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Infection and Immunity, October 2001, p. 6084-6090, Vol. 69, No. 10
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 CTXPhi Genome instead of CTXPhi Lysogens in Adult Rabbits

Shah M. Faruque,1,* M. Mostafizur Rahman,1 A. K. M. Mahbub Hasan,1 G. Balakrish Nair,1 John J. Mekalanos,2 and David A. Sack1

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 CTXPhi , a filamentous bacteriophage which encodes cholera toxin (CT). Following infection of recipient V. cholerae cells by CTXPhi , 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 CTXPhi and examined the diarrheagenic potential of the strains carrying the RF of the CTXPhi genome using the adult rabbit diarrhea model. Under laboratory conditions, strains carrying the RF of CTXPhi 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 CTXPhi genome as the RF) were either negative or produced mild diarrhea, whereas the attRS-positive strains with integrated CTXPhi 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 CTXPhi 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 CTXPhi genome. These results may have implications for the development of live V. cholerae vaccine candidates impaired in chromosomal integration of CTXPhi . 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.


Infection and Immunity, October 2001, p. 6084-6090, Vol. 69, No. 10
0019-9567/01/$04.00+0   DOI: 10.1128/IAI.69.10.6084-6090.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.



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Copyright © 2001 by the American Society for Microbiology. All rights reserved.