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Cited by 1,879

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Lysogenic Conversion by a Filamentous Phage Encoding Cholera Toxin

Waldor, Matthew K., Mekalanos, John J.·1996·Science

Abstract

Vibrio cholerae , the causative agent of cholera, requires two coordinately regulated factors for full virulence: cholera toxin (CT), a potent enterotoxin, and toxin-coregulated pili (TCP), surface organelles required for intestinal colonization. The structural genes for CT are shown here to be encoded by a filamentous bacteriophage (designated CTXφ), which is related to coliphage M13. The CTXφ genome chromosomally integrated or replicated as a plasmid. CTXφ used TCP as its receptor and infected V. cholerae cells within the gastrointestinal tracts of mice more efficiently than under laboratory conditions. Thus, the emergence of toxigenic V. cholerae involves horizontal gene transfer that may depend on in vivo gene expression.

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    Altschul, S. F., Gish, W., Miller, W., Myers, E. W., & Lipman, D. J. (1990) · Journal of Molecular Biology · doi:10.1006/jmbi.1990.9999 · Cited by 98,669

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Metadata

Authors
Waldor, M. K., & Mekalanos, J. J.
Venue
Science
Published
1996-06-28
Volume
272
Issue
5270
Pages
1910-1914
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W1977151336
Cited by
1,879
References
1
FWCI
38.96
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Lysogenic Conversion by a Filamentous Phage Encoding Cholera Toxin. https://app.cochat.ai/papers/10.1126/science.272.5270.1910
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Waldor, M. K., & Mekalanos, J. J. (1996). Lysogenic Conversion by a Filamentous Phage Encoding Cholera Toxin. Science. https://doi.org/10.1126/science.272.5270.1910

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.