrying the RF of the CTX
genome using the adult rabbit diarrhea model. Under laboratory
conditions, strains carrying the RF of CTX
produced more CT than
corresponding lysogens as assayed by a GM1-based enzyme-linked immunosorbent assay and by fluid accumulation in ligated
ileal loops of rabbits. However, when tested for diarrhea in rabbits,
the attRS-negative strains (which carried the CTX
genome as the RF) were either negative or produced mild diarrhea, whereas the attRS-positive strains with integrated
CTX
produced severe fatal diarrhea. Analysis of the strains after
intestinal passage showed that the attRS-negative
strains lost the phage genome at approximately a fivefold higher
frequency than under in vitro conditions, and 75 to 90% of cells
recovered from challenged rabbits after 24 h were CT negative.
These results suggested that strains carrying the RF of CTX
are
unable to cause severe disease due to rapid loss of the phage in vivo,
and the gastrointestinal environment thus provides selection of
toxigenic strains with an integrated CTX
genome. These results may
have implications for the development of live V.
cholerae vaccine candidates impaired in chromosomal integration
of CTX
. These findings may also contribute to understanding of the
etiology of diarrhea occasionally associated with nontoxigenic
V. cholerae strains.
*
Corresponding author. Mailing address: Molecular
Genetics Laboratory, Laboratory Sciences Division, ICDDR,B. GPO Box
128, Dhaka-1000, Bangladesh. Phone: 880 2 8811751 to 880 2 8811760. Fax: 880 2 8812529 and 880 2 8823116. E-mail:
faruque{at}icddrb.org.
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